Variant report

Variant	esv3390407
Chromosome Location	chr16:75701870-75751074
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	chr16:75712246-75712407	K562	blood:	n/a	n/a
2	ARID3A	chr16:75736196-75736523	K562	blood:	n/a	n/a
3	ARID3A	chr16:75729665-75729864	K562	blood:	n/a	n/a
4	ATF1	chr16:75712144-75712338	K562	blood:	n/a	n/a
5	ATF1	chr16:75736223-75736529	K562	blood:	n/a	n/a
6	ATF2	chr16:75721345-75721610	GM12878	blood:	n/a	n/a
7	ATF2	chr16:75721203-75721690	GM12878	blood:	n/a	n/a
8	ATF3	chr16:75736081-75736463	K562	blood:	n/a	n/a
9	ATF3	chr16:75736274-75736505	K562	blood:	n/a	n/a
10	BHLHE40	chr16:75736172-75736583	K562	blood:	n/a	n/a
11	BHLHE40	chr16:75706726-75707061	K562	blood:	n/a	n/a
12	CBX3	chr16:75729603-75729953	K562	blood:	n/a	n/a
13	CBX3	chr16:75744276-75744592	K562	blood:	n/a	n/a
14	CBX3	chr16:75744358-75744644	K562	blood:	n/a	n/a
15	CBX3	chr16:75736125-75736537	K562	blood:	n/a	n/a
16	CCNT2	chr16:75736019-75736466	K562	blood:	n/a	n/a
17	CEBPB	chr16:75716249-75716441	HepG2	liver:	n/a	chr16:75716369-75716380 chr16:75716271-75716284
18	CEBPB	chr16:75716191-75716550	HepG2	liver:	n/a	chr16:75716369-75716380 chr16:75716271-75716284
19	CEBPB	chr16:75716901-75717008	HepG2	liver:	n/a	n/a
20	CEBPB	chr16:75736103-75736430	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr16:75736051-75736568	K562	blood:	n/a	n/a
22	CEBPB	chr16:75716187-75716563	HepG2	liver:	n/a	chr16:75716369-75716380 chr16:75716271-75716284
23	CEBPB	chr16:75713381-75713627	HepG2	liver:	n/a	n/a
24	CEBPB	chr16:75736059-75736453	K562	blood:	n/a	n/a
25	CEBPB	chr16:75736206-75736323	HepG2	liver:	n/a	n/a
26	CEBPD	chr16:75712016-75712441	K562	blood:	n/a	n/a
27	CEBPD	chr16:75712165-75712496	K562	blood:	n/a	n/a
28	CEBPD	chr16:75736111-75736580	K562	blood:	n/a	n/a
29	CEBPD	chr16:75736102-75736520	K562	blood:	n/a	n/a
30	CTCF	chr16:75729740-75729890	HEK293	kidney:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
31	CTCF	chr16:75739220-75739370	HEK293	kidney:	n/a	n/a
32	CTCF	chr16:75729739-75729884	GM13977	blood:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
33	CTCF	chr16:75729740-75729890	HCT-116	colon:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
34	CTCF	chr16:75729600-75729750	HRE	kidney:	n/a	n/a
35	CTCF	chr16:75729660-75729810	HAc	cerebellar:	n/a	chr16:75729801-75729810
36	CTCF	chr16:75730000-75730150	GM12864	blood:	n/a	chr16:75730111-75730124
37	CTCF	chr16:75729780-75729930	AG09319	gingival:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
38	CTCF	chr16:75729720-75729870	HepG2	liver:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
39	CTCF	chr16:75729680-75729830	Caco-2	colon:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
40	CTCF	chr16:75729693-75729935	K562	blood:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
41	CTCF	chr16:75729680-75729830	GM12864	blood:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
42	CTCF	chr16:75729745-75729878	GM12878	blood:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
43	CTCF	chr16:75729700-75729850	GM06990	blood:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
44	CTCF	chr16:75729740-75729890	AG10803	skin:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
45	CTCF	chr16:75729760-75729910	MCF-7	breast:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
46	CTCF	chr16:75729680-75729830	K562	blood:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
47	CTCF	chr16:75729716-75729852	A549	lung:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
48	CTCF	chr16:75729740-75729890	BE2_C	brain:	n/a	chr16:75729798-75729816 chr16:75729800-75729821 chr16:75729801-75729810 chr16:75729801-75729814
49	CTCF	chr16:75729380-75729530	WI-38	lung:	n/a	n/a
50	CTCF	chr16:75709947-75710075	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75735341-75735391	MCF10A-Er-Src	breast:	n/a
2	chr16:75735341-75735391	HIPEpiC	eye:	n/a
3	chr16:75735341-75735391	AG04449	skin:	fetal
4	chr16:75735341-75735391	HCT-116	colon:	n/a
5	chr16:75735341-75735391	HRPEpiC	eye:	n/a
6	chr16:75735341-75735391	A549	lung:	n/a
7	chr16:75735341-75735391	IMR90	lung:	fetal
8	chr16:75735341-75735391	Caco-2	colon:	n/a
9	chr16:75735341-75735391	U87	brain:	n/a
10	chr16:75735341-75735391	NT2-D1	testis:	n/a
11	chr16:75735341-75735391	HCM	heart:	n/a
12	chr16:75735341-75735391	CMK	blood:	n/a
13	chr16:75735341-75735391	AG09319	gingival:	n/a
14	chr16:75735341-75735391	HEK293	kidney:	embryo
15	chr16:75735341-75735391	PFSK-1	brain:	n/a
16	chr16:75735341-75735391	RPTEC	kidney:	n/a
17	chr16:75735341-75735391	NH-A	brain:	n/a
18	chr16:75735341-75735391	T-47D	breast:	n/a
19	chr16:75735341-75735391	HL-60	blood:	n/a
20	chr16:75735341-75735391	AoSMC	blood vessel:	n/a
21	chr16:75735341-75735391	NB4	blood:	n/a
22	chr16:75735341-75735391	GM12891	blood:	n/a
23	chr16:75735341-75735391	BJ	skin:	n/a
24	chr16:75735341-75735391	PANC-1	pancreas:	n/a
25	chr16:75735341-75735391	SKMC	muscle:	n/a
26	chr16:75735341-75735391	AG10803	skin:	n/a
27	chr16:75735341-75735391	GM06990	blood:	n/a
28	chr16:75735341-75735391	BE2_C	brain:	n/a
29	chr16:75735341-75735391	NHBE	bronchial:	n/a
30	chr16:75735341-75735391	AG09309	skin:	n/a
31	chr16:75735341-75735391	HEEpiC	esophagus:	n/a
32	chr16:75735341-75735391	K562	blood:	n/a
33	chr16:75735341-75735391	ovcar-3	ovarian:	n/a
34	chr16:75735341-75735391	LNCaP	prostate:	n/a
35	chr16:75735341-75735391	HNPCEpiC	eye:	n/a
36	chr16:75735341-75735391	HPAEpiC	pulmonary alveolar:	n/a
37	chr16:75735341-75735391	SAEC	small airway:	n/a
38	chr16:75735341-75735391	AG04450	lung:	fetal
39	chr16:75735341-75735391	HCPEpiC	choroid plexus:	n/a
40	chr16:75735341-75735391	NHDF-neo	bronchial:	n/a
41	chr16:75735341-75735391	GM12878	blood:	n/a
42	chr16:75735341-75735391	HepG2	liver:	n/a
43	chr16:75735341-75735391	Hepatocyte	liver:	n/a
44	chr16:75735341-75735391	HUVEC	blood vessel:	n/a
45	chr16:75735341-75735391	HAEpiC	amniotic membrane:	n/a
46	chr16:75735341-75735391	PrEC	prostate:	n/a
47	chr16:75735341-75735391	SK-N-SH	brain:	n/a
48	chr16:75735341-75735391	HRCEpiC	kidney:	n/a
49	chr16:75735341-75735391	Jurkat	blood:	n/a
50	chr16:75735341-75735391	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:75681022..75683493-chr16:75704929..75707383,3	MCF-7	breast:
2	chr16:75738452..75740473-chr16:75740490..75742244,2	MCF-7	breast:
3	chr16:75696333..75698717-chr16:75701380..75703728,2	K562	blood:
4	chr16:75720417..75720999-chr16:75797794..75798298,2	MCF-7	breast:
5	chr16:75680353..75682515-chr16:75712211..75714863,2	K562	blood:
6	chr16:75688504..75690013-chr16:75704731..75707189,2	K562	blood:
7	chr16:75682678..75684338-chr16:75706932..75709259,2	MCF-7	breast:
8	chr16:75736237..75738500-chr16:75741844..75744257,2	K562	blood:
9	chr16:75729730..75730247-chr16:75797702..75798331,2	MCF-7	breast:
10	chr16:75747750..75749880-chr16:75752084..75754247,2	K562	blood:
11	chr16:75680353..75682568-chr16:75712211..75713793,2	K562	blood:
12	chr16:75728474..75730726-chr16:75731491..75733375,2	K562	blood:
13	chr16:75739275..75740832-chr16:75744437..75746332,2	K562	blood:
14	chr16:75681120..75683833-chr16:75746001..75749575,3	MCF-7	breast:
15	chr16:75723045..75725785-chr16:75728359..75730585,2	K562	blood:
16	chr16:75729621..75730494-chr16:75797798..75798445,2	MCF-7	breast:
17	chr16:75681726..75683717-chr16:75721135..75723322,2	K562	blood:
18	chr16:75730757..75732886-chr16:75734189..75736396,2	K562	blood:
19	chr16:75723045..75725785-chr16:75728359..75730585,2	K562	blood:
20	chr16:75741611..75743630-chr16:75751631..75753594,2	K562	blood:
21	chr16:75739275..75740832-chr16:75744437..75746332,2	K562	blood:
22	chr16:75738452..75740473-chr16:75740490..75742244,2	MCF-7	breast:
23	chr16:75675467..75677135-chr16:75707523..75710179,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GABARAPL2-4	chr16:75708250-75712036	NONHSAT143757
2	lnc-GABARAPL2-6	chr16:75724213-75724972	NONHSAT143760
3	lnc-GABARAPL2-5	chr16:75723031-75723233	NONHSAT143759
4	lnc-KARS-1	chr16:75732431-75732728	NONHSAT143761
5	lnc-GABARAPL2-7	chr16:75720338-75721987	NONHSAT143758
6	lnc-GABARAPL2-7	chr16:75725151-75725424	NONHSAT143758

Variant related genes	Relation type
ENSG00000214325	TF binding region
ATP5F1P7	TF binding region
RN7SL520P	TF binding region
ENSG00000214325	CpG island
ATP5F1P7	CpG island
RN7SL520P	CpG island
ENSG00000166848	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000240199	chromatin interactions
ENSG00000261424	chromatin interactions

Extended variants
information (count: 1988 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1988 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554048389	chr16:75701906-75701907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576971711	chr16:75701918-75701919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184065465	chr16:75701934-75701935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556208949	chr16:75701945-75701946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367555276	chr16:75702004-75702005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575960747	chr16:75702026-75702027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541461625	chr16:75702046-75702047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs16942274	chr16:75702047-75702048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185071550	chr16:75702048-75702049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114240518	chr16:75702058-75702059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149520848	chr16:75702096-75702097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552987846	chr16:75702099-75702100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572851669	chr16:75702107-75702108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35775620	chr16:75702109-75702110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12447600	chr16:75702111-75702112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189875829	chr16:75702113-75702114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9783794	chr16:75702122-75702123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9783763	chr16:75702124-75702125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201839745	chr16:75702127-75702128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs60465691	chr16:75702129-75702130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34756627	chr16:75702130-75702131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28538249	chr16:75702131-75702132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397856087	chr16:75702144-75702145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187137305	chr16:75702157-75702158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368396651	chr16:75702158-75702159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535077058	chr16:75702176-75702177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191784960	chr16:75702187-75702188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9285360	chr16:75702240-75702241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183305620	chr16:75702265-75702266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188705341	chr16:75702273-75702274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576289363	chr16:75702284-75702285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147546524	chr16:75702360-75702361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs193003665	chr16:75702366-75702367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571718968	chr16:75702374-75702375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540680314	chr16:75702375-75702376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564040363	chr16:75702393-75702394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533553189	chr16:75702405-75702406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543682175	chr16:75702407-75702408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185865354	chr16:75702410-75702411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529651966	chr16:75702412-75702413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148138782	chr16:75702414-75702415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528560064	chr16:75702415-75702416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539006725	chr16:75702438-75702439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542043257	chr16:75702439-75702440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528515236	chr16:75702450-75702451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551819713	chr16:75702455-75702456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559006779	chr16:75702506-75702507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188238129	chr16:75702588-75702589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561915959	chr16:75702589-75702590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538362895	chr16:75702591-75702592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75692400-75704000	Weak transcription	Psoas Muscle	Psoas
2	chr16:75693800-75723200	Weak transcription	Ovary	ovary
3	chr16:75694400-75705800	Weak transcription	Pancreas	Pancrea
4	chr16:75695000-75702200	Weak transcription	Spleen	Spleen
5	chr16:75695600-75704600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr16:75695600-75713200	Weak transcription	Right Atrium	heart
7	chr16:75696000-75706400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr16:75696000-75713200	Weak transcription	Left Ventricle	heart
9	chr16:75696000-75716200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr16:75696200-75712400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr16:75696400-75706000	Weak transcription	Aorta	Aorta
12	chr16:75702200-75702400	Enhancers	Spleen	Spleen
13	chr16:75704200-75704400	Enhancers	HepG2	liver
14	chr16:75709000-75712600	Weak transcription	Placenta	Placenta
15	chr16:75710800-75712600	Enhancers	Fetal Heart	heart
16	chr16:75711200-75713600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr16:75712400-75712800	Enhancers	Brain Substantia Nigra	brain
18	chr16:75712400-75713400	Enhancers	Brain Cingulate Gyrus	brain
19	chr16:75712400-75713400	Enhancers	Brain Hippocampus Middle	brain
20	chr16:75712400-75713400	Bivalent Enhancer	Stomach Mucosa	stomach
21	chr16:75712400-75713600	Enhancers	Brain Anterior Caudate	brain
22	chr16:75712600-75712800	Enhancers	Placenta	Placenta
23	chr16:75712600-75713200	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr16:75712600-75713400	Enhancers	Gastric	stomach
25	chr16:75712600-75713600	Enhancers	Lung	lung
26	chr16:75712600-75714000	Weak transcription	Fetal Heart	heart
27	chr16:75713200-75713400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr16:75713200-75713400	Weak transcription	Spleen	Spleen
29	chr16:75713200-75713600	Enhancers	Left Ventricle	heart
30	chr16:75713200-75713600	Enhancers	Right Atrium	heart
31	chr16:75713400-75713600	Enhancers	Spleen	Spleen
32	chr16:75713400-75715400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr16:75713600-75718800	Weak transcription	Spleen	Spleen
34	chr16:75714000-75714600	Enhancers	Fetal Heart	heart
35	chr16:75714600-75720000	Weak transcription	Fetal Heart	heart
36	chr16:75716200-75716400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr16:75716200-75716400	Bivalent/Poised TSS	HepG2	liver
38	chr16:75716400-75716600	Flanking Bivalent TSS/Enh	HepG2	liver
39	chr16:75716600-75716800	Bivalent Enhancer	HepG2	liver
40	chr16:75720000-75722000	Enhancers	Fetal Heart	heart
41	chr16:75721200-75721600	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr16:75725200-75725400	Enhancers	Pancreas	Pancrea
43	chr16:75725600-75725800	Bivalent Enhancer	Stomach Mucosa	stomach
44	chr16:75726000-75726200	Enhancers	Pancreas	Pancrea
45	chr16:75730600-75731200	Enhancers	Brain Cingulate Gyrus	brain
46	chr16:75730800-75731200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr16:75730800-75731200	Enhancers	Brain Anterior Caudate	brain
48	chr16:75730800-75731200	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr16:75730800-75731800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr16:75731200-75733600	Weak transcription	Brain Inferior Temporal Lobe	brain

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