Variant report

Variant	nsv912584
Chromosome Location	chr20:896012-926397
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	BRCA1	chr20:921731-921791	HepG2	liver:	n/a	n/a
2	CBX3	chr20:912147-912383	HCT-116	colon:	n/a	n/a
3	CEBPB	chr20:905306-905575	K562	blood:	n/a	chr20:905412-905423
4	CEBPB	chr20:896245-896512	HepG2	liver:	n/a	chr20:896378-896389 chr20:896380-896391 chr20:896378-896391
5	CEBPB	chr20:905276-905535	HepG2	liver:	n/a	chr20:905412-905423
6	CEBPZ	chr20:912151-912386	HepG2	liver:	n/a	n/a
7	CHD2	chr20:925496-925746	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr20:915056-915452	H1-hESC	embryonic stem cell:	n/a	chr20:915287-915305
9	CTCF	chr20:896822-896914	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr20:920640-920790	GM12871	blood:	n/a	n/a
11	CTCF	chr20:900580-900730	HPAF	blood vessel:	n/a	chr20:900711-900720
12	CTCF	chr20:915248-915324	K562	blood:	n/a	chr20:915287-915305
13	CTCF	chr20:896460-896610	HEK293	kidney:	n/a	n/a
14	CTCF	chr20:915223-915307	K562	blood:	n/a	chr20:915287-915305
15	CTCF	chr20:915178-915401	H1-hESC	embryonic stem cell:	n/a	chr20:915287-915305
16	CTCF	chr20:915240-915390	WERI-Rb-1	eye:	n/a	chr20:915287-915305
17	CTCF	chr20:900695-900722	H1-hESC	embryonic stem cell:	n/a	chr20:900711-900720
18	CTCF	chr20:915063-915450	H1-hESC	embryonic stem cell:	n/a	chr20:915287-915305
19	CTCF	chr20:915160-915310	HEK293	kidney:	n/a	chr20:915287-915305
20	CTCF	chr20:920740-920890	HepG2	liver:	n/a	n/a
21	EBF1	chr20:907499-907707	GM12878	blood:	n/a	n/a
22	EGR1	chr20:900165-900333	K562	blood:	n/a	n/a
23	EGR1	chr20:900164-900373	K562	blood:	n/a	n/a
24	FOS	chr20:900993-901322	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr20:901067-901267	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr20:900993-901267	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr20:900993-901300	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr20:899938-900135	MCF10A-Er-Src	breast:	n/a	n/a
29	GATA1	chr20:913654-914090	K562	blood:	n/a	n/a
30	GATA1	chr20:913628-913961	PBDE	blood:	n/a	n/a
31	GATA3	chr20:900321-900511	MCF-7	breast:	n/a	n/a
32	GTF2F1	chr20:915170-915322	H1-hESC	embryonic stem cell:	n/a	n/a
33	IRF1	chr20:913718-914084	K562	blood:	n/a	chr20:913901-913915 chr20:913901-913911 chr20:913893-913913 chr20:913899-913912 chr20:913901-913912 chr20:913897-913911 chr20:913899-913912 chr20:913895-913916 chr20:913900-913917 chr20:913898-913915 chr20:913902-913913 chr20:913898-913912 chr20:913900-913912 chr20:913899-913912
34	IRF1	chr20:913725-913992	K562	blood:	n/a	chr20:913901-913915 chr20:913901-913911 chr20:913893-913913 chr20:913899-913912 chr20:913901-913912 chr20:913897-913911 chr20:913899-913912 chr20:913895-913916 chr20:913900-913917 chr20:913898-913915 chr20:913902-913913 chr20:913898-913912 chr20:913900-913912 chr20:913899-913912
35	IRF1	chr20:913716-914094	K562	blood:	n/a	chr20:913901-913915 chr20:913901-913911 chr20:913893-913913 chr20:913899-913912 chr20:913901-913912 chr20:913897-913911 chr20:913899-913912 chr20:913895-913916 chr20:913900-913917 chr20:913898-913915 chr20:913902-913913 chr20:913898-913912 chr20:913900-913912 chr20:913899-913912
36	JUND	chr20:897511-897796	H1-hESC	embryonic stem cell:	n/a	n/a
37	KAP1	chr20:911996-912398	K562	blood:	n/a	n/a
38	MAFF	chr20:905409-905579	HepG2	liver:	n/a	chr20:905517-905535
39	MAFK	chr20:905424-905595	HepG2	liver:	n/a	chr20:905519-905534
40	MAFK	chr20:905387-905573	HepG2	liver:	n/a	chr20:905519-905534
41	MAX	chr20:905338-905717	NB4	blood:	n/a	chr20:905535-905545
42	MAX	chr20:905449-905624	H1-hESC	embryonic stem cell:	n/a	chr20:905535-905545
43	MAX	chr20:905530-905595	K562	blood:	n/a	chr20:905535-905545
44	MAZ	chr20:912222-912239	HepG2	liver:	n/a	n/a
45	MYC	chr20:901323-901437	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr20:899025-899401	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr20:899025-899450	H1-neurons	neurons:	n/a	n/a
48	RAD21	chr20:915129-915503	H1-hESC	embryonic stem cell:	n/a	n/a
49	RAD21	chr20:915124-915496	H1-hESC	embryonic stem cell:	n/a	n/a
50	RAD21	chr20:915024-915515	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:897600-897650	Hela-S3	cervix:	n/a
2	chr20:897600-897650	Hela-S3	cervix:	n/a
3	chr20:897024-897074	HCT-116	colon:	n/a
4	chr20:896981-897031	HepG2	liver:	n/a
5	chr20:897600-897650	HEEpiC	esophagus:	n/a
6	chr20:896981-897031	Hela-S3	cervix:	n/a
7	chr20:897545-897595	ProgFib	skin:	n/a
8	chr20:897024-897074	HEEpiC	esophagus:	n/a
9	chr20:896876-896926	NB4	blood:	n/a
10	chr20:896564-896614	HNPCEpiC	eye:	n/a
11	chr20:897024-897074	HNPCEpiC	eye:	n/a
12	chr20:897050-897100	BJ	skin:	n/a
13	chr20:897050-897100	PANC-1	pancreas:	n/a
14	chr20:897024-897074	AG04449	skin:	fetal
15	chr20:896876-896926	H1-hESC	embryonic stem cell:	embryo
16	chr20:897050-897100	SAEC	small airway:	n/a
17	chr20:897545-897595	H1-hESC	embryonic stem cell:	embryo
18	chr20:897545-897595	HRCEpiC	kidney:	n/a
19	chr20:896564-896614	HRPEpiC	eye:	n/a
20	chr20:897024-897074	AoSMC	blood vessel:	n/a
21	chr20:896349-896399	HepG2	liver:	n/a
22	chr20:896876-896926	BJ	skin:	n/a
23	chr20:897545-897595	GM12891	blood:	n/a
24	chr20:896349-896399	Hela-S3	cervix:	n/a
25	chr20:897545-897595	SK-N-SH	brain:	n/a
26	chr20:896349-896399	BE2_C	brain:	n/a
27	chr20:896981-897031	NHBE	bronchial:	n/a
28	chr20:897050-897100	AG09319	gingival:	n/a
29	chr20:896564-896614	NHDF-neo	bronchial:	n/a
30	chr20:896876-896926	MCF10A-Er-Src	breast:	n/a
31	chr20:897024-897074	HRCEpiC	kidney:	n/a
32	chr20:896876-896926	ovcar-3	ovarian:	n/a
33	chr20:897024-897074	HAEpiC	amniotic membrane:	n/a
34	chr20:897050-897100	LNCaP	prostate:	n/a
35	chr20:897545-897595	AG10803	skin:	n/a
36	chr20:897024-897074	NH-A	brain:	n/a
37	chr20:896981-897031	AG10803	skin:	n/a
38	chr20:897600-897650	ovcar-3	ovarian:	n/a
39	chr20:896981-897031	K562	blood:	n/a
40	chr20:897050-897100	GM06990	blood:	n/a
41	chr20:897545-897595	SK-N-SH_RA	brain:	n/a
42	chr20:896981-897031	U87	brain:	n/a
43	chr20:896981-897031	HCT-116	colon:	n/a
44	chr20:896564-896614	GM12891	blood:	n/a
45	chr20:897050-897100	BE2_C	brain:	n/a
46	chr20:897600-897650	BE2_C	brain:	n/a
47	chr20:897545-897595	AG09319	gingival:	n/a
48	chr20:896981-897031	AG09309	skin:	n/a
49	chr20:897050-897100	H1-hESC	embryonic stem cell:	embryo
50	chr20:897024-897074	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:897191..899627-chr20:903602..905719,2	MCF-7	breast:
2	chr20:836809..839072-chr20:903298..905274,2	K562	blood:
3	chr20:899077..901728-chr20:908752..911161,2	K562	blood:
4	chr20:925330..928261-chr20:941058..943608,3	K562	blood:
5	chr20:914281..915061-chr3:49059512..49060483,2	NB4	blood:
6	chr20:921972..923694-chr20:931266..933420,2	K562	blood:
7	chr20:825224..827249-chr20:896016..898725,2	MCF-7	breast:
8	chr20:847957..850389-chr20:899044..901532,2	K562	blood:
9	chr20:899077..901728-chr20:908752..911161,2	K562	blood:
10	chr20:897191..899627-chr20:903602..905719,2	MCF-7	breast:

Variant related genes	Relation type
ANGPT4	TF binding region
ANGPT4	CpG island
ENSG00000178149	chromatin interactions
ENSG00000125898	chromatin interactions
ENSG00000178057	chromatin interactions

Extended variants
information (count: 1414 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1414 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs478451	chr20:896012-896013	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558437209	chr20:896025-896026	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181620885	chr20:896052-896053	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185958904	chr20:896061-896062	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs117794389	chr20:896070-896071	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189979417	chr20:896074-896075	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs73565264	chr20:896155-896156	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543026141	chr20:896208-896209	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559207833	chr20:896221-896222	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181135420	chr20:896245-896246	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116496474	chr20:896254-896255	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs386811561	chr20:896267-896268	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73892544	chr20:896268-896269	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs502522	chr20:896299-896300	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs6086450	chr20:896303-896304	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs567376848	chr20:896313-896314	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535836791	chr20:896315-896316	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185575962	chr20:896331-896332	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528615515	chr20:896344-896345	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566374948	chr20:896350-896351	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535381473	chr20:896388-896389	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558498313	chr20:896412-896413	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375134979	chr20:896413-896414	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377130281	chr20:896435-896436	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562175835	chr20:896496-896497	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370336882	chr20:896504-896505	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369518796	chr20:896513-896514	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369649721	chr20:896539-896540	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73565266	chr20:896545-896546	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs377149306	chr20:896565-896566	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116327782	chr20:896574-896575	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs199745156	chr20:896579-896580	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139001653	chr20:896590-896591	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149874461	chr20:896605-896606	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574115140	chr20:896633-896634	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs146463028	chr20:896641-896642	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140900541	chr20:896658-896659	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201720367	chr20:896672-896673	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200815484	chr20:896686-896687	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144442482	chr20:896688-896689	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146594844	chr20:896715-896716	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs199886060	chr20:896742-896743	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs17702306	chr20:896753-896754	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369053720	chr20:896772-896773	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200170732	chr20:896790-896791	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs372508631	chr20:896821-896822	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201487067	chr20:896866-896867	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs376436931	chr20:896872-896873	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs370905563	chr20:896876-896877	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs373183124	chr20:896877-896878	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	17426248	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:888000-896400	Weak transcription	Right Atrium	heart
2	chr20:893200-896200	Weak transcription	Adipose Nuclei	Adipose
3	chr20:893600-896600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr20:894600-896200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr20:894600-897400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr20:894600-897400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr20:894800-897000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr20:894800-897600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr20:895200-896200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr20:895200-896200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr20:895200-898000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr20:895200-898200	Enhancers	Ovary	ovary
13	chr20:895600-896400	Weak transcription	Osteobl	bone
14	chr20:895600-897400	Enhancers	Brain Substantia Nigra	brain
15	chr20:895800-897800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr20:895800-897800	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr20:895800-900200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr20:896000-896600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr20:896000-897000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
20	chr20:896000-897800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr20:896200-896800	Enhancers	Brain Hippocampus Middle	brain
22	chr20:896200-897000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr20:896200-897400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr20:896200-897400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr20:896200-897400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr20:896200-897400	Enhancers	Right Ventricle	heart
27	chr20:896200-897600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr20:896200-897800	Enhancers	Adipose Nuclei	Adipose
29	chr20:896400-897000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
30	chr20:896400-897000	Enhancers	Osteobl	bone
31	chr20:896400-897400	Enhancers	Right Atrium	heart
32	chr20:896400-897600	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr20:896400-898000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr20:896600-896800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
35	chr20:896600-897000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr20:896600-897000	Enhancers	Brain Cingulate Gyrus	brain
37	chr20:896600-897000	Bivalent Enhancer	Fetal Stomach	stomach
38	chr20:896600-897600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr20:896600-897800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr20:896600-898000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr20:896600-898000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr20:896600-898000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:896600-898400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr20:896600-898800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr20:896800-897000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr20:896800-897000	Bivalent Enhancer	Placenta	Placenta
47	chr20:896800-897400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr20:896800-897800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
49	chr20:897000-897200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr20:897000-897200	Bivalent Enhancer	HSMMtube	muscle

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