Variant report

Variant	nsv964369
Chromosome Location	chr20:1615768-1617546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:93)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:93 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:1617304-1617678	HepG2	liver:	n/a	n/a
2	CEBPB	chr20:1617435-1617633	HepG2	liver:	n/a	n/a
3	CHD2	chr20:1617533-1617678	HepG2	liver:	n/a	n/a
4	CTCF	chr20:1617460-1617610	RPTEC	kidney:	n/a	n/a
5	CTCF	chr20:1617492-1617657	GM12891	blood:	n/a	n/a
6	CTCF	chr20:1617480-1617630	HUVEC	blood vessel:	n/a	n/a
7	CTCF	chr20:1617488-1617659	GM19240	blood:	n/a	n/a
8	CTCF	chr20:1617507-1617617	K562	blood:	n/a	n/a
9	CTCF	chr20:1617508-1617635	A549	lung:	n/a	n/a
10	CTCF	chr20:1617494-1617651	GM19238	blood:	n/a	n/a
11	CTCF	chr20:1617460-1617610	GM12874	blood:	n/a	n/a
12	CTCF	chr20:1617391-1617692	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr20:1617393-1617760	HepG2	liver:	n/a	n/a
14	CTCF	chr20:1617403-1617664	HepG2	liver:	n/a	n/a
15	CTCF	chr20:1617465-1617671	NHEK	skin:	n/a	n/a
16	CTCF	chr20:1617500-1617650	GM12868	blood:	n/a	n/a
17	CTCF	chr20:1617480-1617630	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr20:1617460-1617610	SAEC	small airway:	n/a	n/a
19	CTCF	chr20:1617486-1617639	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr20:1617460-1617610	GM12873	blood:	n/a	n/a
21	CTCF	chr20:1617485-1617631	GM12878	blood:	n/a	n/a
22	CTCF	chr20:1617500-1617650	GM12874	blood:	n/a	n/a
23	CTCF	chr20:1617530-1617612	MCF-7	breast:	n/a	n/a
24	CTCF	chr20:1617504-1617619	K562	blood:	n/a	n/a
25	CTCF	chr20:1617515-1617625	Gliobla	brain:	n/a	n/a
26	CTCF	chr20:1617323-1617708	HCT-116	colon:	n/a	n/a
27	CTCF	chr20:1617540-1617690	HepG2	liver:	n/a	n/a
28	CTCF	chr20:1617322-1617717	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr20:1617462-1617661	HepG2	liver:	n/a	n/a
30	CTCF	chr20:1617460-1617610	HEK293	kidney:	n/a	n/a
31	CTCF	chr20:1617520-1617670	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr20:1617500-1617605	Fibrobl	skin:	n/a	n/a
33	CTCF	chr20:1617500-1617650	GM12865	blood:	n/a	n/a
34	CTCF	chr20:1617500-1617650	GM12871	blood:	n/a	n/a
35	CTCF	chr20:1617523-1617639	GM19239	blood:	n/a	n/a
36	CTCF	chr20:1617500-1617650	NHEK	skin:	n/a	n/a
37	CTCF	chr20:1617492-1617644	MCF-7	breast:	n/a	n/a
38	CTCF	chr20:1617429-1617717	GM12878	blood:	n/a	n/a
39	CTCF	chr20:1617541-1617635	MCF-7	breast:	n/a	n/a
40	CTCF	chr20:1617500-1617650	HepG2	liver:	n/a	n/a
41	CTCF	chr20:1617500-1617643	GM12892	blood:	n/a	n/a
42	CTCF	chr20:1617480-1617630	GM12878	blood:	n/a	n/a
43	CTCF	chr20:1617480-1617630	NB4	blood:	n/a	n/a
44	CTCF	chr20:1617500-1617650	HRE	kidney:	n/a	n/a
45	CTCF	chr20:1617280-1617430	A549	lung:	n/a	n/a
46	CTCF	chr20:1617493-1617649	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr20:1617529-1617629	GM13977	blood:	n/a	n/a
48	CTCF	chr20:1617460-1617610	GM12869	blood:	n/a	n/a
49	CTCF	chr20:1617511-1617642	GM10266	blood:	n/a	n/a
50	CTCF	chr20:1617485-1617673	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1616387-1616437	AG10803	skin:	n/a
2	chr20:1616387-1616437	HUVEC	blood vessel:	n/a
3	chr20:1616387-1616437	HRCEpiC	kidney:	n/a
4	chr20:1616387-1616437	MCF-7	breast:	n/a
5	chr20:1616387-1616437	AG09309	skin:	n/a
6	chr20:1616387-1616437	Jurkat	blood:	n/a
7	chr20:1616387-1616437	HepG2	liver:	n/a
8	chr20:1616387-1616437	HCM	heart:	n/a
9	chr20:1616387-1616437	BJ	skin:	n/a
10	chr20:1616387-1616437	HL-60	blood:	n/a
11	chr20:1616387-1616437	Caco-2	colon:	n/a
12	chr20:1616387-1616437	GM06990	blood:	n/a
13	chr20:1616387-1616437	HRPEpiC	eye:	n/a
14	chr20:1616387-1616437	AG04450	lung:	fetal
15	chr20:1616387-1616437	AG04449	skin:	fetal
16	chr20:1616387-1616437	LNCaP	prostate:	n/a
17	chr20:1616387-1616437	HNPCEpiC	eye:	n/a
18	chr20:1616387-1616437	BE2_C	brain:	n/a
19	chr20:1616387-1616437	SK-N-SH	brain:	n/a
20	chr20:1616387-1616437	HRE	kidney:	n/a
21	chr20:1616387-1616437	NH-A	brain:	n/a
22	chr20:1616387-1616437	PrEC	prostate:	n/a
23	chr20:1616387-1616437	RPTEC	kidney:	n/a
24	chr20:1616387-1616437	MCF10A-Er-Src	breast:	n/a
25	chr20:1616387-1616437	ECC-1	luminal epithelium:	n/a
26	chr20:1616387-1616437	PANC-1	pancreas:	n/a
27	chr20:1616387-1616437	GM12891	blood:	n/a
28	chr20:1616387-1616437	CMK	blood:	n/a
29	chr20:1616387-1616437	SAEC	small airway:	n/a
30	chr20:1616387-1616437	GM12878	blood:	n/a
31	chr20:1616387-1616437	AG09319	gingival:	n/a
32	chr20:1616387-1616437	U87	brain:	n/a
33	chr20:1616387-1616437	K562	blood:	n/a
34	chr20:1616387-1616437	AoSMC	blood vessel:	n/a
35	chr20:1616387-1616437	HIPEpiC	eye:	n/a
36	chr20:1616387-1616437	HAEpiC	amniotic membrane:	n/a
37	chr20:1616387-1616437	NHDF-neo	bronchial:	n/a
38	chr20:1616387-1616437	GM12892	blood:	n/a
39	chr20:1616387-1616437	H1-hESC	embryonic stem cell:	embryo
40	chr20:1616387-1616437	NB4	blood:	n/a
41	chr20:1616387-1616437	ovcar-3	ovarian:	n/a
42	chr20:1616387-1616437	HCPEpiC	choroid plexus:	n/a
43	chr20:1616387-1616437	HPAEpiC	pulmonary alveolar:	n/a
44	chr20:1616387-1616437	HEEpiC	esophagus:	n/a
45	chr20:1616387-1616437	IMR90	lung:	fetal
46	chr20:1616387-1616437	NT2-D1	testis:	n/a
47	chr20:1616387-1616437	SK-N-SH_RA	brain:	n/a
48	chr20:1616387-1616437	SKMC	muscle:	n/a
49	chr20:1616387-1616437	SK-N-MC	brain:	n/a
50	chr20:1616387-1616437	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:1484085..1484840-chr20:1617080..1618039,2	MCF-7	breast:

No data

Variant related genes	Relation type
SIRPG	TF binding region
SIRPG	CpG island

Extended variants
information (count: 123 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:123 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530396365	chr20:1615770-1615771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79366176	chr20:1615771-1615772	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567241655	chr20:1615774-1615775	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531255093	chr20:1615780-1615781	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549855268	chr20:1615789-1615790	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571373231	chr20:1615808-1615809	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs62186948	chr20:1615835-1615836	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369020325	chr20:1615844-1615845	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs62186949	chr20:1615883-1615884	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547634798	chr20:1615915-1615916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147969759	chr20:1615929-1615930	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs78053816	chr20:1615934-1615935	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs9305125	chr20:1615959-1615960	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs369760423	chr20:1615964-1615965	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs148596804	chr20:1615970-1615971	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs147655438	chr20:1615980-1615981	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs41275434	chr20:1615981-1615982	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs370938397	chr20:1615986-1615987	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs149789805	chr20:1615989-1615990	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs145754609	chr20:1615990-1615991	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs373199508	chr20:1615994-1615995	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs576944150	chr20:1615996-1615997	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs376291488	chr20:1616013-1616014	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201051307	chr20:1616026-1616027	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs41275436	chr20:1616048-1616049	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200982024	chr20:1616050-1616051	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs574972022	chr20:1616054-1616055	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs370713827	chr20:1616064-1616065	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs542506528	chr20:1616081-1616082	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs148883600	chr20:1616096-1616097	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs145447195	chr20:1616101-1616102	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374114001	chr20:1616103-1616104	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs9974013	chr20:1616118-1616119	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs141069067	chr20:1616123-1616124	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs114922972	chr20:1616136-1616137	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs6034239	chr20:1616137-1616138	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs142972068	chr20:1616138-1616139	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs367852522	chr20:1616139-1616140	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs547549347	chr20:1616143-1616144	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538901849	chr20:1616196-1616197	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs181987018	chr20:1616205-1616206	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs6043409	chr20:1616206-1616207	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs200055053	chr20:1616207-1616208	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs548420665	chr20:1616213-1616214	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370231533	chr20:1616221-1616222	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201625579	chr20:1616226-1616227	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs374181477	chr20:1616262-1616263	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs368583183	chr20:1616274-1616275	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs548604272	chr20:1616329-1616330	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs565315312	chr20:1616339-1616340	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	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
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
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1605200-1631800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr20:1607600-1627600	Weak transcription	Fetal Thymus	thymus
3	chr20:1607600-1632000	Weak transcription	Spleen	Spleen
4	chr20:1608400-1616800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr20:1611600-1624800	Weak transcription	Thymus	Thymus
6	chr20:1612200-1615800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr20:1612400-1616000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr20:1612600-1616200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr20:1612800-1617600	Weak transcription	HUVEC	blood vessel
10	chr20:1613200-1616200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr20:1613400-1616000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr20:1613600-1616000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr20:1614400-1618800	Strong transcription	Primary T cells from cord blood	blood
14	chr20:1614600-1616000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr20:1614600-1616000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
16	chr20:1614600-1616000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr20:1614800-1615800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr20:1614800-1615800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr20:1614800-1615800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr20:1614800-1615800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr20:1614800-1616000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr20:1614800-1616000	Weak transcription	HepG2	liver
23	chr20:1614800-1617400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr20:1614800-1617800	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr20:1614800-1618200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr20:1614800-1618400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr20:1615400-1616000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr20:1615800-1616600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr20:1615800-1616800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr20:1615800-1617400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
31	chr20:1615800-1617400	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr20:1615800-1617600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr20:1616000-1616200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
34	chr20:1616000-1616400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr20:1616000-1616600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr20:1616000-1616600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr20:1616000-1616600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
38	chr20:1616000-1616800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr20:1616000-1617000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr20:1616000-1618600	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr20:1616000-1619200	Enhancers	HepG2	liver
42	chr20:1616200-1616800	Enhancers	H9 Cell Line	embryonic stem cell
43	chr20:1616200-1617200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr20:1616200-1617600	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr20:1616400-1617400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr20:1616600-1621200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr20:1616600-1625200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr20:1616800-1617800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr20:1616800-1618000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr20:1616800-1621200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links