Variant report

Variant	esv1812605
Chromosome Location	chr20:1544966-1560140
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	chr20:1550229-1550409	K562	blood:	n/a	n/a
2	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
3	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
4	BHLHE40	chr20:1549969-1550250	K562	blood:	n/a	n/a
5	BRCA1	chr20:1550123-1550444	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr20:1550060-1550411	MCF-7	breast:	n/a	n/a
7	CEBPB	chr20:1557313-1557606	Hela-S3	cervix:	n/a	chr20:1557460-1557471
8	CEBPB	chr20:1557320-1557574	A549	lung:	n/a	chr20:1557460-1557471
9	CEBPB	chr20:1550062-1550405	A549	lung:	n/a	n/a
10	CEBPB	chr20:1550079-1550429	K562	blood:	n/a	n/a
11	CEBPB	chr20:1548089-1548620	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr20:1549987-1550512	A549	lung:	n/a	n/a
13	CEBPB	chr20:1550069-1550318	K562	blood:	n/a	n/a
14	CEBPB	chr20:1550076-1550409	HepG2	liver:	n/a	n/a
15	CEBPB	chr20:1557318-1557553	HepG2	liver:	n/a	chr20:1557460-1557471
16	CEBPB	chr20:1549872-1550575	HCT-116	colon:	n/a	chr20:1549945-1549956
17	CEBPB	chr20:1550085-1550450	A549	lung:	n/a	n/a
18	CEBPB	chr20:1550121-1550426	IMR90	lung:	n/a	n/a
19	CEBPB	chr20:1549828-1550670	HCT-116	colon:	n/a	chr20:1549945-1549956
20	CEBPB	chr20:1549993-1550495	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr20:1548232-1548651	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr20:1550074-1550408	Hela-S3	cervix:	n/a	n/a
23	CREB1	chr20:1550008-1550399	K562	blood:	n/a	n/a
24	CTCF	chr20:1550471-1550587	K562	blood:	n/a	n/a
25	CTCF	chr20:1552670-1552733	GM10266	blood:	n/a	n/a
26	CTCF	chr20:1556774-1556880	NHEK	skin:	n/a	n/a
27	CTCF	chr20:1550540-1550690	NB4	blood:	n/a	n/a
28	E2F4	chr20:1550155-1550481	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr20:1550067-1550405	K562	blood:	n/a	n/a
30	EP300	chr20:1549951-1550436	Hela-S3	cervix:	n/a	n/a
31	EP300	chr20:1548112-1548657	Hela-S3	cervix:	n/a	n/a
32	FOS	chr20:1549958-1550474	MCF10A-Er-Src	breast:	n/a	chr20:1550241-1550249 chr20:1550240-1550250 chr20:1550239-1550251 chr20:1550239-1550250
33	FOS	chr20:1547412-1547722	MCF10A-Er-Src	breast:	n/a	chr20:1547544-1547552 chr20:1547547-1547555 chr20:1547416-1547428
34	FOS	chr20:1550024-1550457	MCF10A-Er-Src	breast:	n/a	chr20:1550241-1550249 chr20:1550240-1550250 chr20:1550239-1550251 chr20:1550239-1550250
35	FOS	chr20:1557393-1557685	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr20:1548038-1549064	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr20:1556802-1556896	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr20:1548179-1549018	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr20:1550023-1550434	HUVEC	blood vessel:	n/a	chr20:1550241-1550249 chr20:1550240-1550250 chr20:1550239-1550251 chr20:1550239-1550250
40	FOS	chr20:1549885-1550514	MCF10A-Er-Src	breast:	n/a	chr20:1550241-1550249 chr20:1550240-1550250 chr20:1550239-1550251 chr20:1550239-1550250
41	FOS	chr20:1547453-1547679	MCF10A-Er-Src	breast:	n/a	chr20:1547544-1547552 chr20:1547547-1547555
42	FOS	chr20:1547417-1547722	MCF10A-Er-Src	breast:	n/a	chr20:1547544-1547552 chr20:1547547-1547555
43	FOS	chr20:1547896-1548917	HUVEC	blood vessel:	n/a	n/a
44	FOS	chr20:1549982-1550478	MCF10A-Er-Src	breast:	n/a	chr20:1550241-1550249 chr20:1550240-1550250 chr20:1550239-1550251 chr20:1550239-1550250
45	FOS	chr20:1547519-1547719	MCF10A-Er-Src	breast:	n/a	chr20:1547544-1547552 chr20:1547547-1547555
46	FOS	chr20:1557387-1557630	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr20:1548080-1548657	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr20:1548038-1549062	MCF10A-Er-Src	breast:	n/a	n/a
49	FOSL1	chr20:1549851-1550618	HCT-116	colon:	n/a	chr20:1550241-1550249 chr20:1550240-1550250 chr20:1550239-1550251
50	FOSL1	chr20:1549873-1550579	HCT-116	colon:	n/a	chr20:1550241-1550249 chr20:1550240-1550250 chr20:1550239-1550251

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1546019-1546069	SK-N-MC	brain:	n/a
2	chr20:1546019-1546069	PANC-1	pancreas:	n/a
3	chr20:1546019-1546069	HEEpiC	esophagus:	n/a
4	chr20:1546019-1546069	Jurkat	blood:	n/a
5	chr20:1546019-1546069	Hela-S3	cervix:	n/a
6	chr20:1546019-1546069	NHDF-neo	bronchial:	n/a
7	chr20:1546019-1546069	RPTEC	kidney:	n/a
8	chr20:1546019-1546069	T-47D	breast:	n/a
9	chr20:1546019-1546069	CMK	blood:	n/a
10	chr20:1546019-1546069	AG04450	lung:	fetal
11	chr20:1546019-1546069	SK-N-SH_RA	brain:	n/a
12	chr20:1546019-1546069	GM19239	blood:	n/a
13	chr20:1546019-1546069	NB4	blood:	n/a
14	chr20:1546019-1546069	K562	blood:	n/a
15	chr20:1546019-1546069	AG04449	skin:	fetal
16	chr20:1546019-1546069	GM06990	blood:	n/a
17	chr20:1546019-1546069	HCPEpiC	choroid plexus:	n/a
18	chr20:1546019-1546069	HCM	heart:	n/a
19	chr20:1546019-1546069	ProgFib	skin:	n/a
20	chr20:1546019-1546069	HIPEpiC	eye:	n/a
21	chr20:1546019-1546069	GM12891	blood:	n/a
22	chr20:1546019-1546069	IMR90	lung:	fetal
23	chr20:1546019-1546069	AG09309	skin:	n/a
24	chr20:1546019-1546069	HRCEpiC	kidney:	n/a
25	chr20:1546019-1546069	Caco-2	colon:	n/a
26	chr20:1546019-1546069	LNCaP	prostate:	n/a
27	chr20:1546019-1546069	HPAEpiC	pulmonary alveolar:	n/a
28	chr20:1546019-1546069	NH-A	brain:	n/a
29	chr20:1546019-1546069	HRPEpiC	eye:	n/a
30	chr20:1546019-1546069	HEK293	kidney:	embryo
31	chr20:1546019-1546069	ovcar-3	ovarian:	n/a
32	chr20:1546019-1546069	PrEC	prostate:	n/a
33	chr20:1546019-1546069	SAEC	small airway:	n/a
34	chr20:1546019-1546069	HCT-116	colon:	n/a
35	chr20:1546019-1546069	HRE	kidney:	n/a
36	chr20:1546019-1546069	GM12878	blood:	n/a
37	chr20:1546019-1546069	MCF-7	breast:	n/a
38	chr20:1546019-1546069	HL-60	blood:	n/a
39	chr20:1546019-1546069	HMEC	breast:	n/a
40	chr20:1546019-1546069	HepG2	liver:	n/a
41	chr20:1546019-1546069	H1-hESC	embryonic stem cell:	embryo
42	chr20:1546019-1546069	HAEpiC	amniotic membrane:	n/a
43	chr20:1546019-1546069	Hepatocyte	liver:	n/a
44	chr20:1546019-1546069	U87	brain:	n/a
45	chr20:1546019-1546069	HUVEC	blood vessel:	n/a
46	chr20:1546019-1546069	GM12892	blood:	n/a
47	chr20:1546019-1546069	NT2-D1	testis:	n/a
48	chr20:1546019-1546069	HCF	heart:	n/a
49	chr20:1546019-1546069	HNPCEpiC	eye:	n/a
50	chr20:1546019-1546069	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:
2	chr20:1547054..1548894-chr20:1756067..1757690,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1

Variant related genes	Relation type
SIRPB1	TF binding region
SIRPB1	CpG island

Extended variants
information (count: 574 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538450087	chr20:1544995-1544996	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184925039	chr20:1545028-1545029	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs373462740	chr20:1545076-1545077	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs146013755	chr20:1545080-1545081	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs139920459	chr20:1545089-1545090	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs572798438	chr20:1545117-1545118	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs188981426	chr20:1545133-1545134	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs544907957	chr20:1545166-1545167	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs149708397	chr20:1545186-1545187	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs573689204	chr20:1545208-1545209	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs544374358	chr20:1545293-1545294	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs375137247	chr20:1545387-1545388	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs181069766	chr20:1545406-1545407	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577507288	chr20:1545409-1545410	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185518072	chr20:1545462-1545463	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2253693	chr20:1545468-1545469	Genic enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs45512895	chr20:1545529-1545530	Genic enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549177731	chr20:1545541-1545542	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2253698	chr20:1545617-1545618	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs6105340	chr20:1545635-1545636	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550385271	chr20:1545669-1545670	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200979171	chr20:1545690-1545691	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571877913	chr20:1545691-1545692	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536410483	chr20:1545718-1545719	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189597232	chr20:1545727-1545728	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531589523	chr20:1545745-1545746	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372470630	chr20:1545794-1545795	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs16995228	chr20:1545857-1545858	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566308622	chr20:1545941-1545942	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533766481	chr20:1545980-1545981	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145520796	chr20:1545981-1545982	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371415442	chr20:1546012-1546013	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs114721859	chr20:1546020-1546021	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs373144814	chr20:1546030-1546031	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs570931302	chr20:1546035-1546036	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs577419882	chr20:1546086-1546087	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs544878020	chr20:1546093-1546094	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs536615314	chr20:1546135-1546136	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs572287257	chr20:1546148-1546149	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs2253814	chr20:1546175-1546176	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs2253815	chr20:1546207-1546208	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs74321032	chr20:1546229-1546230	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs536542704	chr20:1546233-1546234	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs181521523	chr20:1546248-1546249	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs148842400	chr20:1546256-1546257	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs552931485	chr20:1546263-1546264	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs142523875	chr20:1546274-1546275	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs11907473	chr20:1546350-1546351	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs147557710	chr20:1546352-1546353	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs566340787	chr20:1546353-1546354	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Prostate cancer	21551127	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1532800-1545400	Weak transcription	Spleen	Spleen
2	chr20:1537000-1551600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr20:1541800-1545200	Weak transcription	Primary T cells from cord blood	blood
4	chr20:1543000-1545000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
5	chr20:1543200-1550400	Weak transcription	Thymus	Thymus
6	chr20:1543600-1548600	Genic enhancers	Primary monocytes fromperipheralblood	blood
7	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr20:1544000-1545000	Genic enhancers	Monocytes-CD14+_RO01746	blood
9	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr20:1544800-1548200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr20:1545000-1545400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
12	chr20:1545000-1548000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr20:1545200-1547400	Strong transcription	Primary T cells from cord blood	blood
14	chr20:1545400-1546200	Genic enhancers	Monocytes-CD14+_RO01746	blood
15	chr20:1545400-1546600	Strong transcription	Spleen	Spleen
16	chr20:1545600-1545800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr20:1545800-1546800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr20:1545800-1549400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr20:1546000-1547000	ZNF genes & repeats	Lung	lung
20	chr20:1546200-1547800	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr20:1546600-1551200	Enhancers	Hela-S3	cervix
22	chr20:1546600-1551400	Weak transcription	Spleen	Spleen
23	chr20:1546800-1550800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr20:1546800-1551000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr20:1547000-1547800	Enhancers	NHEK	skin
26	chr20:1547000-1550800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr20:1547000-1551000	Enhancers	HMEC	breast
28	chr20:1547200-1549000	Enhancers	NH-A	brain
29	chr20:1547200-1549400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr20:1547200-1551000	Enhancers	HUVEC	blood vessel
31	chr20:1547400-1548000	Enhancers	A549	lung
32	chr20:1547400-1548800	Weak transcription	Primary T cells from cord blood	blood
33	chr20:1547400-1549000	Enhancers	Osteobl	bone
34	chr20:1547800-1548000	Genic enhancers	Monocytes-CD14+_RO01746	blood
35	chr20:1547800-1548200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr20:1547800-1548600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr20:1547800-1548800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr20:1547800-1548800	Flanking Active TSS	NHEK	skin
39	chr20:1547800-1550200	Enhancers	NHDF-Ad	bronchial
40	chr20:1548000-1548200	Active TSS	A549	lung
41	chr20:1548000-1548400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr20:1548000-1548400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
43	chr20:1548000-1548400	Enhancers	Esophagus	oesophagus
44	chr20:1548000-1548400	Enhancers	NHLF	lung
45	chr20:1548000-1548800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr20:1548000-1549000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr20:1548000-1549000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr20:1548000-1549000	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
49	chr20:1548200-1548600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr20:1548200-1548600	Flanking Active TSS	A549	lung

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