Variant report

Variant	nsv828708
Chromosome Location	chr20:25223895-25231601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:859)
CpG islands
(count:794)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25227258-25228233	HepG2	liver:	n/a	n/a
2	BACH1	chr20:25227720-25229538	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr20:25228408-25229146	A549	lung:	n/a	n/a
4	BCL3	chr20:25227616-25228336	A549	lung:	n/a	n/a
5	BCLAF1	chr20:25228639-25229050	GM12878	blood:	n/a	n/a
6	BCLAF1	chr20:25228642-25229149	GM12878	blood:	n/a	n/a
7	BHLHE40	chr20:25227761-25229052	HepG2	liver:	n/a	chr20:25228438-25228454
8	BHLHE40	chr20:25227796-25229055	K562	blood:	n/a	chr20:25228438-25228454
9	BHLHE40	chr20:25228728-25229226	GM12878	blood:	n/a	chr20:25229111-25229127
10	BRCA1	chr20:25228757-25229169	HepG2	liver:	n/a	n/a
11	BRCA1	chr20:25228718-25228943	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr20:25228181-25228459	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr20:25227868-25228449	HepG2	liver:	n/a	n/a
14	CCNT2	chr20:25227947-25229451	K562	blood:	n/a	chr20:25229398-25229407
15	CEBPB	chr20:25227254-25227523	K562	blood:	n/a	chr20:25227370-25227381
16	CEBPB	chr20:25227202-25227559	HepG2	liver:	n/a	chr20:25227370-25227381 chr20:25227249-25227260 chr20:25227249-25227260
17	CEBPB	chr20:25228390-25228629	HepG2	liver:	n/a	n/a
18	CEBPB	chr20:25226231-25226431	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr20:25226950-25227737	A549	lung:	n/a	chr20:25227370-25227381 chr20:25227249-25227260 chr20:25227249-25227260
20	CEBPB	chr20:25227196-25227565	A549	lung:	n/a	chr20:25227370-25227381 chr20:25227249-25227260 chr20:25227249-25227260
21	CEBPB	chr20:25228696-25228897	Hela-S3	cervix:	n/a	n/a
22	CEBPD	chr20:25228549-25228843	HepG2	liver:	n/a	n/a
23	CEBPD	chr20:25228294-25228991	HepG2	liver:	n/a	n/a
24	CHD1	chr20:25228722-25229205	GM12878	blood:	n/a	n/a
25	CHD1	chr20:25228742-25228934	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr20:25227574-25230347	IMR90	lung:	n/a	chr20:25229396-25229406
27	CHD2	chr20:25228364-25228995	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr20:25228724-25229502	H1-hESC	embryonic stem cell:	n/a	chr20:25229396-25229406
29	CHD2	chr20:25228344-25229036	GM12878	blood:	n/a	n/a
30	CHD2	chr20:25227746-25228149	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr20:25229343-25229412	GM12878	blood:	n/a	chr20:25229396-25229406
32	CHD2	chr20:25229301-25229432	HepG2	liver:	n/a	chr20:25229396-25229406
33	CHD2	chr20:25227939-25228073	HepG2	liver:	n/a	n/a
34	CHD2	chr20:25228318-25229085	HepG2	liver:	n/a	n/a
35	CHD2	chr20:25228746-25228987	K562	blood:	n/a	n/a
36	CHD2	chr20:25227864-25228120	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr20:25227792-25228118	A549	lung:	n/a	n/a
38	CREB1	chr20:25227471-25229630	HepG2	liver:	n/a	n/a
39	CREB1	chr20:25227264-25229533	A549	lung:	n/a	n/a
40	CREB1	chr20:25228644-25229178	GM12878	blood:	n/a	n/a
41	CREB1	chr20:25228664-25229154	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTBP2	chr20:25227752-25228531	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr20:25228791-25229405	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr20:25227761-25228002	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr20:25228903-25228909	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr20:25229940-25230090	RPTEC	kidney:	n/a	n/a
47	CTCF	chr20:25227780-25227930	GM12869	blood:	n/a	n/a
48	CTCF	chr20:25229940-25230090	HMF	breast:	n/a	n/a
49	CTCF	chr20:25229920-25230070	HPF	lung:	n/a	n/a
50	CTCF	chr20:25229900-25230050	HCFaa	heart:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25228575-25228625	HCPEpiC	choroid plexus:	n/a
2	chr20:25228575-25228625	HCPEpiC	choroid plexus:	n/a
3	chr20:25228558-25228608	AG04450	lung:	fetal
4	chr20:25229376-25229426	RPTEC	kidney:	n/a
5	chr20:25228558-25228608	Hela-S3	cervix:	n/a
6	chr20:25228558-25228608	HNPCEpiC	eye:	n/a
7	chr20:25229376-25229426	ovcar-3	ovarian:	n/a
8	chr20:25227488-25227538	IMR90	lung:	fetal
9	chr20:25230959-25231009	GM12891	blood:	n/a
10	chr20:25225861-25225911	HUVEC	blood vessel:	n/a
11	chr20:25228575-25228625	IMR90	lung:	fetal
12	chr20:25225861-25225911	SK-N-SH_RA	brain:	n/a
13	chr20:25227488-25227538	HRE	kidney:	n/a
14	chr20:25230959-25231009	IMR90	lung:	fetal
15	chr20:25227488-25227538	BE2_C	brain:	n/a
16	chr20:25228580-25228630	AG04450	lung:	fetal
17	chr20:25228575-25228625	NHBE	bronchial:	n/a
18	chr20:25228575-25228625	SK-N-MC	brain:	n/a
19	chr20:25228305-25228355	HepG2	liver:	n/a
20	chr20:25228731-25228781	HEEpiC	esophagus:	n/a
21	chr20:25228305-25228355	HEEpiC	esophagus:	n/a
22	chr20:25228580-25228630	NHDF-neo	bronchial:	n/a
23	chr20:25228251-25228301	SKMC	muscle:	n/a
24	chr20:25228251-25228301	CMK	blood:	n/a
25	chr20:25229376-25229426	GM19239	blood:	n/a
26	chr20:25225861-25225911	GM06990	blood:	n/a
27	chr20:25228615-25228665	BJ	skin:	n/a
28	chr20:25228569-25228619	ovcar-3	ovarian:	n/a
29	chr20:25228615-25228665	HUVEC	blood vessel:	n/a
30	chr20:25230959-25231009	NT2-D1	testis:	n/a
31	chr20:25228305-25228355	MCF10A-Er-Src	breast:	n/a
32	chr20:25225861-25225911	PFSK-1	brain:	n/a
33	chr20:25228575-25228625	SK-N-SH	brain:	n/a
34	chr20:25228251-25228301	ECC-1	luminal epithelium:	n/a
35	chr20:25228558-25228608	SK-N-SH	brain:	n/a
36	chr20:25228731-25228781	AG09309	skin:	n/a
37	chr20:25228558-25228608	GM12878	blood:	n/a
38	chr20:25228305-25228355	SK-N-SH_RA	brain:	n/a
39	chr20:25228899-25228949	T-47D	breast:	n/a
40	chr20:25230959-25231009	HMEC	breast:	n/a
41	chr20:25228575-25228625	MCF-7	breast:	n/a
42	chr20:25227488-25227538	NH-A	brain:	n/a
43	chr20:25228251-25228301	AG04449	skin:	fetal
44	chr20:25227488-25227538	AG10803	skin:	n/a
45	chr20:25229376-25229426	AG09309	skin:	n/a
46	chr20:25228615-25228665	U87	brain:	n/a
47	chr20:25228558-25228608	Jurkat	blood:	n/a
48	chr20:25228580-25228630	HEK293	kidney:	embryo
49	chr20:25228580-25228630	AoSMC	blood vessel:	n/a
50	chr20:25228615-25228665	HAEpiC	amniotic membrane:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:25228549..25230437-chr20:25281061..25283760,2	MCF-7	breast:
2	chr20:25226994..25230316-chr20:25230894..25234790,8	K562	blood:
3	chr20:25203499..25204385-chr20:25227516..25228200,3	MCF-7	breast:
4	chr20:25228557..25231308-chr20:25476839..25479017,2	MCF-7	breast:
5	chr17:80186667..80187466-chr20:25228580..25229101,2	HCT-116	colon:
6	chr20:25057289..25058975-chr20:25226619..25228863,2	MCF-7	breast:
7	chr20:25204037..25205721-chr20:25227160..25229400,2	K562	blood:
8	chr20:25119092..25121344-chr20:25229044..25231163,2	MCF-7	breast:
9	chr20:25226304..25227809-chr20:25275139..25278038,2	MCF-7	breast:
10	chr12:104531363..104532174-chr20:25228138..25229130,2	NB4	blood:
11	chr20:25223963..25226805-chr20:25228679..25230694,3	K562	blood:
12	chr20:25119470..25120469-chr20:25227465..25228346,4	MCF-7	breast:
13	chr20:25200007..25207026-chr20:25227086..25230373,11	MCF-7	breast:
14	chr20:25189131..25190922-chr20:25228814..25231748,2	MCF-7	breast:
15	chr20:25201569..25205371-chr20:25224362..25226841,4	MCF-7	breast:
16	chr20:25174010..25179528-chr20:25225802..25231331,13	MCF-7	breast:
17	chr2:198364442..198365011-chr20:25228269..25228983,2	HCT-116	colon:
18	chr20:24971946..24973582-chr20:25227704..25229248,2	MCF-7	breast:
19	chr20:25231045..25233817-chr20:25255982..25257750,2	MCF-7	breast:
20	chr11:78285600..78286417-chr20:25228512..25229228,2	NB4	blood:
21	chr20:25208292..25210129-chr20:25227027..25228548,2	MCF-7	breast:
22	chr20:25204221..25206637-chr20:25227058..25229400,2	K562	blood:
23	chr20:24971839..24974533-chr20:25228512..25230139,2	MCF-7	breast:
24	chr20:25174902..25179249-chr20:25225017..25231959,9	MCF-7	breast:
25	chr20:25202506..25206898-chr20:25226343..25231297,7	MCF-7	breast:
26	chr12:53339776..53342666-chr20:25227973..25230849,2	MCF-7	breast:
27	chr20:25217672..25220139-chr20:25231086..25234075,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABHD12-1	chr20:25227084-25227480	XLOC_013706
2	lnc-ABHD12-1	chr20:25225790-25225982	XLOC_013706

No data

Variant related genes	Relation type
PYGB	TF binding region
PYGB	CpG island
ENSG00000115541	chromatin interactions
ENSG00000144381	chromatin interactions
ENSG00000197586	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000120837	chromatin interactions
ENSG00000111057	chromatin interactions
ENSG00000101474	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000101004	chromatin interactions
ENSG00000100987	chromatin interactions
ENSG00000137513	chromatin interactions
C15orf17	miRNA target sites
ZNRF3	miRNA target sites

Extended variants
information (count: 317 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147249664	chr20:25223938-25223939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557154833	chr20:25223939-25223940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569572209	chr20:25224014-25224015	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs139021431	chr20:25224069-25224070	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554770564	chr20:25224107-25224108	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552469929	chr20:25224153-25224154	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs79090114	chr20:25224162-25224163	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553839741	chr20:25224201-25224202	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs576817506	chr20:25224210-25224211	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs545830692	chr20:25224244-25224245	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555878010	chr20:25224308-25224309	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576440905	chr20:25224310-25224311	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs6050480	chr20:25224370-25224371	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs35067790	chr20:25224394-25224395	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs190662820	chr20:25224406-25224407	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs181855448	chr20:25224422-25224423	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs560679891	chr20:25224423-25224424	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs532489002	chr20:25224450-25224451	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs552573777	chr20:25224547-25224548	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs369789628	chr20:25224549-25224550	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs562717627	chr20:25224566-25224567	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs6050481	chr20:25224580-25224581	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs548487291	chr20:25224621-25224622	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs144732332	chr20:25224703-25224704	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs68154819	chr20:25224803-25224804	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs186059012	chr20:25224889-25224890	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs570568490	chr20:25224980-25224981	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539144946	chr20:25224987-25224988	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs556154762	chr20:25225001-25225002	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs148571037	chr20:25225018-25225019	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs188863107	chr20:25225076-25225077	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs541721425	chr20:25225116-25225117	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs113176394	chr20:25225130-25225131	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs28496800	chr20:25225171-25225172	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs557633051	chr20:25225210-25225211	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs542719685	chr20:25225213-25225214	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs577293176	chr20:25225315-25225316	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs181313960	chr20:25225347-25225348	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs4815395	chr20:25225354-25225355	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186624854	chr20:25225363-25225364	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs543280284	chr20:25225379-25225380	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs191073066	chr20:25225461-25225462	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs112867514	chr20:25225482-25225483	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs562092132	chr20:25225484-25225485	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs371556082	chr20:25225502-25225503	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs35984147	chr20:25225634-25225635	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs548005095	chr20:25225653-25225654	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182864460	chr20:25225654-25225655	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs539997153	chr20:25225669-25225670	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs570896300	chr20:25225753-25225754	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
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
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:831 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25217600-25227600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr20:25219000-25226000	Weak transcription	Colonic Mucosa	Colon
3	chr20:25219000-25227400	Weak transcription	Colon Smooth Muscle	Colon
4	chr20:25219400-25226800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr20:25219400-25226800	Weak transcription	Right Ventricle	heart
6	chr20:25219400-25227600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr20:25219400-25228000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr20:25219600-25227000	Weak transcription	NHDF-Ad	bronchial
9	chr20:25219800-25227400	Weak transcription	NHLF	lung
10	chr20:25220200-25227000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr20:25220400-25227400	Weak transcription	Esophagus	oesophagus
12	chr20:25220600-25226800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr20:25220600-25227200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr20:25220800-25226000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr20:25221800-25224200	Weak transcription	Fetal Intestine Large	intestine
16	chr20:25221800-25225800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr20:25221800-25226000	Weak transcription	Fetal Heart	heart
18	chr20:25221800-25226800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr20:25221800-25226800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr20:25222000-25226200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr20:25222000-25226800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr20:25222000-25227000	Weak transcription	HSMM	muscle
23	chr20:25222000-25227200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr20:25222000-25227400	Weak transcription	Fetal Kidney	kidney
25	chr20:25222000-25227400	Weak transcription	HSMMtube	muscle
26	chr20:25222000-25227600	Weak transcription	Fetal Lung	lung
27	chr20:25222400-25227000	Weak transcription	K562	blood
28	chr20:25222400-25227400	Weak transcription	NH-A	brain
29	chr20:25222600-25224400	Enhancers	HMEC	breast
30	chr20:25223000-25225400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr20:25223200-25224400	Weak transcription	A549	lung
32	chr20:25223200-25227400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr20:25223400-25224000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr20:25223400-25226000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr20:25223400-25227400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr20:25223600-25225800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr20:25223600-25227800	Weak transcription	Brain Germinal Matrix	brain
38	chr20:25223800-25224000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr20:25223800-25227600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr20:25224000-25224200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr20:25224200-25224600	ZNF genes & repeats	Fetal Intestine Large	intestine
42	chr20:25224200-25225200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr20:25224400-25224800	ZNF genes & repeats	A549	lung
44	chr20:25224400-25225800	Weak transcription	HMEC	breast
45	chr20:25224600-25226200	Weak transcription	Fetal Intestine Large	intestine
46	chr20:25224800-25225800	Weak transcription	A549	lung
47	chr20:25225200-25225800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr20:25225800-25226000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr20:25225800-25226800	Enhancers	A549	lung
50	chr20:25225800-25226800	Enhancers	HMEC	breast

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