Variant report

Variant	nsv878752
Chromosome Location	chr4:22414023-22501043
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	chr4:22437299-22437741	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:22476377-22477117	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:22455972-22456260	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:22457970-22458493	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:22461719-22462382	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:22436571-22436819	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:22489028-22489337	HepG2	liver:	n/a	n/a
8	ATF2	chr4:22485174-22485556	GM12878	blood:	n/a	n/a
9	BACH1	chr4:22465025-22465108	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:22467709-22468003	GM12878	blood:	n/a	n/a
11	BATF	chr4:22485171-22485506	GM12878	blood:	n/a	n/a
12	BATF	chr4:22456697-22456973	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:22497824-22497994	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:22480127-22480357	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:22485135-22485505	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:22480635-22480793	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:22485182-22485421	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:22429384-22429649	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:22480094-22480806	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:22485205-22485500	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:22456620-22456873	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:22488879-22489010	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:22476315-22476977	HepG2	liver:	n/a	n/a
24	CBX3	chr4:22436583-22436925	HCT-116	colon:	n/a	n/a
25	CEBPB	chr4:22458027-22458258	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:22457973-22458338	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:22437242-22437704	HepG2	liver:	n/a	chr4:22437570-22437583 chr4:22437392-22437405 chr4:22437392-22437403
28	CEBPB	chr4:22485188-22485613	IMR90	lung:	n/a	chr4:22485401-22485412
29	CEBPB	chr4:22485220-22485600	Hela-S3	cervix:	n/a	chr4:22485401-22485412
30	CEBPB	chr4:22476253-22476646	HepG2	liver:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
31	CEBPB	chr4:22476298-22476627	Hela-S3	cervix:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
32	CEBPB	chr4:22474914-22475282	IMR90	lung:	n/a	chr4:22475101-22475112
33	CEBPB	chr4:22475010-22475226	K562	blood:	n/a	chr4:22475101-22475112
34	CEBPB	chr4:22485276-22485494	HepG2	liver:	n/a	chr4:22485401-22485412
35	CEBPB	chr4:22474919-22475425	HCT-116	colon:	n/a	chr4:22475101-22475112
36	CEBPB	chr4:22474955-22475186	K562	blood:	n/a	chr4:22475101-22475112
37	CEBPB	chr4:22474370-22474636	HepG2	liver:	n/a	chr4:22474479-22474492 chr4:22474480-22474491
38	CEBPB	chr4:22498049-22498440	IMR90	lung:	n/a	chr4:22498236-22498249 chr4:22498236-22498249
39	CEBPB	chr4:22476284-22476644	H1-hESC	embryonic stem cell:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
40	CEBPB	chr4:22476270-22476653	HepG2	liver:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
41	CEBPB	chr4:22458032-22458354	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:22474830-22475399	HCT-116	colon:	n/a	chr4:22475101-22475112
43	CEBPB	chr4:22476127-22477207	HCT-116	colon:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
44	CEBPB	chr4:22476288-22477066	IMR90	lung:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
45	CEBPB	chr4:22474907-22475304	Hela-S3	cervix:	n/a	chr4:22475101-22475112
46	CEBPB	chr4:22476256-22476577	HepG2	liver:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
47	CEBPB	chr4:22474313-22474652	IMR90	lung:	n/a	chr4:22474479-22474492 chr4:22474480-22474491
48	CEBPB	chr4:22476363-22476538	HepG2	liver:	n/a	chr4:22476452-22476465 chr4:22476454-22476465 chr4:22476452-22476463 chr4:22476454-22476465 chr4:22476452-22476465
49	CEBPB	chr4:22439558-22439755	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:22484146-22484392	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22483053-22483103	PANC-1	pancreas:	n/a
2	chr4:22483053-22483103	HepG2	liver:	n/a
3	chr4:22437783-22437833	Hepatocyte	liver:	n/a
4	chr4:22437783-22437833	ProgFib	skin:	n/a
5	chr4:22437783-22437833	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:22437783-22437833	NHDF-neo	bronchial:	n/a
7	chr4:22437783-22437833	IMR90	lung:	fetal
8	chr4:22437783-22437833	NHBE	bronchial:	n/a
9	chr4:22461750-22461800	PFSK-1	brain:	n/a
10	chr4:22437783-22437833	HRE	kidney:	n/a
11	chr4:22493281-22493331	T-47D	breast:	n/a
12	chr4:22476976-22477026	HUVEC	blood vessel:	n/a
13	chr4:22493281-22493331	HCF	heart:	n/a
14	chr4:22461750-22461800	BE2_C	brain:	n/a
15	chr4:22437783-22437833	CMK	blood:	n/a
16	chr4:22437783-22437833	BJ	skin:	n/a
17	chr4:22461750-22461800	H1-hESC	embryonic stem cell:	embryo
18	chr4:22493281-22493331	HepG2	liver:	n/a
19	chr4:22476976-22477026	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:22476976-22477026	CMK	blood:	n/a
21	chr4:22461750-22461800	ProgFib	skin:	n/a
22	chr4:22493281-22493331	HEEpiC	esophagus:	n/a
23	chr4:22483053-22483103	NHDF-neo	bronchial:	n/a
24	chr4:22493281-22493331	NT2-D1	testis:	n/a
25	chr4:22437783-22437833	Hela-S3	cervix:	n/a
26	chr4:22476976-22477026	HRCEpiC	kidney:	n/a
27	chr4:22483053-22483103	SKMC	muscle:	n/a
28	chr4:22476976-22477026	BE2_C	brain:	n/a
29	chr4:22493281-22493331	SKMC	muscle:	n/a
30	chr4:22437783-22437833	SKMC	muscle:	n/a
31	chr4:22476976-22477026	NT2-D1	testis:	n/a
32	chr4:22476976-22477026	SK-N-SH	brain:	n/a
33	chr4:22476976-22477026	AG04450	lung:	fetal
34	chr4:22476976-22477026	NHBE	bronchial:	n/a
35	chr4:22437783-22437833	MCF-7	breast:	n/a
36	chr4:22461750-22461800	K562	blood:	n/a
37	chr4:22483053-22483103	AG10803	skin:	n/a
38	chr4:22483053-22483103	GM06990	blood:	n/a
39	chr4:22461750-22461800	Jurkat	blood:	n/a
40	chr4:22437783-22437833	HEK293	kidney:	embryo
41	chr4:22476976-22477026	MCF-7	breast:	n/a
42	chr4:22483053-22483103	AG04450	lung:	fetal
43	chr4:22493281-22493331	NHBE	bronchial:	n/a
44	chr4:22493281-22493331	HCM	heart:	n/a
45	chr4:22476976-22477026	K562	blood:	n/a
46	chr4:22461750-22461800	HRPEpiC	eye:	n/a
47	chr4:22461750-22461800	HCPEpiC	choroid plexus:	n/a
48	chr4:22461750-22461800	SAEC	small airway:	n/a
49	chr4:22437783-22437833	HRCEpiC	kidney:	n/a
50	chr4:22493281-22493331	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:22486301..22488142-chr4:22490876..22493757,2	MCF-7	breast:
2	chr4:22425322..22428021-chr4:22430037..22432573,2	MCF-7	breast:
3	chr4:22436354..22437178-chr4:22608677..22609430,4	MCF-7	breast:
4	chr4:22487743..22489336-chr4:22491654..22493275,2	K562	blood:
5	chr4:22433445..22435816-chr4:22516699..22518877,2	MCF-7	breast:
6	chr4:22452403..22454410-chr4:22458067..22459809,2	MCF-7	breast:
7	chr4:22488399..22490950-chr4:22493521..22495053,2	MCF-7	breast:
8	chr4:22466142..22467676-chr4:22473054..22475391,2	K562	blood:
9	chr4:22486301..22488142-chr4:22490876..22493757,2	MCF-7	breast:
10	chr4:22500720..22505653-chr4:22515837..22519334,6	MCF-7	breast:
11	chr4:22425322..22428021-chr4:22430037..22432573,2	MCF-7	breast:
12	chr4:22487490..22489243-chr4:22491775..22493390,2	K562	blood:
13	chr4:22466667..22470398-chr4:22474006..22476709,3	MCF-7	breast:
14	chr4:22449726..22452368-chr4:22458347..22461364,3	MCF-7	breast:
15	chr4:22465182..22467125-chr4:22517057..22519339,2	MCF-7	breast:
16	chr4:22487490..22489243-chr4:22491775..22493390,2	K562	blood:
17	chr4:22491618..22493227-chr4:22516915..22519248,2	MCF-7	breast:
18	chr4:22449726..22452368-chr4:22458347..22461364,3	MCF-7	breast:
19	chr4:22487743..22489336-chr4:22491654..22493275,2	K562	blood:
20	chr4:22471253..22472855-chr4:22515638..22517354,2	MCF-7	breast:
21	chr4:22435935..22438268-chr4:22516437..22518541,2	MCF-7	breast:
22	chr4:22427307..22429305-chr4:22435269..22437253,2	K562	blood:
23	chr4:22452403..22454410-chr4:22458067..22459809,2	MCF-7	breast:
24	chr4:22466142..22467676-chr4:22473054..22475391,2	K562	blood:
25	chr4:22497592..22500394-chr4:22516759..22518508,2	MCF-7	breast:
26	chr10:75007030..75007602-chr4:22476562..22477062,2	Hela-S3	cervix:
27	chr4:22437735..22439383-chr4:22516765..22518580,2	MCF-7	breast:
28	chr4:22457536..22463707-chr4:22514115..22518559,7	MCF-7	breast:
29	chr4:22427307..22429305-chr4:22435269..22437253,2	K562	blood:
30	chr4:22488399..22490950-chr4:22493521..22495053,2	MCF-7	breast:

Variant related genes	Relation type
GPR125	TF binding region
GPR125	CpG island
ENSG00000251516	chromatin interactions
ENSG00000152990	chromatin interactions
ENSG00000236756	chromatin interactions

Extended variants
information (count: 3655 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3655 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10002842	chr4:22414023-22414024	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529114064	chr4:22414094-22414095	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs34067286	chr4:22414156-22414157	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs12331257	chr4:22414210-22414211	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs565837213	chr4:22414262-22414263	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534057863	chr4:22414263-22414264	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552208548	chr4:22414265-22414266	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs36064474	chr4:22414267-22414268	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570522879	chr4:22414272-22414273	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577097528	chr4:22414328-22414329	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7435129	chr4:22414376-22414377	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556464821	chr4:22414386-22414387	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186728042	chr4:22414388-22414389	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545678598	chr4:22414397-22414398	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77074438	chr4:22414416-22414417	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191588803	chr4:22414468-22414469	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150600021	chr4:22414546-22414547	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73800936	chr4:22414554-22414555	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576154493	chr4:22414573-22414574	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17531579	chr4:22414608-22414609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562050228	chr4:22414616-22414617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529193066	chr4:22414654-22414655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200069328	chr4:22414699-22414700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547643846	chr4:22414706-22414707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75149073	chr4:22414707-22414708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7697042	chr4:22414708-22414709	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs533110107	chr4:22414709-22414710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552298310	chr4:22414710-22414711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74406494	chr4:22414712-22414713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372272654	chr4:22414715-22414716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367721102	chr4:22414722-22414723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150998541	chr4:22414723-22414724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570588434	chr4:22414726-22414727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537881005	chr4:22414728-22414729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549776155	chr4:22414731-22414732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568414776	chr4:22414748-22414749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369954722	chr4:22414755-22414756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535776386	chr4:22414765-22414766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372551119	chr4:22414766-22414767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374821325	chr4:22414775-22414776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368930660	chr4:22414780-22414781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370462836	chr4:22414788-22414789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372920953	chr4:22414834-22414835	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs61736470	chr4:22414862-22414863	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372587041	chr4:22414866-22414867	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140116910	chr4:22414873-22414874	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561661155	chr4:22414875-22414876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142367791	chr4:22414916-22414917	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs151265183	chr4:22414919-22414920	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572591405	chr4:22414932-22414933	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22368800-22418600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:22371600-22449800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:22383200-22438000	Weak transcription	Lung	lung
4	chr4:22383600-22442800	Weak transcription	A549	lung
5	chr4:22385400-22430400	Weak transcription	Psoas Muscle	Psoas
6	chr4:22386000-22446600	Weak transcription	Fetal Thymus	thymus
7	chr4:22388000-22416600	Weak transcription	NHLF	lung
8	chr4:22388200-22432400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:22388200-22442800	Weak transcription	Brain Germinal Matrix	brain
10	chr4:22388400-22417800	Weak transcription	HUVEC	blood vessel
11	chr4:22388400-22473600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr4:22388800-22469600	Weak transcription	Colonic Mucosa	Colon
13	chr4:22389200-22473600	Weak transcription	Fetal Brain Male	brain
14	chr4:22390200-22414800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:22390600-22423600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr4:22390600-22439600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr4:22390600-22456200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr4:22390600-22459800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr4:22390800-22418000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:22390800-22420400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr4:22390800-22421400	Weak transcription	HepG2	liver
22	chr4:22390800-22429400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:22391400-22415400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:22393000-22435200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:22393400-22444800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr4:22393600-22459800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:22393800-22418000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:22393800-22446400	Weak transcription	NH-A	brain
29	chr4:22393800-22453000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:22397000-22428400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:22398400-22423200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:22399000-22416800	Strong transcription	Liver	Liver
33	chr4:22399800-22442800	Weak transcription	Fetal Brain Female	brain
34	chr4:22400000-22448000	Weak transcription	Left Ventricle	heart
35	chr4:22400600-22419800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr4:22400800-22422000	Weak transcription	HSMMtube	muscle
37	chr4:22400800-22429200	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr4:22400800-22430000	Weak transcription	Adipose Nuclei	Adipose
39	chr4:22400800-22449600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:22400800-22461800	Weak transcription	Gastric	stomach
41	chr4:22401000-22419600	Weak transcription	Aorta	Aorta
42	chr4:22401000-22425000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:22401200-22431000	Weak transcription	Ovary	ovary
44	chr4:22401400-22423600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:22401600-22418000	Weak transcription	Colon Smooth Muscle	Colon
46	chr4:22402400-22419800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr4:22404600-22414800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:22405000-22424200	Weak transcription	Fetal Kidney	kidney
49	chr4:22405200-22414400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr4:22405400-22422600	Weak transcription	NHEK	skin

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