Variant report

Variant	nsv901592
Chromosome Location	chr14:32093548-32267323
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	chr14:32256644-32256965	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:32186760-32187276	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:32256749-32256838	K562	blood:	n/a	n/a
4	ARID3A	chr14:32153639-32153640	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:32217355-32217854	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:32094871-32095254	HepG2	liver:	n/a	chr14:32095223-32095239 chr14:32095224-32095240
7	ATF3	chr14:32256603-32256876	K562	blood:	n/a	n/a
8	BATF	chr14:32222145-32222496	GM12878	blood:	n/a	chr14:32222322-32222333
9	BATF	chr14:32222193-32222405	GM12878	blood:	n/a	chr14:32222322-32222333
10	BHLHE40	chr14:32186771-32187135	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:32186621-32187204	HepG2	liver:	n/a	n/a
12	BRCA1	chr14:32144763-32144831	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr14:32122437-32122625	K562	blood:	n/a	n/a
14	CBX3	chr14:32250769-32251134	HCT-116	colon:	n/a	n/a
15	CEBPB	chr14:32175933-32176008	A549	lung:	n/a	n/a
16	CEBPB	chr14:32239633-32239833	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:32162063-32162385	HepG2	liver:	n/a	chr14:32162190-32162207
18	CEBPB	chr14:32217458-32217785	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:32244074-32244421	IMR90	lung:	n/a	chr14:32244239-32244250
20	CEBPB	chr14:32169086-32169350	A549	lung:	n/a	chr14:32169236-32169247 chr14:32169195-32169206
21	CEBPB	chr14:32239392-32239922	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:32186739-32187242	HepG2	liver:	n/a	chr14:32186929-32186942 chr14:32186931-32186942
23	CEBPB	chr14:32186672-32187188	HepG2	liver:	n/a	chr14:32186929-32186942 chr14:32186931-32186942
24	CEBPB	chr14:32243986-32244377	HepG2	liver:	n/a	chr14:32244239-32244250
25	CEBPB	chr14:32094855-32095184	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:32239723-32239825	A549	lung:	n/a	n/a
27	CEBPB	chr14:32120554-32120775	A549	lung:	n/a	chr14:32120672-32120681 chr14:32120670-32120681 chr14:32120671-32120682 chr14:32120669-32120686
28	CEBPB	chr14:32186755-32187113	HepG2	liver:	n/a	chr14:32186929-32186942 chr14:32186931-32186942
29	CEBPB	chr14:32141932-32142313	HepG2	liver:	n/a	chr14:32142101-32142110 chr14:32142099-32142110 chr14:32142101-32142110 chr14:32142099-32142112 chr14:32142099-32142112 chr14:32142101-32142112 chr14:32142101-32142110 chr14:32142101-32142110
30	CEBPB	chr14:32227682-32227948	HepG2	liver:	n/a	chr14:32227828-32227839 chr14:32227827-32227838 chr14:32227798-32227809
31	CEBPB	chr14:32212588-32212735	HepG2	liver:	n/a	chr14:32212641-32212652
32	CEBPB	chr14:32118207-32118445	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:32142001-32142217	A549	lung:	n/a	chr14:32142101-32142110 chr14:32142099-32142110 chr14:32142101-32142110 chr14:32142099-32142112 chr14:32142099-32142112 chr14:32142101-32142112 chr14:32142101-32142110 chr14:32142101-32142110
34	CEBPB	chr14:32164080-32164384	IMR90	lung:	n/a	chr14:32164212-32164221 chr14:32164211-32164222
35	CEBPB	chr14:32164170-32164372	A549	lung:	n/a	chr14:32164212-32164221 chr14:32164211-32164222
36	CEBPB	chr14:32186819-32187100	HepG2	liver:	n/a	chr14:32186929-32186942 chr14:32186931-32186942
37	CEBPB	chr14:32244108-32244346	A549	lung:	n/a	chr14:32244239-32244250
38	CEBPB	chr14:32120512-32120823	HepG2	liver:	n/a	chr14:32120672-32120681 chr14:32120670-32120681 chr14:32120671-32120682 chr14:32120669-32120686
39	CEBPB	chr14:32169057-32169356	HepG2	liver:	n/a	chr14:32169236-32169247 chr14:32169195-32169206
40	CEBPB	chr14:32239638-32239883	K562	blood:	n/a	n/a
41	CEBPB	chr14:32164045-32164380	HepG2	liver:	n/a	chr14:32164212-32164221 chr14:32164211-32164222
42	CEBPB	chr14:32120587-32120791	K562	blood:	n/a	chr14:32120672-32120681 chr14:32120670-32120681 chr14:32120671-32120682 chr14:32120669-32120686
43	CEBPB	chr14:32120539-32120750	IMR90	lung:	n/a	chr14:32120672-32120681 chr14:32120670-32120681 chr14:32120671-32120682 chr14:32120669-32120686
44	CEBPB	chr14:32217421-32217831	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:32118165-32118498	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:32141936-32142271	IMR90	lung:	n/a	chr14:32142101-32142110 chr14:32142099-32142110 chr14:32142101-32142110 chr14:32142099-32142112 chr14:32142099-32142112 chr14:32142101-32142112 chr14:32142101-32142110 chr14:32142101-32142110
47	CEBPD	chr14:32186726-32187123	HepG2	liver:	n/a	chr14:32186930-32186941
48	CEBPZ	chr14:32209927-32209942	HepG2	liver:	n/a	n/a
49	CHD2	chr14:32137943-32138054	HepG2	liver:	n/a	n/a
50	CHD2	chr14:32222097-32222319	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32180736-32180786	GM12891	blood:	n/a
2	chr14:32169802-32169852	AG10803	skin:	n/a
3	chr14:32109281-32109331	AoSMC	blood vessel:	n/a
4	chr14:32180736-32180786	PFSK-1	brain:	n/a
5	chr14:32170077-32170127	SK-N-SH	brain:	n/a
6	chr14:32181048-32181098	NHDF-neo	bronchial:	n/a
7	chr14:32180736-32180786	HAEpiC	amniotic membrane:	n/a
8	chr14:32180736-32180786	ProgFib	skin:	n/a
9	chr14:32170077-32170127	HCPEpiC	choroid plexus:	n/a
10	chr14:32169802-32169852	LNCaP	prostate:	n/a
11	chr14:32169802-32169852	MCF10A-Er-Src	breast:	n/a
12	chr14:32181048-32181098	HAEpiC	amniotic membrane:	n/a
13	chr14:32181048-32181098	GM06990	blood:	n/a
14	chr14:32181048-32181098	HMEC	breast:	n/a
15	chr14:32181048-32181098	HL-60	blood:	n/a
16	chr14:32170077-32170127	AG04449	skin:	fetal
17	chr14:32170077-32170127	GM12878	blood:	n/a
18	chr14:32109281-32109331	PFSK-1	brain:	n/a
19	chr14:32109281-32109331	K562	blood:	n/a
20	chr14:32170077-32170127	HUVEC	blood vessel:	n/a
21	chr14:32169802-32169852	SK-N-SH	brain:	n/a
22	chr14:32181048-32181098	AG04450	lung:	fetal
23	chr14:32109281-32109331	SK-N-SH_RA	brain:	n/a
24	chr14:32109281-32109331	HMEC	breast:	n/a
25	chr14:32180736-32180786	AG04449	skin:	fetal
26	chr14:32169802-32169852	HNPCEpiC	eye:	n/a
27	chr14:32181048-32181098	AG09309	skin:	n/a
28	chr14:32181048-32181098	HEEpiC	esophagus:	n/a
29	chr14:32170077-32170127	HCT-116	colon:	n/a
30	chr14:32180736-32180786	AG09309	skin:	n/a
31	chr14:32109281-32109331	AG04450	lung:	fetal
32	chr14:32181048-32181098	MCF-7	breast:	n/a
33	chr14:32109281-32109331	SKMC	muscle:	n/a
34	chr14:32169802-32169852	AG04449	skin:	fetal
35	chr14:32180736-32180786	HCPEpiC	choroid plexus:	n/a
36	chr14:32170077-32170127	SKMC	muscle:	n/a
37	chr14:32181048-32181098	K562	blood:	n/a
38	chr14:32181048-32181098	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:32170077-32170127	AG09319	gingival:	n/a
40	chr14:32169802-32169852	SK-N-SH_RA	brain:	n/a
41	chr14:32180736-32180786	HNPCEpiC	eye:	n/a
42	chr14:32169802-32169852	GM12878	blood:	n/a
43	chr14:32170077-32170127	IMR90	lung:	fetal
44	chr14:32169802-32169852	A549	lung:	n/a
45	chr14:32181048-32181098	IMR90	lung:	fetal
46	chr14:32109281-32109331	Hela-S3	cervix:	n/a
47	chr14:32180736-32180786	RPTEC	kidney:	n/a
48	chr14:32170077-32170127	SK-N-SH_RA	brain:	n/a
49	chr14:32109281-32109331	AG09309	skin:	n/a
50	chr14:32169802-32169852	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:32123058..32124663-chr14:32126123..32128762,2	K562	blood:
2	chr14:32247374..32249738-chr14:32259732..32262061,2	MCF-7	breast:
3	chr14:32146895..32147481-chr14:32713372..32714254,2	MCF-7	breast:
4	chr14:32123058..32124663-chr14:32126123..32128762,2	K562	blood:
5	chr14:32195719..32197688-chr14:32198704..32200404,2	MCF-7	breast:
6	chr14:32195719..32197688-chr14:32198704..32200404,2	MCF-7	breast:
7	chr14:32250042..32252755-chr14:32254053..32255704,2	MCF-7	breast:
8	chr14:31979147..31979905-chr14:32256388..32256891,2	MCF-7	breast:
9	chr14:32250042..32252755-chr14:32254053..32255704,2	MCF-7	breast:
10	chr14:32247374..32249738-chr14:32259732..32262061,2	MCF-7	breast:

Variant related genes	Relation type
NUBPL	TF binding region
RNU6-602P	TF binding region
RNU6-455P	TF binding region
NUBPL	CpG island
RNU6-602P	CpG island
RNU6-455P	CpG island

Extended variants
information (count: 7060 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7060 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7142881	chr14:32093548-32093549	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs74589678	chr14:32093554-32093555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61995634	chr14:32093631-32093632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192525499	chr14:32093700-32093701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575658120	chr14:32093745-32093746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543697484	chr14:32093747-32093748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184232012	chr14:32093763-32093764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533958673	chr14:32093818-32093819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34897588	chr14:32093854-32093855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576927228	chr14:32093857-32093858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540870454	chr14:32093866-32093867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376661563	chr14:32093895-32093896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188339975	chr14:32093896-32093897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7143323	chr14:32093915-32093916	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs561244640	chr14:32093916-32093917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs193188227	chr14:32093944-32093945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550443348	chr14:32094013-32094014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145182880	chr14:32094014-32094015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373006611	chr14:32094016-32094017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113043168	chr14:32094024-32094025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532694469	chr14:32094039-32094040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374952298	chr14:32094056-32094057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547686938	chr14:32094061-32094062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574264584	chr14:32094096-32094097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542260713	chr14:32094100-32094101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565965206	chr14:32094115-32094116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184659432	chr14:32094150-32094151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535918442	chr14:32094158-32094159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116779111	chr14:32094169-32094170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs80221314	chr14:32094190-32094191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10133316	chr14:32094206-32094207	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188635952	chr14:32094280-32094281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12885499	chr14:32094309-32094310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147583553	chr14:32094332-32094333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12885660	chr14:32094381-32094382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142204459	chr14:32094400-32094401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571641839	chr14:32094454-32094455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143772305	chr14:32094455-32094456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149710157	chr14:32094463-32094464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543141219	chr14:32094471-32094472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561411102	chr14:32094490-32094491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191148936	chr14:32094501-32094502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556405779	chr14:32094523-32094524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183657056	chr14:32094552-32094553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565547085	chr14:32094561-32094562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189151820	chr14:32094575-32094576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548095961	chr14:32094578-32094579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376099876	chr14:32094639-32094640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145648417	chr14:32094643-32094644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530271211	chr14:32094648-32094649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32046200-32110600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:32069600-32102800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr14:32088000-32093600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr14:32092000-32096000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr14:32092000-32096400	Weak transcription	Fetal Lung	lung
6	chr14:32092200-32093800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:32092200-32099000	Weak transcription	Aorta	Aorta
8	chr14:32092200-32099600	Weak transcription	Brain Hippocampus Middle	brain
9	chr14:32092200-32100400	Weak transcription	Rectal Smooth Muscle	rectum
10	chr14:32092400-32094800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr14:32092400-32100600	Weak transcription	Left Ventricle	heart
12	chr14:32092400-32103000	Weak transcription	Primary T cells from cord blood	blood
13	chr14:32092800-32094200	Weak transcription	Fetal Intestine Large	intestine
14	chr14:32092800-32096000	Weak transcription	Fetal Intestine Small	intestine
15	chr14:32092800-32096200	Weak transcription	Lung	lung
16	chr14:32093200-32094200	Weak transcription	HepG2	liver
17	chr14:32093200-32102800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr14:32094200-32095800	Enhancers	HepG2	liver
19	chr14:32095000-32096200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:32096000-32096200	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr14:32096200-32096800	Active TSS	Colon Smooth Muscle	Colon
22	chr14:32096400-32096800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr14:32096400-32097000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:32096800-32097800	Weak transcription	Colon Smooth Muscle	Colon
25	chr14:32097800-32098200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr14:32097800-32098200	Enhancers	Colon Smooth Muscle	Colon
27	chr14:32098200-32099800	Weak transcription	Colon Smooth Muscle	Colon
28	chr14:32099800-32100800	Enhancers	Colon Smooth Muscle	Colon
29	chr14:32100200-32101000	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr14:32100400-32100800	Enhancers	Rectal Smooth Muscle	rectum
31	chr14:32100600-32100800	Enhancers	Brain Hippocampus Middle	brain
32	chr14:32101200-32101600	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr14:32101800-32102200	Weak transcription	Aorta	Aorta
34	chr14:32102200-32102800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr14:32102800-32103200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
36	chr14:32102800-32103200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr14:32103000-32103200	Active TSS	Primary T cells from cord blood	blood
38	chr14:32109200-32109600	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr14:32109200-32109800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:32109800-32115400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr14:32110600-32112200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:32112200-32123200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:32114000-32116200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:32114200-32120400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr14:32115200-32115800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
46	chr14:32115400-32115600	ZNF genes & repeats	Pancreas	Pancrea
47	chr14:32115400-32115800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:32115600-32116800	Weak transcription	Pancreas	Pancrea
49	chr14:32116600-32117800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:32116600-32125000	Weak transcription	Fetal Kidney	kidney

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