Variant report

Variant	esv1803430
Chromosome Location	chr14:81995306-82009830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:586)
CpG islands
(count:1038)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:82003417-82004185	HepG2	liver:	n/a	chr14:82003589-82003605
2	ARID3A	chr14:82000249-82000685	K562	blood:	n/a	n/a
3	ARID3A	chr14:82003648-82003859	K562	blood:	n/a	n/a
4	ARID3A	chr14:81999976-82001256	HepG2	liver:	n/a	n/a
5	ATF1	chr14:81995798-81996176	K562	blood:	n/a	n/a
6	ATF1	chr14:82000051-82000615	K562	blood:	n/a	n/a
7	ATF2	chr14:82001761-82002273	GM12878	blood:	n/a	n/a
8	ATF3	chr14:81995829-81996157	K562	blood:	n/a	n/a
9	ATF3	chr14:82000359-82000584	K562	blood:	n/a	n/a
10	ATF3	chr14:82000349-82000523	GM12878	blood:	n/a	n/a
11	BACH1	chr14:81999825-81999934	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr14:82001872-82002208	GM12878	blood:	n/a	n/a
13	BCL3	chr14:82006719-82006925	GM12878	blood:	n/a	n/a
14	BCLAF1	chr14:82000223-82000656	GM12878	blood:	n/a	chr14:82000303-82000312
15	BHLHE40	chr14:82000973-82001263	HepG2	liver:	n/a	n/a
16	BHLHE40	chr14:81996007-81996179	GM12878	blood:	n/a	n/a
17	BHLHE40	chr14:81999999-82001251	GM12878	blood:	n/a	n/a
18	BHLHE40	chr14:82003563-82003817	HepG2	liver:	n/a	n/a
19	BHLHE40	chr14:82001765-82002283	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:81999989-82000660	K562	blood:	n/a	n/a
21	BHLHE40	chr14:82000008-82000666	HepG2	liver:	n/a	n/a
22	BRCA1	chr14:82000068-82000707	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr14:82000010-82000330	HepG2	liver:	n/a	n/a
24	CBX3	chr14:82004543-82004882	K562	blood:	n/a	n/a
25	CBX3	chr14:82000142-82000685	K562	blood:	n/a	n/a
26	CBX3	chr14:82004585-82004855	K562	blood:	n/a	n/a
27	CCNT2	chr14:81995877-81996051	K562	blood:	n/a	n/a
28	CCNT2	chr14:81999899-82000409	K562	blood:	n/a	n/a
29	CEBPB	chr14:81995711-81996261	HCT-116	colon:	n/a	chr14:81995790-81995803 chr14:81995978-81995995 chr14:81995981-81995992
30	CEBPB	chr14:82000204-82000641	A549	lung:	n/a	n/a
31	CEBPB	chr14:81995799-81996178	IMR90	lung:	n/a	chr14:81995978-81995995 chr14:81995981-81995992
32	CEBPB	chr14:82000023-82000670	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:81995794-81996160	HepG2	liver:	n/a	chr14:81995978-81995995 chr14:81995981-81995992
34	CEBPB	chr14:82000079-82000696	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:82003583-82003925	HepG2	liver:	n/a	n/a
36	CEBPB	chr14:81995710-81996188	Hela-S3	cervix:	n/a	chr14:81995790-81995803 chr14:81995978-81995995 chr14:81995981-81995992
37	CEBPB	chr14:81995874-81996049	H1-hESC	embryonic stem cell:	n/a	chr14:81995978-81995995 chr14:81995981-81995992
38	CEBPB	chr14:81995729-81996216	K562	blood:	n/a	chr14:81995790-81995803 chr14:81995978-81995995 chr14:81995981-81995992
39	CEBPB	chr14:82000147-82000700	K562	blood:	n/a	n/a
40	CEBPB	chr14:81995791-81996176	K562	blood:	n/a	chr14:81995978-81995995 chr14:81995981-81995992
41	CEBPB	chr14:81999999-82000678	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr14:82003689-82003813	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:82002777-82003216	MCF-7	breast:	n/a	n/a
44	CEBPB	chr14:81995800-81996141	A549	lung:	n/a	chr14:81995978-81995995 chr14:81995981-81995992
45	CEBPB	chr14:81995679-81996222	HCT-116	colon:	n/a	chr14:81995790-81995803 chr14:81995978-81995995 chr14:81995981-81995992
46	CEBPB	chr14:81995842-81996123	K562	blood:	n/a	chr14:81995978-81995995 chr14:81995981-81995992
47	CEBPD	chr14:81999996-82000348	HepG2	liver:	n/a	n/a
48	CHD1	chr14:81999933-82000204	GM12878	blood:	n/a	chr14:82000164-82000174
49	CHD1	chr14:81999115-81999492	GM12878	blood:	n/a	n/a
50	CHD2	chr14:82001905-82002406	GM12878	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81999924-81999974	BJ	skin:	n/a
2	chr14:81999924-81999974	BJ	skin:	n/a
3	chr14:82000312-82000362	HRCEpiC	kidney:	n/a
4	chr14:82000246-82000296	HAEpiC	amniotic membrane:	n/a
5	chr14:82000050-82000100	AoSMC	blood vessel:	n/a
6	chr14:81998796-81998846	HRCEpiC	kidney:	n/a
7	chr14:82000382-82000432	ovcar-3	ovarian:	n/a
8	chr14:82000431-82000481	BJ	skin:	n/a
9	chr14:81999924-81999974	BE2_C	brain:	n/a
10	chr14:81999503-81999553	HCM	heart:	n/a
11	chr14:81999503-81999553	PFSK-1	brain:	n/a
12	chr14:82000431-82000481	ovcar-3	ovarian:	n/a
13	chr14:82000536-82000586	GM12892	blood:	n/a
14	chr14:81999924-81999974	HCF	heart:	n/a
15	chr14:82000250-82000300	HRPEpiC	eye:	n/a
16	chr14:82000026-82000076	BJ	skin:	n/a
17	chr14:82000431-82000481	MCF-7	breast:	n/a
18	chr14:82000050-82000100	ovcar-3	ovarian:	n/a
19	chr14:82000250-82000300	HCF	heart:	n/a
20	chr14:82000858-82000908	HRCEpiC	kidney:	n/a
21	chr14:82000382-82000432	Caco-2	colon:	n/a
22	chr14:82000050-82000100	PrEC	prostate:	n/a
23	chr14:82000258-82000308	ovcar-3	ovarian:	n/a
24	chr14:81998796-81998846	HEEpiC	esophagus:	n/a
25	chr14:82000312-82000362	H1-hESC	embryonic stem cell:	embryo
26	chr14:82000382-82000432	BE2_C	brain:	n/a
27	chr14:82000431-82000481	HRPEpiC	eye:	n/a
28	chr14:82000858-82000908	PFSK-1	brain:	n/a
29	chr14:82000433-82000483	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:82000312-82000362	NT2-D1	testis:	n/a
31	chr14:82000026-82000076	HUVEC	blood vessel:	n/a
32	chr14:81998796-81998846	CMK	blood:	n/a
33	chr14:81998796-81998846	T-47D	breast:	n/a
34	chr14:82000258-82000308	HUVEC	blood vessel:	n/a
35	chr14:82000312-82000362	HCPEpiC	choroid plexus:	n/a
36	chr14:82000246-82000296	IMR90	lung:	fetal
37	chr14:82002568-82002618	SK-N-SH	brain:	n/a
38	chr14:82000431-82000481	HRCEpiC	kidney:	n/a
39	chr14:82000858-82000908	BJ	skin:	n/a
40	chr14:82000382-82000432	NH-A	brain:	n/a
41	chr14:81999924-81999974	MCF-7	breast:	n/a
42	chr14:82000256-82000306	HL-60	blood:	n/a
43	chr14:82000382-82000432	SK-N-SH_RA	brain:	n/a
44	chr14:81999924-81999974	AG09309	skin:	n/a
45	chr14:82000026-82000076	HMEC	breast:	n/a
46	chr14:81997731-81997781	AG04449	skin:	fetal
47	chr14:82000258-82000308	MCF10A-Er-Src	breast:	n/a
48	chr14:81999503-81999553	HRCEpiC	kidney:	n/a
49	chr14:82000050-82000100	BE2_C	brain:	n/a
50	chr14:81998796-81998846	MCF-7	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81684769..81687229-chr14:81994691..81996758,3	MCF-7	breast:
2	chr14:81685821..81688367-chr14:81994101..81997507,5	K562	blood:
3	chr14:81686218..81688258-chr14:81998585..82000595,3	MCF-7	breast:
4	chr14:81982519..81985151-chr14:81994400..81995945,2	K562	blood:
5	chr14:81999215..82002071-chr14:82007539..82010769,3	MCF-7	breast:
6	chr14:81998367..82001361-chr15:65596794..65598307,2	MCF-7	breast:
7	chr14:81929424..81932136-chr14:81997102..81999064,2	K562	blood:
8	chr14:81998522..82000521-chr14:82004123..82005693,2	MCF-7	breast:
9	chr14:81995745..81998818-chr14:81999880..82001620,3	K562	blood:

No data

Variant related genes	Relation type
SEL1L	TF binding region
SEL1L	CpG island
ENSG00000165417	chromatin interactions
ENSG00000071537	chromatin interactions
ENSG00000200156	chromatin interactions

Extended variants
information (count: 568 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:568 , 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	rs1998386	chr14:81995306-81995307	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530616531	chr14:81995349-81995350	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527781067	chr14:81995526-81995527	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs138880858	chr14:81995541-81995542	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370016394	chr14:81995568-81995569	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs548766514	chr14:81995657-81995658	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs140573326	chr14:81995695-81995696	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs114761746	chr14:81995848-81995849	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs532802768	chr14:81995854-81995855	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs548014330	chr14:81995863-81995864	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572298342	chr14:81995894-81995895	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547740625	chr14:81995943-81995944	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs180768221	chr14:81995992-81995993	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533667170	chr14:81995994-81995995	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs116658691	chr14:81996002-81996003	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567180907	chr14:81996009-81996010	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs565921375	chr14:81996031-81996032	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538130399	chr14:81996032-81996033	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs185423290	chr14:81996049-81996050	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs577411479	chr14:81996051-81996052	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs575223672	chr14:81996075-81996076	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144779964	chr14:81996116-81996117	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs541576427	chr14:81996181-81996182	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs138586928	chr14:81996192-81996193	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs564544590	chr14:81996194-81996195	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542775566	chr14:81996318-81996319	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561312726	chr14:81996325-81996326	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs4903985	chr14:81996369-81996370	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34486996	chr14:81996386-81996387	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560644182	chr14:81996387-81996388	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190186471	chr14:81996421-81996422	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565531991	chr14:81996434-81996435	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs551787215	chr14:81996446-81996447	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs78245965	chr14:81996453-81996454	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs547977273	chr14:81996469-81996470	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566301427	chr14:81996495-81996496	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs181405046	chr14:81996547-81996548	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs78139975	chr14:81996589-81996590	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs567245953	chr14:81996614-81996615	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111601926	chr14:81996646-81996647	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs3069889	chr14:81996674-81996675	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs34289277	chr14:81996675-81996676	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs2371804	chr14:81996676-81996677	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs113823197	chr14:81996769-81996770	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs549367475	chr14:81996794-81996795	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186082098	chr14:81996798-81996799	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs571165552	chr14:81996820-81996821	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs375962222	chr14:81996842-81996843	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs35094352	chr14:81996863-81996864	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs1951607	chr14:81996878-81996879	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

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
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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81967600-81999600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:81973800-81999400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:81973800-81999400	Weak transcription	Esophagus	oesophagus
4	chr14:81974800-81998200	Weak transcription	Fetal Brain Male	brain
5	chr14:81981200-81999400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr14:81983200-81999400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:81983800-81999400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr14:81984000-81998800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:81984200-81999200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr14:81984400-81999400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr14:81986000-81998600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr14:81986400-81996600	Weak transcription	Psoas Muscle	Psoas
13	chr14:81986400-81997200	Weak transcription	Fetal Heart	heart
14	chr14:81986400-81998800	Weak transcription	Hela-S3	cervix
15	chr14:81987000-81998200	Weak transcription	Small Intestine	intestine
16	chr14:81987400-81998200	Weak transcription	Brain Angular Gyrus	brain
17	chr14:81987600-81998800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr14:81988000-81998400	Weak transcription	Stomach Mucosa	stomach
19	chr14:81988000-81998600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr14:81988200-81995600	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr14:81988600-81995400	Weak transcription	K562	blood
22	chr14:81989600-81998600	Weak transcription	Osteobl	bone
23	chr14:81989800-81999200	Weak transcription	Colonic Mucosa	Colon
24	chr14:81990000-81998600	Weak transcription	NHLF	lung
25	chr14:81990200-81998000	Weak transcription	Gastric	stomach
26	chr14:81990200-81998000	Weak transcription	Spleen	Spleen
27	chr14:81990200-81998600	Weak transcription	HMEC	breast
28	chr14:81990200-81999200	Weak transcription	Aorta	Aorta
29	chr14:81990800-81997200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr14:81990800-81999400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr14:81991200-81998200	Weak transcription	Thymus	Thymus
32	chr14:81991200-81998600	Weak transcription	Fetal Stomach	stomach
33	chr14:81991200-81998800	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr14:81991200-81999400	Weak transcription	Lung	lung
35	chr14:81991400-81995800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr14:81991400-81997800	Weak transcription	Right Ventricle	heart
37	chr14:81991400-81999000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr14:81991600-81995800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr14:81991600-81997000	Weak transcription	Fetal Brain Female	brain
40	chr14:81991600-81997800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr14:81991600-81997800	Weak transcription	Ovary	ovary
42	chr14:81991600-81998200	Weak transcription	Brain Germinal Matrix	brain
43	chr14:81991600-81998400	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr14:81991600-81998400	Weak transcription	Fetal Kidney	kidney
45	chr14:81991600-81998600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr14:81991600-81999400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:81991800-81996400	Weak transcription	Primary B cells from cord blood	blood
48	chr14:81991800-81996600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr14:81991800-81997600	Weak transcription	Fetal Intestine Small	intestine
50	chr14:81991800-81999200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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