Variant report

Variant	esv3390097
Chromosome Location	chr14:65002586-65009255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:1954)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:65006955-65007349	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr14:65006929-65007426	GM12878	blood:	n/a	n/a
3	BACH1	chr14:65006887-65007225	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr14:65007183-65008002	A549	lung:	n/a	n/a
5	BCLAF1	chr14:65006901-65007368	GM12878	blood:	n/a	chr14:65006939-65006948
6	BHLHE40	chr14:65006894-65007608	A549	lung:	n/a	chr14:65007383-65007399
7	BHLHE40	chr14:65006864-65007301	HepG2	liver:	n/a	n/a
8	BHLHE40	chr14:65006699-65007391	GM12878	blood:	n/a	n/a
9	BRCA1	chr14:65006860-65007383	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr14:65007118-65007280	HepG2	liver:	n/a	n/a
11	BRCA1	chr14:65007071-65007269	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:65005451-65005759	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr14:65003387-65003912	A549	lung:	n/a	chr14:65003702-65003713
14	CEBPB	chr14:65006967-65007205	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:65003134-65004052	A549	lung:	n/a	chr14:65003702-65003713
16	CEBPB	chr14:65005436-65005751	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:65003608-65003918	HepG2	liver:	n/a	chr14:65003702-65003713
18	CEBPB	chr14:65005360-65005853	MCF-7	breast:	n/a	n/a
19	CEBPB	chr14:65005448-65005772	IMR90	lung:	n/a	n/a
20	CEBPB	chr14:65005431-65005756	A549	lung:	n/a	n/a
21	CEBPB	chr14:65005461-65005981	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:65003586-65003980	A549	lung:	n/a	chr14:65003702-65003713
23	CEBPB	chr14:65003593-65003944	Hela-S3	cervix:	n/a	chr14:65003702-65003713
24	CEBPB	chr14:65003668-65003902	H1-hESC	embryonic stem cell:	n/a	chr14:65003702-65003713
25	CEBPB	chr14:65003352-65003950	IMR90	lung:	n/a	chr14:65003702-65003713
26	CEBPB	chr14:65006862-65007359	Hela-S3	cervix:	n/a	n/a
27	CHD1	chr14:65006145-65006370	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr14:65006153-65006344	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr14:65006939-65007621	GM12878	blood:	n/a	chr14:65007446-65007456
30	CHD2	chr14:65006788-65007514	Hela-S3	cervix:	n/a	chr14:65007446-65007456
31	CHD2	chr14:65006994-65007214	HepG2	liver:	n/a	n/a
32	CHD2	chr14:65006762-65007757	H1-hESC	embryonic stem cell:	n/a	chr14:65007446-65007456
33	CREB1	chr14:65006811-65007456	HepG2	liver:	n/a	n/a
34	CREB1	chr14:65006850-65007375	ECC-1	luminal epithelium:	n/a	n/a
35	CREB1	chr14:65006830-65007578	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr14:65006790-65007684	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr14:65006715-65007802	A549	lung:	n/a	n/a
38	CREB1	chr14:65006901-65007286	A549	lung:	n/a	n/a
39	CREB1	chr14:65006801-65007544	GM12878	blood:	n/a	n/a
40	CREB1	chr14:65007297-65007570	A549	lung:	n/a	n/a
41	CREB1	chr14:65006841-65007573	HepG2	liver:	n/a	n/a
42	CTCF	chr14:65007120-65007270	GM12864	blood:	n/a	chr14:65007186-65007199 chr14:65007189-65007202
43	CTCF	chr14:65007080-65007230	AG09309	skin:	n/a	chr14:65007186-65007199 chr14:65007189-65007202
44	CTCF	chr14:65007566-65007571	NHEK	skin:	n/a	n/a
45	CTCF	chr14:65007080-65007230	NHDF-neo	bronchial:	n/a	chr14:65007186-65007199 chr14:65007189-65007202
46	CTCF	chr14:65006760-65006910	GM12870	blood:	n/a	n/a
47	CTCF	chr14:65007048-65007306	ProgFib	skin:	n/a	chr14:65007186-65007199 chr14:65007189-65007202
48	CTCF	chr14:65007100-65007250	GM12869	blood:	n/a	chr14:65007186-65007199 chr14:65007189-65007202
49	CTCF	chr14:65007120-65007270	A549	lung:	n/a	chr14:65007186-65007199 chr14:65007189-65007202
50	CTCF	chr14:65007015-65007332	Fibrobl	skin:	n/a	chr14:65007186-65007199 chr14:65007189-65007202

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65006720-65006770	H1-hESC	embryonic stem cell:	embryo
2	chr14:65007437-65007487	HAEpiC	amniotic membrane:	n/a
3	chr14:65006720-65006770	H1-hESC	embryonic stem cell:	embryo
4	chr14:65007437-65007487	HAEpiC	amniotic membrane:	n/a
5	chr14:65007061-65007111	NHDF-neo	bronchial:	n/a
6	chr14:65007171-65007221	Hela-S3	cervix:	n/a
7	chr14:65008641-65008691	HAEpiC	amniotic membrane:	n/a
8	chr14:65006875-65006925	GM19239	blood:	n/a
9	chr14:65007512-65007562	BE2_C	brain:	n/a
10	chr14:65006720-65006770	AG09319	gingival:	n/a
11	chr14:65007050-65007100	BJ	skin:	n/a
12	chr14:65006716-65006766	SK-N-SH_RA	brain:	n/a
13	chr14:65008641-65008691	NH-A	brain:	n/a
14	chr14:65006943-65006993	SK-N-MC	brain:	n/a
15	chr14:65006881-65006931	HCT-116	colon:	n/a
16	chr14:65006041-65006091	ProgFib	skin:	n/a
17	chr14:65006965-65007015	SK-N-SH	brain:	n/a
18	chr14:65006071-65006121	NHDF-neo	bronchial:	n/a
19	chr14:65006875-65006925	PrEC	prostate:	n/a
20	chr14:65006688-65006738	SKMC	muscle:	n/a
21	chr14:65007061-65007111	HIPEpiC	eye:	n/a
22	chr14:65006204-65006254	T-47D	breast:	n/a
23	chr14:65006041-65006091	PANC-1	pancreas:	n/a
24	chr14:65007327-65007377	HCM	heart:	n/a
25	chr14:65006170-65006220	HUVEC	blood vessel:	n/a
26	chr14:65007066-65007116	Hela-S3	cervix:	n/a
27	chr14:65006041-65006091	SK-N-SH_RA	brain:	n/a
28	chr14:65007512-65007562	HMEC	breast:	n/a
29	chr14:65007066-65007116	ProgFib	skin:	n/a
30	chr14:65006204-65006254	GM12891	blood:	n/a
31	chr14:65005951-65006001	Jurkat	blood:	n/a
32	chr14:65006951-65007001	HL-60	blood:	n/a
33	chr14:65006720-65006770	SK-N-SH	brain:	n/a
34	chr14:65006943-65006993	GM12878	blood:	n/a
35	chr14:65007061-65007111	SAEC	small airway:	n/a
36	chr14:65007096-65007146	Caco-2	colon:	n/a
37	chr14:65006053-65006103	CMK	blood:	n/a
38	chr14:65006943-65006993	BJ	skin:	n/a
39	chr14:65006071-65006121	HUVEC	blood vessel:	n/a
40	chr14:65007050-65007100	ovcar-3	ovarian:	n/a
41	chr14:65006823-65006873	HCPEpiC	choroid plexus:	n/a
42	chr14:65007512-65007562	HEEpiC	esophagus:	n/a
43	chr14:65007096-65007146	GM12892	blood:	n/a
44	chr14:65006222-65006272	GM12878	blood:	n/a
45	chr14:65006222-65006272	Caco-2	colon:	n/a
46	chr14:65006053-65006103	AG09309	skin:	n/a
47	chr14:65006965-65007015	MCF10A-Er-Src	breast:	n/a
48	chr14:65006716-65006766	MCF10A-Er-Src	breast:	n/a
49	chr14:65006716-65006766	MCF-7	breast:	n/a
50	chr14:65006359-65006409	PrEC	prostate:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65006312..65006877-chr18:3653628..3654511,2	HCT-116	colon:
2	chr14:65007817..65010307-chr14:65107845..65109704,2	MCF-7	breast:
3	chr14:65005458..65007740-chr14:65223841..65226148,2	MCF-7	breast:
4	chr14:65005138..65007971-chr14:65016762..65019337,2	MCF-7	breast:
5	chr14:65005373..65008937-chr14:65014849..65020282,8	MCF-7	breast:
6	chr14:64803941..64806112-chr14:65005957..65008329,2	MCF-7	breast:
7	chr14:65005088..65007392-chr14:65188450..65190752,3	MCF-7	breast:
8	chr14:64967941..64976890-chr14:65001097..65012463,31	MCF-7	breast:
9	chr14:64988143..64990019-chr14:65005055..65006993,2	MCF-7	breast:
10	chr14:64969721..64971407-chr14:65001897..65003648,2	K562	blood:
11	chr14:64969536..64972010-chr14:65003528..65005468,3	MCF-7	breast:
12	chr14:65006111..65008789-chr14:65009033..65011662,5	MCF-7	breast:
13	chr14:65006752..65008464-chr14:65051582..65054161,2	MCF-7	breast:
14	chr14:64969034..64974113-chr14:65005478..65010690,22	MCF-7	breast:
15	chr14:65006961..65009286-chr14:65016299..65018796,2	K562	blood:
16	chr14:65008751..65009279-chr14:65103132..65103948,2	MCF-7	breast:
17	chr14:64969193..64971407-chr14:65001217..65003397,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB25-3	chr14:65007035-65007086	NR_110550
2	lnc-ZBTB25-3	chr14:65007035-65007086	ENSG00000259116.1

No data

Variant related genes	Relation type
HSPA2	TF binding region
ENSG00000259116	TF binding region
ENSG00000259160	TF binding region
HSPA2	CpG island
ENSG00000259116	CpG island
ENSG00000259160	CpG island
ENSG00000126804	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000126822	chromatin interactions
ENSG00000140009	chromatin interactions
ENSG00000126803	chromatin interactions
ENSG00000165807	chromatin interactions
ENSG00000214770	chromatin interactions
ENSG00000070182	chromatin interactions
ENSG00000259116	chromatin interactions

Extended variants
information (count: 291 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534941142	chr14:65002586-65002587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs373952253	chr14:65002595-65002596	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368471143	chr14:65002597-65002598	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371970863	chr14:65002598-65002599	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376957033	chr14:65002599-65002600	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs45469496	chr14:65002600-65002601	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs190390335	chr14:65002605-65002606	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554422875	chr14:65002620-65002621	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs45625140	chr14:65002635-65002636	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147557907	chr14:65002636-65002637	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs556744601	chr14:65002657-65002658	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs531556709	chr14:65002661-65002662	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576488022	chr14:65002662-65002663	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs545384602	chr14:65002672-65002673	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs45559537	chr14:65002700-65002701	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs572601977	chr14:65002755-65002756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs45486597	chr14:65002919-65002920	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs150093128	chr14:65002998-65002999	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12432891	chr14:65003005-65003006	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs45457592	chr14:65003021-65003022	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563077725	chr14:65003025-65003026	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532092639	chr14:65003083-65003084	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551860660	chr14:65003194-65003195	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs149220285	chr14:65003195-65003196	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs528336267	chr14:65003271-65003272	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs548507186	chr14:65003276-65003277	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs45503604	chr14:65003335-65003336	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs537273190	chr14:65003344-65003345	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs546795624	chr14:65003371-65003372	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs565993359	chr14:65003392-65003393	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs45502099	chr14:65003393-65003394	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs546619581	chr14:65003460-65003461	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs570134710	chr14:65003521-65003522	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs539135769	chr14:65003605-65003606	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs143337874	chr14:65003652-65003653	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs185411743	chr14:65003668-65003669	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs555270986	chr14:65003670-65003671	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs574676846	chr14:65003702-65003703	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs547118806	chr14:65003742-65003743	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs7151628	chr14:65003747-65003748	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs554587700	chr14:65003826-65003827	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs7151976	chr14:65003891-65003892	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559078730	chr14:65003921-65003922	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs528138335	chr14:65003928-65003929	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs138989120	chr14:65003929-65003930	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs561926893	chr14:65003971-65003972	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs368587662	chr14:65003997-65003998	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs190221151	chr14:65004016-65004017	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs550746148	chr14:65004050-65004051	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs570667779	chr14:65004064-65004065	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Hematopoietic stem cell	20738155	CNVD
Cancer	17440070	CNVD
Intracranial arachnoid cysts	20187927	CNVD

Chromatin state (count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64974800-65006000	Weak transcription	Ovary	ovary
2	chr14:64976000-65006000	Weak transcription	Brain Germinal Matrix	brain
3	chr14:64978200-65006000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:64979200-65005800	Weak transcription	Brain Anterior Caudate	brain
5	chr14:64982000-65005800	Weak transcription	Fetal Heart	heart
6	chr14:64987800-65005000	Weak transcription	Pancreas	Pancrea
7	chr14:64989200-65006000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr14:64989800-65005800	Weak transcription	Right Ventricle	heart
9	chr14:64990200-65003400	Weak transcription	HSMMtube	muscle
10	chr14:64990200-65003400	Weak transcription	NHLF	lung
11	chr14:64990200-65005800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr14:64990200-65005800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr14:64990200-65005800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr14:64990200-65006000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr14:64990200-65006000	Weak transcription	Aorta	Aorta
16	chr14:64990200-65006000	Weak transcription	Fetal Muscle Leg	muscle
17	chr14:64990200-65006000	Weak transcription	Left Ventricle	heart
18	chr14:64990200-65006200	Weak transcription	Small Intestine	intestine
19	chr14:64990400-65003600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr14:64990400-65005800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr14:64990400-65005800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr14:64990400-65005800	Weak transcription	Adipose Nuclei	Adipose
23	chr14:64990400-65005800	Weak transcription	Fetal Kidney	kidney
24	chr14:64990400-65005800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:64990400-65005800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr14:64990400-65006000	Weak transcription	Fetal Intestine Large	intestine
27	chr14:64990600-65005800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr14:64990800-65005800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr14:64991000-65005600	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr14:64991000-65005600	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr14:64991400-65003200	Weak transcription	NHDF-Ad	bronchial
32	chr14:64992000-65005800	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr14:64992200-65005800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:64992400-65003400	Weak transcription	A549	lung
35	chr14:64992400-65003600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:64993200-65003400	Weak transcription	Hela-S3	cervix
37	chr14:64993400-65005800	Weak transcription	NH-A	brain
38	chr14:64993400-65005800	Weak transcription	NHEK	skin
39	chr14:64993600-65006000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr14:64993800-65003000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr14:64993800-65003200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:64993800-65003200	Weak transcription	Placenta	Placenta
43	chr14:64993800-65005400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr14:64993800-65005600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr14:64993800-65005800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr14:64993800-65005800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:64993800-65005800	Weak transcription	Fetal Intestine Small	intestine
48	chr14:64993800-65005800	Weak transcription	GM12878-XiMat	blood
49	chr14:64993800-65006000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr14:64993800-65006000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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