Variant report

Variant	nsv901979
Chromosome Location	chr14:56740554-56802610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:384)
CpG islands
(count:429)
Chromatin interactive
region (count:15)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:56800461-56800677	K562	blood:	n/a	n/a
2	ATF1	chr14:56800409-56800721	K562	blood:	n/a	n/a
3	BACH1	chr14:56780639-56780839	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr14:56792219-56792416	K562	blood:	n/a	n/a
5	BHLHE40	chr14:56780626-56780753	K562	blood:	n/a	n/a
6	BHLHE40	chr14:56762527-56762767	K562	blood:	n/a	n/a
7	CBX3	chr14:56800296-56800855	HCT-116	colon:	n/a	n/a
8	CBX3	chr14:56785141-56785460	K562	blood:	n/a	n/a
9	CEBPB	chr14:56800481-56801059	IMR90	lung:	n/a	chr14:56800896-56800905
10	CEBPB	chr14:56790186-56790260	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:56798113-56798264	A549	lung:	n/a	n/a
12	CEBPB	chr14:56789236-56789524	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:56767257-56767550	IMR90	lung:	n/a	n/a
14	CEBPB	chr14:56758629-56758926	IMR90	lung:	n/a	chr14:56758786-56758797 chr14:56758788-56758797
15	CEBPB	chr14:56758653-56758955	HepG2	liver:	n/a	chr14:56758786-56758797 chr14:56758788-56758797
16	CEBPB	chr14:56798143-56798223	IMR90	lung:	n/a	n/a
17	CEBPB	chr14:56790106-56790315	IMR90	lung:	n/a	n/a
18	CEBPB	chr14:56792097-56792569	IMR90	lung:	n/a	chr14:56792376-56792387
19	CTCF	chr14:56756331-56756553	K562	blood:	n/a	chr14:56756449-56756465
20	CTCF	chr14:56760960-56761110	HBMEC	blood vessel:	n/a	chr14:56761039-56761052
21	CTCF	chr14:56747680-56747830	AG04450	lung:	n/a	n/a
22	CTCF	chr14:56747700-56747850	BE2_C	brain:	n/a	n/a
23	CTCF	chr14:56747700-56747850	GM12873	blood:	n/a	n/a
24	CTCF	chr14:56747720-56747870	AG04449	skin:	n/a	n/a
25	CTCF	chr14:56801340-56801490	HCM	heart:	n/a	n/a
26	CTCF	chr14:56766380-56766530	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr14:56756380-56756479	GM12892	blood:	n/a	chr14:56756449-56756465
28	CTCF	chr14:56760980-56761130	SAEC	small airway:	n/a	chr14:56761039-56761052
29	CTCF	chr14:56760940-56761090	NHLF	lung:	n/a	chr14:56761039-56761052
30	CTCF	chr14:56760960-56761110	GM12873	blood:	n/a	chr14:56761039-56761052
31	CTCF	chr14:56747880-56748030	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr14:56760980-56761130	GM12871	blood:	n/a	chr14:56761039-56761052
33	CTCF	chr14:56747720-56747870	HMEC	breast:	n/a	n/a
34	CTCF	chr14:56756405-56756456	GM19238	blood:	n/a	n/a
35	CTCF	chr14:56747660-56747810	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr14:56747720-56747870	AG10803	skin:	n/a	n/a
37	CTCF	chr14:56747740-56747890	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:56760920-56761070	RPTEC	kidney:	n/a	chr14:56761039-56761052
39	CTCF	chr14:56747731-56747832	HepG2	liver:	n/a	n/a
40	CTCF	chr14:56747720-56747870	GM12874	blood:	n/a	n/a
41	CTCF	chr14:56766440-56766590	AG09319	gingival:	n/a	n/a
42	CTCF	chr14:56766340-56766490	RPTEC	kidney:	n/a	n/a
43	CTCF	chr14:56760948-56761169	MCF-7	breast:	n/a	chr14:56761039-56761052
44	CTCF	chr14:56766463-56766524	K562	blood:	n/a	n/a
45	CTCF	chr14:56766360-56766510	AG04450	lung:	n/a	n/a
46	CTCF	chr14:56747740-56747890	BE2_C	brain:	n/a	n/a
47	CTCF	chr14:56760960-56761110	HRE	kidney:	n/a	chr14:56761039-56761052
48	CTCF	chr14:56747720-56747870	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr14:56798700-56798850	GM12866	blood:	n/a	n/a
50	CTCF	chr14:56760960-56761110	GM12865	blood:	n/a	chr14:56761039-56761052

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56740867-56740917	MCF10A-Er-Src	breast:	n/a
2	chr14:56800153-56800203	NB4	blood:	n/a
3	chr14:56740867-56740917	MCF10A-Er-Src	breast:	n/a
4	chr14:56800153-56800203	NB4	blood:	n/a
5	chr14:56800153-56800203	SKMC	muscle:	n/a
6	chr14:56792319-56792369	T-47D	breast:	n/a
7	chr14:56777251-56777301	Hela-S3	cervix:	n/a
8	chr14:56755262-56755312	MCF-7	breast:	n/a
9	chr14:56800153-56800203	NH-A	brain:	n/a
10	chr14:56777251-56777301	H1-hESC	embryonic stem cell:	embryo
11	chr14:56792319-56792369	HMEC	breast:	n/a
12	chr14:56740867-56740917	HIPEpiC	eye:	n/a
13	chr14:56800153-56800203	MCF-7	breast:	n/a
14	chr14:56792319-56792369	GM12892	blood:	n/a
15	chr14:56766873-56766923	AoSMC	blood vessel:	n/a
16	chr14:56777251-56777301	CMK	blood:	n/a
17	chr14:56777251-56777301	HCM	heart:	n/a
18	chr14:56766873-56766923	Caco-2	colon:	n/a
19	chr14:56755262-56755312	PrEC	prostate:	n/a
20	chr14:56792319-56792369	MCF-7	breast:	n/a
21	chr14:56766873-56766923	HCPEpiC	choroid plexus:	n/a
22	chr14:56766873-56766923	CMK	blood:	n/a
23	chr14:56755226-56755276	A549	lung:	n/a
24	chr14:56755226-56755276	Hepatocyte	liver:	n/a
25	chr14:56766873-56766923	HMEC	breast:	n/a
26	chr14:56777251-56777301	HCT-116	colon:	n/a
27	chr14:56777251-56777301	MCF10A-Er-Src	breast:	n/a
28	chr14:56755262-56755312	PANC-1	pancreas:	n/a
29	chr14:56800153-56800203	HCF	heart:	n/a
30	chr14:56777251-56777301	HRPEpiC	eye:	n/a
31	chr14:56755262-56755312	GM12878	blood:	n/a
32	chr14:56777251-56777301	Jurkat	blood:	n/a
33	chr14:56800153-56800203	GM12892	blood:	n/a
34	chr14:56755262-56755312	AG09319	gingival:	n/a
35	chr14:56766873-56766923	HNPCEpiC	eye:	n/a
36	chr14:56755262-56755312	A549	lung:	n/a
37	chr14:56755262-56755312	SAEC	small airway:	n/a
38	chr14:56740867-56740917	ECC-1	luminal epithelium:	n/a
39	chr14:56755226-56755276	NHDF-neo	bronchial:	n/a
40	chr14:56800153-56800203	GM19239	blood:	n/a
41	chr14:56800153-56800203	IMR90	lung:	fetal
42	chr14:56755262-56755312	GM19239	blood:	n/a
43	chr14:56766873-56766923	HL-60	blood:	n/a
44	chr14:56755262-56755312	H1-hESC	embryonic stem cell:	embryo
45	chr14:56777251-56777301	Hepatocyte	liver:	n/a
46	chr14:56800153-56800203	HUVEC	blood vessel:	n/a
47	chr14:56755226-56755276	Caco-2	colon:	n/a
48	chr14:56800153-56800203	AG04450	lung:	fetal
49	chr14:56755226-56755276	AG10803	skin:	n/a
50	chr14:56755226-56755276	HAEpiC	amniotic membrane:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:56769713..56772001-chr14:56773071..56775429,2	K562	blood:
2	chr14:56798962..56800809-chr14:56842457..56844323,2	K562	blood:
3	chr14:56221789..56224702-chr14:56769776..56771612,2	K562	blood:
4	chr14:56681835..56684539-chr14:56756557..56758766,2	K562	blood:
5	chr14:56794620..56796149-chr14:56801330..56803015,2	K562	blood:
6	chr14:56682968..56684539-chr14:56757092..56758766,2	K562	blood:
7	chr14:56735282..56738108-chr14:56741731..56743329,2	K562	blood:
8	chr14:56800511..56802640-chr14:56807027..56808554,2	K562	blood:
9	chr14:56331802..56332310-chr14:56747361..56748275,2	MCF-7	breast:
10	chr14:56714179..56714751-chr14:56760641..56761350,3	MCF-7	breast:
11	chr14:56656212..56658616-chr14:56744495..56746783,2	K562	blood:
12	chr14:56794620..56796149-chr14:56801330..56803015,2	K562	blood:
13	chr14:56769713..56772001-chr14:56773071..56775429,2	K562	blood:
14	chr14:56802231..56804890-chr14:56805110..56807908,2	K562	blood:
15	chr14:56643693..56645416-chr14:56800419..56803265,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PELI2-2	chr14:56777654-56777820	ENSG00000259719.1
2	lnc-PELI2-2	chr14:56777598-56777820	ENSG00000259719.1
3	lnc-PELI2-2	chr14:56788204-56788329	ENSG00000259719.1
4	lnc-RP11-1085N6.3.1-3	chr14:56770208-56770387	ENSG00000259483.1
5	lnc-PELI2-2	chr14:56794901-56795079	ENSG00000259719.1
6	lnc-PELI2-1	chr14:56776790-56776977	XLOC_010839
7	lnc-PELI2-2	chr14:56797140-56797205	ENSG00000259719.1
8	lnc-PELI2-2	chr14:56792822-56793190	NONHSAT037041
9	lnc-PELI2-2	chr14:56788204-56788329	NONHSAT037041
10	lnc-RP11-1085N6.3.1-3	chr14:56776819-56776931	ENSG00000259483.1
11	lnc-PELI2-2	chr14:56784610-56784804	ENSG00000259719.1
12	lnc-RP11-1085N6.3.1-3	chr14:56775457-56775627	ENSG00000259483.1
13	lnc-RP11-1085N6.3.1-3	chr14:56777427-56777479	ENSG00000259483.1
14	lnc-PELI2-1	chr14:56777422-56777445	XLOC_010839
15	lnc-PELI2-2	chr14:56792898-56792926	ENSG00000259719.1
16	lnc-PELI2-2	chr14:56788204-56788329	ENSG00000259719.1
17	lnc-PELI2-2	chr14:56777598-56777820	NONHSAT037041

No data

Variant related genes	Relation type
ENSG00000259719	TF binding region
ENSG00000259483	TF binding region
ENSG00000259719	CpG island
ENSG00000259483	CpG island

Extended variants
information (count: 2416 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2416 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3783682	chr14:56740554-56740555	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576181173	chr14:56740658-56740659	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs532177543	chr14:56740674-56740675	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs545157022	chr14:56740685-56740686	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs566399874	chr14:56740701-56740702	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs536925981	chr14:56740745-56740746	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs369550737	chr14:56740758-56740759	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs548825531	chr14:56740763-56740764	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs549240541	chr14:56740798-56740799	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs564862874	chr14:56740815-56740816	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs17091196	chr14:56740833-56740834	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs541271335	chr14:56740836-56740837	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs558963771	chr14:56740837-56740838	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs577265680	chr14:56740850-56740851	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs374103026	chr14:56740882-56740883	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs372873802	chr14:56740890-56740891	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs242589	chr14:56740917-56740918	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs71291822	chr14:56740921-56740922	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs34580608	chr14:56740922-56740923	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs200581598	chr14:56740923-56740924	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs150774055	chr14:56740975-56740976	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs572326634	chr14:56740996-56740997	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs542479421	chr14:56741012-56741013	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs560756308	chr14:56741013-56741014	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs575782538	chr14:56741206-56741207	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs543207964	chr14:56741234-56741235	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs189527181	chr14:56741235-56741236	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs367635359	chr14:56741236-56741237	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs532095124	chr14:56741272-56741273	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs117245420	chr14:56741312-56741313	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs115760032	chr14:56741313-56741314	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs548860479	chr14:56741349-56741350	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181065227	chr14:56741350-56741351	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs537690470	chr14:56741377-56741378	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs139626412	chr14:56741435-56741436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185226203	chr14:56741453-56741454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191174107	chr14:56741480-56741481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371509642	chr14:56741514-56741515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs17091199	chr14:56741515-56741516	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs144741666	chr14:56741533-56741534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554486627	chr14:56741606-56741607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10483656	chr14:56741625-56741626	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183447728	chr14:56741646-56741647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147910357	chr14:56741671-56741672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187085269	chr14:56741680-56741681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540737731	chr14:56741705-56741706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551508391	chr14:56741722-56741723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35868839	chr14:56741785-56741786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs72720013	chr14:56741788-56741789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397806317	chr14:56741808-56741809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Endometrioid adenocarcinoma	16974079	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	21633010	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56717800-56749600	Weak transcription	Fetal Thymus	thymus
2	chr14:56717800-56765400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:56718400-56755800	Weak transcription	Ovary	ovary
4	chr14:56718800-56751400	Weak transcription	Primary B cells from cord blood	blood
5	chr14:56724600-56755200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr14:56725400-56746800	Weak transcription	Dnd41	blood
7	chr14:56725600-56742200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:56729200-56740600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr14:56731200-56747800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr14:56731400-56748000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr14:56733200-56744000	Weak transcription	Gastric	stomach
12	chr14:56733800-56746400	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr14:56734000-56750000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr14:56734800-56740800	Weak transcription	Esophagus	oesophagus
15	chr14:56735200-56755200	Weak transcription	Adipose Nuclei	Adipose
16	chr14:56735400-56741200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr14:56735800-56741800	Weak transcription	Fetal Intestine Small	intestine
18	chr14:56735800-56750200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr14:56735800-56751800	Weak transcription	Primary T cells from cord blood	blood
20	chr14:56735800-56765800	Weak transcription	NHLF	lung
21	chr14:56737400-56755800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr14:56738200-56741800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr14:56738200-56741800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:56738400-56741400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr14:56738400-56741600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr14:56738400-56741800	Enhancers	NHDF-Ad	bronchial
27	chr14:56738400-56742000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:56738600-56740800	Enhancers	HSMMtube	muscle
29	chr14:56738800-56741000	Enhancers	HUVEC	blood vessel
30	chr14:56738800-56755800	Weak transcription	Lung	lung
31	chr14:56738800-56766000	Weak transcription	Brain Angular Gyrus	brain
32	chr14:56738800-56775600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr14:56739000-56746800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr14:56739200-56740800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr14:56739200-56741800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr14:56739200-56741800	Weak transcription	Pancreas	Pancrea
37	chr14:56739200-56742000	Enhancers	Osteobl	bone
38	chr14:56739400-56743000	Weak transcription	Thymus	Thymus
39	chr14:56739600-56740600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr14:56739800-56740600	Weak transcription	Fetal Stomach	stomach
41	chr14:56740000-56740800	Enhancers	Stomach Smooth Muscle	stomach
42	chr14:56740000-56756000	Weak transcription	Brain Hippocampus Middle	brain
43	chr14:56740000-56757000	Weak transcription	Left Ventricle	heart
44	chr14:56740000-56764800	Weak transcription	Right Ventricle	heart
45	chr14:56740400-56740600	Enhancers	Aorta	Aorta
46	chr14:56740600-56740800	Flanking Active TSS	Aorta	Aorta
47	chr14:56740600-56740800	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr14:56740600-56741000	Enhancers	Fetal Stomach	stomach
49	chr14:56740600-56741400	Enhancers	Colon Smooth Muscle	Colon
50	chr14:56740600-56741600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links