Variant report

Variant	nsv520826
Chromosome Location	chr14:104837237-104872237
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	ATF2	chr14:104853315-104853690	GM12878	blood:	n/a	n/a
2	BATF	chr14:104853348-104853593	GM12878	blood:	n/a	n/a
3	BCL11A	chr14:104853356-104853621	GM12878	blood:	n/a	chr14:104853461-104853470
4	BCL3	chr14:104853374-104853619	GM12878	blood:	n/a	chr14:104853461-104853470
5	BCL3	chr14:104850568-104850914	GM12878	blood:	n/a	chr14:104850648-104850657
6	BCL3	chr14:104850572-104850917	GM12878	blood:	n/a	chr14:104850648-104850657
7	BCLAF1	chr14:104853385-104853683	GM12878	blood:	n/a	chr14:104853461-104853470
8	CEBPB	chr14:104862635-104863004	MCF-7	breast:	n/a	chr14:104862810-104862823
9	CEBPB	chr14:104836980-104837263	A549	lung:	n/a	n/a
10	CEBPB	chr14:104862645-104863007	H1-hESC	embryonic stem cell:	n/a	chr14:104862810-104862823
11	CEBPB	chr14:104862743-104862899	A549	lung:	n/a	chr14:104862810-104862823
12	CEBPB	chr14:104862673-104862964	HepG2	liver:	n/a	chr14:104862810-104862823
13	CEBPB	chr14:104837024-104837262	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:104862712-104862901	Hela-S3	cervix:	n/a	chr14:104862810-104862823
15	CTCF	chr14:104866340-104866460	GM12878	blood:	n/a	n/a
16	CTCF	chr14:104866340-104866490	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr14:104866080-104866230	MCF-7	breast:	n/a	n/a
18	CTCF	chr14:104852820-104852970	GM12870	blood:	n/a	n/a
19	CTCF	chr14:104852660-104852810	GM12875	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
20	CTCF	chr14:104858260-104858410	HepG2	liver:	n/a	n/a
21	CTCF	chr14:104852642-104852767	H1-hESC	embryonic stem cell:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
22	CTCF	chr14:104852640-104852790	GM12874	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
23	CTCF	chr14:104866338-104866481	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:104869832-104869875	Fibrobl	skin:	n/a	n/a
25	CTCF	chr14:104858364-104858407	GM12891	blood:	n/a	n/a
26	CTCF	chr14:104858260-104858410	GM12875	blood:	n/a	n/a
27	CTCF	chr14:104852580-104852730	GM12864	blood:	n/a	chr14:104852711-104852720 chr14:104852630-104852643
28	CTCF	chr14:104852750-104852756	GM12878	blood:	n/a	n/a
29	CTCF	chr14:104852620-104852770	GM12874	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751 chr14:104852630-104852643
30	CTCF	chr14:104858340-104858490	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr14:104865434-104865517	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr14:104852660-104852810	GM12873	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
33	CTCF	chr14:104866325-104866476	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr14:104852540-104852824	H1-hESC	embryonic stem cell:	n/a	chr14:104852711-104852720 chr14:104852742-104852751 chr14:104852630-104852643
35	CTCF	chr14:104866349-104866470	GM12892	blood:	n/a	n/a
36	CTCF	chr14:104858335-104858444	GM19238	blood:	n/a	n/a
37	CTCF	chr14:104852620-104852770	GM12869	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751 chr14:104852630-104852643
38	CTCF	chr14:104866341-104866476	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:104866331-104866492	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:104852640-104852790	GM12866	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
41	CTCF	chr14:104865873-104866814	SK-N-SH	brain:	n/a	n/a
42	CTCF	chr14:104852655-104852745	GM12878	blood:	n/a	chr14:104852711-104852720
43	CTCF	chr14:104850560-104850710	BE2_C	brain:	n/a	n/a
44	CTCF	chr14:104852700-104852850	GM12864	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
45	CTCF	chr14:104852600-104852750	GM12870	blood:	n/a	chr14:104852711-104852720 chr14:104852630-104852643
46	CTCF	chr14:104852680-104852830	GM12867	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
47	CTCF	chr14:104852640-104852790	GM12875	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
48	CTCF	chr14:104866330-104866491	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:104852660-104852810	GM12872	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
50	CTCF	chr14:104852612-104852802	GM12878	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751 chr14:104852630-104852643

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104865112-104865162	AG09309	skin:	n/a
2	chr14:104865112-104865162	AG09309	skin:	n/a
3	chr14:104837550-104837600	AG10803	skin:	n/a
4	chr14:104862680-104862730	HRCEpiC	kidney:	n/a
5	chr14:104851832-104851882	HRCEpiC	kidney:	n/a
6	chr14:104862559-104862609	SK-N-SH_RA	brain:	n/a
7	chr14:104856500-104856550	SK-N-MC	brain:	n/a
8	chr14:104856500-104856550	SAEC	small airway:	n/a
9	chr14:104837363-104837413	AG10803	skin:	n/a
10	chr14:104864723-104864773	ECC-1	luminal epithelium:	n/a
11	chr14:104864723-104864773	AoSMC	blood vessel:	n/a
12	chr14:104852775-104852825	PANC-1	pancreas:	n/a
13	chr14:104866284-104866334	Caco-2	colon:	n/a
14	chr14:104852104-104852154	NB4	blood:	n/a
15	chr14:104837550-104837600	A549	lung:	n/a
16	chr14:104864723-104864773	SAEC	small airway:	n/a
17	chr14:104837550-104837600	HCM	heart:	n/a
18	chr14:104837550-104837600	SKMC	muscle:	n/a
19	chr14:104852775-104852825	HIPEpiC	eye:	n/a
20	chr14:104864723-104864773	BE2_C	brain:	n/a
21	chr14:104854940-104854990	H1-hESC	embryonic stem cell:	embryo
22	chr14:104842040-104842090	AG09319	gingival:	n/a
23	chr14:104854790-104854840	NT2-D1	testis:	n/a
24	chr14:104854790-104854840	ECC-1	luminal epithelium:	n/a
25	chr14:104842040-104842090	U87	brain:	n/a
26	chr14:104837541-104837591	AG09319	gingival:	n/a
27	chr14:104865792-104865842	AG10803	skin:	n/a
28	chr14:104870666-104870716	HCT-116	colon:	n/a
29	chr14:104862680-104862730	HCT-116	colon:	n/a
30	chr14:104866636-104866686	AG10803	skin:	n/a
31	chr14:104837363-104837413	NHDF-neo	bronchial:	n/a
32	chr14:104856500-104856550	MCF-7	breast:	n/a
33	chr14:104851903-104851953	PrEC	prostate:	n/a
34	chr14:104837363-104837413	Caco-2	colon:	n/a
35	chr14:104856872-104856922	HCPEpiC	choroid plexus:	n/a
36	chr14:104852775-104852825	HAEpiC	amniotic membrane:	n/a
37	chr14:104837541-104837591	Jurkat	blood:	n/a
38	chr14:104842040-104842090	SK-N-MC	brain:	n/a
39	chr14:104850405-104850455	GM12892	blood:	n/a
40	chr14:104862680-104862730	HCPEpiC	choroid plexus:	n/a
41	chr14:104866636-104866686	H1-hESC	embryonic stem cell:	embryo
42	chr14:104856667-104856717	RPTEC	kidney:	n/a
43	chr14:104854711-104854761	HCPEpiC	choroid plexus:	n/a
44	chr14:104837550-104837600	Hela-S3	cervix:	n/a
45	chr14:104856667-104856717	A549	lung:	n/a
46	chr14:104865112-104865162	NH-A	brain:	n/a
47	chr14:104851903-104851953	NHDF-neo	bronchial:	n/a
48	chr14:104865112-104865162	Hela-S3	cervix:	n/a
49	chr14:104852706-104852756	HRPEpiC	eye:	n/a
50	chr14:104856500-104856550	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:104841247..104842926-chr14:104851671..104854407,2	MCF-7	breast:
2	chr14:104841247..104842926-chr14:104851671..104854407,2	MCF-7	breast:
3	chr14:104846626..104850072-chr14:104851431..104854716,4	MCF-7	breast:
4	chr14:104852349..104854257-chr14:104854522..104857044,2	MCF-7	breast:
5	chr14:104839152..104841523-chr14:104843087..104845999,3	MCF-7	breast:
6	chr14:104852349..104854257-chr14:104854522..104857044,2	MCF-7	breast:
7	chr14:104860512..104862041-chr14:104863587..104866008,2	K562	blood:
8	chr14:104837762..104840619-chr14:104842293..104845118,2	MCF-7	breast:
9	chr14:104842421..104844937-chr14:104846124..104848778,2	K562	blood:
10	chr14:104837762..104840619-chr14:104842293..104845118,2	MCF-7	breast:
11	chr14:104827640..104830097-chr14:104849702..104851434,2	MCF-7	breast:
12	chr14:104808137..104810517-chr14:104838226..104840189,2	MCF-7	breast:
13	chr14:104846626..104850072-chr14:104851431..104854716,4	MCF-7	breast:
14	chr14:104810225..104812544-chr14:104838511..104840510,3	MCF-7	breast:
15	chr14:104862114..104865269-chr14:104866594..104868712,3	MCF-7	breast:
16	chr14:104865956..104868004-chr14:104868266..104870745,2	K562	blood:
17	chr14:104604366..104607521-chr14:104837580..104840047,4	MCF-7	breast:
18	chr14:104860512..104862041-chr14:104863587..104866008,2	K562	blood:
19	chr14:104842421..104844937-chr14:104846124..104848778,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-614O9.3.1-1	chr14:104842867-104843033	ENSG00000258598
2	lnc-RP11-614O9.3.1-1	chr14:104843878-104844157	ENSG00000258598
3	lnc-RP11-614O9.3.1-1	chr14:104845218-104845288	ENSG00000258598

Variant related genes	Relation type
RNU6-684P	TF binding region
ENSG00000258598	TF binding region
RNU6-684P	CpG island
ENSG00000258598	CpG island
ENSG00000258598	chromatin interactions
ENSG00000066735	chromatin interactions
ENSG00000222761	chromatin interactions

Extended variants
information (count: 1633 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1633 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7152431	chr14:104837237-104837238	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541114250	chr14:104837258-104837259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563971673	chr14:104837290-104837291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577393478	chr14:104837291-104837292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543223023	chr14:104837314-104837315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563614427	chr14:104837345-104837346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529134731	chr14:104837350-104837351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77218735	chr14:104837364-104837365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559387178	chr14:104837370-104837371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528230769	chr14:104837411-104837412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148292904	chr14:104837435-104837436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7153433	chr14:104837477-104837478	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs61577366	chr14:104837529-104837530	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550068867	chr14:104837541-104837542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570333424	chr14:104837550-104837551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141379458	chr14:104837622-104837623	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112341963	chr14:104837633-104837634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565719230	chr14:104837643-104837644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374497735	chr14:104837647-104837648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534817669	chr14:104837697-104837698	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147428118	chr14:104837706-104837707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs578007050	chr14:104837742-104837743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543612261	chr14:104837755-104837756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116307652	chr14:104837764-104837765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573925380	chr14:104837774-104837775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189262503	chr14:104837783-104837784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528115995	chr14:104837825-104837826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544988466	chr14:104837832-104837833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373482199	chr14:104837840-104837841	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs61603240	chr14:104837909-104837910	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs574504562	chr14:104837915-104837916	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs550398738	chr14:104837954-104837955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570143614	chr14:104837955-104837956	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs558632573	chr14:104838049-104838050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529624159	chr14:104838050-104838051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549240854	chr14:104838078-104838079	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373153775	chr14:104838085-104838086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566002190	chr14:104838123-104838124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs8021437	chr14:104838124-104838125	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557688171	chr14:104838130-104838131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs571716117	chr14:104838132-104838133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs112150875	chr14:104838133-104838134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557160291	chr14:104838157-104838158	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs8020156	chr14:104838158-104838159	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs8020667	chr14:104838191-104838192	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs181533072	chr14:104838205-104838206	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs186551750	chr14:104838282-104838283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575326564	chr14:104838283-104838284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545027029	chr14:104838307-104838308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs139710396	chr14:104838328-104838329	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	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
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104831000-104842000	Weak transcription	Gastric	stomach
2	chr14:104831400-104838800	Weak transcription	Fetal Intestine Small	intestine
3	chr14:104833400-104837600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:104834600-104838600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:104835400-104842000	Weak transcription	Fetal Brain Male	brain
6	chr14:104836400-104839200	Weak transcription	Brain Germinal Matrix	brain
7	chr14:104837600-104840200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:104838400-104839600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr14:104838400-104839600	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr14:104838600-104839400	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr14:104838600-104839600	Enhancers	Primary T cells fromperipheralblood	blood
12	chr14:104838600-104839600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr14:104838800-104839200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr14:104838800-104839600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr14:104838800-104840000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr14:104838800-104840000	Enhancers	Fetal Intestine Small	intestine
17	chr14:104839000-104839400	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr14:104839000-104839400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr14:104839000-104839400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:104839000-104839600	Enhancers	Fetal Intestine Large	intestine
21	chr14:104839200-104840000	Enhancers	Brain Germinal Matrix	brain
22	chr14:104839600-104839800	Bivalent Enhancer	Fetal Lung	lung
23	chr14:104840200-104842000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr14:104840800-104841000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr14:104842000-104842200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr14:104842000-104842600	Enhancers	Gastric	stomach
27	chr14:104842000-104843000	Enhancers	Brain Germinal Matrix	brain
28	chr14:104842000-104847400	Enhancers	Fetal Brain Male	brain
29	chr14:104842200-104842800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:104842400-104843400	Enhancers	Adipose Nuclei	Adipose
31	chr14:104842600-104850400	Weak transcription	Gastric	stomach
32	chr14:104842800-104843000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
33	chr14:104842800-104843000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
34	chr14:104842800-104846800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr14:104843000-104843400	Weak transcription	Brain Germinal Matrix	brain
36	chr14:104843400-104845000	Enhancers	Brain Germinal Matrix	brain
37	chr14:104843800-104845800	Enhancers	Fetal Brain Female	brain
38	chr14:104845000-104845200	Flanking Active TSS	Brain Germinal Matrix	brain
39	chr14:104845200-104845400	Enhancers	Brain Germinal Matrix	brain
40	chr14:104845400-104845600	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr14:104845400-104845800	Enhancers	Fetal Stomach	stomach
42	chr14:104845600-104846200	Enhancers	Brain Germinal Matrix	brain
43	chr14:104845800-104846000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
44	chr14:104845800-104849200	Weak transcription	Fetal Brain Female	brain
45	chr14:104846800-104847400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:104847400-104849000	Weak transcription	Fetal Brain Male	brain
47	chr14:104847400-104849800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:104848400-104849800	Enhancers	Brain Germinal Matrix	brain
49	chr14:104849000-104849800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr14:104849000-104850000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain

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