Variant report

Variant	nsv1050985
Chromosome Location	chr14:41770445-42004827
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	ATF1	chr14:41852997-41853203	K562	blood:	n/a	n/a
2	ATF3	chr14:41831395-41831637	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:41853134-41853209	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:41974666-41975084	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr14:41968204-41968590	HepG2	liver:	n/a	chr14:41968396-41968407
6	CEBPB	chr14:41918185-41918765	MCF-7	breast:	n/a	n/a
7	CEBPB	chr14:41843358-41843671	IMR90	lung:	n/a	n/a
8	CEBPB	chr14:41918168-41918773	MCF-7	breast:	n/a	n/a
9	CEBPB	chr14:41968235-41968518	A549	lung:	n/a	chr14:41968396-41968407
10	CEBPB	chr14:41771959-41772333	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr14:41968335-41968511	HepG2	liver:	n/a	chr14:41968396-41968407
12	CEBPB	chr14:41991038-41991570	MCF-7	breast:	n/a	n/a
13	CEBPB	chr14:41974777-41974995	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:41956608-41956944	HepG2	liver:	n/a	chr14:41956807-41956819 chr14:41956753-41956766 chr14:41956753-41956764
15	CEBPB	chr14:41968204-41968593	Hela-S3	cervix:	n/a	chr14:41968396-41968407
16	CEBPB	chr14:41938215-41938415	H1-hESC	embryonic stem cell:	n/a	chr14:41938372-41938383
17	CEBPB	chr14:41968213-41968567	A549	lung:	n/a	chr14:41968396-41968407
18	CEBPB	chr14:41998657-41999192	HepG2	liver:	n/a	chr14:41998801-41998812
19	CEBPB	chr14:41772728-41772983	K562	blood:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
20	CEBPB	chr14:41938247-41938466	HepG2	liver:	n/a	chr14:41938372-41938383
21	CEBPB	chr14:41962541-41962898	IMR90	lung:	n/a	chr14:41962714-41962725
22	CEBPB	chr14:41881269-41881541	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:41801056-41801376	HepG2	liver:	n/a	chr14:41801209-41801220
24	CEBPB	chr14:41843406-41843570	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:41843283-41843667	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:41772715-41773048	A549	lung:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
27	CEBPB	chr14:41907194-41907541	HepG2	liver:	n/a	chr14:41907363-41907374
28	CEBPB	chr14:41959271-41959420	HepG2	liver:	n/a	chr14:41959353-41959370
29	CEBPB	chr14:41968203-41968594	IMR90	lung:	n/a	chr14:41968396-41968407
30	CEBPB	chr14:41772732-41773141	IMR90	lung:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
31	CEBPB	chr14:41962596-41962849	HepG2	liver:	n/a	chr14:41962714-41962725
32	CEBPB	chr14:41968172-41968600	ECC-1	luminal epithelium:	n/a	chr14:41968396-41968407
33	CEBPB	chr14:41968103-41968573	MCF-7	breast:	n/a	chr14:41968396-41968407
34	CEBPB	chr14:41825972-41826222	HepG2	liver:	n/a	chr14:41826057-41826068
35	CEBPB	chr14:41772781-41773093	ECC-1	luminal epithelium:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
36	CEBPB	chr14:41920034-41920186	HepG2	liver:	n/a	chr14:41920090-41920101 chr14:41920090-41920101 chr14:41920088-41920099
37	CEBPB	chr14:41998662-41999216	IMR90	lung:	n/a	chr14:41998801-41998812
38	CEBPB	chr14:41772723-41773057	ECC-1	luminal epithelium:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
39	CEBPB	chr14:41900404-41900704	HepG2	liver:	n/a	chr14:41900564-41900575
40	CEBPB	chr14:41855036-41855437	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr14:41974406-41974723	HepG2	liver:	n/a	chr14:41974564-41974575
42	CEBPB	chr14:41919045-41919549	MCF-7	breast:	n/a	n/a
43	CEBPB	chr14:41962635-41962791	A549	lung:	n/a	chr14:41962714-41962725
44	CEBPB	chr14:41843343-41843675	MCF-7	breast:	n/a	n/a
45	CEBPB	chr14:41887814-41888122	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:41860008-41860342	HepG2	liver:	n/a	chr14:41860189-41860200
47	CEBPB	chr14:41968164-41968716	MCF-7	breast:	n/a	chr14:41968396-41968407
48	CEBPB	chr14:41900498-41900583	A549	lung:	n/a	chr14:41900564-41900575
49	CEBPB	chr14:41968217-41968577	K562	blood:	n/a	chr14:41968396-41968407
50	CEBPB	chr14:41968176-41968591	H1-hESC	embryonic stem cell:	n/a	chr14:41968396-41968407

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:41771257-41771307	HEEpiC	esophagus:	n/a
2	chr14:41771257-41771307	HEEpiC	esophagus:	n/a
3	chr14:41771257-41771307	AG09319	gingival:	n/a
4	chr14:41771257-41771307	SAEC	small airway:	n/a
5	chr14:41771257-41771307	K562	blood:	n/a
6	chr14:41771257-41771307	SK-N-MC	brain:	n/a
7	chr14:41771257-41771307	GM12892	blood:	n/a
8	chr14:41771257-41771307	HMEC	breast:	n/a
9	chr14:41771257-41771307	ovcar-3	ovarian:	n/a
10	chr14:41771257-41771307	GM06990	blood:	n/a
11	chr14:41771257-41771307	CMK	blood:	n/a
12	chr14:41771257-41771307	ProgFib	skin:	n/a
13	chr14:41771257-41771307	HepG2	liver:	n/a
14	chr14:41771257-41771307	H1-hESC	embryonic stem cell:	embryo
15	chr14:41771257-41771307	HUVEC	blood vessel:	n/a
16	chr14:41771257-41771307	AG09309	skin:	n/a
17	chr14:41771257-41771307	HL-60	blood:	n/a
18	chr14:41771257-41771307	Jurkat	blood:	n/a
19	chr14:41771257-41771307	LNCaP	prostate:	n/a
20	chr14:41771257-41771307	HCPEpiC	choroid plexus:	n/a
21	chr14:41771257-41771307	PrEC	prostate:	n/a
22	chr14:41771257-41771307	IMR90	lung:	fetal
23	chr14:41771257-41771307	GM12878	blood:	n/a
24	chr14:41771257-41771307	HAEpiC	amniotic membrane:	n/a
25	chr14:41771257-41771307	NH-A	brain:	n/a
26	chr14:41771257-41771307	BJ	skin:	n/a
27	chr14:41771257-41771307	AG10803	skin:	n/a
28	chr14:41771257-41771307	U87	brain:	n/a
29	chr14:41771257-41771307	Hepatocyte	liver:	n/a
30	chr14:41771257-41771307	A549	lung:	n/a
31	chr14:41771257-41771307	NHBE	bronchial:	n/a
32	chr14:41771257-41771307	HRPEpiC	eye:	n/a
33	chr14:41771257-41771307	HRE	kidney:	n/a
34	chr14:41771257-41771307	PANC-1	pancreas:	n/a
35	chr14:41771257-41771307	RPTEC	kidney:	n/a
36	chr14:41771257-41771307	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:41771257-41771307	T-47D	breast:	n/a
38	chr14:41771257-41771307	NB4	blood:	n/a
39	chr14:41771257-41771307	MCF-7	breast:	n/a
40	chr14:41771257-41771307	HNPCEpiC	eye:	n/a
41	chr14:41771257-41771307	Caco-2	colon:	n/a
42	chr14:41771257-41771307	SKMC	muscle:	n/a
43	chr14:41771257-41771307	HRCEpiC	kidney:	n/a
44	chr14:41771257-41771307	SK-N-SH_RA	brain:	n/a
45	chr14:41771257-41771307	HEK293	kidney:	embryo
46	chr14:41771257-41771307	AoSMC	blood vessel:	n/a
47	chr14:41771257-41771307	HCT-116	colon:	n/a
48	chr14:41771257-41771307	SK-N-SH	brain:	n/a
49	chr14:41771257-41771307	HCM	heart:	n/a
50	chr14:41771257-41771307	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:167600671..167603478-chr14:41990511..41992655,2	MCF-7	breast:
2	chr14:41931064..41933309-chr14:41934938..41936692,2	MCF-7	breast:
3	chr14:41931064..41933309-chr14:41934938..41936692,2	MCF-7	breast:
4	chr14:41792593..41793113-chr2:63668078..63668598,2	MCF-7	breast:
5	chr14:41856073..41858584-chr14:41859093..41860987,2	MCF-7	breast:
6	chr14:41873770..41876020-chr14:41877862..41880665,2	MCF-7	breast:
7	chr14:41956888..41958612-chr14:41960214..41961890,2	MCF-7	breast:
8	chr14:41916762..41919309-chr14:41919759..41921480,2	K562	blood:
9	chr14:41956888..41958612-chr14:41960214..41961890,2	MCF-7	breast:
10	chr14:41285689..41286269-chr14:41888680..41889346,2	MCF-7	breast:
11	chr14:41952601..41955142-chr4:3784821..3786920,2	MCF-7	breast:
12	chr14:41873770..41876020-chr14:41877862..41880665,2	MCF-7	breast:
13	chr14:41916762..41919309-chr14:41919759..41921480,2	K562	blood:
14	chr14:41856073..41858584-chr14:41859093..41860987,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRFN5-4	chr14:41995891-41995949	NONHSAT036571
2	lnc-FBXO33-5	chr14:41984175-41984554	NONHSAT036570
3	lnc-LRFN5-4	chr14:41989726-41989971	NONHSAT036571

Variant related genes	Relation type
ENSG00000221695	TF binding region
ENSG00000221695	CpG island
ENSG00000143951	chromatin interactions

Extended variants
information (count: 4098 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4098 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2802067	chr14:41770523-41770524	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113600203	chr14:41770627-41770628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35273218	chr14:41770696-41770697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186088026	chr14:41770737-41770738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536488424	chr14:41770740-41770741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543926871	chr14:41770964-41770965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562060066	chr14:41771001-41771002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375799318	chr14:41771050-41771051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188197192	chr14:41771138-41771139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559948468	chr14:41771140-41771141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533711783	chr14:41771145-41771146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552101248	chr14:41771151-41771152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570489768	chr14:41771158-41771159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75357576	chr14:41771174-41771175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576216970	chr14:41771264-41771265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568065083	chr14:41771314-41771315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535490902	chr14:41771373-41771374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369466011	chr14:41771420-41771421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181423880	chr14:41771429-41771430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10135526	chr14:41771455-41771456	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs113674698	chr14:41771489-41771490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557612313	chr14:41771524-41771525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185745401	chr14:41771546-41771547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543476112	chr14:41771557-41771558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141018305	chr14:41771609-41771610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574061817	chr14:41771641-41771642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190062612	chr14:41771743-41771744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541530618	chr14:41771751-41771752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200587698	chr14:41771754-41771755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183528977	chr14:41771844-41771845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186837878	chr14:41771877-41771878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552137985	chr14:41771969-41771970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192086381	chr14:41771999-41772000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577909719	chr14:41772007-41772008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4899908	chr14:41772027-41772028	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs370462469	chr14:41772055-41772056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183980379	chr14:41772080-41772081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187780232	chr14:41772138-41772139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535217786	chr14:41772154-41772155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547067187	chr14:41772157-41772158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565570197	chr14:41772168-41772169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561859343	chr14:41772177-41772178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532150418	chr14:41772179-41772180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539263133	chr14:41772191-41772192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1782165	chr14:41772214-41772215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2798983	chr14:41772233-41772234	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs371444115	chr14:41772308-41772309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572382727	chr14:41772324-41772325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555521299	chr14:41772338-41772339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552383208	chr14:41772341-41772342	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Colorectal cancer	16774939	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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41769400-41770800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr14:41770000-41770600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr14:41770000-41770800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr14:41770000-41772000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr14:41770000-41772400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr14:41770200-41770800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:41770200-41772200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr14:41770400-41771800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:41770400-41773000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:41770600-41771600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr14:41770600-41771800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:41770800-41771200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr14:41770800-41771200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr14:41770800-41771200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr14:41771200-41772400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr14:41771200-41772400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr14:41771200-41772400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:41771600-41772400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr14:41771600-41773200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:41771800-41772400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr14:41772400-41773600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:41773600-41774000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr14:41799200-41799600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr14:41817200-41818600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr14:41817200-41818800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:41818400-41819000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:41819400-41820000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr14:41819800-41820000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr14:41824400-41825800	Enhancers	Fetal Lung	lung
30	chr14:41837200-41837400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:41837400-41837600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:41837400-41837600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
33	chr14:41855000-41855400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr14:41866400-41867400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr14:41866400-41868000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:41866600-41867600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:41866600-41868600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr14:41866800-41868000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr14:41866800-41868800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr14:41867000-41867600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:41867200-41867400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:41867200-41867400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr14:41867200-41867600	Enhancers	Fetal Brain Male	brain
44	chr14:41867400-41870600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr14:41867400-41870800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr14:41867600-41869400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:41868000-41868200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:41868000-41868200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr14:41868000-41869200	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr14:41868000-41870800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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