Variant report

Variant	nsv564470
Chromosome Location	chr14:41405093-41539775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:348)
CpG islands
(count:123)
Chromatin interactive
region (count:2)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:41407165-41407367	K562	blood:	n/a	n/a
2	BHLHE40	chr14:41407166-41407365	K562	blood:	n/a	n/a
3	BHLHE40	chr14:41516318-41516387	HepG2	liver:	n/a	n/a
4	CCNT2	chr14:41407166-41407534	K562	blood:	n/a	n/a
5	CEBPB	chr14:41454815-41455173	IMR90	lung:	n/a	chr14:41454980-41454991
6	CEBPB	chr14:41492158-41492509	ECC-1	luminal epithelium:	n/a	chr14:41492338-41492349
7	CEBPB	chr14:41416310-41416495	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:41454834-41455142	H1-hESC	embryonic stem cell:	n/a	chr14:41454980-41454991
9	CEBPB	chr14:41454866-41455145	K562	blood:	n/a	chr14:41454980-41454991
10	CEBPB	chr14:41492127-41492510	MCF-7	breast:	n/a	chr14:41492338-41492349
11	CEBPB	chr14:41529969-41530252	HepG2	liver:	n/a	chr14:41530112-41530123
12	CEBPB	chr14:41492165-41492433	ECC-1	luminal epithelium:	n/a	chr14:41492338-41492349
13	CEBPB	chr14:41431432-41431774	HepG2	liver:	n/a	chr14:41431587-41431598 chr14:41431719-41431730 chr14:41431440-41431451
14	CEBPB	chr14:41492185-41492478	A549	lung:	n/a	chr14:41492338-41492349
15	CEBPB	chr14:41454805-41455171	HepG2	liver:	n/a	chr14:41454980-41454991
16	CEBPB	chr14:41454786-41455174	MCF-7	breast:	n/a	chr14:41454980-41454991
17	CEBPB	chr14:41483360-41483610	HepG2	liver:	n/a	chr14:41483484-41483495
18	CEBPB	chr14:41453098-41453237	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:41492186-41492556	MCF-7	breast:	n/a	chr14:41492338-41492349
20	CEBPB	chr14:41492158-41492502	IMR90	lung:	n/a	chr14:41492338-41492349
21	CEBPB	chr14:41410937-41411137	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:41470919-41471096	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr14:41454796-41455168	A549	lung:	n/a	chr14:41454980-41454991
24	CEBPB	chr14:41492163-41492521	HepG2	liver:	n/a	chr14:41492338-41492349
25	CEBPB	chr14:41454765-41455264	MCF-7	breast:	n/a	chr14:41454980-41454991
26	CEBPB	chr14:41515324-41515615	HepG2	liver:	n/a	chr14:41515462-41515473
27	CEBPB	chr14:41530050-41530203	A549	lung:	n/a	chr14:41530112-41530123
28	CEBPB	chr14:41526762-41526943	HepG2	liver:	n/a	chr14:41526861-41526872
29	CEBPB	chr14:41450414-41450779	MCF-7	breast:	n/a	n/a
30	CEBPB	chr14:41534322-41534484	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:41495427-41495773	IMR90	lung:	n/a	chr14:41495750-41495762
32	CEBPB	chr14:41470999-41471090	HepG2	liver:	n/a	n/a
33	CHD1	chr14:41424252-41424603	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr14:41521060-41521210	MCF-7	breast:	n/a	n/a
35	CTCF	chr14:41444320-41444470	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr14:41500852-41500868	GM10266	blood:	n/a	n/a
37	CTCF	chr14:41521123-41521271	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr14:41521200-41521350	HRE	kidney:	n/a	n/a
39	CTCF	chr14:41474939-41474960	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr14:41423959-41424077	Fibrobl	skin:	n/a	n/a
41	CTCF	chr14:41450480-41450630	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:41519336-41519355	GM20000	blood:	n/a	n/a
43	CTCF	chr14:41464827-41464917	GM20000	blood:	n/a	n/a
44	CTCF	chr14:41485041-41485072	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:41407165-41407535	K562	blood:	n/a	n/a
46	E2F4	chr14:41458069-41458092	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr14:41505336-41505490	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr14:41407167-41407535	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr14:41408071-41408178	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr14:41450622-41450685	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:41423839-41423889	LNCaP	prostate:	n/a
2	chr14:41423839-41423889	LNCaP	prostate:	n/a
3	chr14:41423839-41423889	SKMC	muscle:	n/a
4	chr14:41469306-41469356	HL-60	blood:	n/a
5	chr14:41469306-41469356	ECC-1	luminal epithelium:	n/a
6	chr14:41469306-41469356	MCF10A-Er-Src	breast:	n/a
7	chr14:41423839-41423889	AG04450	lung:	fetal
8	chr14:41423839-41423889	HNPCEpiC	eye:	n/a
9	chr14:41423839-41423889	NH-A	brain:	n/a
10	chr14:41423839-41423889	HCPEpiC	choroid plexus:	n/a
11	chr14:41469306-41469356	SK-N-SH	brain:	n/a
12	chr14:41469306-41469356	ovcar-3	ovarian:	n/a
13	chr14:41469306-41469356	HRE	kidney:	n/a
14	chr14:41469306-41469356	HRPEpiC	eye:	n/a
15	chr14:41423839-41423889	RPTEC	kidney:	n/a
16	chr14:41469306-41469356	U87	brain:	n/a
17	chr14:41423839-41423889	NHBE	bronchial:	n/a
18	chr14:41423839-41423889	U87	brain:	n/a
19	chr14:41423839-41423889	ECC-1	luminal epithelium:	n/a
20	chr14:41469306-41469356	AG09309	skin:	n/a
21	chr14:41469306-41469356	ProgFib	skin:	n/a
22	chr14:41423839-41423889	HRE	kidney:	n/a
23	chr14:41423839-41423889	GM12892	blood:	n/a
24	chr14:41423839-41423889	Jurkat	blood:	n/a
25	chr14:41423839-41423889	HEK293	kidney:	embryo
26	chr14:41423839-41423889	BE2_C	brain:	n/a
27	chr14:41423839-41423889	HL-60	blood:	n/a
28	chr14:41423839-41423889	Hela-S3	cervix:	n/a
29	chr14:41423839-41423889	A549	lung:	n/a
30	chr14:41423839-41423889	HepG2	liver:	n/a
31	chr14:41469306-41469356	HCM	heart:	n/a
32	chr14:41423839-41423889	HPAEpiC	pulmonary alveolar:	n/a
33	chr14:41469306-41469356	Hepatocyte	liver:	n/a
34	chr14:41423839-41423889	AG09319	gingival:	n/a
35	chr14:41423839-41423889	HIPEpiC	eye:	n/a
36	chr14:41469306-41469356	IMR90	lung:	fetal
37	chr14:41423839-41423889	MCF10A-Er-Src	breast:	n/a
38	chr14:41423839-41423889	ovcar-3	ovarian:	n/a
39	chr14:41423839-41423889	PFSK-1	brain:	n/a
40	chr14:41423839-41423889	Caco-2	colon:	n/a
41	chr14:41423839-41423889	MCF-7	breast:	n/a
42	chr14:41423839-41423889	HCF	heart:	n/a
43	chr14:41469306-41469356	PrEC	prostate:	n/a
44	chr14:41423839-41423889	HEEpiC	esophagus:	n/a
45	chr14:41469306-41469356	HIPEpiC	eye:	n/a
46	chr14:41469306-41469356	SK-N-MC	brain:	n/a
47	chr14:41469306-41469356	NH-A	brain:	n/a
48	chr14:41423839-41423889	AoSMC	blood vessel:	n/a
49	chr14:41469306-41469356	NHBE	bronchial:	n/a
50	chr14:41423839-41423889	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:41377936..41380382-chr14:41413256..41415527,2	MCF-7	breast:
2	chr14:41488666..41490358-chr14:41674438..41676053,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRFN5-1	chr14:41423916-41424157	NR_109758
2	lnc-LRFN5-1	chr14:41424103-41424157	ENSG00000251363
3	lnc-LRFN5-1	chr14:41423916-41424157	NR_109757
4	lnc-LRFN5-1	chr14:41431995-41432050	XLOC_010813
5	lnc-LRFN5-1	chr14:41443545-41443595	ENSG00000251363
6	lnc-LRFN5-1	chr14:41431995-41432047	ENSG00000251363
7	lnc-LRFN5-1	chr14:41444546-41445070	XLOC_010813
8	lnc-LRFN5-1	chr14:41431995-41432047	NR_109758
9	lnc-LRFN5-1	chr14:41431995-41432047	NR_109757
10	lnc-LRFN5-1	chr14:41494725-41494994	NR_109757
11	lnc-LRFN5-1	chr14:41431995-41432047	XLOC_010813
12	lnc-LRFN5-1	chr14:41443545-41443595	NR_109757
13	lnc-LRFN5-1	chr14:41423822-41424157	XLOC_010813
14	lnc-LRFN5-1	chr14:41443545-41443595	ENSG00000251363
15	lnc-LRFN5-1	chr14:41431995-41432047	XLOC_010813
16	lnc-LRFN5-1	chr14:41444546-41445068	ENSG00000251363
17	lnc-LRFN5-1	chr14:41444546-41445082	ENSG00000251363
18	lnc-LRFN5-1	chr14:41423916-41424157	XLOC_010813
19	lnc-LRFN5-1	chr14:41443545-41443814	XLOC_010813
20	lnc-LRFN5-1	chr14:41423916-41424157	ENSG00000251363
21	lnc-LRFN5-1	chr14:41443545-41443595	NR_109758
22	lnc-LRFN5-1	chr14:41443545-41443595	XLOC_010813
23	lnc-LRFN5-1	chr14:41431994-41432047	ENSG00000251363
24	lnc-LRFN5-1	chr14:41424123-41424157	XLOC_010813

No data

Variant related genes	Relation type
ENSG00000251363	TF binding region
ENSG00000251363	CpG island
KLHL28	miRNA target sites
SLC25A22	miRNA target sites
ARID4B	miRNA target sites
APBB2	miRNA target sites
SLC25A1	miRNA target sites
SLC25A15	miRNA target sites

Extended variants
information (count: 2589 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2589 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546049444	chr14:41413650-41413651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367845563	chr14:41413702-41413703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1182565	chr14:41413712-41413713	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs74044549	chr14:41413747-41413748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187779033	chr14:41413769-41413770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76176858	chr14:41413817-41413818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200988624	chr14:41413846-41413847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78565733	chr14:41413856-41413857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs202039675	chr14:41413857-41413858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199868939	chr14:41413859-41413860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529822901	chr14:41413877-41413878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs71409967	chr14:41413918-41413919	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs566698689	chr14:41413981-41413982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533756604	chr14:41413987-41413988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376380741	chr14:41423354-41423355	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368293768	chr14:41423363-41423364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs28827806	chr14:41423371-41423372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs374926032	chr14:41423396-41423397	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs559400503	chr14:41423399-41423400	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533298986	chr14:41423428-41423429	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs369069613	chr14:41423459-41423460	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs551942878	chr14:41423468-41423469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570110843	chr14:41423485-41423486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs537655209	chr14:41423497-41423498	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs549377927	chr14:41423507-41423508	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs567983030	chr14:41423523-41423524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs61987195	chr14:41423530-41423531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs535419415	chr14:41423547-41423548	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs372386898	chr14:41423572-41423573	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs539497232	chr14:41423649-41423650	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs557835522	chr14:41423678-41423679	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs112414125	chr14:41423715-41423716	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs576126247	chr14:41423716-41423717	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs543622457	chr14:41423759-41423760	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs532992242	chr14:41423762-41423763	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561821943	chr14:41423764-41423765	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs573628235	chr14:41423771-41423772	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs541026166	chr14:41423788-41423789	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs546709628	chr14:41423793-41423794	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs559362213	chr14:41423797-41423798	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs566581070	chr14:41423812-41423813	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs533165515	chr14:41423820-41423821	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs192836297	chr14:41423822-41423823	Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs142538767	chr14:41423834-41423835	Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs530995864	chr14:41423836-41423837	Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs549580963	chr14:41423839-41423840	Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs567955127	chr14:41423847-41423848	Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs528832922	chr14:41423871-41423872	Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs547325199	chr14:41423872-41423873	Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs185778685	chr14:41423885-41423886	Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41413600-41414000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr14:41423600-41425000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr14:41423600-41426000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:41423800-41425600	Active TSS	H1 Cell Line	embryonic stem cell
5	chr14:41423800-41426000	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr14:41424000-41424400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:41424000-41425000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr14:41424000-41425000	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr14:41424000-41425200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:41424000-41425200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
11	chr14:41424000-41425400	Active TSS	H9 Cell Line	embryonic stem cell
12	chr14:41424000-41425400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:41424000-41425400	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr14:41424000-41425600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr14:41424000-41425800	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr14:41424000-41425800	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr14:41424000-41426200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:41424000-41426400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:41424000-41426400	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr14:41424000-41426400	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr14:41424000-41426600	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr14:41424200-41424600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr14:41424200-41424600	Active TSS	Right Ventricle	heart
24	chr14:41424200-41424800	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr14:41424200-41424800	Active TSS	Placenta	Placenta
26	chr14:41424200-41424800	Active TSS	HUVEC	blood vessel
27	chr14:41424200-41424800	Active TSS	K562	blood
28	chr14:41424400-41428400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr14:41425000-41425400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr14:41425000-41425600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr14:41425200-41425400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:41425200-41428400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr14:41425400-41425600	Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr14:41425400-41427600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:41425400-41427800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr14:41425400-41428400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr14:41425600-41425800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr14:41425600-41426400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr14:41425600-41427800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr14:41425600-41427800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr14:41425800-41426000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr14:41425800-41427800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr14:41426000-41426200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:41426000-41426400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr14:41426000-41426400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr14:41426200-41426600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr14:41426200-41426600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr14:41426200-41430000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr14:41426400-41426800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr14:41426400-41426800	Weak transcription	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links