Variant report

Variant	nsv1048363
Chromosome Location	chr14:41647223-41770505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 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	chr14:41754536-41754724	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:41760911-41761210	HepG2	liver:	n/a	chr14:41761068-41761079
3	CEBPB	chr14:41694658-41695011	HepG2	liver:	n/a	chr14:41694823-41694834
4	CEBPB	chr14:41704794-41705110	HepG2	liver:	n/a	chr14:41704949-41704960
5	CEBPB	chr14:41670220-41670485	HepG2	liver:	n/a	chr14:41670353-41670364
6	CEBPB	chr14:41694700-41694938	K562	blood:	n/a	chr14:41694823-41694834
7	CEBPB	chr14:41744045-41744376	IMR90	lung:	n/a	n/a
8	CEBPB	chr14:41752395-41752683	HepG2	liver:	n/a	chr14:41752499-41752510
9	CEBPB	chr14:41699855-41700184	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:41699864-41700151	A549	lung:	n/a	n/a
11	CEBPB	chr14:41704769-41705059	MCF-7	breast:	n/a	chr14:41704949-41704960
12	CEBPB	chr14:41753829-41753973	A549	lung:	n/a	n/a
13	CEBPB	chr14:41694681-41694991	A549	lung:	n/a	chr14:41694823-41694834
14	CEBPB	chr14:41699865-41700180	IMR90	lung:	n/a	n/a
15	CEBPB	chr14:41694722-41694926	H1-hESC	embryonic stem cell:	n/a	chr14:41694823-41694834
16	CEBPB	chr14:41763615-41763815	HepG2	liver:	n/a	chr14:41763736-41763747
17	CEBPB	chr14:41760922-41761122	A549	lung:	n/a	chr14:41761068-41761079
18	CEBPB	chr14:41743982-41744316	MCF-7	breast:	n/a	n/a
19	CEBPB	chr14:41744035-41744421	MCF-7	breast:	n/a	n/a
20	CEBPB	chr14:41722516-41722685	HepG2	liver:	n/a	chr14:41722556-41722567
21	CEBPB	chr14:41744022-41744392	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:41760907-41761197	IMR90	lung:	n/a	chr14:41761068-41761079
23	CEBPB	chr14:41694665-41694996	IMR90	lung:	n/a	chr14:41694823-41694834
24	CEBPB	chr14:41709687-41709929	HepG2	liver:	n/a	chr14:41709816-41709827 chr14:41709816-41709829
25	CEBPB	chr14:41744057-41744308	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:41699224-41699528	HepG2	liver:	n/a	chr14:41699378-41699389
27	CEBPB	chr14:41711186-41711386	HepG2	liver:	n/a	chr14:41711294-41711305
28	CEBPB	chr14:41700013-41700163	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr14:41763620-41763791	A549	lung:	n/a	chr14:41763736-41763747
30	CEBPB	chr14:41699862-41700157	MCF-7	breast:	n/a	n/a
31	CEBPB	chr14:41744058-41744361	A549	lung:	n/a	n/a
32	CEBPB	chr14:41744898-41745141	HepG2	liver:	n/a	n/a
33	CTCF	chr14:41750120-41750270	NHEK	skin:	n/a	n/a
34	CTCF	chr14:41750140-41750290	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr14:41750140-41750290	AG10803	skin:	n/a	n/a
36	CTCF	chr14:41750100-41750250	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr14:41750460-41750610	HepG2	liver:	n/a	n/a
38	CTCF	chr14:41677401-41677435	GM13976	blood:	n/a	n/a
39	CTCF	chr14:41769258-41769351	Gliobla	brain:	n/a	n/a
40	CTCF	chr14:41750020-41750170	AG04450	lung:	n/a	n/a
41	CTCF	chr14:41769260-41769410	HepG2	liver:	n/a	n/a
42	CTCF	chr14:41750080-41750230	HCT-116	colon:	n/a	n/a
43	CTCF	chr14:41749908-41750477	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:41750100-41750250	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr14:41750020-41750170	HCM	heart:	n/a	n/a
46	CTCF	chr14:41750100-41750250	HCFaa	heart:	n/a	n/a
47	CTCF	chr14:41750080-41750230	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr14:41750120-41750270	GM12878	blood:	n/a	n/a
49	CTCF	chr14:41750080-41750230	GM12872	blood:	n/a	n/a
50	CTCF	chr14:41750100-41750250	HMF	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:41684218-41684268	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:41684218-41684268	HEEpiC	esophagus:	n/a
3	chr14:41684218-41684268	A549	lung:	n/a
4	chr14:41684218-41684268	ECC-1	luminal epithelium:	n/a
5	chr14:41684218-41684268	AG04450	lung:	fetal
6	chr14:41684218-41684268	H1-hESC	embryonic stem cell:	embryo
7	chr14:41684218-41684268	HCM	heart:	n/a
8	chr14:41684218-41684268	RPTEC	kidney:	n/a
9	chr14:41684218-41684268	SK-N-SH	brain:	n/a
10	chr14:41684218-41684268	NT2-D1	testis:	n/a
11	chr14:41684218-41684268	HCF	heart:	n/a
12	chr14:41684218-41684268	GM19239	blood:	n/a
13	chr14:41684218-41684268	GM12892	blood:	n/a
14	chr14:41684218-41684268	HRPEpiC	eye:	n/a
15	chr14:41684218-41684268	Hela-S3	cervix:	n/a
16	chr14:41684218-41684268	Caco-2	colon:	n/a
17	chr14:41684218-41684268	CMK	blood:	n/a
18	chr14:41684218-41684268	BE2_C	brain:	n/a
19	chr14:41684218-41684268	HRCEpiC	kidney:	n/a
20	chr14:41684218-41684268	HRE	kidney:	n/a
21	chr14:41684218-41684268	HCPEpiC	choroid plexus:	n/a
22	chr14:41684218-41684268	ovcar-3	ovarian:	n/a
23	chr14:41684218-41684268	SK-N-MC	brain:	n/a
24	chr14:41684218-41684268	PFSK-1	brain:	n/a
25	chr14:41684218-41684268	AoSMC	blood vessel:	n/a
26	chr14:41684218-41684268	HCT-116	colon:	n/a
27	chr14:41684218-41684268	U87	brain:	n/a
28	chr14:41684218-41684268	HUVEC	blood vessel:	n/a
29	chr14:41684218-41684268	PrEC	prostate:	n/a
30	chr14:41684218-41684268	HepG2	liver:	n/a
31	chr14:41684218-41684268	AG09309	skin:	n/a
32	chr14:41684218-41684268	MCF-7	breast:	n/a
33	chr14:41684218-41684268	K562	blood:	n/a
34	chr14:41684218-41684268	Jurkat	blood:	n/a
35	chr14:41684218-41684268	NHBE	bronchial:	n/a
36	chr14:41684218-41684268	HMEC	breast:	n/a
37	chr14:41684218-41684268	IMR90	lung:	fetal
38	chr14:41684218-41684268	GM12891	blood:	n/a
39	chr14:41684218-41684268	NH-A	brain:	n/a
40	chr14:41684218-41684268	HEK293	kidney:	embryo
41	chr14:41684218-41684268	T-47D	breast:	n/a
42	chr14:41684218-41684268	GM12878	blood:	n/a
43	chr14:41684218-41684268	GM06990	blood:	n/a
44	chr14:41684218-41684268	SK-N-SH_RA	brain:	n/a
45	chr14:41684218-41684268	PANC-1	pancreas:	n/a
46	chr14:41684218-41684268	NB4	blood:	n/a
47	chr14:41684218-41684268	ProgFib	skin:	n/a
48	chr14:41684218-41684268	SKMC	muscle:	n/a
49	chr14:41684218-41684268	NHDF-neo	bronchial:	n/a
50	chr14:41684218-41684268	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:41749762..41750647-chr14:42069299..42070355,5	MCF-7	breast:
2	chr14:41488666..41490358-chr14:41674438..41676053,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRFN5-5	chr14:41765489-41767937	NONHSAT036568

No data

Variant related genes	Relation type
ENSG00000258385	TF binding region
ENSG00000258385	CpG island

Extended variants
information (count: 1578 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1578 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148447981	chr14:41669608-41669609	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs529842886	chr14:41669624-41669625	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs547664670	chr14:41669645-41669646	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs77101571	chr14:41669696-41669697	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs536217153	chr14:41669728-41669729	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs74803015	chr14:41669730-41669731	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs527448952	chr14:41669748-41669749	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs552454997	chr14:41669755-41669756	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs369923900	chr14:41669767-41669768	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs147630406	chr14:41669769-41669770	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs188703517	chr14:41669791-41669792	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs116869753	chr14:41669797-41669798	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs183485592	chr14:41673026-41673027	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs528692099	chr14:41673031-41673032	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs547146192	chr14:41673110-41673111	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs115050914	chr14:41673128-41673129	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs187268069	chr14:41673141-41673142	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs550855354	chr14:41673170-41673171	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs17111545	chr14:41673195-41673196	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs184994729	chr14:41674409-41674410	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs138230627	chr14:41674413-41674414	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs1782169	chr14:41674426-41674427	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs561119227	chr14:41674434-41674435	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs187917721	chr14:41674435-41674436	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs192845360	chr14:41674460-41674461	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs149551606	chr14:41674481-41674482	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs568946118	chr14:41674508-41674509	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs536592140	chr14:41674513-41674514	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs185258452	chr14:41674517-41674518	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs207474704	chr14:41674551-41674552	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs566863794	chr14:41674554-41674555	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs201317544	chr14:41674566-41674567	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs112446490	chr14:41674580-41674581	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs188893132	chr14:41674581-41674582	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs148336632	chr14:41674589-41674590	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs556379827	chr14:41674619-41674620	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs141462716	chr14:41674686-41674687	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs369190971	chr14:41674691-41674692	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs542510998	chr14:41674721-41674722	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs530353006	chr14:41674739-41674740	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
41	rs560580836	chr14:41674776-41674777	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
42	rs192554948	chr14:41674813-41674814	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs540204486	chr14:41674838-41674839	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs564851052	chr14:41674875-41674876	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs1782170	chr14:41674903-41674904	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550689366	chr14:41674914-41674915	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs184888045	chr14:41674917-41674918	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs529805854	chr14:41674956-41674957	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs75668612	chr14:41674957-41674958	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs566616775	chr14:41674991-41674992	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41669600-41669800	Bivalent Enhancer	Left Ventricle	heart
2	chr14:41673000-41673200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:41674400-41674600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
4	chr14:41674400-41675000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:41674400-41675000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:41674400-41675200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr14:41674600-41674800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
8	chr14:41674800-41675000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr14:41674800-41675200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr14:41674800-41675400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr14:41674800-41675600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr14:41675000-41679600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:41675200-41675400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr14:41675200-41675400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
15	chr14:41675400-41675600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr14:41696200-41696800	Enhancers	Liver	Liver
17	chr14:41696400-41696800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:41696800-41699800	Weak transcription	Liver	Liver
19	chr14:41699800-41700400	Enhancers	Liver	Liver
20	chr14:41700400-41703800	Weak transcription	Liver	Liver
21	chr14:41703800-41705600	Enhancers	Liver	Liver
22	chr14:41715400-41716000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr14:41715400-41716000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr14:41722000-41722400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr14:41722000-41722400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr14:41722000-41723000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:41722000-41723200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:41723200-41734200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:41726400-41727200	Enhancers	Liver	Liver
30	chr14:41734200-41734600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:41736400-41737800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr14:41736600-41738400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr14:41738000-41738400	Active TSS	Fetal Heart	heart
34	chr14:41747000-41747400	Enhancers	Fetal Brain Female	brain
35	chr14:41747000-41747600	Enhancers	Fetal Brain Male	brain
36	chr14:41750200-41750800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr14:41754600-41755000	Enhancers	Brain Germinal Matrix	brain
38	chr14:41762800-41763600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:41764400-41766200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr14:41766200-41767200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr14:41766800-41767200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr14:41766800-41767600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr14:41767000-41767400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr14:41767400-41767800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr14:41767400-41767800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr14:41767600-41770400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:41769000-41769600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr14:41769200-41769400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr14:41769400-41770000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr14:41769400-41770800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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