Variant report

Variant	nsv983769
Chromosome Location	chr14:40823617-40852104
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	CEBPB	chr14:40840907-40841139	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr14:40844308-40844652	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:40844299-40844655	A549	lung:	n/a	n/a
4	CEBPB	chr14:40844357-40844564	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr14:40844332-40844672	IMR90	lung:	n/a	n/a
6	CEBPB	chr14:40840922-40841392	HepG2	liver:	n/a	chr14:40841265-40841278 chr14:40841265-40841276 chr14:40841267-40841276
7	CTCF	chr14:40836292-40836352	GM13976	blood:	n/a	n/a
8	CTCF	chr14:40841280-40841430	HPF	lung:	n/a	n/a
9	ELF1	chr14:40834427-40835016	MCF-7	breast:	n/a	chr14:40834998-40835009
10	EP300	chr14:40837572-40837846	T-47D	breast:	n/a	chr14:40837821-40837831 chr14:40837726-40837736
11	EP300	chr14:40837426-40838012	T-47D	breast:	n/a	chr14:40837896-40837910 chr14:40837821-40837831 chr14:40837471-40837485 chr14:40837991-40838000 chr14:40837465-40837479 chr14:40837726-40837736
12	EP300	chr14:40834404-40834981	MCF-7	breast:	n/a	chr14:40834946-40834960 chr14:40834908-40834917
13	EP300	chr14:40837523-40838000	MCF-7	breast:	n/a	chr14:40837896-40837910 chr14:40837821-40837831 chr14:40837991-40838000 chr14:40837726-40837736
14	FOS	chr14:40840281-40840506	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr14:40836951-40837247	MCF10A-Er-Src	breast:	n/a	chr14:40837151-40837158 chr14:40837151-40837159 chr14:40837152-40837163
16	FOS	chr14:40840310-40840509	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr14:40840331-40840587	MCF10A-Er-Src	breast:	n/a	n/a
18	FOSL2	chr14:40836876-40837352	MCF-7	breast:	n/a	chr14:40837151-40837158 chr14:40837151-40837159 chr14:40837152-40837163
19	FOSL2	chr14:40837479-40837975	MCF-7	breast:	n/a	chr14:40837744-40837753
20	FOXA1	chr14:40831261-40831604	T-47D	breast:	n/a	n/a
21	FOXA1	chr14:40837526-40837914	T-47D	breast:	n/a	chr14:40837725-40837740 chr14:40837818-40837830
22	FOXA1	chr14:40837436-40838037	T-47D	breast:	n/a	chr14:40837725-40837740 chr14:40837818-40837830
23	FOXA1	chr14:40837487-40837940	HepG2	liver:	n/a	chr14:40837725-40837740 chr14:40837818-40837830
24	FOXM1	chr14:40837059-40838074	MCF-7	breast:	n/a	n/a
25	FOXM1	chr14:40834444-40834925	MCF-7	breast:	n/a	n/a
26	FOXM1	chr14:40834310-40835125	MCF-7	breast:	n/a	n/a
27	GATA3	chr14:40837192-40838103	MCF-7	breast:	n/a	chr14:40837426-40837434 chr14:40837992-40838002
28	GATA3	chr14:40836848-40838128	MCF-7	breast:	n/a	chr14:40837426-40837434 chr14:40837992-40838002
29	GATA3	chr14:40834480-40834887	T-47D	breast:	n/a	chr14:40834678-40834685 chr14:40834678-40834687 chr14:40834677-40834685 chr14:40834671-40834692 chr14:40834677-40834687
30	GATA3	chr14:40836968-40838452	MCF-7	breast:	n/a	chr14:40837426-40837434 chr14:40837992-40838002
31	GATA3	chr14:40834374-40835023	MCF-7	breast:	n/a	chr14:40834909-40834919 chr14:40834678-40834685 chr14:40834678-40834687 chr14:40834677-40834685 chr14:40834671-40834692 chr14:40834677-40834687
32	GATA3	chr14:40834230-40835352	MCF-7	breast:	n/a	chr14:40834909-40834919 chr14:40834678-40834685 chr14:40834678-40834687 chr14:40834677-40834685 chr14:40834671-40834692 chr14:40834677-40834687
33	GATA3	chr14:40834531-40834946	MCF-7	breast:	n/a	chr14:40834909-40834919 chr14:40834678-40834685 chr14:40834678-40834687 chr14:40834677-40834685 chr14:40834671-40834692 chr14:40834677-40834687
34	GATA3	chr14:40834468-40834807	T-47D	breast:	n/a	chr14:40834678-40834685 chr14:40834678-40834687 chr14:40834677-40834685 chr14:40834671-40834692 chr14:40834677-40834687
35	GATA3	chr14:40837450-40837879	T-47D	breast:	n/a	n/a
36	GATA3	chr14:40837413-40838004	T-47D	breast:	n/a	chr14:40837426-40837434 chr14:40837992-40838002
37	GATA3	chr14:40834188-40835195	MCF-7	breast:	n/a	chr14:40834909-40834919 chr14:40834678-40834685 chr14:40834678-40834687 chr14:40834677-40834685 chr14:40834671-40834692 chr14:40834677-40834687
38	GATA3	chr14:40837288-40837901	MCF-7	breast:	n/a	chr14:40837426-40837434
39	HDAC2	chr14:40834470-40834944	MCF-7	breast:	n/a	chr14:40834677-40834686
40	HDAC2	chr14:40837448-40838120	MCF-7	breast:	n/a	chr14:40837473-40837487 chr14:40837727-40837736 chr14:40837469-40837483 chr14:40837821-40837830 chr14:40837876-40837890 chr14:40837472-40837486 chr14:40837871-40837885 chr14:40837474-40837488
41	HDAC2	chr14:40837566-40838013	MCF-7	breast:	n/a	chr14:40837727-40837736 chr14:40837821-40837830 chr14:40837876-40837890 chr14:40837871-40837885
42	JUND	chr14:40837447-40838007	MCF-7	breast:	n/a	chr14:40837744-40837753
43	JUND	chr14:40834455-40834998	MCF-7	breast:	n/a	n/a
44	JUND	chr14:40837394-40838038	T-47D	breast:	n/a	chr14:40837744-40837753
45	MAFF	chr14:40840008-40840193	HepG2	liver:	n/a	chr14:40840042-40840060
46	MAFF	chr14:40834327-40834528	HepG2	liver:	n/a	n/a
47	MAFK	chr14:40839968-40840213	HepG2	liver:	n/a	chr14:40840039-40840056
48	MAFK	chr14:40839867-40840225	HepG2	liver:	n/a	chr14:40840039-40840056
49	MAFK	chr14:40840018-40840187	IMR90	lung:	n/a	chr14:40840039-40840056
50	MAFK	chr14:40839664-40839761	H1-hESC	embryonic stem cell:	n/a	chr14:40839673-40839687

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:40832309-40832359	NHDF-neo	bronchial:	n/a
2	chr14:40832309-40832359	NHDF-neo	bronchial:	n/a
3	chr14:40832309-40832359	Caco-2	colon:	n/a
4	chr14:40832309-40832359	HEEpiC	esophagus:	n/a
5	chr14:40832309-40832359	HRCEpiC	kidney:	n/a
6	chr14:40832309-40832359	HUVEC	blood vessel:	n/a
7	chr14:40832309-40832359	MCF-7	breast:	n/a
8	chr14:40832309-40832359	ProgFib	skin:	n/a
9	chr14:40832309-40832359	LNCaP	prostate:	n/a
10	chr14:40832309-40832359	U87	brain:	n/a
11	chr14:40832309-40832359	HMEC	breast:	n/a
12	chr14:40832309-40832359	NH-A	brain:	n/a
13	chr14:40832309-40832359	HRE	kidney:	n/a
14	chr14:40832309-40832359	AG04450	lung:	fetal
15	chr14:40832309-40832359	SK-N-MC	brain:	n/a
16	chr14:40832309-40832359	BE2_C	brain:	n/a
17	chr14:40832309-40832359	Hela-S3	cervix:	n/a
18	chr14:40832309-40832359	SAEC	small airway:	n/a
19	chr14:40832309-40832359	GM06990	blood:	n/a
20	chr14:40832309-40832359	SK-N-SH	brain:	n/a
21	chr14:40832309-40832359	HepG2	liver:	n/a
22	chr14:40832309-40832359	AG09319	gingival:	n/a
23	chr14:40832309-40832359	AG04449	skin:	fetal
24	chr14:40832309-40832359	HL-60	blood:	n/a
25	chr14:40832309-40832359	K562	blood:	n/a
26	chr14:40832309-40832359	Hepatocyte	liver:	n/a
27	chr14:40832309-40832359	PrEC	prostate:	n/a
28	chr14:40832309-40832359	GM12892	blood:	n/a
29	chr14:40832309-40832359	AG09309	skin:	n/a
30	chr14:40832309-40832359	ovcar-3	ovarian:	n/a
31	chr14:40832309-40832359	SK-N-SH_RA	brain:	n/a
32	chr14:40832309-40832359	T-47D	breast:	n/a
33	chr14:40832309-40832359	CMK	blood:	n/a
34	chr14:40832309-40832359	GM19239	blood:	n/a
35	chr14:40832309-40832359	BJ	skin:	n/a
36	chr14:40832309-40832359	ECC-1	luminal epithelium:	n/a
37	chr14:40832309-40832359	Jurkat	blood:	n/a
38	chr14:40832309-40832359	IMR90	lung:	fetal
39	chr14:40832309-40832359	HIPEpiC	eye:	n/a
40	chr14:40832309-40832359	HAEpiC	amniotic membrane:	n/a
41	chr14:40832309-40832359	SKMC	muscle:	n/a
42	chr14:40832309-40832359	HPAEpiC	pulmonary alveolar:	n/a
43	chr14:40832309-40832359	H1-hESC	embryonic stem cell:	embryo
44	chr14:40832309-40832359	GM12891	blood:	n/a
45	chr14:40832309-40832359	PANC-1	pancreas:	n/a
46	chr14:40832309-40832359	A549	lung:	n/a
47	chr14:40832309-40832359	HCM	heart:	n/a
48	chr14:40832309-40832359	NB4	blood:	n/a
49	chr14:40832309-40832359	PFSK-1	brain:	n/a
50	chr14:40832309-40832359	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:40839183..40841621-chr14:40841712..40843758,2	MCF-7	breast:
2	chr14:40839183..40841621-chr14:40841712..40843758,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000258418	TF binding region
ENSG00000258480	TF binding region
ENSG00000258418	CpG island
ENSG00000258480	CpG island

Extended variants
information (count: 531 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538887893	chr14:40823619-40823620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191174400	chr14:40823630-40823631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572487092	chr14:40823666-40823667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541468502	chr14:40823671-40823672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138827208	chr14:40823707-40823708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140495006	chr14:40823708-40823709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150439325	chr14:40823731-40823732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543823785	chr14:40823766-40823767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138221278	chr14:40823777-40823778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532435812	chr14:40823785-40823786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545723027	chr14:40823847-40823848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183049021	chr14:40823848-40823849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528174267	chr14:40823864-40823865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548236648	chr14:40823877-40823878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113003083	chr14:40823887-40823888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542062651	chr14:40823890-40823891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187385562	chr14:40823940-40823941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201832860	chr14:40823992-40823993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192576096	chr14:40824022-40824023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539310270	chr14:40824024-40824025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368783518	chr14:40824029-40824030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371046135	chr14:40824048-40824049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558894746	chr14:40824072-40824073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1955551	chr14:40824125-40824126	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs149291057	chr14:40824142-40824143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184812001	chr14:40824159-40824160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147409441	chr14:40824201-40824202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138192480	chr14:40824207-40824208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188695593	chr14:40824221-40824222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370894090	chr14:40824344-40824345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192788547	chr14:40824390-40824391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538371554	chr14:40824395-40824396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557385920	chr14:40824402-40824403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530626731	chr14:40824437-40824438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545481688	chr14:40824443-40824444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577074453	chr14:40824458-40824459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546028705	chr14:40824459-40824460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12891314	chr14:40824491-40824492	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs184301386	chr14:40824524-40824525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368301819	chr14:40824560-40824561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77673762	chr14:40824566-40824567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201782399	chr14:40824627-40824628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200545090	chr14:40824634-40824635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576366153	chr14:40824636-40824637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530516530	chr14:40824638-40824639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374793847	chr14:40824658-40824659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532681206	chr14:40824695-40824696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564069204	chr14:40824701-40824702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190024526	chr14:40824726-40824727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548099971	chr14:40824732-40824733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Invasive pancreatic ductal carcinoma	16982739	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
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:40823600-40823800	Enhancers	H9 Cell Line	embryonic stem cell
2	chr14:40823600-40825200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr14:40823600-40825200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr14:40823600-40825400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr14:40823600-40825400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:40823600-40825400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr14:40823800-40825200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr14:40824200-40824400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr14:40824400-40825200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr14:40825200-40825400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr14:40825200-40825600	Enhancers	H9 Cell Line	embryonic stem cell
12	chr14:40826800-40828200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr14:40827800-40828200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr14:40828600-40829200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:40828600-40829400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr14:40828800-40829200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
17	chr14:40828800-40829400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr14:40829400-40831200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr14:40829400-40831800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:40830200-40830600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:40830600-40831600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:40831200-40832800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr14:40831200-40833000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr14:40831200-40833200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr14:40831200-40835800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr14:40831400-40831600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr14:40831400-40832800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr14:40831600-40832200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:40831600-40832800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr14:40831800-40832200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:40831800-40832600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr14:40832000-40832600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr14:40832000-40832600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:40832200-40832400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr14:40832200-40832600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr14:40832400-40832600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr14:40832400-40833000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr14:40832600-40833800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr14:40833800-40835000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:40834200-40834800	Enhancers	Brain Germinal Matrix	brain
41	chr14:40834400-40835400	Enhancers	Dnd41	blood
42	chr14:40837600-40838000	Enhancers	Fetal Kidney	kidney
43	chr14:40837600-40838200	Enhancers	Liver	Liver
44	chr14:40837800-40838400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr14:40840400-40841600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr14:40840800-40841200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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