Variant report

Variant	nsv564385
Chromosome Location	chr14:38246440-38321607
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	ARID3A	chr14:38318201-38318889	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:38257325-38257703	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:38288259-38289246	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:38303625-38303740	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:38260485-38261042	HepG2	liver:	n/a	chr14:38260596-38260612 chr14:38260595-38260611
6	ARID3A	chr14:38246221-38246634	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:38266043-38266686	HepG2	liver:	n/a	n/a
8	BHLHE40	chr14:38257273-38257648	HepG2	liver:	n/a	n/a
9	BHLHE40	chr14:38288516-38288820	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:38247669-38247776	HepG2	liver:	n/a	chr14:38247739-38247750
11	CEBPB	chr14:38313446-38313776	A549	lung:	n/a	chr14:38313601-38313612
12	CEBPB	chr14:38313413-38313788	K562	blood:	n/a	chr14:38313601-38313612
13	CEBPB	chr14:38270344-38270683	HepG2	liver:	n/a	chr14:38270486-38270497 chr14:38270509-38270520
14	CEBPB	chr14:38288369-38288896	HepG2	liver:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
15	CEBPB	chr14:38320301-38320598	HepG2	liver:	n/a	chr14:38320452-38320463 chr14:38320451-38320462
16	CEBPB	chr14:38257352-38257584	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:38257305-38257887	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:38313447-38313772	Hela-S3	cervix:	n/a	chr14:38313601-38313612
19	CEBPB	chr14:38265449-38265658	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:38288563-38288893	Hela-S3	cervix:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
21	CEBPB	chr14:38290660-38290925	HepG2	liver:	n/a	chr14:38290789-38290800
22	CEBPB	chr14:38289638-38289968	HepG2	liver:	n/a	chr14:38289796-38289807 chr14:38289795-38289808
23	CEBPB	chr14:38289657-38289831	H1-hESC	embryonic stem cell:	n/a	chr14:38289796-38289807 chr14:38289795-38289808
24	CEBPB	chr14:38288344-38288897	IMR90	lung:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
25	CEBPB	chr14:38313415-38313793	HepG2	liver:	n/a	chr14:38313601-38313612
26	CEBPB	chr14:38288627-38288842	HepG2	liver:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
27	CEBPB	chr14:38271918-38271998	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr14:38257326-38257980	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:38313423-38313757	IMR90	lung:	n/a	chr14:38313601-38313612
30	CEBPB	chr14:38288248-38288936	HepG2	liver:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
31	CEBPB	chr14:38288405-38288863	A549	lung:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
32	CEBPB	chr14:38313496-38313703	H1-hESC	embryonic stem cell:	n/a	chr14:38313601-38313612
33	CEBPB	chr14:38288659-38288825	MCF-7	breast:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
34	CEBPB	chr14:38313521-38313730	HepG2	liver:	n/a	chr14:38313601-38313612
35	CEBPB	chr14:38270353-38270644	A549	lung:	n/a	chr14:38270486-38270497 chr14:38270509-38270520
36	CEBPB	chr14:38313359-38313792	HepG2	liver:	n/a	chr14:38313601-38313612
37	CEBPB	chr14:38288592-38288863	H1-hESC	embryonic stem cell:	n/a	chr14:38288740-38288751 chr14:38288742-38288753
38	CEBPB	chr14:38313389-38313845	A549	lung:	n/a	chr14:38313601-38313612
39	CEBPB	chr14:38318261-38318533	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:38313457-38313687	ECC-1	luminal epithelium:	n/a	chr14:38313601-38313612
41	CEBPB	chr14:38313369-38313818	MCF-7	breast:	n/a	chr14:38313601-38313612
42	CEBPD	chr14:38313484-38313708	HepG2	liver:	n/a	n/a
43	CTCF	chr14:38294680-38294830	GM06990	blood:	n/a	n/a
44	CTCF	chr14:38247620-38247770	HepG2	liver:	n/a	n/a
45	CTCF	chr14:38320552-38320585	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr14:38292112-38292162	Lung_OC	lung:	n/a	n/a
47	CTCF	chr14:38290318-38290354	GM10248	blood:	n/a	n/a
48	CTCF	chr14:38280570-38280700	Medullo	brain:	n/a	n/a
49	CTCF	chr14:38247308-38247370	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:38247900-38248050	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38263141-38263191	ovcar-3	ovarian:	n/a
2	chr14:38263141-38263191	SAEC	small airway:	n/a
3	chr14:38279064-38279114	K562	blood:	n/a
4	chr14:38279064-38279114	AG04449	skin:	fetal
5	chr14:38263617-38263667	NB4	blood:	n/a
6	chr14:38263141-38263191	BE2_C	brain:	n/a
7	chr14:38279064-38279114	HMEC	breast:	n/a
8	chr14:38263617-38263667	H1-hESC	embryonic stem cell:	embryo
9	chr14:38263617-38263667	GM12891	blood:	n/a
10	chr14:38279064-38279114	HEEpiC	esophagus:	n/a
11	chr14:38279064-38279114	GM19239	blood:	n/a
12	chr14:38263617-38263667	HEK293	kidney:	embryo
13	chr14:38263617-38263667	MCF-7	breast:	n/a
14	chr14:38263617-38263667	HIPEpiC	eye:	n/a
15	chr14:38263617-38263667	HCF	heart:	n/a
16	chr14:38279064-38279114	AG09309	skin:	n/a
17	chr14:38279064-38279114	SK-N-MC	brain:	n/a
18	chr14:38263617-38263667	T-47D	breast:	n/a
19	chr14:38263617-38263667	NHBE	bronchial:	n/a
20	chr14:38263141-38263191	T-47D	breast:	n/a
21	chr14:38263141-38263191	GM19239	blood:	n/a
22	chr14:38263141-38263191	Jurkat	blood:	n/a
23	chr14:38279064-38279114	Hepatocyte	liver:	n/a
24	chr14:38263141-38263191	IMR90	lung:	fetal
25	chr14:38263141-38263191	MCF10A-Er-Src	breast:	n/a
26	chr14:38263141-38263191	AG09309	skin:	n/a
27	chr14:38263617-38263667	GM12878	blood:	n/a
28	chr14:38279064-38279114	ECC-1	luminal epithelium:	n/a
29	chr14:38279064-38279114	HRCEpiC	kidney:	n/a
30	chr14:38279064-38279114	HIPEpiC	eye:	n/a
31	chr14:38263141-38263191	HNPCEpiC	eye:	n/a
32	chr14:38279064-38279114	HPAEpiC	pulmonary alveolar:	n/a
33	chr14:38263617-38263667	HCT-116	colon:	n/a
34	chr14:38279064-38279114	BJ	skin:	n/a
35	chr14:38279064-38279114	Caco-2	colon:	n/a
36	chr14:38263141-38263191	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:38263141-38263191	AG09319	gingival:	n/a
38	chr14:38263617-38263667	HRPEpiC	eye:	n/a
39	chr14:38263141-38263191	HUVEC	blood vessel:	n/a
40	chr14:38263617-38263667	HCM	heart:	n/a
41	chr14:38263617-38263667	HRE	kidney:	n/a
42	chr14:38263141-38263191	HCT-116	colon:	n/a
43	chr14:38279064-38279114	PrEC	prostate:	n/a
44	chr14:38279064-38279114	CMK	blood:	n/a
45	chr14:38263141-38263191	NH-A	brain:	n/a
46	chr14:38279064-38279114	HCM	heart:	n/a
47	chr14:38279064-38279114	HCF	heart:	n/a
48	chr14:38263617-38263667	HMEC	breast:	n/a
49	chr14:38279064-38279114	SKMC	muscle:	n/a
50	chr14:38279064-38279114	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:38273224..38275723-chr14:38279510..38281745,2	K562	blood:
2	chr14:38063353..38065330-chr14:38297774..38300460,2	MCF-7	breast:
3	chr14:38317873..38320611-chr14:38331977..38333787,2	MCF-7	breast:
4	chr14:38273224..38275723-chr14:38279510..38281745,2	K562	blood:
5	chr14:38288642..38290464-chr14:38293057..38295277,2	MCF-7	breast:
6	chr14:38288642..38290464-chr14:38293057..38295277,2	MCF-7	breast:
7	chr14:38063198..38065699-chr14:38312720..38314688,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MIPOL1-6	chr14:38320042-38321184	NONHSAT036473

Variant related genes	Relation type
TTC6	TF binding region
RNU6-1277P	TF binding region
TTC6	CpG island
RNU6-1277P	CpG island
ENSG00000139865	chromatin interactions
ENSG00000129514	chromatin interactions

Extended variants
information (count: 2381 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8016889	chr14:38246440-38246441	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533246980	chr14:38246462-38246463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534204082	chr14:38246496-38246497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182763149	chr14:38246507-38246508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80104243	chr14:38246564-38246565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs57518151	chr14:38246565-38246566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147890680	chr14:38246566-38246567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567261822	chr14:38246571-38246572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536301195	chr14:38246576-38246577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556200384	chr14:38246598-38246599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544258344	chr14:38246614-38246615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186111194	chr14:38246616-38246617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538744728	chr14:38246617-38246618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370973691	chr14:38246618-38246619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533298935	chr14:38246698-38246699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs58001960	chr14:38246706-38246707	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs4901251	chr14:38246748-38246749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11851121	chr14:38246841-38246842	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560894252	chr14:38246844-38246845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574393491	chr14:38246855-38246856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542571486	chr14:38246856-38246857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115986040	chr14:38246866-38246867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs36194865	chr14:38246870-38246871	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs190089349	chr14:38246883-38246884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145205901	chr14:38246921-38246922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200979750	chr14:38246976-38246977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376967421	chr14:38246977-38246978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147694593	chr14:38247021-38247022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35609632	chr14:38247069-38247070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78963000	chr14:38247109-38247110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567912607	chr14:38247128-38247129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149162284	chr14:38247131-38247132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79013727	chr14:38247132-38247133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182535686	chr14:38247147-38247148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569657661	chr14:38247177-38247178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77562934	chr14:38247184-38247185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143262032	chr14:38247203-38247204	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571408744	chr14:38247228-38247229	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565730690	chr14:38247245-38247246	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534461752	chr14:38247265-38247266	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554351499	chr14:38247275-38247276	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574355531	chr14:38247293-38247294	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187229946	chr14:38247338-38247339	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543333861	chr14:38247354-38247355	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538699674	chr14:38247373-38247374	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538049390	chr14:38247393-38247394	Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77025879	chr14:38247419-38247420	ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576418071	chr14:38247464-38247465	ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371675993	chr14:38247476-38247477	ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550044948	chr14:38247486-38247487	ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38241800-38247200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:38242000-38247600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:38246200-38247400	Enhancers	HepG2	liver
4	chr14:38247200-38247600	ZNF genes & repeats	Fetal Intestine Small	intestine
5	chr14:38247200-38247800	ZNF genes & repeats	Gastric	stomach
6	chr14:38247200-38247800	ZNF genes & repeats	Pancreas	Pancrea
7	chr14:38247200-38248000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:38247400-38247600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:38247600-38247800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:38247800-38249400	Weak transcription	Gastric	stomach
11	chr14:38248000-38248400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:38253000-38255200	Enhancers	HepG2	liver
13	chr14:38255200-38255600	ZNF genes & repeats	Fetal Stomach	stomach
14	chr14:38255200-38256600	Weak transcription	HepG2	liver
15	chr14:38256600-38257800	Enhancers	HepG2	liver
16	chr14:38257800-38258000	Flanking Active TSS	HepG2	liver
17	chr14:38258000-38258400	Enhancers	HepG2	liver
18	chr14:38258400-38259400	Weak transcription	HepG2	liver
19	chr14:38259400-38259600	ZNF genes & repeats	Pancreas	Pancrea
20	chr14:38259400-38261600	Enhancers	HepG2	liver
21	chr14:38259600-38260000	Weak transcription	Fetal Intestine Small	intestine
22	chr14:38260200-38260600	Enhancers	Liver	Liver
23	chr14:38260600-38261200	Flanking Active TSS	Liver	Liver
24	chr14:38260600-38261200	Enhancers	Stomach Mucosa	stomach
25	chr14:38261200-38261400	Enhancers	Liver	Liver
26	chr14:38261600-38266000	Weak transcription	HepG2	liver
27	chr14:38266000-38266600	Enhancers	HepG2	liver
28	chr14:38266600-38279400	Weak transcription	HepG2	liver
29	chr14:38268600-38269800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:38269600-38269800	Enhancers	Fetal Lung	lung
31	chr14:38269800-38279000	Weak transcription	Fetal Lung	lung
32	chr14:38276400-38279600	Weak transcription	Stomach Mucosa	stomach
33	chr14:38278800-38279000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:38278800-38279800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:38278800-38280000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr14:38278800-38280000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr14:38278800-38280000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr14:38278800-38280000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr14:38278800-38280200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr14:38278800-38280200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr14:38279000-38279600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr14:38279000-38279800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr14:38279000-38280000	Enhancers	H9 Cell Line	embryonic stem cell
44	chr14:38279000-38280000	Enhancers	Fetal Lung	lung
45	chr14:38279000-38280200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:38279000-38289000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:38279200-38280000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr14:38279200-38280200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr14:38279200-38280400	Enhancers	Liver	Liver
50	chr14:38279400-38280800	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links