Variant report

Variant	nsv983949
Chromosome Location	chr14:32604484-32618641
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	chr14:32607253-32607349	HepG2	liver:	n/a	n/a
2	BHLHE40	chr14:32610137-32610142	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:32605248-32605604	HepG2	liver:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
4	CEBPB	chr14:32605257-32605608	A549	lung:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
5	CEBPB	chr14:32605246-32605621	MCF-7	breast:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
6	CEBPB	chr14:32605342-32605520	K562	blood:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
7	CEBPB	chr14:32605273-32605582	IMR90	lung:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
8	CEBPB	chr14:32605244-32605593	A549	lung:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
9	CEBPB	chr14:32605137-32605698	A549	lung:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
10	CEBPB	chr14:32603507-32604682	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr14:32605177-32605650	Hela-S3	cervix:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
12	CEBPB	chr14:32605249-32605610	ECC-1	luminal epithelium:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
13	CEBPB	chr14:32605278-32605602	ECC-1	luminal epithelium:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
14	CEBPB	chr14:32605283-32605572	K562	blood:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
15	CEBPB	chr14:32605160-32605648	MCF-7	breast:	n/a	chr14:32605409-32605420 chr14:32605429-32605440
16	CTCF	chr14:32618380-32618530	HepG2	liver:	n/a	n/a
17	CTCF	chr14:32613220-32613370	HepG2	liver:	n/a	n/a
18	CTCF	chr14:32609548-32609607	Spleen_OC	spleen:	n/a	n/a
19	E2F4	chr14:32617884-32618170	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr14:32605065-32605486	MCF10A-Er-Src	breast:	n/a	n/a
21	ELF1	chr14:32603770-32604791	MCF-7	breast:	n/a	chr14:32604539-32604550
22	EP300	chr14:32603398-32604519	A549	lung:	n/a	n/a
23	EP300	chr14:32603608-32604486	ECC-1	luminal epithelium:	n/a	n/a
24	FOS	chr14:32605401-32605544	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr14:32611214-32611455	HUVEC	blood vessel:	n/a	chr14:32611340-32611351
26	FOXA1	chr14:32609846-32610257	HepG2	liver:	n/a	n/a
27	FOXA1	chr14:32605681-32605941	T-47D	breast:	n/a	n/a
28	FOXA2	chr14:32609894-32610173	HepG2	liver:	n/a	n/a
29	GABPA	chr14:32609253-32609341	HepG2	liver:	n/a	n/a
30	GATA3	chr14:32603549-32604590	SK-N-SH	brain:	n/a	chr14:32603678-32603690
31	GATA3	chr14:32603471-32604550	MCF-7	breast:	n/a	chr14:32603678-32603690
32	GATA3	chr14:32607145-32607404	MCF-7	breast:	n/a	n/a
33	GATA3	chr14:32603522-32604638	A549	lung:	n/a	chr14:32603678-32603690
34	GATA3	chr14:32603322-32604673	MCF-7	breast:	n/a	chr14:32603678-32603690
35	GATA3	chr14:32603777-32604546	MCF-7	breast:	n/a	n/a
36	GATA3	chr14:32603592-32604496	SK-N-SH	brain:	n/a	chr14:32603678-32603690
37	JUN	chr14:32612114-32612196	HepG2	liver:	n/a	chr14:32612121-32612134
38	JUND	chr14:32611850-32612270	HepG2	liver:	n/a	n/a
39	KAP1	chr14:32607200-32607516	HEK293	kidney:	n/a	n/a
40	KAP1	chr14:32603477-32604621	HEK293	kidney:	n/a	n/a
41	KAP1	chr14:32603534-32604568	U2OS	brain:	n/a	n/a
42	KAP1	chr14:32607325-32607472	U2OS	brain:	n/a	n/a
43	MAFK	chr14:32611246-32611426	HepG2	liver:	n/a	n/a
44	MAFK	chr14:32603600-32604601	Hela-S3	cervix:	n/a	n/a
45	MAFK	chr14:32608235-32608478	HepG2	liver:	n/a	n/a
46	MAFK	chr14:32611301-32611387	HepG2	liver:	n/a	n/a
47	MXI1	chr14:32616775-32616807	K562	blood:	n/a	n/a
48	NR2F2	chr14:32603636-32604502	MCF-7	breast:	n/a	n/a
49	PBX3	chr14:32603671-32604486	SK-N-SH	brain:	n/a	n/a
50	POLR2A	chr14:32604548-32604560	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:32564399..32566977-chr14:32602689..32605048,2	MCF-7	breast:
2	chr14:32602399..32605082-chr14:32670593..32672756,2	MCF-7	breast:
3	chr14:32543954..32548342-chr14:32602314..32606365,7	MCF-7	breast:
4	chr14:32614081..32616307-chr14:32620214..32621864,2	MCF-7	breast:
5	chr14:32597351..32599387-chr14:32602127..32605349,3	MCF-7	breast:
6	chr14:32614093..32616573-chr14:32619305..32621843,3	K562	blood:
7	chr14:32555055..32558113-chr14:32603507..32605288,3	MCF-7	breast:

Variant related genes	Relation type
ARHGAP5	TF binding region
ENSG00000100852	chromatin interactions
ENSG00000258655	chromatin interactions
ENSG00000201654	chromatin interactions
ENSG00000202337	chromatin interactions

Extended variants
information (count: 545 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:545 , 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	rs551598565	chr14:32604494-32604495	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs566525902	chr14:32604529-32604530	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs528618918	chr14:32604543-32604544	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs546792044	chr14:32604560-32604561	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs571854691	chr14:32604562-32604563	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs535832958	chr14:32604565-32604566	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs142165948	chr14:32604586-32604587	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs186581140	chr14:32604607-32604608	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs8010167	chr14:32604638-32604639	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539725421	chr14:32604659-32604660	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs144558229	chr14:32604667-32604668	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs573375539	chr14:32604689-32604690	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs551003879	chr14:32604715-32604716	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs555506451	chr14:32604733-32604734	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs192795824	chr14:32604735-32604736	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs61427077	chr14:32604769-32604770	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148930017	chr14:32604770-32604771	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs551448037	chr14:32604808-32604809	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs185400638	chr14:32604860-32604861	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs531661325	chr14:32604928-32604929	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs143641127	chr14:32604944-32604945	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs189064048	chr14:32604962-32604963	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs549112668	chr14:32604972-32604973	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs148118044	chr14:32604982-32604983	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs115763619	chr14:32604999-32605000	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs550591903	chr14:32605088-32605089	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs568896948	chr14:32605093-32605094	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs533662606	chr14:32605117-32605118	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539789467	chr14:32605141-32605142	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs1952488	chr14:32605219-32605220	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567108684	chr14:32605230-32605231	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576234454	chr14:32605242-32605243	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543673307	chr14:32605264-32605265	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112566848	chr14:32605291-32605292	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs200296336	chr14:32605328-32605329	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs555987908	chr14:32605375-32605376	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs573826839	chr14:32605468-32605469	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141009543	chr14:32605503-32605504	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145044321	chr14:32605516-32605517	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs184587211	chr14:32605588-32605589	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs189197596	chr14:32605608-32605609	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs560189690	chr14:32605636-32605637	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113529171	chr14:32605703-32605704	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542451204	chr14:32605730-32605731	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs114684644	chr14:32605739-32605740	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577071138	chr14:32605747-32605748	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550678724	chr14:32605768-32605769	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562975088	chr14:32605775-32605776	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs533176922	chr14:32605801-32605802	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551713349	chr14:32605839-32605840	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	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
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32571800-32606800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr14:32571800-32614400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr14:32574400-32615600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr14:32577200-32605400	Weak transcription	Primary T cells from cord blood	blood
5	chr14:32577400-32625000	Weak transcription	Small Intestine	intestine
6	chr14:32590000-32623000	Weak transcription	HSMMtube	muscle
7	chr14:32591600-32621200	Weak transcription	NHLF	lung
8	chr14:32592200-32606400	Weak transcription	Brain Substantia Nigra	brain
9	chr14:32592800-32614400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr14:32593600-32606400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr14:32593800-32607200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr14:32595800-32605600	Weak transcription	Primary B cells from cord blood	blood
13	chr14:32595800-32605600	Weak transcription	Fetal Lung	lung
14	chr14:32595800-32605800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr14:32596000-32605600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr14:32596000-32606600	Weak transcription	Brain Angular Gyrus	brain
17	chr14:32596000-32622800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr14:32596200-32605400	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr14:32596200-32605800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr14:32596400-32620400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr14:32596600-32616200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr14:32597600-32606400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr14:32597800-32605200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr14:32597800-32607200	Weak transcription	Ovary	ovary
25	chr14:32597800-32607400	Weak transcription	Lung	lung
26	chr14:32597800-32616600	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr14:32597800-32619600	Weak transcription	Esophagus	oesophagus
28	chr14:32598000-32604600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr14:32598000-32605800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr14:32598000-32606800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr14:32598000-32606800	Weak transcription	Fetal Thymus	thymus
32	chr14:32598000-32614200	Weak transcription	Pancreas	Pancrea
33	chr14:32598000-32618400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr14:32598000-32629000	Weak transcription	Gastric	stomach
35	chr14:32598800-32605400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr14:32598800-32605600	Weak transcription	Adipose Nuclei	Adipose
37	chr14:32599000-32605800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr14:32599000-32606400	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr14:32599000-32607400	Weak transcription	Brain Anterior Caudate	brain
40	chr14:32599200-32605600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:32599200-32605800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr14:32599200-32605800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr14:32599200-32605800	Weak transcription	HSMM	muscle
44	chr14:32599200-32606400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr14:32599200-32606800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr14:32599200-32615200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr14:32599200-32619600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr14:32599200-32623400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr14:32599600-32605200	Weak transcription	HepG2	liver
50	chr14:32600200-32604800	Weak transcription	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links