Variant report

Variant	nsv902054
Chromosome Location	chr14:67253035-67364763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:67305949-67305970	K562	blood:	n/a	n/a
2	BRCA1	chr14:67288110-67288222	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr14:67280308-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
4	CEBPB	chr14:67353631-67353964	HepG2	liver:	n/a	chr14:67353794-67353805
5	CEBPB	chr14:67280291-67280680	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
6	CEBPB	chr14:67280194-67280806	MCF-7	breast:	n/a	chr14:67280486-67280497
7	CEBPB	chr14:67280214-67280811	MCF-7	breast:	n/a	chr14:67280486-67280497
8	CEBPB	chr14:67280182-67280792	A549	lung:	n/a	chr14:67280486-67280497
9	CEBPB	chr14:67280306-67280665	H1-hESC	embryonic stem cell:	n/a	chr14:67280486-67280497
10	CEBPB	chr14:67326093-67326355	A549	lung:	n/a	n/a
11	CEBPB	chr14:67353634-67353973	A549	lung:	n/a	chr14:67353794-67353805
12	CEBPB	chr14:67280360-67280549	HepG2	liver:	n/a	chr14:67280486-67280497
13	CEBPB	chr14:67280261-67280604	HepG2	liver:	n/a	chr14:67280486-67280497
14	CEBPB	chr14:67326120-67326325	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:67359417-67359654	IMR90	lung:	n/a	n/a
16	CEBPB	chr14:67326212-67326326	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:67326090-67326343	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:67258805-67259057	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:67359441-67359647	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:67325909-67326408	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:67280297-67280677	A549	lung:	n/a	chr14:67280486-67280497
22	CEBPB	chr14:67290364-67290658	IMR90	lung:	n/a	n/a
23	CEBPB	chr14:67359428-67359672	A549	lung:	n/a	n/a
24	CEBPB	chr14:67280318-67280671	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
25	CEBPB	chr14:67359463-67359648	K562	blood:	n/a	n/a
26	CEBPB	chr14:67290366-67290605	A549	lung:	n/a	n/a
27	CEBPB	chr14:67353631-67353953	IMR90	lung:	n/a	chr14:67353794-67353805
28	CEBPB	chr14:67280274-67280662	A549	lung:	n/a	chr14:67280486-67280497
29	CEBPB	chr14:67280292-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
30	CEBPB	chr14:67280298-67280687	IMR90	lung:	n/a	chr14:67280486-67280497
31	CEBPB	chr14:67310889-67310923	A549	lung:	n/a	n/a
32	CEBPB	chr14:67280301-67280681	K562	blood:	n/a	chr14:67280486-67280497
33	CEBPB	chr14:67280307-67280679	Hela-S3	cervix:	n/a	chr14:67280486-67280497
34	CEBPB	chr14:67326052-67326430	HepG2	liver:	n/a	n/a
35	CTCF	chr14:67334720-67334870	HCM	heart:	n/a	n/a
36	CTCF	chr14:67334900-67334906	Lung_OC	lung:	n/a	n/a
37	CTCF	chr14:67334760-67334910	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr14:67257939-67258039	GM13976	blood:	n/a	n/a
39	CTCF	chr14:67326697-67326714	GM13976	blood:	n/a	n/a
40	CTCF	chr14:67268780-67268930	HepG2	liver:	n/a	n/a
41	CTCF	chr14:67259096-67259130	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr14:67334874-67334990	LNCaP	prostate:	n/a	chr14:67334895-67334913 chr14:67334897-67334918 chr14:67334896-67334912
43	CTCF	chr14:67334813-67334897	Lung_OC	lung:	n/a	n/a
44	CTCF	chr14:67254153-67254203	Lung_OC	lung:	n/a	n/a
45	CTCF	chr14:67295888-67295970	GM13976	blood:	n/a	n/a
46	CTCF	chr14:67298860-67299010	HCFaa	heart:	n/a	n/a
47	CTCF	chr14:67362679-67362734	LNCaP	prostate:	n/a	n/a
48	CTCF	chr14:67334780-67334930	HMEC	breast:	n/a	chr14:67334895-67334913 chr14:67334897-67334918 chr14:67334896-67334912
49	CTCF	chr14:67341775-67341817	LNCaP	prostate:	n/a	n/a
50	CTCF	chr14:67280631-67280687	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67292488-67292538	HCM	heart:	n/a
2	chr14:67292488-67292538	LNCaP	prostate:	n/a
3	chr14:67292488-67292538	ECC-1	luminal epithelium:	n/a
4	chr14:67292488-67292538	HepG2	liver:	n/a
5	chr14:67292488-67292538	SK-N-SH_RA	brain:	n/a
6	chr14:67292488-67292538	U87	brain:	n/a
7	chr14:67292488-67292538	HAEpiC	amniotic membrane:	n/a
8	chr14:67292488-67292538	AG04449	skin:	fetal
9	chr14:67292488-67292538	NHDF-neo	bronchial:	n/a
10	chr14:67292488-67292538	HNPCEpiC	eye:	n/a
11	chr14:67292488-67292538	AG10803	skin:	n/a
12	chr14:67292488-67292538	NB4	blood:	n/a
13	chr14:67292488-67292538	ovcar-3	ovarian:	n/a
14	chr14:67292488-67292538	HRPEpiC	eye:	n/a
15	chr14:67292488-67292538	HIPEpiC	eye:	n/a
16	chr14:67292488-67292538	HRE	kidney:	n/a
17	chr14:67292488-67292538	HPAEpiC	pulmonary alveolar:	n/a
18	chr14:67292488-67292538	HL-60	blood:	n/a
19	chr14:67292488-67292538	GM12891	blood:	n/a
20	chr14:67292488-67292538	MCF10A-Er-Src	breast:	n/a
21	chr14:67292488-67292538	BJ	skin:	n/a
22	chr14:67292488-67292538	HRCEpiC	kidney:	n/a
23	chr14:67292488-67292538	SK-N-SH	brain:	n/a
24	chr14:67292488-67292538	RPTEC	kidney:	n/a
25	chr14:67292488-67292538	ProgFib	skin:	n/a
26	chr14:67292488-67292538	AG09309	skin:	n/a
27	chr14:67292488-67292538	MCF-7	breast:	n/a
28	chr14:67292488-67292538	HEEpiC	esophagus:	n/a
29	chr14:67292488-67292538	HCT-116	colon:	n/a
30	chr14:67292488-67292538	CMK	blood:	n/a
31	chr14:67292488-67292538	HCF	heart:	n/a
32	chr14:67292488-67292538	SKMC	muscle:	n/a
33	chr14:67292488-67292538	AoSMC	blood vessel:	n/a
34	chr14:67292488-67292538	HUVEC	blood vessel:	n/a
35	chr14:67292488-67292538	PrEC	prostate:	n/a
36	chr14:67292488-67292538	Caco-2	colon:	n/a
37	chr14:67292488-67292538	K562	blood:	n/a
38	chr14:67292488-67292538	GM12878	blood:	n/a
39	chr14:67292488-67292538	AG09319	gingival:	n/a
40	chr14:67292488-67292538	T-47D	breast:	n/a
41	chr14:67292488-67292538	AG04450	lung:	fetal
42	chr14:67292488-67292538	BE2_C	brain:	n/a
43	chr14:67292488-67292538	HCPEpiC	choroid plexus:	n/a
44	chr14:67292488-67292538	GM06990	blood:	n/a
45	chr14:67292488-67292538	HMEC	breast:	n/a
46	chr14:67292488-67292538	GM12892	blood:	n/a
47	chr14:67292488-67292538	SK-N-MC	brain:	n/a
48	chr14:67292488-67292538	Jurkat	blood:	n/a
49	chr14:67292488-67292538	IMR90	lung:	fetal
50	chr14:67292488-67292538	H1-hESC	embryonic stem cell:	embryo

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
2	chr14:67347067..67349521-chr14:67447070..67449089,2	MCF-7	breast:
3	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:
4	chr14:67297492..67297992-chr6:10786994..10787529,2	MCF-7	breast:
5	chr14:67290864..67292814-chr14:67296432..67298009,2	MCF-7	breast:
6	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:
7	chr14:67247462..67249948-chr14:67251250..67254048,2	MCF-7	breast:
8	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
9	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
10	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:

No data

Variant related genes	Relation type
GPHN	TF binding region
GPHN	CpG island
ENSG00000171723	chromatin interactions

Extended variants
information (count: 3898 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3898 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8022328	chr14:67253035-67253036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192424468	chr14:67253042-67253043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148535917	chr14:67253052-67253053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536766405	chr14:67253093-67253094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142845962	chr14:67253165-67253166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184399550	chr14:67253175-67253176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111470529	chr14:67253243-67253244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572487774	chr14:67253271-67253272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112904832	chr14:67253278-67253279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561259611	chr14:67253302-67253303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79866586	chr14:67253341-67253342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12897449	chr14:67253393-67253394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543664694	chr14:67253394-67253395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562045671	chr14:67253410-67253411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147679655	chr14:67253427-67253428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12897486	chr14:67253448-67253449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541412886	chr14:67253451-67253452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559925722	chr14:67253456-67253457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79041142	chr14:67253474-67253475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548948968	chr14:67253508-67253509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146228761	chr14:67253527-67253528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147844749	chr14:67253569-67253570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550047231	chr14:67253604-67253605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568354101	chr14:67253605-67253606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189067172	chr14:67253714-67253715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535784022	chr14:67253727-67253728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547749286	chr14:67253779-67253780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565964627	chr14:67253827-67253828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557054516	chr14:67253839-67253840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111975876	chr14:67253901-67253902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140372092	chr14:67253959-67253960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs118023734	chr14:67253968-67253969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576530286	chr14:67254091-67254092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75203429	chr14:67254249-67254250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375397279	chr14:67254281-67254282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563235724	chr14:67254303-67254304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573977731	chr14:67254328-67254329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561553530	chr14:67254329-67254330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577330399	chr14:67254386-67254387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541351553	chr14:67254396-67254397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77240816	chr14:67254406-67254407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181938337	chr14:67254487-67254488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554568137	chr14:67254490-67254491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553261342	chr14:67254576-67254577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186312892	chr14:67254603-67254604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189243550	chr14:67254607-67254608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564023799	chr14:67254615-67254616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150354193	chr14:67254634-67254635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181591223	chr14:67254642-67254643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138014435	chr14:67254646-67254647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Autism	22495309	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67225400-67256400	Weak transcription	Pancreas	Pancrea
2	chr14:67237600-67258800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:67238200-67256400	Weak transcription	Liver	Liver
4	chr14:67240000-67254800	Weak transcription	Fetal Intestine Small	intestine
5	chr14:67242600-67256200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr14:67248400-67259000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:67250400-67261000	Weak transcription	Left Ventricle	heart
8	chr14:67250800-67266400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:67254800-67255600	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr14:67255600-67280000	Weak transcription	Gastric	stomach
11	chr14:67256200-67256600	ZNF genes & repeats	Ovary	ovary
12	chr14:67256400-67256600	ZNF genes & repeats	Liver	Liver
13	chr14:67256400-67256600	ZNF genes & repeats	Pancreas	Pancrea
14	chr14:67256600-67261000	Weak transcription	Pancreas	Pancrea
15	chr14:67256600-67262400	Weak transcription	Liver	Liver
16	chr14:67256600-67272600	Weak transcription	Ovary	ovary
17	chr14:67257000-67258000	ZNF genes & repeats	GM12878-XiMat	blood
18	chr14:67257600-67282000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr14:67258800-67259400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:67259000-67259400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:67259400-67259800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr14:67259400-67260800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr14:67259800-67263800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:67260800-67261000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:67261000-67261200	Enhancers	Left Ventricle	heart
26	chr14:67261000-67261200	ZNF genes & repeats	Pancreas	Pancrea
27	chr14:67261000-67280000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:67261200-67268400	Weak transcription	Pancreas	Pancrea
29	chr14:67262400-67263200	Strong transcription	Liver	Liver
30	chr14:67263200-67272400	Weak transcription	Liver	Liver
31	chr14:67267200-67280000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr14:67267400-67280000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr14:67268000-67268200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr14:67268200-67268400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:67268200-67270200	ZNF genes & repeats	Fetal Intestine Small	intestine
36	chr14:67268200-67272200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr14:67268400-67268600	ZNF genes & repeats	Aorta	Aorta
38	chr14:67268400-67268600	Enhancers	Right Ventricle	heart
39	chr14:67268400-67268800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:67268400-67268800	ZNF genes & repeats	Pancreas	Pancrea
41	chr14:67268400-67269000	ZNF genes & repeats	Esophagus	oesophagus
42	chr14:67268400-67269200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr14:67268400-67271600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:67268600-67268800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr14:67268600-67280000	Weak transcription	Aorta	Aorta
46	chr14:67268600-67280000	Weak transcription	Right Ventricle	heart
47	chr14:67268800-67269000	ZNF genes & repeats	Fetal Stomach	stomach
48	chr14:67268800-67280000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr14:67268800-67280000	Weak transcription	Pancreas	Pancrea
50	chr14:67269000-67269400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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