Variant report

Variant	nsv980715
Chromosome Location	chr5:114545011-114548142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:102)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:102 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:114544930-114545454	GM12878	blood:	n/a	n/a
2	ATF2	chr5:114544786-114545434	GM12878	blood:	n/a	n/a
3	BATF	chr5:114544874-114545373	GM12878	blood:	n/a	n/a
4	BATF	chr5:114544925-114545244	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:114544903-114545448	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:114544908-114545320	GM12878	blood:	n/a	n/a
7	BCLAF1	chr5:114544838-114545432	GM12878	blood:	n/a	n/a
8	BCLAF1	chr5:114544913-114545425	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:114544953-114545360	GM12878	blood:	n/a	n/a
10	BRCA1	chr5:114545258-114545280	GM12878	blood:	n/a	n/a
11	CEBPB	chr5:114546595-114546795	A549	lung:	n/a	n/a
12	CEBPB	chr5:114544794-114545484	GM12878	blood:	n/a	n/a
13	CEBPB	chr5:114544950-114545400	GM12878	blood:	n/a	n/a
14	CHD1	chr5:114544974-114545298	GM12878	blood:	n/a	n/a
15	CHD2	chr5:114544930-114545355	GM12878	blood:	n/a	n/a
16	CTCF	chr5:114545129-114545339	GM12878	blood:	n/a	n/a
17	CTCF	chr5:114547078-114547151	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr5:114545140-114545290	GM06990	blood:	n/a	n/a
19	CTCF	chr5:114545290-114545328	Lung_OC	lung:	n/a	n/a
20	CTCF	chr5:114545180-114545330	GM12871	blood:	n/a	n/a
21	CTCF	chr5:114545208-114545228	Spleen_OC	spleen:	n/a	n/a
22	CUX1	chr5:114544991-114545254	GM12878	blood:	n/a	n/a
23	EBF1	chr5:114544913-114545341	GM12878	blood:	n/a	n/a
24	EBF1	chr5:114544967-114545366	GM12878	blood:	n/a	n/a
25	EBF1	chr5:114545007-114545330	GM12878	blood:	n/a	n/a
26	ELK1	chr5:114545070-114545191	GM12878	blood:	n/a	n/a
27	EP300	chr5:114544930-114545363	GM12878	blood:	n/a	n/a
28	EP300	chr5:114544974-114545337	GM12878	blood:	n/a	n/a
29	EP300	chr5:114544977-114545348	GM12878	blood:	n/a	n/a
30	EP300	chr5:114544894-114545426	GM12878	blood:	n/a	n/a
31	FOXM1	chr5:114544715-114545512	GM12878	blood:	n/a	n/a
32	FOXM1	chr5:114544788-114545439	GM12878	blood:	n/a	n/a
33	IKZF1	chr5:114544970-114545419	GM12878	blood:	n/a	n/a
34	IRF3	chr5:114545042-114545242	GM12878	blood:	n/a	chr5:114545209-114545222 chr5:114545209-114545222 chr5:114545085-114545099 chr5:114545208-114545222 chr5:114545209-114545222 chr5:114545084-114545104
35	IRF4	chr5:114544882-114545453	GM12878	blood:	n/a	chr5:114545209-114545223
36	IRF4	chr5:114544876-114545332	GM12878	blood:	n/a	chr5:114545209-114545223
37	MAX	chr5:114544966-114545244	NB4	blood:	n/a	n/a
38	MAX	chr5:114544973-114545314	GM12878	blood:	n/a	n/a
39	MAZ	chr5:114544966-114545310	GM12878	blood:	n/a	n/a
40	MEF2A	chr5:114544813-114545371	GM12878	blood:	n/a	n/a
41	MTA3	chr5:114544764-114545436	GM12878	blood:	n/a	n/a
42	MTA3	chr5:114544829-114545378	GM12878	blood:	n/a	n/a
43	MXI1	chr5:114544973-114545323	GM12878	blood:	n/a	n/a
44	MYC	chr5:114545035-114545214	NB4	blood:	n/a	n/a
45	NFATC1	chr5:114544850-114545390	GM12878	blood:	n/a	n/a
46	NFATC1	chr5:114544841-114545452	GM12878	blood:	n/a	n/a
47	NFIC	chr5:114544805-114545550	GM12878	blood:	n/a	chr5:114545151-114545179
48	NFIC	chr5:114544765-114545566	GM12878	blood:	n/a	chr5:114545151-114545179
49	NFYB	chr5:114544947-114545244	GM12878	blood:	n/a	n/a
50	PAX5	chr5:114544869-114545341	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114547039-114547089	K562	blood:	n/a
2	chr5:114547039-114547089	BE2_C	brain:	n/a
3	chr5:114547039-114547089	Hepatocyte	liver:	n/a
4	chr5:114547039-114547089	AG09319	gingival:	n/a
5	chr5:114547039-114547089	HL-60	blood:	n/a
6	chr5:114547039-114547089	HEK293	kidney:	embryo
7	chr5:114547039-114547089	GM06990	blood:	n/a
8	chr5:114547039-114547089	NH-A	brain:	n/a
9	chr5:114547039-114547089	HRPEpiC	eye:	n/a
10	chr5:114547039-114547089	GM12878	blood:	n/a
11	chr5:114547039-114547089	PANC-1	pancreas:	n/a
12	chr5:114547039-114547089	AG04450	lung:	fetal
13	chr5:114547039-114547089	HRE	kidney:	n/a
14	chr5:114547039-114547089	Jurkat	blood:	n/a
15	chr5:114547039-114547089	AG04449	skin:	fetal
16	chr5:114547039-114547089	HMEC	breast:	n/a
17	chr5:114547039-114547089	HUVEC	blood vessel:	n/a
18	chr5:114547039-114547089	RPTEC	kidney:	n/a
19	chr5:114547039-114547089	MCF-7	breast:	n/a
20	chr5:114547039-114547089	AG09309	skin:	n/a
21	chr5:114547039-114547089	U87	brain:	n/a
22	chr5:114547039-114547089	BJ	skin:	n/a
23	chr5:114547039-114547089	T-47D	breast:	n/a
24	chr5:114547039-114547089	A549	lung:	n/a
25	chr5:114547039-114547089	SK-N-SH_RA	brain:	n/a
26	chr5:114547039-114547089	SK-N-MC	brain:	n/a
27	chr5:114547039-114547089	SAEC	small airway:	n/a
28	chr5:114547039-114547089	SKMC	muscle:	n/a
29	chr5:114547039-114547089	GM12892	blood:	n/a
30	chr5:114547039-114547089	Hela-S3	cervix:	n/a
31	chr5:114547039-114547089	HCF	heart:	n/a
32	chr5:114547039-114547089	Caco-2	colon:	n/a
33	chr5:114547039-114547089	HCPEpiC	choroid plexus:	n/a
34	chr5:114547039-114547089	PrEC	prostate:	n/a
35	chr5:114547039-114547089	SK-N-SH	brain:	n/a
36	chr5:114547039-114547089	HNPCEpiC	eye:	n/a
37	chr5:114547039-114547089	NT2-D1	testis:	n/a
38	chr5:114547039-114547089	HCT-116	colon:	n/a
39	chr5:114547039-114547089	PFSK-1	brain:	n/a
40	chr5:114547039-114547089	HCM	heart:	n/a
41	chr5:114547039-114547089	ECC-1	luminal epithelium:	n/a
42	chr5:114547039-114547089	HepG2	liver:	n/a
43	chr5:114547039-114547089	GM19239	blood:	n/a
44	chr5:114547039-114547089	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:114547039-114547089	ProgFib	skin:	n/a
46	chr5:114547039-114547089	HRCEpiC	kidney:	n/a
47	chr5:114547039-114547089	H1-hESC	embryonic stem cell:	embryo
48	chr5:114547039-114547089	GM12891	blood:	n/a
49	chr5:114547039-114547089	HEEpiC	esophagus:	n/a
50	chr5:114547039-114547089	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:114545341..114547918-chr5:114548363..114550045,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PGGT1B	hsa-miR-124-3p	chr5:114547316-114547335

Variant related genes	Relation type
ENSG00000248175	TF binding region
ENSG00000248175	CpG island

Extended variants
information (count: 114 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565067553	chr5:114545066-114545067	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs536775805	chr5:114545107-114545108	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs185481279	chr5:114545115-114545116	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs113588728	chr5:114545120-114545121	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs542956873	chr5:114545128-114545129	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs371404287	chr5:114545146-114545147	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs558199567	chr5:114545154-114545155	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs7725831	chr5:114545170-114545171	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs147069424	chr5:114545213-114545214	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550502782	chr5:114545289-114545290	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs568860007	chr5:114545290-114545291	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs188828833	chr5:114545298-114545299	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs557865050	chr5:114545379-114545380	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs540581061	chr5:114545391-114545392	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs10463668	chr5:114545511-114545512	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs7708472	chr5:114545548-114545549	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs181590715	chr5:114545561-114545562	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186198888	chr5:114545566-114545567	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150691608	chr5:114545637-114545638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576010266	chr5:114545647-114545648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545038464	chr5:114545673-114545674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192418695	chr5:114545758-114545759	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370331514	chr5:114545796-114545797	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574685950	chr5:114545811-114545812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180850687	chr5:114545864-114545865	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561281935	chr5:114545881-114545882	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs202247716	chr5:114545889-114545890	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75833544	chr5:114545898-114545899	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77478402	chr5:114545899-114545900	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186254949	chr5:114545916-114545917	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569496411	chr5:114545947-114545948	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530357720	chr5:114545972-114545973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375245372	chr5:114545976-114545977	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190826537	chr5:114545981-114545982	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75310694	chr5:114545999-114546000	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79499482	chr5:114546029-114546030	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182515790	chr5:114546050-114546051	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571225770	chr5:114546105-114546106	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112851891	chr5:114546112-114546113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs17132480	chr5:114546116-114546117	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs142099523	chr5:114546134-114546135	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546774049	chr5:114546168-114546169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567347952	chr5:114546201-114546202	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs265420	chr5:114546251-114546252	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs556026382	chr5:114546285-114546286	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575900315	chr5:114546316-114546317	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374108924	chr5:114546329-114546330	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200311969	chr5:114546344-114546345	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558629637	chr5:114546393-114546394	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187261123	chr5:114546417-114546418	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114523400-114576200	Weak transcription	Psoas Muscle	Psoas
2	chr5:114528000-114563000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:114529200-114562600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr5:114529800-114551000	Weak transcription	Left Ventricle	heart
5	chr5:114530200-114562600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr5:114530200-114562600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr5:114530600-114548600	Weak transcription	Fetal Intestine Large	intestine
8	chr5:114530600-114594400	Weak transcription	Pancreas	Pancrea
9	chr5:114530800-114548000	Weak transcription	Adipose Nuclei	Adipose
10	chr5:114530800-114565200	Weak transcription	NHDF-Ad	bronchial
11	chr5:114531000-114546400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:114531000-114547600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:114531000-114551200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:114531000-114558800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr5:114531200-114546400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:114531200-114548200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr5:114532000-114547000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr5:114533600-114551200	Weak transcription	HSMM	muscle
19	chr5:114533800-114549000	Weak transcription	Aorta	Aorta
20	chr5:114535200-114551200	Weak transcription	HSMMtube	muscle
21	chr5:114536000-114556000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:114538200-114548600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:114538200-114551800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr5:114538400-114548000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr5:114538400-114548200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr5:114538400-114567000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:114538400-114572000	Weak transcription	Lung	lung
28	chr5:114538600-114555200	Weak transcription	Placenta	Placenta
29	chr5:114538800-114550800	Weak transcription	Fetal Stomach	stomach
30	chr5:114539200-114580200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr5:114539400-114547400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:114539400-114548000	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr5:114539800-114566000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr5:114540200-114546800	Weak transcription	HMEC	breast
35	chr5:114540800-114567600	Weak transcription	Hela-S3	cervix
36	chr5:114541000-114562000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr5:114541200-114548000	Weak transcription	Duodenum Mucosa	Duodenum
38	chr5:114541400-114548200	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr5:114541600-114545200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:114541600-114551200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr5:114541800-114548800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr5:114541800-114549000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:114541800-114573400	Weak transcription	NHLF	lung
44	chr5:114542000-114575800	Weak transcription	Small Intestine	intestine
45	chr5:114542600-114549000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:114543200-114548800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:114543400-114548600	Weak transcription	Ovary	ovary
48	chr5:114543400-114549800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:114543600-114548000	Weak transcription	Fetal Muscle Leg	muscle
50	chr5:114543600-114551200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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