Variant report

Variant	nsv4708
Chromosome Location	chr5:9245266-9290172
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr5:9267391-9267543	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr5:9251520-9251933	IMR90	lung:	n/a	n/a
3	CEBPB	chr5:9265870-9266281	H1-hESC	embryonic stem cell:	n/a	chr5:9266152-9266165 chr5:9266062-9266075
4	CEBPB	chr5:9266077-9266080	A549	lung:	n/a	n/a
5	CEBPB	chr5:9283153-9283457	IMR90	lung:	n/a	n/a
6	CEBPB	chr5:9265621-9266327	IMR90	lung:	n/a	chr5:9266152-9266165 chr5:9266062-9266075
7	CHD2	chr5:9265797-9266115	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr5:9265757-9266281	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr5:9283640-9283790	HPAF	blood vessel:	n/a	n/a
10	CTCF	chr5:9283700-9283850	GM12866	blood:	n/a	n/a
11	CTCF	chr5:9265600-9265750	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr5:9288520-9288670	NHLF	lung:	n/a	chr5:9288578-9288591 chr5:9288575-9288593 chr5:9288576-9288592
13	CTCF	chr5:9288540-9288690	AoAF	blood vessel:	n/a	chr5:9288578-9288591 chr5:9288575-9288593 chr5:9288576-9288592
14	CTCF	chr5:9265780-9265930	AG09319	gingival:	n/a	n/a
15	CTCF	chr5:9288473-9288661	Fibrobl	skin:	n/a	chr5:9288578-9288591 chr5:9288575-9288593 chr5:9288576-9288592
16	CTCF	chr5:9265860-9266010	HMF	breast:	n/a	n/a
17	CTCF	chr5:9283660-9283810	HCFaa	heart:	n/a	n/a
18	CTCF	chr5:9283699-9283823	GM12878	blood:	n/a	n/a
19	CTCF	chr5:9283580-9283730	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr5:9283620-9283770	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr5:9269280-9269430	HMEC	breast:	n/a	n/a
22	CTCF	chr5:9283640-9283790	GM12871	blood:	n/a	n/a
23	CTCF	chr5:9283640-9283790	HMF	breast:	n/a	n/a
24	CTCF	chr5:9283740-9283890	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr5:9283700-9283850	GM12870	blood:	n/a	n/a
26	CTCF	chr5:9283680-9283830	AG09309	skin:	n/a	n/a
27	CTCF	chr5:9283640-9283790	HAc	cerebellar:	n/a	n/a
28	CTCF	chr5:9265560-9265710	AG04449	skin:	n/a	n/a
29	CTCF	chr5:9283720-9283870	HPF	lung:	n/a	n/a
30	CTCF	chr5:9283740-9283890	HRE	kidney:	n/a	n/a
31	CTCF	chr5:9283760-9283910	NHEK	skin:	n/a	n/a
32	CTCF	chr5:9288491-9288646	MCF-7	breast:	n/a	chr5:9288578-9288591 chr5:9288575-9288593 chr5:9288576-9288592
33	CTCF	chr5:9265840-9265990	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr5:9288440-9288590	HVMF	connective:	n/a	n/a
35	CTCF	chr5:9283500-9283650	GM12874	blood:	n/a	n/a
36	CTCF	chr5:9283680-9283830	GM12875	blood:	n/a	n/a
37	CTCF	chr5:9265780-9265930	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr5:9283620-9283770	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr5:9288494-9288681	LNCaP	prostate:	n/a	chr5:9288578-9288591 chr5:9288575-9288593 chr5:9288576-9288592
40	CTCF	chr5:9267678-9267741	GM20000	blood:	n/a	n/a
41	CTCF	chr5:9283680-9283830	HMF	breast:	n/a	n/a
42	CTCF	chr5:9283720-9283870	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr5:9283680-9283830	GM12878	blood:	n/a	n/a
44	CTCF	chr5:9265900-9266050	HMEC	breast:	n/a	n/a
45	CTCF	chr5:9265860-9266010	HMEC	breast:	n/a	n/a
46	CTCF	chr5:9283660-9283810	Caco-2	colon:	n/a	n/a
47	CTCF	chr5:9265800-9265950	BJ	skin:	n/a	n/a
48	CTCF	chr5:9283660-9283810	GM12869	blood:	n/a	n/a
49	CTCF	chr5:9283700-9283850	NB4	blood:	n/a	n/a
50	CTCF	chr5:9283720-9283870	AG09319	gingival:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:9265636-9265686	HCPEpiC	choroid plexus:	n/a
2	chr5:9265636-9265686	BE2_C	brain:	n/a
3	chr5:9265636-9265686	HCF	heart:	n/a
4	chr5:9265636-9265686	GM12878	blood:	n/a
5	chr5:9265636-9265686	ProgFib	skin:	n/a
6	chr5:9265636-9265686	NB4	blood:	n/a
7	chr5:9265636-9265686	PANC-1	pancreas:	n/a
8	chr5:9265636-9265686	HEK293	kidney:	embryo
9	chr5:9265636-9265686	SAEC	small airway:	n/a
10	chr5:9265636-9265686	CMK	blood:	n/a
11	chr5:9265636-9265686	ECC-1	luminal epithelium:	n/a
12	chr5:9265636-9265686	AG04450	lung:	fetal
13	chr5:9265636-9265686	AG09319	gingival:	n/a
14	chr5:9265636-9265686	AG04449	skin:	fetal
15	chr5:9265636-9265686	K562	blood:	n/a
16	chr5:9265636-9265686	SK-N-SH_RA	brain:	n/a
17	chr5:9265636-9265686	T-47D	breast:	n/a
18	chr5:9265636-9265686	HNPCEpiC	eye:	n/a
19	chr5:9265636-9265686	MCF-7	breast:	n/a
20	chr5:9265636-9265686	ovcar-3	ovarian:	n/a
21	chr5:9265636-9265686	SK-N-MC	brain:	n/a
22	chr5:9265636-9265686	MCF10A-Er-Src	breast:	n/a
23	chr5:9265636-9265686	SKMC	muscle:	n/a
24	chr5:9265636-9265686	HL-60	blood:	n/a
25	chr5:9265636-9265686	HUVEC	blood vessel:	n/a
26	chr5:9265636-9265686	GM06990	blood:	n/a
27	chr5:9265636-9265686	IMR90	lung:	fetal
28	chr5:9265636-9265686	NH-A	brain:	n/a
29	chr5:9265636-9265686	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:9265636-9265686	SK-N-SH	brain:	n/a
31	chr5:9265636-9265686	HCT-116	colon:	n/a
32	chr5:9265636-9265686	PFSK-1	brain:	n/a
33	chr5:9265636-9265686	GM19239	blood:	n/a
34	chr5:9265636-9265686	Caco-2	colon:	n/a
35	chr5:9265636-9265686	HRPEpiC	eye:	n/a
36	chr5:9265636-9265686	HRE	kidney:	n/a
37	chr5:9265636-9265686	A549	lung:	n/a
38	chr5:9265636-9265686	HCM	heart:	n/a
39	chr5:9265636-9265686	HEEpiC	esophagus:	n/a
40	chr5:9265636-9265686	HMEC	breast:	n/a
41	chr5:9265636-9265686	Hela-S3	cervix:	n/a
42	chr5:9265636-9265686	LNCaP	prostate:	n/a
43	chr5:9265636-9265686	AG10803	skin:	n/a
44	chr5:9265636-9265686	HAEpiC	amniotic membrane:	n/a
45	chr5:9265636-9265686	HRCEpiC	kidney:	n/a
46	chr5:9265636-9265686	HIPEpiC	eye:	n/a
47	chr5:9265636-9265686	GM12891	blood:	n/a
48	chr5:9265636-9265686	AG09309	skin:	n/a
49	chr5:9265636-9265686	GM12892	blood:	n/a
50	chr5:9265636-9265686	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:9250420..9251966-chr5:9252760..9255699,2	MCF-7	breast:
2	chr5:9250420..9251966-chr5:9252760..9255699,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAS2R1-15	chr5:9285164-9285428	NONHSAT100347
2	lnc-TAS2R1-14	chr5:9286515-9286787	NONHSAT100348
3	lnc-TAS2R1-17	chr5:9250167-9250464	NONHSAT100344
4	lnc-CCT5-21	chr5:9265653-9265979	NONHSAT100346
5	lnc-TAS2R1-16	chr5:9257233-9257479	NONHSAT100345

No data

Variant related genes	Relation type
SEMA5A	TF binding region
SEMA5A	CpG island

Extended variants
information (count: 1695 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1695 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35009977	chr5:9245337-9245338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537596527	chr5:9245339-9245340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73742614	chr5:9245347-9245348	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs577401668	chr5:9245355-9245356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180992463	chr5:9245359-9245360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs3777296	chr5:9245441-9245442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs116488299	chr5:9245479-9245480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533123099	chr5:9245495-9245496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573238685	chr5:9245496-9245497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542252040	chr5:9245506-9245507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551507517	chr5:9245515-9245516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562115638	chr5:9245571-9245572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144214734	chr5:9245575-9245576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370138970	chr5:9245591-9245592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372311094	chr5:9245597-9245598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564108013	chr5:9245625-9245626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373898939	chr5:9245629-9245630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114366788	chr5:9245722-9245723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150603301	chr5:9245724-9245725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528551276	chr5:9245772-9245773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376580760	chr5:9245822-9245823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185425686	chr5:9245851-9245852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1805999	chr5:9245893-9245894	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs374722549	chr5:9245960-9245961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540788308	chr5:9245970-9245971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546709360	chr5:9246031-9246032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1805998	chr5:9246036-9246037	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs139998014	chr5:9246047-9246048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1805953	chr5:9246081-9246082	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs373193137	chr5:9246086-9246087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1610875	chr5:9246100-9246101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373321862	chr5:9246107-9246108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71611369	chr5:9246117-9246118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1805997	chr5:9246152-9246153	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs149849980	chr5:9246171-9246172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs199635380	chr5:9246210-9246211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190574275	chr5:9246219-9246220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182239445	chr5:9246226-9246227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555785560	chr5:9246311-9246312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575738776	chr5:9246312-9246313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112823555	chr5:9246332-9246333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556974722	chr5:9246337-9246338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145840029	chr5:9246363-9246364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141731995	chr5:9246366-9246367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539634185	chr5:9246377-9246378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377227234	chr5:9246385-9246386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34560450	chr5:9246387-9246388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369219790	chr5:9246451-9246452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577724778	chr5:9246452-9246453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540426131	chr5:9246481-9246482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Lung adenocarcinoma	17982442	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:9185400-9264600	Weak transcription	Left Ventricle	heart
2	chr5:9225200-9258600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr5:9226400-9254000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr5:9229000-9250400	Weak transcription	Fetal Muscle Leg	muscle
5	chr5:9234600-9249400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:9234600-9249800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:9234600-9250200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:9234600-9251600	Weak transcription	Fetal Stomach	stomach
9	chr5:9234800-9263400	Weak transcription	Fetal Heart	heart
10	chr5:9238400-9254400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:9240200-9249200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:9240200-9251200	Weak transcription	NHLF	lung
13	chr5:9240600-9249400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:9240800-9246400	Weak transcription	NH-A	brain
15	chr5:9240800-9249400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr5:9242600-9249800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr5:9242800-9246000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr5:9243400-9245400	Enhancers	Brain Hippocampus Middle	brain
19	chr5:9243400-9265400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:9243600-9248000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:9243800-9245600	Enhancers	Brain Cingulate Gyrus	brain
22	chr5:9243800-9246000	Enhancers	Placenta Amnion	Placenta Amnion
23	chr5:9244000-9245400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr5:9244000-9245400	Weak transcription	NHDF-Ad	bronchial
25	chr5:9244600-9245600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:9244600-9245600	Enhancers	HMEC	breast
27	chr5:9245000-9245600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:9245000-9264600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:9245200-9245600	Enhancers	Osteobl	bone
30	chr5:9245200-9245800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:9245200-9265200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr5:9245400-9245800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr5:9245400-9245800	Enhancers	NHDF-Ad	bronchial
34	chr5:9245600-9249400	Weak transcription	Osteobl	bone
35	chr5:9245600-9249800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:9245600-9251000	Weak transcription	HMEC	breast
37	chr5:9245600-9251400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:9245800-9246000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:9245800-9250200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:9245800-9251200	Weak transcription	NHDF-Ad	bronchial
41	chr5:9246000-9249400	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr5:9246000-9249800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr5:9247000-9247200	Enhancers	Brain Hippocampus Middle	brain
44	chr5:9248000-9248800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:9248200-9248600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:9248200-9248600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:9248800-9249000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:9249000-9249600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:9249200-9250200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr5:9249400-9249600	Enhancers	Muscle Satellite Cultured Cells	--

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