Variant report

Variant	nsv968108
Chromosome Location	chr5:99981282-99993998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:99982017-99982085	K562	blood:	n/a	n/a
2	ARID3A	chr5:99983489-99983958	K562	blood:	n/a	n/a
3	ARID3A	chr5:99990630-99990941	K562	blood:	n/a	n/a
4	ATF1	chr5:99990201-99990376	K562	blood:	n/a	n/a
5	BHLHE40	chr5:99990719-99990919	K562	blood:	n/a	n/a
6	BHLHE40	chr5:99983105-99983921	K562	blood:	n/a	n/a
7	BRCA1	chr5:99981848-99981913	GM12878	blood:	n/a	n/a
8	BRCA1	chr5:99983490-99983559	GM12878	blood:	n/a	n/a
9	CCNT2	chr5:99990726-99991000	K562	blood:	n/a	chr5:99990744-99990764
10	CEBPB	chr5:99983315-99983876	K562	blood:	n/a	n/a
11	CEBPB	chr5:99980653-99981420	HepG2	liver:	n/a	chr5:99981235-99981246
12	CEBPB	chr5:99980697-99981417	K562	blood:	n/a	chr5:99981235-99981246
13	CEBPB	chr5:99983312-99983748	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:99983195-99983759	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr5:99980650-99981422	A549	lung:	n/a	chr5:99981235-99981246
16	CEBPB	chr5:99983151-99983762	MCF-7	breast:	n/a	n/a
17	CEBPD	chr5:99990624-99990996	K562	blood:	n/a	n/a
18	CTCF	chr5:99992854-99992942	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr5:99985079-99985182	GM10248	blood:	n/a	chr5:99985158-99985165
20	CTCF	chr5:99985578-99985642	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr5:99992493-99992530	GM10266	blood:	n/a	n/a
22	CUX1	chr5:99983809-99984184	K562	blood:	n/a	n/a
23	CUX1	chr5:99990821-99990898	K562	blood:	n/a	n/a
24	E2F4	chr5:99983304-99983597	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr5:99981755-99981955	GM12878	blood:	n/a	chr5:99981891-99981902
26	EBF1	chr5:99981749-99982029	GM12878	blood:	n/a	chr5:99981891-99981902
27	EBF1	chr5:99983050-99983186	GM12878	blood:	n/a	n/a
28	EBF1	chr5:99981773-99982012	GM12878	blood:	n/a	chr5:99981891-99981902
29	EGR1	chr5:99983071-99983345	K562	blood:	n/a	n/a
30	EP300	chr5:99983076-99983846	MCF-7	breast:	n/a	chr5:99983519-99983532
31	EP300	chr5:99990703-99990920	K562	blood:	n/a	n/a
32	EP300	chr5:99983103-99983789	MCF-7	breast:	n/a	chr5:99983519-99983532
33	EP300	chr5:99982932-99983907	ECC-1	luminal epithelium:	n/a	chr5:99983519-99983532
34	EP300	chr5:99990581-99990958	K562	blood:	n/a	chr5:99990631-99990645
35	EP300	chr5:99983141-99984003	K562	blood:	n/a	chr5:99983519-99983532
36	EP300	chr5:99983150-99983639	ECC-1	luminal epithelium:	n/a	chr5:99983519-99983532
37	EP300	chr5:99981783-99982504	K562	blood:	n/a	n/a
38	ESR1	chr5:99983130-99983734	T-47D	breast:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
39	ESR1	chr5:99983174-99983787	T-47D	breast:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
40	ESR1	chr5:99983069-99983750	ECC-1	luminal epithelium:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
41	ESR1	chr5:99983018-99983720	ECC-1	luminal epithelium:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
42	ESR1	chr5:99983140-99983777	ECC-1	luminal epithelium:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
43	ESR1	chr5:99983136-99983750	ECC-1	luminal epithelium:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
44	ESR1	chr5:99983026-99983784	ECC-1	luminal epithelium:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
45	ESR1	chr5:99981749-99982127	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr5:99983193-99983729	T-47D	breast:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
47	ESR1	chr5:99983180-99983709	T-47D	breast:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
48	ESR1	chr5:99981721-99982077	ECC-1	luminal epithelium:	n/a	n/a
49	ESR1	chr5:99983290-99983645	T-47D	breast:	n/a	chr5:99983477-99983494 chr5:99983476-99983493
50	ESR1	chr5:99981690-99982187	ECC-1	luminal epithelium:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99993323-99993373	HPAEpiC	pulmonary alveolar:	n/a
2	chr5:99993323-99993373	HL-60	blood:	n/a
3	chr5:99993323-99993373	NH-A	brain:	n/a
4	chr5:99993323-99993373	GM06990	blood:	n/a
5	chr5:99993323-99993373	AG10803	skin:	n/a
6	chr5:99993323-99993373	HepG2	liver:	n/a
7	chr5:99993323-99993373	GM12878	blood:	n/a
8	chr5:99993323-99993373	NHDF-neo	bronchial:	n/a
9	chr5:99993323-99993373	AoSMC	blood vessel:	n/a
10	chr5:99993323-99993373	AG04449	skin:	fetal
11	chr5:99993323-99993373	AG09319	gingival:	n/a
12	chr5:99993323-99993373	H1-hESC	embryonic stem cell:	embryo
13	chr5:99993323-99993373	Hepatocyte	liver:	n/a
14	chr5:99993323-99993373	AG09309	skin:	n/a
15	chr5:99993323-99993373	GM12891	blood:	n/a
16	chr5:99993323-99993373	SKMC	muscle:	n/a
17	chr5:99993323-99993373	Jurkat	blood:	n/a
18	chr5:99993323-99993373	SAEC	small airway:	n/a
19	chr5:99993323-99993373	IMR90	lung:	fetal
20	chr5:99993323-99993373	PFSK-1	brain:	n/a
21	chr5:99993323-99993373	HCT-116	colon:	n/a
22	chr5:99993323-99993373	A549	lung:	n/a
23	chr5:99993323-99993373	HUVEC	blood vessel:	n/a
24	chr5:99993323-99993373	HAEpiC	amniotic membrane:	n/a
25	chr5:99993323-99993373	MCF-7	breast:	n/a
26	chr5:99993323-99993373	GM12892	blood:	n/a
27	chr5:99993323-99993373	HRE	kidney:	n/a
28	chr5:99993323-99993373	HCM	heart:	n/a
29	chr5:99993323-99993373	T-47D	breast:	n/a
30	chr5:99993323-99993373	U87	brain:	n/a
31	chr5:99993323-99993373	SK-N-SH	brain:	n/a
32	chr5:99993323-99993373	HCF	heart:	n/a
33	chr5:99993323-99993373	NHBE	bronchial:	n/a
34	chr5:99993323-99993373	Hela-S3	cervix:	n/a
35	chr5:99993323-99993373	ovcar-3	ovarian:	n/a
36	chr5:99993323-99993373	PANC-1	pancreas:	n/a
37	chr5:99993323-99993373	BE2_C	brain:	n/a
38	chr5:99993323-99993373	RPTEC	kidney:	n/a
39	chr5:99993323-99993373	HIPEpiC	eye:	n/a
40	chr5:99993323-99993373	ProgFib	skin:	n/a
41	chr5:99993323-99993373	HNPCEpiC	eye:	n/a
42	chr5:99993323-99993373	Caco-2	colon:	n/a
43	chr5:99993323-99993373	MCF10A-Er-Src	breast:	n/a
44	chr5:99993323-99993373	NT2-D1	testis:	n/a
45	chr5:99993323-99993373	HEK293	kidney:	embryo
46	chr5:99993323-99993373	HRCEpiC	kidney:	n/a
47	chr5:99993323-99993373	PrEC	prostate:	n/a
48	chr5:99993323-99993373	LNCaP	prostate:	n/a
49	chr5:99993323-99993373	K562	blood:	n/a
50	chr5:99993323-99993373	HCPEpiC	choroid plexus:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:99979051..99981832-chr5:99981912..99985691,4	MCF-7	breast:
2	chr5:99984054..99985811-chr5:99989132..99991041,2	K562	blood:
3	chr5:99975585..99977874-chr5:99980709..99983188,3	K562	blood:
4	chr5:99984054..99985811-chr5:99989132..99991041,2	K562	blood:
5	chr5:99989812..99991852-chr5:99993776..99996637,2	K562	blood:
6	chr5:99983058..99983589-chr5:100699944..100700904,2	MCF-7	breast:
7	chr5:25503170..25504042-chr5:99982844..99983480,2	MCF-7	breast:
8	chr5:99982875..99983980-chr5:100090231..100091716,20	MCF-7	breast:
9	chr5:99969436..99971759-chr5:99981835..99984130,2	MCF-7	breast:
10	chr5:99983206..99984911-chr8:101906981..101908614,2	MCF-7	breast:
11	chr5:99979324..99981672-chr5:99983886..99985398,2	K562	blood:
12	chr5:99989812..99991852-chr5:99993776..99996637,2	K562	blood:
13	chr5:99983045..99983930-chr5:100117214..100117742,2	MCF-7	breast:
14	chr5:99983062..99983901-chr5:100090730..100091412,3	MCF-7	breast:
15	chr5:99979051..99981832-chr5:99981912..99985691,4	MCF-7	breast:
16	chr5:99978477..99981448-chr5:99989522..99992251,2	MCF-7	breast:
17	chr5:99983166..99984736-chr5:100011479..100013209,2	MCF-7	breast:
18	chr5:99979324..99981672-chr5:99983886..99985398,2	K562	blood:
19	chr5:99982908..99983980-chr5:100090394..100091716,11	MCF-7	breast:
20	chr5:99978477..99981448-chr5:99989522..99992251,2	MCF-7	breast:
21	chr5:99978017..99980273-chr5:99982713..99984242,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA4-2	chr5:99993523-99993674	XLOC_004939
2	lnc-ST8SIA4-2	chr5:99992117-99992230	XLOC_004939
3	lnc-ST8SIA4-2	chr5:99991144-99991208	XLOC_004939
4	lnc-ST8SIA4-2	chr5:99991144-99991179	XLOC_004939
5	lnc-ST8SIA4-2	chr5:99989792-99990096	XLOC_004939
6	lnc-ST8SIA4-2	chr5:99993523-99993674	XLOC_004939
7	lnc-ST8SIA4-2	chr5:99989816-99990096	XLOC_004939

No data

Variant related genes	Relation type
ENSG00000250806	TF binding region
ENSG00000250806	CpG island
ENSG00000212994	chromatin interactions
RBFOX2	miRNA target sites

Extended variants
information (count: 439 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7734712	chr5:99981346-99981347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548007751	chr5:99981401-99981402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116034990	chr5:99981442-99981443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534774050	chr5:99981453-99981454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs137976592	chr5:99981476-99981477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112815285	chr5:99981477-99981478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553453737	chr5:99981486-99981487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6896187	chr5:99981493-99981494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368010440	chr5:99981507-99981508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539076785	chr5:99981538-99981539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557685237	chr5:99981548-99981549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554416937	chr5:99981552-99981553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139655561	chr5:99981615-99981616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs58915163	chr5:99981616-99981617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201127685	chr5:99981619-99981620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199963191	chr5:99981625-99981626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200766947	chr5:99981628-99981629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201608527	chr5:99981629-99981630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147485516	chr5:99981630-99981631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs58363152	chr5:99981631-99981632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62385933	chr5:99981633-99981634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543230524	chr5:99981635-99981636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565176037	chr5:99981685-99981686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577267031	chr5:99981692-99981693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573409719	chr5:99981694-99981695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539905034	chr5:99981710-99981711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564999131	chr5:99981742-99981743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34128745	chr5:99981793-99981794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56083896	chr5:99981801-99981802	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs73155157	chr5:99981820-99981821	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs562419218	chr5:99981821-99981822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529969882	chr5:99981822-99981823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79977193	chr5:99981858-99981859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566520391	chr5:99981889-99981890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375603054	chr5:99981904-99981905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11960094	chr5:99981926-99981927	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs58571109	chr5:99981958-99981959	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs571760325	chr5:99981967-99981968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539013190	chr5:99982121-99982122	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs557426469	chr5:99982136-99982137	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs578210891	chr5:99982158-99982159	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs575726306	chr5:99982204-99982205	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs182833011	chr5:99982243-99982244	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555250304	chr5:99982256-99982257	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs147766681	chr5:99982278-99982279	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs540859775	chr5:99982290-99982291	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs10059478	chr5:99982292-99982293	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs141085998	chr5:99982338-99982339	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs371874461	chr5:99982387-99982388	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs372246616	chr5:99982401-99982402	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99978000-99983000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:99978000-99983200	Weak transcription	Placenta	Placenta
3	chr5:99978400-99983000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr5:99979400-99983200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:99979600-99983000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:99980000-99983000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr5:99980000-99983200	Weak transcription	HMEC	breast
8	chr5:99980200-99981800	Weak transcription	Fetal Kidney	kidney
9	chr5:99980200-99982800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr5:99980200-99983000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:99980200-99983000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:99980200-99983000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr5:99980200-99983400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr5:99980200-99985000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:99980400-99983400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:99980600-99983000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:99981200-99982000	Enhancers	K562	blood
18	chr5:99981800-99982200	Enhancers	Fetal Thymus	thymus
19	chr5:99981800-99982200	Enhancers	GM12878-XiMat	blood
20	chr5:99981800-99983000	Enhancers	Dnd41	blood
21	chr5:99981800-99983400	Enhancers	Fetal Kidney	kidney
22	chr5:99982000-99982600	Flanking Active TSS	K562	blood
23	chr5:99982200-99983000	Weak transcription	GM12878-XiMat	blood
24	chr5:99982200-99983200	Weak transcription	Fetal Thymus	thymus
25	chr5:99982600-99983000	Enhancers	K562	blood
26	chr5:99982800-99983000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr5:99982800-99985600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr5:99983000-99983200	Active TSS	Rectal Smooth Muscle	rectum
29	chr5:99983000-99983200	Enhancers	A549	lung
30	chr5:99983000-99983200	Enhancers	Hela-S3	cervix
31	chr5:99983000-99983200	Enhancers	NHEK	skin
32	chr5:99983000-99983400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr5:99983000-99983400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
34	chr5:99983000-99983400	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr5:99983000-99983400	Flanking Active TSS	K562	blood
36	chr5:99983000-99983600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:99983000-99983600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr5:99983000-99983600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr5:99983000-99983600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr5:99983000-99983600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:99983000-99983800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr5:99983000-99983800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr5:99983000-99983800	Flanking Active TSS	Dnd41	blood
44	chr5:99983000-99983800	Enhancers	GM12878-XiMat	blood
45	chr5:99983000-99984000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr5:99983000-99984000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr5:99983000-99984000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr5:99983000-99984000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr5:99983000-99985400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:99983200-99983400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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