Variant report

Variant	nsv5286
Chromosome Location	chr6:44865290-44909915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:269)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:269 , 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	ARID3A	chr6:44907927-44908749	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:44900932-44900942	K562	blood:	n/a	n/a
3	ARID3A	chr6:44888556-44889970	HepG2	liver:	n/a	n/a
4	ATF1	chr6:44888645-44888963	K562	blood:	n/a	n/a
5	ATF1	chr6:44876296-44876496	K562	blood:	n/a	n/a
6	ATF1	chr6:44893099-44893531	K562	blood:	n/a	n/a
7	BHLHE40	chr6:44891304-44891474	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:44888678-44889228	HepG2	liver:	n/a	n/a
9	CBX3	chr6:44889457-44889879	HCT-116	colon:	n/a	n/a
10	CCNT2	chr6:44893177-44893452	K562	blood:	n/a	n/a
11	CCNT2	chr6:44888713-44888911	K562	blood:	n/a	chr6:44888832-44888852
12	CEBPB	chr6:44908161-44908502	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:44888558-44889173	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:44888597-44889189	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:44893092-44893440	K562	blood:	n/a	n/a
16	CEBPB	chr6:44888607-44888936	K562	blood:	n/a	n/a
17	CEBPB	chr6:44888661-44888811	HepG2	liver:	n/a	n/a
18	CTCF	chr6:44889692-44889801	GM12878	blood:	n/a	n/a
19	CTCF	chr6:44889620-44889770	Caco-2	colon:	n/a	n/a
20	CTCF	chr6:44889692-44889835	NHEK	skin:	n/a	n/a
21	CTCF	chr6:44889550-44889982	HCT-116	colon:	n/a	n/a
22	CTCF	chr6:44889700-44889850	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr6:44889665-44889848	MCF-7	breast:	n/a	n/a
24	CTCF	chr6:44889761-44889791	GM10266	blood:	n/a	n/a
25	CTCF	chr6:44889740-44889890	HRE	kidney:	n/a	n/a
26	CTCF	chr6:44889600-44889750	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr6:44889680-44889830	HMEC	breast:	n/a	n/a
28	CTCF	chr6:44889700-44889850	GM06990	blood:	n/a	n/a
29	CTCF	chr6:44889708-44889778	LNCaP	prostate:	n/a	n/a
30	CTCF	chr6:44889660-44889810	HMEC	breast:	n/a	n/a
31	CTCF	chr6:44889720-44889870	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr6:44868280-44868430	K562	blood:	n/a	n/a
33	CTCF	chr6:44889600-44889750	RPTEC	kidney:	n/a	n/a
34	CTCF	chr6:44889693-44889796	Lung_OC	lung:	n/a	n/a
35	CTCF	chr6:44900404-44900477	Fibrobl	skin:	n/a	n/a
36	CTCF	chr6:44889540-44889690	Caco-2	colon:	n/a	n/a
37	CTCF	chr6:44889690-44889807	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr6:44889635-44889860	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:44889725-44889799	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr6:44889780-44889930	HepG2	liver:	n/a	n/a
41	CTCF	chr6:44889741-44889759	GM10266	blood:	n/a	n/a
42	CTCF	chr6:44889520-44889670	GM12872	blood:	n/a	n/a
43	CTCF	chr6:44889740-44889753	GM19238	blood:	n/a	n/a
44	CTCF	chr6:44889533-44889842	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:44889640-44889790	HEK293	kidney:	n/a	n/a
46	CTCF	chr6:44889680-44889830	RPTEC	kidney:	n/a	n/a
47	CTCF	chr6:44889640-44889790	HCT-116	colon:	n/a	n/a
48	CTCF	chr6:44889633-44889846	HepG2	liver:	n/a	n/a
49	CTCF	chr6:44889640-44889790	HepG2	liver:	n/a	n/a
50	CTCF	chr6:44874685-44874739	GM10266	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44866054-44866104	HEEpiC	esophagus:	n/a
2	chr6:44866054-44866104	HEK293	kidney:	embryo
3	chr6:44866054-44866104	GM12892	blood:	n/a
4	chr6:44866054-44866104	T-47D	breast:	n/a
5	chr6:44866054-44866104	Jurkat	blood:	n/a
6	chr6:44866054-44866104	SK-N-SH_RA	brain:	n/a
7	chr6:44866054-44866104	PrEC	prostate:	n/a
8	chr6:44866054-44866104	AG09319	gingival:	n/a
9	chr6:44866054-44866104	LNCaP	prostate:	n/a
10	chr6:44866054-44866104	NT2-D1	testis:	n/a
11	chr6:44866054-44866104	HNPCEpiC	eye:	n/a
12	chr6:44866054-44866104	AoSMC	blood vessel:	n/a
13	chr6:44866054-44866104	NHDF-neo	bronchial:	n/a
14	chr6:44866054-44866104	Hela-S3	cervix:	n/a
15	chr6:44866054-44866104	HepG2	liver:	n/a
16	chr6:44866054-44866104	Caco-2	colon:	n/a
17	chr6:44866054-44866104	H1-hESC	embryonic stem cell:	embryo
18	chr6:44866054-44866104	HMEC	breast:	n/a
19	chr6:44866054-44866104	HIPEpiC	eye:	n/a
20	chr6:44866054-44866104	GM06990	blood:	n/a
21	chr6:44866054-44866104	A549	lung:	n/a
22	chr6:44866054-44866104	GM12891	blood:	n/a
23	chr6:44866054-44866104	ovcar-3	ovarian:	n/a
24	chr6:44866054-44866104	K562	blood:	n/a
25	chr6:44866054-44866104	SK-N-SH	brain:	n/a
26	chr6:44866054-44866104	AG09309	skin:	n/a
27	chr6:44866054-44866104	NB4	blood:	n/a
28	chr6:44866054-44866104	CMK	blood:	n/a
29	chr6:44866054-44866104	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:44866054-44866104	HRCEpiC	kidney:	n/a
31	chr6:44866054-44866104	PANC-1	pancreas:	n/a
32	chr6:44866054-44866104	SAEC	small airway:	n/a
33	chr6:44866054-44866104	HRE	kidney:	n/a
34	chr6:44866054-44866104	HCPEpiC	choroid plexus:	n/a
35	chr6:44866054-44866104	ECC-1	luminal epithelium:	n/a
36	chr6:44866054-44866104	GM19239	blood:	n/a
37	chr6:44866054-44866104	MCF10A-Er-Src	breast:	n/a
38	chr6:44866054-44866104	Hepatocyte	liver:	n/a
39	chr6:44866054-44866104	AG10803	skin:	n/a
40	chr6:44866054-44866104	BJ	skin:	n/a
41	chr6:44866054-44866104	HAEpiC	amniotic membrane:	n/a
42	chr6:44866054-44866104	GM12878	blood:	n/a
43	chr6:44866054-44866104	U87	brain:	n/a
44	chr6:44866054-44866104	NH-A	brain:	n/a
45	chr6:44866054-44866104	HRPEpiC	eye:	n/a
46	chr6:44866054-44866104	MCF-7	breast:	n/a
47	chr6:44866054-44866104	HCF	heart:	n/a
48	chr6:44866054-44866104	AG04450	lung:	fetal
49	chr6:44866054-44866104	IMR90	lung:	fetal
50	chr6:44866054-44866104	HCM	heart:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
2	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:
3	chr6:44874731..44877061-chr6:44885216..44887016,2	K562	blood:
4	chr6:44863793..44865900-chr6:44866802..44868640,2	K562	blood:
5	chr6:44863539..44865317-chr6:44876149..44878495,2	K562	blood:
6	chr6:44888776..44891351-chr6:45344894..45347692,2	K562	blood:
7	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
8	chr6:44874731..44877061-chr6:44885216..44887016,2	K562	blood:
9	chr6:44863539..44865317-chr6:44876149..44878495,2	K562	blood:
10	chr6:44863793..44865900-chr6:44866802..44868640,2	K562	blood:
11	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-5	chr6:44866448-44867032	NONHSAT112969

No data

Variant related genes	Relation type
NUDT19P4	TF binding region
NUDT19P4	CpG island
ENSG00000196284	chromatin interactions

Extended variants
information (count: 1825 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539562589	chr6:44865329-44865330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558188215	chr6:44865343-44865344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372970258	chr6:44865357-44865358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115866650	chr6:44865380-44865381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189940901	chr6:44865385-44865386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181628964	chr6:44865421-44865422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573969706	chr6:44865466-44865467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184542631	chr6:44865471-44865472	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs559711666	chr6:44865478-44865479	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs12529522	chr6:44865520-44865521	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs545581990	chr6:44865531-44865532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189351430	chr6:44865609-44865610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531242895	chr6:44865629-44865630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560576818	chr6:44865683-44865684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543422311	chr6:44865684-44865685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561640402	chr6:44865693-44865694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529220501	chr6:44865717-44865718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146975255	chr6:44865737-44865738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565742800	chr6:44865757-44865758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533149323	chr6:44865773-44865774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551625584	chr6:44865784-44865785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530312024	chr6:44865807-44865808	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570118316	chr6:44865843-44865844	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537073349	chr6:44865844-44865845	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138098617	chr6:44865853-44865854	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143554005	chr6:44865891-44865892	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181967752	chr6:44865911-44865912	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs114605214	chr6:44865933-44865934	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs563726755	chr6:44865967-44865968	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs578143467	chr6:44865969-44865970	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs148622712	chr6:44865976-44865977	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs557596674	chr6:44865985-44865986	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs576228860	chr6:44865989-44865990	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372193585	chr6:44866010-44866011	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185251621	chr6:44866026-44866027	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs112719968	chr6:44866065-44866066	Enhancers Weak transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs141128906	chr6:44866092-44866093	Enhancers Weak transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs528850988	chr6:44866096-44866097	Enhancers Weak transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs541017483	chr6:44866111-44866112	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs559590944	chr6:44866125-44866126	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs533015932	chr6:44866148-44866149	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs533099351	chr6:44866161-44866162	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs551529867	chr6:44866162-44866163	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs59526039	chr6:44866192-44866193	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs532690411	chr6:44866196-44866197	Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs552508788	chr6:44866227-44866228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569721619	chr6:44866309-44866310	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs12530016	chr6:44866322-44866323	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs191215533	chr6:44866358-44866359	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs375220495	chr6:44866360-44866361	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44854600-44866200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:44859200-44889400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:44862600-44889400	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr6:44863000-44865600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:44863200-44866600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:44863600-44870400	Weak transcription	Aorta	Aorta
7	chr6:44864000-44866600	Enhancers	Fetal Lung	lung
8	chr6:44864200-44866600	Enhancers	Fetal Stomach	stomach
9	chr6:44864800-44888400	Weak transcription	Primary T cells from cord blood	blood
10	chr6:44865000-44865800	Weak transcription	HSMM	muscle
11	chr6:44865800-44866200	Genic enhancers	HSMM	muscle
12	chr6:44866000-44866200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr6:44866000-44866600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:44866000-44866600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr6:44866000-44866600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:44866000-44866600	Enhancers	Gastric	stomach
17	chr6:44866000-44866600	Enhancers	HSMMtube	muscle
18	chr6:44866000-44866600	Enhancers	NHDF-Ad	bronchial
19	chr6:44866000-44866600	Enhancers	NHLF	lung
20	chr6:44866200-44866400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr6:44866200-44866600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:44866200-44866600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:44866200-44866600	Enhancers	Placenta	Placenta
24	chr6:44866200-44866600	Enhancers	NH-A	brain
25	chr6:44866200-44866800	Enhancers	HSMM	muscle
26	chr6:44866400-44866600	Enhancers	Pancreas	Pancrea
27	chr6:44866400-44868600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr6:44866600-44869600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:44866600-44879600	Weak transcription	Pancreas	Pancrea
30	chr6:44867400-44868000	Enhancers	K562	blood
31	chr6:44867600-44868000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:44867800-44868800	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr6:44868000-44874600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:44868600-44868800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr6:44868800-44869000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr6:44868800-44870200	Weak transcription	Fetal Intestine Small	intestine
37	chr6:44873200-44888000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr6:44874400-44874800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr6:44874600-44874800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:44874800-44889400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr6:44875000-44888800	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr6:44877800-44892800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:44879000-44888000	Weak transcription	HepG2	liver
44	chr6:44880600-44888000	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr6:44881000-44881200	Enhancers	Fetal Intestine Small	intestine
46	chr6:44881000-44894600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr6:44881200-44882200	Weak transcription	Fetal Intestine Small	intestine
48	chr6:44882000-44882800	Enhancers	Fetal Intestine Large	intestine
49	chr6:44882200-44882600	Enhancers	Fetal Intestine Small	intestine
50	chr6:44882400-44886400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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