Variant report

Variant	nsv5180
Chromosome Location	chr6:5389197-5434354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:725)
CpG islands
(count:305)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:5398731-5399051	K562	blood:	n/a	n/a
2	ATF1	chr6:5400979-5401008	K562	blood:	n/a	n/a
3	BRCA1	chr6:5411934-5412037	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:5394543-5394882	K562	blood:	n/a	chr6:5394716-5394727
5	CEBPB	chr6:5394541-5394893	IMR90	lung:	n/a	chr6:5394716-5394727
6	CEBPB	chr6:5394562-5394904	A549	lung:	n/a	chr6:5394716-5394727
7	CEBPB	chr6:5394562-5394950	MCF-7	breast:	n/a	chr6:5394716-5394727
8	CEBPB	chr6:5394603-5394931	MCF-7	breast:	n/a	chr6:5394716-5394727
9	CEBPB	chr6:5398872-5399134	A549	lung:	n/a	n/a
10	CEBPB	chr6:5394513-5394800	K562	blood:	n/a	chr6:5394716-5394727
11	CEBPB	chr6:5412316-5412616	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:5394553-5394878	Hela-S3	cervix:	n/a	chr6:5394716-5394727
13	CEBPB	chr6:5426867-5426988	HepG2	liver:	n/a	chr6:5426914-5426925
14	CEBPB	chr6:5402661-5402938	K562	blood:	n/a	n/a
15	CEBPB	chr6:5394537-5394883	HepG2	liver:	n/a	chr6:5394716-5394727
16	CEBPB	chr6:5394578-5394817	H1-hESC	embryonic stem cell:	n/a	chr6:5394716-5394727
17	CTBP2	chr6:5412246-5412718	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr6:5422620-5422770	GM06990	blood:	n/a	n/a
19	CTCF	chr6:5395920-5396070	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr6:5398800-5398950	HMEC	breast:	n/a	n/a
21	CTCF	chr6:5422680-5422830	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr6:5402600-5402750	RPTEC	kidney:	n/a	n/a
23	CTCF	chr6:5422640-5422790	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr6:5398800-5398950	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr6:5402720-5402870	GM12801	blood:	n/a	n/a
26	CTCF	chr6:5422640-5422790	WI-38	lung:	n/a	n/a
27	CTCF	chr6:5422680-5422830	AG09319	gingival:	n/a	n/a
28	CTCF	chr6:5422628-5422851	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr6:5422560-5422948	GM12878	blood:	n/a	n/a
30	CTCF	chr6:5402680-5402830	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr6:5402720-5402870	GM12868	blood:	n/a	n/a
32	CTCF	chr6:5398800-5398950	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr6:5413760-5413910	GM12871	blood:	n/a	n/a
34	CTCF	chr6:5396880-5397030	AG04450	lung:	n/a	n/a
35	CTCF	chr6:5422611-5422886	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:5422680-5422830	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:5396080-5396230	AG10803	skin:	n/a	chr6:5396148-5396155 chr6:5396136-5396157
38	CTCF	chr6:5422660-5422810	GM12866	blood:	n/a	n/a
39	CTCF	chr6:5402602-5402917	ECC-1	luminal epithelium:	n/a	n/a
40	CTCF	chr6:5402586-5402974	IMR90	lung:	n/a	n/a
41	CTCF	chr6:5396000-5396150	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr6:5398780-5398930	HVMF	connective:	n/a	n/a
43	CTCF	chr6:5422640-5422790	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr6:5398780-5398930	GM12878	blood:	n/a	n/a
45	CTCF	chr6:5422623-5422875	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:5402680-5402830	SAEC	small airway:	n/a	n/a
47	CTCF	chr6:5402740-5402890	GM12868	blood:	n/a	n/a
48	CTCF	chr6:5402662-5402895	LNCaP	prostate:	n/a	n/a
49	CTCF	chr6:5402680-5402830	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr6:5422640-5422790	HVMF	connective:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5412087-5412137	NT2-D1	testis:	n/a
2	chr6:5406020-5406070	PFSK-1	brain:	n/a
3	chr6:5404958-5405008	LNCaP	prostate:	n/a
4	chr6:5412087-5412137	GM06990	blood:	n/a
5	chr6:5404958-5405008	NH-A	brain:	n/a
6	chr6:5425832-5425882	ovcar-3	ovarian:	n/a
7	chr6:5412087-5412137	PANC-1	pancreas:	n/a
8	chr6:5412087-5412137	ECC-1	luminal epithelium:	n/a
9	chr6:5425832-5425882	AG09319	gingival:	n/a
10	chr6:5431669-5431719	HIPEpiC	eye:	n/a
11	chr6:5404958-5405008	PrEC	prostate:	n/a
12	chr6:5412087-5412137	ovcar-3	ovarian:	n/a
13	chr6:5404958-5405008	GM12892	blood:	n/a
14	chr6:5412087-5412137	HepG2	liver:	n/a
15	chr6:5412087-5412137	AoSMC	blood vessel:	n/a
16	chr6:5431669-5431719	HUVEC	blood vessel:	n/a
17	chr6:5425832-5425882	HIPEpiC	eye:	n/a
18	chr6:5412087-5412137	HUVEC	blood vessel:	n/a
19	chr6:5431669-5431719	NH-A	brain:	n/a
20	chr6:5431669-5431719	MCF10A-Er-Src	breast:	n/a
21	chr6:5412087-5412137	GM12892	blood:	n/a
22	chr6:5425832-5425882	SAEC	small airway:	n/a
23	chr6:5412087-5412137	Caco-2	colon:	n/a
24	chr6:5425832-5425882	CMK	blood:	n/a
25	chr6:5406020-5406070	HCF	heart:	n/a
26	chr6:5412087-5412137	HRCEpiC	kidney:	n/a
27	chr6:5404958-5405008	PANC-1	pancreas:	n/a
28	chr6:5431669-5431719	NHBE	bronchial:	n/a
29	chr6:5412087-5412137	Jurkat	blood:	n/a
30	chr6:5404958-5405008	NT2-D1	testis:	n/a
31	chr6:5425832-5425882	ECC-1	luminal epithelium:	n/a
32	chr6:5425832-5425882	GM12891	blood:	n/a
33	chr6:5425832-5425882	MCF-7	breast:	n/a
34	chr6:5425832-5425882	HL-60	blood:	n/a
35	chr6:5431669-5431719	Hepatocyte	liver:	n/a
36	chr6:5406020-5406070	AG09319	gingival:	n/a
37	chr6:5412087-5412137	HCM	heart:	n/a
38	chr6:5431669-5431719	HMEC	breast:	n/a
39	chr6:5425832-5425882	PFSK-1	brain:	n/a
40	chr6:5412087-5412137	K562	blood:	n/a
41	chr6:5425832-5425882	AG04450	lung:	fetal
42	chr6:5404958-5405008	HNPCEpiC	eye:	n/a
43	chr6:5412087-5412137	NH-A	brain:	n/a
44	chr6:5412087-5412137	IMR90	lung:	fetal
45	chr6:5425832-5425882	LNCaP	prostate:	n/a
46	chr6:5431669-5431719	BE2_C	brain:	n/a
47	chr6:5404958-5405008	HL-60	blood:	n/a
48	chr6:5406020-5406070	GM19239	blood:	n/a
49	chr6:5406020-5406070	H1-hESC	embryonic stem cell:	embryo
50	chr6:5404958-5405008	AG09319	gingival:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:5415440..5417820-chr6:5418569..5420285,2	K562	blood:
2	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
3	chr6:5143575..5144138-chr6:5398465..5399339,2	K562	blood:
4	chr6:5424951..5427870-chr6:5732837..5734922,2	MCF-7	breast:
5	chr6:5422309..5423241-chr6:6547390..6547945,3	MCF-7	breast:
6	chr6:5143322..5144392-chr6:5398327..5399283,4	MCF-7	breast:
7	chr6:5135691..5136262-chr6:5402310..5402817,2	K562	blood:
8	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
9	chr6:5143546..5144516-chr6:5402052..5403264,7	K562	blood:
10	chr6:5214686..5215658-chr6:5401229..5403280,10	K562	blood:
11	chr6:5422389..5423223-chr6:5898415..5898938,2	MCF-7	breast:
12	chr6:5415440..5417820-chr6:5418569..5420285,2	K562	blood:
13	chr15:91040281..91042340-chr6:5395615..5398410,2	MCF-7	breast:
14	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
15	chr6:5214744..5215638-chr6:5398420..5399368,7	K562	blood:
16	chr6:5143921..5144506-chr6:5398809..5399361,2	MCF-7	breast:
17	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
18	chr6:5380009..5381908-chr6:5391068..5392911,2	K562	blood:
19	chr6:5431881..5436604-chr6:5436753..5441713,4	K562	blood:
20	chr6:5143607..5144647-chr6:5402160..5403231,5	MCF-7	breast:
21	chr6:5056624..5057532-chr6:5398465..5398983,2	K562	blood:
22	chr6:4957603..4958360-chr6:5398859..5399468,2	MCF-7	breast:

No data

Variant related genes	Relation type
FARS2	TF binding region
FARS2	CpG island

Extended variants
information (count: 1940 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73350536	chr6:5389218-5389219	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570002871	chr6:5389229-5389230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115839776	chr6:5389247-5389248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35967844	chr6:5389386-5389387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397950662	chr6:5389392-5389393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143485597	chr6:5389393-5389394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148016550	chr6:5389395-5389396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73350538	chr6:5389403-5389404	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2503811	chr6:5389418-5389419	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs116837005	chr6:5389423-5389424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542435244	chr6:5389460-5389461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73718088	chr6:5389484-5389485	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs73718089	chr6:5389488-5389489	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs12525112	chr6:5389499-5389500	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs540451107	chr6:5389502-5389503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140705909	chr6:5389539-5389540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6938599	chr6:5389574-5389575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113400111	chr6:5389597-5389598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565796638	chr6:5389625-5389626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150088958	chr6:5389676-5389677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1895646	chr6:5389729-5389730	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs138994408	chr6:5389748-5389749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537297293	chr6:5389750-5389751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17140384	chr6:5389764-5389765	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs187050328	chr6:5389804-5389805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564940705	chr6:5389812-5389813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553168659	chr6:5389829-5389830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142264103	chr6:5389840-5389841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542046976	chr6:5389851-5389852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1895645	chr6:5389883-5389884	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191540837	chr6:5389887-5389888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550673703	chr6:5389946-5389947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546053642	chr6:5389949-5389950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551739273	chr6:5389968-5389969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1895644	chr6:5389970-5389971	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs34436906	chr6:5390088-5390089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs397811361	chr6:5390090-5390091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs13215188	chr6:5390091-5390092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201988030	chr6:5390097-5390098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185258581	chr6:5390131-5390132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538138474	chr6:5390139-5390140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541057748	chr6:5390151-5390152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111659275	chr6:5390174-5390175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559175612	chr6:5390188-5390189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146356747	chr6:5390199-5390200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138400240	chr6:5390202-5390203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190177828	chr6:5390223-5390224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530738271	chr6:5390244-5390245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116826727	chr6:5390246-5390247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570785966	chr6:5390247-5390248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5368400-5398600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:5369400-5419800	Weak transcription	Aorta	Aorta
3	chr6:5369600-5417400	Weak transcription	Fetal Intestine Small	intestine
4	chr6:5371000-5411400	Weak transcription	Ovary	ovary
5	chr6:5374400-5431400	Weak transcription	Primary B cells from cord blood	blood
6	chr6:5380200-5395800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr6:5385200-5391800	Weak transcription	Primary T cells from cord blood	blood
8	chr6:5385600-5390600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:5388000-5389200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr6:5388000-5389400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:5388600-5390000	Enhancers	Brain Cingulate Gyrus	brain
12	chr6:5388600-5390000	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr6:5388600-5390000	Enhancers	Brain Substantia Nigra	brain
14	chr6:5388800-5389800	Enhancers	Brain Hippocampus Middle	brain
15	chr6:5389000-5390000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:5389000-5390000	Enhancers	Brain Angular Gyrus	brain
17	chr6:5389000-5390000	Enhancers	Brain Anterior Caudate	brain
18	chr6:5389000-5390400	Enhancers	Psoas Muscle	Psoas
19	chr6:5389200-5389800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:5389400-5389800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr6:5389400-5390000	Enhancers	Colon Smooth Muscle	Colon
22	chr6:5389600-5389800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr6:5389600-5390400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr6:5389800-5390600	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:5390600-5391200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:5392400-5392600	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr6:5392400-5392800	Enhancers	Fetal Heart	heart
28	chr6:5395200-5395400	Enhancers	Left Ventricle	heart
29	chr6:5395400-5431200	Weak transcription	Left Ventricle	heart
30	chr6:5395800-5397200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr6:5396800-5397000	Enhancers	Fetal Muscle Trunk	muscle
32	chr6:5397000-5397200	Enhancers	Rectal Smooth Muscle	rectum
33	chr6:5397200-5398800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr6:5398600-5399200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:5398600-5399200	Enhancers	NHEK	skin
36	chr6:5398800-5399200	Enhancers	Rectal Smooth Muscle	rectum
37	chr6:5399000-5399200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:5399000-5399200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr6:5399200-5403000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:5399200-5415800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr6:5399200-5440000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:5399400-5399800	Weak transcription	NHEK	skin
43	chr6:5400000-5400600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr6:5401200-5402600	Weak transcription	NHEK	skin
45	chr6:5402200-5402400	Active TSS	Primary hematopoietic stem cells	blood
46	chr6:5402400-5406000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr6:5402600-5408400	Weak transcription	Primary T cells from cord blood	blood
48	chr6:5402800-5403400	Enhancers	NHEK	skin
49	chr6:5403000-5403200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:5403000-5403200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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