Variant report

Variant	nsv886935
Chromosome Location	chr6:166704744-166726566
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:1526)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:166715322-166715710	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:166715159-166715246	K562	blood:	n/a	n/a
3	ARID3A	chr6:166719692-166720195	HepG2	liver:	n/a	n/a
4	BACH1	chr6:166720441-166720971	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:166721825-166721891	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:166714035-166714049	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:166721222-166721264	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr6:166721858-166722322	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:166721860-166722417	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:166720543-166720920	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:166721775-166722393	GM12878	blood:	n/a	chr6:166722082-166722098
12	BHLHE40	chr6:166723852-166724052	K562	blood:	n/a	n/a
13	CBX3	chr6:166708859-166709162	K562	blood:	n/a	n/a
14	CCNT2	chr6:166720752-166720895	K562	blood:	n/a	n/a
15	CEBPB	chr6:166715429-166715728	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:166717465-166717732	HepG2	liver:	n/a	chr6:166717567-166717578
17	CEBPB	chr6:166719901-166720100	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:166726327-166727013	K562	blood:	n/a	n/a
19	CEBPB	chr6:166719805-166720185	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:166726449-166726942	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:166724290-166724467	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPD	chr6:166724820-166725242	K562	blood:	n/a	n/a
23	CHD1	chr6:166721944-166722338	GM12878	blood:	n/a	n/a
24	CHD2	chr6:166719301-166719320	HepG2	liver:	n/a	n/a
25	CHD2	chr6:166720755-166720759	GM12878	blood:	n/a	n/a
26	CHD2	chr6:166722786-166722894	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr6:166721801-166721879	HepG2	liver:	n/a	chr6:166721862-166721872
28	CTCF	chr6:166720859-166720925	NHEK	skin:	n/a	n/a
29	CTCF	chr6:166709800-166709950	GM12871	blood:	n/a	n/a
30	CTCF	chr6:166720507-166721020	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr6:166720580-166720730	GM12871	blood:	n/a	n/a
32	CTCF	chr6:166722000-166722150	SK-N-SH_RA	brain:	n/a	chr6:166722081-166722094 chr6:166722141-166722150
33	CTCF	chr6:166717682-166717800	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr6:166720578-166720701	GM19238	blood:	n/a	n/a
35	CTCF	chr6:166717660-166717810	HepG2	liver:	n/a	n/a
36	CTCF	chr6:166720631-166720658	GM12878	blood:	n/a	n/a
37	CTCF	chr6:166720800-166721003	GM12891	blood:	n/a	n/a
38	CTCF	chr6:166720904-166720922	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr6:166722820-166722970	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr6:166720480-166720630	GM06990	blood:	n/a	n/a
41	CTCF	chr6:166720500-166720650	GM12864	blood:	n/a	n/a
42	CTCF	chr6:166707220-166707370	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr6:166721960-166722110	GM12871	blood:	n/a	chr6:166722081-166722094
44	CTCF	chr6:166720860-166721010	GM12867	blood:	n/a	n/a
45	CTCF	chr6:166720888-166720948	GM10248	blood:	n/a	n/a
46	CTCF	chr6:166720880-166721030	GM12870	blood:	n/a	n/a
47	CTCF	chr6:166722824-166722976	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:166720795-166720805	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr6:166720900-166721050	GM12871	blood:	n/a	n/a
50	CTCF	chr6:166720560-166720710	GM12870	blood:	n/a	n/a

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166722248-166722298	SK-N-SH	brain:	n/a
2	chr6:166722248-166722298	SK-N-SH	brain:	n/a
3	chr6:166720997-166721047	PrEC	prostate:	n/a
4	chr6:166720114-166720164	HRPEpiC	eye:	n/a
5	chr6:166711138-166711188	Hepatocyte	liver:	n/a
6	chr6:166720997-166721047	SKMC	muscle:	n/a
7	chr6:166720092-166720142	HMEC	breast:	n/a
8	chr6:166720092-166720142	GM12892	blood:	n/a
9	chr6:166720749-166720799	IMR90	lung:	fetal
10	chr6:166720092-166720142	AG10803	skin:	n/a
11	chr6:166715306-166715356	RPTEC	kidney:	n/a
12	chr6:166711291-166711341	SKMC	muscle:	n/a
13	chr6:166722058-166722108	A549	lung:	n/a
14	chr6:166717758-166717808	A549	lung:	n/a
15	chr6:166722060-166722110	GM12878	blood:	n/a
16	chr6:166720749-166720799	AG04449	skin:	fetal
17	chr6:166722165-166722215	AG09319	gingival:	n/a
18	chr6:166721155-166721205	U87	brain:	n/a
19	chr6:166722060-166722110	AoSMC	blood vessel:	n/a
20	chr6:166722053-166722103	HEEpiC	esophagus:	n/a
21	chr6:166722165-166722215	AG04449	skin:	fetal
22	chr6:166724408-166724458	RPTEC	kidney:	n/a
23	chr6:166711291-166711341	NB4	blood:	n/a
24	chr6:166720114-166720164	AG09309	skin:	n/a
25	chr6:166721759-166721809	CMK	blood:	n/a
26	chr6:166721155-166721205	Jurkat	blood:	n/a
27	chr6:166711488-166711538	SK-N-MC	brain:	n/a
28	chr6:166722165-166722215	HEK293	kidney:	embryo
29	chr6:166720433-166720483	H1-hESC	embryonic stem cell:	embryo
30	chr6:166722062-166722112	AG09319	gingival:	n/a
31	chr6:166722058-166722108	T-47D	breast:	n/a
32	chr6:166711442-166711492	HNPCEpiC	eye:	n/a
33	chr6:166715306-166715356	SK-N-MC	brain:	n/a
34	chr6:166720749-166720799	SK-N-SH	brain:	n/a
35	chr6:166707834-166707884	IMR90	lung:	fetal
36	chr6:166721155-166721205	HCF	heart:	n/a
37	chr6:166720092-166720142	NT2-D1	testis:	n/a
38	chr6:166711381-166711431	ovcar-3	ovarian:	n/a
39	chr6:166722248-166722298	MCF-7	breast:	n/a
40	chr6:166721155-166721205	HEEpiC	esophagus:	n/a
41	chr6:166722060-166722110	Jurkat	blood:	n/a
42	chr6:166722053-166722103	GM06990	blood:	n/a
43	chr6:166707834-166707884	HRPEpiC	eye:	n/a
44	chr6:166721759-166721809	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:166711488-166711538	HUVEC	blood vessel:	n/a
46	chr6:166721644-166721694	A549	lung:	n/a
47	chr6:166722060-166722110	HMEC	breast:	n/a
48	chr6:166711381-166711431	Jurkat	blood:	n/a
49	chr6:166722248-166722298	Hepatocyte	liver:	n/a
50	chr6:166722053-166722103	AG04450	lung:	fetal

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166710025..166712273-chr6:166716005..166718139,2	K562	blood:
2	chr6:166718072..166719641-chr6:166743205..166745434,2	K562	blood:
3	chr6:166726414..166727356-chr6:166813994..166814993,6	K562	blood:
4	chr6:166712983..166714666-chr6:166752860..166755099,2	K562	blood:
5	chr6:166726149..166728361-chr6:166730618..166732594,2	K562	blood:
6	chr6:166722484..166724020-chr6:166795532..166798475,2	K562	blood:
7	chr6:166719852..166722547-chr6:166755922..166758056,2	K562	blood:
8	chr6:166709970..166712406-chr6:166716038..166718668,2	K562	blood:
9	chr6:166722635..166726585-chr6:166755013..166756920,3	K562	blood:
10	chr6:166722256..166724406-chr6:166752301..166754007,2	MCF-7	breast:
11	chr6:166722651..166724604-chr6:166784233..166785851,2	K562	blood:
12	chr6:166709970..166712406-chr6:166716038..166718668,2	K562	blood:
13	chr6:166726357..166727438-chr6:166794885..166795636,3	K562	blood:
14	chr6:166713905..166716781-chr6:166720409..166722328,2	K562	blood:
15	chr6:166710025..166712273-chr6:166716005..166718139,2	K562	blood:
16	chr6:166706226..166707823-chr6:166795283..166798156,2	K562	blood:
17	chr6:166720530..166722265-chr6:166724559..166726140,2	K562	blood:

No data

Variant related genes	Relation type
PRR18	TF binding region
PRR18	CpG island
ENSG00000261420	chromatin interactions
ENSG00000198818	chromatin interactions
ENSG00000060762	chromatin interactions
ENSG00000176381	chromatin interactions

Extended variants
information (count: 1024 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10946151	chr6:166704744-166704745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558372972	chr6:166704758-166704759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149552309	chr6:166704815-166704816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534747653	chr6:166704936-166704937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190000348	chr6:166705078-166705079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534622082	chr6:166705133-166705134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373440433	chr6:166705136-166705137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574164307	chr6:166705183-166705184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372153856	chr6:166705198-166705199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs117858846	chr6:166705221-166705222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556497286	chr6:166705228-166705229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374953742	chr6:166705236-166705237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191776045	chr6:166705361-166705362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376071795	chr6:166705371-166705372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369366706	chr6:166705406-166705407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545775911	chr6:166705415-166705416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532905767	chr6:166705424-166705425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113442328	chr6:166705430-166705431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1884957	chr6:166705512-166705513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs35637071	chr6:166705515-166705516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528258438	chr6:166705516-166705517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540396274	chr6:166705524-166705525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546249957	chr6:166705633-166705634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562187110	chr6:166705634-166705635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529362503	chr6:166705648-166705649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551005254	chr6:166705674-166705675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562733886	chr6:166705691-166705692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563298377	chr6:166705695-166705696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551769077	chr6:166705735-166705736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567116835	chr6:166705761-166705762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534148933	chr6:166705788-166705789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183895967	chr6:166705789-166705790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148494246	chr6:166705843-166705844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535166748	chr6:166705857-166705858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556585379	chr6:166705862-166705863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143721989	chr6:166705863-166705864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6934274	chr6:166705902-166705903	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs147201547	chr6:166705935-166705936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573065249	chr6:166706025-166706026	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs540432514	chr6:166706073-166706074	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs561827115	chr6:166706074-166706075	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574228013	chr6:166706075-166706076	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs6934656	chr6:166706121-166706122	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs77671697	chr6:166706144-166706145	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs6915183	chr6:166706169-166706170	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
46	rs188227871	chr6:166706218-166706219	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs560623360	chr6:166706233-166706234	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376055253	chr6:166706247-166706248	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs527936769	chr6:166706268-166706269	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs549204020	chr6:166706276-166706277	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166687600-166704800	Weak transcription	Right Atrium	heart
2	chr6:166691200-166706000	Weak transcription	Brain Anterior Caudate	brain
3	chr6:166698400-166705800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr6:166705800-166706000	Enhancers	Brain Hippocampus Middle	brain
5	chr6:166705800-166709400	Enhancers	Brain Cingulate Gyrus	brain
6	chr6:166706000-166706200	Enhancers	Brain Anterior Caudate	brain
7	chr6:166706000-166706400	Flanking Active TSS	Brain Hippocampus Middle	brain
8	chr6:166706000-166706400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr6:166706000-166706800	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr6:166706000-166711000	Enhancers	Brain Substantia Nigra	brain
11	chr6:166706200-166706600	Weak transcription	Brain Anterior Caudate	brain
12	chr6:166706200-166710600	Enhancers	Brain Angular Gyrus	brain
13	chr6:166706400-166706600	Bivalent Enhancer	HepG2	liver
14	chr6:166706400-166707800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr6:166706400-166709400	Enhancers	Brain Hippocampus Middle	brain
16	chr6:166706600-166709600	Enhancers	Brain Anterior Caudate	brain
17	chr6:166706800-166707200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr6:166707200-166708400	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr6:166707400-166709000	Enhancers	Fetal Intestine Large	intestine
20	chr6:166707400-166709000	Enhancers	Fetal Thymus	thymus
21	chr6:166707600-166708200	Enhancers	Duodenum Mucosa	Duodenum
22	chr6:166707600-166708600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:166707600-166708600	Enhancers	Fetal Intestine Small	intestine
24	chr6:166707600-166708800	Enhancers	Primary hematopoietic stem cells	blood
25	chr6:166707800-166708200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr6:166707800-166709400	Enhancers	Primary B cells from cord blood	blood
27	chr6:166707800-166709400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr6:166708000-166709000	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:166708000-166709200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:166708200-166712000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:166708400-166708800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr6:166708800-166709000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr6:166708800-166709200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr6:166709000-166709800	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr6:166709200-166709800	Enhancers	Primary hematopoietic stem cells	blood
36	chr6:166709400-166709600	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr6:166709400-166711000	Flanking Active TSS	Brain Hippocampus Middle	brain
38	chr6:166709600-166710000	Flanking Active TSS	Brain Anterior Caudate	brain
39	chr6:166709600-166710400	Active TSS	Brain Cingulate Gyrus	brain
40	chr6:166709800-166710000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:166709800-166711000	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr6:166710000-166710200	Active TSS	Brain Anterior Caudate	brain
43	chr6:166710200-166710400	Flanking Active TSS	Brain Anterior Caudate	brain
44	chr6:166710400-166710800	Enhancers	Brain Anterior Caudate	brain
45	chr6:166710400-166710800	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr6:166710600-166712000	Weak transcription	Brain Angular Gyrus	brain
47	chr6:166710800-166711600	Active TSS	Brain Cingulate Gyrus	brain
48	chr6:166710800-166712000	Weak transcription	Brain Anterior Caudate	brain
49	chr6:166711000-166712000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr6:166711000-166712000	Weak transcription	Brain Substantia Nigra	brain

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