Variant report

Variant	esv1796475
Chromosome Location	chr6:163822296-163836689
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:965)
CpG islands
(count:796)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:163830843-163831145	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163833393-163835195	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:163826851-163827481	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:163831964-163831984	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:163834674-163835193	K562	blood:	n/a	n/a
6	ARID3A	chr6:163829506-163830620	HepG2	liver:	n/a	chr6:163830036-163830052 chr6:163829655-163829671 chr6:163829654-163829670
7	ARID3A	chr6:163832278-163832521	HepG2	liver:	n/a	n/a
8	ATF1	chr6:163833475-163833658	K562	blood:	n/a	n/a
9	ATF2	chr6:163833939-163834675	GM12878	blood:	n/a	n/a
10	ATF2	chr6:163834688-163835329	GM12878	blood:	n/a	n/a
11	ATF2	chr6:163834078-163834503	GM12878	blood:	n/a	n/a
12	ATF2	chr6:163834922-163835269	GM12878	blood:	n/a	n/a
13	ATF3	chr6:163834928-163835250	K562	blood:	n/a	n/a
14	ATF3	chr6:163834927-163835263	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr6:163834850-163835290	GM12878	blood:	n/a	n/a
16	ATF3	chr6:163834497-163834859	K562	blood:	n/a	n/a
17	ATF3	chr6:163834904-163835255	HepG2	liver:	n/a	n/a
18	ATF3	chr6:163834816-163835317	HepG2	liver:	n/a	n/a
19	ATF3	chr6:163835011-163835162	GM12878	blood:	n/a	n/a
20	ATF3	chr6:163834976-163835190	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:163833884-163835210	K562	blood:	n/a	n/a
22	BACH1	chr6:163834314-163835318	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL3	chr6:163828532-163828884	GM12878	blood:	n/a	n/a
24	BCL3	chr6:163828521-163828887	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:163834193-163835293	GM12878	blood:	n/a	chr6:163834831-163834840
26	BCLAF1	chr6:163834227-163835276	GM12878	blood:	n/a	chr6:163834831-163834840
27	BCLAF1	chr6:163834461-163835301	K562	blood:	n/a	chr6:163834831-163834840 chr6:163835287-163835300
28	BCLAF1	chr6:163835600-163835941	GM12878	blood:	n/a	chr6:163835760-163835773 chr6:163835781-163835790 chr6:163835779-163835792
29	BHLHE40	chr6:163836622-163837133	K562	blood:	n/a	n/a
30	BHLHE40	chr6:163835608-163835832	GM12878	blood:	n/a	chr6:163835760-163835776 chr6:163835757-163835773
31	BHLHE40	chr6:163825335-163825610	K562	blood:	n/a	chr6:163825456-163825465
32	BHLHE40	chr6:163834242-163835307	K562	blood:	n/a	n/a
33	BHLHE40	chr6:163834536-163834943	A549	lung:	n/a	n/a
34	BHLHE40	chr6:163833621-163835329	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:163834344-163835354	HepG2	liver:	n/a	n/a
36	BHLHE40	chr6:163835658-163835902	K562	blood:	n/a	chr6:163835760-163835776 chr6:163835757-163835773
37	BRCA1	chr6:163834833-163835219	GM12878	blood:	n/a	n/a
38	BRCA1	chr6:163834883-163835128	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:163834975-163835254	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr6:163834088-163835319	K562	blood:	n/a	n/a
41	CBX3	chr6:163834516-163834893	K562	blood:	n/a	n/a
42	CCNT2	chr6:163833862-163837213	K562	blood:	n/a	chr6:163837081-163837090
43	CEBPB	chr6:163833449-163834753	K562	blood:	n/a	n/a
44	CEBPB	chr6:163834950-163835319	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:163826037-163826239	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:163834962-163835251	K562	blood:	n/a	n/a
47	CEBPB	chr6:163826053-163826267	K562	blood:	n/a	n/a
48	CEBPB	chr6:163829675-163830035	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:163825981-163826369	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:163834959-163835331	A549	lung:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163835395-163835445	HRCEpiC	kidney:	n/a
2	chr6:163835117-163835167	K562	blood:	n/a
3	chr6:163836245-163836295	Caco-2	colon:	n/a
4	chr6:163835395-163835445	HRCEpiC	kidney:	n/a
5	chr6:163835117-163835167	K562	blood:	n/a
6	chr6:163836245-163836295	Caco-2	colon:	n/a
7	chr6:163834903-163834953	SKMC	muscle:	n/a
8	chr6:163834924-163834974	NHDF-neo	bronchial:	n/a
9	chr6:163834903-163834953	HCPEpiC	choroid plexus:	n/a
10	chr6:163834924-163834974	Jurkat	blood:	n/a
11	chr6:163834158-163834208	PANC-1	pancreas:	n/a
12	chr6:163834158-163834208	K562	blood:	n/a
13	chr6:163826969-163827019	MCF10A-Er-Src	breast:	n/a
14	chr6:163834872-163834922	HUVEC	blood vessel:	n/a
15	chr6:163835251-163835301	ovcar-3	ovarian:	n/a
16	chr6:163834176-163834226	GM12878	blood:	n/a
17	chr6:163834452-163834502	GM12892	blood:	n/a
18	chr6:163834452-163834502	K562	blood:	n/a
19	chr6:163835117-163835167	A549	lung:	n/a
20	chr6:163834158-163834208	NHBE	bronchial:	n/a
21	chr6:163834924-163834974	HNPCEpiC	eye:	n/a
22	chr6:163834924-163834974	NH-A	brain:	n/a
23	chr6:163835251-163835301	SK-N-SH_RA	brain:	n/a
24	chr6:163835395-163835445	IMR90	lung:	fetal
25	chr6:163836245-163836295	HepG2	liver:	n/a
26	chr6:163835395-163835445	RPTEC	kidney:	n/a
27	chr6:163836348-163836398	Hela-S3	cervix:	n/a
28	chr6:163836245-163836295	HIPEpiC	eye:	n/a
29	chr6:163835117-163835167	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:163834924-163834974	SK-N-MC	brain:	n/a
31	chr6:163836348-163836398	NHBE	bronchial:	n/a
32	chr6:163835117-163835167	U87	brain:	n/a
33	chr6:163836348-163836398	MCF10A-Er-Src	breast:	n/a
34	chr6:163834176-163834226	NT2-D1	testis:	n/a
35	chr6:163834452-163834502	GM06990	blood:	n/a
36	chr6:163836348-163836398	SAEC	small airway:	n/a
37	chr6:163834872-163834922	Hepatocyte	liver:	n/a
38	chr6:163835582-163835632	NH-A	brain:	n/a
39	chr6:163834924-163834974	BE2_C	brain:	n/a
40	chr6:163826969-163827019	HNPCEpiC	eye:	n/a
41	chr6:163836245-163836295	K562	blood:	n/a
42	chr6:163835117-163835167	Caco-2	colon:	n/a
43	chr6:163835582-163835632	HRCEpiC	kidney:	n/a
44	chr6:163834176-163834226	SK-N-SH_RA	brain:	n/a
45	chr6:163835395-163835445	PrEC	prostate:	n/a
46	chr6:163836348-163836398	PANC-1	pancreas:	n/a
47	chr6:163826969-163827019	HUVEC	blood vessel:	n/a
48	chr6:163834158-163834208	LNCaP	prostate:	n/a
49	chr6:163834872-163834922	PFSK-1	brain:	n/a
50	chr6:163834903-163834953	AG04449	skin:	fetal

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:163707215..163709135-chr6:163832836..163834940,2	MCF-7	breast:
2	chr6:163831740..163833588-chr6:164102782..164105266,2	K562	blood:
3	chr5:34007852..34008601-chr6:163834316..163835107,2	Hela-S3	cervix:
4	chr6:163833988..163836212-chr6:163848529..163850044,2	MCF-7	breast:
5	chr6:163820462..163822214-chr6:163823879..163825565,2	K562	blood:
6	chr6:163824877..163830472-chr6:163836413..163839637,4	MCF-7	breast:
7	chr6:163834433..163837014-chr6:163986395..163988827,2	K562	blood:
8	chr6:163825837..163828170-chr6:163829514..163831485,3	MCF-7	breast:
9	chr6:163825837..163828170-chr6:163829514..163831485,3	MCF-7	breast:
10	chr6:163836144..163840696-chr6:163983068..163987938,4	K562	blood:
11	chr6:163828630..163831846-chr6:163832456..163835653,4	MCF-7	breast:
12	chr6:163832712..163834333-chr6:164408971..164410917,2	K562	blood:
13	chr6:163725918..163727720-chr6:163831906..163834070,2	K562	blood:
14	chr17:8075909..8076789-chr6:163834187..163834895,2	Hela-S3	cervix:
15	chr6:163820034..163822360-chr6:163835389..163837208,2	MCF-7	breast:
16	chr6:163822459..163825061-chr6:163833454..163835896,2	MCF-7	breast:
17	chr6:163680711..163682973-chr6:163830679..163833543,2	K562	blood:
18	chr6:163804907..163807228-chr6:163823895..163826768,2	K562	blood:
19	chr6:163832850..163838270-chr6:163950827..163956360,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QKI-6	chr6:163833646-163833771	NONHSAT115961
2	lnc-QKI-6	chr6:163832465-163832741	NONHSAT115961

No data

Variant related genes	Relation type
QKI	TF binding region
CAHM	TF binding region
QKI	CpG island
CAHM	CpG island
ENSG00000242110	chromatin interactions
ENSG00000112531	chromatin interactions
ENSG00000270419	chromatin interactions

Extended variants
information (count: 551 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4263561	chr6:163822296-163822297	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542375298	chr6:163822297-163822298	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2259477	chr6:163822380-163822381	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs116631453	chr6:163822386-163822387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551361743	chr6:163822387-163822388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2259476	chr6:163822396-163822397	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs530388873	chr6:163822417-163822418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547973658	chr6:163822434-163822435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566381322	chr6:163822437-163822438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184726768	chr6:163822454-163822455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139486231	chr6:163822455-163822456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34026669	chr6:163822518-163822519	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs533641811	chr6:163822530-163822531	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs149242092	chr6:163822543-163822544	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12663137	chr6:163822564-163822565	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs377320134	chr6:163822595-163822596	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546758381	chr6:163822598-163822599	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs78312257	chr6:163822676-163822677	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs535266830	chr6:163822677-163822678	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558132618	chr6:163822680-163822681	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs570462624	chr6:163822686-163822687	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144419924	chr6:163822697-163822698	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536997973	chr6:163822725-163822726	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs557331513	chr6:163822736-163822737	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148435560	chr6:163822747-163822748	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542706939	chr6:163822759-163822760	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539757307	chr6:163822778-163822779	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147782302	chr6:163822801-163822802	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537422668	chr6:163822867-163822868	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs189509334	chr6:163822875-163822876	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73244744	chr6:163822888-163822889	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545207147	chr6:163822937-163822938	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs34384803	chr6:163822974-163822975	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs6901705	chr6:163823051-163823052	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs73013591	chr6:163823087-163823088	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558164063	chr6:163823088-163823089	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144024698	chr6:163823106-163823107	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75727935	chr6:163823109-163823110	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs529762352	chr6:163823170-163823171	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs181535006	chr6:163823178-163823179	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs566587106	chr6:163823188-163823189	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528649354	chr6:163823202-163823203	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551953054	chr6:163823203-163823204	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs375050177	chr6:163823405-163823406	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186927322	chr6:163823433-163823434	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs557413189	chr6:163823452-163823453	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs146617918	chr6:163823509-163823510	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7754420	chr6:163823535-163823536	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573025466	chr6:163823542-163823543	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs111407675	chr6:163823567-163823568	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Renal cell carcinoma	18592004	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
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163809800-163825600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:163818000-163822600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:163818000-163826800	Weak transcription	Gastric	stomach
4	chr6:163818200-163825600	Weak transcription	Lung	lung
5	chr6:163818200-163826200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr6:163818200-163826800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:163818400-163825200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr6:163818400-163825400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:163818400-163825400	Weak transcription	Right Atrium	heart
10	chr6:163818600-163823400	Weak transcription	Fetal Heart	heart
11	chr6:163818800-163825800	Weak transcription	Colon Smooth Muscle	Colon
12	chr6:163818800-163826400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:163819000-163824000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:163819400-163822600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:163819600-163822400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:163819800-163825000	Enhancers	Placenta	Placenta
17	chr6:163820000-163825600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr6:163820200-163823000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr6:163820200-163823000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr6:163820200-163823200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:163820200-163825600	Weak transcription	Spleen	Spleen
22	chr6:163820200-163825800	Weak transcription	Psoas Muscle	Psoas
23	chr6:163820200-163826000	Weak transcription	Brain Germinal Matrix	brain
24	chr6:163820200-163826000	Weak transcription	Fetal Brain Female	brain
25	chr6:163820200-163826800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr6:163820400-163822400	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr6:163820400-163822600	Weak transcription	Brain Anterior Caudate	brain
28	chr6:163820400-163822600	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr6:163820400-163823000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr6:163820400-163824600	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr6:163820400-163824600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr6:163820400-163824800	Weak transcription	Brain Angular Gyrus	brain
33	chr6:163820400-163825600	Weak transcription	Fetal Muscle Leg	muscle
34	chr6:163820400-163826000	Weak transcription	Ovary	ovary
35	chr6:163820400-163826800	Weak transcription	GM12878-XiMat	blood
36	chr6:163820600-163825400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:163820600-163826600	Weak transcription	Fetal Brain Male	brain
38	chr6:163820800-163823400	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr6:163820800-163825600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:163821000-163822400	Weak transcription	Brain Substantia Nigra	brain
41	chr6:163821200-163823200	Weak transcription	Brain Hippocampus Middle	brain
42	chr6:163821400-163824600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr6:163821400-163827000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:163821800-163823000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr6:163821800-163823400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr6:163821800-163824400	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr6:163822000-163823000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr6:163822000-163825400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:163822000-163825400	Weak transcription	Adipose Nuclei	Adipose
50	chr6:163822200-163822600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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