Variant report

Variant	nsv605195
Chromosome Location	chr6:163824864-163836634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:948)
CpG islands
(count:793)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:163826851-163827481	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163829506-163830620	HepG2	liver:	n/a	chr6:163830036-163830052 chr6:163829655-163829671 chr6:163829654-163829670
3	ARID3A	chr6:163832278-163832521	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:163830843-163831145	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:163834674-163835193	K562	blood:	n/a	n/a
6	ARID3A	chr6:163833393-163835195	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:163831964-163831984	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	chr6:163834922-163835269	GM12878	blood:	n/a	n/a
11	ATF2	chr6:163834688-163835329	GM12878	blood:	n/a	n/a
12	ATF2	chr6:163834078-163834503	GM12878	blood:	n/a	n/a
13	ATF3	chr6:163834976-163835190	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr6:163834928-163835250	K562	blood:	n/a	n/a
15	ATF3	chr6:163835011-163835162	GM12878	blood:	n/a	n/a
16	ATF3	chr6:163834497-163834859	K562	blood:	n/a	n/a
17	ATF3	chr6:163834816-163835317	HepG2	liver:	n/a	n/a
18	ATF3	chr6:163834850-163835290	GM12878	blood:	n/a	n/a
19	ATF3	chr6:163834927-163835263	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr6:163834904-163835255	HepG2	liver:	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	chr6:163828521-163828887	GM12878	blood:	n/a	n/a
24	BCL3	chr6:163828532-163828884	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:163835600-163835941	GM12878	blood:	n/a	chr6:163835760-163835773 chr6:163835781-163835790 chr6:163835779-163835792
26	BCLAF1	chr6:163834461-163835301	K562	blood:	n/a	chr6:163834831-163834840 chr6:163835287-163835300
27	BCLAF1	chr6:163834193-163835293	GM12878	blood:	n/a	chr6:163834831-163834840
28	BCLAF1	chr6:163834227-163835276	GM12878	blood:	n/a	chr6:163834831-163834840
29	BHLHE40	chr6:163834536-163834943	A549	lung:	n/a	n/a
30	BHLHE40	chr6:163833621-163835329	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:163834344-163835354	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:163836622-163837133	K562	blood:	n/a	n/a
33	BHLHE40	chr6:163835608-163835832	GM12878	blood:	n/a	chr6:163835760-163835776 chr6:163835757-163835773
34	BHLHE40	chr6:163834242-163835307	K562	blood:	n/a	n/a
35	BHLHE40	chr6:163825335-163825610	K562	blood:	n/a	chr6:163825456-163825465
36	BHLHE40	chr6:163835658-163835902	K562	blood:	n/a	chr6:163835760-163835776 chr6:163835757-163835773
37	BRCA1	chr6:163834883-163835128	HepG2	liver:	n/a	n/a
38	BRCA1	chr6:163834975-163835254	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr6:163834833-163835219	GM12878	blood:	n/a	n/a
40	CBX3	chr6:163834516-163834893	K562	blood:	n/a	n/a
41	CBX3	chr6:163834088-163835319	K562	blood:	n/a	n/a
42	CCNT2	chr6:163833862-163837213	K562	blood:	n/a	chr6:163837081-163837090
43	CEBPB	chr6:163834947-163835336	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:163834962-163835251	K562	blood:	n/a	n/a
45	CEBPB	chr6:163829732-163829940	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:163833837-163834672	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:163834232-163835874	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:163834950-163835319	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:163833449-163834753	K562	blood:	n/a	n/a
50	CEBPB	chr6:163835037-163835191	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163834924-163834974	K562	blood:	n/a
2	chr6:163835117-163835167	BE2_C	brain:	n/a
3	chr6:163834452-163834502	T-47D	breast:	n/a
4	chr6:163836245-163836295	HAEpiC	amniotic membrane:	n/a
5	chr6:163836245-163836295	GM12892	blood:	n/a
6	chr6:163834924-163834974	HIPEpiC	eye:	n/a
7	chr6:163834176-163834226	T-47D	breast:	n/a
8	chr6:163834872-163834922	HRE	kidney:	n/a
9	chr6:163834176-163834226	GM12878	blood:	n/a
10	chr6:163834872-163834922	HNPCEpiC	eye:	n/a
11	chr6:163834872-163834922	NHDF-neo	bronchial:	n/a
12	chr6:163834924-163834974	AG09309	skin:	n/a
13	chr6:163835582-163835632	NH-A	brain:	n/a
14	chr6:163835117-163835167	HL-60	blood:	n/a
15	chr6:163834903-163834953	AG09319	gingival:	n/a
16	chr6:163835582-163835632	T-47D	breast:	n/a
17	chr6:163835251-163835301	HEK293	kidney:	embryo
18	chr6:163826969-163827019	PFSK-1	brain:	n/a
19	chr6:163834176-163834226	GM12892	blood:	n/a
20	chr6:163834158-163834208	CMK	blood:	n/a
21	chr6:163835395-163835445	MCF-7	breast:	n/a
22	chr6:163835395-163835445	CMK	blood:	n/a
23	chr6:163836348-163836398	GM06990	blood:	n/a
24	chr6:163835582-163835632	PrEC	prostate:	n/a
25	chr6:163835117-163835167	LNCaP	prostate:	n/a
26	chr6:163834158-163834208	HEK293	kidney:	embryo
27	chr6:163835117-163835167	AG09319	gingival:	n/a
28	chr6:163834158-163834208	NHDF-neo	bronchial:	n/a
29	chr6:163835395-163835445	HUVEC	blood vessel:	n/a
30	chr6:163835117-163835167	AoSMC	blood vessel:	n/a
31	chr6:163834924-163834974	SK-N-MC	brain:	n/a
32	chr6:163835582-163835632	BE2_C	brain:	n/a
33	chr6:163834176-163834226	PrEC	prostate:	n/a
34	chr6:163826969-163827019	HL-60	blood:	n/a
35	chr6:163835395-163835445	Caco-2	colon:	n/a
36	chr6:163834452-163834502	Hepatocyte	liver:	n/a
37	chr6:163835251-163835301	HepG2	liver:	n/a
38	chr6:163834158-163834208	IMR90	lung:	fetal
39	chr6:163834872-163834922	H1-hESC	embryonic stem cell:	embryo
40	chr6:163835117-163835167	MCF-7	breast:	n/a
41	chr6:163826969-163827019	AG04450	lung:	fetal
42	chr6:163835117-163835167	Jurkat	blood:	n/a
43	chr6:163835395-163835445	LNCaP	prostate:	n/a
44	chr6:163834452-163834502	IMR90	lung:	fetal
45	chr6:163836348-163836398	SKMC	muscle:	n/a
46	chr6:163834924-163834974	NT2-D1	testis:	n/a
47	chr6:163835117-163835167	HEEpiC	esophagus:	n/a
48	chr6:163834924-163834974	AG04449	skin:	fetal
49	chr6:163836348-163836398	BJ	skin:	n/a
50	chr6:163835251-163835301	HEEpiC	esophagus:	n/a

(count:18 , 50 per page) page: 1

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

(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
CAHM	TF binding region
QKI	TF binding region
CAHM	CpG island
QKI	CpG island
ENSG00000112531	chromatin interactions
ENSG00000242110	chromatin interactions
ENSG00000270419	chromatin interactions

Extended variants
information (count: 447 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:447 , 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	rs113385245	chr6:163824864-163824865	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs79584775	chr6:163824873-163824874	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554812894	chr6:163824910-163824911	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs145167385	chr6:163824916-163824917	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142449856	chr6:163824924-163824925	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs191161778	chr6:163824936-163824937	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs146517359	chr6:163825018-163825019	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543447752	chr6:163825020-163825021	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545494145	chr6:163825031-163825032	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562578357	chr6:163825059-163825060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs6928861	chr6:163825064-163825065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576061597	chr6:163825073-163825074	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs562248428	chr6:163825075-163825076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544360842	chr6:163825143-163825144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143622511	chr6:163825165-163825166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs530279260	chr6:163825223-163825224	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146238630	chr6:163825318-163825319	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560656603	chr6:163825406-163825407	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148274979	chr6:163825414-163825415	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552291873	chr6:163825436-163825437	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183577238	chr6:163825438-163825439	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76805616	chr6:163825446-163825447	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2757575	chr6:163825508-163825509	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs548745584	chr6:163825517-163825518	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188462308	chr6:163825536-163825537	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116130370	chr6:163825619-163825620	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs553996577	chr6:163825735-163825736	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577088419	chr6:163825742-163825743	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192842545	chr6:163825772-163825773	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539373907	chr6:163825862-163825863	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559954732	chr6:163825868-163825869	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150723372	chr6:163825878-163825879	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115200158	chr6:163825882-163825883	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541522843	chr6:163825906-163825907	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183041661	chr6:163825912-163825913	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs139024110	chr6:163825941-163825942	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs574676779	chr6:163825966-163825967	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186474104	chr6:163825967-163825968	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375777978	chr6:163825978-163825979	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560791579	chr6:163825998-163825999	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532703695	chr6:163826020-163826021	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546514679	chr6:163826044-163826045	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552080398	chr6:163826123-163826124	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562736028	chr6:163826139-163826140	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78172877	chr6:163826161-163826162	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs142489785	chr6:163826162-163826163	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568581804	chr6:163826172-163826173	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs2757576	chr6:163826210-163826211	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs145969076	chr6:163826243-163826244	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs570687911	chr6:163826246-163826247	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 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:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163809800-163825600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:163818000-163826800	Weak transcription	Gastric	stomach
3	chr6:163818200-163825600	Weak transcription	Lung	lung
4	chr6:163818200-163826200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr6:163818200-163826800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:163818400-163825200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:163818400-163825400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:163818400-163825400	Weak transcription	Right Atrium	heart
9	chr6:163818800-163825800	Weak transcription	Colon Smooth Muscle	Colon
10	chr6:163818800-163826400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:163819800-163825000	Enhancers	Placenta	Placenta
12	chr6:163820000-163825600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr6:163820200-163825600	Weak transcription	Spleen	Spleen
14	chr6:163820200-163825800	Weak transcription	Psoas Muscle	Psoas
15	chr6:163820200-163826000	Weak transcription	Brain Germinal Matrix	brain
16	chr6:163820200-163826000	Weak transcription	Fetal Brain Female	brain
17	chr6:163820200-163826800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:163820400-163825600	Weak transcription	Fetal Muscle Leg	muscle
19	chr6:163820400-163826000	Weak transcription	Ovary	ovary
20	chr6:163820400-163826800	Weak transcription	GM12878-XiMat	blood
21	chr6:163820600-163825400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:163820600-163826600	Weak transcription	Fetal Brain Male	brain
23	chr6:163820800-163825600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr6:163821400-163827000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:163822000-163825400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:163822000-163825400	Weak transcription	Adipose Nuclei	Adipose
27	chr6:163822400-163826200	Enhancers	Brain Substantia Nigra	brain
28	chr6:163822400-163826400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr6:163823000-163826600	Enhancers	Brain Cingulate Gyrus	brain
30	chr6:163823000-163827000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:163823000-163827200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr6:163823000-163827200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr6:163823200-163826400	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr6:163823200-163826800	Enhancers	Brain Hippocampus Middle	brain
35	chr6:163823400-163825600	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr6:163823400-163826200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:163823400-163826600	Enhancers	Fetal Heart	heart
38	chr6:163823400-163826800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr6:163823400-163826800	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr6:163824000-163825200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:163824000-163825200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr6:163824000-163825600	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr6:163824000-163826800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:163824200-163825200	Weak transcription	HepG2	liver
45	chr6:163824400-163825200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr6:163824400-163825600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:163824400-163825600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr6:163824400-163825800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr6:163824600-163825000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr6:163824600-163825000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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