Variant report

Variant	nsv823691
Chromosome Location	chr6:53918427-53978766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:230)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:230 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:53962447-53962872	HepG2	liver:	n/a	n/a
2	BACH1	chr6:53968331-53968637	K562	blood:	n/a	n/a
3	BACH1	chr6:53968321-53968664	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:53936826-53937112	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr6:53962611-53962857	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:53972403-53972554	HepG2	liver:	n/a	chr6:53972454-53972463 chr6:53972454-53972463 chr6:53972455-53972464 chr6:53972448-53972469
7	BRCA1	chr6:53918522-53919323	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr6:53918781-53919330	HCT-116	colon:	n/a	n/a
9	CEBPB	chr6:53941007-53941256	HepG2	liver:	n/a	n/a
10	CEBPB	chr6:53962505-53962816	A549	lung:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
11	CEBPB	chr6:53962593-53962858	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
12	CEBPB	chr6:53937815-53937982	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr6:53936663-53937131	HepG2	liver:	n/a	chr6:53937019-53937030
14	CEBPB	chr6:53962535-53962901	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
15	CEBPB	chr6:53936979-53937060	A549	lung:	n/a	chr6:53937019-53937030
16	CEBPB	chr6:53936747-53937174	IMR90	lung:	n/a	chr6:53937019-53937030
17	CEBPB	chr6:53918742-53919509	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:53918732-53919431	HCT-116	colon:	n/a	n/a
19	CEBPB	chr6:53918783-53919309	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:53925043-53925338	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:53941019-53941213	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:53921912-53922227	HepG2	liver:	n/a	chr6:53922081-53922094 chr6:53922081-53922092 chr6:53922082-53922093 chr6:53922081-53922094 chr6:53922081-53922092
23	CEBPB	chr6:53937860-53938018	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:53936791-53937133	H1-hESC	embryonic stem cell:	n/a	chr6:53937019-53937030
25	CEBPB	chr6:53925120-53925332	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:53962546-53962803	Hela-S3	cervix:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
27	CEBPB	chr6:53962549-53962950	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
28	CEBPB	chr6:53962398-53962934	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
29	CEBPB	chr6:53922006-53922164	HepG2	liver:	n/a	chr6:53922081-53922094 chr6:53922081-53922092 chr6:53922082-53922093 chr6:53922081-53922094 chr6:53922081-53922092
30	CEBPD	chr6:53962610-53962878	HepG2	liver:	n/a	chr6:53962728-53962739
31	CHD2	chr6:53918780-53919224	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr6:53952359-53952466	GM19238	blood:	n/a	n/a
33	CTCF	chr6:53933664-53933744	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr6:53952383-53952462	GM12892	blood:	n/a	n/a
35	CTCF	chr6:53920580-53920730	HepG2	liver:	n/a	n/a
36	CTCF	chr6:53975180-53975247	Lung_OC	lung:	n/a	n/a
37	CTCF	chr6:53935242-53935284	GM20000	blood:	n/a	n/a
38	CTCF	chr6:53952379-53952456	GM19239	blood:	n/a	n/a
39	CTCF	chr6:53952320-53952470	HEK293	kidney:	n/a	n/a
40	CTCF	chr6:53926060-53926210	HEK293	kidney:	n/a	n/a
41	CTCF	chr6:53952412-53952425	GM19240	blood:	n/a	n/a
42	CTCF	chr6:53933580-53933730	HMEC	breast:	n/a	n/a
43	CTCF	chr6:53950460-53950610	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr6:53920520-53920670	HEK293	kidney:	n/a	n/a
45	CTCF	chr6:53948280-53948430	AG10803	skin:	n/a	n/a
46	CTCF	chr6:53933620-53933770	RPTEC	kidney:	n/a	n/a
47	CTCF	chr6:53952310-53952497	GM12878	blood:	n/a	n/a
48	CUX1	chr6:53965712-53965730	GM12878	blood:	n/a	n/a
49	E2F4	chr6:53918687-53919226	MCF10A-Er-Src	breast:	n/a	n/a
50	ELK1	chr6:53967800-53967839	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:53919041-53919091	PANC-1	pancreas:	n/a
2	chr6:53939321-53939371	HEEpiC	esophagus:	n/a
3	chr6:53950838-53950888	PFSK-1	brain:	n/a
4	chr6:53939321-53939371	U87	brain:	n/a
5	chr6:53939321-53939371	HAEpiC	amniotic membrane:	n/a
6	chr6:53919041-53919091	HIPEpiC	eye:	n/a
7	chr6:53939321-53939371	AG04450	lung:	fetal
8	chr6:53919041-53919091	HCT-116	colon:	n/a
9	chr6:53919041-53919091	GM12878	blood:	n/a
10	chr6:53939321-53939371	SAEC	small airway:	n/a
11	chr6:53919041-53919091	ovcar-3	ovarian:	n/a
12	chr6:53919041-53919091	Caco-2	colon:	n/a
13	chr6:53939321-53939371	Hela-S3	cervix:	n/a
14	chr6:53939321-53939371	Caco-2	colon:	n/a
15	chr6:53950838-53950888	HNPCEpiC	eye:	n/a
16	chr6:53919041-53919091	HMEC	breast:	n/a
17	chr6:53950838-53950888	ovcar-3	ovarian:	n/a
18	chr6:53939321-53939371	CMK	blood:	n/a
19	chr6:53919041-53919091	GM06990	blood:	n/a
20	chr6:53939321-53939371	SK-N-MC	brain:	n/a
21	chr6:53950838-53950888	AG04450	lung:	fetal
22	chr6:53939321-53939371	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:53950838-53950888	GM06990	blood:	n/a
24	chr6:53939321-53939371	GM12878	blood:	n/a
25	chr6:53950838-53950888	BJ	skin:	n/a
26	chr6:53950838-53950888	ECC-1	luminal epithelium:	n/a
27	chr6:53919041-53919091	ProgFib	skin:	n/a
28	chr6:53939321-53939371	HepG2	liver:	n/a
29	chr6:53939321-53939371	Hepatocyte	liver:	n/a
30	chr6:53939321-53939371	AG10803	skin:	n/a
31	chr6:53919041-53919091	HEK293	kidney:	embryo
32	chr6:53939321-53939371	HRE	kidney:	n/a
33	chr6:53919041-53919091	MCF10A-Er-Src	breast:	n/a
34	chr6:53939321-53939371	AG09319	gingival:	n/a
35	chr6:53939321-53939371	HMEC	breast:	n/a
36	chr6:53919041-53919091	T-47D	breast:	n/a
37	chr6:53950838-53950888	AG10803	skin:	n/a
38	chr6:53939321-53939371	IMR90	lung:	fetal
39	chr6:53939321-53939371	GM12892	blood:	n/a
40	chr6:53919041-53919091	HAEpiC	amniotic membrane:	n/a
41	chr6:53939321-53939371	NHDF-neo	bronchial:	n/a
42	chr6:53939321-53939371	HRCEpiC	kidney:	n/a
43	chr6:53939321-53939371	Jurkat	blood:	n/a
44	chr6:53939321-53939371	RPTEC	kidney:	n/a
45	chr6:53939321-53939371	PFSK-1	brain:	n/a
46	chr6:53939321-53939371	HRPEpiC	eye:	n/a
47	chr6:53950838-53950888	MCF10A-Er-Src	breast:	n/a
48	chr6:53950838-53950888	HMEC	breast:	n/a
49	chr6:53950838-53950888	Jurkat	blood:	n/a
50	chr6:53950838-53950888	SAEC	small airway:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:53918180..53920698-chr6:53921750..53923879,2	K562	blood:
2	chr6:53857425..53857943-chr6:53933277..53933955,2	MCF-7	breast:
3	chr6:53918180..53920698-chr6:53921750..53923879,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC1-8	chr6:53967721-53970052	NONHSAT113215
2	lnc-LRRC1-8	chr6:53967547-53967621	ucscGeneNc_uc003pce_2
3	lnc-LRRC1-9	chr6:53971647-53971816	NONHSAT113221
4	lnc-LRRC1-8	chr6:53955515-53955607	ucscGeneNc_uc003pce_2
5	lnc-LRRC1-9	chr6:53973667-53973851	NONHSAT113221
6	lnc-KLHL31-10	chr6:53927754-53927853	NONHSAT113220
7	lnc-KLHL31-3	chr6:53923720-53923768	ENSG00000235050.2
8	lnc-LRRC1-8	chr6:53967547-53967621	NONHSAT113215
9	lnc-LRRC1-8	chr6:53955515-53955607	NONHSAT113215
10	lnc-KLHL31-3	chr6:53944324-53944524	ENSG00000235050.2
11	lnc-LRRC1-8	chr6:53967721-53970422	ucscGeneNc_uc003pce_2
12	lnc-KLHL31-10	chr6:53927195-53927695	NONHSAT113220
13	lnc-LRRC1-9	chr6:53975371-53975476	NONHSAT113221
14	lnc-KLHL31-3	chr6:53922745-53922798	ENSG00000235050.2

No data

Variant related genes	Relation type
MLIP-AS1	TF binding region
MLIP	TF binding region
MLIP-AS1	CpG island
MLIP	CpG island

Extended variants
information (count: 2131 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2131 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189616568	chr6:53918434-53918435	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs9474719	chr6:53918458-53918459	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549902969	chr6:53918525-53918526	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs71558853	chr6:53918837-53918838	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs145300513	chr6:53918888-53918889	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs541463415	chr6:53918946-53918947	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs555758150	chr6:53919042-53919043	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs566379774	chr6:53919043-53919044	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs149194784	chr6:53919051-53919052	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs182697106	chr6:53919180-53919181	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs72955958	chr6:53919185-53919186	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs148455872	chr6:53919218-53919219	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs374597265	chr6:53919226-53919227	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs376207103	chr6:53919228-53919229	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs370289077	chr6:53919229-53919230	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs398001622	chr6:53919246-53919247	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs543525880	chr6:53919268-53919269	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs557120034	chr6:53919286-53919287	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs573649879	chr6:53919302-53919303	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs542659414	chr6:53919323-53919324	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs188217448	chr6:53919324-53919325	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs528390149	chr6:53919340-53919341	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs141505279	chr6:53919360-53919361	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576424286	chr6:53919400-53919401	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs16884654	chr6:53919407-53919408	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145278582	chr6:53919529-53919530	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs144797331	chr6:53919586-53919587	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs117318275	chr6:53919644-53919645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569838400	chr6:53919655-53919656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546315534	chr6:53919690-53919691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs56830731	chr6:53919703-53919704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529217655	chr6:53919745-53919746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549370291	chr6:53919767-53919768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566198650	chr6:53919789-53919790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367920305	chr6:53919834-53919835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558199791	chr6:53919847-53919848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572169896	chr6:53919854-53919855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571845195	chr6:53919905-53919906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537661946	chr6:53919927-53919928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs377359864	chr6:53919935-53919936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573788223	chr6:53919953-53919954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192794364	chr6:53919961-53919962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115738440	chr6:53919964-53919965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572790181	chr6:53919974-53919975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185089121	chr6:53919978-53919979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17631709	chr6:53920022-53920023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7739196	chr6:53920024-53920025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs138116930	chr6:53920042-53920043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563403967	chr6:53920046-53920047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374918235	chr6:53920114-53920115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	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
Autism	22495311	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Neuroblastoma	18923191	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD

Chromatin state (count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53913600-53918800	Weak transcription	Psoas Muscle	Psoas
2	chr6:53913600-53926000	Weak transcription	Left Ventricle	heart
3	chr6:53915600-53918600	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:53916000-53918800	Weak transcription	Right Atrium	heart
5	chr6:53916200-53918600	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr6:53916400-53918800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:53916400-53919200	Enhancers	Fetal Heart	heart
8	chr6:53917200-53919200	Weak transcription	Right Ventricle	heart
9	chr6:53917800-53918600	Enhancers	HMEC	breast
10	chr6:53917800-53918800	Enhancers	Hela-S3	cervix
11	chr6:53917800-53919000	Enhancers	HSMM	muscle
12	chr6:53917800-53919200	Active TSS	Skeletal Muscle Female	skeletal muscle
13	chr6:53918000-53918600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:53918000-53918600	Enhancers	HSMMtube	muscle
15	chr6:53918000-53923200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:53918200-53918600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:53918200-53918800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:53918200-53919000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:53918200-53919200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:53918200-53919600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:53918400-53918600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:53918400-53918600	Enhancers	NH-A	brain
23	chr6:53918400-53918600	Enhancers	Osteobl	bone
24	chr6:53918400-53918800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr6:53918400-53918800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:53918400-53918800	Enhancers	Colon Smooth Muscle	Colon
27	chr6:53918400-53918800	Enhancers	NHEK	skin
28	chr6:53918400-53919000	Enhancers	Duodenum Mucosa	Duodenum
29	chr6:53918400-53919000	Enhancers	Fetal Intestine Large	intestine
30	chr6:53918400-53919000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr6:53918400-53919400	Active TSS	Aorta	Aorta
32	chr6:53918400-53919600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:53918400-53919600	Enhancers	Colonic Mucosa	Colon
34	chr6:53918400-53919600	Enhancers	Fetal Intestine Small	intestine
35	chr6:53918600-53918800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:53918600-53918800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:53918600-53918800	Enhancers	Adipose Nuclei	Adipose
38	chr6:53918600-53918800	Enhancers	Brain Anterior Caudate	brain
39	chr6:53918600-53918800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr6:53918600-53918800	Enhancers	Fetal Muscle Leg	muscle
41	chr6:53918600-53918800	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr6:53918600-53918800	Enhancers	HUVEC	blood vessel
43	chr6:53918600-53918800	Enhancers	NHLF	lung
44	chr6:53918600-53919000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr6:53918600-53919000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:53918600-53919000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr6:53918600-53919000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr6:53918600-53919000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr6:53918600-53919000	Enhancers	Stomach Mucosa	stomach
50	chr6:53918600-53919000	Flanking Active TSS	HSMMtube	muscle

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