Variant report

Variant	nsv883538
Chromosome Location	chr6:29748206-29760819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:2380)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29758519-29758625	HepG2	liver:	n/a	n/a
2	BACH1	chr6:29759860-29760583	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr6:29758482-29758496	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:29758432-29758726	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr6:29757089-29757337	HepG2	liver:	n/a	chr6:29757235-29757246
6	CEBPB	chr6:29757214-29757216	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr6:29758960-29759205	Hela-S3	cervix:	n/a	n/a
8	CHD1	chr6:29760250-29760494	GM12878	blood:	n/a	n/a
9	CTCF	chr6:29760540-29760690	HVMF	connective:	n/a	n/a
10	CTCF	chr6:29760380-29760530	GM12869	blood:	n/a	n/a
11	CTCF	chr6:29760280-29760430	GM12864	blood:	n/a	n/a
12	CTCF	chr6:29756480-29756630	HCT-116	colon:	n/a	n/a
13	CTCF	chr6:29760340-29760490	A549	lung:	n/a	n/a
14	CTCF	chr6:29760260-29760410	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr6:29760240-29760390	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr6:29760280-29760430	AG09309	skin:	n/a	n/a
17	CTCF	chr6:29760193-29760454	NHEK	skin:	n/a	n/a
18	CTCF	chr6:29760220-29760370	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr6:29760295-29760394	GM20000	blood:	n/a	n/a
20	CTCF	chr6:29759921-29760630	MCF-7	breast:	n/a	n/a
21	CTCF	chr6:29760220-29760370	GM12874	blood:	n/a	n/a
22	CTCF	chr6:29760240-29760390	BJ	skin:	n/a	n/a
23	CTCF	chr6:29756840-29756990	GM12875	blood:	n/a	n/a
24	CTCF	chr6:29760280-29760430	NHEK	skin:	n/a	n/a
25	CTCF	chr6:29760200-29760350	GM12866	blood:	n/a	n/a
26	CTCF	chr6:29760066-29760110	GM10266	blood:	n/a	n/a
27	CTCF	chr6:29760220-29760370	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr6:29760500-29760650	GM12864	blood:	n/a	n/a
29	CTCF	chr6:29756560-29756710	HEK293	kidney:	n/a	n/a
30	CTCF	chr6:29760280-29760430	Caco-2	colon:	n/a	n/a
31	CTCF	chr6:29760240-29760390	HEK293	kidney:	n/a	n/a
32	CTCF	chr6:29760320-29760470	HAc	cerebellar:	n/a	n/a
33	CTCF	chr6:29756560-29756710	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr6:29760160-29760310	GM12871	blood:	n/a	n/a
35	CTCF	chr6:29760237-29760446	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr6:29760034-29760486	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:29760220-29760370	HRE	kidney:	n/a	n/a
38	CTCF	chr6:29760200-29760451	LNCaP	prostate:	n/a	n/a
39	CTCF	chr6:29760260-29760410	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr6:29760240-29760390	Caco-2	colon:	n/a	n/a
41	CTCF	chr6:29760240-29760445	GM13976	blood:	n/a	n/a
42	CTCF	chr6:29760240-29760390	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr6:29760219-29760447	GM12891	blood:	n/a	n/a
44	CTCF	chr6:29760260-29760410	GM12869	blood:	n/a	n/a
45	CTCF	chr6:29760220-29760370	SAEC	small airway:	n/a	n/a
46	CTCF	chr6:29760200-29760350	GM12875	blood:	n/a	n/a
47	CTCF	chr6:29756540-29756690	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr6:29760280-29760430	AG09319	gingival:	n/a	n/a
49	CTCF	chr6:29758965-29759069	GM13976	blood:	n/a	n/a
50	CTCF	chr6:29760220-29760370	GM12865	blood:	n/a	n/a

(count:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29760782-29760832	SK-N-MC	brain:	n/a
2	chr6:29760782-29760832	SK-N-MC	brain:	n/a
3	chr6:29760765-29760815	SAEC	small airway:	n/a
4	chr6:29760805-29760855	ECC-1	luminal epithelium:	n/a
5	chr6:29759972-29760022	HAEpiC	amniotic membrane:	n/a
6	chr6:29760495-29760545	HRPEpiC	eye:	n/a
7	chr6:29759972-29760022	HRPEpiC	eye:	n/a
8	chr6:29760634-29760684	PrEC	prostate:	n/a
9	chr6:29760609-29760659	SK-N-SH_RA	brain:	n/a
10	chr6:29760028-29760078	GM12892	blood:	n/a
11	chr6:29759955-29760005	ovcar-3	ovarian:	n/a
12	chr6:29759197-29759247	AG09319	gingival:	n/a
13	chr6:29760769-29760819	K562	blood:	n/a
14	chr6:29760096-29760146	HEEpiC	esophagus:	n/a
15	chr6:29760634-29760684	GM12892	blood:	n/a
16	chr6:29760158-29760208	HEK293	kidney:	embryo
17	chr6:29760435-29760485	AoSMC	blood vessel:	n/a
18	chr6:29760164-29760214	HMEC	breast:	n/a
19	chr6:29756503-29756553	HEK293	kidney:	embryo
20	chr6:29760158-29760208	GM12891	blood:	n/a
21	chr6:29760096-29760146	GM06990	blood:	n/a
22	chr6:29760090-29760140	HCPEpiC	choroid plexus:	n/a
23	chr6:29760634-29760684	GM12891	blood:	n/a
24	chr6:29756503-29756553	MCF10A-Er-Src	breast:	n/a
25	chr6:29760158-29760208	SK-N-SH_RA	brain:	n/a
26	chr6:29760148-29760198	ovcar-3	ovarian:	n/a
27	chr6:29759197-29759247	HCPEpiC	choroid plexus:	n/a
28	chr6:29756503-29756553	Jurkat	blood:	n/a
29	chr6:29759804-29759854	AG04450	lung:	fetal
30	chr6:29758527-29758577	GM12892	blood:	n/a
31	chr6:29760148-29760198	GM12891	blood:	n/a
32	chr6:29760028-29760078	HUVEC	blood vessel:	n/a
33	chr6:29759972-29760022	Jurkat	blood:	n/a
34	chr6:29760695-29760745	AG10803	skin:	n/a
35	chr6:29760754-29760804	GM12891	blood:	n/a
36	chr6:29760675-29760725	GM12892	blood:	n/a
37	chr6:29760435-29760485	K562	blood:	n/a
38	chr6:29760784-29760834	NB4	blood:	n/a
39	chr6:29760782-29760832	HRE	kidney:	n/a
40	chr6:29760688-29760738	AG09309	skin:	n/a
41	chr6:29760681-29760731	HRCEpiC	kidney:	n/a
42	chr6:29760784-29760834	BJ	skin:	n/a
43	chr6:29760435-29760485	NHDF-neo	bronchial:	n/a
44	chr6:29760713-29760763	GM12891	blood:	n/a
45	chr6:29760148-29760198	GM19239	blood:	n/a
46	chr6:29760023-29760073	NHBE	bronchial:	n/a
47	chr6:29760765-29760815	HEEpiC	esophagus:	n/a
48	chr6:29759972-29760022	T-47D	breast:	n/a
49	chr6:29760754-29760804	SK-N-SH	brain:	n/a
50	chr6:29760447-29760497	CMK	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29755459..29758755-chr6:29758827..29760410,3	MCF-7	breast:
2	chr6:29755459..29758755-chr6:29758827..29760410,3	MCF-7	breast:
3	chr6:29755654..29758226-chr6:29780556..29783054,2	MCF-7	breast:
4	chr6:29759731..29760249-chr6:31324546..31325250,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP57-14	chr6:29759530-29760527	NONHSAT108553
2	lnc-ZFP57-14	chr6:29758808-29760850	NONHSAT108552

No data

Variant related genes	Relation type
HCG4	TF binding region
HLA-V	TF binding region
HCG4	CpG island
HLA-V	CpG island
ENSG00000234745	chromatin interactions
ENSG00000181126	chromatin interactions

Extended variants
information (count: 684 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1611229	chr6:29748206-29748207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs180951464	chr6:29748240-29748241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145026403	chr6:29748264-29748265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544524129	chr6:29748303-29748304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185073512	chr6:29748304-29748305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1611230	chr6:29748308-29748309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs138766651	chr6:29748313-29748314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544833628	chr6:29748324-29748325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs80334281	chr6:29748329-29748330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191056972	chr6:29748336-29748337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141913213	chr6:29748373-29748374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112442053	chr6:29748394-29748395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376460960	chr6:29748395-29748396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148112094	chr6:29748410-29748411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181760262	chr6:29748417-29748418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569257933	chr6:29748423-29748424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141912740	chr6:29748454-29748455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370508051	chr6:29748472-29748473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150663034	chr6:29748495-29748496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569086345	chr6:29748500-29748501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139910383	chr6:29748509-29748510	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
22	rs1611233	chr6:29748523-29748524	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs568043237	chr6:29748529-29748530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147526123	chr6:29748540-29748541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186780647	chr6:29748571-29748572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576483454	chr6:29748611-29748612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560081183	chr6:29748613-29748614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537884371	chr6:29748633-29748634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1611234	chr6:29748641-29748642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs146526194	chr6:29748646-29748647	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs545187777	chr6:29748683-29748684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560316503	chr6:29748685-29748686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1611236	chr6:29748690-29748691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1611237	chr6:29748691-29748692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540593216	chr6:29748714-29748715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191709605	chr6:29748715-29748716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573208908	chr6:29748728-29748729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183055863	chr6:29748734-29748735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552735989	chr6:29748748-29748749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569009160	chr6:29748751-29748752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553328517	chr6:29748755-29748756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145482715	chr6:29748812-29748813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111296608	chr6:29748837-29748838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188392443	chr6:29748843-29748844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9468610	chr6:29748856-29748857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs190151402	chr6:29748862-29748863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570127905	chr6:29748863-29748864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539132011	chr6:29748902-29748903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551657931	chr6:29748943-29748944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11759669	chr6:29748945-29748946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29733600-29755800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:29739000-29753600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:29753600-29754000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:29754000-29757600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:29756000-29756200	Enhancers	Placenta Amnion	Placenta Amnion
6	chr6:29756000-29758600	Weak transcription	Pancreas	Pancrea
7	chr6:29756200-29756800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr6:29756400-29756800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:29756800-29757000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:29756800-29757000	Enhancers	Placenta Amnion	Placenta Amnion
11	chr6:29756800-29757400	Weak transcription	NHEK	skin
12	chr6:29756800-29758400	Enhancers	HMEC	breast
13	chr6:29757000-29757200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:29757000-29758000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:29757000-29758600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr6:29757200-29758600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr6:29757400-29758000	Enhancers	NHEK	skin
18	chr6:29757400-29759000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:29757600-29757800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr6:29757600-29758000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:29757800-29758000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
22	chr6:29757800-29758400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:29757800-29758800	Enhancers	Hela-S3	cervix
24	chr6:29758000-29758200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
25	chr6:29758000-29758200	Flanking Active TSS	NHEK	skin
26	chr6:29758000-29758400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:29758000-29759000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:29758200-29758600	Enhancers	NHEK	skin
29	chr6:29758400-29759000	Flanking Active TSS	HMEC	breast
30	chr6:29758400-29759400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:29758400-29760000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:29758600-29758800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:29758600-29758800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:29758600-29758800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr6:29758600-29758800	Enhancers	Gastric	stomach
36	chr6:29758600-29759000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr6:29758600-29759200	Flanking Active TSS	NHEK	skin
38	chr6:29758600-29759400	Enhancers	Esophagus	oesophagus
39	chr6:29758600-29759400	Enhancers	Pancreas	Pancrea
40	chr6:29758600-29759600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:29758600-29759800	Bivalent Enhancer	Stomach Mucosa	stomach
42	chr6:29758600-29760600	Active TSS	Placenta Amnion	Placenta Amnion
43	chr6:29758800-29759000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr6:29758800-29759600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr6:29758800-29759600	Enhancers	Duodenum Mucosa	Duodenum
46	chr6:29758800-29759600	Flanking Active TSS	Hela-S3	cervix
47	chr6:29759000-29759200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr6:29759000-29759200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr6:29759000-29759200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:29759000-29759200	Enhancers	Brain Angular Gyrus	brain

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