Variant report

Variant	nsv883536
Chromosome Location	chr6:29746023-29760819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:2387)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 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	chr6:29757089-29757337	HepG2	liver:	n/a	chr6:29757235-29757246
5	CEBPB	chr6:29757214-29757216	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr6:29758960-29759205	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:29745784-29746100	HepG2	liver:	n/a	chr6:29745937-29745948
8	CEBPB	chr6:29758432-29758726	Hela-S3	cervix:	n/a	n/a
9	CHD1	chr6:29760250-29760494	GM12878	blood:	n/a	n/a
10	CTCF	chr6:29760238-29760433	LNCaP	prostate:	n/a	n/a
11	CTCF	chr6:29760078-29760538	MCF-7	breast:	n/a	n/a
12	CTCF	chr6:29760212-29760397	A549	lung:	n/a	n/a
13	CTCF	chr6:29760360-29760510	GM12872	blood:	n/a	n/a
14	CTCF	chr6:29756000-29756150	GM12874	blood:	n/a	n/a
15	CTCF	chr6:29760220-29760370	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr6:29760179-29760476	MCF-7	breast:	n/a	n/a
17	CTCF	chr6:29760240-29760390	AG04449	skin:	n/a	n/a
18	CTCF	chr6:29760500-29760650	GM12864	blood:	n/a	n/a
19	CTCF	chr6:29760295-29760394	GM20000	blood:	n/a	n/a
20	CTCF	chr6:29760120-29760270	HCM	heart:	n/a	n/a
21	CTCF	chr6:29760240-29760390	HPF	lung:	n/a	n/a
22	CTCF	chr6:29760340-29760490	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr6:29760180-29760330	RPTEC	kidney:	n/a	n/a
24	CTCF	chr6:29760176-29760469	MCF-7	breast:	n/a	n/a
25	CTCF	chr6:29756560-29756710	HMEC	breast:	n/a	n/a
26	CTCF	chr6:29760260-29760410	AG04449	skin:	n/a	n/a
27	CTCF	chr6:29760220-29760370	GM06990	blood:	n/a	n/a
28	CTCF	chr6:29756480-29756630	HCT-116	colon:	n/a	n/a
29	CTCF	chr6:29760200-29760350	GM12864	blood:	n/a	n/a
30	CTCF	chr6:29760220-29760370	NHEK	skin:	n/a	n/a
31	CTCF	chr6:29760220-29760370	GM12865	blood:	n/a	n/a
32	CTCF	chr6:29760280-29760430	GM12865	blood:	n/a	n/a
33	CTCF	chr6:29760240-29760390	BJ	skin:	n/a	n/a
34	CTCF	chr6:29760200-29760471	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr6:29760260-29760410	GM12875	blood:	n/a	n/a
36	CTCF	chr6:29760148-29760510	IMR90	lung:	n/a	n/a
37	CTCF	chr6:29760280-29760430	NHEK	skin:	n/a	n/a
38	CTCF	chr6:29760280-29760430	AG09319	gingival:	n/a	n/a
39	CTCF	chr6:29760260-29760410	HVMF	connective:	n/a	n/a
40	CTCF	chr6:29760280-29760430	AG09309	skin:	n/a	n/a
41	CTCF	chr6:29760280-29760430	GM06990	blood:	n/a	n/a
42	CTCF	chr6:29760066-29760110	GM10266	blood:	n/a	n/a
43	CTCF	chr6:29760280-29760430	GM12866	blood:	n/a	n/a
44	CTCF	chr6:29760120-29760270	A549	lung:	n/a	n/a
45	CTCF	chr6:29760260-29760410	AG09309	skin:	n/a	n/a
46	CTCF	chr6:29760245-29760433	GM10248	blood:	n/a	n/a
47	CTCF	chr6:29760040-29760190	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr6:29760240-29760445	GM13976	blood:	n/a	n/a
49	CTCF	chr6:29760220-29760370	HEK293	kidney:	n/a	n/a
50	CTCF	chr6:29760180-29760330	GM12872	blood:	n/a	n/a

(count:2387 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29760784-29760834	SKMC	muscle:	n/a
2	chr6:29760609-29760659	GM19239	blood:	n/a
3	chr6:29760023-29760073	BE2_C	brain:	n/a
4	chr6:29759947-29759997	ovcar-3	ovarian:	n/a
5	chr6:29760659-29760709	HCF	heart:	n/a
6	chr6:29756503-29756553	HUVEC	blood vessel:	n/a
7	chr6:29760784-29760834	HCM	heart:	n/a
8	chr6:29759949-29759999	HEEpiC	esophagus:	n/a
9	chr6:29760784-29760834	SKMC	muscle:	n/a
10	chr6:29760609-29760659	GM19239	blood:	n/a
11	chr6:29760023-29760073	BE2_C	brain:	n/a
12	chr6:29759947-29759997	ovcar-3	ovarian:	n/a
13	chr6:29760659-29760709	HCF	heart:	n/a
14	chr6:29756503-29756553	HUVEC	blood vessel:	n/a
15	chr6:29760784-29760834	HCM	heart:	n/a
16	chr6:29759949-29759999	HEEpiC	esophagus:	n/a
17	chr6:29760148-29760198	GM06990	blood:	n/a
18	chr6:29759804-29759854	NB4	blood:	n/a
19	chr6:29760782-29760832	HepG2	liver:	n/a
20	chr6:29760757-29760807	SKMC	muscle:	n/a
21	chr6:29760675-29760725	NT2-D1	testis:	n/a
22	chr6:29759729-29759779	BE2_C	brain:	n/a
23	chr6:29759197-29759247	HL-60	blood:	n/a
24	chr6:29760659-29760709	HRCEpiC	kidney:	n/a
25	chr6:29760090-29760140	SAEC	small airway:	n/a
26	chr6:29756503-29756553	HRE	kidney:	n/a
27	chr6:29760713-29760763	BJ	skin:	n/a
28	chr6:29760688-29760738	BE2_C	brain:	n/a
29	chr6:29759078-29759128	PANC-1	pancreas:	n/a
30	chr6:29760634-29760684	NT2-D1	testis:	n/a
31	chr6:29760765-29760815	BE2_C	brain:	n/a
32	chr6:29760447-29760497	HNPCEpiC	eye:	n/a
33	chr6:29760505-29760555	Hela-S3	cervix:	n/a
34	chr6:29760695-29760745	PrEC	prostate:	n/a
35	chr6:29760028-29760078	K562	blood:	n/a
36	chr6:29759197-29759247	GM19239	blood:	n/a
37	chr6:29759718-29759768	SK-N-SH	brain:	n/a
38	chr6:29760410-29760460	PANC-1	pancreas:	n/a
39	chr6:29756503-29756553	HCM	heart:	n/a
40	chr6:29760695-29760745	Hepatocyte	liver:	n/a
41	chr6:29760754-29760804	SK-N-SH_RA	brain:	n/a
42	chr6:29760754-29760804	AG10803	skin:	n/a
43	chr6:29759197-29759247	AoSMC	blood vessel:	n/a
44	chr6:29759972-29760022	HRCEpiC	kidney:	n/a
45	chr6:29760090-29760140	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:29760695-29760745	HCF	heart:	n/a
47	chr6:29760435-29760485	SKMC	muscle:	n/a
48	chr6:29760713-29760763	NT2-D1	testis:	n/a
49	chr6:29760028-29760078	HRE	kidney:	n/a
50	chr6:29759718-29759768	K562	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	chr6:29755654..29758226-chr6:29780556..29783054,2	MCF-7	breast:
3	chr6:29759731..29760249-chr6:31324546..31325250,2	HCT-116	colon:
4	chr6:29755459..29758755-chr6:29758827..29760410,3	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 806 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149550517	chr6:29746097-29746098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188633345	chr6:29746117-29746118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577642143	chr6:29746129-29746130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111725565	chr6:29746138-29746139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374944344	chr6:29746154-29746155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369735795	chr6:29746159-29746160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146076326	chr6:29746198-29746199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577528597	chr6:29746253-29746254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367959217	chr6:29746284-29746285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540121645	chr6:29746286-29746287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1633029	chr6:29746305-29746306	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs140074250	chr6:29746312-29746313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541899775	chr6:29746321-29746322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562123622	chr6:29746345-29746346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1633028	chr6:29746367-29746368	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs143734791	chr6:29746374-29746375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146358640	chr6:29746430-29746431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1633027	chr6:29746462-29746463	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549644779	chr6:29746471-29746472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200178180	chr6:29746472-29746473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1633026	chr6:29746515-29746516	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1633025	chr6:29746527-29746528	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs192731419	chr6:29746537-29746538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139662924	chr6:29746543-29746544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534383428	chr6:29746546-29746547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56091723	chr6:29746552-29746553	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs76779442	chr6:29746566-29746567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114178056	chr6:29746568-29746569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142930762	chr6:29746633-29746634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1633024	chr6:29746657-29746658	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536150639	chr6:29746750-29746751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151104836	chr6:29746782-29746783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1633023	chr6:29746794-29746795	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1633022	chr6:29746803-29746804	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs557859889	chr6:29746818-29746819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1633021	chr6:29746869-29746870	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs141098200	chr6:29746878-29746879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183054327	chr6:29746886-29746887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187659023	chr6:29746894-29746895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112807308	chr6:29746896-29746897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542921950	chr6:29746897-29746898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191280943	chr6:29746899-29746900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183717540	chr6:29746908-29746909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117485577	chr6:29746939-29746940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17178658	chr6:29746963-29746964	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs17178665	chr6:29747011-29747012	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs149877322	chr6:29747018-29747019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147573077	chr6:29747032-29747033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535740172	chr6:29747057-29747058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142046362	chr6:29747074-29747075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Gastric cancer	16891809	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:368 , 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	chr6:29745600-29746200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:29745600-29747200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr6:29745600-29747200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr6:29746000-29746200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:29746000-29746400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:29746200-29746600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:29746200-29747200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr6:29746400-29747200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr6:29746600-29747000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:29746600-29747000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:29746600-29747200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:29746800-29747200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr6:29747000-29748000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:29747600-29747800	Flanking Active TSS	K562	blood
17	chr6:29753600-29754000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:29754000-29757600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr6:29756000-29756200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr6:29756000-29758600	Weak transcription	Pancreas	Pancrea
21	chr6:29756200-29756800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr6:29756400-29756800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:29756800-29757000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:29756800-29757000	Enhancers	Placenta Amnion	Placenta Amnion
25	chr6:29756800-29757400	Weak transcription	NHEK	skin
26	chr6:29756800-29758400	Enhancers	HMEC	breast
27	chr6:29757000-29757200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr6:29757000-29758000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:29757000-29758600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr6:29757200-29758600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr6:29757400-29758000	Enhancers	NHEK	skin
32	chr6:29757400-29759000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:29757600-29757800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:29757600-29758000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:29757800-29758000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr6:29757800-29758400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:29757800-29758800	Enhancers	Hela-S3	cervix
38	chr6:29758000-29758200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr6:29758000-29758200	Flanking Active TSS	NHEK	skin
40	chr6:29758000-29758400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:29758000-29759000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:29758200-29758600	Enhancers	NHEK	skin
43	chr6:29758400-29759000	Flanking Active TSS	HMEC	breast
44	chr6:29758400-29759400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:29758400-29760000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:29758600-29758800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr6:29758600-29758800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr6:29758600-29758800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr6:29758600-29758800	Enhancers	Gastric	stomach
50	chr6:29758600-29759000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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