Variant report

Variant	nsv969390
Chromosome Location	chr6:35428276-35434702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:62)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:43 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:35428920-35429443	MCF-7	breast:	n/a	chr6:35429294-35429305
2	CEBPB	chr6:35429116-35429466	ECC-1	luminal epithelium:	n/a	chr6:35429294-35429305
3	CEBPB	chr6:35429094-35429439	ECC-1	luminal epithelium:	n/a	chr6:35429294-35429305
4	CEBPB	chr6:35429181-35429381	HepG2	liver:	n/a	chr6:35429294-35429305
5	CEBPB	chr6:35428995-35429434	MCF-7	breast:	n/a	chr6:35429294-35429305
6	CEBPB	chr6:35429159-35429350	Hela-S3	cervix:	n/a	chr6:35429294-35429305
7	CEBPB	chr6:35429137-35429357	K562	blood:	n/a	chr6:35429294-35429305
8	CEBPB	chr6:35429185-35429350	IMR90	lung:	n/a	chr6:35429294-35429305
9	CEBPB	chr6:35429154-35429393	K562	blood:	n/a	chr6:35429294-35429305
10	CTCF	chr6:35429003-35429097	LNCaP	prostate:	n/a	n/a
11	ELF1	chr6:35428918-35429401	MCF-7	breast:	n/a	n/a
12	EP300	chr6:35428941-35429443	MCF-7	breast:	n/a	n/a
13	EP300	chr6:35429039-35429425	T-47D	breast:	n/a	n/a
14	FOXA1	chr6:35429121-35429323	T-47D	breast:	n/a	n/a
15	FOXM1	chr6:35428980-35429377	MCF-7	breast:	n/a	n/a
16	GATA3	chr6:35428829-35429479	MCF-7	breast:	n/a	n/a
17	GATA3	chr6:35429100-35429420	MCF-7	breast:	n/a	n/a
18	GATA3	chr6:35428970-35429464	T-47D	breast:	n/a	n/a
19	GATA3	chr6:35431097-35431474	MCF-7	breast:	n/a	n/a
20	GATA3	chr6:35429018-35429396	MCF-7	breast:	n/a	n/a
21	GATA3	chr6:35429033-35429399	T-47D	breast:	n/a	n/a
22	GATA3	chr6:35428856-35429580	MCF-7	breast:	n/a	n/a
23	HDAC2	chr6:35428943-35429471	MCF-7	breast:	n/a	n/a
24	HDAC2	chr6:35429012-35429444	MCF-7	breast:	n/a	n/a
25	JUND	chr6:35428909-35429440	MCF-7	breast:	n/a	n/a
26	MAX	chr6:35428926-35429427	MCF-7	breast:	n/a	n/a
27	MAX	chr6:35428853-35429517	MCF-7	breast:	n/a	n/a
28	NR2F2	chr6:35431083-35431462	MCF-7	breast:	n/a	n/a
29	NR2F2	chr6:35428807-35429493	MCF-7	breast:	n/a	n/a
30	NR2F2	chr6:35428806-35429413	MCF-7	breast:	n/a	n/a
31	POLR2A	chr6:35430483-35430712	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr6:35430529-35430807	K562	blood:	n/a	n/a
33	POLR2A	chr6:35433258-35433329	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr6:35432023-35432152	K562	blood:	n/a	n/a
35	POLR2A	chr6:35431660-35431740	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr6:35434651-35434752	K562	blood:	n/a	n/a
37	POLR2A	chr6:35434639-35434738	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr6:35433006-35433017	K562	blood:	n/a	n/a
39	POLR2A	chr6:35434144-35434280	Hela-S3	cervix:	n/a	n/a
40	SIN3AK20	chr6:35428784-35429564	MCF-7	breast:	n/a	n/a
41	SIN3AK20	chr6:35428963-35429511	MCF-7	breast:	n/a	n/a
42	TCF7L2	chr6:35429111-35429249	MCF-7	breast:	n/a	n/a
43	ZNF217	chr6:35429013-35429373	MCF-7	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35432435-35432485	GM12892	blood:	n/a
2	chr6:35432435-35432485	GM12892	blood:	n/a
3	chr6:35432435-35432485	NHBE	bronchial:	n/a
4	chr6:35432435-35432485	SK-N-SH_RA	brain:	n/a
5	chr6:35432435-35432485	HEEpiC	esophagus:	n/a
6	chr6:35432435-35432485	HRCEpiC	kidney:	n/a
7	chr6:35432435-35432485	SKMC	muscle:	n/a
8	chr6:35432435-35432485	HNPCEpiC	eye:	n/a
9	chr6:35432435-35432485	NB4	blood:	n/a
10	chr6:35432435-35432485	GM12891	blood:	n/a
11	chr6:35432435-35432485	GM12878	blood:	n/a
12	chr6:35432435-35432485	Hepatocyte	liver:	n/a
13	chr6:35432435-35432485	RPTEC	kidney:	n/a
14	chr6:35432435-35432485	HL-60	blood:	n/a
15	chr6:35432435-35432485	HAEpiC	amniotic membrane:	n/a
16	chr6:35432435-35432485	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:35432435-35432485	ovcar-3	ovarian:	n/a
18	chr6:35432435-35432485	SK-N-SH	brain:	n/a
19	chr6:35432435-35432485	HepG2	liver:	n/a
20	chr6:35432435-35432485	AG10803	skin:	n/a
21	chr6:35432435-35432485	ECC-1	luminal epithelium:	n/a
22	chr6:35432435-35432485	NT2-D1	testis:	n/a
23	chr6:35432435-35432485	ProgFib	skin:	n/a
24	chr6:35432435-35432485	GM19239	blood:	n/a
25	chr6:35432435-35432485	CMK	blood:	n/a
26	chr6:35432435-35432485	K562	blood:	n/a
27	chr6:35432435-35432485	HEK293	kidney:	embryo
28	chr6:35432435-35432485	PANC-1	pancreas:	n/a
29	chr6:35432435-35432485	BE2_C	brain:	n/a
30	chr6:35432435-35432485	AoSMC	blood vessel:	n/a
31	chr6:35432435-35432485	GM06990	blood:	n/a
32	chr6:35432435-35432485	AG04449	skin:	fetal
33	chr6:35432435-35432485	HCPEpiC	choroid plexus:	n/a
34	chr6:35432435-35432485	HRPEpiC	eye:	n/a
35	chr6:35432435-35432485	AG09319	gingival:	n/a
36	chr6:35432435-35432485	HIPEpiC	eye:	n/a
37	chr6:35432435-35432485	HCF	heart:	n/a
38	chr6:35432435-35432485	SAEC	small airway:	n/a
39	chr6:35432435-35432485	BJ	skin:	n/a
40	chr6:35432435-35432485	Hela-S3	cervix:	n/a
41	chr6:35432435-35432485	IMR90	lung:	fetal
42	chr6:35432435-35432485	MCF-7	breast:	n/a
43	chr6:35432435-35432485	Caco-2	colon:	n/a
44	chr6:35432435-35432485	H1-hESC	embryonic stem cell:	embryo
45	chr6:35432435-35432485	PFSK-1	brain:	n/a
46	chr6:35432435-35432485	HUVEC	blood vessel:	n/a
47	chr6:35432435-35432485	T-47D	breast:	n/a
48	chr6:35432435-35432485	Jurkat	blood:	n/a
49	chr6:35432435-35432485	U87	brain:	n/a
50	chr6:35432435-35432485	NH-A	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:35257372..35267692-chr6:35433856..35438688,25	K562	blood:
2	chr6:35309215..35314259-chr6:35432456..35439068,10	MCF-7	breast:
3	chr6:35415818..35424678-chr6:35432486..35440672,36	K562	blood:
4	chr6:35427059..35428930-chr6:35434282..35437196,3	MCF-7	breast:
5	chr11:2397606..2400001-chr6:35434655..35437647,2	K562	blood:
6	chr6:35419142..35422512-chr6:35424570..35429105,6	MCF-7	breast:
7	chr6:35419072..35422959-chr6:35429759..35431880,3	K562	blood:
8	chr6:35308405..35313609-chr6:35434054..35440248,12	K562	blood:
9	chr6:35226066..35229330-chr6:35434346..35438215,4	K562	blood:
10	chr6:35424729..35431814-chr6:35432688..35440099,20	K562	blood:
11	chr6:35423275..35426107-chr6:35428625..35431307,2	MCF-7	breast:
12	chr6:35433822..35437754-chr6:35703135..35706478,6	K562	blood:
13	chr6:35308378..35313609-chr6:35433550..35439145,12	K562	blood:
14	chr6:35429670..35431283-chr6:35435809..35438144,3	MCF-7	breast:
15	chr6:35419072..35421261-chr6:35429401..35431880,2	K562	blood:
16	chr6:35257372..35267871-chr6:35433266..35439192,25	K562	blood:
17	chr6:35227094..35229802-chr6:35433183..35436613,4	K562	blood:
18	chr6:35429000..35431728-chr6:35441899..35443827,3	K562	blood:
19	chr6:35418617..35424875-chr6:35434196..35438070,12	MCF-7	breast:
20	chr6:35427041..35429819-chr6:35457117..35459807,2	K562	blood:
21	chr6:35225661..35227762-chr6:35430266..35431804,2	K562	blood:
22	chr6:35260730..35269335-chr6:35433870..35444063,22	MCF-7	breast:
23	chr6:35432131..35435121-chr6:35435197..35437523,2	K562	blood:

No data

Variant related genes	Relation type
RPL10A	TF binding region
RPL10A	CpG island
ENSG00000232909	chromatin interactions
ENSG00000110651	chromatin interactions
ENSG00000157343	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000023892	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000112033	chromatin interactions
ENSG00000238184	chromatin interactions
ENSG00000112039	chromatin interactions

Extended variants
information (count: 262 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537489416	chr6:35428277-35428278	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs559046656	chr6:35428278-35428279	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs367566975	chr6:35428300-35428301	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs55992713	chr6:35428309-35428310	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147572271	chr6:35428318-35428319	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534777587	chr6:35428344-35428345	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs141551053	chr6:35428345-35428346	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs201970876	chr6:35428361-35428362	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs200535245	chr6:35428390-35428391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541746126	chr6:35428391-35428392	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557260261	chr6:35428439-35428440	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376666455	chr6:35428445-35428446	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs574888545	chr6:35428489-35428490	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs45488897	chr6:35428607-35428608	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs540979664	chr6:35428611-35428612	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528189577	chr6:35428614-35428615	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs7746718	chr6:35428627-35428628	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559671030	chr6:35428639-35428640	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs62402087	chr6:35428697-35428698	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs67491477	chr6:35428700-35428701	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530353406	chr6:35428729-35428730	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140698585	chr6:35428743-35428744	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10947550	chr6:35428782-35428783	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs530885932	chr6:35428840-35428841	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs375966321	chr6:35428845-35428846	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570928477	chr6:35428892-35428893	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs535097729	chr6:35428895-35428896	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs6457824	chr6:35428900-35428901	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573395410	chr6:35428952-35428953	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs45478097	chr6:35428953-35428954	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs148878755	chr6:35428956-35428957	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs143531331	chr6:35428957-35428958	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs569808324	chr6:35429081-35429082	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575183802	chr6:35429092-35429093	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs118006603	chr6:35429137-35429138	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs45465100	chr6:35429155-35429156	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs138339574	chr6:35429171-35429172	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536802000	chr6:35429186-35429187	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs6914178	chr6:35429225-35429226	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs371615282	chr6:35429271-35429272	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs45466692	chr6:35429300-35429301	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574888294	chr6:35429304-35429305	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542418609	chr6:35429318-35429319	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563935698	chr6:35429370-35429371	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs45532239	chr6:35429384-35429385	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552930176	chr6:35429411-35429412	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs71540107	chr6:35429428-35429429	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs186268386	chr6:35429526-35429527	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs34731739	chr6:35429557-35429558	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192020820	chr6:35429572-35429573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	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
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35421000-35435400	Weak transcription	Colon Smooth Muscle	Colon
2	chr6:35421200-35435200	Weak transcription	Brain Angular Gyrus	brain
3	chr6:35421200-35435400	Weak transcription	Brain Anterior Caudate	brain
4	chr6:35421400-35435400	Weak transcription	Colonic Mucosa	Colon
5	chr6:35421400-35435400	Weak transcription	Fetal Kidney	kidney
6	chr6:35421400-35435400	Weak transcription	Pancreas	Pancrea
7	chr6:35421600-35433800	Weak transcription	HUVEC	blood vessel
8	chr6:35421600-35435200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr6:35421600-35435200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr6:35421600-35435400	Weak transcription	A549	lung
11	chr6:35421600-35435400	Weak transcription	NH-A	brain
12	chr6:35421800-35431000	Weak transcription	Liver	Liver
13	chr6:35422000-35430200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:35422200-35435200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr6:35422200-35435400	Weak transcription	Small Intestine	intestine
16	chr6:35422400-35430200	Weak transcription	HSMM	muscle
17	chr6:35422400-35434800	Strong transcription	Fetal Intestine Small	intestine
18	chr6:35422600-35429200	Strong transcription	Dnd41	blood
19	chr6:35422600-35435400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr6:35422800-35431000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:35422800-35434800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:35422800-35434800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr6:35422800-35435200	Weak transcription	Fetal Thymus	thymus
24	chr6:35422800-35435400	Weak transcription	Fetal Brain Male	brain
25	chr6:35422800-35435600	Weak transcription	Right Atrium	heart
26	chr6:35423000-35428400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:35423000-35428600	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr6:35423000-35435200	Weak transcription	Fetal Heart	heart
29	chr6:35423000-35435200	Strong transcription	Fetal Stomach	stomach
30	chr6:35423000-35435400	Weak transcription	NHDF-Ad	bronchial
31	chr6:35423200-35429200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:35423200-35432200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr6:35423200-35435200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:35423400-35428400	Genic enhancers	Placenta	Placenta
35	chr6:35423400-35428600	Strong transcription	Lung	lung
36	chr6:35423400-35428600	Strong transcription	NHEK	skin
37	chr6:35423400-35428800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:35423400-35429000	Strong transcription	Spleen	Spleen
39	chr6:35423400-35429200	Strong transcription	Ovary	ovary
40	chr6:35423400-35429400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:35423400-35430800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr6:35423400-35431400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr6:35423400-35431400	Strong transcription	Brain Germinal Matrix	brain
44	chr6:35423400-35431400	Strong transcription	Fetal Lung	lung
45	chr6:35423400-35431800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:35423400-35431800	Strong transcription	Fetal Intestine Large	intestine
47	chr6:35423400-35432000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:35423400-35432000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:35423400-35434600	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr6:35423400-35434800	Strong transcription	HUES6 Cell Line	embryonic stem cell

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