Variant report

Variant	nsv965762
Chromosome Location	chr6:127669294-127698325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:192)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:192 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:127687627-127688469	K562	blood:	n/a	n/a
2	ATF1	chr6:127688105-127688305	K562	blood:	n/a	n/a
3	ATF3	chr6:127687291-127688018	HCT-116	colon:	n/a	n/a
4	ATF3	chr6:127687513-127687859	K562	blood:	n/a	n/a
5	ATF3	chr6:127687224-127688167	HCT-116	colon:	n/a	n/a
6	BACH1	chr6:127687937-127688526	K562	blood:	n/a	n/a
7	BATF	chr6:127688257-127688496	GM12878	blood:	n/a	chr6:127688345-127688356
8	CBX3	chr6:127687333-127687814	K562	blood:	n/a	n/a
9	CBX3	chr6:127687970-127688623	K562	blood:	n/a	n/a
10	CBX3	chr6:127671186-127671380	K562	blood:	n/a	n/a
11	CBX3	chr6:127671128-127671490	K562	blood:	n/a	n/a
12	CCNT2	chr6:127688243-127688443	K562	blood:	n/a	n/a
13	CEBPB	chr6:127687528-127687704	HepG2	liver:	n/a	chr6:127687637-127687648
14	CEBPB	chr6:127687343-127687838	A549	lung:	n/a	chr6:127687637-127687648
15	CEBPB	chr6:127687400-127687782	MCF-7	breast:	n/a	chr6:127687637-127687648
16	CEBPB	chr6:127687483-127687808	H1-hESC	embryonic stem cell:	n/a	chr6:127687637-127687648
17	CEBPB	chr6:127687286-127688051	A549	lung:	n/a	chr6:127687637-127687648
18	CEBPB	chr6:127687412-127687877	ECC-1	luminal epithelium:	n/a	chr6:127687637-127687648
19	CEBPB	chr6:127687452-127687821	K562	blood:	n/a	chr6:127687637-127687648
20	CEBPB	chr6:127687330-127687845	IMR90	lung:	n/a	chr6:127687637-127687648
21	CEBPB	chr6:127687245-127688427	HCT-116	colon:	n/a	chr6:127687637-127687648
22	CEBPB	chr6:127687372-127687806	MCF-7	breast:	n/a	chr6:127687637-127687648
23	CEBPB	chr6:127687408-127687827	A549	lung:	n/a	chr6:127687637-127687648
24	CEBPB	chr6:127687287-127688036	HCT-116	colon:	n/a	chr6:127687637-127687648
25	CEBPB	chr6:127687390-127687865	Hela-S3	cervix:	n/a	chr6:127687637-127687648
26	CEBPB	chr6:127687439-127687819	K562	blood:	n/a	chr6:127687637-127687648
27	CHD2	chr6:127687387-127687816	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr6:127687570-127687584	NHEK	skin:	n/a	n/a
29	CTCF	chr6:127677113-127677203	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr6:127669234-127669434	GM12878	blood:	n/a	n/a
31	CTCF	chr6:127669314-127669386	LNCaP	prostate:	n/a	n/a
32	CTCF	chr6:127684207-127684229	GM10248	blood:	n/a	n/a
33	CTCF	chr6:127669260-127669410	HMEC	breast:	n/a	n/a
34	CTCF	chr6:127669280-127669430	NHEK	skin:	n/a	n/a
35	CTCF	chr6:127669260-127669410	SAEC	small airway:	n/a	n/a
36	CTCF	chr6:127669220-127669370	HEEpiC	esophagus:	n/a	n/a
37	CUX1	chr6:127687595-127687789	K562	blood:	n/a	n/a
38	E2F4	chr6:127688275-127688557	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr6:127687513-127687847	MCF10A-Er-Src	breast:	n/a	n/a
40	EP300	chr6:127688037-127688577	K562	blood:	n/a	n/a
41	EP300	chr6:127687386-127687832	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr6:127687243-127688045	SK-N-SH	brain:	n/a	n/a
43	EP300	chr6:127687457-127687725	K562	blood:	n/a	n/a
44	EP300	chr6:127687396-127687845	Hela-S3	cervix:	n/a	n/a
45	EP300	chr6:127687408-127687776	SK-N-SH_RA	brain:	n/a	n/a
46	FOS	chr6:127687462-127687988	MCF10A-Er-Src	breast:	n/a	chr6:127687715-127687726
47	FOS	chr6:127687473-127687905	Hela-S3	cervix:	n/a	chr6:127687715-127687726
48	FOS	chr6:127687448-127688100	MCF10A-Er-Src	breast:	n/a	chr6:127687715-127687726
49	FOS	chr6:127687482-127687932	HUVEC	blood vessel:	n/a	chr6:127687715-127687726
50	FOS	chr6:127687409-127688568	MCF10A-Er-Src	breast:	n/a	chr6:127687715-127687726

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:127687368-127687418	HNPCEpiC	eye:	n/a
2	chr6:127687368-127687418	HCM	heart:	n/a
3	chr6:127687368-127687418	HEK293	kidney:	embryo
4	chr6:127687368-127687418	HEEpiC	esophagus:	n/a
5	chr6:127687368-127687418	AG10803	skin:	n/a
6	chr6:127687368-127687418	SKMC	muscle:	n/a
7	chr6:127687368-127687418	Hepatocyte	liver:	n/a
8	chr6:127687368-127687418	HRCEpiC	kidney:	n/a
9	chr6:127687368-127687418	AG04450	lung:	fetal
10	chr6:127687368-127687418	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:127687368-127687418	BE2_C	brain:	n/a
12	chr6:127687368-127687418	HMEC	breast:	n/a
13	chr6:127687368-127687418	GM12892	blood:	n/a
14	chr6:127687368-127687418	GM19239	blood:	n/a
15	chr6:127687368-127687418	U87	brain:	n/a
16	chr6:127687368-127687418	HAEpiC	amniotic membrane:	n/a
17	chr6:127687368-127687418	HepG2	liver:	n/a
18	chr6:127687368-127687418	AG09309	skin:	n/a
19	chr6:127687368-127687418	AG04449	skin:	fetal
20	chr6:127687368-127687418	ProgFib	skin:	n/a
21	chr6:127687368-127687418	LNCaP	prostate:	n/a
22	chr6:127687368-127687418	NT2-D1	testis:	n/a
23	chr6:127687368-127687418	PANC-1	pancreas:	n/a
24	chr6:127687368-127687418	K562	blood:	n/a
25	chr6:127687368-127687418	HIPEpiC	eye:	n/a
26	chr6:127687368-127687418	AoSMC	blood vessel:	n/a
27	chr6:127687368-127687418	GM12878	blood:	n/a
28	chr6:127687368-127687418	PFSK-1	brain:	n/a
29	chr6:127687368-127687418	IMR90	lung:	fetal
30	chr6:127687368-127687418	A549	lung:	n/a
31	chr6:127687368-127687418	H1-hESC	embryonic stem cell:	embryo
32	chr6:127687368-127687418	BJ	skin:	n/a
33	chr6:127687368-127687418	NHDF-neo	bronchial:	n/a
34	chr6:127687368-127687418	HCF	heart:	n/a
35	chr6:127687368-127687418	HUVEC	blood vessel:	n/a
36	chr6:127687368-127687418	MCF10A-Er-Src	breast:	n/a
37	chr6:127687368-127687418	AG09319	gingival:	n/a
38	chr6:127687368-127687418	ECC-1	luminal epithelium:	n/a
39	chr6:127687368-127687418	HL-60	blood:	n/a
40	chr6:127687368-127687418	RPTEC	kidney:	n/a
41	chr6:127687368-127687418	T-47D	breast:	n/a
42	chr6:127687368-127687418	GM12891	blood:	n/a
43	chr6:127687368-127687418	HCT-116	colon:	n/a
44	chr6:127687368-127687418	Jurkat	blood:	n/a
45	chr6:127687368-127687418	HRPEpiC	eye:	n/a
46	chr6:127687368-127687418	NB4	blood:	n/a
47	chr6:127687368-127687418	CMK	blood:	n/a
48	chr6:127687368-127687418	NHBE	bronchial:	n/a
49	chr6:127687368-127687418	MCF-7	breast:	n/a
50	chr6:127687368-127687418	SK-N-SH_RA	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:127664700..127666398-chr6:127672661..127675455,3	K562	blood:
2	chr6:127669193..127671594-chr6:127672805..127674451,2	MCF-7	breast:
3	chr6:127663265..127666547-chr6:127687239..127690914,3	K562	blood:
4	chr6:127668521..127671464-chr6:127672769..127675041,2	MCF-7	breast:
5	chr6:127690026..127691959-chr6:127695076..127697504,2	K562	blood:
6	chr6:127663032..127665224-chr6:127677771..127679403,2	K562	blood:
7	chr6:127681859..127685536-chr6:127685894..127688986,4	MCF-7	breast:
8	chr6:127663267..127665190-chr6:127682385..127684934,2	MCF-7	breast:
9	chr6:127690026..127691959-chr6:127695076..127697504,2	K562	blood:
10	chr6:127668521..127671464-chr6:127672769..127675041,2	MCF-7	breast:
11	chr6:127661647..127664364-chr6:127693030..127695790,2	K562	blood:
12	chr6:127661647..127664491-chr6:127692305..127695790,3	K562	blood:
13	chr6:127663265..127666606-chr6:127686732..127691150,6	K562	blood:
14	chr6:127669193..127671594-chr6:127672805..127674451,2	MCF-7	breast:
15	chr6:127587591..127589201-chr6:127668421..127670620,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF146-4	chr6:127694677-127695126	NONHSAT114851
2	lnc-RNF146-5	chr6:127695203-127695771	NONHSAT114852

No data

Variant related genes	Relation type
ECHDC1	TF binding region
RPL5P18	TF binding region
YWHAZP4	TF binding region
ECHDC1	CpG island
RPL5P18	CpG island
YWHAZP4	CpG island
ENSG00000093144	chromatin interactions
ENSG00000118518	chromatin interactions
ENSG00000220744	chromatin interactions

Extended variants
information (count: 1055 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553351194	chr6:127669427-127669428	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs34414466	chr6:127669430-127669431	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs577705437	chr6:127669431-127669432	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs397759320	chr6:127669442-127669443	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75090107	chr6:127669443-127669444	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375398286	chr6:127669450-127669451	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544984320	chr6:127669455-127669456	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562212181	chr6:127669487-127669488	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575223885	chr6:127669489-127669490	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542720009	chr6:127669511-127669512	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs561306067	chr6:127669512-127669513	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189948427	chr6:127669519-127669520	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs144813870	chr6:127669520-127669521	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs562690582	chr6:127669526-127669527	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs144033201	chr6:127669583-127669584	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532675528	chr6:127669596-127669597	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550513836	chr6:127669683-127669684	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147294203	chr6:127669694-127669695	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs551150309	chr6:127669714-127669715	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs9398840	chr6:127669744-127669745	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs182177063	chr6:127669755-127669756	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534855905	chr6:127669775-127669776	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs140845287	chr6:127669792-127669793	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs73771682	chr6:127669823-127669824	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs144691884	chr6:127669979-127669980	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185374656	chr6:127669991-127669992	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs575228334	chr6:127669993-127669994	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs151252038	chr6:127670003-127670004	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs139231414	chr6:127670013-127670014	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149982971	chr6:127670023-127670024	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs55633254	chr6:127670033-127670034	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs565140403	chr6:127670040-127670041	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140388722	chr6:127670050-127670051	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145484564	chr6:127670058-127670059	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562719752	chr6:127670059-127670060	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530154974	chr6:127670080-127670081	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs377057330	chr6:127670092-127670093	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566586700	chr6:127670104-127670105	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566918843	chr6:127670106-127670107	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9398841	chr6:127670134-127670135	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs546790900	chr6:127670141-127670142	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs571485338	chr6:127670194-127670195	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555355008	chr6:127670217-127670218	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538917464	chr6:127670317-127670318	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550878762	chr6:127670319-127670320	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs568755013	chr6:127670323-127670324	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536283577	chr6:127670331-127670332	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567193467	chr6:127670449-127670450	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554277495	chr6:127670509-127670510	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572556220	chr6:127670529-127670530	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Neurocytoma	17123091	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21958427	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17847001	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:127665800-127669600	Weak transcription	Gastric	stomach
2	chr6:127665800-127670000	Weak transcription	Esophagus	oesophagus
3	chr6:127665800-127670800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:127665800-127671200	Weak transcription	Right Ventricle	heart
5	chr6:127665800-127671800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:127665800-127672400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:127666000-127669400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:127666000-127669400	Weak transcription	Fetal Intestine Small	intestine
9	chr6:127666000-127669400	Weak transcription	Small Intestine	intestine
10	chr6:127666000-127669800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr6:127666000-127670000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr6:127666000-127670000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:127666000-127670400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:127666000-127671400	Weak transcription	Fetal Lung	lung
15	chr6:127666000-127672400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:127666000-127679200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:127666000-127704000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr6:127666200-127669600	Weak transcription	Adipose Nuclei	Adipose
19	chr6:127666200-127671800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:127666200-127673400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:127666200-127676800	Weak transcription	Right Atrium	heart
22	chr6:127666200-127687000	Weak transcription	HSMM	muscle
23	chr6:127666400-127670400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:127666400-127670400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr6:127666600-127669800	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr6:127666600-127670400	Weak transcription	Dnd41	blood
27	chr6:127667000-127671200	Weak transcription	K562	blood
28	chr6:127667200-127669600	Weak transcription	Lung	lung
29	chr6:127667200-127670600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:127667600-127669400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr6:127667600-127676200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:127667800-127669600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:127668000-127669400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:127668000-127673400	Weak transcription	Primary B cells from cord blood	blood
35	chr6:127668800-127675800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr6:127669400-127669600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:127669400-127670200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:127669400-127670200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr6:127669400-127670800	ZNF genes & repeats	Fetal Intestine Small	intestine
40	chr6:127669400-127671800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:127669600-127670000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:127669600-127670000	Enhancers	Adipose Nuclei	Adipose
43	chr6:127669600-127670000	Strong transcription	Gastric	stomach
44	chr6:127669600-127670600	Enhancers	Lung	lung
45	chr6:127669800-127670800	ZNF genes & repeats	Fetal Muscle Leg	muscle
46	chr6:127669800-127673200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr6:127670000-127670600	ZNF genes & repeats	Esophagus	oesophagus
48	chr6:127670000-127670800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:127670000-127672000	Weak transcription	Gastric	stomach
50	chr6:127670200-127670600	Weak transcription	Monocytes-CD14+_RO01746	blood

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