Variant report

Variant	nsv965718
Chromosome Location	chr6:35512668-35527452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:35521071-35521413	K562	blood:	n/a	n/a
2	ATF3	chr6:35521065-35521374	K562	blood:	n/a	n/a
3	BATF	chr6:35526391-35526712	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:35526387-35526609	GM12878	blood:	n/a	n/a
5	CBX3	chr6:35518128-35518651	HCT-116	colon:	n/a	n/a
6	CBX3	chr6:35519985-35520460	K562	blood:	n/a	n/a
7	CBX3	chr6:35518192-35518630	K562	blood:	n/a	n/a
8	CBX3	chr6:35520960-35521489	K562	blood:	n/a	n/a
9	CBX3	chr6:35519991-35520537	K562	blood:	n/a	n/a
10	CBX3	chr6:35518217-35518567	K562	blood:	n/a	n/a
11	CEBPB	chr6:35512597-35513014	MCF-7	breast:	n/a	n/a
12	CEBPB	chr6:35512717-35512917	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr6:35521009-35521553	K562	blood:	n/a	n/a
14	CREB1	chr6:35521039-35521540	K562	blood:	n/a	n/a
15	CTCF	chr6:35512625-35512766	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:35520142-35520398	Gliobla	brain:	n/a	n/a
17	CTCF	chr6:35521176-35521417	K562	blood:	n/a	n/a
18	CTCF	chr6:35520200-35520350	GM12867	blood:	n/a	n/a
19	CTCF	chr6:35512601-35512795	MCF-7	breast:	n/a	n/a
20	CTCF	chr6:35520086-35520420	GM12878	blood:	n/a	n/a
21	CTCF	chr6:35520160-35520310	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr6:35520140-35520290	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr6:35520089-35520394	HepG2	liver:	n/a	n/a
24	CTCF	chr6:35520065-35520478	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr6:35520190-35520365	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:35512602-35512811	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:35520112-35520420	K562	blood:	n/a	n/a
28	CTCF	chr6:35520043-35520465	K562	blood:	n/a	n/a
29	CTCF	chr6:35519999-35520626	SK-N-SH	brain:	n/a	n/a
30	CTCF	chr6:35520180-35520330	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:35519987-35520504	A549	lung:	n/a	n/a
32	CTCF	chr6:35520130-35520370	A549	lung:	n/a	n/a
33	CTCF	chr6:35520200-35520350	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr6:35520220-35520370	GM12865	blood:	n/a	n/a
35	CTCF	chr6:35520102-35520396	ECC-1	luminal epithelium:	n/a	n/a
36	CTCF	chr6:35520153-35520308	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr6:35520200-35520350	SAEC	small airway:	n/a	n/a
38	CTCF	chr6:35520180-35520330	GM12872	blood:	n/a	n/a
39	CTCF	chr6:35520115-35520400	Medullo	brain:	n/a	n/a
40	CTCF	chr6:35520177-35520377	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:35520180-35520330	K562	blood:	n/a	n/a
42	CTCF	chr6:35520160-35520310	GM12875	blood:	n/a	n/a
43	CTCF	chr6:35520161-35520394	GM12891	blood:	n/a	n/a
44	CTCF	chr6:35520500-35520650	GM12874	blood:	n/a	n/a
45	CTCF	chr6:35520144-35520425	GM19238	blood:	n/a	n/a
46	CTCF	chr6:35520200-35520350	A549	lung:	n/a	n/a
47	CTCF	chr6:35520160-35520310	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr6:35520200-35520350	GM12871	blood:	n/a	n/a
49	CTCF	chr6:35520200-35520350	HepG2	liver:	n/a	n/a
50	CTCF	chr6:35520099-35520352	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35523700-35523750	CMK	blood:	n/a
2	chr6:35523700-35523750	RPTEC	kidney:	n/a
3	chr6:35523658-35523708	NHDF-neo	bronchial:	n/a
4	chr6:35523700-35523750	HNPCEpiC	eye:	n/a
5	chr6:35523658-35523708	GM06990	blood:	n/a
6	chr6:35523700-35523750	AG09319	gingival:	n/a
7	chr6:35523700-35523750	GM12892	blood:	n/a
8	chr6:35523658-35523708	HCF	heart:	n/a
9	chr6:35523658-35523708	PANC-1	pancreas:	n/a
10	chr6:35523700-35523750	GM19239	blood:	n/a
11	chr6:35523658-35523708	Hela-S3	cervix:	n/a
12	chr6:35523735-35523785	SK-N-SH_RA	brain:	n/a
13	chr6:35523700-35523750	SK-N-MC	brain:	n/a
14	chr6:35523735-35523785	AG04450	lung:	fetal
15	chr6:35523658-35523708	HRE	kidney:	n/a
16	chr6:35523658-35523708	ovcar-3	ovarian:	n/a
17	chr6:35523735-35523785	A549	lung:	n/a
18	chr6:35523735-35523785	LNCaP	prostate:	n/a
19	chr6:35523735-35523785	HCT-116	colon:	n/a
20	chr6:35523735-35523785	NHBE	bronchial:	n/a
21	chr6:35523658-35523708	HCT-116	colon:	n/a
22	chr6:35523735-35523785	GM19239	blood:	n/a
23	chr6:35523700-35523750	AoSMC	blood vessel:	n/a
24	chr6:35523658-35523708	HCM	heart:	n/a
25	chr6:35523658-35523708	SK-N-SH_RA	brain:	n/a
26	chr6:35523658-35523708	MCF-7	breast:	n/a
27	chr6:35523700-35523750	GM06990	blood:	n/a
28	chr6:35523700-35523750	PrEC	prostate:	n/a
29	chr6:35523658-35523708	HL-60	blood:	n/a
30	chr6:35523735-35523785	K562	blood:	n/a
31	chr6:35523735-35523785	NB4	blood:	n/a
32	chr6:35523700-35523750	Hela-S3	cervix:	n/a
33	chr6:35523658-35523708	GM12878	blood:	n/a
34	chr6:35523700-35523750	HAEpiC	amniotic membrane:	n/a
35	chr6:35523700-35523750	HL-60	blood:	n/a
36	chr6:35523735-35523785	GM12891	blood:	n/a
37	chr6:35523735-35523785	HNPCEpiC	eye:	n/a
38	chr6:35523658-35523708	HRCEpiC	kidney:	n/a
39	chr6:35523700-35523750	NT2-D1	testis:	n/a
40	chr6:35523658-35523708	SAEC	small airway:	n/a
41	chr6:35523658-35523708	HRPEpiC	eye:	n/a
42	chr6:35523735-35523785	AG10803	skin:	n/a
43	chr6:35523658-35523708	HEEpiC	esophagus:	n/a
44	chr6:35523658-35523708	BE2_C	brain:	n/a
45	chr6:35523700-35523750	Hepatocyte	liver:	n/a
46	chr6:35523735-35523785	PrEC	prostate:	n/a
47	chr6:35523700-35523750	A549	lung:	n/a
48	chr6:35523700-35523750	U87	brain:	n/a
49	chr6:35523735-35523785	AG04449	skin:	fetal
50	chr6:35523700-35523750	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:35525249..35527797-chr6:35704384..35706200,2	MCF-7	breast:
2	chr6:35519589..35521210-chr6:35531779..35534325,2	K562	blood:
3	chr6:35514449..35517152-chr6:35520311..35522822,2	MCF-7	breast:
4	chr6:35518936..35520877-chr6:35523519..35525721,2	K562	blood:
5	chr6:35516983..35519769-chr6:35528825..35530443,2	K562	blood:
6	chr6:35265779..35267633-chr6:35521296..35523516,2	K562	blood:
7	chr6:35439431..35441944-chr6:35514105..35515809,2	MCF-7	breast:
8	chr6:35490502..35491010-chr6:35519931..35520659,2	K562	blood:
9	chr6:35514449..35517152-chr6:35520311..35522822,2	MCF-7	breast:
10	chr6:35490359..35491197-chr6:35519826..35520699,4	MCF-7	breast:
11	chr6:35435984..35437834-chr6:35513145..35515787,2	MCF-7	breast:
12	chr6:35511057..35513907-chr6:35704750..35707121,2	K562	blood:
13	chr6:35490356..35491291-chr6:35519797..35520709,4	MCF-7	breast:
14	chr6:35441574..35443877-chr6:35520480..35522030,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL10A-1	chr6:35512992-35513446	ENSG00000228559
2	lnc-RPL10A-1	chr6:35512645-35512710	ENSG00000228559

No data

Variant related genes	Relation type
ENSG00000219023	TF binding region
ENSG00000219023	CpG island
ENSG00000157343	chromatin interactions
ENSG00000232909	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000219023	chromatin interactions

Extended variants
information (count: 618 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565494371	chr6:35512678-35512679	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs186597437	chr6:35512685-35512686	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs529372745	chr6:35512687-35512688	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs550814213	chr6:35512689-35512690	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs568799306	chr6:35512691-35512692	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs568984551	chr6:35512692-35512693	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs539263917	chr6:35512697-35512698	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs538169640	chr6:35512698-35512699	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs143399150	chr6:35512706-35512707	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs375935433	chr6:35512759-35512760	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs533531104	chr6:35512782-35512783	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554911070	chr6:35512842-35512843	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188854586	chr6:35512846-35512847	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537899248	chr6:35512847-35512848	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12195290	chr6:35512849-35512850	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs115233865	chr6:35512851-35512852	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546126133	chr6:35512889-35512890	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs12529688	chr6:35512925-35512926	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs3807050	chr6:35512926-35512927	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs540943136	chr6:35512935-35512936	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs3807049	chr6:35512955-35512956	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs148368145	chr6:35512974-35512975	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs10947556	chr6:35512979-35512980	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs562879460	chr6:35512983-35512984	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs58708511	chr6:35512987-35512988	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs12213536	chr6:35512993-35512994	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs3807048	chr6:35513016-35513017	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs533811107	chr6:35513032-35513033	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs114838524	chr6:35513066-35513067	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs78669151	chr6:35513115-35513116	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs181991470	chr6:35513116-35513117	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs73746465	chr6:35513176-35513177	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs369829076	chr6:35513244-35513245	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs571281475	chr6:35513330-35513331	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs540007256	chr6:35513381-35513382	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs73415680	chr6:35513416-35513417	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs141774688	chr6:35513443-35513444	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs147095608	chr6:35513549-35513550	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560255834	chr6:35513562-35513563	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556102377	chr6:35513566-35513567	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs531067683	chr6:35513568-35513569	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201273545	chr6:35513584-35513585	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149752545	chr6:35513592-35513593	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs575191264	chr6:35513595-35513596	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs143013269	chr6:35513596-35513597	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs552153834	chr6:35513599-35513600	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376089288	chr6:35513600-35513601	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs56140933	chr6:35513602-35513603	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs398110022	chr6:35513603-35513604	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544324948	chr6:35513622-35513623	Enhancers Weak transcription	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
Lung cancer	19153074	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35511200-35513400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr6:35511200-35514200	Enhancers	Placenta	Placenta
3	chr6:35511400-35513400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:35511600-35512800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr6:35512000-35513400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:35512200-35513200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:35512200-35513200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:35512200-35513400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:35512200-35513400	Enhancers	NHEK	skin
10	chr6:35512400-35513000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:35512400-35513000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:35512400-35513200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:35512400-35513200	Enhancers	HMEC	breast
14	chr6:35512400-35513400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:35512400-35513400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:35512400-35513400	Enhancers	Esophagus	oesophagus
17	chr6:35512400-35513400	Enhancers	Placenta Amnion	Placenta Amnion
18	chr6:35512400-35513800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:35512400-35513800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:35512600-35512800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:35512600-35512800	Enhancers	Fetal Brain Male	brain
22	chr6:35512600-35513000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:35512600-35513200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr6:35512600-35513200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:35512800-35513200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr6:35512800-35513200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:35512800-35513200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:35513000-35513400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:35513000-35513600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:35513000-35513600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:35513200-35515400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:35513400-35517400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:35513400-35517600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:35513400-35534200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:35513600-35513800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:35513800-35515200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:35514200-35515200	Weak transcription	Placenta	Placenta
38	chr6:35515200-35515600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:35515200-35516400	Enhancers	Placenta	Placenta
40	chr6:35515400-35516000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:35515400-35516000	Bivalent Enhancer	HepG2	liver
42	chr6:35515600-35515800	Bivalent/Poised TSS	Fetal Brain Male	brain
43	chr6:35515800-35516000	Active TSS	Fetal Brain Male	brain
44	chr6:35517400-35517800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:35517600-35517800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:35517800-35521000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr6:35519800-35520200	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr6:35520400-35524600	Weak transcription	Right Atrium	heart
49	chr6:35521000-35521400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:35522600-35523000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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