Variant report

Variant	nsv884058
Chromosome Location	chr6:30182395-30202429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:434)
CpG islands
(count:305)
Chromatin interactive
region (count:26)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:30186939-30187273	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:30186958-30187227	K562	blood:	n/a	n/a
3	ATF2	chr6:30180810-30182485	GM12878	blood:	n/a	chr6:30181297-30181308 chr6:30181959-30181970
4	BATF	chr6:30202214-30202520	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:30195665-30195980	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:30186999-30187199	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:30187102-30187161	K562	blood:	n/a	n/a
8	BRCA1	chr6:30187010-30187210	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:30201895-30202361	Hela-S3	cervix:	n/a	chr6:30202280-30202291
10	CEBPB	chr6:30202194-30202412	HepG2	liver:	n/a	chr6:30202280-30202291
11	CEBPB	chr6:30202205-30202406	IMR90	lung:	n/a	chr6:30202280-30202291
12	CEBPB	chr6:30182363-30182424	A549	lung:	n/a	chr6:30182375-30182388
13	CEBPB	chr6:30182258-30182538	HepG2	liver:	n/a	chr6:30182375-30182388
14	CEBPB	chr6:30182045-30182472	Hela-S3	cervix:	n/a	chr6:30182375-30182388
15	CHD1	chr6:30186997-30187159	GM12878	blood:	n/a	n/a
16	CHD2	chr6:30180781-30182509	GM12878	blood:	n/a	n/a
17	CHD2	chr6:30187095-30187313	GM12878	blood:	n/a	n/a
18	CREB1	chr6:30180777-30182461	GM12878	blood:	n/a	n/a
19	CREB1	chr6:30180791-30182464	GM12878	blood:	n/a	n/a
20	CREB1	chr6:30180668-30182533	HepG2	liver:	n/a	n/a
21	CREB1	chr6:30187082-30187339	A549	lung:	n/a	n/a
22	CREB1	chr6:30180668-30182724	HepG2	liver:	n/a	n/a
23	CTCF	chr6:30187040-30187190	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr6:30187080-30187230	GM12864	blood:	n/a	n/a
25	CTCF	chr6:30187040-30187190	AG04450	lung:	n/a	n/a
26	CTCF	chr6:30187040-30187190	AG04449	skin:	n/a	n/a
27	CTCF	chr6:30187040-30187190	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr6:30186918-30187372	K562	blood:	n/a	n/a
29	CTCF	chr6:30187073-30187278	GM12891	blood:	n/a	n/a
30	CTCF	chr6:30187060-30187210	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr6:30187040-30187190	BE2_C	brain:	n/a	n/a
32	CTCF	chr6:30187080-30187230	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr6:30187040-30187190	SAEC	small airway:	n/a	n/a
34	CTCF	chr6:30186939-30187286	HepG2	liver:	n/a	n/a
35	CTCF	chr6:30187026-30187286	GM19238	blood:	n/a	n/a
36	CTCF	chr6:30186863-30187499	HCT-116	colon:	n/a	n/a
37	CTCF	chr6:30187080-30187230	GM12870	blood:	n/a	n/a
38	CTCF	chr6:30187040-30187190	NHEK	skin:	n/a	n/a
39	CTCF	chr6:30187060-30187210	Caco-2	colon:	n/a	n/a
40	CTCF	chr6:30182260-30182410	GM12864	blood:	n/a	n/a
41	CTCF	chr6:30187060-30187210	HCFaa	heart:	n/a	n/a
42	CTCF	chr6:30187080-30187230	GM12871	blood:	n/a	n/a
43	CTCF	chr6:30187020-30187170	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr6:30186916-30187321	IMR90	lung:	n/a	n/a
45	CTCF	chr6:30187040-30187190	AG10803	skin:	n/a	n/a
46	CTCF	chr6:30186935-30187318	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr6:30187100-30187250	GM12875	blood:	n/a	n/a
48	CTCF	chr6:30187060-30187210	GM12874	blood:	n/a	n/a
49	CTCF	chr6:30187060-30187210	GM12864	blood:	n/a	n/a
50	CTCF	chr6:30186985-30187270	Lung_OC	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30182518-30182568	PrEC	prostate:	n/a
2	chr6:30182349-30182399	HIPEpiC	eye:	n/a
3	chr6:30182563-30182613	RPTEC	kidney:	n/a
4	chr6:30182349-30182399	NB4	blood:	n/a
5	chr6:30182349-30182399	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:30182349-30182399	HRPEpiC	eye:	n/a
7	chr6:30185818-30185868	HEK293	kidney:	embryo
8	chr6:30182349-30182399	Caco-2	colon:	n/a
9	chr6:30182349-30182399	NHDF-neo	bronchial:	n/a
10	chr6:30182507-30182557	SAEC	small airway:	n/a
11	chr6:30182349-30182399	SK-N-MC	brain:	n/a
12	chr6:30182349-30182399	RPTEC	kidney:	n/a
13	chr6:30182507-30182557	HCT-116	colon:	n/a
14	chr6:30182507-30182557	GM12878	blood:	n/a
15	chr6:30182563-30182613	HIPEpiC	eye:	n/a
16	chr6:30182507-30182557	CMK	blood:	n/a
17	chr6:30182349-30182399	HAEpiC	amniotic membrane:	n/a
18	chr6:30182518-30182568	HUVEC	blood vessel:	n/a
19	chr6:30182563-30182613	SK-N-SH	brain:	n/a
20	chr6:30182518-30182568	HRE	kidney:	n/a
21	chr6:30182518-30182568	HCM	heart:	n/a
22	chr6:30182563-30182613	Hela-S3	cervix:	n/a
23	chr6:30182563-30182613	HRCEpiC	kidney:	n/a
24	chr6:30185818-30185868	HCM	heart:	n/a
25	chr6:30182507-30182557	HMEC	breast:	n/a
26	chr6:30182507-30182557	HCF	heart:	n/a
27	chr6:30182563-30182613	AG04450	lung:	fetal
28	chr6:30182563-30182613	PFSK-1	brain:	n/a
29	chr6:30182563-30182613	NT2-D1	testis:	n/a
30	chr6:30185818-30185868	SK-N-MC	brain:	n/a
31	chr6:30182349-30182399	GM12892	blood:	n/a
32	chr6:30182349-30182399	HMEC	breast:	n/a
33	chr6:30182507-30182557	GM06990	blood:	n/a
34	chr6:30182563-30182613	HMEC	breast:	n/a
35	chr6:30182349-30182399	U87	brain:	n/a
36	chr6:30185818-30185868	NT2-D1	testis:	n/a
37	chr6:30182563-30182613	NH-A	brain:	n/a
38	chr6:30182563-30182613	NHDF-neo	bronchial:	n/a
39	chr6:30182518-30182568	AG10803	skin:	n/a
40	chr6:30185818-30185868	K562	blood:	n/a
41	chr6:30182518-30182568	HCPEpiC	choroid plexus:	n/a
42	chr6:30182518-30182568	SAEC	small airway:	n/a
43	chr6:30182349-30182399	HCPEpiC	choroid plexus:	n/a
44	chr6:30182518-30182568	A549	lung:	n/a
45	chr6:30182349-30182399	HNPCEpiC	eye:	n/a
46	chr6:30182518-30182568	PFSK-1	brain:	n/a
47	chr6:30182507-30182557	AG09319	gingival:	n/a
48	chr6:30182349-30182399	HCT-116	colon:	n/a
49	chr6:30182349-30182399	ovcar-3	ovarian:	n/a
50	chr6:30182563-30182613	BE2_C	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30182391..30184727-chr6:30190494..30193163,2	MCF-7	breast:
2	chr6:30032989..30035787-chr6:30185731..30187917,2	MCF-7	breast:
3	chr6:30186843..30187585-chr6:30364587..30365117,2	MCF-7	breast:
4	chr6:30180733..30183619-chr6:30310467..30312981,3	MCF-7	breast:
5	chr17:27052665..27053186-chr6:30181676..30182430,2	Hela-S3	cervix:
6	chr6:30182772..30184809-chr6:30214077..30216863,2	K562	blood:
7	chr6:30188017..30189614-chr6:30314561..30316760,2	MCF-7	breast:
8	chr6:30194307..30196564-chr6:30200875..30202443,2	K562	blood:
9	chr6:30172695..30175243-chr6:30183856..30185988,2	K562	blood:
10	chr6:30156337..30158600-chr6:30180750..30182606,2	MCF-7	breast:
11	chr6:30187236..30189646-chr6:30189831..30192507,2	K562	blood:
12	chr6:30068684..30075353-chr6:30179679..30184952,7	MCF-7	breast:
13	chr2:149810082..149810583-chr6:30185481..30185981,2	Hela-S3	cervix:
14	chr6:30182145..30184666-chr6:30223310..30225294,2	MCF-7	breast:
15	chr6:30187236..30189646-chr6:30189831..30192507,2	K562	blood:
16	chr6:30175583..30179292-chr6:30184478..30187344,3	K562	blood:
17	chr6:30181485..30183400-chr6:30291563..30295527,5	MCF-7	breast:
18	chr6:30200513..30202643-chr6:30293738..30295917,2	MCF-7	breast:
19	chr6:30178310..30184484-chr6:30311860..30320436,13	MCF-7	breast:
20	chr6:30178635..30184988-chr6:30292357..30296104,9	MCF-7	breast:
21	chr6:30185779..30188163-chr6:30312459..30314446,2	MCF-7	breast:
22	chr16:931776..932561-chr6:30187031..30187732,2	MCF-7	breast:
23	chr15:75744964..75747465-chr6:30180922..30182722,2	MCF-7	breast:
24	chr6:30182391..30184727-chr6:30190494..30193163,2	MCF-7	breast:
25	chr6:30186670..30187594-chr6:30364355..30365372,7	K562	blood:
26	chr6:30033185..30035212-chr6:30180473..30182741,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM26-2	chr6:30201166-30203164	ucscGeneNc_uc003npj_2
2	lnc-TRIM26-2	chr6:30202135-30202227	ENSG00000242996
3	lnc-TRIM26-2	chr6:30201816-30202045	ENSG00000242996
4	lnc-TRIM26-2	chr6:30202135-30202254	ENSG00000242996
5	lnc-TRIM26-2	chr6:30201816-30202045	ENSG00000242996

No data

Variant related genes	Relation type
HCG17	TF binding region
TRIM26	TF binding region
TRIM26BP	TF binding region
HCG17	CpG island
TRIM26	CpG island
TRIM26BP	CpG island
ENSG00000160602	chromatin interactions
ENSG00000224372	chromatin interactions
ENSG00000231226	chromatin interactions
ENSG00000233892	chromatin interactions
ENSG00000231074	chromatin interactions
ENSG00000241370	chromatin interactions
ENSG00000270604	chromatin interactions
ENSG00000204616	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000234127	chromatin interactions
ENSG00000204599	chromatin interactions
ENSG00000204619	chromatin interactions

Extended variants
information (count: 507 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1345229	chr6:30182395-30182396	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529842818	chr6:30182458-30182459	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs546261621	chr6:30182508-30182509	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs566247207	chr6:30182623-30182624	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs532143751	chr6:30182679-30182680	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs552131454	chr6:30182680-30182681	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs568808563	chr6:30182684-30182685	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs529836804	chr6:30182717-30182718	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs549107595	chr6:30182744-30182745	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs371913763	chr6:30182764-30182765	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs77417865	chr6:30182808-30182809	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs77088087	chr6:30182810-30182811	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs537881738	chr6:30182816-30182817	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs3132669	chr6:30182826-30182827	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs571862408	chr6:30182827-30182828	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs182057965	chr6:30182829-30182830	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs575239395	chr6:30183029-30183030	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs575804373	chr6:30183060-30183061	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs368042018	chr6:30183061-30183062	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs546033599	chr6:30183124-30183125	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs564336047	chr6:30183153-30183154	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs573359622	chr6:30183177-30183178	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs545198792	chr6:30183222-30183223	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs558902600	chr6:30183244-30183245	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs200341406	chr6:30183307-30183308	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs149847286	chr6:30183312-30183313	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs186269773	chr6:30183423-30183424	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs190454750	chr6:30183424-30183425	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs529808118	chr6:30183460-30183461	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs540025201	chr6:30183463-30183464	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs144854735	chr6:30183487-30183488	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs532233596	chr6:30183523-30183524	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs552024135	chr6:30183566-30183567	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs554409878	chr6:30183638-30183639	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs4713300	chr6:30183667-30183668	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs4713301	chr6:30183668-30183669	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs182707942	chr6:30183674-30183675	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs113271514	chr6:30183675-30183676	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs185557674	chr6:30183721-30183722	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs371811214	chr6:30183727-30183728	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs531210326	chr6:30183737-30183738	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs190854542	chr6:30183776-30183777	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs567975197	chr6:30183807-30183808	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs536979134	chr6:30183871-30183872	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs555865554	chr6:30183885-30183886	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs182953702	chr6:30183889-30183890	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs187541717	chr6:30183969-30183970	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs201309891	chr6:30184133-30184134	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs2523723	chr6:30184176-30184177	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs73726125	chr6:30184180-30184181	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:111)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung 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
Ovarian cancer	21781307	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
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	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
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	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
Myelofibrosis	22110671	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
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30179400-30182400	Active TSS	Fetal Intestine Small	intestine
2	chr6:30179600-30182400	Active TSS	Esophagus	oesophagus
3	chr6:30179800-30182400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:30179800-30182400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:30179800-30182400	Active TSS	Aorta	Aorta
6	chr6:30179800-30182400	Active TSS	A549	lung
7	chr6:30179800-30182600	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr6:30179800-30182600	Active TSS	Lung	lung
9	chr6:30180000-30182400	Active TSS	H1 Cell Line	embryonic stem cell
10	chr6:30180000-30182400	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr6:30180000-30182400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:30180000-30182400	Active TSS	Fetal Intestine Large	intestine
13	chr6:30180000-30182400	Active TSS	Right Ventricle	heart
14	chr6:30180000-30182600	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr6:30180000-30182600	Active TSS	H9 Cell Line	embryonic stem cell
16	chr6:30180000-30182600	Active TSS	Psoas Muscle	Psoas
17	chr6:30180000-30182600	Active TSS	Right Atrium	heart
18	chr6:30180200-30182400	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr6:30180200-30182400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:30180200-30182400	Active TSS	Brain Substantia Nigra	brain
21	chr6:30180200-30182400	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr6:30180200-30182400	Active TSS	Stomach Mucosa	stomach
23	chr6:30180200-30182400	Active TSS	NHDF-Ad	bronchial
24	chr6:30180200-30182400	Active TSS	NHLF	lung
25	chr6:30180200-30182600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:30180200-30182600	Active TSS	Fetal Lung	lung
27	chr6:30180200-30182600	Active TSS	HSMMtube	muscle
28	chr6:30180200-30182800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:30180400-30182400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr6:30180400-30182400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:30180400-30182400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:30180400-30182400	Active TSS	Primary T killer memory cells from peripheral blood	blood
33	chr6:30180400-30182400	Active TSS	Brain Cingulate Gyrus	brain
34	chr6:30180400-30182400	Active TSS	Duodenum Mucosa	Duodenum
35	chr6:30180400-30182400	Active TSS	Left Ventricle	heart
36	chr6:30180400-30182400	Active TSS	Ovary	ovary
37	chr6:30180400-30182400	Active TSS	Placenta Amnion	Placenta Amnion
38	chr6:30180400-30182400	Active TSS	Sigmoid Colon	Sigmoid Colon
39	chr6:30180400-30182600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
40	chr6:30180400-30182600	Active TSS	Brain Angular Gyrus	brain
41	chr6:30180400-30182600	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr6:30180400-30182600	Active TSS	Small Intestine	intestine
43	chr6:30180400-30182800	Active TSS	HSMM	muscle
44	chr6:30180600-30182400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr6:30180600-30182400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:30180600-30182400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:30180600-30182400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:30180600-30182400	Active TSS	Fetal Kidney	kidney
49	chr6:30180600-30182600	Active TSS	Pancreas	Pancrea
50	chr6:30180600-30182800	Active TSS	HUES64 Cell Line	embryonic stem cell

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