Variant report

Variant	esv2607475
Chromosome Location	chr6:15664805-15717086
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:602)
CpG islands
(count:367)
Chromatin interactive
region (count:99)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:15691365-15691874	K562	blood:	n/a	n/a
2	ARID3A	chr6:15691499-15691880	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:15698603-15699017	K562	blood:	n/a	n/a
4	ARID3A	chr6:15683225-15683480	K562	blood:	n/a	n/a
5	ARID3A	chr6:15683822-15683870	HepG2	liver:	n/a	n/a
6	ATF2	chr6:15691375-15691973	GM12878	blood:	n/a	n/a
7	ATF2	chr6:15691400-15691898	GM12878	blood:	n/a	n/a
8	ATF2	chr6:15691380-15691878	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr6:15691538-15691799	GM12878	blood:	n/a	n/a
10	ATF3	chr6:15691420-15691769	GM12878	blood:	n/a	chr6:15691501-15691511
11	ATF3	chr6:15698676-15699089	K562	blood:	n/a	n/a
12	BATF	chr6:15691483-15691834	GM12878	blood:	n/a	n/a
13	BATF	chr6:15678015-15678371	GM12878	blood:	n/a	n/a
14	BCLAF1	chr6:15691403-15691896	GM12878	blood:	n/a	chr6:15691691-15691700
15	BCLAF1	chr6:15691317-15691909	GM12878	blood:	n/a	chr6:15691691-15691700
16	BHLHE40	chr6:15691518-15691915	K562	blood:	n/a	n/a
17	BHLHE40	chr6:15683772-15684015	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:15691396-15691895	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:15688540-15688747	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:15698805-15698919	K562	blood:	n/a	n/a
21	BRCA1	chr6:15691452-15691834	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr6:15665612-15665662	HepG2	liver:	n/a	n/a
23	BRCA1	chr6:15691522-15691791	HepG2	liver:	n/a	n/a
24	BRCA1	chr6:15691474-15691837	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr6:15716963-15717523	K562	blood:	n/a	n/a
26	CBX3	chr6:15691376-15692144	K562	blood:	n/a	n/a
27	CBX3	chr6:15698634-15699221	K562	blood:	n/a	n/a
28	CBX3	chr6:15691461-15691900	K562	blood:	n/a	n/a
29	CBX3	chr6:15698207-15699204	K562	blood:	n/a	n/a
30	CCNT2	chr6:15691587-15691804	K562	blood:	n/a	n/a
31	CCNT2	chr6:15698772-15699124	K562	blood:	n/a	n/a
32	CEBPB	chr6:15691476-15691858	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:15690193-15690343	IMR90	lung:	n/a	chr6:15690268-15690279
34	CEBPB	chr6:15694184-15694221	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr6:15698667-15699088	K562	blood:	n/a	n/a
36	CEBPB	chr6:15690138-15690366	HepG2	liver:	n/a	chr6:15690268-15690279
37	CEBPB	chr6:15698611-15699098	K562	blood:	n/a	n/a
38	CEBPB	chr6:15690143-15690359	A549	lung:	n/a	chr6:15690268-15690279
39	CEBPB	chr6:15691593-15691749	K562	blood:	n/a	n/a
40	CEBPD	chr6:15698605-15699207	K562	blood:	n/a	n/a
41	CEBPD	chr6:15698567-15699226	K562	blood:	n/a	n/a
42	CHD2	chr6:15683538-15684126	GM12878	blood:	n/a	n/a
43	CHD2	chr6:15691473-15691850	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr6:15691572-15691900	HepG2	liver:	n/a	n/a
45	CHD2	chr6:15691495-15691900	GM12878	blood:	n/a	n/a
46	CHD2	chr6:15691507-15691828	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr6:15691483-15691832	K562	blood:	n/a	n/a
48	CREB1	chr6:15691378-15691961	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr6:15691558-15691902	A549	lung:	n/a	n/a
50	CREB1	chr6:15691477-15691865	H1-hESC	embryonic stem cell:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:15666243-15666293	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:15666243-15666293	HPAEpiC	pulmonary alveolar:	n/a
3	chr6:15675176-15675226	Caco-2	colon:	n/a
4	chr6:15666243-15666293	NH-A	brain:	n/a
5	chr6:15691717-15691767	SAEC	small airway:	n/a
6	chr6:15691800-15691850	LNCaP	prostate:	n/a
7	chr6:15675176-15675226	IMR90	lung:	fetal
8	chr6:15691800-15691850	HCPEpiC	choroid plexus:	n/a
9	chr6:15691717-15691767	Hela-S3	cervix:	n/a
10	chr6:15691717-15691767	NHBE	bronchial:	n/a
11	chr6:15691800-15691850	HEK293	kidney:	embryo
12	chr6:15691258-15691308	GM12891	blood:	n/a
13	chr6:15691717-15691767	NH-A	brain:	n/a
14	chr6:15666243-15666293	ECC-1	luminal epithelium:	n/a
15	chr6:15691258-15691308	HNPCEpiC	eye:	n/a
16	chr6:15691717-15691767	HMEC	breast:	n/a
17	chr6:15691800-15691850	HAEpiC	amniotic membrane:	n/a
18	chr6:15675176-15675226	SK-N-MC	brain:	n/a
19	chr6:15691705-15691755	HAEpiC	amniotic membrane:	n/a
20	chr6:15691717-15691767	T-47D	breast:	n/a
21	chr6:15666243-15666293	ovcar-3	ovarian:	n/a
22	chr6:15675176-15675226	HCPEpiC	choroid plexus:	n/a
23	chr6:15675176-15675226	HCF	heart:	n/a
24	chr6:15691705-15691755	AG04450	lung:	fetal
25	chr6:15691800-15691850	HRE	kidney:	n/a
26	chr6:15691800-15691850	U87	brain:	n/a
27	chr6:15666243-15666293	BJ	skin:	n/a
28	chr6:15691717-15691767	LNCaP	prostate:	n/a
29	chr6:15691800-15691850	GM06990	blood:	n/a
30	chr6:15666243-15666293	HCM	heart:	n/a
31	chr6:15691258-15691308	NHBE	bronchial:	n/a
32	chr6:15675176-15675226	CMK	blood:	n/a
33	chr6:15691258-15691308	NHDF-neo	bronchial:	n/a
34	chr6:15691258-15691308	HEEpiC	esophagus:	n/a
35	chr6:15691705-15691755	ovcar-3	ovarian:	n/a
36	chr6:15666243-15666293	HEEpiC	esophagus:	n/a
37	chr6:15691717-15691767	HEEpiC	esophagus:	n/a
38	chr6:15691717-15691767	HAEpiC	amniotic membrane:	n/a
39	chr6:15691258-15691308	A549	lung:	n/a
40	chr6:15666243-15666293	HL-60	blood:	n/a
41	chr6:15691717-15691767	NT2-D1	testis:	n/a
42	chr6:15691800-15691850	SK-N-MC	brain:	n/a
43	chr6:15691258-15691308	ProgFib	skin:	n/a
44	chr6:15675176-15675226	ProgFib	skin:	n/a
45	chr6:15675176-15675226	MCF-7	breast:	n/a
46	chr6:15691717-15691767	GM19239	blood:	n/a
47	chr6:15675176-15675226	ECC-1	luminal epithelium:	n/a
48	chr6:15666243-15666293	PrEC	prostate:	n/a
49	chr6:15691717-15691767	A549	lung:	n/a
50	chr6:15691800-15691850	NH-A	brain:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:15696754..15698975-chr6:15892314..15894571,2	K562	blood:
2	chr6:15708630..15712705-chr6:16139075..16141924,3	K562	blood:
3	chr6:15681708..15684305-chr6:15689801..15691675,2	K562	blood:
4	chr6:15672874..15675125-chr6:15675945..15678266,2	K562	blood:
5	chr6:15676839..15679833-chr6:16153654..16155926,2	K562	blood:
6	chr6:15680559..15683188-chr6:16129427..16132579,3	K562	blood:
7	chr6:15683311..15685899-chr6:16128191..16130449,3	K562	blood:
8	chr6:15688875..15695962-chr6:16127988..16134034,16	MCF-7	breast:
9	chr6:15686242..15688880-chr6:15691006..15692946,2	K562	blood:
10	chr6:15689774..15693088-chr6:16205829..16209132,3	K562	blood:
11	chr6:15668138..15670397-chr6:15673156..15674994,2	K562	blood:
12	chr6:15696979..15700313-chr6:15702500..15706211,4	K562	blood:
13	chr6:15686282..15689020-chr6:16128019..16129871,2	K562	blood:
14	chr6:15690304..15694051-chr6:16129108..16131986,7	K562	blood:
15	chr6:15676701..15679445-chr6:16128067..16130744,3	K562	blood:
16	chr6:15691584..15692147-chr6:16171307..16172061,2	MCF-7	breast:
17	chr6:15668138..15670397-chr6:15673156..15674994,2	K562	blood:
18	chr6:15689426..15691062-chr6:16188089..16190345,2	K562	blood:
19	chr6:15691034..15692122-chr6:16128597..16129547,5	K562	blood:
20	chr6:15674092..15676465-chr6:16128146..16130347,2	MCF-7	breast:
21	chr6:15692594..15695303-chr6:15695960..15699366,3	K562	blood:
22	chr6:15628080..15630749-chr6:15690393..15693220,2	K562	blood:
23	chr6:15697857..15699700-chr6:16052665..16055384,2	K562	blood:
24	chr6:15704050..15705965-chr6:16130583..16132835,2	K562	blood:
25	chr6:15657500..15659223-chr6:15666722..15668599,2	K562	blood:
26	chr6:15691382..15692187-chr6:16036682..16037471,3	MCF-7	breast:
27	chr6:15665975..15668458-chr6:16128792..16131070,2	MCF-7	breast:
28	chr6:15716067..15718297-chr6:15719116..15720796,2	K562	blood:
29	chr6:15712668..15715344-chr6:15716824..15719119,3	K562	blood:
30	chr6:15690815..15692594-chr6:16152230..16153735,2	K562	blood:
31	chr6:15704434..15705965-chr6:16129192..16132083,2	K562	blood:
32	chr6:15707898..15710276-chr6:15713020..15715412,2	K562	blood:
33	chr6:15696361..15699402-chr6:16127550..16130271,4	K562	blood:
34	chr6:15689750..15690620-chr6:16183530..16184123,2	MCF-7	breast:
35	chr6:15713813..15717822-chr6:16126996..16131137,5	K562	blood:
36	chr6:15707898..15710276-chr6:15713020..15715412,2	K562	blood:
37	chr6:15691148..15692183-chr6:16168724..16169738,7	MCF-7	breast:
38	chr6:15678826..15681687-chr6:16136285..16138589,3	K562	blood:
39	chr6:15710538..15713074-chr6:16127901..16130794,2	MCF-7	breast:
40	chr6:15670461..15672032-chr6:15680372..15682046,2	K562	blood:
41	chr6:15711716..15714538-chr6:15724011..15725713,2	K562	blood:
42	chr6:15682633..15685781-chr6:15685826..15688802,3	K562	blood:
43	chr6:15678420..15680634-chr6:15684808..15686738,2	K562	blood:
44	chr6:15661124..15663645-chr6:15690658..15693451,3	K562	blood:
45	chr6:15692594..15695303-chr6:15695960..15699366,3	K562	blood:
46	chr6:15676527..15678703-chr6:16128031..16129735,2	MCF-7	breast:
47	chr6:15660394..15662870-chr6:15679792..15681475,2	K562	blood:
48	chr6:15691300..15692107-chr6:16168761..16169885,4	MCF-7	breast:
49	chr6:15712668..15715344-chr6:15716824..15719119,3	K562	blood:
50	chr6:15670461..15672032-chr6:15680372..15682046,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTNBP1-7	chr6:15708809-15709169	NONHSAT107877
2	lnc-DTNBP1-1	chr6:15674470-15675115	XLOC_005620
3	lnc-DTNBP1-7	chr6:15708733-15708781	NONHSAT107877
4	lnc-DTNBP1-2	chr6:15695349-15695670	XLOC_005621
5	lnc-DTNBP1-1	chr6:15682235-15682336	XLOC_005620

No data

Variant related genes	Relation type
DTNBP1	TF binding region
DTNBP1	CpG island
ENSG00000047579	chromatin interactions
ENSG00000216364	chromatin interactions
ENSG00000263712	chromatin interactions
ENSG00000007944	chromatin interactions
ENSG00000271888	chromatin interactions

Extended variants
information (count: 1937 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1937 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369910133	chr6:15664813-15664814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371523621	chr6:15664817-15664818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192989096	chr6:15664824-15664825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184532642	chr6:15664837-15664838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557065530	chr6:15664997-15664998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571154656	chr6:15665040-15665041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539719003	chr6:15665101-15665102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538281737	chr6:15665104-15665105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553622375	chr6:15665108-15665109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187350469	chr6:15665162-15665163	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs541950315	chr6:15665166-15665167	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555548760	chr6:15665173-15665174	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs533123758	chr6:15665193-15665194	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12204704	chr6:15665205-15665206	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
15	rs2619538	chr6:15665209-15665210	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs533277667	chr6:15665230-15665231	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs540099599	chr6:15665231-15665232	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs559923199	chr6:15665259-15665260	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs529004688	chr6:15665296-15665297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548760969	chr6:15665355-15665356	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs568578184	chr6:15665422-15665423	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs368421194	chr6:15665438-15665439	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552212137	chr6:15665448-15665449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192540626	chr6:15665449-15665450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550976898	chr6:15665489-15665490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570725020	chr6:15665519-15665520	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs567761902	chr6:15665523-15665524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs370315725	chr6:15665529-15665530	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs76260455	chr6:15665648-15665649	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs527255795	chr6:15665695-15665696	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553658058	chr6:15665702-15665703	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs57847117	chr6:15665721-15665722	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536096805	chr6:15665802-15665803	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs547010674	chr6:15665859-15665860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555979926	chr6:15665864-15665865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541130280	chr6:15665874-15665875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184768560	chr6:15666020-15666021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189250157	chr6:15666025-15666026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557749760	chr6:15666051-15666052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs367566919	chr6:15666089-15666090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs540137770	chr6:15666129-15666130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs567168027	chr6:15666235-15666236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538934709	chr6:15666237-15666238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559198330	chr6:15666238-15666239	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373634943	chr6:15666244-15666245	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559781580	chr6:15666300-15666301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs562756953	chr6:15666303-15666304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs62395006	chr6:15666439-15666440	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550758933	chr6:15666480-15666481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs180797130	chr6:15666489-15666490	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	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
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17142309	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian cancer	20844748	CNVD
Developmental delay	19490664	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15663800-15665200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:15664000-15668200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:15664200-15668400	Weak transcription	K562	blood
4	chr6:15668200-15668600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr6:15668400-15668600	Enhancers	K562	blood
6	chr6:15668600-15669400	Weak transcription	K562	blood
7	chr6:15669400-15669600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:15669400-15669600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr6:15669400-15669600	Enhancers	K562	blood
10	chr6:15671400-15672200	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr6:15671800-15672600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr6:15671800-15673400	Enhancers	Fetal Muscle Leg	muscle
13	chr6:15671800-15674800	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr6:15672000-15673200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr6:15672000-15673600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr6:15672200-15672400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:15672200-15672600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr6:15672200-15672800	Enhancers	Psoas Muscle	Psoas
19	chr6:15672200-15673200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr6:15672400-15672800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:15672400-15672800	Enhancers	Esophagus	oesophagus
22	chr6:15672400-15675200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:15672600-15672800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:15672600-15674800	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:15672800-15674400	Weak transcription	Psoas Muscle	Psoas
26	chr6:15672800-15674600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr6:15672800-15674800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:15672800-15677200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:15673200-15674400	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr6:15673200-15674600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr6:15673200-15677400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:15673400-15673800	Weak transcription	Fetal Muscle Leg	muscle
33	chr6:15673600-15674000	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr6:15673800-15676400	Enhancers	Fetal Muscle Leg	muscle
35	chr6:15674000-15674200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
36	chr6:15674000-15677000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr6:15674400-15675000	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr6:15674400-15675200	Enhancers	Fetal Muscle Trunk	muscle
39	chr6:15674400-15676600	Enhancers	Psoas Muscle	Psoas
40	chr6:15674600-15676400	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr6:15674600-15676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:15674800-15675200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr6:15674800-15675600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr6:15674800-15675800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr6:15674800-15676200	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr6:15674800-15676600	Enhancers	Primary hematopoietic stem cells	blood
47	chr6:15674800-15676600	Enhancers	Brain Anterior Caudate	brain
48	chr6:15674800-15676800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:15675000-15675200	Bivalent Enhancer	Small Intestine	intestine
50	chr6:15675000-15675400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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