Variant report

Variant	esv3384463
Chromosome Location	chr6:28759027-28776259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:676)
CpG islands
(count:488)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:28762543-28762667	K562	blood:	n/a	n/a
2	ARID3A	chr6:28770404-28770887	K562	blood:	n/a	n/a
3	ARID3A	chr6:28763610-28764071	K562	blood:	n/a	n/a
4	ARID3A	chr6:28770461-28770741	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:28763574-28764023	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:28775492-28775915	K562	blood:	n/a	n/a
7	ATF1	chr6:28775513-28775854	K562	blood:	n/a	n/a
8	ATF1	chr6:28762398-28762773	K562	blood:	n/a	n/a
9	ATF1	chr6:28771747-28771919	K562	blood:	n/a	n/a
10	ATF1	chr6:28770452-28770723	K562	blood:	n/a	n/a
11	ATF1	chr6:28763618-28763987	K562	blood:	n/a	n/a
12	ATF2	chr6:28763561-28763996	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr6:28775485-28775878	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:28763620-28764042	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr6:28763329-28764114	A549	lung:	n/a	n/a
16	ATF3	chr6:28770218-28770915	A549	lung:	n/a	n/a
17	ATF3	chr6:28758277-28759227	K562	blood:	n/a	n/a
18	ATF3	chr6:28770324-28770803	HCT-116	colon:	n/a	n/a
19	ATF3	chr6:28763426-28764070	HCT-116	colon:	n/a	n/a
20	ATF3	chr6:28770240-28770785	HCT-116	colon:	n/a	n/a
21	ATF3	chr6:28763482-28764170	HCT-116	colon:	n/a	n/a
22	ATF3	chr6:28770153-28770948	A549	lung:	n/a	n/a
23	ATF3	chr6:28775377-28775970	A549	lung:	n/a	n/a
24	ATF3	chr6:28775351-28776014	K562	blood:	n/a	n/a
25	ATF3	chr6:28763298-28764145	A549	lung:	n/a	n/a
26	ATF3	chr6:28770191-28770826	K562	blood:	n/a	n/a
27	ATF3	chr6:28775354-28776109	A549	lung:	n/a	n/a
28	ATF3	chr6:28775486-28775995	HCT-116	colon:	n/a	n/a
29	ATF3	chr6:28775382-28775972	HCT-116	colon:	n/a	n/a
30	ATF3	chr6:28763359-28764090	K562	blood:	n/a	n/a
31	BATF	chr6:28775490-28775810	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:28770522-28770819	GM12878	blood:	n/a	chr6:28770688-28770697
33	BDP1	chr6:28775505-28775933	Hela-S3	cervix:	n/a	n/a
34	BDP1	chr6:28775501-28775941	K562	blood:	n/a	n/a
35	BDP1	chr6:28763621-28764049	K562	blood:	n/a	n/a
36	BDP1	chr6:28770461-28770892	K562	blood:	n/a	n/a
37	BDP1	chr6:28770463-28770856	Hela-S3	cervix:	n/a	n/a
38	BDP1	chr6:28763601-28764051	Hela-S3	cervix:	n/a	n/a
39	BHLHE40	chr6:28763641-28763988	K562	blood:	n/a	n/a
40	BHLHE40	chr6:28762434-28762748	K562	blood:	n/a	n/a
41	BHLHE40	chr6:28763665-28763926	HepG2	liver:	n/a	n/a
42	BHLHE40	chr6:28770487-28770671	HepG2	liver:	n/a	n/a
43	BRCA1	chr6:28763607-28763979	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr6:28775528-28775859	Hela-S3	cervix:	n/a	chr6:28775765-28775772
45	BRCA1	chr6:28770480-28770733	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr6:28775529-28775782	H1-hESC	embryonic stem cell:	n/a	chr6:28775765-28775772
47	BRF1	chr6:28763679-28763999	Hela-S3	cervix:	n/a	n/a
48	BRF1	chr6:28775531-28775882	Hela-S3	cervix:	n/a	n/a
49	BRF1	chr6:28763655-28764010	K562	blood:	n/a	n/a
50	BRF1	chr6:28775524-28775880	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:28770623-28770673	HCT-116	colon:	n/a
2	chr6:28762288-28762338	AG10803	skin:	n/a
3	chr6:28770623-28770673	GM12891	blood:	n/a
4	chr6:28770623-28770673	Jurkat	blood:	n/a
5	chr6:28762471-28762521	HCM	heart:	n/a
6	chr6:28762288-28762338	HEK293	kidney:	embryo
7	chr6:28761989-28762039	AG04450	lung:	fetal
8	chr6:28762552-28762602	ECC-1	luminal epithelium:	n/a
9	chr6:28761989-28762039	Caco-2	colon:	n/a
10	chr6:28761989-28762039	PrEC	prostate:	n/a
11	chr6:28762552-28762602	PANC-1	pancreas:	n/a
12	chr6:28761989-28762039	H1-hESC	embryonic stem cell:	embryo
13	chr6:28761989-28762039	HAEpiC	amniotic membrane:	n/a
14	chr6:28770593-28770643	PFSK-1	brain:	n/a
15	chr6:28762552-28762602	HEK293	kidney:	embryo
16	chr6:28770623-28770673	BE2_C	brain:	n/a
17	chr6:28762288-28762338	GM12891	blood:	n/a
18	chr6:28770623-28770673	GM06990	blood:	n/a
19	chr6:28762471-28762521	HCPEpiC	choroid plexus:	n/a
20	chr6:28770623-28770673	NHDF-neo	bronchial:	n/a
21	chr6:28762125-28762175	HEK293	kidney:	embryo
22	chr6:28762288-28762338	GM19239	blood:	n/a
23	chr6:28770593-28770643	T-47D	breast:	n/a
24	chr6:28762544-28762594	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:28762471-28762521	HEK293	kidney:	embryo
26	chr6:28762288-28762338	BE2_C	brain:	n/a
27	chr6:28761989-28762039	MCF10A-Er-Src	breast:	n/a
28	chr6:28762288-28762338	NHDF-neo	bronchial:	n/a
29	chr6:28770593-28770643	HEK293	kidney:	embryo
30	chr6:28770593-28770643	IMR90	lung:	fetal
31	chr6:28762288-28762338	SK-N-SH_RA	brain:	n/a
32	chr6:28770593-28770643	PrEC	prostate:	n/a
33	chr6:28762288-28762338	HEEpiC	esophagus:	n/a
34	chr6:28762288-28762338	Hepatocyte	liver:	n/a
35	chr6:28762544-28762594	GM12878	blood:	n/a
36	chr6:28770623-28770673	BJ	skin:	n/a
37	chr6:28762125-28762175	A549	lung:	n/a
38	chr6:28770593-28770643	HCPEpiC	choroid plexus:	n/a
39	chr6:28761989-28762039	A549	lung:	n/a
40	chr6:28762552-28762602	GM12878	blood:	n/a
41	chr6:28762544-28762594	HMEC	breast:	n/a
42	chr6:28770623-28770673	HNPCEpiC	eye:	n/a
43	chr6:28762288-28762338	ovcar-3	ovarian:	n/a
44	chr6:28770623-28770673	AG10803	skin:	n/a
45	chr6:28770623-28770673	PANC-1	pancreas:	n/a
46	chr6:28770623-28770673	H1-hESC	embryonic stem cell:	embryo
47	chr6:28770623-28770673	SK-N-MC	brain:	n/a
48	chr6:28770593-28770643	Hela-S3	cervix:	n/a
49	chr6:28761989-28762039	GM19239	blood:	n/a
50	chr6:28762544-28762594	K562	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:28757752..28760408-chr6:28765977..28767794,2	K562	blood:
2	chr6:28691994..28695396-chr6:28761030..28763739,3	K562	blood:
3	chr6:28757752..28760408-chr6:28765977..28767794,2	K562	blood:
4	chr6:28760359..28762539-chr6:28774291..28776179,2	K562	blood:
5	chr6:28758828..28759555-chr9:136657868..136658790,2	MCF-7	breast:
6	chr6:28774860..28778003-chr6:28805367..28807894,3	K562	blood:
7	chr6:28734776..28737188-chr6:28758091..28759724,2	K562	blood:
8	chr6:28774872..28779186-chr6:28780865..28786550,9	K562	blood:
9	chr6:28761882..28764605-chr6:28861705..28864953,3	K562	blood:
10	chr6:28756425..28760621-chr6:28761088..28764506,5	K562	blood:
11	chr6:28755863..28759570-chr6:28911484..28914475,3	K562	blood:
12	chr6:28739775..28742884-chr6:28756307..28759477,3	K562	blood:
13	chr6:28761012..28764011-chr6:28768099..28770643,2	K562	blood:
14	chr6:28770520..28773672-chr6:28829844..28832870,3	K562	blood:
15	chr6:28771451..28773263-chr6:28777101..28779175,2	K562	blood:
16	chr6:28761080..28764011-chr6:28767880..28769599,2	K562	blood:
17	chr6:28723125..28726078-chr6:28775767..28777359,2	K562	blood:
18	chr6:28695047..28697144-chr6:28756622..28759292,2	K562	blood:
19	chr6:28692257..28693945-chr6:28757387..28759135,2	K562	blood:
20	chr6:28770558..28773254-chr6:28806737..28808772,2	K562	blood:
21	chr6:28725484..28727930-chr6:28757614..28759136,2	K562	blood:
22	chr6:28756573..28759569-chr6:28769791..28772080,4	K562	blood:
23	chr6:28686813..28689115-chr6:28758010..28760174,2	K562	blood:
24	chr6:28769803..28772263-chr6:28862688..28865946,3	MCF-7	breast:
25	chr6:28762168..28764957-chr6:28971752..28974125,2	K562	blood:
26	chr6:28767356..28769263-chr6:28782865..28784537,2	K562	blood:
27	chr6:28768996..28771268-chr6:28774440..28778213,3	K562	blood:
28	chr6:28760359..28762539-chr6:28774291..28776179,2	K562	blood:
29	chr6:28772556..28774593-chr6:28785044..28786627,2	K562	blood:
30	chr6:28752766..28756379-chr6:28756550..28759154,4	K562	blood:
31	chr6:28768996..28771268-chr6:28774440..28778213,3	K562	blood:
32	chr6:28775179..28778043-chr6:28889400..28891921,3	MCF-7	breast:
33	chr6:28756573..28759569-chr6:28769791..28772080,4	K562	blood:
34	chr6:28769403..28772112-chr6:28910261..28912768,2	K562	blood:
35	chr6:28771461..28773672-chr6:28829844..28832711,2	K562	blood:
36	chr6:28760359..28764219-chr6:28771578..28776179,5	K562	blood:
37	chr6:28743173..28744938-chr6:28758816..28760398,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM27-18	chr6:28773744-28776603	NONHSAT108486
2	lnc-TRIM27-19	chr6:28770349-28770592	NONHSAT108485

No data

Variant related genes	Relation type
ENSG00000265764	TF binding region
ENSG00000265764	CpG island
ENSG00000204713	chromatin interactions
ENSG00000265764	chromatin interactions
ENSG00000224157	chromatin interactions
ENSG00000221191	chromatin interactions
ENSG00000225595	chromatin interactions
ENSG00000225173	chromatin interactions
ENSG00000197935	chromatin interactions
ENSG00000204709	chromatin interactions

Extended variants
information (count: 722 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190527249	chr6:28759077-28759078	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs556041747	chr6:28759241-28759242	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs138166366	chr6:28759245-28759246	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs574717372	chr6:28759251-28759252	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs539910555	chr6:28759266-28759267	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141828575	chr6:28759284-28759285	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs576384856	chr6:28759291-28759292	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs545830916	chr6:28759319-28759320	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs150623849	chr6:28759330-28759331	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs138770320	chr6:28759363-28759364	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs149382265	chr6:28759421-28759422	Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs561831002	chr6:28759524-28759525	Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs116010379	chr6:28759594-28759595	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547067026	chr6:28759635-28759636	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182231459	chr6:28759644-28759645	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532390439	chr6:28759691-28759692	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs12665150	chr6:28759703-28759704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528539267	chr6:28759758-28759759	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544146725	chr6:28759780-28759781	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372931596	chr6:28759781-28759782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs552573814	chr6:28759815-28759816	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569425481	chr6:28759828-28759829	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs538500505	chr6:28759841-28759842	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs116361574	chr6:28759854-28759855	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs147496605	chr6:28759889-28759890	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186036602	chr6:28759899-28759900	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370218824	chr6:28759904-28759905	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs529330434	chr6:28759906-28759907	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372992458	chr6:28759933-28759934	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576912846	chr6:28759967-28759968	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190798079	chr6:28759968-28759969	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545467945	chr6:28759982-28759983	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs556152835	chr6:28759999-28760000	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575970632	chr6:28760017-28760018	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374193501	chr6:28760030-28760031	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111463907	chr6:28760123-28760124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs533538404	chr6:28760133-28760134	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs9280472	chr6:28760137-28760138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561966064	chr6:28760200-28760201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs537871337	chr6:28760303-28760304	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs148852436	chr6:28760340-28760341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553007298	chr6:28760349-28760350	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181607555	chr6:28760392-28760393	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541267859	chr6:28760466-28760467	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185541218	chr6:28760484-28760485	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560550069	chr6:28760523-28760524	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191242763	chr6:28760546-28760547	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs2754761	chr6:28760601-28760602	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs569201877	chr6:28760608-28760609	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140090646	chr6:28760615-28760616	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	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
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
Breast cancer	22032731	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
T-cell lymphomas	19863542	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
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	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

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28756400-28759200	Active TSS	A549	lung
2	chr6:28756800-28759200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
3	chr6:28757400-28759200	Active TSS	H9 Cell Line	embryonic stem cell
4	chr6:28757600-28759200	Active TSS	Hela-S3	cervix
5	chr6:28758200-28761600	Weak transcription	HMEC	breast
6	chr6:28758400-28761600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:28758400-28761800	Weak transcription	HSMMtube	muscle
8	chr6:28758600-28759200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:28758600-28759600	Flanking Active TSS	HepG2	liver
10	chr6:28758800-28759200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
11	chr6:28758800-28759200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:28758800-28759200	Enhancers	NHEK	skin
13	chr6:28758800-28761800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:28758800-28761800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:28759000-28759200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr6:28759000-28759200	Flanking Active TSS	Placenta	Placenta
17	chr6:28759000-28759200	Enhancers	GM12878-XiMat	blood
18	chr6:28759000-28759400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr6:28759000-28759400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
20	chr6:28759000-28759400	Enhancers	Osteobl	bone
21	chr6:28759000-28759600	Flanking Active TSS	K562	blood
22	chr6:28759200-28759400	Flanking Active TSS	A549	lung
23	chr6:28759200-28759600	Flanking Active TSS	Hela-S3	cervix
24	chr6:28759400-28761800	Weak transcription	A549	lung
25	chr6:28759600-28760200	Enhancers	HepG2	liver
26	chr6:28759600-28760200	Enhancers	K562	blood
27	chr6:28759600-28763600	Weak transcription	Hela-S3	cervix
28	chr6:28760200-28761400	Weak transcription	HepG2	liver
29	chr6:28760200-28761400	Weak transcription	K562	blood
30	chr6:28760400-28761400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
31	chr6:28761400-28761600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:28761400-28761600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:28761400-28761800	Enhancers	HepG2	liver
34	chr6:28761400-28761800	Enhancers	K562	blood
35	chr6:28761600-28761800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:28761600-28762200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:28761600-28762400	Active TSS	HMEC	breast
38	chr6:28761600-28762600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr6:28761600-28762600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:28761600-28762800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:28761600-28762800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:28761600-28763000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
43	chr6:28761600-28763000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
44	chr6:28761600-28763800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
45	chr6:28761600-28764600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr6:28761800-28762000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:28761800-28762000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
48	chr6:28761800-28762000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
49	chr6:28761800-28762000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:28761800-28762000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain

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