Variant report

Variant	nsv1012903
Chromosome Location	chr3:49978765-50071878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:264)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:50010077-50010258	HepG2	liver:	n/a	n/a
2	ATF1	chr3:49998077-49998258	K562	blood:	n/a	n/a
3	ATF2	chr3:49984110-49984569	GM12878	blood:	n/a	n/a
4	BCL3	chr3:50007112-50007395	GM12878	blood:	n/a	n/a
5	BCL3	chr3:50021819-50022276	GM12878	blood:	n/a	n/a
6	BCL3	chr3:50007049-50007308	GM12878	blood:	n/a	n/a
7	BCL3	chr3:50021837-50022242	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:49984582-49984855	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:50035994-50036087	GM12878	blood:	n/a	n/a
10	CEBPB	chr3:50010037-50010374	HepG2	liver:	n/a	chr3:50010201-50010212 chr3:50010201-50010210 chr3:50010199-50010210
11	CEBPB	chr3:49979844-49979969	K562	blood:	n/a	n/a
12	CEBPB	chr3:50007699-50007754	K562	blood:	n/a	chr3:50007703-50007714
13	CEBPB	chr3:49995214-49995414	HepG2	liver:	n/a	chr3:49995320-49995331
14	CEBPB	chr3:50010036-50010338	IMR90	lung:	n/a	chr3:50010201-50010212 chr3:50010201-50010210 chr3:50010199-50010210
15	CEBPB	chr3:50007594-50007814	HepG2	liver:	n/a	chr3:50007703-50007714
16	CEBPB	chr3:49995211-49995383	K562	blood:	n/a	chr3:49995320-49995331
17	CEBPB	chr3:50010651-50011119	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:50016463-50016773	Hela-S3	cervix:	n/a	chr3:50016616-50016627
19	CEBPB	chr3:50016444-50016811	K562	blood:	n/a	chr3:50016616-50016627
20	CEBPB	chr3:50016444-50016803	IMR90	lung:	n/a	chr3:50016616-50016627
21	CEBPB	chr3:50016452-50016777	HepG2	liver:	n/a	chr3:50016616-50016627
22	CEBPB	chr3:50021981-50022233	HepG2	liver:	n/a	chr3:50022094-50022105
23	CEBPB	chr3:50016473-50016753	A549	lung:	n/a	chr3:50016616-50016627
24	CEBPB	chr3:50027530-50027686	HepG2	liver:	n/a	chr3:50027573-50027584
25	CREB1	chr3:50021884-50022195	GM12878	blood:	n/a	n/a
26	CREB1	chr3:49984170-49984513	GM12878	blood:	n/a	n/a
27	CREB1	chr3:50021905-50022198	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr3:50035960-50036110	BJ	skin:	n/a	n/a
29	CTCF	chr3:50021991-50022106	GM19239	blood:	n/a	n/a
30	CTCF	chr3:50035890-50035997	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr3:50058971-50058993	GM13976	blood:	n/a	n/a
32	CTCF	chr3:50035851-50036006	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr3:50035922-50035961	LNCaP	prostate:	n/a	n/a
34	CTCF	chr3:50035840-50035990	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:49986085-49986202	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr3:50015678-50015738	LNCaP	prostate:	n/a	n/a
37	CTCF	chr3:50022012-50022031	GM12891	blood:	n/a	n/a
38	CTCF	chr3:50035780-50035930	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:50035820-50035970	AG10803	skin:	n/a	n/a
40	CTCF	chr3:50035880-50036030	NHEK	skin:	n/a	n/a
41	CTCF	chr3:50035880-50036030	AG09319	gingival:	n/a	n/a
42	CTCF	chr3:50035852-50035990	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:50035740-50035890	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr3:50035860-50035965	LNCaP	prostate:	n/a	n/a
45	CTCF	chr3:50035860-50035927	Fibrobl	skin:	n/a	n/a
46	CTCF	chr3:50035887-50035989	ProgFib	skin:	n/a	n/a
47	CTCF	chr3:50035859-50035992	Gliobla	brain:	n/a	n/a
48	CTCF	chr3:50006305-50006332	GM10248	blood:	n/a	n/a
49	CTCF	chr3:50035873-50035990	NHEK	skin:	n/a	n/a
50	CTCF	chr3:49994321-49994392	Medullo	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:49987589-49987639	Hepatocyte	liver:	n/a
2	chr3:49987589-49987639	LNCaP	prostate:	n/a
3	chr3:49987589-49987639	U87	brain:	n/a
4	chr3:49987589-49987639	GM12878	blood:	n/a
5	chr3:49987589-49987639	HEK293	kidney:	embryo
6	chr3:49987589-49987639	AG04449	skin:	fetal
7	chr3:49987589-49987639	HRPEpiC	eye:	n/a
8	chr3:49987589-49987639	Caco-2	colon:	n/a
9	chr3:49987589-49987639	K562	blood:	n/a
10	chr3:49987589-49987639	H1-hESC	embryonic stem cell:	embryo
11	chr3:49987589-49987639	NH-A	brain:	n/a
12	chr3:49987589-49987639	A549	lung:	n/a
13	chr3:49987589-49987639	HRE	kidney:	n/a
14	chr3:49987589-49987639	HL-60	blood:	n/a
15	chr3:49987589-49987639	HepG2	liver:	n/a
16	chr3:49987589-49987639	Jurkat	blood:	n/a
17	chr3:49987589-49987639	NT2-D1	testis:	n/a
18	chr3:49987589-49987639	ProgFib	skin:	n/a
19	chr3:49987589-49987639	SK-N-SH_RA	brain:	n/a
20	chr3:49987589-49987639	HUVEC	blood vessel:	n/a
21	chr3:49987589-49987639	SK-N-SH	brain:	n/a
22	chr3:49987589-49987639	IMR90	lung:	fetal
23	chr3:49987589-49987639	GM06990	blood:	n/a
24	chr3:49987589-49987639	MCF-7	breast:	n/a
25	chr3:49987589-49987639	HCT-116	colon:	n/a
26	chr3:49987589-49987639	AG10803	skin:	n/a
27	chr3:49987589-49987639	BE2_C	brain:	n/a
28	chr3:49987589-49987639	SAEC	small airway:	n/a
29	chr3:49987589-49987639	AG09319	gingival:	n/a
30	chr3:49987589-49987639	Hela-S3	cervix:	n/a
31	chr3:49987589-49987639	HRCEpiC	kidney:	n/a
32	chr3:49987589-49987639	PANC-1	pancreas:	n/a
33	chr3:49987589-49987639	AG09309	skin:	n/a
34	chr3:49987589-49987639	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:49987589-49987639	GM19239	blood:	n/a
36	chr3:49987589-49987639	NB4	blood:	n/a
37	chr3:49987589-49987639	GM12891	blood:	n/a
38	chr3:49987589-49987639	NHDF-neo	bronchial:	n/a
39	chr3:49987589-49987639	HEEpiC	esophagus:	n/a
40	chr3:49987589-49987639	BJ	skin:	n/a
41	chr3:49987589-49987639	HCF	heart:	n/a
42	chr3:49987589-49987639	RPTEC	kidney:	n/a
43	chr3:49987589-49987639	CMK	blood:	n/a
44	chr3:49987589-49987639	PFSK-1	brain:	n/a
45	chr3:49987589-49987639	HIPEpiC	eye:	n/a
46	chr3:49987589-49987639	HNPCEpiC	eye:	n/a
47	chr3:49987589-49987639	NHBE	bronchial:	n/a
48	chr3:49987589-49987639	HCM	heart:	n/a
49	chr3:49987589-49987639	SKMC	muscle:	n/a
50	chr3:49987589-49987639	SK-N-MC	brain:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49977495..49980410-chr3:49985163..49987874,2	K562	blood:
2	chr3:50060113..50061890-chr3:50064863..50067741,2	K562	blood:
3	chr3:50027643..50030377-chr3:50031655..50033615,2	K562	blood:
4	chr3:50037509..50039299-chr3:50062748..50064702,2	MCF-7	breast:
5	chr3:49977713..49979508-chr3:49980727..49984411,5	K562	blood:
6	chr3:49977713..49979804-chr3:49979930..49983021,3	K562	blood:
7	chr3:49978223..49979811-chr3:50003793..50005372,2	K562	blood:
8	chr3:49977058..49978995-chr3:49986374..49988156,2	K562	blood:
9	chr3:49976300..49979550-chr3:50125389..50128777,3	K562	blood:
10	chr3:49965505..49970003-chr3:49975811..49980300,11	K562	blood:
11	chr3:49978223..49979811-chr3:50003793..50005372,2	K562	blood:
12	chr3:49976777..49979438-chr3:49981879..49983606,2	MCF-7	breast:
13	chr3:49976087..49977817-chr3:49983493..49984999,2	K562	blood:
14	chr3:50057660..50059872-chr6:31709500..31711893,2	K562	blood:
15	chr3:49976672..49978991-chr3:50012976..50015141,2	MCF-7	breast:
16	chr3:50060113..50061890-chr3:50064863..50067741,2	K562	blood:
17	chr3:50001120..50002746-chr3:50007377..50010218,2	K562	blood:
18	chr3:49943520..49945282-chr3:50028077..50030089,2	K562	blood:
19	chr3:50029898..50031827-chr3:50035708..50038441,2	K562	blood:
20	chr3:49823173..49825666-chr3:49976602..49979269,2	MCF-7	breast:
21	chr3:49977360..49980004-chr3:50009456..50011405,3	K562	blood:
22	chr3:50037509..50039299-chr3:50062748..50064702,2	MCF-7	breast:
23	chr3:50027643..50030377-chr3:50031655..50033615,2	K562	blood:
24	chr3:49966957..49970009-chr3:49975972..49978983,5	MCF-7	breast:
25	chr3:50035315..50037436-chr3:50045585..50047929,2	MCF-7	breast:
26	chr3:49965505..49970003-chr3:49974970..49980028,17	K562	blood:
27	chr3:49965568..49971141-chr3:49975411..49979217,7	MCF-7	breast:
28	chr3:50001120..50002746-chr3:50007377..50010218,2	K562	blood:

No data

Variant related genes	Relation type
RBM6	TF binding region
RBM6	CpG island
ENSG00000204410	chromatin interactions
ENSG00000003756	chromatin interactions
ENSG00000164077	chromatin interactions
ENSG00000004534	chromatin interactions
ENSG00000176095	chromatin interactions

Extended variants
information (count: 3134 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3134 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565126460	chr3:49978790-49978791	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs9862242	chr3:49978801-49978802	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs111590526	chr3:49978871-49978872	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs11917527	chr3:49978875-49978876	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs111765900	chr3:49978891-49978892	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs532163814	chr3:49978977-49978978	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs551865234	chr3:49978994-49978995	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs566820979	chr3:49978997-49978998	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs527706813	chr3:49979029-49979030	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs13081092	chr3:49979097-49979098	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs539177991	chr3:49979143-49979144	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs73079033	chr3:49979174-49979175	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs111281011	chr3:49979197-49979198	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs367829744	chr3:49979198-49979199	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs556434137	chr3:49979201-49979202	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs62262099	chr3:49979205-49979206	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs538815634	chr3:49979206-49979207	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs553845545	chr3:49979258-49979259	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs572015248	chr3:49979297-49979298	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542720829	chr3:49979307-49979308	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs71325002	chr3:49979315-49979316	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535133659	chr3:49979354-49979355	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs113889758	chr3:49979372-49979373	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs140423996	chr3:49979457-49979458	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs375768438	chr3:49979466-49979467	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576105633	chr3:49979491-49979492	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78310267	chr3:49979531-49979532	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs398051930	chr3:49979544-49979545	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs543744908	chr3:49979637-49979638	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370111086	chr3:49979645-49979646	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371886576	chr3:49979685-49979686	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576985440	chr3:49979689-49979690	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35170106	chr3:49979704-49979705	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559477582	chr3:49979705-49979706	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs527816013	chr3:49979718-49979719	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11717829	chr3:49979727-49979728	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs560993093	chr3:49979746-49979747	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531550495	chr3:49979848-49979849	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550070236	chr3:49979861-49979862	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369194404	chr3:49979870-49979871	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189559218	chr3:49979871-49979872	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142562147	chr3:49979908-49979909	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551319785	chr3:49979929-49979930	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561309110	chr3:49979930-49979931	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs55814616	chr3:49979946-49979947	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs566245940	chr3:49979954-49979955	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559379209	chr3:49980033-49980034	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536390624	chr3:49980040-49980041	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373904086	chr3:49980094-49980095	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs571076735	chr3:49980147-49980148	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD

Chromatin state (count:2805 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49977000-49978800	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr3:49977000-49978800	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr3:49977000-49978800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr3:49977000-49978800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:49977000-49978800	Active TSS	Psoas Muscle	Psoas
6	chr3:49977000-49978800	Active TSS	A549	lung
7	chr3:49977000-49979000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr3:49977200-49978800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr3:49977200-49978800	Active TSS	H9 Cell Line	embryonic stem cell
10	chr3:49977200-49978800	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr3:49977200-49979000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:49977400-49978800	Active TSS	H1 Cell Line	embryonic stem cell
13	chr3:49977400-49978800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr3:49977400-49978800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr3:49977400-49978800	Active TSS	Placenta Amnion	Placenta Amnion
16	chr3:49977400-49979000	Active TSS	Muscle Satellite Cultured Cells	--
17	chr3:49977400-49979000	Active TSS	HSMM	muscle
18	chr3:49977400-49979000	Active TSS	NHDF-Ad	bronchial
19	chr3:49977400-49979200	Active TSS	GM12878-XiMat	blood
20	chr3:49977800-49978800	Active TSS	Right Atrium	heart
21	chr3:49977800-49979400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr3:49978000-49978800	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr3:49978000-49978800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
24	chr3:49978000-49978800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
25	chr3:49978000-49978800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr3:49978000-49978800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr3:49978000-49978800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr3:49978000-49978800	Flanking Active TSS	Liver	Liver
29	chr3:49978000-49978800	Bivalent/Poised TSS	HepG2	liver
30	chr3:49978000-49979000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr3:49978000-49979000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr3:49978200-49978800	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr3:49978200-49978800	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr3:49978200-49978800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
35	chr3:49978200-49978800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr3:49978200-49978800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
37	chr3:49978200-49978800	Flanking Active TSS	Adipose Nuclei	Adipose
38	chr3:49978200-49978800	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr3:49978200-49978800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr3:49978200-49978800	Flanking Active TSS	Fetal Brain Male	brain
41	chr3:49978200-49978800	Flanking Active TSS	Fetal Lung	lung
42	chr3:49978200-49978800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
43	chr3:49978200-49978800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr3:49978200-49978800	Flanking Active TSS	Rectal Smooth Muscle	rectum
45	chr3:49978200-49979000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr3:49978200-49979000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:49978200-49979000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr3:49978200-49979000	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr3:49978200-49979000	Flanking Active TSS	Fetal Brain Female	brain
50	chr3:49978200-49979000	Flanking Active TSS	Stomach Smooth Muscle	stomach

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