Variant report

Variant	nsv1061412
Chromosome Location	chr20:24629468-24887869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1782)
CpG islands
(count:183)
Chromatin interactive
region (count:99)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1782 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:24736101-24736599	HepG2	liver:	n/a	n/a
2	ATF1	chr20:24823984-24824053	K562	blood:	n/a	n/a
3	ATF2	chr20:24823428-24824067	GM12878	blood:	n/a	n/a
4	ATF2	chr20:24823358-24824230	GM12878	blood:	n/a	n/a
5	ATF2	chr20:24819759-24820167	GM12878	blood:	n/a	n/a
6	ATF2	chr20:24819858-24820201	GM12878	blood:	n/a	n/a
7	ATF3	chr20:24631670-24632182	A549	lung:	n/a	n/a
8	BACH1	chr20:24726894-24727261	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr20:24819766-24820179	GM12878	blood:	n/a	chr20:24820001-24820012 chr20:24820002-24820012
10	BATF	chr20:24819764-24820201	GM12878	blood:	n/a	chr20:24820001-24820012 chr20:24820002-24820012
11	BATF	chr20:24823482-24824089	GM12878	blood:	n/a	n/a
12	BATF	chr20:24823367-24824107	GM12878	blood:	n/a	n/a
13	BCL11A	chr20:24823488-24824038	GM12878	blood:	n/a	n/a
14	BCL11A	chr20:24823419-24824114	GM12878	blood:	n/a	n/a
15	BCL3	chr20:24823484-24823990	GM12878	blood:	n/a	n/a
16	BCL3	chr20:24793446-24794245	GM12878	blood:	n/a	n/a
17	BCL3	chr20:24823543-24824000	GM12878	blood:	n/a	n/a
18	BCL3	chr20:24793533-24794095	GM12878	blood:	n/a	n/a
19	BCLAF1	chr20:24823274-24824117	GM12878	blood:	n/a	n/a
20	BCLAF1	chr20:24823395-24823968	GM12878	blood:	n/a	n/a
21	BHLHE40	chr20:24789382-24789495	K562	blood:	n/a	n/a
22	BHLHE40	chr20:24789440-24789585	GM12878	blood:	n/a	n/a
23	BHLHE40	chr20:24797734-24797766	K562	blood:	n/a	n/a
24	BHLHE40	chr20:24823388-24824112	GM12878	blood:	n/a	n/a
25	BHLHE40	chr20:24632352-24632357	K562	blood:	n/a	n/a
26	BRCA1	chr20:24709520-24709714	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr20:24845427-24845689	K562	blood:	n/a	n/a
28	CEBPB	chr20:24887677-24887995	A549	lung:	n/a	chr20:24887827-24887838
29	CEBPB	chr20:24630567-24631429	IMR90	lung:	n/a	n/a
30	CEBPB	chr20:24631792-24632236	HCT-116	colon:	n/a	chr20:24631991-24632002
31	CEBPB	chr20:24736080-24736660	HepG2	liver:	n/a	n/a
32	CEBPB	chr20:24843980-24844269	HepG2	liver:	n/a	chr20:24844130-24844141
33	CEBPB	chr20:24887690-24888000	IMR90	lung:	n/a	chr20:24887827-24887838
34	CEBPB	chr20:24807869-24808090	HepG2	liver:	n/a	n/a
35	CEBPB	chr20:24772384-24772681	A549	lung:	n/a	n/a
36	CEBPB	chr20:24736057-24736558	HepG2	liver:	n/a	n/a
37	CEBPB	chr20:24778500-24778861	HepG2	liver:	n/a	chr20:24778671-24778684 chr20:24778673-24778684 chr20:24778671-24778682
38	CEBPB	chr20:24633869-24634241	A549	lung:	n/a	chr20:24633987-24634004
39	CEBPB	chr20:24654123-24654740	IMR90	lung:	n/a	chr20:24654273-24654286
40	CEBPB	chr20:24701415-24702039	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:24769985-24770271	HepG2	liver:	n/a	chr20:24770163-24770180
42	CEBPB	chr20:24856012-24856061	HepG2	liver:	n/a	n/a
43	CEBPB	chr20:24778562-24778822	IMR90	lung:	n/a	chr20:24778671-24778684 chr20:24778673-24778684 chr20:24778671-24778682
44	CEBPB	chr20:24701432-24702039	A549	lung:	n/a	n/a
45	CEBPB	chr20:24843998-24844266	A549	lung:	n/a	chr20:24844130-24844141
46	CEBPB	chr20:24736092-24736631	HepG2	liver:	n/a	n/a
47	CEBPB	chr20:24830229-24830481	A549	lung:	n/a	chr20:24830356-24830367
48	CEBPB	chr20:24691218-24691482	HepG2	liver:	n/a	chr20:24691356-24691367
49	CEBPB	chr20:24631818-24632144	Hela-S3	cervix:	n/a	chr20:24631991-24632002
50	CEBPB	chr20:24676162-24676507	A549	lung:	n/a	chr20:24676333-24676344 chr20:24676332-24676349 chr20:24676334-24676345 chr20:24676333-24676346 chr20:24676335-24676344

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:24784216-24784266	HMEC	breast:	n/a
2	chr20:24784136-24784186	H1-hESC	embryonic stem cell:	embryo
3	chr20:24784136-24784186	AG09319	gingival:	n/a
4	chr20:24784216-24784266	HCT-116	colon:	n/a
5	chr20:24646600-24646650	HCF	heart:	n/a
6	chr20:24784216-24784266	HepG2	liver:	n/a
7	chr20:24646600-24646650	SKMC	muscle:	n/a
8	chr20:24646600-24646650	T-47D	breast:	n/a
9	chr20:24646600-24646650	HPAEpiC	pulmonary alveolar:	n/a
10	chr20:24646600-24646650	HNPCEpiC	eye:	n/a
11	chr20:24784216-24784266	PFSK-1	brain:	n/a
12	chr20:24784136-24784186	HIPEpiC	eye:	n/a
13	chr20:24784216-24784266	HEEpiC	esophagus:	n/a
14	chr20:24646600-24646650	MCF10A-Er-Src	breast:	n/a
15	chr20:24646600-24646650	A549	lung:	n/a
16	chr20:24784216-24784266	HRCEpiC	kidney:	n/a
17	chr20:24646600-24646650	U87	brain:	n/a
18	chr20:24784216-24784266	HRPEpiC	eye:	n/a
19	chr20:24646600-24646650	NH-A	brain:	n/a
20	chr20:24784136-24784186	HepG2	liver:	n/a
21	chr20:24784216-24784266	IMR90	lung:	fetal
22	chr20:24784136-24784186	A549	lung:	n/a
23	chr20:24784216-24784266	HCF	heart:	n/a
24	chr20:24784136-24784186	Hela-S3	cervix:	n/a
25	chr20:24784216-24784266	HNPCEpiC	eye:	n/a
26	chr20:24646600-24646650	SAEC	small airway:	n/a
27	chr20:24784136-24784186	HCM	heart:	n/a
28	chr20:24784216-24784266	HEK293	kidney:	embryo
29	chr20:24646600-24646650	MCF-7	breast:	n/a
30	chr20:24784136-24784186	GM19239	blood:	n/a
31	chr20:24784136-24784186	HL-60	blood:	n/a
32	chr20:24646600-24646650	BJ	skin:	n/a
33	chr20:24784136-24784186	SKMC	muscle:	n/a
34	chr20:24784216-24784266	Hela-S3	cervix:	n/a
35	chr20:24646600-24646650	ProgFib	skin:	n/a
36	chr20:24646600-24646650	K562	blood:	n/a
37	chr20:24784136-24784186	NB4	blood:	n/a
38	chr20:24784216-24784266	HUVEC	blood vessel:	n/a
39	chr20:24784136-24784186	SAEC	small airway:	n/a
40	chr20:24784216-24784266	T-47D	breast:	n/a
41	chr20:24784216-24784266	GM12891	blood:	n/a
42	chr20:24784136-24784186	HCT-116	colon:	n/a
43	chr20:24784216-24784266	Jurkat	blood:	n/a
44	chr20:24646600-24646650	AG04449	skin:	fetal
45	chr20:24784136-24784186	SK-N-MC	brain:	n/a
46	chr20:24784136-24784186	NH-A	brain:	n/a
47	chr20:24784136-24784186	AG04450	lung:	fetal
48	chr20:24784136-24784186	LNCaP	prostate:	n/a
49	chr20:24784216-24784266	A549	lung:	n/a
50	chr20:24646600-24646650	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr20:24629904..24632760-chr20:24759535..24761078,2	MCF-7	breast:
2	chr20:24746739..24748935-chr20:24753285..24754881,2	MCF-7	breast:
3	chr20:24726357..24729522-chr20:24732233..24738144,6	MCF-7	breast:
4	chr20:24630307..24631279-chr20:24640279..24641332,14	MCF-7	breast:
5	chr20:24763298..24765600-chr20:24898179..24900035,23	MCF-7	breast:
6	chr20:24654225..24656073-chr20:24661737..24664471,2	MCF-7	breast:
7	chr20:24797658..24800025-chr20:24806940..24809429,2	MCF-7	breast:
8	chr20:24671407..24673133-chr20:24673157..24675510,2	K562	blood:
9	chr20:24630261..24631279-chr20:24640264..24641332,21	MCF-7	breast:
10	chr20:24716951..24718615-chr20:24720507..24722408,2	MCF-7	breast:
11	chr20:24764889..24765421-chr20:24919390..24920112,2	MCF-7	breast:
12	chr20:24751479..24753898-chr20:24757094..24759323,2	MCF-7	breast:
13	chr20:24630253..24631426-chr20:24640312..24641216,7	MCF-7	breast:
14	chr20:24631593..24633850-chr20:24634510..24636557,2	MCF-7	breast:
15	chr20:24448836..24451309-chr20:24629831..24631551,2	MCF-7	breast:
16	chr20:24780843..24782788-chr20:24791141..24793003,2	MCF-7	breast:
17	chr20:24631399..24634097-chr20:24646074..24647990,2	MCF-7	breast:
18	chr20:24651840..24653392-chr20:24727209..24728729,2	MCF-7	breast:
19	chr20:24869298..24871986-chr20:24874096..24876314,2	MCF-7	breast:
20	chr20:24755822..24758667-chr20:24759812..24761777,2	MCF-7	breast:
21	chr20:24612466..24614630-chr20:24629800..24632618,2	MCF-7	breast:
22	chr20:24630307..24631279-chr20:24640279..24641332,14	MCF-7	breast:
23	chr20:24716951..24718615-chr20:24720507..24722408,2	MCF-7	breast:
24	chr20:24630442..24631150-chr20:24777044..24777861,2	MCF-7	breast:
25	chr20:24623933..24625636-chr20:24628321..24630040,2	MCF-7	breast:
26	chr20:24645518..24647041-chr20:24652515..24654778,2	MCF-7	breast:
27	chr20:24654225..24656073-chr20:24661737..24664471,2	MCF-7	breast:
28	chr20:24625629..24628366-chr20:24631832..24633768,2	MCF-7	breast:
29	chr20:24633208..24634877-chr20:24753642..24755749,2	MCF-7	breast:
30	chr20:24630371..24631127-chr20:24753147..24753931,3	MCF-7	breast:
31	chr20:24237902..24238701-chr20:24630250..24631153,4	MCF-7	breast:
32	chr20:24363369..24365498-chr20:24749184..24751241,2	MCF-7	breast:
33	chr20:24633208..24634877-chr20:24753642..24755749,2	MCF-7	breast:
34	chr20:24820307..24822750-chr20:24822757..24824794,2	K562	blood:
35	chr20:24786455..24788540-chr20:24788618..24791423,2	MCF-7	breast:
36	chr20:24616131..24617827-chr20:24647064..24649863,2	MCF-7	breast:
37	chr20:24630419..24630929-chr20:24722844..24723588,2	MCF-7	breast:
38	chr20:24778826..24780956-chr20:24782590..24785406,2	MCF-7	breast:
39	chr20:24887755..24889606-chr20:24897276..24899425,2	K562	blood:
40	chr20:24760897..24762927-chr20:24971923..24974297,2	MCF-7	breast:
41	chr20:24671407..24673133-chr20:24673157..24675510,2	K562	blood:
42	chr20:24826869..24829135-chr20:24829517..24831916,2	MCF-7	breast:
43	chr20:24189074..24189575-chr20:24761714..24762521,2	MCF-7	breast:
44	chr20:24630391..24631212-chr20:24752974..24753906,2	MCF-7	breast:
45	chr20:24630442..24631150-chr20:24777044..24777861,2	MCF-7	breast:
46	chr20:24602331..24603843-chr20:24632177..24634998,2	MCF-7	breast:
47	chr20:24140940..24141858-chr20:24761680..24762579,3	MCF-7	breast:
48	chr20:24764506..24765162-chr20:24897617..24898498,2	MCF-7	breast:
49	chr20:24651840..24653392-chr20:24727209..24728729,2	MCF-7	breast:
50	chr20:24826869..24829135-chr20:24829517..24831916,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SYNDIG1-1	chr20:24660183-24660300	XLOC_013498
2	lnc-SYNDIG1-1	chr20:24660941-24661627	XLOC_013498
3	lnc-C20orf3-2	chr20:24860976-24861148	XLOC_013702
4	lnc-C20orf3-2	chr20:24860690-24860879	XLOC_013702

No data

Variant related genes	Relation type
ENSG00000231015	TF binding region
ENSG00000231015	CpG island
ENSG00000101474	chromatin interactions
ENSG00000101463	chromatin interactions
ENSG00000109089	chromatin interactions
DCAF8	miRNA target sites

Extended variants
information (count: 10625 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:10625 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114152783	chr20:24629468-24629469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559307742	chr20:24629471-24629472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528631704	chr20:24629472-24629473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551585727	chr20:24629513-24629514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189234379	chr20:24629575-24629576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180777306	chr20:24629617-24629618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551164667	chr20:24629620-24629621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567985534	chr20:24629626-24629627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143097736	chr20:24629728-24629729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6049830	chr20:24629748-24629749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11904965	chr20:24629772-24629773	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs538584175	chr20:24629783-24629784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11087473	chr20:24629794-24629795	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs151167325	chr20:24629812-24629813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537672539	chr20:24629813-24629814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140367403	chr20:24629823-24629824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574427000	chr20:24629840-24629841	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540127589	chr20:24629853-24629854	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7261028	chr20:24629867-24629868	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560346941	chr20:24629881-24629882	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573164200	chr20:24629903-24629904	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545352740	chr20:24629927-24629928	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565257253	chr20:24629948-24629949	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531010977	chr20:24629949-24629950	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs550139068	chr20:24629961-24629962	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184998511	chr20:24629963-24629964	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs34582067	chr20:24629971-24629972	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs729577	chr20:24629972-24629973	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550356505	chr20:24629979-24629980	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530462444	chr20:24630031-24630032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191044121	chr20:24630089-24630090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567114929	chr20:24630090-24630091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145405105	chr20:24630105-24630106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552125258	chr20:24630127-24630128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532834371	chr20:24630158-24630159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74861164	chr20:24630198-24630199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554384488	chr20:24630206-24630207	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536125347	chr20:24630216-24630217	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs202172027	chr20:24630224-24630225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551072237	chr20:24630311-24630312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs4815295	chr20:24630360-24630361	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs146971571	chr20:24630388-24630389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533698490	chr20:24630422-24630423	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553797641	chr20:24630484-24630485	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577038949	chr20:24630502-24630503	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113394442	chr20:24630531-24630532	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375743517	chr20:24630569-24630570	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs62215323	chr20:24630642-24630643	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558892556	chr20:24630715-24630716	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575846452	chr20:24630730-24630731	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1477 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24615400-24633800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr20:24616200-24639600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr20:24616400-24630200	Weak transcription	Brain Angular Gyrus	brain
4	chr20:24620000-24641200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:24625200-24630600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr20:24625600-24633800	Weak transcription	Spleen	Spleen
7	chr20:24626000-24629600	Enhancers	Fetal Thymus	thymus
8	chr20:24627400-24630200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr20:24628000-24633600	Enhancers	Fetal Brain Male	brain
10	chr20:24628600-24630800	Enhancers	Brain Substantia Nigra	brain
11	chr20:24628600-24631000	Enhancers	Brain Hippocampus Middle	brain
12	chr20:24628600-24631600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr20:24628600-24631800	Weak transcription	HMEC	breast
14	chr20:24628800-24630000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr20:24628800-24631000	Enhancers	Primary B cells from peripheral blood	blood
16	chr20:24629000-24630200	Weak transcription	Colon Smooth Muscle	Colon
17	chr20:24629000-24633600	Enhancers	NHLF	lung
18	chr20:24629200-24630200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr20:24629200-24631000	Enhancers	GM12878-XiMat	blood
20	chr20:24629200-24634600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr20:24629200-24642600	Weak transcription	Right Atrium	heart
22	chr20:24629400-24629600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr20:24629400-24629600	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr20:24629400-24629600	Enhancers	Osteobl	bone
25	chr20:24629400-24630600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr20:24629400-24630800	Weak transcription	Fetal Muscle Leg	muscle
27	chr20:24629400-24632600	Enhancers	Fetal Brain Female	brain
28	chr20:24629400-24641000	Weak transcription	Right Ventricle	heart
29	chr20:24629600-24629800	Enhancers	Brain Anterior Caudate	brain
30	chr20:24629600-24630000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr20:24629600-24630000	Weak transcription	Fetal Stomach	stomach
32	chr20:24629600-24630000	Weak transcription	Osteobl	bone
33	chr20:24629600-24631000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr20:24629800-24630400	Weak transcription	Brain Anterior Caudate	brain
35	chr20:24630000-24630400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr20:24630000-24630600	Enhancers	Osteobl	bone
37	chr20:24630000-24631000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr20:24630000-24631800	Enhancers	Fetal Stomach	stomach
39	chr20:24630200-24630400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr20:24630200-24630600	Enhancers	Stomach Smooth Muscle	stomach
41	chr20:24630200-24631000	Enhancers	Brain Angular Gyrus	brain
42	chr20:24630200-24631400	Enhancers	Colon Smooth Muscle	Colon
43	chr20:24630200-24631600	Enhancers	Fetal Lung	lung
44	chr20:24630200-24631600	Enhancers	Ovary	ovary
45	chr20:24630200-24631600	Enhancers	HSMMtube	muscle
46	chr20:24630200-24634600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr20:24630200-24634800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr20:24630400-24630800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr20:24630400-24631200	Enhancers	Brain Anterior Caudate	brain
50	chr20:24630400-24631600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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