Variant report

Variant	esv34905
Chromosome Location	chr1:225631404-225676582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1947)
CpG islands
(count:1285)
Chromatin interactive
region (count:121)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1947 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225632560-225633003	K562	blood:	n/a	n/a
2	ARID3A	chr1:225632590-225633025	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:225642531-225642726	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:225647151-225647298	K562	blood:	n/a	n/a
5	ARID3A	chr1:225662672-225662961	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:225638306-225638710	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:225641860-225642234	HepG2	liver:	n/a	n/a
8	ATF1	chr1:225632536-225633005	K562	blood:	n/a	n/a
9	ATF2	chr1:225654627-225655750	GM12878	blood:	n/a	n/a
10	ATF2	chr1:225632446-225633105	GM12878	blood:	n/a	n/a
11	ATF2	chr1:225654702-225655834	GM12878	blood:	n/a	n/a
12	ATF2	chr1:225662522-225663052	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:225632483-225633006	GM12878	blood:	n/a	n/a
14	ATF2	chr1:225662618-225663049	GM12878	blood:	n/a	n/a
15	ATF3	chr1:225632559-225632878	K562	blood:	n/a	n/a
16	ATF3	chr1:225662504-225663165	A549	lung:	n/a	n/a
17	ATF3	chr1:225642475-225642816	K562	blood:	n/a	n/a
18	ATF3	chr1:225662673-225663001	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr1:225662733-225662914	GM12878	blood:	n/a	n/a
20	ATF3	chr1:225642548-225642761	K562	blood:	n/a	n/a
21	ATF3	chr1:225668678-225668889	K562	blood:	n/a	n/a
22	ATF3	chr1:225662673-225662962	K562	blood:	n/a	n/a
23	ATF3	chr1:225662524-225663048	A549	lung:	n/a	n/a
24	ATF3	chr1:225632468-225633035	K562	blood:	n/a	n/a
25	ATF3	chr1:225662670-225662973	K562	blood:	n/a	n/a
26	ATF3	chr1:225662710-225662979	HepG2	liver:	n/a	n/a
27	BACH1	chr1:225632751-225633067	K562	blood:	n/a	n/a
28	BACH1	chr1:225662493-225662984	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr1:225668564-225668953	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr1:225632487-225632947	GM12878	blood:	n/a	n/a
31	BATF	chr1:225654740-225655157	GM12878	blood:	n/a	n/a
32	BATF	chr1:225664360-225664601	GM12878	blood:	n/a	n/a
33	BATF	chr1:225664356-225664634	GM12878	blood:	n/a	n/a
34	BCL3	chr1:225672714-225673679	A549	lung:	n/a	chr1:225672752-225672765 chr1:225672761-225672769
35	BCL3	chr1:225662472-225663091	A549	lung:	n/a	chr1:225662827-225662840
36	BCLAF1	chr1:225632422-225632979	GM12878	blood:	n/a	chr1:225632738-225632747
37	BCLAF1	chr1:225654674-225655751	GM12878	blood:	n/a	chr1:225655522-225655531 chr1:225655480-225655493
38	BCLAF1	chr1:225654577-225655721	GM12878	blood:	n/a	chr1:225655522-225655531 chr1:225655480-225655493
39	BCLAF1	chr1:225632345-225633085	K562	blood:	n/a	chr1:225632738-225632747
40	BHLHE40	chr1:225632542-225632851	HepG2	liver:	n/a	chr1:225632727-225632740 chr1:225632723-225632744 chr1:225632728-225632737 chr1:225632729-225632738 chr1:225632729-225632738
41	BHLHE40	chr1:225641858-225642258	HepG2	liver:	n/a	n/a
42	BHLHE40	chr1:225654779-225655825	GM12878	blood:	n/a	chr1:225655162-225655178 chr1:225655462-225655478
43	BHLHE40	chr1:225632582-225632919	A549	lung:	n/a	chr1:225632727-225632740 chr1:225632723-225632744 chr1:225632728-225632737 chr1:225632729-225632738 chr1:225632729-225632738
44	BHLHE40	chr1:225662623-225663196	HepG2	liver:	n/a	n/a
45	BHLHE40	chr1:225658456-225658583	K562	blood:	n/a	n/a
46	BHLHE40	chr1:225638249-225638549	HepG2	liver:	n/a	n/a
47	BHLHE40	chr1:225647129-225647268	K562	blood:	n/a	n/a
48	BHLHE40	chr1:225635935-225636211	HepG2	liver:	n/a	n/a
49	BHLHE40	chr1:225632468-225633033	HepG2	liver:	n/a	chr1:225632727-225632740 chr1:225632723-225632744 chr1:225632728-225632737 chr1:225632729-225632738 chr1:225632729-225632738
50	BHLHE40	chr1:225631402-225631424	K562	blood:	n/a	n/a

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225659296-225659346	RPTEC	kidney:	n/a
2	chr1:225663401-225663451	GM12878	blood:	n/a
3	chr1:225662606-225662656	GM12892	blood:	n/a
4	chr1:225651959-225652009	HCM	heart:	n/a
5	chr1:225659296-225659346	RPTEC	kidney:	n/a
6	chr1:225663401-225663451	GM12878	blood:	n/a
7	chr1:225662606-225662656	GM12892	blood:	n/a
8	chr1:225651959-225652009	HCM	heart:	n/a
9	chr1:225663401-225663451	NHBE	bronchial:	n/a
10	chr1:225659296-225659346	Hepatocyte	liver:	n/a
11	chr1:225651959-225652009	Jurkat	blood:	n/a
12	chr1:225662606-225662656	NHBE	bronchial:	n/a
13	chr1:225671904-225671954	IMR90	lung:	fetal
14	chr1:225662766-225662816	HCT-116	colon:	n/a
15	chr1:225651959-225652009	HepG2	liver:	n/a
16	chr1:225632889-225632939	ProgFib	skin:	n/a
17	chr1:225662606-225662656	CMK	blood:	n/a
18	chr1:225659296-225659346	AG09309	skin:	n/a
19	chr1:225663401-225663451	SKMC	muscle:	n/a
20	chr1:225642746-225642796	HRE	kidney:	n/a
21	chr1:225671904-225671954	SK-N-SH	brain:	n/a
22	chr1:225632889-225632939	Hela-S3	cervix:	n/a
23	chr1:225658745-225658795	SK-N-SH	brain:	n/a
24	chr1:225655154-225655204	AG10803	skin:	n/a
25	chr1:225671862-225671912	SK-N-SH	brain:	n/a
26	chr1:225659296-225659346	GM12878	blood:	n/a
27	chr1:225676425-225676475	AG09309	skin:	n/a
28	chr1:225651959-225652009	NH-A	brain:	n/a
29	chr1:225671904-225671954	HCPEpiC	choroid plexus:	n/a
30	chr1:225642746-225642796	MCF-7	breast:	n/a
31	chr1:225665763-225665813	PrEC	prostate:	n/a
32	chr1:225634976-225635026	U87	brain:	n/a
33	chr1:225671990-225672040	BJ	skin:	n/a
34	chr1:225632889-225632939	SK-N-MC	brain:	n/a
35	chr1:225632889-225632939	GM19239	blood:	n/a
36	chr1:225648715-225648765	GM19239	blood:	n/a
37	chr1:225671432-225671482	HCM	heart:	n/a
38	chr1:225661446-225661496	GM12878	blood:	n/a
39	chr1:225658651-225658701	HAEpiC	amniotic membrane:	n/a
40	chr1:225661446-225661496	ovcar-3	ovarian:	n/a
41	chr1:225658745-225658795	RPTEC	kidney:	n/a
42	chr1:225632889-225632939	NHBE	bronchial:	n/a
43	chr1:225648715-225648765	T-47D	breast:	n/a
44	chr1:225651959-225652009	MCF10A-Er-Src	breast:	n/a
45	chr1:225671432-225671482	GM12891	blood:	n/a
46	chr1:225659296-225659346	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:225632889-225632939	HCPEpiC	choroid plexus:	n/a
48	chr1:225632889-225632939	NH-A	brain:	n/a
49	chr1:225651959-225652009	BE2_C	brain:	n/a
50	chr1:225655154-225655204	LNCaP	prostate:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:225662379..225663286-chr1:226163400..226164300,7	K562	blood:
2	chr1:225660270..225662835-chr1:225667398..225670221,2	MCF-7	breast:
3	chr1:225662381..225663188-chr1:226098805..226099681,6	MCF-7	breast:
4	chr1:225666757..225668833-chr1:226110294..226111958,2	MCF-7	breast:
5	chr1:225633065..225638606-chr1:225639136..225643843,7	MCF-7	breast:
6	chr1:225662402..225663343-chr1:226032820..226034152,12	MCF-7	breast:
7	chr1:225662701..225663242-chr1:226175273..226175841,2	MCF-7	breast:
8	chr1:225637801..225642696-chr1:225647950..225650939,4	K562	blood:
9	chr1:225662383..225663164-chr1:225958651..225959497,2	MCF-7	breast:
10	chr1:225652465..225653214-chr21:44312715..44313565,2	Hela-S3	cervix:
11	chr1:225660989..225663497-chr1:226070471..226072090,2	K562	blood:
12	chr1:225613873..225616554-chr1:225637686..225639961,3	MCF-7	breast:
13	chr1:225662710..225663336-chr1:226154888..226155470,2	MCF-7	breast:
14	chr1:225668756..225671445-chr1:225674981..225676551,3	K562	blood:
15	chr1:225631906..225634098-chr1:225666664..225668819,2	K562	blood:
16	chr1:225662349..225663258-chr1:225740687..225742425,6	K562	blood:
17	chr1:225597626..225599804-chr1:225650818..225652643,2	K562	blood:
18	chr1:225662353..225663278-chr1:226308878..226309804,6	K562	blood:
19	chr1:225662368..225663228-chr1:226027050..226027785,2	K562	blood:
20	chr1:225665630..225667137-chr1:226308801..226311216,2	K562	blood:
21	chr1:225652711..225653212-chr6:26216728..26217456,2	Hela-S3	cervix:
22	chr1:225662607..225663273-chr1:225994915..225995627,2	K562	blood:
23	chr1:225657432..225660259-chr1:225660834..225662970,2	K562	blood:
24	chr1:225632782..225636036-chr1:225646050..225649453,3	K562	blood:
25	chr1:225655109..225657230-chr1:226022691..226024869,2	K562	blood:
26	chr1:225662457..225663199-chr1:225705258..225705789,2	MCF-7	breast:
27	chr1:225662746..225665144-chr1:225672666..225674544,2	MCF-7	breast:
28	chr1:225662375..225662892-chr1:226154381..226155127,2	K562	blood:
29	chr1:225611259..225613937-chr1:225629471..225632737,4	K562	blood:
30	chr1:225636376..225639030-chr1:225641511..225643648,3	K562	blood:
31	chr1:225654995..225657413-chr1:226069983..226072182,2	MCF-7	breast:
32	chr1:225658101..225659665-chr1:226308804..226311081,2	K562	blood:
33	chr1:225633065..225638606-chr1:225639136..225643843,7	MCF-7	breast:
34	chr1:225674280..225677221-chr1:225997663..226000316,2	MCF-7	breast:
35	chr1:225632657..225635050-chr1:226182326..226184522,2	MCF-7	breast:
36	chr1:225664099..225665880-chr1:226167899..226170601,2	K562	blood:
37	chr1:225662357..225662998-chr1:225754575..225755137,2	K562	blood:
38	chr1:225616757..225618444-chr1:225653517..225655559,2	K562	blood:
39	chr1:225637530..225639456-chr1:225642105..225644098,3	K562	blood:
40	chr1:225668021..225670369-chr1:226148124..226150238,2	MCF-7	breast:
41	chr1:225668772..225671386-chr1:225671515..225673412,2	K562	blood:
42	chr1:225614179..225618111-chr1:225627420..225635153,13	K562	blood:
43	chr1:225626720..225628379-chr1:225647904..225650755,2	K562	blood:
44	chr1:225629716..225632443-chr1:225636032..225637800,2	MCF-7	breast:
45	chr1:225636376..225639030-chr1:225641511..225643648,3	K562	blood:
46	chr1:225615091..225616977-chr1:225649695..225651542,2	MCF-7	breast:
47	chr1:225652849..225654996-chr1:225964946..225967311,2	MCF-7	breast:
48	chr1:225661061..225665257-chr1:226163112..226166318,3	K562	blood:
49	chr1:225668756..225671445-chr1:225674981..225676551,3	K562	blood:
50	chr1:225625683..225626268-chr1:225662425..225662953,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LBR-1	chr1:225649243-225649287	XLOC_001230
2	lnc-AC092811.1-1	chr1:225659565-225660157	XLOC_000585
3	lnc-LBR-1	chr1:225652925-225652985	XLOC_001230
4	lnc-AC092811.1-1	chr1:225657547-225659222	XLOC_000585
5	lnc-LBR-1	chr1:225635693-225636287	XLOC_001230
6	lnc-LBR-1	chr1:225636128-225636287	XLOC_001230

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ENAH	hsa-miR-124-3p	chr1:225674888-225674882

Variant related genes	Relation type
ENSG00000234476	TF binding region
ENSG00000234476	CpG island
ENSG00000143742	chromatin interactions
ENSG00000163041	chromatin interactions
ENSG00000143815	chromatin interactions
ENSG00000242861	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000143819	chromatin interactions
ENSG00000143751	chromatin interactions
ENSG00000243709	chromatin interactions
ENSG00000122482	chromatin interactions
ENSG00000196187	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000143811	chromatin interactions
ENSG00000234476	chromatin interactions
ENSG00000160194	chromatin interactions
ARL8B	miRNA target sites
CBL	miRNA target sites
CBLL1	miRNA target sites

Extended variants
information (count: 1738 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1738 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1340865	chr1:225631404-225631405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372296593	chr1:225631423-225631424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12744205	chr1:225631432-225631433	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs181483469	chr1:225631441-225631442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72750890	chr1:225631465-225631466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs71170084	chr1:225631513-225631514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12022807	chr1:225631547-225631548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370112575	chr1:225631555-225631556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559243095	chr1:225631567-225631568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185954443	chr1:225631622-225631623	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs112524171	chr1:225631633-225631634	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149017629	chr1:225631644-225631645	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559752231	chr1:225631658-225631659	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560925749	chr1:225631676-225631677	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12025279	chr1:225631709-225631710	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528610635	chr1:225631712-225631713	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531759831	chr1:225631726-225631727	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550242014	chr1:225631748-225631749	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541989543	chr1:225631763-225631764	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs571611302	chr1:225631768-225631769	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539228519	chr1:225631779-225631780	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188420473	chr1:225631806-225631807	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566407781	chr1:225631812-225631813	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143823822	chr1:225631821-225631822	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs554649761	chr1:225631857-225631858	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575979578	chr1:225631943-225631944	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536601213	chr1:225632043-225632044	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558621154	chr1:225632090-225632091	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs368520663	chr1:225632097-225632098	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540844175	chr1:225632132-225632133	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138376161	chr1:225632135-225632136	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs562192631	chr1:225632186-225632187	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75904298	chr1:225632191-225632192	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs74937252	chr1:225632192-225632193	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181146265	chr1:225632198-225632199	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs79647080	chr1:225632200-225632201	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78758999	chr1:225632204-225632205	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs78753195	chr1:225632214-225632215	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs80255996	chr1:225632226-225632227	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs75967044	chr1:225632231-225632232	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371272404	chr1:225632266-225632267	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11578604	chr1:225632270-225632271	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs534953402	chr1:225632290-225632291	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541720086	chr1:225632299-225632300	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs112995106	chr1:225632353-225632354	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs141361809	chr1:225632398-225632399	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531741692	chr1:225632402-225632403	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549864318	chr1:225632403-225632404	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565403037	chr1:225632404-225632405	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145312907	chr1:225632413-225632414	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1923 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225625400-225636000	Enhancers	Colon Smooth Muscle	Colon
2	chr1:225626000-225636200	Enhancers	Fetal Intestine Large	intestine
3	chr1:225627600-225632400	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr1:225627800-225631800	Enhancers	Stomach Mucosa	stomach
5	chr1:225627800-225632400	Enhancers	Stomach Smooth Muscle	stomach
6	chr1:225628000-225632400	Enhancers	Fetal Thymus	thymus
7	chr1:225628800-225632400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr1:225628800-225632400	Enhancers	K562	blood
9	chr1:225628800-225633000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr1:225629000-225632000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr1:225629000-225632200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr1:225629000-225632400	Enhancers	Primary B cells from cord blood	blood
13	chr1:225629000-225632400	Enhancers	Primary T cells fromperipheralblood	blood
14	chr1:225629000-225632400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:225629200-225632400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr1:225629200-225632600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:225629200-225633000	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr1:225629200-225636400	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr1:225629400-225632400	Enhancers	Primary B cells from peripheral blood	blood
20	chr1:225629400-225635600	Enhancers	Primary hematopoietic stem cells	blood
21	chr1:225629400-225635600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:225629600-225634000	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr1:225629600-225634200	Enhancers	Spleen	Spleen
24	chr1:225629800-225631600	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr1:225629800-225632200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:225629800-225632400	Enhancers	Adipose Nuclei	Adipose
27	chr1:225629800-225634800	Enhancers	HUVEC	blood vessel
28	chr1:225630000-225632200	Enhancers	Left Ventricle	heart
29	chr1:225630000-225632400	Enhancers	Primary T cells from cord blood	blood
30	chr1:225630000-225632400	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr1:225630000-225632400	Enhancers	Thymus	Thymus
32	chr1:225630000-225632600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr1:225630200-225632200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr1:225630200-225632400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr1:225630200-225632400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:225630200-225632400	Enhancers	Duodenum Mucosa	Duodenum
37	chr1:225630200-225632400	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr1:225630200-225632400	Enhancers	GM12878-XiMat	blood
39	chr1:225630200-225633200	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr1:225630200-225633400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr1:225630200-225634600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:225630200-225635200	Enhancers	Liver	Liver
43	chr1:225630200-225636400	Enhancers	Fetal Intestine Small	intestine
44	chr1:225630400-225632000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr1:225630400-225632400	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr1:225630600-225631600	Enhancers	Right Ventricle	heart
47	chr1:225630600-225632400	Enhancers	Hela-S3	cervix
48	chr1:225630800-225631800	Enhancers	Rectal Smooth Muscle	rectum
49	chr1:225630800-225633800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr1:225630800-225636600	Enhancers	Fetal Muscle Leg	muscle

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