Variant report

Variant	nsv1021229
Chromosome Location	chr8:130887132-131057897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4489)
CpG islands
(count:2562)
Chromatin interactive
region (count:241)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4489 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130983807-130984435	K562	blood:	n/a	n/a
2	ARID3A	chr8:131009008-131009301	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:130985812-130985978	K562	blood:	n/a	n/a
4	ARID3A	chr8:131012944-131013054	K562	blood:	n/a	n/a
5	ARID3A	chr8:130930739-130930879	K562	blood:	n/a	n/a
6	ARID3A	chr8:130952428-130952564	K562	blood:	n/a	n/a
7	ARID3A	chr8:131045172-131045208	K562	blood:	n/a	n/a
8	ARID3A	chr8:130982576-130982644	K562	blood:	n/a	n/a
9	ARID3A	chr8:131004638-131005192	K562	blood:	n/a	n/a
10	ARID3A	chr8:130903869-130904188	K562	blood:	n/a	n/a
11	ARID3A	chr8:131028825-131028876	K562	blood:	n/a	n/a
12	ARID3A	chr8:130951844-130952495	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:131014808-131014920	K562	blood:	n/a	n/a
14	ARID3A	chr8:131054553-131055003	K562	blood:	n/a	n/a
15	ARID3A	chr8:131027514-131028077	K562	blood:	n/a	n/a
16	ATF1	chr8:130929452-130929512	K562	blood:	n/a	n/a
17	ATF1	chr8:131004594-131005276	K562	blood:	n/a	n/a
18	ATF1	chr8:131054462-131054889	K562	blood:	n/a	n/a
19	ATF1	chr8:130985712-130985982	K562	blood:	n/a	n/a
20	ATF1	chr8:131044987-131045295	K562	blood:	n/a	n/a
21	ATF1	chr8:130897746-130898286	K562	blood:	n/a	n/a
22	ATF2	chr8:131027349-131027901	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr8:130900217-130900979	GM12878	blood:	n/a	n/a
24	ATF2	chr8:131027340-131027895	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr8:130951753-130952113	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr8:130996350-130996810	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr8:130897836-130898390	GM12878	blood:	n/a	n/a
28	ATF2	chr8:131020655-131021478	GM12878	blood:	n/a	n/a
29	ATF2	chr8:130983715-130984457	GM12878	blood:	n/a	n/a
30	ATF2	chr8:131048950-131049454	GM12878	blood:	n/a	n/a
31	ATF2	chr8:131054448-131055257	GM12878	blood:	n/a	n/a
32	ATF2	chr8:130952286-130952758	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr8:131054272-131055347	GM12878	blood:	n/a	n/a
34	ATF2	chr8:130897880-130898426	GM12878	blood:	n/a	n/a
35	ATF2	chr8:131041198-131041650	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr8:130951842-130952140	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr8:130951803-130952373	GM12878	blood:	n/a	n/a
38	ATF2	chr8:131020554-131021539	GM12878	blood:	n/a	n/a
39	ATF2	chr8:130983740-130984525	GM12878	blood:	n/a	n/a
40	ATF3	chr8:130996575-130996805	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF3	chr8:131012045-131012531	K562	blood:	n/a	n/a
42	ATF3	chr8:130951834-130952614	A549	lung:	n/a	chr8:130952151-130952160 chr8:130952247-130952256
43	ATF3	chr8:130983720-130984152	K562	blood:	n/a	n/a
44	ATF3	chr8:131008717-131009228	A549	lung:	n/a	n/a
45	ATF3	chr8:131054457-131054915	K562	blood:	n/a	n/a
46	ATF3	chr8:130996418-130996972	A549	lung:	n/a	n/a
47	ATF3	chr8:130996482-130996875	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF3	chr8:130996579-130996822	K562	blood:	n/a	n/a
49	ATF3	chr8:131027039-131028066	A549	lung:	n/a	chr8:131027168-131027181
50	ATF3	chr8:131044974-131045354	K562	blood:	n/a	n/a

(count:2562 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130951373-130951423	IMR90	lung:	fetal
2	chr8:131028232-131028282	GM06990	blood:	n/a
3	chr8:130952075-130952125	ProgFib	skin:	n/a
4	chr8:131031752-131031802	HCF	heart:	n/a
5	chr8:131028985-131029035	GM06990	blood:	n/a
6	chr8:130995417-130995467	AG04449	skin:	fetal
7	chr8:130898833-130898883	CMK	blood:	n/a
8	chr8:130998171-130998221	Caco-2	colon:	n/a
9	chr8:131000261-131000311	GM12892	blood:	n/a
10	chr8:130994109-130994159	GM12878	blood:	n/a
11	chr8:130930889-130930939	H1-hESC	embryonic stem cell:	embryo
12	chr8:131028985-131029035	IMR90	lung:	fetal
13	chr8:131029139-131029189	A549	lung:	n/a
14	chr8:130995990-130996040	HMEC	breast:	n/a
15	chr8:130952330-130952380	NH-A	brain:	n/a
16	chr8:130976125-130976175	GM12891	blood:	n/a
17	chr8:130995990-130996040	PrEC	prostate:	n/a
18	chr8:130954845-130954895	HL-60	blood:	n/a
19	chr8:131054408-131054458	A549	lung:	n/a
20	chr8:130998171-130998221	GM12891	blood:	n/a
21	chr8:130952078-130952128	PANC-1	pancreas:	n/a
22	chr8:131028232-131028282	PrEC	prostate:	n/a
23	chr8:130994109-130994159	Jurkat	blood:	n/a
24	chr8:130995417-130995467	CMK	blood:	n/a
25	chr8:130952137-130952187	ECC-1	luminal epithelium:	n/a
26	chr8:131000415-131000465	MCF10A-Er-Src	breast:	n/a
27	chr8:131027724-131027774	GM12891	blood:	n/a
28	chr8:131027724-131027774	SAEC	small airway:	n/a
29	chr8:131000521-131000571	Caco-2	colon:	n/a
30	chr8:130952330-130952380	HEEpiC	esophagus:	n/a
31	chr8:130952644-130952694	NT2-D1	testis:	n/a
32	chr8:131008537-131008587	Hela-S3	cervix:	n/a
33	chr8:131028990-131029040	AG10803	skin:	n/a
34	chr8:131028985-131029035	GM12891	blood:	n/a
35	chr8:130923773-130923823	A549	lung:	n/a
36	chr8:131000261-131000311	Hela-S3	cervix:	n/a
37	chr8:130925897-130925947	NB4	blood:	n/a
38	chr8:130952742-130952792	GM06990	blood:	n/a
39	chr8:130925897-130925947	GM12878	blood:	n/a
40	chr8:130952137-130952187	AG09309	skin:	n/a
41	chr8:130952075-130952125	NHBE	bronchial:	n/a
42	chr8:130930889-130930939	GM19239	blood:	n/a
43	chr8:130952333-130952383	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:131000521-131000571	AG09309	skin:	n/a
45	chr8:130945857-130945907	HEEpiC	esophagus:	n/a
46	chr8:130947389-130947439	BJ	skin:	n/a
47	chr8:130952075-130952125	RPTEC	kidney:	n/a
48	chr8:130952742-130952792	NH-A	brain:	n/a
49	chr8:131028232-131028282	HCPEpiC	choroid plexus:	n/a
50	chr8:131027724-131027774	Caco-2	colon:	n/a

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:130954709..130956974-chr8:130965501..130967949,2	K562	blood:
2	chr8:130959510..130961740-chr8:130964129..130966017,2	K562	blood:
3	chr8:131045657..131048618-chr8:131053552..131056058,2	K562	blood:
4	chr8:131047199..131051287-chr8:131052494..131054886,3	MCF-7	breast:
5	chr8:130926539..130930830-chr8:130934319..130938827,6	K562	blood:
6	chr8:130996752..130999185-chr8:131000348..131002341,2	MCF-7	breast:
7	chr8:130910934..130912844-chr8:130917105..130920578,4	MCF-7	breast:
8	chr8:130994883..130996522-chr8:131001539..131003623,2	K562	blood:
9	chr8:130958128..130959766-chr8:130960080..130961800,2	MCF-7	breast:
10	chr8:130908195..130912113-chr8:130924701..130928264,3	K562	blood:
11	chr4:152329639..152330392-chr8:130951751..130952461,2	HCT-116	colon:
12	chr8:131007021..131009238-chr8:131011453..131013766,3	MCF-7	breast:
13	chr8:131032809..131035482-chr8:131037784..131039457,2	K562	blood:
14	chr8:130975036..130977455-chr8:130978942..130980656,2	K562	blood:
15	chr8:130937201..130939813-chr8:130948093..130951512,3	K562	blood:
16	chr8:131011363..131013823-chr8:131017566..131020563,3	MCF-7	breast:
17	chr8:130838576..130840911-chr8:130898985..130901514,2	K562	blood:
18	chr8:130967769..130969893-chr8:131027217..131029473,2	K562	blood:
19	chr8:130999535..131002267-chr8:131027934..131030613,2	MCF-7	breast:
20	chr8:130908607..130911071-chr8:131026510..131028615,2	MCF-7	breast:
21	chr8:131025540..131027750-chr8:131037896..131040382,2	MCF-7	breast:
22	chr8:130965774..130967791-chr8:130974900..130977591,2	K562	blood:
23	chr8:131045657..131048618-chr8:131053552..131056058,2	K562	blood:
24	chr8:130984372..130987995-chr8:130999430..131001156,3	K562	blood:
25	chr8:130931267..130935486-chr8:130937892..130940092,5	K562	blood:
26	chr8:130949943..130953390-chr8:131026093..131029581,5	K562	blood:
27	chr8:130950627..130952678-chr8:131014268..131017998,3	K562	blood:
28	chr8:131035060..131037464-chr8:131038992..131041654,2	K562	blood:
29	chr8:130933216..130934839-chr8:130941023..130942716,2	K562	blood:
30	chr8:130926539..130930830-chr8:130934319..130938827,6	K562	blood:
31	chr8:130981588..130985969-chr8:131027661..131030801,4	K562	blood:
32	chr8:130966871..130968440-chr8:130972283..130975022,2	K562	blood:
33	chr8:130935896..130938185-chr8:130950448..130952343,2	MCF-7	breast:
34	chr8:130911413..130914047-chr8:130914470..130917225,2	K562	blood:
35	chr8:130951528..130952250-chr8:131028470..131029127,2	MCF-7	breast:
36	chr8:131027601..131029228-chr8:131030030..131032966,2	MCF-7	breast:
37	chr8:130960320..130961292-chr8:131027438..131028472,5	MCF-7	breast:
38	chr8:130996585..131001100-chr8:131002410..131006763,8	K562	blood:
39	chr8:130950792..130953797-chr8:130957137..130959742,3	K562	blood:
40	chr8:130927294..130929703-chr8:130944717..130947284,2	K562	blood:
41	chr8:131031108..131033473-chr8:131036840..131039215,2	MCF-7	breast:
42	chr8:131003704..131005230-chr8:131007280..131008801,2	K562	blood:
43	chr8:131021262..131023800-chr8:131023935..131026265,2	MCF-7	breast:
44	chr8:130889604..130891485-chr8:130894789..130897188,2	K562	blood:
45	chr8:130880795..130883192-chr8:130906423..130908284,2	K562	blood:
46	chr8:130983642..130985327-chr8:131033782..131036207,2	MCF-7	breast:
47	chr8:130996925..130998430-chr8:131034711..131036563,2	MCF-7	breast:
48	chr8:130949943..130953390-chr8:131026093..131029581,5	K562	blood:
49	chr8:130927994..130929549-chr8:131028328..131029984,2	K562	blood:
50	chr8:130937344..130939463-chr8:130940607..130943087,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFR3A-5	chr8:130902711-130902901	ENSG00000254263
2	lnc-EFR3A-4	chr8:130960070-130960209	ENSG00000253720
3	lnc-GSDMC-5	chr8:130951854-130952017	NONHSAT129139
4	lnc-EFR3A-4	chr8:130952102-130952164	ENSG00000253720
5	lnc-EFR3A-4	chr8:130960795-130960944	ENSG00000253720
6	lnc-GSDMC-5	chr8:130982755-130983241	NONHSAT129141
7	lnc-GSDMC-5	chr8:130915207-130915596	NONHSAT129139
8	lnc-EFR3A-5	chr8:130913729-130914004	ENSG00000254263
9	lnc-EFR3A-4	chr8:130961445-130961640	ENSG00000253720
10	lnc-GSDMC-5	chr8:131028853-131028898	NONHSAT129141

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5194	chr8:131020606-131020627	MIMAT0021125

No data

Variant related genes	Relation type
ENSG00000253720	TF binding region
ENSG00000254263	TF binding region
MIR5194	TF binding region
FAM49B	TF binding region
RNU7-181P	TF binding region
ENSG00000253720	CpG island
ENSG00000254263	CpG island
MIR5194	CpG island
FAM49B	CpG island
RNU7-181P	CpG island
ENSG00000253043	chromatin interactions
ENSG00000153310	chromatin interactions
ENSG00000200075	chromatin interactions
ENSG00000264653	chromatin interactions
ENSG00000124126	chromatin interactions
ENSG00000251611	chromatin interactions
ENSG00000253720	chromatin interactions
ENSG00000164142	chromatin interactions

Extended variants
information (count: 6449 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:6449 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76123272	chr8:130887138-130887139	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs562665794	chr8:130887145-130887146	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs191934729	chr8:130887180-130887181	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs560947469	chr8:130887226-130887227	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs528431287	chr8:130887247-130887248	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs540437732	chr8:130887265-130887266	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs540730955	chr8:130887304-130887305	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs565180538	chr8:130887318-130887319	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565200689	chr8:130887377-130887378	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs149550463	chr8:130887392-130887393	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs533176162	chr8:130887411-130887412	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79904357	chr8:130887435-130887436	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563614186	chr8:130887477-130887478	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111608907	chr8:130887511-130887512	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200118510	chr8:130887513-130887514	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116084824	chr8:130887515-130887516	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182303975	chr8:130887568-130887569	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559916628	chr8:130887595-130887596	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201200567	chr8:130887620-130887621	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534286519	chr8:130887626-130887627	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77869638	chr8:130887627-130887628	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78347246	chr8:130887636-130887637	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547205179	chr8:130887645-130887646	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571230990	chr8:130887711-130887712	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186571501	chr8:130887757-130887758	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs80261908	chr8:130887758-130887759	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73710955	chr8:130887811-130887812	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536554577	chr8:130887850-130887851	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554805201	chr8:130887858-130887859	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144728377	chr8:130887893-130887894	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190183699	chr8:130887910-130887911	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28593681	chr8:130887933-130887934	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs143459733	chr8:130888005-130888006	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116316854	chr8:130888028-130888029	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182406527	chr8:130888058-130888059	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545269653	chr8:130888177-130888178	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188398131	chr8:130888208-130888209	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530683492	chr8:130888215-130888216	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375101729	chr8:130888253-130888254	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560994493	chr8:130888337-130888338	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528115414	chr8:130888342-130888343	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200991109	chr8:130888362-130888363	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs298610	chr8:130888404-130888405	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs571362066	chr8:130888411-130888412	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146766035	chr8:130888424-130888425	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139296039	chr8:130888492-130888493	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561168860	chr8:130888504-130888505	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554704458	chr8:130888631-130888632	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569120483	chr8:130888647-130888648	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193202893	chr8:130888695-130888696	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5901 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130864400-130903600	Weak transcription	Colon Smooth Muscle	Colon
2	chr8:130864600-130888200	Weak transcription	Small Intestine	intestine
3	chr8:130864800-130898200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr8:130865000-130897400	Weak transcription	Psoas Muscle	Psoas
5	chr8:130865200-130887200	Weak transcription	Fetal Kidney	kidney
6	chr8:130865200-130897600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr8:130865400-130899200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr8:130865600-130907600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr8:130866000-130894800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr8:130866400-130891600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr8:130868000-130891400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr8:130869800-130895800	Weak transcription	HepG2	liver
13	chr8:130869800-130897600	Weak transcription	Brain Angular Gyrus	brain
14	chr8:130871200-130887600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:130871200-130896000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr8:130873600-130895600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr8:130873800-130887600	Weak transcription	Fetal Stomach	stomach
18	chr8:130874000-130899000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr8:130874600-130897600	Weak transcription	Brain Hippocampus Middle	brain
20	chr8:130875200-130897400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr8:130875800-130899400	Weak transcription	Fetal Intestine Large	intestine
22	chr8:130877200-130897400	Weak transcription	Fetal Intestine Small	intestine
23	chr8:130877200-130898800	Weak transcription	Lung	lung
24	chr8:130881800-130887800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr8:130882000-130887600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr8:130882600-130888400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:130882600-130889400	Weak transcription	K562	blood
28	chr8:130882800-130887200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:130882800-130887600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:130882800-130896000	Weak transcription	Pancreas	Pancrea
31	chr8:130882800-130897600	Weak transcription	Right Ventricle	heart
32	chr8:130882800-130898800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:130883000-130887200	Weak transcription	NHLF	lung
34	chr8:130883000-130887800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:130883000-130888000	Weak transcription	Aorta	Aorta
36	chr8:130883000-130891400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr8:130883000-130895600	Weak transcription	Fetal Muscle Leg	muscle
38	chr8:130883000-130897400	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr8:130883000-130897400	Weak transcription	Gastric	stomach
40	chr8:130883000-130897400	Weak transcription	Thymus	Thymus
41	chr8:130883000-130897800	Weak transcription	Esophagus	oesophagus
42	chr8:130883000-130897800	Weak transcription	Spleen	Spleen
43	chr8:130883200-130891600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr8:130883200-130899000	Weak transcription	Placenta	Placenta
45	chr8:130883200-130899200	Weak transcription	Fetal Muscle Trunk	muscle
46	chr8:130883400-130887600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr8:130883400-130890800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr8:130883400-130891200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr8:130883400-130892400	Weak transcription	Primary B cells from cord blood	blood
50	chr8:130883400-130895800	Weak transcription	Left Ventricle	heart

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