Variant report

Variant	nsv6315
Chromosome Location	chr8:96216465-96261671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1323)
CpG islands
(count:122)
Chromatin interactive
region (count:161)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1323 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:96223744-96224151	HepG2	liver:	n/a	chr8:96223906-96223922 chr8:96223905-96223921
2	ARID3A	chr8:96260867-96261286	K562	blood:	n/a	chr8:96260887-96260903 chr8:96260886-96260902
3	ARID3A	chr8:96235911-96236248	K562	blood:	n/a	n/a
4	ARID3A	chr8:96237312-96237625	K562	blood:	n/a	n/a
5	ARID3A	chr8:96238736-96239118	K562	blood:	n/a	n/a
6	ARID3A	chr8:96237680-96238075	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:96260945-96261297	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:96237833-96237936	K562	blood:	n/a	n/a
9	ARID3A	chr8:96224165-96224531	K562	blood:	n/a	n/a
10	ARID3A	chr8:96222407-96222791	HepG2	liver:	n/a	n/a
11	ATF1	chr8:96241079-96241401	K562	blood:	n/a	n/a
12	ATF1	chr8:96249430-96249693	K562	blood:	n/a	n/a
13	ATF1	chr8:96221867-96222148	K562	blood:	n/a	n/a
14	ATF1	chr8:96235725-96236095	K562	blood:	n/a	n/a
15	ATF1	chr8:96238705-96239049	K562	blood:	n/a	n/a
16	ATF2	chr8:96249960-96250581	GM12878	blood:	n/a	n/a
17	ATF2	chr8:96240355-96240989	GM12878	blood:	n/a	n/a
18	ATF2	chr8:96260917-96261308	GM12878	blood:	n/a	n/a
19	ATF2	chr8:96240481-96240886	GM12878	blood:	n/a	n/a
20	ATF2	chr8:96226054-96226497	GM12878	blood:	n/a	n/a
21	ATF2	chr8:96260868-96261328	GM12878	blood:	n/a	n/a
22	ATF2	chr8:96249930-96250564	GM12878	blood:	n/a	n/a
23	ATF3	chr8:96241002-96241334	K562	blood:	n/a	n/a
24	ATF3	chr8:96238640-96239042	K562	blood:	n/a	n/a
25	ATF3	chr8:96249280-96249710	K562	blood:	n/a	n/a
26	ATF3	chr8:96241722-96242193	GM12878	blood:	n/a	n/a
27	ATF3	chr8:96241845-96242061	GM12878	blood:	n/a	n/a
28	ATF3	chr8:96241832-96242128	K562	blood:	n/a	n/a
29	BACH1	chr8:96237741-96238307	K562	blood:	n/a	n/a
30	BACH1	chr8:96238683-96239045	K562	blood:	n/a	n/a
31	BACH1	chr8:96237898-96237955	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr8:96249947-96250642	GM12878	blood:	n/a	n/a
33	BATF	chr8:96240535-96240805	GM12878	blood:	n/a	n/a
34	BATF	chr8:96250042-96250356	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:96240502-96240757	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:96240489-96240847	GM12878	blood:	n/a	n/a
37	BCL3	chr8:96248125-96248419	GM12878	blood:	n/a	n/a
38	BCL3	chr8:96229221-96229625	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:96249896-96250659	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:96260979-96261212	GM12878	blood:	n/a	n/a
41	BCLAF1	chr8:96240458-96241034	GM12878	blood:	n/a	n/a
42	BCLAF1	chr8:96260961-96261367	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:96250046-96250483	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:96235734-96236401	K562	blood:	n/a	n/a
45	BHLHE40	chr8:96241057-96241691	K562	blood:	n/a	n/a
46	BHLHE40	chr8:96240570-96240977	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:96249427-96249693	K562	blood:	n/a	n/a
48	BHLHE40	chr8:96224599-96224903	K562	blood:	n/a	n/a
49	BHLHE40	chr8:96238650-96239057	K562	blood:	n/a	n/a
50	BHLHE40	chr8:96243632-96243648	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96258496-96258546	Hepatocyte	liver:	n/a
2	chr8:96226844-96226894	HEK293	kidney:	embryo
3	chr8:96258496-96258546	LNCaP	prostate:	n/a
4	chr8:96226844-96226894	HNPCEpiC	eye:	n/a
5	chr8:96258496-96258546	RPTEC	kidney:	n/a
6	chr8:96258496-96258546	SKMC	muscle:	n/a
7	chr8:96258496-96258546	Caco-2	colon:	n/a
8	chr8:96226844-96226894	HCT-116	colon:	n/a
9	chr8:96258496-96258546	SAEC	small airway:	n/a
10	chr8:96226844-96226894	AG04450	lung:	fetal
11	chr8:96226844-96226894	HEEpiC	esophagus:	n/a
12	chr8:96258496-96258546	NHBE	bronchial:	n/a
13	chr8:96226844-96226894	SK-N-MC	brain:	n/a
14	chr8:96258496-96258546	Jurkat	blood:	n/a
15	chr8:96258496-96258546	T-47D	breast:	n/a
16	chr8:96258496-96258546	NHDF-neo	bronchial:	n/a
17	chr8:96258496-96258546	GM12892	blood:	n/a
18	chr8:96258496-96258546	BJ	skin:	n/a
19	chr8:96226844-96226894	HepG2	liver:	n/a
20	chr8:96226844-96226894	HRCEpiC	kidney:	n/a
21	chr8:96258496-96258546	HIPEpiC	eye:	n/a
22	chr8:96226844-96226894	AG09309	skin:	n/a
23	chr8:96226844-96226894	NH-A	brain:	n/a
24	chr8:96258496-96258546	SK-N-SH	brain:	n/a
25	chr8:96226844-96226894	K562	blood:	n/a
26	chr8:96226844-96226894	A549	lung:	n/a
27	chr8:96226844-96226894	ECC-1	luminal epithelium:	n/a
28	chr8:96226844-96226894	SK-N-SH	brain:	n/a
29	chr8:96226844-96226894	GM12878	blood:	n/a
30	chr8:96226844-96226894	NT2-D1	testis:	n/a
31	chr8:96226844-96226894	HUVEC	blood vessel:	n/a
32	chr8:96258496-96258546	ovcar-3	ovarian:	n/a
33	chr8:96258496-96258546	GM19239	blood:	n/a
34	chr8:96258496-96258546	AG09309	skin:	n/a
35	chr8:96226844-96226894	MCF10A-Er-Src	breast:	n/a
36	chr8:96258496-96258546	AG04449	skin:	fetal
37	chr8:96258496-96258546	Hela-S3	cervix:	n/a
38	chr8:96226844-96226894	Caco-2	colon:	n/a
39	chr8:96226844-96226894	GM12892	blood:	n/a
40	chr8:96226844-96226894	ProgFib	skin:	n/a
41	chr8:96258496-96258546	HUVEC	blood vessel:	n/a
42	chr8:96258496-96258546	AG04450	lung:	fetal
43	chr8:96226844-96226894	U87	brain:	n/a
44	chr8:96226844-96226894	RPTEC	kidney:	n/a
45	chr8:96226844-96226894	Jurkat	blood:	n/a
46	chr8:96226844-96226894	HMEC	breast:	n/a
47	chr8:96258496-96258546	HEK293	kidney:	embryo
48	chr8:96258496-96258546	AG10803	skin:	n/a
49	chr8:96226844-96226894	HCPEpiC	choroid plexus:	n/a
50	chr8:96258496-96258546	HNPCEpiC	eye:	n/a

(count:161 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:96236807..96240008-chr8:96246119..96247780,3	MCF-7	breast:
2	chr8:96037192..96039493-chr8:96242564..96245463,2	MCF-7	breast:
3	chr8:96222002..96228732-chr8:96228964..96237755,16	MCF-7	breast:
4	chr8:96210702..96213000-chr8:96259520..96261197,2	MCF-7	breast:
5	chr8:96214177..96216026-chr8:96245562..96248226,2	MCF-7	breast:
6	chr8:96221181..96226002-chr8:96248062..96252220,6	MCF-7	breast:
7	chr8:96229389..96231464-chr8:96247771..96249721,2	K562	blood:
8	chr8:96123802..96126736-chr8:96258433..96260604,2	MCF-7	breast:
9	chr8:96239351..96241151-chr8:96247805..96249381,2	MCF-7	breast:
10	chr8:96218443..96220891-chr8:96249353..96251227,2	MCF-7	breast:
11	chr8:96230420..96235229-chr8:96280327..96282960,4	MCF-7	breast:
12	chr8:96249492..96251130-chr8:96256592..96259030,2	K562	blood:
13	chr8:96218170..96221837-chr8:96222580..96225075,3	MCF-7	breast:
14	chr8:96243081..96246840-chr8:96248821..96252281,5	K562	blood:
15	chr8:96068887..96069501-chr8:96260956..96261535,2	K562	blood:
16	chr8:95912286..95913059-chr8:96260714..96261265,2	MCF-7	breast:
17	chr8:96240965..96243166-chr8:96252025..96254042,3	K562	blood:
18	chr8:96145311..96147896-chr8:96222063..96224775,3	MCF-7	breast:
19	chr8:96206048..96207695-chr8:96222331..96224850,2	MCF-7	breast:
20	chr8:96238086..96240049-chr8:96241356..96243074,2	K562	blood:
21	chr8:96219891..96220754-chr8:96235921..96236812,8	MCF-7	breast:
22	chr8:96260878..96262975-chr8:96277953..96279731,2	K562	blood:
23	chr8:96239351..96241151-chr8:96247805..96249381,2	MCF-7	breast:
24	chr8:96087772..96089911-chr8:96238508..96240959,2	MCF-7	breast:
25	chr8:96249665..96253673-chr8:96259430..96262765,4	K562	blood:
26	chr8:96228952..96231247-chr8:96237951..96240683,3	MCF-7	breast:
27	chr8:96232022..96234358-chr8:96242400..96245249,2	K562	blood:
28	chr8:96256620..96258806-chr8:96280344..96282393,2	MCF-7	breast:
29	chr8:96236593..96238582-chr8:96243971..96246452,2	K562	blood:
30	chr8:96055071..96057640-chr8:96260633..96262435,2	MCF-7	breast:
31	chr8:96145482..96148403-chr8:96241783..96244505,2	MCF-7	breast:
32	chr8:96245615..96247830-chr8:96279996..96282391,2	MCF-7	breast:
33	chr8:96222030..96225621-chr8:96235538..96238037,4	MCF-7	breast:
34	chr8:96084881..96087733-chr8:96239867..96242215,3	MCF-7	breast:
35	chr8:96236593..96238582-chr8:96243971..96246452,2	K562	blood:
36	chr8:96069257..96069944-chr8:96260679..96261427,2	MCF-7	breast:
37	chr8:96124242..96126154-chr8:96223005..96225325,2	MCF-7	breast:
38	chr8:96234462..96239842-chr8:96279058..96283088,6	K562	blood:
39	chr8:96221181..96226002-chr8:96248062..96252220,6	MCF-7	breast:
40	chr8:96220160..96222982-chr8:96225240..96226907,2	K562	blood:
41	chr8:96247598..96249978-chr8:96254089..96255776,2	K562	blood:
42	chr8:96233041..96235359-chr8:96238288..96241007,3	K562	blood:
43	chr8:96204194..96207440-chr8:96236906..96239736,3	MCF-7	breast:
44	chr8:96203164..96205455-chr8:96217318..96219508,3	MCF-7	breast:
45	chr8:96219891..96220818-chr8:96235921..96236731,3	MCF-7	breast:
46	chr8:96206515..96208115-chr8:96256638..96258375,2	MCF-7	breast:
47	chr8:96221802..96225274-chr8:96226379..96230011,4	K562	blood:
48	chr8:96218874..96220553-chr8:96227342..96228870,2	MCF-7	breast:
49	chr8:96224254..96224982-chr8:96236085..96236596,2	MCF-7	breast:
50	chr8:96167676..96169648-chr8:96260449..96262617,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf37-1	chr8:96220713-96220767	NONHSAT127827
2	lnc-C8orf37-1	chr8:96220647-96220806	ENSG00000253351
3	lnc-PLEKHF2-2	chr8:96216684-96217151	ENSG00000253773.1
4	lnc-C8orf37-1	chr8:96228546-96228602	ENSG00000253351
5	lnc-C8orf37-1	chr8:96228546-96228743	NONHSAT127827
6	lnc-PLEKHF2-2	chr8:96217488-96217540	ENSG00000253773.1
7	lnc-C8orf37-1	chr8:96219235-96219536	ENSG00000253351

No data

Variant related genes	Relation type
ENSG00000253351	TF binding region
ENSG00000253773	TF binding region
ENSG00000253351	CpG island
ENSG00000253773	CpG island
ENSG00000254248	chromatin interactions
ENSG00000156170	chromatin interactions
ENSG00000175305	chromatin interactions
ENSG00000253351	chromatin interactions
ENSG00000253773	chromatin interactions
ENSG00000156469	chromatin interactions
ENSG00000245080	chromatin interactions
ENSG00000253878	chromatin interactions
ENSG00000156471	chromatin interactions
ENSG00000164938	chromatin interactions
ENSG00000175895	chromatin interactions
ENSG00000156172	chromatin interactions

Extended variants
information (count: 1656 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75643353	chr8:96216470-96216471	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs114936995	chr8:96216514-96216515	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs144228827	chr8:96216519-96216520	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148706187	chr8:96216537-96216538	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs575625558	chr8:96216543-96216544	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs544727576	chr8:96216561-96216562	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs192218097	chr8:96216569-96216570	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185004787	chr8:96216578-96216579	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs117882618	chr8:96216629-96216630	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141469181	chr8:96216645-96216646	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147476403	chr8:96216654-96216655	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs77969221	chr8:96216655-96216656	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs140099218	chr8:96216749-96216750	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs532515149	chr8:96216760-96216761	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs552322689	chr8:96216817-96216818	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs189853315	chr8:96216827-96216828	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs76231040	chr8:96216829-96216830	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs34840818	chr8:96216832-96216833	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs114986217	chr8:96216865-96216866	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs547144790	chr8:96216879-96216880	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs567134788	chr8:96216914-96216915	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs536085231	chr8:96216918-96216919	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs535067623	chr8:96216923-96216924	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs192800315	chr8:96216930-96216931	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs371560632	chr8:96216935-96216936	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs2514564	chr8:96216940-96216941	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs11987379	chr8:96216955-96216956	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145538532	chr8:96216970-96216971	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs184853440	chr8:96217041-96217042	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs2514565	chr8:96217043-96217044	Weak transcription Enhancers Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs554743817	chr8:96217091-96217092	Weak transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
32	rs542454025	chr8:96217183-96217184	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs75101003	chr8:96217192-96217193	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs147752642	chr8:96217204-96217205	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs114485878	chr8:96217209-96217210	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs139986585	chr8:96217210-96217211	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs546151191	chr8:96217217-96217218	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs189312261	chr8:96217222-96217223	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs149889762	chr8:96217252-96217253	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs75660269	chr8:96217284-96217285	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs561895476	chr8:96217291-96217292	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs552247918	chr8:96217312-96217313	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs144898914	chr8:96217318-96217319	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs180765398	chr8:96217330-96217331	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs11987491	chr8:96217351-96217352	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs11987496	chr8:96217379-96217380	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs552108854	chr8:96217385-96217386	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs372081909	chr8:96217386-96217387	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs189200399	chr8:96217416-96217417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553897351	chr8:96217442-96217443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:862 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96209000-96220000	Weak transcription	Right Ventricle	heart
2	chr8:96212000-96218000	Enhancers	Primary B cells from peripheral blood	blood
3	chr8:96212400-96217000	Enhancers	Fetal Thymus	thymus
4	chr8:96214000-96217000	Enhancers	HepG2	liver
5	chr8:96214200-96220000	Weak transcription	HMEC	breast
6	chr8:96214200-96226400	Weak transcription	Right Atrium	heart
7	chr8:96214400-96233400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:96214600-96217200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr8:96215200-96220400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr8:96215400-96217000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr8:96215400-96219400	Weak transcription	Placenta	Placenta
12	chr8:96215600-96220000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:96215800-96220800	Weak transcription	Primary B cells from cord blood	blood
14	chr8:96215800-96220800	Weak transcription	Thymus	Thymus
15	chr8:96216000-96217400	Enhancers	K562	blood
16	chr8:96216200-96216600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:96216200-96217800	Enhancers	Pancreas	Pancrea
18	chr8:96216200-96220000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:96216400-96216600	Weak transcription	Esophagus	oesophagus
20	chr8:96216400-96216600	Enhancers	Gastric	stomach
21	chr8:96216600-96216800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:96216600-96216800	Enhancers	Esophagus	oesophagus
23	chr8:96216600-96217000	Weak transcription	Gastric	stomach
24	chr8:96216800-96217000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr8:96216800-96218000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:96216800-96220000	Weak transcription	Esophagus	oesophagus
27	chr8:96217000-96217200	Enhancers	Gastric	stomach
28	chr8:96217000-96217400	Bivalent Enhancer	HepG2	liver
29	chr8:96217000-96219400	Weak transcription	Fetal Thymus	thymus
30	chr8:96217200-96217800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:96217200-96220600	Weak transcription	Gastric	stomach
32	chr8:96217400-96220200	Weak transcription	K562	blood
33	chr8:96217800-96218800	Weak transcription	Pancreas	Pancrea
34	chr8:96217800-96220000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:96218000-96219200	Weak transcription	Primary B cells from peripheral blood	blood
36	chr8:96218000-96220000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:96218800-96227000	Enhancers	Pancreas	Pancrea
38	chr8:96219200-96219400	Enhancers	Primary B cells from peripheral blood	blood
39	chr8:96219400-96219800	Weak transcription	Primary B cells from peripheral blood	blood
40	chr8:96219400-96220600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr8:96219400-96221400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:96219400-96222400	Enhancers	Placenta	Placenta
43	chr8:96219400-96229600	Enhancers	Fetal Thymus	thymus
44	chr8:96219800-96225600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr8:96219800-96251800	Enhancers	Primary B cells from peripheral blood	blood
46	chr8:96220000-96220200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:96220000-96220200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:96220000-96220200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr8:96220000-96220200	Enhancers	Spleen	Spleen
50	chr8:96220000-96220400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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