Variant report

Variant	nsv889512
Chromosome Location	chr7:153088772-153662151
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1747)
CpG islands
(count:2445)
Chromatin interactive
region (count:275)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:153143735-153143934	K562	blood:	n/a	n/a
2	ARID3A	chr7:153108540-153108589	K562	blood:	n/a	n/a
3	ARID3A	chr7:153103753-153104234	K562	blood:	n/a	n/a
4	ARID3A	chr7:153109096-153109296	K562	blood:	n/a	n/a
5	ARID3A	chr7:153130385-153130583	K562	blood:	n/a	n/a
6	ARID3A	chr7:153103307-153103458	K562	blood:	n/a	n/a
7	ARID3A	chr7:153531658-153531679	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:153110322-153112174	K562	blood:	n/a	n/a
9	ARID3A	chr7:153104655-153106258	K562	blood:	n/a	n/a
10	ARID3A	chr7:153590800-153590804	K562	blood:	n/a	n/a
11	ARID3A	chr7:153109739-153110062	K562	blood:	n/a	n/a
12	ATF1	chr7:153104526-153104952	K562	blood:	n/a	n/a
13	ATF1	chr7:153110923-153111307	K562	blood:	n/a	n/a
14	ATF1	chr7:153308996-153309145	K562	blood:	n/a	n/a
15	ATF1	chr7:153154941-153155221	K562	blood:	n/a	n/a
16	ATF1	chr7:153130251-153130554	K562	blood:	n/a	n/a
17	ATF1	chr7:153119688-153120319	K562	blood:	n/a	n/a
18	ATF1	chr7:153112718-153113068	K562	blood:	n/a	n/a
19	ATF1	chr7:153545773-153545921	K562	blood:	n/a	n/a
20	ATF3	chr7:153119989-153120275	K562	blood:	n/a	n/a
21	BACH1	chr7:153539559-153539602	K562	blood:	n/a	n/a
22	BACH1	chr7:153203925-153204059	K562	blood:	n/a	n/a
23	BACH1	chr7:153097892-153097911	K562	blood:	n/a	n/a
24	BACH1	chr7:153108498-153108636	K562	blood:	n/a	n/a
25	BACH1	chr7:153463065-153463215	K562	blood:	n/a	n/a
26	BACH1	chr7:153591752-153591756	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:153111122-153111267	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:153100843-153101026	K562	blood:	n/a	n/a
29	BACH1	chr7:153109751-153110110	K562	blood:	n/a	n/a
30	BACH1	chr7:153200611-153200865	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr7:153244736-153244872	K562	blood:	n/a	n/a
32	BACH1	chr7:153133123-153133319	K562	blood:	n/a	n/a
33	BACH1	chr7:153583560-153584651	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr7:153631881-153631909	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr7:153110739-153112141	K562	blood:	n/a	n/a
36	BACH1	chr7:153099558-153099965	K562	blood:	n/a	n/a
37	BACH1	chr7:153113244-153113564	K562	blood:	n/a	n/a
38	BATF	chr7:153337705-153337995	GM12878	blood:	n/a	n/a
39	BATF	chr7:153337727-153337979	GM12878	blood:	n/a	n/a
40	BATF	chr7:153474050-153474399	GM12878	blood:	n/a	chr7:153474228-153474239
41	BCL11A	chr7:153474048-153474497	GM12878	blood:	n/a	n/a
42	BCL3	chr7:153505225-153505579	GM12878	blood:	n/a	n/a
43	BCL3	chr7:153104489-153105071	K562	blood:	n/a	n/a
44	BCL3	chr7:153103242-153103537	K562	blood:	n/a	n/a
45	BCL3	chr7:153109499-153110250	K562	blood:	n/a	n/a
46	BCL3	chr7:153505233-153505545	GM12878	blood:	n/a	n/a
47	BCL3	chr7:153105524-153106503	K562	blood:	n/a	n/a
48	BCL3	chr7:153101811-153102227	K562	blood:	n/a	n/a
49	BCLAF1	chr7:153110402-153111174	K562	blood:	n/a	n/a
50	BCLAF1	chr7:153104261-153105189	K562	blood:	n/a	n/a

(count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153442389-153442439	Hepatocyte	liver:	n/a
2	chr7:153583867-153583917	HIPEpiC	eye:	n/a
3	chr7:153449200-153449250	K562	blood:	n/a
4	chr7:153108642-153108692	BE2_C	brain:	n/a
5	chr7:153641267-153641317	AG04450	lung:	fetal
6	chr7:153442389-153442439	Hepatocyte	liver:	n/a
7	chr7:153583867-153583917	HIPEpiC	eye:	n/a
8	chr7:153449200-153449250	K562	blood:	n/a
9	chr7:153108642-153108692	BE2_C	brain:	n/a
10	chr7:153641267-153641317	AG04450	lung:	fetal
11	chr7:153586592-153586642	NB4	blood:	n/a
12	chr7:153641307-153641357	A549	lung:	n/a
13	chr7:153584416-153584466	BJ	skin:	n/a
14	chr7:153583563-153583613	GM06990	blood:	n/a
15	chr7:153584748-153584798	SAEC	small airway:	n/a
16	chr7:153582285-153582335	HepG2	liver:	n/a
17	chr7:153586207-153586257	ECC-1	luminal epithelium:	n/a
18	chr7:153641267-153641317	SKMC	muscle:	n/a
19	chr7:153108642-153108692	GM12878	blood:	n/a
20	chr7:153586592-153586642	Jurkat	blood:	n/a
21	chr7:153108726-153108776	AG09319	gingival:	n/a
22	chr7:153582285-153582335	HCF	heart:	n/a
23	chr7:153586022-153586072	HCPEpiC	choroid plexus:	n/a
24	chr7:153584416-153584466	NHBE	bronchial:	n/a
25	chr7:153108642-153108692	ovcar-3	ovarian:	n/a
26	chr7:153287752-153287802	AG09309	skin:	n/a
27	chr7:153109375-153109425	HNPCEpiC	eye:	n/a
28	chr7:153443930-153443980	ECC-1	luminal epithelium:	n/a
29	chr7:153446256-153446306	SK-N-SH_RA	brain:	n/a
30	chr7:153449200-153449250	BJ	skin:	n/a
31	chr7:153287752-153287802	MCF10A-Er-Src	breast:	n/a
32	chr7:153110492-153110542	GM12892	blood:	n/a
33	chr7:153446256-153446306	Hela-S3	cervix:	n/a
34	chr7:153641307-153641357	H1-hESC	embryonic stem cell:	embryo
35	chr7:153110762-153110812	NB4	blood:	n/a
36	chr7:153110762-153110812	AG04449	skin:	fetal
37	chr7:153109375-153109425	Jurkat	blood:	n/a
38	chr7:153584873-153584923	HRPEpiC	eye:	n/a
39	chr7:153109375-153109425	HRPEpiC	eye:	n/a
40	chr7:153446256-153446306	SAEC	small airway:	n/a
41	chr7:153641267-153641317	HRE	kidney:	n/a
42	chr7:153579447-153579497	T-47D	breast:	n/a
43	chr7:153287752-153287802	GM06990	blood:	n/a
44	chr7:153586130-153586180	BJ	skin:	n/a
45	chr7:153589306-153589356	LNCaP	prostate:	n/a
46	chr7:153583867-153583917	GM06990	blood:	n/a
47	chr7:153287591-153287641	HCF	heart:	n/a
48	chr7:153109538-153109588	HEEpiC	esophagus:	n/a
49	chr7:153446810-153446860	SAEC	small airway:	n/a
50	chr7:153109538-153109588	SKMC	muscle:	n/a

(count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:153106936..153109083-chr7:153612449..153615319,2	K562	blood:
2	chr7:152592588..152594175-chr7:153102302..153103832,2	K562	blood:
3	chr7:153103747..153106321-chr7:153180376..153182318,2	K562	blood:
4	chr7:153102564..153104715-chr7:153192183..153194069,2	K562	blood:
5	chr7:153091082..153093692-chr7:153327387..153329268,2	K562	blood:
6	chr7:153286479..153288377-chr7:153294913..153296439,2	K562	blood:
7	chr7:153103413..153106073-chr7:153238288..153241221,2	K562	blood:
8	chr7:152981185..152983494-chr7:153101027..153103155,2	K562	blood:
9	chr7:152886507..152888458-chr7:153102294..153104030,2	K562	blood:
10	chr7:153094372..153097321-chr7:153253930..153256627,2	K562	blood:
11	chr7:153212579..153217619-chr7:153220846..153223669,4	K562	blood:
12	chr7:153353677..153355280-chr7:153357292..153359740,2	K562	blood:
13	chr7:153111734..153114146-chr7:153170231..153173109,2	K562	blood:
14	chr7:153168042..153171876-chr7:153172518..153177517,5	K562	blood:
15	chr7:153103515..153106229-chr7:153225211..153227248,2	K562	blood:
16	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
17	chr7:153078567..153079314-chr7:153528933..153530177,7	MCF-7	breast:
18	chr7:153636605..153638915-chr7:153643180..153645983,3	K562	blood:
19	chr7:153102808..153104376-chr7:153215788..153218674,2	K562	blood:
20	chr7:153244368..153246054-chr7:153249661..153252423,2	K562	blood:
21	chr7:153380114..153381790-chr7:153386652..153388674,2	K562	blood:
22	chr7:153100820..153103410-chr7:153246584..153249087,2	K562	blood:
23	chr7:153366174..153368925-chr7:153372775..153374765,2	K562	blood:
24	chr7:153168042..153171876-chr7:153172518..153177517,5	K562	blood:
25	chr7:153119320..153121928-chr7:153170985..153172845,2	K562	blood:
26	chr7:64299266..64299795-chr7:153109659..153110240,2	K562	blood:
27	chr7:153095496..153100083-chr7:153227240..153231404,4	K562	blood:
28	chr7:153100820..153103410-chr7:153246584..153249087,2	K562	blood:
29	chr7:152938733..152940838-chr7:153103273..153105378,2	K562	blood:
30	chr7:153250299..153251916-chr7:153251980..153254318,2	K562	blood:
31	chr7:152947748..152949504-chr7:153104988..153107669,2	K562	blood:
32	chr7:153439451..153439951-chr8:111669137..111669684,2	MCF-7	breast:
33	chr7:153168165..153169692-chr7:153180801..153182343,2	K562	blood:
34	chr7:153528295..153530118-chr7:153531328..153534242,2	K562	blood:
35	chr7:153207860..153209582-chr7:153211240..153212900,2	K562	blood:
36	chr7:152890055..152890585-chr7:153532359..153532887,2	MCF-7	breast:
37	chr7:153105650..153108822-chr7:153162776..153165855,3	K562	blood:
38	chr7:153608416..153611349-chr7:153614803..153616522,2	K562	blood:
39	chr7:153055542..153057416-chr7:153103974..153105838,2	K562	blood:
40	chr7:153103375..153106774-chr7:153173661..153176724,3	K562	blood:
41	chr7:153078444..153079476-chr7:153379433..153380748,5	MCF-7	breast:
42	chr7:153089054..153091644-chr7:153185631..153188291,2	K562	blood:
43	chr7:153102849..153104905-chr7:153187331..153188983,2	K562	blood:
44	chr7:153358262..153360123-chr7:153364415..153366361,2	K562	blood:
45	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
46	chr7:153524660..153527227-chr7:153530341..153532970,2	K562	blood:
47	chr7:153535667..153538318-chr7:153542041..153544226,2	K562	blood:
48	chr7:153102849..153104905-chr7:153187331..153188983,2	K562	blood:
49	chr7:153094563..153096914-chr7:153326913..153328518,2	K562	blood:
50	chr7:153109911..153112162-chr7:153199634..153201415,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XRCC2-3	chr7:153221094-153221300	XLOC_006658
2	lnc-XRCC2-1	chr7:153109178-153109319	ENSG00000234722
3	lnc-XRCC2-4	chr7:153413334-153413531	XLOC_006659
4	lnc-DPP6-2	chr7:153120526-153120601	XLOC_006298
5	lnc-DPP6-3	chr7:153092498-153092703	XLOC_006297
6	lnc-DPP6-3	chr7:153093149-153093207	XLOC_006297
7	lnc-DPP6-2	chr7:153119376-153119626	XLOC_006298
8	lnc-XRCC2-3	chr7:153220300-153220910	XLOC_006658
9	lnc-XRCC2-1	chr7:153109176-153109319	ENSG00000234722.3
10	lnc-XRCC2-1	chr7:153104041-153104171	ENSG00000234722
11	lnc-XRCC2-2	chr7:153125396-153125424	XLOC_006657
12	lnc-XRCC2-1	chr7:153102578-153102683	ENSG00000234722
13	lnc-XRCC2-1	chr7:153110698-153111021	ENSG00000234722
14	lnc-DPP6-3	chr7:153092527-153092639	XLOC_006297
15	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722
16	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722.3
17	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722.3
18	lnc-DPP6-7	chr7:153146514-153146960	NONHSAT124301
19	lnc-XRCC2-1	chr7:153104041-153104169	ENSG00000234722.3
20	lnc-XRCC2-4	chr7:153406738-153407404	XLOC_006659
21	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722
22	lnc-XRCC2-2	chr7:153120803-153121101	XLOC_006657

No data

Variant related genes	Relation type
DPP6	TF binding region
ENSG00000233489	TF binding region
ENSG00000234722	TF binding region
DPP6	CpG island
ENSG00000233489	CpG island
ENSG00000234722	CpG island
ENSG00000261455	chromatin interactions
ENSG00000130226	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000223700	chromatin interactions
ENSG00000197774	chromatin interactions
ENSG00000236198	chromatin interactions
ENSG00000234722	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000233489	chromatin interactions
ENSG00000234338	chromatin interactions
ENSG00000171222	chromatin interactions
CDKN1A	miRNA target sites
APAF1	miRNA target sites
DHX57	miRNA target sites
LRRC1	miRNA target sites
CCT2	miRNA target sites

Extended variants
information (count: 10493 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:10493 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10271744	chr7:153088772-153088773	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555875862	chr7:153088789-153088790	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185753312	chr7:153088791-153088792	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569538521	chr7:153088805-153088806	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540121870	chr7:153088822-153088823	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529236405	chr7:153088842-153088843	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138847263	chr7:153088877-153088878	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190901374	chr7:153088878-153088879	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552753974	chr7:153088897-153088898	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574481442	chr7:153088940-153088941	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541436018	chr7:153088963-153088964	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556521655	chr7:153088964-153088965	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574919234	chr7:153088972-153088973	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183090726	chr7:153088986-153088987	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564078124	chr7:153089015-153089016	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187730540	chr7:153089082-153089083	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540423936	chr7:153089101-153089102	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191008209	chr7:153089103-153089104	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183108367	chr7:153089139-153089140	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577700467	chr7:153089150-153089151	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11768904	chr7:153089250-153089251	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs374333039	chr7:153089268-153089269	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149339836	chr7:153089354-153089355	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188190047	chr7:153089385-153089386	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552095050	chr7:153089437-153089438	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200371948	chr7:153089442-153089443	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567183703	chr7:153089445-153089446	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376262664	chr7:153089491-153089492	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534088328	chr7:153089493-153089494	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10808003	chr7:153089510-153089511	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191672524	chr7:153089521-153089522	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535509659	chr7:153089579-153089580	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184626563	chr7:153089630-153089631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10808004	chr7:153089729-153089730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs10246760	chr7:153089742-153089743	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187371794	chr7:153089746-153089747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573113524	chr7:153089805-153089806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35946327	chr7:153089808-153089809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs56884852	chr7:153089810-153089811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71182099	chr7:153089813-153089814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs398067431	chr7:153089815-153089816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540018601	chr7:153089847-153089848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561905428	chr7:153089877-153089878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529104753	chr7:153089900-153089901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192553659	chr7:153089960-153089961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544716220	chr7:153089999-153090000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563012538	chr7:153090076-153090077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533326260	chr7:153090096-153090097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551804343	chr7:153090097-153090098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2312353	chr7:153090137-153090138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Autism	22495309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153084400-153089600	Strong transcription	K562	blood
2	chr7:153089600-153091000	Weak transcription	K562	blood
3	chr7:153090200-153092800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:153091000-153091400	ZNF genes & repeats	K562	blood
5	chr7:153091400-153092600	Weak transcription	K562	blood
6	chr7:153092600-153095800	Strong transcription	K562	blood
7	chr7:153094200-153094600	Enhancers	Lung	lung
8	chr7:153094600-153094800	Weak transcription	Lung	lung
9	chr7:153094800-153095200	Enhancers	Lung	lung
10	chr7:153095200-153096000	Weak transcription	Lung	lung
11	chr7:153095800-153096600	Weak transcription	K562	blood
12	chr7:153096000-153096200	Enhancers	Lung	lung
13	chr7:153096000-153096400	Enhancers	Adipose Nuclei	Adipose
14	chr7:153096600-153098200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:153096600-153104000	Strong transcription	K562	blood
16	chr7:153099800-153100200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:153099800-153100400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:153103400-153104800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:153103800-153104800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr7:153103800-153105000	Enhancers	Brain Germinal Matrix	brain
21	chr7:153104000-153105800	Weak transcription	K562	blood
22	chr7:153105800-153106800	Genic enhancers	K562	blood
23	chr7:153106800-153110000	Transcr. at gene 5' and 3'	K562	blood
24	chr7:153110000-153111000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:153110000-153111400	Active TSS	K562	blood
26	chr7:153111400-153112000	Flanking Active TSS	K562	blood
27	chr7:153112000-153113200	Enhancers	K562	blood
28	chr7:153112800-153113200	Enhancers	Fetal Kidney	kidney
29	chr7:153117600-153118000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr7:153119000-153120000	Enhancers	Adipose Nuclei	Adipose
31	chr7:153119000-153121200	Enhancers	Colon Smooth Muscle	Colon
32	chr7:153119200-153121000	Enhancers	Dnd41	blood
33	chr7:153119400-153119600	Enhancers	Rectal Smooth Muscle	rectum
34	chr7:153119400-153120200	Bivalent Enhancer	K562	blood
35	chr7:153119600-153120600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr7:153120600-153120800	Bivalent Enhancer	K562	blood
37	chr7:153120600-153121000	Enhancers	Rectal Smooth Muscle	rectum
38	chr7:153120800-153121600	Enhancers	Fetal Kidney	kidney
39	chr7:153127000-153127800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr7:153127000-153127800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
41	chr7:153127400-153127600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr7:153128200-153128400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:153128200-153128600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:153128200-153128600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:153128400-153129800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
46	chr7:153128800-153129600	Bivalent Enhancer	K562	blood
47	chr7:153129000-153129400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr7:153129000-153129800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr7:153129200-153129800	Enhancers	Fetal Kidney	kidney
50	chr7:153129200-153129800	Enhancers	Stomach Smooth Muscle	stomach

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