Variant report

Variant	nsv970441
Chromosome Location	chr7:6039097-6048842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:719)
CpG islands
(count:427)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6048573-6048736	K562	blood:	n/a	n/a
2	ARID3A	chr7:6043356-6043411	K562	blood:	n/a	n/a
3	ARID3A	chr7:6048396-6049266	HepG2	liver:	n/a	n/a
4	ATF1	chr7:6048597-6049112	K562	blood:	n/a	n/a
5	ATF2	chr7:6048715-6049138	GM12878	blood:	n/a	n/a
6	ATF2	chr7:6048405-6049290	GM12878	blood:	n/a	n/a
7	ATF2	chr7:6048690-6049101	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr7:6048394-6049286	A549	lung:	n/a	chr7:6048833-6048844 chr7:6048834-6048841 chr7:6048833-6048841 chr7:6048830-6048845 chr7:6048834-6048844
9	BACH1	chr7:6048388-6048687	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr7:6047227-6047554	GM12878	blood:	n/a	n/a
11	BCL3	chr7:6048341-6049310	A549	lung:	n/a	chr7:6049244-6049257
12	BCLAF1	chr7:6048196-6049185	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:6048295-6049309	K562	blood:	n/a	n/a
14	BHLHE40	chr7:6048306-6049316	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:6048320-6049331	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:6048446-6049104	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr7:6048454-6048953	GM12878	blood:	n/a	n/a
18	BRCA1	chr7:6048377-6049222	HepG2	liver:	n/a	n/a
19	BRCA1	chr7:6048458-6048612	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr7:6048165-6049362	K562	blood:	n/a	n/a
21	CBX3	chr7:6048751-6049119	K562	blood:	n/a	n/a
22	CCNT2	chr7:6048394-6049371	K562	blood:	n/a	n/a
23	CEBPB	chr7:6048414-6048709	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:6048567-6048712	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:6048465-6049054	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:6048634-6048788	K562	blood:	n/a	n/a
27	CEBPB	chr7:6048405-6049220	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:6048451-6049155	IMR90	lung:	n/a	n/a
29	CEBPD	chr7:6048387-6049148	HepG2	liver:	n/a	n/a
30	CEBPD	chr7:6048426-6049214	K562	blood:	n/a	n/a
31	CEBPD	chr7:6048501-6048705	HepG2	liver:	n/a	n/a
32	CHD1	chr7:6048289-6048622	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr7:6047942-6049154	GM12878	blood:	n/a	n/a
34	CHD2	chr7:6048386-6049307	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr7:6048455-6049173	GM12878	blood:	n/a	n/a
36	CHD2	chr7:6048405-6049209	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr7:6048379-6049169	K562	blood:	n/a	n/a
38	CHD2	chr7:6048418-6049249	HepG2	liver:	n/a	n/a
39	CREB1	chr7:6048332-6049310	HepG2	liver:	n/a	n/a
40	CREB1	chr7:6048463-6049387	K562	blood:	n/a	n/a
41	CREB1	chr7:6048624-6049277	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr7:6048607-6049149	ECC-1	luminal epithelium:	n/a	n/a
43	CREB1	chr7:6048574-6049122	ECC-1	luminal epithelium:	n/a	n/a
44	CREB1	chr7:6048599-6049074	A549	lung:	n/a	n/a
45	CREB1	chr7:6048407-6049343	A549	lung:	n/a	n/a
46	CREB1	chr7:6048382-6049188	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr7:6048263-6049334	GM12878	blood:	n/a	n/a
48	CREB1	chr7:6048304-6049464	HepG2	liver:	n/a	n/a
49	CTCF	chr7:6048400-6048550	GM12865	blood:	n/a	chr7:6048502-6048515 chr7:6048499-6048517 chr7:6048502-6048511
50	CTCF	chr7:6048441-6048605	MCF-7	breast:	n/a	chr7:6048502-6048515 chr7:6048499-6048517 chr7:6048502-6048511

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6048832-6048882	CMK	blood:	n/a
2	chr7:6047553-6047603	HMEC	breast:	n/a
3	chr7:6048715-6048765	Hela-S3	cervix:	n/a
4	chr7:6048715-6048765	HRPEpiC	eye:	n/a
5	chr7:6047553-6047603	AG10803	skin:	n/a
6	chr7:6048710-6048760	HCM	heart:	n/a
7	chr7:6048663-6048713	AG10803	skin:	n/a
8	chr7:6048663-6048713	Caco-2	colon:	n/a
9	chr7:6048663-6048713	NT2-D1	testis:	n/a
10	chr7:6048710-6048760	AG10803	skin:	n/a
11	chr7:6047553-6047603	HCF	heart:	n/a
12	chr7:6047553-6047603	HepG2	liver:	n/a
13	chr7:6047553-6047603	HNPCEpiC	eye:	n/a
14	chr7:6048614-6048664	MCF-7	breast:	n/a
15	chr7:6048710-6048760	HL-60	blood:	n/a
16	chr7:6048663-6048713	HCPEpiC	choroid plexus:	n/a
17	chr7:6048614-6048664	HRE	kidney:	n/a
18	chr7:6048832-6048882	A549	lung:	n/a
19	chr7:6048673-6048723	NT2-D1	testis:	n/a
20	chr7:6048614-6048664	NT2-D1	testis:	n/a
21	chr7:6048614-6048664	GM06990	blood:	n/a
22	chr7:6048673-6048723	GM19239	blood:	n/a
23	chr7:6048710-6048760	GM12878	blood:	n/a
24	chr7:6047553-6047603	CMK	blood:	n/a
25	chr7:6047553-6047603	AG04450	lung:	fetal
26	chr7:6048673-6048723	GM12878	blood:	n/a
27	chr7:6048663-6048713	HRE	kidney:	n/a
28	chr7:6048715-6048765	HRE	kidney:	n/a
29	chr7:6048673-6048723	HMEC	breast:	n/a
30	chr7:6048710-6048760	HEEpiC	esophagus:	n/a
31	chr7:6047553-6047603	AG09309	skin:	n/a
32	chr7:6048715-6048765	AG09309	skin:	n/a
33	chr7:6048832-6048882	PFSK-1	brain:	n/a
34	chr7:6048710-6048760	HUVEC	blood vessel:	n/a
35	chr7:6048614-6048664	LNCaP	prostate:	n/a
36	chr7:6048832-6048882	HepG2	liver:	n/a
37	chr7:6048832-6048882	RPTEC	kidney:	n/a
38	chr7:6048832-6048882	AG09309	skin:	n/a
39	chr7:6048832-6048882	AoSMC	blood vessel:	n/a
40	chr7:6048614-6048664	BJ	skin:	n/a
41	chr7:6048663-6048713	SK-N-SH_RA	brain:	n/a
42	chr7:6048710-6048760	AoSMC	blood vessel:	n/a
43	chr7:6048832-6048882	Jurkat	blood:	n/a
44	chr7:6048614-6048664	SK-N-SH_RA	brain:	n/a
45	chr7:6048673-6048723	AG10803	skin:	n/a
46	chr7:6048673-6048723	MCF10A-Er-Src	breast:	n/a
47	chr7:6048832-6048882	BJ	skin:	n/a
48	chr7:6048832-6048882	HCPEpiC	choroid plexus:	n/a
49	chr7:6048663-6048713	GM12891	blood:	n/a
50	chr7:6048663-6048713	PrEC	prostate:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:39845083..39845933-chr7:6048217..6048963,2	NB4	blood:
2	chr7:6048395..6048947-chr7:6768981..6769924,2	NB4	blood:
3	chr12:120729471..120730015-chr7:6048155..6048715,2	NB4	blood:
4	chr11:2950437..2950992-chr7:6048444..6048999,2	Hela-S3	cervix:
5	chr7:6047404..6049912-chr7:6142714..6146343,4	MCF-7	breast:
6	chr11:108093125..108093795-chr7:6048455..6049343,2	Hela-S3	cervix:
7	chr7:6047922..6050389-chr7:6388573..6391369,3	K562	blood:
8	chr7:6047355..6050049-chr7:6209625..6211423,2	MCF-7	breast:
9	chr7:6048462..6049308-chr8:10696898..10697687,2	Hela-S3	cervix:
10	chr7:6041705..6045263-chr7:6045824..6048661,5	MCF-7	breast:
11	chr7:6046534..6048837-chr7:6387102..6390061,2	MCF-7	breast:
12	chr7:6047363..6049354-chr7:6063912..6067391,3	MCF-7	breast:
13	chr15:65588043..65588860-chr7:6048557..6049373,2	Hela-S3	cervix:
14	chr2:20646774..20647429-chr7:6048823..6049727,2	Hela-S3	cervix:
15	chr7:6047930..6051239-chr7:6095534..6098918,6	K562	blood:
16	chr7:6046967..6050535-chr7:6141219..6149580,10	K562	blood:
17	chr16:68002087..68002738-chr7:6048614..6049589,2	Hela-S3	cervix:
18	chr20:25387920..25388819-chr7:6048429..6049127,2	NB4	blood:
19	chr7:6047579..6050679-chr7:6097211..6100186,3	MCF-7	breast:
20	chr1:45987071..45987954-chr7:6048707..6049207,2	Hela-S3	cervix:
21	chr7:6048507..6049135-chr9:35731875..35732703,2	Hela-S3	cervix:
22	chr7:6041705..6045263-chr7:6045824..6048661,5	MCF-7	breast:
23	chr7:6046629..6049121-chr7:6054916..6059212,5	K562	blood:
24	chr7:6038036..6040606-chr7:6387111..6388814,2	MCF-7	breast:
25	chr7:6048837..6049368-chr7:99933514..99934016,2	Hela-S3	cervix:
26	chr7:6047026..6051403-chr7:6141746..6146462,7	K562	blood:
27	chr1:153598961..153599821-chr7:6048148..6049140,2	Hela-S3	cervix:
28	chr5:10307612..10308244-chr7:6048393..6048921,2	Hela-S3	cervix:
29	chr7:6040633..6042270-chr7:6067684..6070514,2	K562	blood:
30	chr7:6044783..6046787-chr7:6047336..6049227,2	K562	blood:
31	chr7:6035718..6038633-chr7:6038935..6040771,2	K562	blood:
32	chr7:6048448..6049112-chr7:66766894..66767462,2	Hela-S3	cervix:
33	chr7:6036139..6038857-chr7:6041101..6043298,3	K562	blood:
34	chr7:6048500..6051239-chr7:6096959..6099959,3	K562	blood:
35	chr7:6047262..6048916-chr7:6096593..6098744,2	MCF-7	breast:
36	chr7:6044783..6046787-chr7:6047336..6049227,2	K562	blood:
37	chr7:6048826..6049627-chr7:6143766..6144544,2	HCT-116	colon:
38	chr7:6035573..6039204-chr7:6386804..6390151,4	MCF-7	breast:
39	chr5:16465324..16466134-chr7:6048690..6049317,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
AIMP2	TF binding region
PMS2	TF binding region
ENSG00000201990	TF binding region
AIMP2	CpG island
PMS2	CpG island
ENSG00000201990	CpG island
ENSG00000202538	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000143878	chromatin interactions
ENSG00000149308	chromatin interactions
ENSG00000252929	chromatin interactions
ENSG00000181649	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000137076	chromatin interactions
ENSG00000008256	chromatin interactions
ENSG00000149311	chromatin interactions
ENSG00000178397	chromatin interactions
ENSG00000207217	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000067601	chromatin interactions
ENSG00000258724	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000189171	chromatin interactions
ENSG00000164237	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000121716	chromatin interactions
ENSG00000272752	chromatin interactions
ENSG00000254093	chromatin interactions
ENSG00000124067	chromatin interactions
ENSG00000242294	chromatin interactions
ENSG00000201990	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000173545	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000107175	chromatin interactions

Extended variants
information (count: 514 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2345060	chr7:6039129-6039130	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142278565	chr7:6039195-6039196	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147891177	chr7:6039196-6039197	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs542003306	chr7:6039211-6039212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554009968	chr7:6039247-6039248	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183113848	chr7:6039266-6039267	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545792163	chr7:6039267-6039268	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564442382	chr7:6039268-6039269	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs397712111	chr7:6039277-6039278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs111412989	chr7:6039288-6039289	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145200498	chr7:6039318-6039319	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561620695	chr7:6039328-6039329	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528966677	chr7:6039341-6039342	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547539552	chr7:6039343-6039344	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547688127	chr7:6039377-6039378	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs79245786	chr7:6039384-6039385	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372206562	chr7:6039401-6039402	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376608343	chr7:6039404-6039405	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116292386	chr7:6039449-6039450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs373438537	chr7:6039453-6039454	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570373212	chr7:6039454-6039455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561535818	chr7:6039497-6039498	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs187444106	chr7:6039501-6039502	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567713296	chr7:6039503-6039504	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535142251	chr7:6039516-6039517	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs58026649	chr7:6039529-6039530	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572256328	chr7:6039537-6039538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539650156	chr7:6039572-6039573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557766703	chr7:6039605-6039606	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs75627652	chr7:6039608-6039609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142213233	chr7:6039648-6039649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543012435	chr7:6039687-6039688	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191888703	chr7:6039696-6039697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573374607	chr7:6039706-6039707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540742320	chr7:6039748-6039749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs535384141	chr7:6039750-6039751	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569456815	chr7:6039753-6039754	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536750721	chr7:6039768-6039769	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559050257	chr7:6039776-6039777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184709361	chr7:6039794-6039795	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551989976	chr7:6039800-6039801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563788127	chr7:6039804-6039805	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531238003	chr7:6039823-6039824	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28384245	chr7:6039848-6039849	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549077675	chr7:6039859-6039860	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567677878	chr7:6039860-6039861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535049342	chr7:6039862-6039863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375153629	chr7:6039863-6039864	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547097394	chr7:6039898-6039899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571818801	chr7:6039927-6039928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6010400-6048000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:6016200-6047600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:6022600-6048000	Weak transcription	NHLF	lung
4	chr7:6025000-6039600	Weak transcription	Esophagus	oesophagus
5	chr7:6025000-6048000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:6025200-6046800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:6025800-6045200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:6026200-6042800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:6026200-6045400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:6026200-6046200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:6026400-6040000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr7:6026400-6042000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:6026400-6043600	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr7:6026400-6043600	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:6026400-6043600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr7:6026400-6044000	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:6026400-6044000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:6026400-6045000	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr7:6026400-6045000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:6026400-6045400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:6026400-6045600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:6026600-6042800	Strong transcription	Fetal Stomach	stomach
23	chr7:6026600-6045400	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr7:6027600-6047200	Weak transcription	Fetal Kidney	kidney
25	chr7:6028000-6048000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr7:6028200-6045000	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr7:6029000-6048000	Weak transcription	Right Ventricle	heart
28	chr7:6029600-6047000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:6030800-6039800	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr7:6031600-6040200	Strong transcription	Fetal Muscle Trunk	muscle
31	chr7:6032200-6042400	Strong transcription	Fetal Intestine Small	intestine
32	chr7:6032200-6045400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr7:6032800-6040200	Strong transcription	Primary T cells from cord blood	blood
34	chr7:6033200-6040600	Strong transcription	Spleen	Spleen
35	chr7:6033400-6040000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:6033400-6043800	Strong transcription	Primary B cells from peripheral blood	blood
37	chr7:6033600-6040200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:6033600-6042800	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr7:6033600-6042800	Strong transcription	Stomach Smooth Muscle	stomach
40	chr7:6033600-6043800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr7:6033600-6045200	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr7:6033600-6045600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr7:6033800-6040200	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr7:6033800-6043600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:6034000-6040000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr7:6034000-6047600	Weak transcription	Small Intestine	intestine
47	chr7:6035000-6039800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
48	chr7:6035200-6039800	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr7:6035200-6041000	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr7:6035200-6041000	Strong transcription	Dnd41	blood

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