Variant report

Variant	nsv887602
Chromosome Location	chr7:11071993-11220846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:122)
Chromatin interactive
region (count:85)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:11122472-11122755	HepG2	liver:	n/a	n/a
2	ATF1	chr7:11128773-11128831	K562	blood:	n/a	n/a
3	ATF2	chr7:11122404-11123057	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:11102229-11102429	K562	blood:	n/a	n/a
5	BACH1	chr7:11175371-11175473	K562	blood:	n/a	n/a
6	BATF	chr7:11118139-11118345	GM12878	blood:	n/a	chr7:11118255-11118265
7	BATF	chr7:11118081-11118314	GM12878	blood:	n/a	chr7:11118255-11118265
8	BATF	chr7:11160374-11160600	GM12878	blood:	n/a	n/a
9	BCL3	chr7:11195043-11195271	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:11210726-11210891	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:11215693-11215816	K562	blood:	n/a	n/a
12	BRCA1	chr7:11167087-11167179	GM12878	blood:	n/a	n/a
13	CCNT2	chr7:11217186-11217420	K562	blood:	n/a	n/a
14	CEBPB	chr7:11115611-11115936	K562	blood:	n/a	n/a
15	CEBPB	chr7:11122652-11122903	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:11108137-11108367	K562	blood:	n/a	chr7:11108241-11108252
17	CEBPB	chr7:11115589-11115882	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:11108217-11108264	H1-hESC	embryonic stem cell:	n/a	chr7:11108241-11108252
19	CEBPB	chr7:11108099-11108373	A549	lung:	n/a	chr7:11108241-11108252
20	CEBPB	chr7:11210548-11210824	A549	lung:	n/a	chr7:11210690-11210701
21	CEBPB	chr7:11115591-11115931	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:11169609-11170090	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:11210526-11210841	IMR90	lung:	n/a	chr7:11210690-11210701
24	CEBPB	chr7:11115586-11115929	A549	lung:	n/a	n/a
25	CEBPB	chr7:11124794-11124970	HepG2	liver:	n/a	chr7:11124881-11124894
26	CEBPB	chr7:11210550-11210871	HepG2	liver:	n/a	chr7:11210690-11210701
27	CEBPB	chr7:11122659-11123159	A549	lung:	n/a	n/a
28	CEBPB	chr7:11108116-11108371	HepG2	liver:	n/a	chr7:11108241-11108252
29	CEBPB	chr7:11115583-11115943	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:11115591-11115952	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:11124748-11125014	K562	blood:	n/a	chr7:11124881-11124894
32	CEBPB	chr7:11210530-11210811	Hela-S3	cervix:	n/a	chr7:11210690-11210701
33	CEBPB	chr7:11115581-11115979	MCF-7	breast:	n/a	n/a
34	CREB1	chr7:11210819-11211347	GM12878	blood:	n/a	n/a
35	CREB1	chr7:11160285-11160708	GM12878	blood:	n/a	n/a
36	CTCF	chr7:11205490-11205605	Hela-S3	cervix:	n/a	chr7:11205529-11205550
37	CTCF	chr7:11193340-11193490	AG10803	skin:	n/a	n/a
38	CTCF	chr7:11205495-11205611	GM12878	blood:	n/a	chr7:11205529-11205550
39	CTCF	chr7:11193426-11193560	Gliobla	brain:	n/a	n/a
40	CTCF	chr7:11193420-11193570	AG09319	gingival:	n/a	n/a
41	CTCF	chr7:11193420-11193527	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr7:11110120-11110270	BJ	skin:	n/a	n/a
43	CTCF	chr7:11193245-11193764	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:11193460-11193610	Caco-2	colon:	n/a	n/a
45	CTCF	chr7:11193400-11193621	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr7:11193323-11193632	K562	blood:	n/a	n/a
47	CTCF	chr7:11095112-11095126	K562	blood:	n/a	n/a
48	CTCF	chr7:11193382-11193624	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:11211560-11211710	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:11193400-11193550	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11091695-11091745	SK-N-SH	brain:	n/a
2	chr7:11101436-11101486	SK-N-MC	brain:	n/a
3	chr7:11091695-11091745	T-47D	breast:	n/a
4	chr7:11091695-11091745	HMEC	breast:	n/a
5	chr7:11101436-11101486	SK-N-SH	brain:	n/a
6	chr7:11091695-11091745	H1-hESC	embryonic stem cell:	embryo
7	chr7:11091695-11091745	ECC-1	luminal epithelium:	n/a
8	chr7:11091695-11091745	AG04450	lung:	fetal
9	chr7:11101436-11101486	HepG2	liver:	n/a
10	chr7:11091695-11091745	HCF	heart:	n/a
11	chr7:11101436-11101486	HIPEpiC	eye:	n/a
12	chr7:11101436-11101486	MCF10A-Er-Src	breast:	n/a
13	chr7:11091695-11091745	PFSK-1	brain:	n/a
14	chr7:11101436-11101486	HUVEC	blood vessel:	n/a
15	chr7:11101436-11101486	MCF-7	breast:	n/a
16	chr7:11091695-11091745	BJ	skin:	n/a
17	chr7:11101436-11101486	BE2_C	brain:	n/a
18	chr7:11101436-11101486	BJ	skin:	n/a
19	chr7:11101436-11101486	U87	brain:	n/a
20	chr7:11101436-11101486	PFSK-1	brain:	n/a
21	chr7:11091695-11091745	GM12891	blood:	n/a
22	chr7:11091695-11091745	LNCaP	prostate:	n/a
23	chr7:11091695-11091745	MCF-7	breast:	n/a
24	chr7:11091695-11091745	ovcar-3	ovarian:	n/a
25	chr7:11101436-11101486	AG09319	gingival:	n/a
26	chr7:11101436-11101486	A549	lung:	n/a
27	chr7:11091695-11091745	HCPEpiC	choroid plexus:	n/a
28	chr7:11101436-11101486	HL-60	blood:	n/a
29	chr7:11101436-11101486	GM06990	blood:	n/a
30	chr7:11091695-11091745	AG09309	skin:	n/a
31	chr7:11091695-11091745	PrEC	prostate:	n/a
32	chr7:11101436-11101486	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:11101436-11101486	SKMC	muscle:	n/a
34	chr7:11091695-11091745	GM19239	blood:	n/a
35	chr7:11101436-11101486	Hela-S3	cervix:	n/a
36	chr7:11091695-11091745	GM12892	blood:	n/a
37	chr7:11101436-11101486	RPTEC	kidney:	n/a
38	chr7:11091695-11091745	AG04449	skin:	fetal
39	chr7:11091695-11091745	IMR90	lung:	fetal
40	chr7:11101436-11101486	HCT-116	colon:	n/a
41	chr7:11091695-11091745	HCT-116	colon:	n/a
42	chr7:11101436-11101486	Caco-2	colon:	n/a
43	chr7:11091695-11091745	K562	blood:	n/a
44	chr7:11091695-11091745	Jurkat	blood:	n/a
45	chr7:11101436-11101486	LNCaP	prostate:	n/a
46	chr7:11101436-11101486	PANC-1	pancreas:	n/a
47	chr7:11101436-11101486	HCF	heart:	n/a
48	chr7:11091695-11091745	HAEpiC	amniotic membrane:	n/a
49	chr7:11101436-11101486	AG04449	skin:	fetal
50	chr7:11101436-11101486	SAEC	small airway:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:11121527..11123973-chr7:11131499..11134132,2	K562	blood:
2	chr7:11126725..11129133-chr7:11132639..11135110,2	MCF-7	breast:
3	chr7:11140028..11142682-chr7:11145035..11147597,3	K562	blood:
4	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
5	chr7:11073711..11075320-chr7:11100379..11102062,2	K562	blood:
6	chr7:11120505..11122093-chr7:11122139..11123895,2	K562	blood:
7	chr7:11196790..11199546-chr7:11202946..11205522,2	K562	blood:
8	chr7:11080726..11082742-chr7:11094808..11097463,2	K562	blood:
9	chr7:11113760..11116450-chr7:11117895..11120001,2	MCF-7	breast:
10	chr7:11169416..11171057-chr7:11171117..11173550,2	K562	blood:
11	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
12	chr7:11193379..11193920-chr7:11380707..11381612,2	MCF-7	breast:
13	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
14	chr7:11022666..11024973-chr7:11118639..11120820,2	K562	blood:
15	chr7:11011539..11015300-chr7:11077351..11081429,5	MCF-7	breast:
16	chr7:5013239..5014028-chr7:11185489..11186384,2	NB4	blood:
17	chr7:11102318..11104655-chr7:11104749..11107010,2	K562	blood:
18	chr7:11196790..11199292-chr7:11202946..11205439,2	K562	blood:
19	chr7:11073711..11075320-chr7:11100379..11102062,2	K562	blood:
20	chr7:11205391..11208108-chr7:11211440..11214054,2	MCF-7	breast:
21	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
22	chr7:11108681..11111650-chr7:11117427..11119548,2	K562	blood:
23	chr7:10978313..10981160-chr7:11099563..11101890,2	K562	blood:
24	chr7:11196790..11199292-chr7:11202946..11205439,2	K562	blood:
25	chr7:11121943..11123973-chr7:11130475..11132999,2	K562	blood:
26	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
27	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
28	chr7:11140028..11142682-chr7:11145035..11146787,2	K562	blood:
29	chr7:11149421..11151035-chr7:11153801..11157843,3	K562	blood:
30	chr7:11121527..11123973-chr7:11131499..11134132,2	K562	blood:
31	chr7:11120505..11122093-chr7:11122139..11123895,2	K562	blood:
32	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
33	chr7:11205391..11208108-chr7:11211440..11214054,2	MCF-7	breast:
34	chr7:11187936..11191247-chr7:11191383..11194500,4	K562	blood:
35	chr7:10978704..10980840-chr7:11097948..11100485,2	MCF-7	breast:
36	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
37	chr7:11012606..11015240-chr7:11166727..11169294,2	MCF-7	breast:
38	chr7:11075307..11077062-chr7:11087663..11089190,2	K562	blood:
39	chr7:11162789..11165137-chr7:11166828..11168631,2	K562	blood:
40	chr7:11136221..11139675-chr7:11144358..11148872,4	K562	blood:
41	chr7:11076840..11078456-chr7:11079311..11081268,2	MCF-7	breast:
42	chr7:11192916..11193961-chr7:11251567..11252421,4	MCF-7	breast:
43	chr7:11088216..11090960-chr7:11126210..11129188,2	K562	blood:
44	chr7:11130768..11133783-chr7:11134322..11137393,4	K562	blood:
45	chr7:11146142..11148658-chr7:11151256..11153162,2	K562	blood:
46	chr7:11104144..11105857-chr7:11109203..11110826,2	K562	blood:
47	chr7:11196790..11199546-chr7:11202946..11205522,2	K562	blood:
48	chr7:11118440..11120387-chr7:11122259..11124478,2	K562	blood:
49	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
50	chr7:11102318..11104655-chr7:11104749..11107010,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF14	hsa-miR-155-5p	chr7:11142799-11142820
2	PHF14	hsa-miR-155-5p	chr7:11142813-11142835
3	PHF14	hsa-miR-155-5p	chr7:11148709-11148731

Variant related genes	Relation type
PHF14	TF binding region
ENSG00000230333	TF binding region
PHF14	CpG island
ENSG00000230333	CpG island
ENSG00000106443	chromatin interactions
ENSG00000189043	chromatin interactions
ENSG00000196204	chromatin interactions
ENSG00000271185	chromatin interactions
ENSG00000176476	chromatin interactions

Extended variants
information (count: 5864 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5864 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17163914	chr7:11071993-11071994	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187887740	chr7:11072061-11072062	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs192977149	chr7:11072111-11072112	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs113622468	chr7:11072125-11072126	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs536319698	chr7:11072146-11072147	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs558217756	chr7:11072168-11072169	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs542485476	chr7:11072175-11072176	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs553883342	chr7:11072178-11072179	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs74679896	chr7:11072183-11072184	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs375028179	chr7:11072200-11072201	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546125308	chr7:11072201-11072202	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs113516970	chr7:11072214-11072215	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs184299612	chr7:11072245-11072246	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs59441504	chr7:11072277-11072278	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566635542	chr7:11072330-11072331	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs542043029	chr7:11072337-11072338	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs2108112	chr7:11072369-11072370	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538501189	chr7:11072467-11072468	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369254700	chr7:11072504-11072505	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574584119	chr7:11072563-11072564	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562277118	chr7:11072576-11072577	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529764796	chr7:11072604-11072605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs57184355	chr7:11072642-11072643	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546630811	chr7:11072685-11072686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559939829	chr7:11072740-11072741	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs115082919	chr7:11072768-11072769	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115829276	chr7:11072804-11072805	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569196482	chr7:11072812-11072813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374833261	chr7:11072825-11072826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs367757665	chr7:11072869-11072870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548092367	chr7:11072906-11072907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs116136011	chr7:11072907-11072908	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534077998	chr7:11072931-11072932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554227444	chr7:11072947-11072948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558802176	chr7:11072982-11072983	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199526779	chr7:11073088-11073089	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539423919	chr7:11073092-11073093	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs145256609	chr7:11073095-11073096	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs576345646	chr7:11073117-11073118	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs189632811	chr7:11073134-11073135	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577293993	chr7:11073182-11073183	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181809146	chr7:11073192-11073193	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555688322	chr7:11073208-11073209	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572598371	chr7:11073220-11073221	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs3779409	chr7:11073225-11073226	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs560178313	chr7:11073308-11073309	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs116741869	chr7:11073361-11073362	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs137906843	chr7:11073402-11073403	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs114584815	chr7:11073415-11073416	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531639954	chr7:11073427-11073428	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD

Chromatin state (count:1310 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11014600-11092000	Weak transcription	Colonic Mucosa	Colon
2	chr7:11014800-11075200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:11014800-11117400	Weak transcription	HSMMtube	muscle
4	chr7:11015200-11108200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr7:11017200-11076000	Weak transcription	HUVEC	blood vessel
6	chr7:11023200-11076200	Weak transcription	NH-A	brain
7	chr7:11031600-11103800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr7:11035800-11076000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:11035800-11092600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:11035800-11113000	Weak transcription	Esophagus	oesophagus
11	chr7:11035800-11113200	Weak transcription	Lung	lung
12	chr7:11035800-11123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:11036000-11101600	Weak transcription	Placenta	Placenta
14	chr7:11036600-11100800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:11039000-11090600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr7:11039000-11108800	Weak transcription	Psoas Muscle	Psoas
17	chr7:11046000-11128600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr7:11046200-11175000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:11046600-11081200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr7:11046600-11103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:11046600-11122600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:11046600-11167800	Weak transcription	Thymus	Thymus
23	chr7:11048200-11098600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:11048200-11113400	Weak transcription	Aorta	Aorta
25	chr7:11051000-11076000	Weak transcription	HMEC	breast
26	chr7:11053600-11078000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr7:11054400-11075200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr7:11054400-11101800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:11054400-11113200	Weak transcription	Pancreas	Pancrea
30	chr7:11054800-11076200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr7:11055200-11076000	Weak transcription	GM12878-XiMat	blood
32	chr7:11055400-11075800	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr7:11055600-11077600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:11056600-11076200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr7:11057800-11190200	Weak transcription	Fetal Brain Male	brain
36	chr7:11064000-11078400	Weak transcription	Brain Angular Gyrus	brain
37	chr7:11064200-11075200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:11064200-11076000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr7:11064200-11076200	Weak transcription	Colon Smooth Muscle	Colon
40	chr7:11064200-11080200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr7:11064200-11093600	Weak transcription	Hela-S3	cervix
42	chr7:11064400-11072200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr7:11064400-11073000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr7:11064400-11074600	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr7:11064400-11075200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:11064400-11075200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:11064400-11075400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr7:11064400-11075400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:11064400-11076200	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr7:11064400-11080600	Weak transcription	Brain Substantia Nigra	brain

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