Variant report

Variant	nsv1032865
Chromosome Location	chr7:11395480-11477467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:11467383-11467617	HepG2	liver:	n/a	n/a
2	BHLHE40	chr7:11434104-11434404	HepG2	liver:	n/a	n/a
3	CEBPB	chr7:11417825-11418031	A549	lung:	n/a	n/a
4	CEBPB	chr7:11413772-11414023	A549	lung:	n/a	n/a
5	CEBPB	chr7:11405805-11406121	K562	blood:	n/a	chr7:11405989-11406001 chr7:11405933-11405944
6	CEBPB	chr7:11403437-11403767	K562	blood:	n/a	chr7:11403591-11403602 chr7:11403593-11403604 chr7:11403591-11403604 chr7:11403632-11403643 chr7:11403591-11403604
7	CEBPB	chr7:11416257-11416524	A549	lung:	n/a	n/a
8	CEBPB	chr7:11402615-11402837	A549	lung:	n/a	chr7:11402703-11402716 chr7:11402703-11402716 chr7:11402820-11402831 chr7:11402703-11402714 chr7:11402703-11402716
9	CEBPB	chr7:11405770-11406098	IMR90	lung:	n/a	chr7:11405989-11406001 chr7:11405933-11405944
10	CEBPB	chr7:11402579-11402858	IMR90	lung:	n/a	chr7:11402703-11402716 chr7:11402703-11402716 chr7:11402820-11402831 chr7:11402703-11402714 chr7:11402703-11402716
11	CEBPB	chr7:11447761-11448027	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:11410103-11410400	IMR90	lung:	n/a	chr7:11410273-11410286 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410274-11410285
13	CEBPB	chr7:11405785-11406066	H1-hESC	embryonic stem cell:	n/a	chr7:11405989-11406001 chr7:11405933-11405944
14	CEBPB	chr7:11410088-11410342	A549	lung:	n/a	chr7:11410273-11410286 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410274-11410285
15	CEBPB	chr7:11447809-11448003	K562	blood:	n/a	n/a
16	CEBPB	chr7:11398126-11398437	HepG2	liver:	n/a	chr7:11398183-11398196 chr7:11398285-11398296
17	CEBPB	chr7:11447917-11447956	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:11410128-11410384	HepG2	liver:	n/a	chr7:11410273-11410286 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410274-11410285
19	CEBPB	chr7:11398157-11398403	K562	blood:	n/a	chr7:11398183-11398196 chr7:11398285-11398296
20	CEBPB	chr7:11405811-11406065	A549	lung:	n/a	chr7:11405989-11406001 chr7:11405933-11405944
21	CEBPB	chr7:11454605-11454883	H1-hESC	embryonic stem cell:	n/a	chr7:11454732-11454743
22	CEBPB	chr7:11403485-11403764	H1-hESC	embryonic stem cell:	n/a	chr7:11403591-11403602 chr7:11403593-11403604 chr7:11403591-11403604 chr7:11403632-11403643 chr7:11403591-11403604
23	CEBPB	chr7:11447750-11448022	A549	lung:	n/a	n/a
24	CEBPB	chr7:11410146-11410382	K562	blood:	n/a	chr7:11410273-11410286 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410274-11410285
25	CEBPB	chr7:11405867-11406064	Hela-S3	cervix:	n/a	chr7:11405989-11406001 chr7:11405933-11405944
26	CEBPB	chr7:11402521-11402882	Hela-S3	cervix:	n/a	chr7:11402703-11402716 chr7:11402703-11402716 chr7:11402820-11402831 chr7:11402703-11402714 chr7:11402703-11402716
27	CEBPB	chr7:11447763-11448043	A549	lung:	n/a	n/a
28	CEBPB	chr7:11447806-11448011	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:11469506-11469923	HepG2	liver:	n/a	chr7:11469588-11469601 chr7:11469588-11469599
30	CEBPB	chr7:11403426-11403800	Hela-S3	cervix:	n/a	chr7:11403591-11403602 chr7:11403593-11403604 chr7:11403591-11403604 chr7:11403632-11403643 chr7:11403591-11403604
31	CEBPB	chr7:11413183-11413511	Hela-S3	cervix:	n/a	chr7:11413210-11413223
32	CEBPB	chr7:11454563-11454929	HepG2	liver:	n/a	chr7:11454732-11454743
33	CEBPB	chr7:11451441-11451640	A549	lung:	n/a	n/a
34	CEBPB	chr7:11454596-11454829	IMR90	lung:	n/a	chr7:11454732-11454743
35	CEBPB	chr7:11403106-11403780	HepG2	liver:	n/a	chr7:11403591-11403602 chr7:11403593-11403604 chr7:11403591-11403604 chr7:11403632-11403643 chr7:11403591-11403604
36	CEBPB	chr7:11398155-11398426	A549	lung:	n/a	chr7:11398183-11398196 chr7:11398285-11398296
37	CEBPB	chr7:11410183-11410375	H1-hESC	embryonic stem cell:	n/a	chr7:11410273-11410286 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410275-11410284 chr7:11410274-11410285
38	CEBPB	chr7:11450224-11450287	A549	lung:	n/a	n/a
39	CEBPB	chr7:11413217-11413587	A549	lung:	n/a	n/a
40	CEBPB	chr7:11469271-11470056	A549	lung:	n/a	chr7:11469588-11469601 chr7:11469588-11469599 chr7:11469274-11469287
41	CEBPB	chr7:11447785-11448092	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:11447781-11448074	A549	lung:	n/a	n/a
43	CEBPB	chr7:11405752-11406092	HepG2	liver:	n/a	chr7:11405989-11406001 chr7:11405933-11405944
44	CEBPB	chr7:11403135-11403782	A549	lung:	n/a	chr7:11403591-11403602 chr7:11403593-11403604 chr7:11403591-11403604 chr7:11403632-11403643 chr7:11403591-11403604
45	CEBPB	chr7:11413745-11414029	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:11454666-11454894	Hela-S3	cervix:	n/a	chr7:11454732-11454743
47	CEBPB	chr7:11454585-11454894	A549	lung:	n/a	chr7:11454732-11454743
48	CEBPB	chr7:11398164-11398436	IMR90	lung:	n/a	chr7:11398183-11398196 chr7:11398285-11398296
49	CEBPB	chr7:11403446-11403767	IMR90	lung:	n/a	chr7:11403591-11403602 chr7:11403593-11403604 chr7:11403591-11403604 chr7:11403632-11403643 chr7:11403591-11403604
50	CTCF	chr7:11413236-11413441	GM10266	blood:	n/a	chr7:11413352-11413370

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11456440-11456490	SK-N-SH_RA	brain:	n/a
2	chr7:11456440-11456490	SK-N-SH_RA	brain:	n/a
3	chr7:11456440-11456490	MCF-7	breast:	n/a
4	chr7:11456440-11456490	HUVEC	blood vessel:	n/a
5	chr7:11456440-11456490	HNPCEpiC	eye:	n/a
6	chr7:11468680-11468730	PrEC	prostate:	n/a
7	chr7:11468680-11468730	NHDF-neo	bronchial:	n/a
8	chr7:11456440-11456490	PrEC	prostate:	n/a
9	chr7:11456440-11456490	HRCEpiC	kidney:	n/a
10	chr7:11456440-11456490	AoSMC	blood vessel:	n/a
11	chr7:11468680-11468730	IMR90	lung:	fetal
12	chr7:11412105-11412155	K562	blood:	n/a
13	chr7:11468680-11468730	HRE	kidney:	n/a
14	chr7:11412105-11412155	GM12891	blood:	n/a
15	chr7:11468680-11468730	GM12892	blood:	n/a
16	chr7:11456440-11456490	GM06990	blood:	n/a
17	chr7:11456440-11456490	RPTEC	kidney:	n/a
18	chr7:11456440-11456490	Jurkat	blood:	n/a
19	chr7:11468680-11468730	RPTEC	kidney:	n/a
20	chr7:11456440-11456490	Hela-S3	cervix:	n/a
21	chr7:11412105-11412155	MCF-7	breast:	n/a
22	chr7:11468680-11468730	ProgFib	skin:	n/a
23	chr7:11468680-11468730	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:11468680-11468730	LNCaP	prostate:	n/a
25	chr7:11412105-11412155	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:11412105-11412155	GM19239	blood:	n/a
27	chr7:11412105-11412155	HAEpiC	amniotic membrane:	n/a
28	chr7:11468680-11468730	AG10803	skin:	n/a
29	chr7:11412105-11412155	HCM	heart:	n/a
30	chr7:11456440-11456490	Caco-2	colon:	n/a
31	chr7:11412105-11412155	NHBE	bronchial:	n/a
32	chr7:11456440-11456490	ovcar-3	ovarian:	n/a
33	chr7:11456440-11456490	CMK	blood:	n/a
34	chr7:11468680-11468730	HAEpiC	amniotic membrane:	n/a
35	chr7:11412105-11412155	HMEC	breast:	n/a
36	chr7:11456440-11456490	GM12892	blood:	n/a
37	chr7:11468680-11468730	NH-A	brain:	n/a
38	chr7:11412105-11412155	AG10803	skin:	n/a
39	chr7:11456440-11456490	ECC-1	luminal epithelium:	n/a
40	chr7:11468680-11468730	HIPEpiC	eye:	n/a
41	chr7:11412105-11412155	HRCEpiC	kidney:	n/a
42	chr7:11412105-11412155	HNPCEpiC	eye:	n/a
43	chr7:11412105-11412155	HUVEC	blood vessel:	n/a
44	chr7:11456440-11456490	NHBE	bronchial:	n/a
45	chr7:11456440-11456490	BE2_C	brain:	n/a
46	chr7:11456440-11456490	NH-A	brain:	n/a
47	chr7:11456440-11456490	HCF	heart:	n/a
48	chr7:11468680-11468730	MCF10A-Er-Src	breast:	n/a
49	chr7:11412105-11412155	CMK	blood:	n/a
50	chr7:11456440-11456490	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:11467204..11469366-chr7:12166192..12168544,2	K562	blood:
2	chr7:11460090..11463607-chr7:11464944..11467497,3	K562	blood:
3	chr7:11467068..11467774-chr7:11597036..11597764,2	MCF-7	breast:
4	chr7:11453079..11455917-chr7:11456610..11459458,2	K562	blood:
5	chr7:11467968..11470082-chr7:11470357..11472664,2	K562	blood:
6	chr7:11460090..11463607-chr7:11464944..11467497,3	K562	blood:
7	chr7:11405882..11407841-chr7:11412022..11414441,2	K562	blood:
8	chr7:11418373..11421193-chr7:11421983..11424358,2	K562	blood:
9	chr7:11405882..11407841-chr7:11412022..11414441,2	K562	blood:
10	chr7:11467968..11470082-chr7:11470357..11472664,2	K562	blood:
11	chr7:11466869..11467685-chr7:12498254..12498786,2	MCF-7	breast:
12	chr7:11453079..11455917-chr7:11456610..11459458,2	K562	blood:
13	chr7:11411369..11413443-chr7:11415999..11418412,2	K562	blood:
14	chr7:11413756..11416647-chr7:11417032..11420437,3	K562	blood:
15	chr7:11467369..11467919-chr7:11871403..11872276,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF14-1	chr7:11418914-11418996	ENSG00000230333.1
2	lnc-THSD7A-1	chr7:11410062-11410947	NONHSAT119219
3	lnc-PHF14-1	chr7:11418914-11418996	ENSG00000230333.1
4	lnc-PHF14-2	chr7:11449918-11450157	NONHSAT119224
5	lnc-PHF14-1	chr7:11423424-11425305	ENSG00000230333.1
6	lnc-PHF14-1	chr7:11417505-11417804	ENSG00000230333.2
7	lnc-PHF14-1	chr7:11418324-11418996	ENSG00000230333.2
8	lnc-PHF14-1	chr7:11423424-11423496	ENSG00000230333.2
9	lnc-PHF14-1	chr7:11423424-11424045	ENSG00000230333.1
10	lnc-PHF14-1	chr7:11418914-11418996	ENSG00000230333.1
11	lnc-PHF14-2	chr7:11453441-11453656	NONHSAT119224
12	lnc-PHF14-1	chr7:11418914-11418993	ENSG00000230333.1
13	lnc-PHF14-1	chr7:11423424-11423535	ENSG00000230333.1
14	lnc-PHF14-1	chr7:11416625-11416708	ENSG00000230333.2

Variant related genes	Relation type
ENSG00000230333	TF binding region
ENSG00000230435	TF binding region
THSD7A	TF binding region
ENSG00000230333	CpG island
ENSG00000230435	CpG island
THSD7A	CpG island
ENSG00000230333	chromatin interactions
ENSG00000005108	chromatin interactions

Extended variants
information (count: 3465 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3465 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149784728	chr7:11395483-11395484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533440232	chr7:11395484-11395485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536422286	chr7:11395500-11395501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558787429	chr7:11395507-11395508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188450872	chr7:11395549-11395550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573451094	chr7:11395583-11395584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545341366	chr7:11395594-11395595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114979678	chr7:11395602-11395603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79492230	chr7:11395657-11395658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544268517	chr7:11395663-11395664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550416129	chr7:11395680-11395681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561249307	chr7:11395707-11395708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547836369	chr7:11395714-11395715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7797993	chr7:11395720-11395721	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs192840802	chr7:11395736-11395737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148484375	chr7:11395748-11395749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184797974	chr7:11395751-11395752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551707410	chr7:11395756-11395757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17164482	chr7:11395808-11395809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs530541777	chr7:11395853-11395854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144131849	chr7:11395885-11395886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370409082	chr7:11395930-11395931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374596820	chr7:11395934-11395935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547061802	chr7:11395957-11395958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146492507	chr7:11395961-11395962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546875983	chr7:11395975-11395976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188095185	chr7:11396002-11396003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538906639	chr7:11396027-11396028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79311581	chr7:11396028-11396029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141039532	chr7:11396040-11396041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570235369	chr7:11396042-11396043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539112959	chr7:11396046-11396047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191592300	chr7:11396062-11396063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367662883	chr7:11396081-11396082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144759321	chr7:11396089-11396090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540722738	chr7:11396099-11396100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184862229	chr7:11396101-11396102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575786614	chr7:11396120-11396121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369578088	chr7:11396123-11396124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189584868	chr7:11396138-11396139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs151179836	chr7:11396150-11396151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74403630	chr7:11396156-11396157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530859194	chr7:11396189-11396190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182218340	chr7:11396213-11396214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140191056	chr7:11396243-11396244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529709683	chr7:11396245-11396246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572234067	chr7:11396257-11396258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546684250	chr7:11396260-11396261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10225132	chr7:11396280-11396281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs538872228	chr7:11396298-11396299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11383800-11397200	Weak transcription	Adipose Nuclei	Adipose
2	chr7:11393000-11401800	Weak transcription	Gastric	stomach
3	chr7:11395200-11395600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:11395600-11396000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:11396000-11396200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:11396200-11400200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:11397800-11398400	Weak transcription	Adipose Nuclei	Adipose
8	chr7:11400200-11401400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:11401800-11402000	Enhancers	Gastric	stomach
10	chr7:11404200-11404400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:11405200-11418800	Weak transcription	Adipose Nuclei	Adipose
12	chr7:11406800-11408200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:11407200-11407600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:11407200-11407800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr7:11407800-11408000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr7:11407800-11408200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:11407800-11408200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr7:11407800-11408200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:11408000-11421000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:11408200-11430600	Weak transcription	Ovary	ovary
21	chr7:11413000-11430200	Weak transcription	Placenta	Placenta
22	chr7:11413200-11430200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr7:11413400-11413600	Enhancers	Fetal Lung	lung
24	chr7:11413400-11413800	Enhancers	A549	lung
25	chr7:11413400-11414000	Enhancers	Liver	Liver
26	chr7:11413600-11414800	Enhancers	Fetal Intestine Small	intestine
27	chr7:11413600-11430000	Weak transcription	Fetal Lung	lung
28	chr7:11413800-11416200	Weak transcription	A549	lung
29	chr7:11414000-11416000	Weak transcription	Liver	Liver
30	chr7:11414400-11414600	Enhancers	Duodenum Mucosa	Duodenum
31	chr7:11414400-11414800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr7:11414600-11415400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr7:11414800-11415000	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr7:11414800-11419200	Weak transcription	Fetal Intestine Small	intestine
35	chr7:11415000-11415800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr7:11415400-11416200	Enhancers	Duodenum Mucosa	Duodenum
37	chr7:11415800-11417200	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr7:11415800-11419200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr7:11416000-11416800	Enhancers	Liver	Liver
40	chr7:11416200-11416600	Flanking Active TSS	A549	lung
41	chr7:11416600-11416800	Enhancers	A549	lung
42	chr7:11416800-11419000	Weak transcription	Liver	Liver
43	chr7:11417000-11418000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:11417000-11440000	Weak transcription	Fetal Kidney	kidney
45	chr7:11418800-11419600	Strong transcription	Adipose Nuclei	Adipose
46	chr7:11419000-11421400	Strong transcription	Liver	Liver
47	chr7:11419200-11419400	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr7:11419400-11422000	Weak transcription	Fetal Intestine Small	intestine
49	chr7:11419600-11430800	Weak transcription	Adipose Nuclei	Adipose
50	chr7:11421400-11425600	Weak transcription	Liver	Liver

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