Variant report

Variant	nsv831006
Chromosome Location	chr7:53769412-53930274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:368)
CpG islands
(count:306)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:53880056-53880500	K562	blood:	n/a	n/a
2	ARID3A	chr7:53878746-53879008	K562	blood:	n/a	chr7:53878805-53878821
3	ARID3A	chr7:53877206-53877492	K562	blood:	n/a	n/a
4	BHLHE40	chr7:53879156-53880313	K562	blood:	n/a	n/a
5	BRCA1	chr7:53919533-53919557	GM12878	blood:	n/a	n/a
6	CCNT2	chr7:53879220-53879790	K562	blood:	n/a	n/a
7	CEBPB	chr7:53769885-53770064	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:53873750-53874089	K562	blood:	n/a	n/a
9	CEBPB	chr7:53812152-53812345	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:53769952-53770117	A549	lung:	n/a	n/a
11	CEBPB	chr7:53879534-53880394	K562	blood:	n/a	n/a
12	CEBPB	chr7:53879553-53879905	K562	blood:	n/a	n/a
13	CEBPB	chr7:53916135-53916381	HepG2	liver:	n/a	chr7:53916256-53916265 chr7:53916254-53916267 chr7:53916255-53916266
14	CEBPB	chr7:53875149-53875349	K562	blood:	n/a	n/a
15	CEBPB	chr7:53799530-53799792	HepG2	liver:	n/a	chr7:53799691-53799702
16	CEBPB	chr7:53795752-53795945	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:53877399-53877749	K562	blood:	n/a	n/a
18	CEBPB	chr7:53799543-53799740	K562	blood:	n/a	chr7:53799691-53799702
19	CEBPB	chr7:53863849-53863877	K562	blood:	n/a	n/a
20	CEBPB	chr7:53923660-53923836	HepG2	liver:	n/a	chr7:53923796-53923807
21	CEBPB	chr7:53929924-53930105	K562	blood:	n/a	n/a
22	CHD2	chr7:53879367-53879877	K562	blood:	n/a	n/a
23	CHD2	chr7:53827893-53827955	HepG2	liver:	n/a	n/a
24	CTCF	chr7:53839560-53839710	Caco-2	colon:	n/a	n/a
25	CTCF	chr7:53812360-53812510	SAEC	small airway:	n/a	n/a
26	CTCF	chr7:53897513-53897566	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr7:53889517-53889542	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:53812320-53812470	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:53921080-53921230	GM12875	blood:	n/a	n/a
30	CTCF	chr7:53812342-53812432	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:53812320-53812470	NHEK	skin:	n/a	n/a
32	CTCF	chr7:53788000-53788150	GM12865	blood:	n/a	n/a
33	CTCF	chr7:53812300-53812450	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:53812342-53812438	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:53798469-53798519	GM10248	blood:	n/a	n/a
36	CTCF	chr7:53812240-53812390	SAEC	small airway:	n/a	n/a
37	CTCF	chr7:53912871-53912924	GM13976	blood:	n/a	n/a
38	CTCF	chr7:53812300-53812450	HMEC	breast:	n/a	n/a
39	CTCF	chr7:53831287-53831358	Medullo	brain:	n/a	n/a
40	CTCF	chr7:53832160-53832258	GM20000	blood:	n/a	n/a
41	CTCF	chr7:53921340-53921490	GM12869	blood:	n/a	n/a
42	CTCF	chr7:53812200-53812350	HMEC	breast:	n/a	n/a
43	CTCF	chr7:53770168-53770236	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr7:53880057-53880327	K562	blood:	n/a	n/a
45	CTCF	chr7:53930032-53930050	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr7:53812420-53812570	HMEC	breast:	n/a	n/a
47	CTCF	chr7:53812310-53812447	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:53812266-53812487	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr7:53812300-53812450	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr7:53812205-53812512	NHEK	skin:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:53879253-53879303	BJ	skin:	n/a
2	chr7:53879253-53879303	BJ	skin:	n/a
3	chr7:53879377-53879427	SKMC	muscle:	n/a
4	chr7:53811402-53811452	AG10803	skin:	n/a
5	chr7:53879422-53879472	ovcar-3	ovarian:	n/a
6	chr7:53879422-53879472	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:53811402-53811452	HIPEpiC	eye:	n/a
8	chr7:53879253-53879303	NT2-D1	testis:	n/a
9	chr7:53879377-53879427	NHBE	bronchial:	n/a
10	chr7:53879422-53879472	AG10803	skin:	n/a
11	chr7:53879253-53879303	HAEpiC	amniotic membrane:	n/a
12	chr7:53879377-53879427	ProgFib	skin:	n/a
13	chr7:53811402-53811452	AG09319	gingival:	n/a
14	chr7:53879377-53879427	H1-hESC	embryonic stem cell:	embryo
15	chr7:53879728-53879778	BJ	skin:	n/a
16	chr7:53811402-53811452	MCF-7	breast:	n/a
17	chr7:53879377-53879427	K562	blood:	n/a
18	chr7:53879377-53879427	GM12878	blood:	n/a
19	chr7:53879422-53879472	HCM	heart:	n/a
20	chr7:53879728-53879778	PrEC	prostate:	n/a
21	chr7:53879253-53879303	BE2_C	brain:	n/a
22	chr7:53879377-53879427	Caco-2	colon:	n/a
23	chr7:53879377-53879427	GM06990	blood:	n/a
24	chr7:53879422-53879472	NH-A	brain:	n/a
25	chr7:53811402-53811452	HRE	kidney:	n/a
26	chr7:53879377-53879427	NT2-D1	testis:	n/a
27	chr7:53879253-53879303	H1-hESC	embryonic stem cell:	embryo
28	chr7:53811402-53811452	K562	blood:	n/a
29	chr7:53811402-53811452	T-47D	breast:	n/a
30	chr7:53879377-53879427	GM12892	blood:	n/a
31	chr7:53879253-53879303	ovcar-3	ovarian:	n/a
32	chr7:53879422-53879472	ProgFib	skin:	n/a
33	chr7:53879253-53879303	K562	blood:	n/a
34	chr7:53811402-53811452	H1-hESC	embryonic stem cell:	embryo
35	chr7:53811402-53811452	BJ	skin:	n/a
36	chr7:53879422-53879472	MCF-7	breast:	n/a
37	chr7:53879422-53879472	PrEC	prostate:	n/a
38	chr7:53879728-53879778	U87	brain:	n/a
39	chr7:53879728-53879778	NHBE	bronchial:	n/a
40	chr7:53811402-53811452	NH-A	brain:	n/a
41	chr7:53879728-53879778	HEK293	kidney:	embryo
42	chr7:53811402-53811452	Caco-2	colon:	n/a
43	chr7:53811402-53811452	ECC-1	luminal epithelium:	n/a
44	chr7:53879728-53879778	HepG2	liver:	n/a
45	chr7:53879728-53879778	SK-N-SH_RA	brain:	n/a
46	chr7:53879422-53879472	GM12878	blood:	n/a
47	chr7:53811402-53811452	HEEpiC	esophagus:	n/a
48	chr7:53879728-53879778	HCF	heart:	n/a
49	chr7:53811402-53811452	GM12891	blood:	n/a
50	chr7:53879422-53879472	SK-N-SH	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:53841458..53843486-chr7:53862183..53865020,2	K562	blood:
2	chr7:53871548..53874105-chr7:53878796..53880658,2	K562	blood:
3	chr7:53848619..53849339-chr7:53918094..53918709,2	MCF-7	breast:
4	chr7:53779269..53780799-chr7:53781860..53784209,2	MCF-7	breast:
5	chr7:53865812..53868107-chr7:53870179..53872741,2	K562	blood:
6	chr7:53841058..53842718-chr7:53850373..53853368,2	K562	blood:
7	chr7:53820582..53822348-chr7:53824215..53825903,2	K562	blood:
8	chr7:53818690..53823967-chr7:53825430..53828073,4	K562	blood:
9	chr7:53820582..53822348-chr7:53824215..53825903,2	K562	blood:
10	chr7:53841058..53842718-chr7:53850373..53853368,2	K562	blood:
11	chr7:53849409..53852274-chr7:53856069..53858017,2	K562	blood:
12	chr7:53870278..53873063-chr7:53876211..53878158,2	K562	blood:
13	chr7:53818690..53823967-chr7:53825430..53828073,4	K562	blood:
14	chr7:53870278..53873063-chr7:53876211..53878158,2	K562	blood:
15	chr7:53779269..53780799-chr7:53781860..53784209,2	MCF-7	breast:
16	chr7:53776017..53777686-chr7:53778643..53780568,2	MCF-7	breast:
17	chr7:53848619..53849339-chr7:53918094..53918709,2	MCF-7	breast:
18	chr7:53827998..53830937-chr7:53834103..53836205,2	K562	blood:
19	chr7:53857172..53859056-chr7:53860252..53862922,2	K562	blood:
20	chr7:53857172..53859056-chr7:53860252..53862922,2	K562	blood:
21	chr7:53827998..53830937-chr7:53834103..53836205,2	K562	blood:
22	chr7:53865812..53868107-chr7:53870179..53872741,2	K562	blood:
23	chr3:73159725..73160594-chr7:53843395..53843920,2	HCT-116	colon:
24	chr7:53776017..53777686-chr7:53778643..53780568,2	MCF-7	breast:
25	chr5:135485656..135486185-chr7:53838517..53839265,2	MCF-7	breast:
26	chr7:53817997..53820497-chr7:53821045..53822573,2	K562	blood:
27	chr7:53841458..53843486-chr7:53862183..53865020,2	K562	blood:
28	chr7:53849409..53852274-chr7:53856069..53858017,2	K562	blood:
29	chr7:53817997..53820497-chr7:53821045..53822573,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POM121L12-9	chr7:53832905-53833852	NONHSAT120640
2	lnc-POM121L12-10	chr7:53847707-53847956	NONHSAT120643
3	lnc-POM121L12-9	chr7:53832374-53832647	NONHSAT120640
4	lnc-POM121L12-10	chr7:53847476-53847617	NONHSAT120643

No data

Variant related genes	Relation type
RNU2-29P	TF binding region
ENSG00000271306	TF binding region
ENSG00000232418	TF binding region
ENSG00000205628	TF binding region
ENSG00000235454	TF binding region
RNU2-29P	CpG island
ENSG00000271306	CpG island
ENSG00000232418	CpG island
ENSG00000205628	CpG island
ENSG00000235454	CpG island
ENSG00000223247	chromatin interactions
ENSG00000205628	chromatin interactions

Extended variants
information (count: 1595 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:1595 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567987570	chr7:53781806-53781807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535948403	chr7:53781840-53781841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554033653	chr7:53781841-53781842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572616947	chr7:53781863-53781864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539718929	chr7:53781959-53781960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573531251	chr7:53781981-53781982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10282338	chr7:53782008-53782009	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs576420485	chr7:53782035-53782036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577106031	chr7:53782054-53782055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75904193	chr7:53782065-53782066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556441249	chr7:53782068-53782069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188884086	chr7:53782069-53782070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562147829	chr7:53782085-53782086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574406681	chr7:53782089-53782090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375433922	chr7:53782114-53782115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs13247788	chr7:53782143-53782144	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs13230883	chr7:53782155-53782156	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530639893	chr7:53782174-53782175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73383366	chr7:53782178-53782179	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs181627753	chr7:53782182-53782183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531737790	chr7:53782200-53782201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550152747	chr7:53782214-53782215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546058947	chr7:53782242-53782243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527887180	chr7:53782252-53782253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144876506	chr7:53782256-53782257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547892799	chr7:53782266-53782267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566125063	chr7:53782347-53782348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370291177	chr7:53782380-53782381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185539540	chr7:53782381-53782382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11980213	chr7:53782431-53782432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149036602	chr7:53782442-53782443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190465133	chr7:53782443-53782444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537354472	chr7:53782473-53782474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35126910	chr7:53782481-53782482	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs34948720	chr7:53782498-53782499	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs182488979	chr7:53782538-53782539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11970846	chr7:53782577-53782578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143057629	chr7:53782595-53782596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185884540	chr7:53782597-53782598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79734017	chr7:53782601-53782602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531595468	chr7:53782704-53782705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6978045	chr7:53782780-53782781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs374300150	chr7:53782790-53782791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6959651	chr7:53782816-53782817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564881802	chr7:53782826-53782827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12667938	chr7:53782842-53782843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138702157	chr7:53782888-53782889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13224150	chr7:53782927-53782928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs17705087	chr7:53782948-53782949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs527298985	chr7:53783056-53783057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21525872	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53781800-53782200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr7:53782200-53783400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr7:53783400-53783800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr7:53783600-53783800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr7:53783800-53789000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:53785400-53785800	Enhancers	Ovary	ovary
7	chr7:53789000-53789200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr7:53807000-53811400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:53811400-53811600	Enhancers	NHEK	skin
10	chr7:53811400-53812000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr7:53811400-53812000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr7:53811400-53812400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr7:53811400-53812400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:53811400-53812400	Enhancers	HMEC	breast
15	chr7:53811400-53812600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr7:53811400-53812600	Enhancers	Esophagus	oesophagus
17	chr7:53811600-53812200	Flanking Active TSS	NHEK	skin
18	chr7:53811600-53812400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:53811800-53812200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:53811800-53812200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:53811800-53812400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr7:53812200-53812600	Active TSS	Spleen	Spleen
23	chr7:53812200-53812600	Enhancers	NHEK	skin
24	chr7:53827800-53828200	Enhancers	Brain Hippocampus Middle	brain
25	chr7:53832000-53837800	Weak transcription	K562	blood
26	chr7:53836200-53836600	Enhancers	Fetal Stomach	stomach
27	chr7:53837800-53839200	Strong transcription	K562	blood
28	chr7:53838200-53838800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:53839000-53839400	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr7:53839200-53847000	Weak transcription	K562	blood
31	chr7:53839400-53844200	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr7:53840400-53840800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:53840800-53843200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:53841200-53842000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:53843200-53843400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:53843400-53843600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:53844000-53844200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:53844200-53844600	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr7:53844600-53844800	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr7:53844800-53845200	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr7:53847000-53847200	Strong transcription	K562	blood
42	chr7:53847200-53848400	Weak transcription	K562	blood
43	chr7:53861800-53862000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:53864000-53864400	Enhancers	K562	blood
45	chr7:53868200-53868800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr7:53877200-53880200	Active TSS	K562	blood
47	chr7:53879000-53879400	Active TSS	NHEK	skin
48	chr7:53879000-53879600	ZNF genes & repeats	Fetal Intestine Large	intestine
49	chr7:53879000-53879600	Active TSS	Fetal Intestine Small	intestine
50	chr7:53879000-53879600	Active TSS	Right Ventricle	heart

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