Variant report

Variant	nsv606905
Chromosome Location	chr7:50544063-50565963
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:184)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 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	chr7:50555462-50555572	K562	blood:	n/a	n/a
2	ARID3A	chr7:50564372-50565500	K562	blood:	n/a	n/a
3	ARID3A	chr7:50545345-50545545	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:50554248-50554550	K562	blood:	n/a	n/a
5	ARID3A	chr7:50549711-50549911	K562	blood:	n/a	n/a
6	ATF1	chr7:50564633-50565134	K562	blood:	n/a	n/a
7	ATF1	chr7:50554229-50554572	K562	blood:	n/a	n/a
8	ATF3	chr7:50564692-50565091	K562	blood:	n/a	n/a
9	BACH1	chr7:50544710-50544993	K562	blood:	n/a	n/a
10	BHLHE40	chr7:50560606-50560748	K562	blood:	n/a	n/a
11	BHLHE40	chr7:50564301-50564408	K562	blood:	n/a	n/a
12	BHLHE40	chr7:50564711-50565125	K562	blood:	n/a	n/a
13	BHLHE40	chr7:50545019-50545114	K562	blood:	n/a	n/a
14	BRCA1	chr7:50564843-50565049	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr7:50565585-50565895	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr7:50564657-50565085	K562	blood:	n/a	n/a
17	CBX3	chr7:50564702-50565073	K562	blood:	n/a	n/a
18	CCNT2	chr7:50560488-50560688	K562	blood:	n/a	n/a
19	CCNT2	chr7:50564647-50565217	K562	blood:	n/a	n/a
20	CCNT2	chr7:50554223-50554732	K562	blood:	n/a	n/a
21	CEBPB	chr7:50557693-50557749	HepG2	liver:	n/a	chr7:50557718-50557729
22	CEBPB	chr7:50562771-50562971	Hela-S3	cervix:	n/a	chr7:50562850-50562861
23	CEBPB	chr7:50549005-50549190	HepG2	liver:	n/a	chr7:50549025-50549036
24	CEBPB	chr7:50565601-50566166	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:50562739-50562939	K562	blood:	n/a	chr7:50562850-50562861
26	CEBPB	chr7:50562789-50563027	HepG2	liver:	n/a	chr7:50562850-50562861
27	CEBPB	chr7:50564597-50565140	K562	blood:	n/a	n/a
28	CEBPB	chr7:50564703-50564954	K562	blood:	n/a	n/a
29	CEBPB	chr7:50564789-50565091	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:50564685-50565086	K562	blood:	n/a	n/a
31	CEBPB	chr7:50564701-50565177	Hela-S3	cervix:	n/a	n/a
32	CEBPD	chr7:50564616-50565212	K562	blood:	n/a	n/a
33	CEBPD	chr7:50564602-50565241	K562	blood:	n/a	n/a
34	CHD2	chr7:50564788-50565129	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr7:50565788-50566147	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr7:50564553-50565418	K562	blood:	n/a	n/a
37	CTCF	chr7:50549820-50549970	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr7:50564380-50564530	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr7:50548440-50548590	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr7:50549640-50549790	GM12872	blood:	n/a	chr7:50549753-50549762
41	CTCF	chr7:50549680-50549830	RPTEC	kidney:	n/a	chr7:50549753-50549762
42	CTCF	chr7:50549699-50549842	Fibrobl	skin:	n/a	chr7:50549753-50549762
43	CTCF	chr7:50549689-50549833	HepG2	liver:	n/a	chr7:50549753-50549762
44	CTCF	chr7:50549668-50549842	Gliobla	brain:	n/a	chr7:50549753-50549762
45	CTCF	chr7:50549660-50549810	MCF-7	breast:	n/a	chr7:50549753-50549762
46	CTCF	chr7:50549660-50549810	WERI-Rb-1	eye:	n/a	chr7:50549753-50549762
47	CTCF	chr7:50564845-50564997	K562	blood:	n/a	chr7:50564898-50564911
48	CTCF	chr7:50564400-50564550	BE2_C	brain:	n/a	n/a
49	CTCF	chr7:50564440-50564590	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr7:50562980-50563130	GM12869	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50560524-50560574	T-47D	breast:	n/a
2	chr7:50560524-50560574	T-47D	breast:	n/a
3	chr7:50560743-50560793	SAEC	small airway:	n/a
4	chr7:50560686-50560736	A549	lung:	n/a
5	chr7:50560743-50560793	BJ	skin:	n/a
6	chr7:50560686-50560736	SK-N-SH_RA	brain:	n/a
7	chr7:50560524-50560574	HEK293	kidney:	embryo
8	chr7:50560743-50560793	PrEC	prostate:	n/a
9	chr7:50560686-50560736	HMEC	breast:	n/a
10	chr7:50560524-50560574	NB4	blood:	n/a
11	chr7:50560524-50560574	HL-60	blood:	n/a
12	chr7:50560686-50560736	HCF	heart:	n/a
13	chr7:50560686-50560736	NHBE	bronchial:	n/a
14	chr7:50560686-50560736	AoSMC	blood vessel:	n/a
15	chr7:50560686-50560736	HUVEC	blood vessel:	n/a
16	chr7:50560743-50560793	SK-N-SH_RA	brain:	n/a
17	chr7:50560524-50560574	SK-N-MC	brain:	n/a
18	chr7:50560743-50560793	LNCaP	prostate:	n/a
19	chr7:50560686-50560736	SAEC	small airway:	n/a
20	chr7:50560743-50560793	BE2_C	brain:	n/a
21	chr7:50560743-50560793	AG10803	skin:	n/a
22	chr7:50560524-50560574	PFSK-1	brain:	n/a
23	chr7:50560686-50560736	SKMC	muscle:	n/a
24	chr7:50560686-50560736	AG04449	skin:	fetal
25	chr7:50560686-50560736	T-47D	breast:	n/a
26	chr7:50560524-50560574	HIPEpiC	eye:	n/a
27	chr7:50560686-50560736	PFSK-1	brain:	n/a
28	chr7:50560686-50560736	SK-N-MC	brain:	n/a
29	chr7:50560524-50560574	H1-hESC	embryonic stem cell:	embryo
30	chr7:50560686-50560736	RPTEC	kidney:	n/a
31	chr7:50560743-50560793	SK-N-MC	brain:	n/a
32	chr7:50560686-50560736	ovcar-3	ovarian:	n/a
33	chr7:50560686-50560736	GM12892	blood:	n/a
34	chr7:50560743-50560793	HAEpiC	amniotic membrane:	n/a
35	chr7:50560743-50560793	HEEpiC	esophagus:	n/a
36	chr7:50560743-50560793	Jurkat	blood:	n/a
37	chr7:50560524-50560574	K562	blood:	n/a
38	chr7:50560524-50560574	SK-N-SH	brain:	n/a
39	chr7:50560524-50560574	HCF	heart:	n/a
40	chr7:50560743-50560793	Hela-S3	cervix:	n/a
41	chr7:50560524-50560574	Hela-S3	cervix:	n/a
42	chr7:50560686-50560736	CMK	blood:	n/a
43	chr7:50560524-50560574	AG04449	skin:	fetal
44	chr7:50560743-50560793	HCF	heart:	n/a
45	chr7:50560686-50560736	HNPCEpiC	eye:	n/a
46	chr7:50560524-50560574	PANC-1	pancreas:	n/a
47	chr7:50560743-50560793	GM12891	blood:	n/a
48	chr7:50560524-50560574	HCPEpiC	choroid plexus:	n/a
49	chr7:50560686-50560736	HL-60	blood:	n/a
50	chr7:50560686-50560736	GM19239	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:50565140..50566781-chr7:50570058..50572270,2	K562	blood:
2	chr7:50538202..50540101-chr7:50549374..50551291,2	K562	blood:
3	chr7:50546772..50548404-chr7:50551410..50554000,2	K562	blood:
4	chr7:50564851..50566745-chr7:50568557..50570240,2	K562	blood:
5	chr7:50537654..50539269-chr7:50553300..50555389,2	K562	blood:

No data

Variant related genes	Relation type
DDC	TF binding region
DDC	CpG island
ENSG00000132437	chromatin interactions

Extended variants
information (count: 909 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:909 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs732215	chr7:50544063-50544064	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs745042	chr7:50544138-50544139	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs539749801	chr7:50544157-50544158	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4143196	chr7:50544159-50544160	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs55711351	chr7:50544178-50544179	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541538969	chr7:50544216-50544217	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187653463	chr7:50544222-50544223	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556473245	chr7:50544246-50544247	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577912070	chr7:50544259-50544260	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369528328	chr7:50544266-50544267	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138923522	chr7:50544270-50544271	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374652761	chr7:50544298-50544299	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4490786	chr7:50544314-50544315	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs201951824	chr7:50544323-50544324	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193227256	chr7:50544347-50544348	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376564036	chr7:50544386-50544387	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370615997	chr7:50544389-50544390	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574871657	chr7:50544433-50544434	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185666044	chr7:50544436-50544437	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187468674	chr7:50544446-50544447	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs731690	chr7:50544461-50544462	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577080995	chr7:50544482-50544483	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192324857	chr7:50544527-50544528	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542334438	chr7:50544602-50544603	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559665091	chr7:50544609-50544610	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528065290	chr7:50544628-50544629	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11575483	chr7:50544663-50544664	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs369598669	chr7:50544665-50544666	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556920232	chr7:50544669-50544670	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11575482	chr7:50544697-50544698	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550750382	chr7:50544717-50544718	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142295888	chr7:50544718-50544719	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs731689	chr7:50544749-50544750	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546913798	chr7:50544786-50544787	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531649639	chr7:50544806-50544807	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566681741	chr7:50544807-50544808	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535001829	chr7:50544900-50544901	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554681767	chr7:50544916-50544917	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573879619	chr7:50544918-50544919	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188499094	chr7:50544931-50544932	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181320236	chr7:50544938-50544939	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2329365	chr7:50544945-50544946	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs6965432	chr7:50544951-50544952	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs4989851	chr7:50544954-50544955	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs3887826	chr7:50544961-50544962	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2329366	chr7:50544966-50544967	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2876827	chr7:50544975-50544976	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs111728225	chr7:50544991-50544992	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11575474	chr7:50544992-50544993	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs896309	chr7:50545022-50545023	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:121)

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
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	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
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50535800-50546800	Weak transcription	Pancreas	Pancrea
2	chr7:50535800-50553200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr7:50536200-50545400	Weak transcription	Right Atrium	heart
4	chr7:50542000-50549600	Weak transcription	Stomach Mucosa	stomach
5	chr7:50542200-50545000	Weak transcription	HepG2	liver
6	chr7:50542200-50546000	Genic enhancers	Fetal Intestine Small	intestine
7	chr7:50542800-50544200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:50542800-50544200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:50543400-50546600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr7:50543600-50595000	Weak transcription	Liver	Liver
11	chr7:50543800-50544200	Genic enhancers	Fetal Intestine Large	intestine
12	chr7:50544000-50544200	Enhancers	Psoas Muscle	Psoas
13	chr7:50544200-50544600	Strong transcription	Fetal Intestine Large	intestine
14	chr7:50544200-50548400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:50544400-50545200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:50544600-50545800	Weak transcription	Fetal Intestine Large	intestine
17	chr7:50545000-50545800	Enhancers	HepG2	liver
18	chr7:50545200-50545400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:50545800-50548800	Strong transcription	Fetal Intestine Large	intestine
20	chr7:50545800-50565800	Weak transcription	HepG2	liver
21	chr7:50546000-50548800	Strong transcription	Fetal Intestine Small	intestine
22	chr7:50546600-50548800	Strong transcription	Duodenum Mucosa	Duodenum
23	chr7:50546800-50547600	Enhancers	Gastric	stomach
24	chr7:50546800-50547600	Enhancers	Pancreas	Pancrea
25	chr7:50548400-50549000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:50548800-50556600	Weak transcription	Fetal Intestine Small	intestine
27	chr7:50548800-50559600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr7:50548800-50559800	Weak transcription	Fetal Intestine Large	intestine
29	chr7:50548800-50564400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr7:50549600-50550400	Enhancers	Stomach Mucosa	stomach
31	chr7:50554000-50554600	Enhancers	K562	blood
32	chr7:50554600-50559800	Weak transcription	K562	blood
33	chr7:50556400-50557400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:50556600-50556800	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chr7:50556800-50559800	Weak transcription	Fetal Intestine Small	intestine
36	chr7:50556800-50561000	Weak transcription	Ovary	ovary
37	chr7:50557000-50557400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr7:50557200-50558600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr7:50557400-50564200	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr7:50558600-50559000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr7:50559000-50560200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr7:50559000-50561000	Enhancers	Stomach Mucosa	stomach
43	chr7:50559200-50559600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:50559200-50559600	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr7:50559400-50559600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr7:50559600-50560200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:50559600-50561200	Strong transcription	Duodenum Mucosa	Duodenum
48	chr7:50559600-50564200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr7:50559600-50564800	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr7:50559800-50561200	Enhancers	K562	blood

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