Variant report

Variant	nsv607034
Chromosome Location	chr7:55974028-56002247
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	BACH1	chr7:55980324-55980655	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:55980363-55980676	K562	blood:	n/a	n/a
3	BHLHE40	chr7:56000099-56000127	K562	blood:	n/a	n/a
4	CTCF	chr7:55999411-55999466	GM13976	blood:	n/a	n/a
5	CTCF	chr7:55995760-55995910	GM06990	blood:	n/a	n/a
6	CTCF	chr7:55995860-55995908	GM12891	blood:	n/a	n/a
7	CTCF	chr7:55987682-55987707	ProgFib	skin:	n/a	n/a
8	CUX1	chr7:55983544-55983550	K562	blood:	n/a	n/a
9	EP300	chr7:55980568-55980869	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr7:55994001-55994319	K562	blood:	n/a	chr7:55994151-55994161
11	FOXA2	chr7:55980603-55980954	A549	lung:	n/a	n/a
12	GTF2F1	chr7:55986813-55986970	H1-hESC	embryonic stem cell:	n/a	n/a
13	HEY1	chr7:55996026-55996627	K562	blood:	n/a	n/a
14	HNF4A	chr7:55999555-55999741	HepG2	liver:	n/a	chr7:55999687-55999702 chr7:55999687-55999701 chr7:55999688-55999700 chr7:55999693-55999701 chr7:55999687-55999702 chr7:55999688-55999701 chr7:55999689-55999701 chr7:55999687-55999702 chr7:55999688-55999700
15	HNF4A	chr7:55999535-55999789	HepG2	liver:	n/a	chr7:55999687-55999702 chr7:55999687-55999701 chr7:55999688-55999700 chr7:55999693-55999701 chr7:55999687-55999702 chr7:55999688-55999701 chr7:55999689-55999701 chr7:55999687-55999702 chr7:55999688-55999700
16	HNF4G	chr7:55999381-55999847	HepG2	liver:	n/a	chr7:55999687-55999702 chr7:55999687-55999701 chr7:55999688-55999700 chr7:55999693-55999701 chr7:55999687-55999702 chr7:55999688-55999701 chr7:55999689-55999701 chr7:55999687-55999702 chr7:55999688-55999700
17	HNF4G	chr7:55999503-55999777	HepG2	liver:	n/a	chr7:55999687-55999702 chr7:55999687-55999701 chr7:55999688-55999700 chr7:55999693-55999701 chr7:55999687-55999702 chr7:55999688-55999701 chr7:55999689-55999701 chr7:55999687-55999702 chr7:55999688-55999700
18	IKZF1	chr7:55981431-55981535	GM12878	blood:	n/a	n/a
19	MAFF	chr7:55980320-55980674	K562	blood:	n/a	chr7:55980488-55980506
20	MAFF	chr7:55980414-55980660	HepG2	liver:	n/a	chr7:55980488-55980506
21	MAFK	chr7:55980325-55980671	K562	blood:	n/a	chr7:55980495-55980504 chr7:55980491-55980502 chr7:55980490-55980505 chr7:55980490-55980501 chr7:55980495-55980505
22	MAFK	chr7:55980346-55980656	IMR90	lung:	n/a	chr7:55980495-55980504 chr7:55980491-55980502 chr7:55980490-55980505 chr7:55980490-55980501 chr7:55980495-55980505
23	MAFK	chr7:55986769-55986823	HepG2	liver:	n/a	n/a
24	MAFK	chr7:55980332-55980647	HepG2	liver:	n/a	chr7:55980495-55980504 chr7:55980491-55980502 chr7:55980490-55980505 chr7:55980490-55980501 chr7:55980495-55980505
25	MAFK	chr7:55980333-55980683	HepG2	liver:	n/a	chr7:55980495-55980504 chr7:55980491-55980502 chr7:55980490-55980505 chr7:55980490-55980501 chr7:55980495-55980505
26	MAX	chr7:55999943-56000192	K562	blood:	n/a	n/a
27	MAX	chr7:55994090-55994325	NB4	blood:	n/a	n/a
28	MAX	chr7:55978924-55979115	NB4	blood:	n/a	chr7:55979050-55979060
29	MAZ	chr7:55975123-55975225	HepG2	liver:	n/a	n/a
30	MYC	chr7:55995114-55995208	MCF-7	breast:	n/a	n/a
31	MYC	chr7:55994053-55994356	NB4	blood:	n/a	n/a
32	MYC	chr7:55978688-55978806	K562	blood:	n/a	n/a
33	PML	chr7:55996063-55996485	K562	blood:	n/a	n/a
34	PML	chr7:55996050-55996522	K562	blood:	n/a	n/a
35	POLR2A	chr7:55996410-55996712	K562	blood:	n/a	n/a
36	POLR2A	chr7:56000277-56000809	K562	blood:	n/a	n/a
37	POLR2A	chr7:55996090-55996514	GM12891	blood:	n/a	n/a
38	POLR2A	chr7:55995953-55996493	K562	blood:	n/a	n/a
39	POLR2A	chr7:55992539-55993230	K562	blood:	n/a	n/a
40	POLR2A	chr7:55996026-55996410	K562	blood:	n/a	n/a
41	POLR2A	chr7:55990126-55990647	K562	blood:	n/a	n/a
42	POLR2A	chr7:55996243-55996479	K562	blood:	n/a	n/a
43	POLR2A	chr7:56001965-56002064	K562	blood:	n/a	n/a
44	POLR2A	chr7:55995772-55996561	Raji	blood:	n/a	n/a
45	POLR2A	chr7:55996100-55996447	GM12891	blood:	n/a	n/a
46	POLR2A	chr7:55991586-55992048	K562	blood:	n/a	n/a
47	POLR2A	chr7:56001119-56001351	K562	blood:	n/a	n/a
48	POLR2A	chr7:55996038-55996319	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr7:55995996-55996565	K562	blood:	n/a	n/a
50	POLR2A	chr7:55996064-55996297	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:55979455-55979505	SK-N-SH	brain:	n/a
2	chr7:55980196-55980246	Jurkat	blood:	n/a
3	chr7:55980165-55980215	SAEC	small airway:	n/a
4	chr7:55979455-55979505	RPTEC	kidney:	n/a
5	chr7:55979455-55979505	NB4	blood:	n/a
6	chr7:55979688-55979738	ProgFib	skin:	n/a
7	chr7:55980136-55980186	ECC-1	luminal epithelium:	n/a
8	chr7:55980165-55980215	GM06990	blood:	n/a
9	chr7:55980652-55980702	GM06990	blood:	n/a
10	chr7:55980136-55980186	SKMC	muscle:	n/a
11	chr7:55979742-55979792	A549	lung:	n/a
12	chr7:55980165-55980215	ECC-1	luminal epithelium:	n/a
13	chr7:55980136-55980186	GM06990	blood:	n/a
14	chr7:55980165-55980215	HRPEpiC	eye:	n/a
15	chr7:55980196-55980246	MCF-7	breast:	n/a
16	chr7:55979455-55979505	PrEC	prostate:	n/a
17	chr7:55979688-55979738	PANC-1	pancreas:	n/a
18	chr7:55980136-55980186	HRPEpiC	eye:	n/a
19	chr7:55980165-55980215	ProgFib	skin:	n/a
20	chr7:55980165-55980215	HAEpiC	amniotic membrane:	n/a
21	chr7:55979455-55979505	AG04450	lung:	fetal
22	chr7:55980196-55980246	HL-60	blood:	n/a
23	chr7:55980165-55980215	LNCaP	prostate:	n/a
24	chr7:55979742-55979792	HAEpiC	amniotic membrane:	n/a
25	chr7:55979455-55979505	HRE	kidney:	n/a
26	chr7:55979455-55979505	PFSK-1	brain:	n/a
27	chr7:55979742-55979792	HCF	heart:	n/a
28	chr7:55979688-55979738	K562	blood:	n/a
29	chr7:55980136-55980186	HEK293	kidney:	embryo
30	chr7:55980136-55980186	PANC-1	pancreas:	n/a
31	chr7:55979455-55979505	PANC-1	pancreas:	n/a
32	chr7:55980196-55980246	BJ	skin:	n/a
33	chr7:55979455-55979505	H1-hESC	embryonic stem cell:	embryo
34	chr7:55980652-55980702	SK-N-SH_RA	brain:	n/a
35	chr7:55979742-55979792	HL-60	blood:	n/a
36	chr7:55979455-55979505	HMEC	breast:	n/a
37	chr7:55979742-55979792	HEK293	kidney:	embryo
38	chr7:55979742-55979792	ProgFib	skin:	n/a
39	chr7:55980136-55980186	SK-N-SH_RA	brain:	n/a
40	chr7:55980165-55980215	BJ	skin:	n/a
41	chr7:55980165-55980215	Hepatocyte	liver:	n/a
42	chr7:55979688-55979738	SK-N-MC	brain:	n/a
43	chr7:55979742-55979792	SAEC	small airway:	n/a
44	chr7:55980136-55980186	AG04450	lung:	fetal
45	chr7:55980165-55980215	Jurkat	blood:	n/a
46	chr7:55980652-55980702	PANC-1	pancreas:	n/a
47	chr7:55980196-55980246	Hela-S3	cervix:	n/a
48	chr7:55979688-55979738	HepG2	liver:	n/a
49	chr7:55979742-55979792	ovcar-3	ovarian:	n/a
50	chr7:55979742-55979792	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:55985004..55987429-chr7:55990598..55992997,2	MCF-7	breast:
2	chr7:55976397..55978018-chr7:56030450..56032406,2	MCF-7	breast:
3	chr7:55979940..55982331-chr7:55990429..55992641,2	K562	blood:
4	chr7:55984149..55986926-chr7:56019516..56021040,2	K562	blood:
5	chr7:55985004..55987429-chr7:55990598..55992997,2	MCF-7	breast:
6	chr7:55973351..55975048-chr7:55990434..55993161,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GBAS-1	chr7:55979309-55979606	NONHSAT120710
2	lnc-GBAS-1	chr7:55973882-55974072	NONHSAT120710

Variant related genes	Relation type
ZNF713	TF binding region
ZNF713	CpG island
ENSG00000146729	chromatin interactions
ENSG00000178665	chromatin interactions
ENSG00000239789	chromatin interactions

Extended variants
information (count: 1066 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2135118	chr7:55974028-55974029	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548326192	chr7:55974047-55974048	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs181936874	chr7:55974072-55974073	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs148575314	chr7:55974095-55974096	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531698223	chr7:55974176-55974177	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142069277	chr7:55974186-55974187	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200479893	chr7:55974227-55974228	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186645294	chr7:55974236-55974237	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538046914	chr7:55974253-55974254	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550384430	chr7:55974269-55974270	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568195365	chr7:55974350-55974351	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535530211	chr7:55974389-55974390	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76559134	chr7:55974411-55974412	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374025454	chr7:55974413-55974414	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545526341	chr7:55974450-55974451	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539865862	chr7:55974556-55974557	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146656916	chr7:55974559-55974560	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577101273	chr7:55974652-55974653	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544054788	chr7:55974679-55974680	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189534108	chr7:55974707-55974708	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376053203	chr7:55974724-55974725	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140224024	chr7:55974742-55974743	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145383448	chr7:55974744-55974745	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112541969	chr7:55974796-55974797	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527285719	chr7:55974852-55974853	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182041386	chr7:55974912-55974913	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6593290	chr7:55974939-55974940	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs567635575	chr7:55974947-55974948	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75712024	chr7:55974964-55974965	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186359280	chr7:55975023-55975024	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568282719	chr7:55975042-55975043	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548680743	chr7:55975076-55975077	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190021336	chr7:55975099-55975100	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146451438	chr7:55975103-55975104	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565873325	chr7:55975180-55975181	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs6943341	chr7:55975182-55975183	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182530970	chr7:55975183-55975184	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs74772901	chr7:55975211-55975212	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs536938183	chr7:55975212-55975213	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538108001	chr7:55975260-55975261	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556506163	chr7:55975301-55975302	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6962038	chr7:55975311-55975312	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs542093248	chr7:55975356-55975357	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560280264	chr7:55975364-55975365	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140855864	chr7:55975375-55975376	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114976839	chr7:55975436-55975437	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186583307	chr7:55975441-55975442	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4518614	chr7:55975442-55975443	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs531224550	chr7:55975499-55975500	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550023103	chr7:55975514-55975515	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	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
Esophageal squamous carcinoma	21637470	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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Glioblastoma multiforme	19115005	CNVD
Breast cancer	17142309	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:55955400-56004200	Weak transcription	Gastric	stomach
2	chr7:55955800-55975000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr7:55955800-55985800	Weak transcription	Esophagus	oesophagus
4	chr7:55956000-55974200	Weak transcription	Aorta	Aorta
5	chr7:55956000-55979600	Weak transcription	Psoas Muscle	Psoas
6	chr7:55956200-55974200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr7:55956200-55975200	Weak transcription	HSMMtube	muscle
8	chr7:55956200-55979400	Weak transcription	Primary T cells from cord blood	blood
9	chr7:55956200-55979600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr7:55956200-55990800	Weak transcription	Thymus	Thymus
11	chr7:55956200-56002200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:55956400-55974400	Weak transcription	Adipose Nuclei	Adipose
13	chr7:55956400-55974800	Weak transcription	Fetal Kidney	kidney
14	chr7:55956400-55975000	Weak transcription	Liver	Liver
15	chr7:55956400-55979000	Weak transcription	Brain Substantia Nigra	brain
16	chr7:55956400-55979600	Weak transcription	Brain Angular Gyrus	brain
17	chr7:55956400-55979800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr7:55956400-55990600	Weak transcription	Brain Anterior Caudate	brain
19	chr7:55956400-55995800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:55956400-55998800	Weak transcription	Colon Smooth Muscle	Colon
21	chr7:55956600-55974600	Weak transcription	Fetal Brain Male	brain
22	chr7:55956600-55979400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr7:55956600-55990800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:55961800-55979400	Weak transcription	Spleen	Spleen
25	chr7:55962000-55990000	Weak transcription	HepG2	liver
26	chr7:55962000-55992800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr7:55962400-55974600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr7:55962600-55977800	Weak transcription	Fetal Heart	heart
29	chr7:55964600-55974600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:55966000-55974200	Weak transcription	Brain Hippocampus Middle	brain
31	chr7:55966600-55983800	Weak transcription	HUVEC	blood vessel
32	chr7:55966800-55979600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr7:55967600-55995800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr7:55968000-55975200	Weak transcription	Duodenum Mucosa	Duodenum
35	chr7:55968200-55975200	Weak transcription	Fetal Intestine Small	intestine
36	chr7:55968600-55995000	Weak transcription	HSMM	muscle
37	chr7:55969000-55974400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:55969000-55975000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:55969000-55985600	Weak transcription	Dnd41	blood
40	chr7:55969600-55974200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:55969600-55974200	Weak transcription	Fetal Thymus	thymus
42	chr7:55969600-55974800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:55969600-55974800	Weak transcription	Fetal Brain Female	brain
44	chr7:55969600-55975000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:55969600-55979400	Weak transcription	Lung	lung
46	chr7:55969800-55979000	Weak transcription	Brain Cingulate Gyrus	brain
47	chr7:55969800-55998200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:55970200-55974200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:55971600-55993400	Weak transcription	Primary B cells from cord blood	blood
50	chr7:55971800-55980200	Weak transcription	Right Ventricle	heart

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