Variant report

Variant	nsv469612
Chromosome Location	chr7:55752394-55876163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1041)
CpG islands
(count:1342)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:55775903-55776100	K562	blood:	n/a	n/a
2	ARID3A	chr7:55870300-55870318	K562	blood:	n/a	n/a
3	ARID3A	chr7:55800487-55800499	K562	blood:	n/a	n/a
4	ARID3A	chr7:55766815-55767160	HepG2	liver:	n/a	n/a
5	ATF1	chr7:55845338-55845367	K562	blood:	n/a	n/a
6	ATF1	chr7:55775814-55776082	K562	blood:	n/a	n/a
7	ATF1	chr7:55797922-55798229	K562	blood:	n/a	n/a
8	ATF1	chr7:55766863-55767175	K562	blood:	n/a	n/a
9	ATF3	chr7:55775794-55776151	K562	blood:	n/a	n/a
10	ATF3	chr7:55798768-55799118	K562	blood:	n/a	n/a
11	BACH1	chr7:55862322-55862529	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:55809638-55809751	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:55810431-55810600	GM12878	blood:	n/a	n/a
14	BATF	chr7:55790556-55790863	GM12878	blood:	n/a	n/a
15	BATF	chr7:55811851-55812057	GM12878	blood:	n/a	n/a
16	BATF	chr7:55809246-55809419	GM12878	blood:	n/a	n/a
17	BATF	chr7:55766911-55767148	GM12878	blood:	n/a	n/a
18	BATF	chr7:55811971-55812164	GM12878	blood:	n/a	n/a
19	BATF	chr7:55820832-55821076	GM12878	blood:	n/a	chr7:55820958-55820969
20	BCL11A	chr7:55809118-55809327	GM12878	blood:	n/a	chr7:55809309-55809322
21	BCL11A	chr7:55811886-55812072	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:55811867-55812100	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:55809240-55809421	GM12878	blood:	n/a	chr7:55809309-55809322
24	BCL11A	chr7:55811571-55811727	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:55810305-55810522	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:55811958-55812177	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:55766540-55767161	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:55806702-55806733	HepG2	liver:	n/a	n/a
29	BHLHE40	chr7:55766975-55767060	K562	blood:	n/a	n/a
30	BHLHE40	chr7:55766892-55767023	GM12878	blood:	n/a	n/a
31	CBX3	chr7:55864948-55865345	HCT-116	colon:	n/a	n/a
32	CBX3	chr7:55864959-55865300	K562	blood:	n/a	n/a
33	CBX3	chr7:55864939-55865388	HCT-116	colon:	n/a	n/a
34	CBX3	chr7:55864935-55865274	K562	blood:	n/a	n/a
35	CEBPB	chr7:55862358-55862505	IMR90	lung:	n/a	chr7:55862399-55862410
36	CEBPB	chr7:55762081-55762121	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:55778109-55778244	A549	lung:	n/a	chr7:55778194-55778205
38	CEBPB	chr7:55859790-55860072	A549	lung:	n/a	chr7:55859941-55859954 chr7:55859941-55859952
39	CEBPB	chr7:55844751-55844845	H1-hESC	embryonic stem cell:	n/a	chr7:55844761-55844772
40	CEBPB	chr7:55788142-55788370	HepG2	liver:	n/a	chr7:55788232-55788243
41	CEBPB	chr7:55766796-55767226	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:55795321-55795465	HepG2	liver:	n/a	chr7:55795450-55795461
43	CEBPB	chr7:55862268-55862679	HCT-116	colon:	n/a	chr7:55862399-55862410
44	CEBPB	chr7:55859780-55860090	K562	blood:	n/a	chr7:55859941-55859954 chr7:55859941-55859952
45	CEBPB	chr7:55862272-55862668	MCF-7	breast:	n/a	chr7:55862399-55862410
46	CEBPB	chr7:55766901-55767048	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:55862234-55862519	K562	blood:	n/a	chr7:55862399-55862410
48	CEBPB	chr7:55788173-55788288	A549	lung:	n/a	chr7:55788232-55788243
49	CEBPB	chr7:55775697-55776151	K562	blood:	n/a	chr7:55775949-55775962
50	CEBPB	chr7:55798699-55798787	K562	blood:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:55811507-55811557	AoSMC	blood vessel:	n/a
2	chr7:55874624-55874674	GM12878	blood:	n/a
3	chr7:55799739-55799789	NHDF-neo	bronchial:	n/a
4	chr7:55840551-55840601	AG04450	lung:	fetal
5	chr7:55799739-55799789	HCPEpiC	choroid plexus:	n/a
6	chr7:55799845-55799895	Hela-S3	cervix:	n/a
7	chr7:55808739-55808789	AG09309	skin:	n/a
8	chr7:55811507-55811557	PrEC	prostate:	n/a
9	chr7:55840551-55840601	HRPEpiC	eye:	n/a
10	chr7:55757158-55757208	NHDF-neo	bronchial:	n/a
11	chr7:55811507-55811557	HL-60	blood:	n/a
12	chr7:55808934-55808984	PFSK-1	brain:	n/a
13	chr7:55817964-55818014	HRPEpiC	eye:	n/a
14	chr7:55757733-55757783	HIPEpiC	eye:	n/a
15	chr7:55808878-55808928	BE2_C	brain:	n/a
16	chr7:55808739-55808789	HL-60	blood:	n/a
17	chr7:55757158-55757208	CMK	blood:	n/a
18	chr7:55805069-55805119	HRPEpiC	eye:	n/a
19	chr7:55805069-55805119	GM06990	blood:	n/a
20	chr7:55805069-55805119	H1-hESC	embryonic stem cell:	embryo
21	chr7:55874624-55874674	GM19239	blood:	n/a
22	chr7:55756911-55756961	SK-N-SH	brain:	n/a
23	chr7:55799845-55799895	RPTEC	kidney:	n/a
24	chr7:55810883-55810933	HRE	kidney:	n/a
25	chr7:55811507-55811557	HMEC	breast:	n/a
26	chr7:55808739-55808789	GM12891	blood:	n/a
27	chr7:55757733-55757783	AG09309	skin:	n/a
28	chr7:55808878-55808928	HRCEpiC	kidney:	n/a
29	chr7:55808934-55808984	SK-N-MC	brain:	n/a
30	chr7:55757158-55757208	HCPEpiC	choroid plexus:	n/a
31	chr7:55808878-55808928	GM19239	blood:	n/a
32	chr7:55807171-55807221	RPTEC	kidney:	n/a
33	chr7:55808739-55808789	NHDF-neo	bronchial:	n/a
34	chr7:55808739-55808789	NB4	blood:	n/a
35	chr7:55810883-55810933	Hela-S3	cervix:	n/a
36	chr7:55812396-55812446	MCF-7	breast:	n/a
37	chr7:55758049-55758099	HCM	heart:	n/a
38	chr7:55757158-55757208	GM12891	blood:	n/a
39	chr7:55840551-55840601	Hepatocyte	liver:	n/a
40	chr7:55756911-55756961	HCPEpiC	choroid plexus:	n/a
41	chr7:55810883-55810933	NT2-D1	testis:	n/a
42	chr7:55816154-55816204	Hepatocyte	liver:	n/a
43	chr7:55812396-55812446	HIPEpiC	eye:	n/a
44	chr7:55773068-55773118	AG04449	skin:	fetal
45	chr7:55808878-55808928	K562	blood:	n/a
46	chr7:55816154-55816204	GM12891	blood:	n/a
47	chr7:55799829-55799879	HL-60	blood:	n/a
48	chr7:55840551-55840601	GM12878	blood:	n/a
49	chr7:55773068-55773118	HUVEC	blood vessel:	n/a
50	chr7:55810883-55810933	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:55845241..55847686-chr7:56031025..56033785,2	K562	blood:
2	chr7:55782873..55785811-chr7:56031209..56033852,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-15K19.2.1-3	chr7:55832485-55832637	NONHSAT120696
2	lnc-SEPT14-2	chr7:55841348-55841546	NONHSAT120699
3	lnc-PSPH-2	chr7:55865639-55866173	NONHSAT120704
4	lnc-RP11-15K19.2.1-3	chr7:55840922-55841211	NONHSAT120702
5	lnc-RP11-15K19.2.1-3	chr7:55840874-55840935	NONHSAT120696
6	lnc-RP11-15K19.2.1-3	chr7:55846506-55846763	NONHSAT120696
7	lnc-RP11-15K19.2.1-3	chr7:55846506-55846745	NONHSAT120700
8	lnc-SEPT14-2	chr7:55840870-55841028	NONHSAT120699
9	lnc-RP11-15K19.2.1-3	chr7:55840872-55840935	NONHSAT120700

No data

Variant related genes	Relation type
FKBP9L	TF binding region
SUMO2P3	TF binding region
CICP11	TF binding region
PSPHP1	TF binding region
RNU6-1126P	TF binding region
RNU6-389P	TF binding region
CICP12	TF binding region
ENSG00000235738	TF binding region
FKBP9L	CpG island
SUMO2P3	CpG island
CICP11	CpG island
PSPHP1	CpG island
RNU6-1126P	CpG island
RNU6-389P	CpG island
CICP12	CpG island
ENSG00000235738	CpG island
ENSG00000146729	chromatin interactions

Extended variants
information (count: 3322 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3322 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557049477	chr7:55752407-55752408	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs2961441	chr7:55752423-55752424	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs111277216	chr7:55752424-55752425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536257127	chr7:55752429-55752430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554921033	chr7:55752521-55752522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4601271	chr7:55752586-55752587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs73701123	chr7:55752597-55752598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148281665	chr7:55752604-55752605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577546913	chr7:55752628-55752629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182019993	chr7:55752646-55752647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563021126	chr7:55752661-55752662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186229889	chr7:55752662-55752663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542211175	chr7:55752674-55752675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs3813851	chr7:55752684-55752685	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs112438899	chr7:55752695-55752696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112735644	chr7:55752733-55752734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559039279	chr7:55752750-55752751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190655692	chr7:55752798-55752799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571086168	chr7:55752826-55752827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532356449	chr7:55752843-55752844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183360404	chr7:55752885-55752886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371376843	chr7:55752891-55752892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374526820	chr7:55752919-55752920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535828421	chr7:55752932-55752933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554548427	chr7:55752958-55752959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566515917	chr7:55752975-55752976	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs367729588	chr7:55752989-55752990	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs559322419	chr7:55752994-55752995	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs185524994	chr7:55753014-55753015	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544806951	chr7:55753023-55753024	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371287365	chr7:55753047-55753048	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs556335788	chr7:55753048-55753049	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs574872825	chr7:55753054-55753055	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs375022291	chr7:55753060-55753061	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs150629241	chr7:55753104-55753105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560098626	chr7:55753115-55753116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113424343	chr7:55753145-55753146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540105676	chr7:55753151-55753152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564849405	chr7:55753154-55753155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528111172	chr7:55753165-55753166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373172623	chr7:55753196-55753197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183180375	chr7:55753235-55753236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187445517	chr7:55753236-55753237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548340401	chr7:55753273-55753274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566454741	chr7:55753291-55753292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533792640	chr7:55753292-55753293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550787018	chr7:55753320-55753321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192441783	chr7:55753328-55753329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571127200	chr7:55753353-55753354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538203043	chr7:55753365-55753366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Lung cancer	18438408	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
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	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
Glioblastoma multiforme	21569311	CNVD
Breast cancer	17142309	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:55745200-55752600	Weak transcription	Pancreas	Pancrea
2	chr7:55752600-55753200	Enhancers	Pancreas	Pancrea
3	chr7:55753200-55756400	Weak transcription	Pancreas	Pancrea
4	chr7:55754600-55754800	Enhancers	K562	blood
5	chr7:55754600-55757800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr7:55755400-55755800	Enhancers	Left Ventricle	heart
7	chr7:55755800-55756200	Weak transcription	Left Ventricle	heart
8	chr7:55755800-55756600	Bivalent Enhancer	HepG2	liver
9	chr7:55756000-55757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:55756000-55757400	Enhancers	Fetal Lung	lung
11	chr7:55756000-55757400	Enhancers	HUVEC	blood vessel
12	chr7:55756000-55757800	Enhancers	Stomach Mucosa	stomach
13	chr7:55756000-55757800	Enhancers	NHEK	skin
14	chr7:55756200-55756800	Enhancers	Left Ventricle	heart
15	chr7:55756200-55757000	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:55756200-55757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:55756400-55756800	Enhancers	Ovary	ovary
18	chr7:55756400-55756800	Enhancers	Pancreas	Pancrea
19	chr7:55756400-55757000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:55756400-55757000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:55756400-55757000	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr7:55756400-55757200	Enhancers	Fetal Muscle Trunk	muscle
23	chr7:55756400-55757200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr7:55756400-55757200	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr7:55756400-55757200	Enhancers	Small Intestine	intestine
26	chr7:55756400-55757200	Enhancers	Spleen	Spleen
27	chr7:55756400-55757400	Enhancers	Fetal Muscle Leg	muscle
28	chr7:55756400-55757400	Enhancers	HMEC	breast
29	chr7:55756400-55757600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr7:55756400-55757800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr7:55756400-55757800	Enhancers	Colon Smooth Muscle	Colon
32	chr7:55756600-55757000	Enhancers	K562	blood
33	chr7:55756600-55757200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr7:55756600-55757200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:55756600-55757400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:55756600-55757800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr7:55756600-55757800	Enhancers	Fetal Kidney	kidney
38	chr7:55756600-55757800	Enhancers	HepG2	liver
39	chr7:55756800-55757000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:55756800-55757200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:55756800-55757200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:55756800-55757200	Enhancers	Colonic Mucosa	Colon
43	chr7:55756800-55757200	Flanking Active TSS	Ovary	ovary
44	chr7:55756800-55757200	Flanking Active TSS	Pancreas	Pancrea
45	chr7:55756800-55757400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:55756800-55757400	Enhancers	Adipose Nuclei	Adipose
47	chr7:55756800-55757800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:55756800-55757800	Enhancers	Fetal Stomach	stomach
49	chr7:55757000-55761400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr7:55757000-55766600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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