Variant report

Variant	nsv1027494
Chromosome Location	chr7:79693976-79760332
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:79757055-79757502	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr7:79756998-79757539	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:79740475-79740488	K562	blood:	n/a	n/a
4	BCL11A	chr7:79757131-79757375	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr7:79757143-79757380	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:79732050-79732083	K562	blood:	n/a	n/a
7	CBX3	chr7:79696058-79696229	K562	blood:	n/a	n/a
8	CEBPB	chr7:79699774-79700006	A549	lung:	n/a	chr7:79699940-79699949 chr7:79699940-79699949
9	CEBPB	chr7:79703373-79703447	HepG2	liver:	n/a	chr7:79703407-79703418
10	CEBPB	chr7:79756724-79756886	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr7:79728101-79728555	MCF-7	breast:	n/a	chr7:79728332-79728343
12	CEBPB	chr7:79719489-79719848	MCF-7	breast:	n/a	n/a
13	CEBPB	chr7:79728182-79728477	K562	blood:	n/a	chr7:79728332-79728343
14	CEBPB	chr7:79728163-79728488	H1-hESC	embryonic stem cell:	n/a	chr7:79728332-79728343
15	CEBPB	chr7:79719468-79719821	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:79699780-79700074	IMR90	lung:	n/a	chr7:79699940-79699949 chr7:79699940-79699949
17	CEBPB	chr7:79718101-79718369	A549	lung:	n/a	n/a
18	CEBPB	chr7:79728163-79728507	HepG2	liver:	n/a	chr7:79728332-79728343
19	CEBPB	chr7:79728179-79728463	Hela-S3	cervix:	n/a	chr7:79728332-79728343
20	CEBPB	chr7:79718711-79719000	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:79744716-79744911	HepG2	liver:	n/a	chr7:79744777-79744788
22	CEBPB	chr7:79719486-79719851	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:79718041-79718404	MCF-7	breast:	n/a	n/a
24	CEBPB	chr7:79719385-79719980	HCT-116	colon:	n/a	n/a
25	CEBPB	chr7:79728050-79728491	A549	lung:	n/a	chr7:79728332-79728343
26	CEBPB	chr7:79728158-79728513	A549	lung:	n/a	chr7:79728332-79728343
27	CEBPB	chr7:79703341-79703560	A549	lung:	n/a	chr7:79703407-79703418
28	CEBPB	chr7:79719521-79719783	A549	lung:	n/a	n/a
29	CEBPB	chr7:79718183-79718348	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:79728220-79728503	IMR90	lung:	n/a	chr7:79728332-79728343
31	CEBPB	chr7:79718048-79718408	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:79727158-79727388	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:79719593-79719632	K562	blood:	n/a	n/a
34	CHD2	chr7:79756952-79757466	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:79728220-79728370	HMEC	breast:	n/a	n/a
36	CTCF	chr7:79728240-79728390	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr7:79724860-79725010	HFF	foreskin:	n/a	n/a
38	CTCF	chr7:79728240-79728390	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr7:79728080-79728230	GM12878	blood:	n/a	n/a
40	CTCF	chr7:79725000-79725150	AG04450	lung:	n/a	chr7:79725050-79725066 chr7:79725049-79725067 chr7:79725051-79725072 chr7:79725053-79725060
41	CTCF	chr7:79728160-79728310	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr7:79728260-79728410	GM12871	blood:	n/a	n/a
43	CTCF	chr7:79728220-79728370	HPF	lung:	n/a	n/a
44	CTCF	chr7:79728160-79728310	GM12864	blood:	n/a	n/a
45	CTCF	chr7:79728220-79728370	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr7:79724960-79725110	HVMF	connective:	n/a	chr7:79725050-79725066 chr7:79725049-79725067 chr7:79725051-79725072 chr7:79725053-79725060
47	CTCF	chr7:79724903-79725113	SK-N-SH_RA	brain:	n/a	chr7:79725050-79725066 chr7:79725049-79725067 chr7:79725051-79725072 chr7:79725053-79725060
48	CTCF	chr7:79708900-79709050	K562	blood:	n/a	n/a
49	CTCF	chr7:79728200-79728350	GM12864	blood:	n/a	n/a
50	CTCF	chr7:79724896-79725194	GM12878	blood:	n/a	chr7:79725050-79725066 chr7:79725049-79725067 chr7:79725051-79725072 chr7:79725053-79725060

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:79754567-79754617	AoSMC	blood vessel:	n/a
2	chr7:79754567-79754617	HRE	kidney:	n/a
3	chr7:79754567-79754617	T-47D	breast:	n/a
4	chr7:79754567-79754617	K562	blood:	n/a
5	chr7:79754567-79754617	HepG2	liver:	n/a
6	chr7:79754567-79754617	SK-N-MC	brain:	n/a
7	chr7:79754567-79754617	NB4	blood:	n/a
8	chr7:79754567-79754617	ovcar-3	ovarian:	n/a
9	chr7:79754567-79754617	AG09309	skin:	n/a
10	chr7:79754567-79754617	HRCEpiC	kidney:	n/a
11	chr7:79754567-79754617	BE2_C	brain:	n/a
12	chr7:79754567-79754617	HRPEpiC	eye:	n/a
13	chr7:79754567-79754617	Jurkat	blood:	n/a
14	chr7:79754567-79754617	GM06990	blood:	n/a
15	chr7:79754567-79754617	Hela-S3	cervix:	n/a
16	chr7:79754567-79754617	AG04449	skin:	fetal
17	chr7:79754567-79754617	LNCaP	prostate:	n/a
18	chr7:79754567-79754617	GM12892	blood:	n/a
19	chr7:79754567-79754617	HEEpiC	esophagus:	n/a
20	chr7:79754567-79754617	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:79754567-79754617	MCF10A-Er-Src	breast:	n/a
22	chr7:79754567-79754617	PFSK-1	brain:	n/a
23	chr7:79754567-79754617	AG09319	gingival:	n/a
24	chr7:79754567-79754617	NHBE	bronchial:	n/a
25	chr7:79754567-79754617	GM12878	blood:	n/a
26	chr7:79754567-79754617	GM12891	blood:	n/a
27	chr7:79754567-79754617	NHDF-neo	bronchial:	n/a
28	chr7:79754567-79754617	CMK	blood:	n/a
29	chr7:79754567-79754617	HCF	heart:	n/a
30	chr7:79754567-79754617	Hepatocyte	liver:	n/a
31	chr7:79754567-79754617	HCPEpiC	choroid plexus:	n/a
32	chr7:79754567-79754617	HNPCEpiC	eye:	n/a
33	chr7:79754567-79754617	PrEC	prostate:	n/a
34	chr7:79754567-79754617	H1-hESC	embryonic stem cell:	embryo
35	chr7:79754567-79754617	AG04450	lung:	fetal
36	chr7:79754567-79754617	IMR90	lung:	fetal
37	chr7:79754567-79754617	RPTEC	kidney:	n/a
38	chr7:79754567-79754617	SK-N-SH	brain:	n/a
39	chr7:79754567-79754617	GM19239	blood:	n/a
40	chr7:79754567-79754617	MCF-7	breast:	n/a
41	chr7:79754567-79754617	HIPEpiC	eye:	n/a
42	chr7:79754567-79754617	HUVEC	blood vessel:	n/a
43	chr7:79754567-79754617	HL-60	blood:	n/a
44	chr7:79754567-79754617	HAEpiC	amniotic membrane:	n/a
45	chr7:79754567-79754617	HMEC	breast:	n/a
46	chr7:79754567-79754617	AG10803	skin:	n/a
47	chr7:79754567-79754617	HEK293	kidney:	embryo
48	chr7:79754567-79754617	Caco-2	colon:	n/a
49	chr7:79754567-79754617	SKMC	muscle:	n/a
50	chr7:79754567-79754617	A549	lung:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:79727798..79730628-chr7:79742506..79744646,2	K562	blood:
2	chr7:79749208..79750718-chr7:79754504..79757482,2	K562	blood:
3	chr7:79727798..79730628-chr7:79742506..79744646,2	K562	blood:
4	chr7:79724662..79725555-chr7:80021287..80022137,2	MCF-7	breast:
5	chr7:79749208..79750718-chr7:79754504..79757482,2	K562	blood:
6	chr7:79705123..79706774-chr7:79709823..79711327,2	K562	blood:
7	chr7:79724626..79725468-chr7:80021262..80022262,4	MCF-7	breast:
8	chr7:79705123..79706774-chr7:79709823..79711327,2	K562	blood:

No data

Variant related genes	Relation type
GNAI1	TF binding region
ENSG00000230853	TF binding region
GNAI1	CpG island
ENSG00000230853	CpG island

Extended variants
information (count: 2489 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2489 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544614324	chr7:79693982-79693983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564493533	chr7:79694000-79694001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527282305	chr7:79694030-79694031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527725573	chr7:79694055-79694056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567927864	chr7:79694072-79694073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530254501	chr7:79694103-79694104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550316796	chr7:79694104-79694105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570174479	chr7:79694107-79694108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148079303	chr7:79694117-79694118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62460689	chr7:79694136-79694137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs566117771	chr7:79694166-79694167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6945977	chr7:79694205-79694206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs188791128	chr7:79694222-79694223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569954289	chr7:79694247-79694248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573850413	chr7:79694250-79694251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542472224	chr7:79694251-79694252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555899409	chr7:79694258-79694259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368629413	chr7:79694282-79694283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58876952	chr7:79694291-79694292	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574515599	chr7:79694301-79694302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs55728156	chr7:79694322-79694323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199891826	chr7:79694339-79694340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375151821	chr7:79694340-79694341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553625636	chr7:79694347-79694348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540994745	chr7:79694351-79694352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373623756	chr7:79694402-79694403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561441549	chr7:79694425-79694426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140196577	chr7:79694444-79694445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550112622	chr7:79694449-79694450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570312824	chr7:79694455-79694456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529501398	chr7:79694507-79694508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12535738	chr7:79694516-79694517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs143796860	chr7:79694528-79694529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566154749	chr7:79694537-79694538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542496390	chr7:79694544-79694545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs193081323	chr7:79694561-79694562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563147842	chr7:79694566-79694567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548527440	chr7:79694582-79694583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567456510	chr7:79694598-79694599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536500048	chr7:79694618-79694619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146377326	chr7:79694620-79694621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10715897	chr7:79694630-79694631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs398085908	chr7:79694637-79694638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184241127	chr7:79694657-79694658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12530785	chr7:79694677-79694678	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs79802805	chr7:79694678-79694679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58762448	chr7:79694681-79694682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533567479	chr7:79694722-79694723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34798943	chr7:79694723-79694724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10486920	chr7:79694753-79694754	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:79)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79690200-79696400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:79695600-79695800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:79695800-79707400	Weak transcription	Psoas Muscle	Psoas
4	chr7:79696000-79696800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:79696600-79696800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:79696800-79707400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:79698400-79699600	Weak transcription	Small Intestine	intestine
8	chr7:79699200-79699800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:79699200-79700800	Enhancers	Adipose Nuclei	Adipose
10	chr7:79699400-79699600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:79699400-79699800	Enhancers	Ovary	ovary
12	chr7:79699600-79699800	Enhancers	Small Intestine	intestine
13	chr7:79699600-79700000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:79699600-79700000	Enhancers	HSMMtube	muscle
15	chr7:79699600-79700000	Enhancers	Osteobl	bone
16	chr7:79699600-79700800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:79699600-79701400	Enhancers	Fetal Lung	lung
18	chr7:79699800-79701000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:79699800-79704400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:79700000-79701200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:79700000-79704400	Weak transcription	Osteobl	bone
22	chr7:79700800-79707400	Weak transcription	Adipose Nuclei	Adipose
23	chr7:79701200-79707400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:79702000-79702400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:79702800-79703200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:79704400-79704800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:79704400-79704800	Enhancers	Osteobl	bone
28	chr7:79704600-79704800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:79704800-79705000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:79704800-79707400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr7:79704800-79707400	Weak transcription	Osteobl	bone
32	chr7:79705000-79707400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:79705800-79706000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr7:79705800-79706600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:79705800-79707200	Enhancers	Primary hematopoietic stem cells	blood
36	chr7:79705800-79707200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:79706000-79707400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr7:79706200-79706400	Enhancers	Fetal Brain Male	brain
39	chr7:79706200-79706400	Enhancers	Fetal Kidney	kidney
40	chr7:79706400-79707200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr7:79707000-79707200	Enhancers	Dnd41	blood
42	chr7:79707200-79707400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr7:79707200-79707400	Enhancers	Primary T cells from cord blood	blood
44	chr7:79707200-79707400	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr7:79707200-79707400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr7:79707200-79707400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:79707200-79707400	Enhancers	Ovary	ovary
48	chr7:79707200-79707400	Enhancers	Hela-S3	cervix
49	chr7:79707200-79707400	Enhancers	HUVEC	blood vessel
50	chr7:79707200-79707400	Active TSS	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links