Variant report

Variant	nsv967348
Chromosome Location	chr7:99930883-99932817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:99931789-99932008	GM12878	blood:	n/a	n/a
2	BATF	chr7:99932699-99932942	GM12878	blood:	n/a	n/a
3	BATF	chr7:99931763-99932072	GM12878	blood:	n/a	n/a
4	BATF	chr7:99931291-99931464	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:99931278-99931549	GM12878	blood:	n/a	chr7:99931369-99931378
6	BCL11A	chr7:99931290-99931519	GM12878	blood:	n/a	chr7:99931369-99931378
7	BCL11A	chr7:99931741-99932177	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:99931855-99932416	GM12878	blood:	n/a	n/a
9	CHD1	chr7:99932051-99932082	GM12878	blood:	n/a	n/a
10	EBF1	chr7:99931284-99931455	GM12878	blood:	n/a	n/a
11	EBF1	chr7:99931769-99932106	GM12878	blood:	n/a	n/a
12	FOSL2	chr7:99931781-99932039	HepG2	liver:	n/a	n/a
13	FOXM1	chr7:99932675-99934097	GM12878	blood:	n/a	n/a
14	FOXM1	chr7:99932696-99933030	GM12878	blood:	n/a	n/a
15	HEY1	chr7:99932481-99933029	K562	blood:	n/a	n/a
16	HEY1	chr7:99932593-99933011	HepG2	liver:	n/a	n/a
17	HEY1	chr7:99931658-99932472	K562	blood:	n/a	n/a
18	IRF4	chr7:99931616-99932382	GM12878	blood:	n/a	n/a
19	IRF4	chr7:99931731-99932412	GM12878	blood:	n/a	n/a
20	IRF4	chr7:99931254-99931571	GM12878	blood:	n/a	n/a
21	IRF4	chr7:99932709-99933032	GM12878	blood:	n/a	n/a
22	MEF2A	chr7:99932736-99933067	GM12878	blood:	n/a	n/a
23	MXI1	chr7:99932702-99934290	SK-N-SH	brain:	n/a	n/a
24	NFIC	chr7:99931949-99932487	GM12878	blood:	n/a	n/a
25	NR2F2	chr7:99932533-99934558	K562	blood:	n/a	chr7:99933729-99933744
26	PAX5	chr7:99931805-99932122	GM12878	blood:	n/a	n/a
27	PAX5	chr7:99931612-99932414	GM12878	blood:	n/a	n/a
28	PAX5	chr7:99931255-99931537	GM12878	blood:	n/a	n/a
29	PAX5	chr7:99932104-99932291	GM12878	blood:	n/a	n/a
30	PAX5	chr7:99931738-99932078	GM12878	blood:	n/a	n/a
31	PBX3	chr7:99931788-99931948	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:99931792-99932055	GM12878	blood:	n/a	n/a
33	POLR2A	chr7:99932561-99934363	GM12892	blood:	n/a	n/a
34	POLR2A	chr7:99931258-99932461	GM12878	blood:	n/a	n/a
35	POLR2A	chr7:99932609-99933047	GM12891	blood:	n/a	n/a
36	POLR2A	chr7:99932017-99932366	GM12891	blood:	n/a	n/a
37	POLR2A	chr7:99931693-99932105	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr7:99931597-99934357	GM12892	blood:	n/a	n/a
39	POLR2A	chr7:99932497-99933042	GM12878	blood:	n/a	n/a
40	POLR2A	chr7:99931612-99934454	GM12891	blood:	n/a	n/a
41	POLR2A	chr7:99932430-99932908	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr7:99930333-99934470	GM12878	blood:	n/a	n/a
43	POLR2A	chr7:99930720-99931068	GM12878	blood:	n/a	n/a
44	POLR2A	chr7:99931798-99932010	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr7:99931662-99932463	GM12891	blood:	n/a	n/a
46	POLR2A	chr7:99931649-99932385	GM12892	blood:	n/a	n/a
47	POLR2A	chr7:99932510-99933060	GM12891	blood:	n/a	n/a
48	POLR2A	chr7:99932816-99933052	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr7:99931748-99932081	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr7:99931792-99932068	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99932089-99932139	BE2_C	brain:	n/a
2	chr7:99932089-99932139	AG04450	lung:	fetal
3	chr7:99932089-99932139	SK-N-MC	brain:	n/a
4	chr7:99932089-99932139	RPTEC	kidney:	n/a
5	chr7:99932089-99932139	SAEC	small airway:	n/a
6	chr7:99932089-99932139	AoSMC	blood vessel:	n/a
7	chr7:99932089-99932139	PrEC	prostate:	n/a
8	chr7:99932089-99932139	H1-hESC	embryonic stem cell:	embryo
9	chr7:99932089-99932139	HEEpiC	esophagus:	n/a
10	chr7:99932089-99932139	LNCaP	prostate:	n/a
11	chr7:99932089-99932139	HRE	kidney:	n/a
12	chr7:99932089-99932139	AG04449	skin:	fetal
13	chr7:99932089-99932139	NHBE	bronchial:	n/a
14	chr7:99932089-99932139	GM06990	blood:	n/a
15	chr7:99932089-99932139	HRPEpiC	eye:	n/a
16	chr7:99932089-99932139	HAEpiC	amniotic membrane:	n/a
17	chr7:99932089-99932139	ECC-1	luminal epithelium:	n/a
18	chr7:99932089-99932139	GM19239	blood:	n/a
19	chr7:99932089-99932139	IMR90	lung:	fetal
20	chr7:99932089-99932139	HCF	heart:	n/a
21	chr7:99932089-99932139	K562	blood:	n/a
22	chr7:99932089-99932139	A549	lung:	n/a
23	chr7:99932089-99932139	ProgFib	skin:	n/a
24	chr7:99932089-99932139	NT2-D1	testis:	n/a
25	chr7:99932089-99932139	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:99932089-99932139	HEK293	kidney:	embryo
27	chr7:99932089-99932139	GM12892	blood:	n/a
28	chr7:99932089-99932139	NB4	blood:	n/a
29	chr7:99932089-99932139	Caco-2	colon:	n/a
30	chr7:99932089-99932139	HRCEpiC	kidney:	n/a
31	chr7:99932089-99932139	ovcar-3	ovarian:	n/a
32	chr7:99932089-99932139	HL-60	blood:	n/a
33	chr7:99932089-99932139	MCF-7	breast:	n/a
34	chr7:99932089-99932139	AG10803	skin:	n/a
35	chr7:99932089-99932139	AG09319	gingival:	n/a
36	chr7:99932089-99932139	HCPEpiC	choroid plexus:	n/a
37	chr7:99932089-99932139	HIPEpiC	eye:	n/a
38	chr7:99932089-99932139	SKMC	muscle:	n/a
39	chr7:99932089-99932139	AG09309	skin:	n/a
40	chr7:99932089-99932139	PFSK-1	brain:	n/a
41	chr7:99932089-99932139	SK-N-SH	brain:	n/a
42	chr7:99932089-99932139	HNPCEpiC	eye:	n/a
43	chr7:99932089-99932139	MCF10A-Er-Src	breast:	n/a
44	chr7:99932089-99932139	Jurkat	blood:	n/a
45	chr7:99932089-99932139	U87	brain:	n/a
46	chr7:99932089-99932139	NH-A	brain:	n/a
47	chr7:99932089-99932139	BJ	skin:	n/a
48	chr7:99932089-99932139	GM12878	blood:	n/a
49	chr7:99932089-99932139	Hela-S3	cervix:	n/a
50	chr7:99932089-99932139	HCM	heart:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99932318..99935048-chr7:100026420..100028378,2	MCF-7	breast:
2	chr7:99931911..99935442-chr7:99938364..99941933,5	MCF-7	breast:
3	chr7:99932234..99937909-chr7:99939373..99942446,6	K562	blood:
4	chr7:99932595..99935080-chr7:100025979..100028387,3	K562	blood:
5	chr7:99932349..99935076-chr7:100025979..100028387,3	K562	blood:
6	chr7:99715815..99718290-chr7:99932504..99934640,2	MCF-7	breast:

No data

Variant related genes	Relation type
PMS2P1	TF binding region
ENSG00000201913	TF binding region
STAG3L5P	TF binding region
PILRB	TF binding region
STAG3L5P-PVRIG2P-PILRB	TF binding region
PMS2P1	CpG island
ENSG00000201913	CpG island
STAG3L5P	CpG island
PILRB	CpG island
STAG3L5P-PVRIG2P-PILRB	CpG island
ENSG00000166997	chromatin interactions
ENSG00000078319	chromatin interactions
ENSG00000106290	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000078487	chromatin interactions

Extended variants
information (count: 70 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146325724	chr7:99930912-99930913	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
2	rs544034126	chr7:99930933-99930934	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
3	rs6955329	chr7:99930974-99930975	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
4	rs6955335	chr7:99930981-99930982	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
5	rs200992503	chr7:99931025-99931026	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
6	rs7788930	chr7:99931044-99931045	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	mRNA abundance
7	rs535509404	chr7:99931045-99931046	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
8	rs577501507	chr7:99931051-99931052	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
9	rs75308375	chr7:99931057-99931058	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
10	rs77993628	chr7:99931058-99931059	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
11	rs576006776	chr7:99931062-99931063	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
12	rs543100490	chr7:99931063-99931064	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
13	rs541688170	chr7:99931086-99931087	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
14	rs559533611	chr7:99931098-99931099	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
15	rs530095011	chr7:99931175-99931176	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
16	rs541779324	chr7:99931189-99931190	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
17	rs563442732	chr7:99931210-99931211	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
18	rs530881604	chr7:99931249-99931250	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
19	rs549583580	chr7:99931269-99931270	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
20	rs571407291	chr7:99931282-99931283	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
21	rs532334705	chr7:99931311-99931312	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
22	rs547668406	chr7:99931317-99931318	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
23	rs113172473	chr7:99931324-99931325	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
24	rs111561533	chr7:99931366-99931367	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
25	rs536255027	chr7:99931459-99931460	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
26	rs199986637	chr7:99931463-99931464	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
27	rs150704750	chr7:99931544-99931545	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
28	rs373670241	chr7:99931556-99931557	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
29	rs375462076	chr7:99931594-99931595	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
30	rs537128212	chr7:99931619-99931620	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
31	rs111261434	chr7:99931627-99931628	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
32	rs559222896	chr7:99931637-99931638	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
33	rs541272192	chr7:99931660-99931661	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
34	rs370100267	chr7:99931737-99931738	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
35	rs147144608	chr7:99931753-99931754	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
36	rs370992343	chr7:99931763-99931764	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
37	rs112294400	chr7:99931772-99931773	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
38	rs535046574	chr7:99931890-99931891	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
39	rs553637060	chr7:99931908-99931909	Weak transcription Enhancers	TF binding region	5 gene(s)	Overlapped CNVs	n/a
40	rs574984418	chr7:99931912-99931913	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs140268702	chr7:99931958-99931959	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs539051533	chr7:99931993-99931994	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs563305526	chr7:99932032-99932033	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs575370217	chr7:99932041-99932042	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs7384878	chr7:99932049-99932050	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs118055848	chr7:99932053-99932054	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs370137622	chr7:99932064-99932065	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs532326767	chr7:99932069-99932070	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs547235901	chr7:99932089-99932090	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs559603139	chr7:99932110-99932111	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99870200-99932800	Weak transcription	Ovary	ovary
2	chr7:99870400-99932600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:99870600-99932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:99874400-99932800	Weak transcription	Brain Angular Gyrus	brain
5	chr7:99887400-99932800	Weak transcription	Brain Anterior Caudate	brain
6	chr7:99896600-99931800	Weak transcription	K562	blood
7	chr7:99897600-99933200	Weak transcription	Pancreas	Pancrea
8	chr7:99898000-99932800	Weak transcription	Brain Substantia Nigra	brain
9	chr7:99902800-99932800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr7:99911800-99932200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:99912600-99933400	Weak transcription	Fetal Brain Male	brain
12	chr7:99914000-99932800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:99914600-99932800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr7:99914600-99932800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr7:99915000-99932800	Weak transcription	Brain Hippocampus Middle	brain
16	chr7:99915200-99932800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr7:99915400-99932000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr7:99915400-99932600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:99915400-99932600	Weak transcription	Primary T cells from cord blood	blood
20	chr7:99915400-99932600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:99915600-99932800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr7:99915600-99932800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr7:99915600-99933200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:99915600-99933200	Weak transcription	Aorta	Aorta
25	chr7:99915800-99931600	Weak transcription	Primary B cells from cord blood	blood
26	chr7:99915800-99932000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr7:99915800-99932800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr7:99915800-99932800	Weak transcription	Rectal Smooth Muscle	rectum
29	chr7:99915800-99933000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr7:99915800-99933200	Weak transcription	Left Ventricle	heart
31	chr7:99916000-99932000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr7:99916000-99932800	Weak transcription	Fetal Kidney	kidney
33	chr7:99916200-99931800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr7:99916200-99932000	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr7:99916200-99932800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:99916400-99932800	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr7:99916600-99932800	Weak transcription	Right Ventricle	heart
38	chr7:99916600-99932800	Weak transcription	HSMM	muscle
39	chr7:99916800-99932800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr7:99916800-99932800	Weak transcription	Esophagus	oesophagus
41	chr7:99917000-99932800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr7:99917400-99932800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:99918400-99931600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr7:99918600-99931600	Weak transcription	Primary B cells from peripheral blood	blood
45	chr7:99918600-99931800	Weak transcription	Dnd41	blood
46	chr7:99918600-99932800	Weak transcription	Brain Cingulate Gyrus	brain
47	chr7:99918600-99932800	Weak transcription	Fetal Brain Female	brain
48	chr7:99918600-99933200	Weak transcription	Lung	lung
49	chr7:99920600-99932800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:99920800-99932800	Weak transcription	HSMMtube	muscle

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