Variant report

Variant	nsv428175
Chromosome Location	chr7:79096786-79253373
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	ARID3A	chr7:79135879-79136195	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:79136530-79136804	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:79237396-79237695	HepG2	liver:	n/a	n/a
4	ATF1	chr7:79168827-79168925	K562	blood:	n/a	n/a
5	ATF1	chr7:79155465-79155511	K562	blood:	n/a	n/a
6	ATF3	chr7:79136418-79136929	A549	lung:	n/a	n/a
7	BCL3	chr7:79135674-79136308	A549	lung:	n/a	n/a
8	BCL3	chr7:79136354-79136969	A549	lung:	n/a	n/a
9	BCL3	chr7:79135704-79136201	A549	lung:	n/a	n/a
10	BCL3	chr7:79136419-79136964	A549	lung:	n/a	n/a
11	BHLHE40	chr7:79154489-79154768	HepG2	liver:	n/a	n/a
12	CCNT2	chr7:79229521-79229760	K562	blood:	n/a	n/a
13	CCNT2	chr7:79109715-79109825	K562	blood:	n/a	n/a
14	CEBPB	chr7:79220570-79220924	HepG2	liver:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
15	CEBPB	chr7:79220629-79220866	H1-hESC	embryonic stem cell:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
16	CEBPB	chr7:79183216-79183696	A549	lung:	n/a	n/a
17	CEBPB	chr7:79176528-79176817	K562	blood:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
18	CEBPB	chr7:79176480-79176829	IMR90	lung:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
19	CEBPB	chr7:79152819-79153052	Hela-S3	cervix:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
20	CEBPB	chr7:79154408-79154729	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:79159144-79159624	IMR90	lung:	n/a	chr7:79159560-79159573
22	CEBPB	chr7:79220583-79220924	K562	blood:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
23	CEBPB	chr7:79142882-79143017	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:79136335-79136839	A549	lung:	n/a	n/a
25	CEBPB	chr7:79152801-79153095	IMR90	lung:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
26	CEBPB	chr7:79177985-79178595	HepG2	liver:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
27	CEBPB	chr7:79177974-79178565	IMR90	lung:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
28	CEBPB	chr7:79176617-79176808	H1-hESC	embryonic stem cell:	n/a	chr7:79176648-79176659
29	CEBPB	chr7:79220593-79220881	A549	lung:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
30	CEBPB	chr7:79220585-79220896	ECC-1	luminal epithelium:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
31	CEBPB	chr7:79220574-79220912	Hela-S3	cervix:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
32	CEBPB	chr7:79124997-79125653	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:79228897-79229115	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:79152796-79153050	A549	lung:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
35	CEBPB	chr7:79161261-79161581	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:79178069-79178269	H1-hESC	embryonic stem cell:	n/a	chr7:79178142-79178153
37	CEBPB	chr7:79209272-79209522	HepG2	liver:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
38	CEBPB	chr7:79176485-79176822	A549	lung:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
39	CEBPB	chr7:79176477-79176825	HepG2	liver:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
40	CEBPB	chr7:79201511-79201650	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:79183187-79183544	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:79135698-79136302	A549	lung:	n/a	n/a
43	CEBPB	chr7:79209289-79209502	IMR90	lung:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
44	CEBPB	chr7:79183179-79183803	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:79238337-79238638	IMR90	lung:	n/a	chr7:79238501-79238512 chr7:79238503-79238512 chr7:79238502-79238513 chr7:79238501-79238514
46	CEBPB	chr7:79168045-79168264	A549	lung:	n/a	chr7:79168183-79168196 chr7:79168183-79168194 chr7:79168183-79168196
47	CEBPB	chr7:79152850-79153090	HepG2	liver:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
48	CEBPB	chr7:79209298-79209544	A549	lung:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
49	CEBPB	chr7:79177973-79178548	A549	lung:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
50	CEBPB	chr7:79154457-79154741	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:79166927-79166977	SAEC	small airway:	n/a
2	chr7:79134707-79134757	Hela-S3	cervix:	n/a
3	chr7:79166927-79166977	CMK	blood:	n/a
4	chr7:79166927-79166977	NT2-D1	testis:	n/a
5	chr7:79134707-79134757	HUVEC	blood vessel:	n/a
6	chr7:79166927-79166977	K562	blood:	n/a
7	chr7:79134707-79134757	BJ	skin:	n/a
8	chr7:79166927-79166977	T-47D	breast:	n/a
9	chr7:79166927-79166977	Hepatocyte	liver:	n/a
10	chr7:79134707-79134757	BE2_C	brain:	n/a
11	chr7:79134707-79134757	IMR90	lung:	fetal
12	chr7:79166927-79166977	U87	brain:	n/a
13	chr7:79134707-79134757	RPTEC	kidney:	n/a
14	chr7:79134707-79134757	GM12892	blood:	n/a
15	chr7:79166927-79166977	GM06990	blood:	n/a
16	chr7:79166927-79166977	HIPEpiC	eye:	n/a
17	chr7:79134707-79134757	LNCaP	prostate:	n/a
18	chr7:79166927-79166977	Jurkat	blood:	n/a
19	chr7:79134707-79134757	SK-N-SH_RA	brain:	n/a
20	chr7:79134707-79134757	MCF10A-Er-Src	breast:	n/a
21	chr7:79166927-79166977	HRE	kidney:	n/a
22	chr7:79166927-79166977	MCF10A-Er-Src	breast:	n/a
23	chr7:79166927-79166977	NB4	blood:	n/a
24	chr7:79134707-79134757	HMEC	breast:	n/a
25	chr7:79134707-79134757	MCF-7	breast:	n/a
26	chr7:79134707-79134757	HAEpiC	amniotic membrane:	n/a
27	chr7:79166927-79166977	GM12892	blood:	n/a
28	chr7:79166927-79166977	ProgFib	skin:	n/a
29	chr7:79166927-79166977	HMEC	breast:	n/a
30	chr7:79134707-79134757	Hepatocyte	liver:	n/a
31	chr7:79134707-79134757	SKMC	muscle:	n/a
32	chr7:79166927-79166977	ovcar-3	ovarian:	n/a
33	chr7:79134707-79134757	GM12891	blood:	n/a
34	chr7:79134707-79134757	AoSMC	blood vessel:	n/a
35	chr7:79166927-79166977	GM12878	blood:	n/a
36	chr7:79134707-79134757	Caco-2	colon:	n/a
37	chr7:79166927-79166977	NHBE	bronchial:	n/a
38	chr7:79134707-79134757	K562	blood:	n/a
39	chr7:79166927-79166977	HCF	heart:	n/a
40	chr7:79134707-79134757	AG04449	skin:	fetal
41	chr7:79166927-79166977	AG09309	skin:	n/a
42	chr7:79134707-79134757	PrEC	prostate:	n/a
43	chr7:79134707-79134757	ProgFib	skin:	n/a
44	chr7:79134707-79134757	HL-60	blood:	n/a
45	chr7:79166927-79166977	HUVEC	blood vessel:	n/a
46	chr7:79134707-79134757	AG04450	lung:	fetal
47	chr7:79134707-79134757	HRE	kidney:	n/a
48	chr7:79134707-79134757	GM12878	blood:	n/a
49	chr7:79166927-79166977	AG09319	gingival:	n/a
50	chr7:79134707-79134757	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:75245963..75246703-chr7:79210691..79211521,2	MCF-7	breast:
2	chr7:79245565..79248038-chr7:79255445..79257541,2	K562	blood:
3	chr7:79095989..79098582-chr7:79174957..79177392,2	K562	blood:
4	chr7:79095989..79098582-chr7:79174957..79177392,2	K562	blood:
5	chr7:79248162..79250464-chr7:79251117..79253224,2	MCF-7	breast:
6	chr7:79171467..79174385-chr7:79176496..79179081,2	K562	blood:
7	chr7:79248162..79250464-chr7:79251117..79253224,2	MCF-7	breast:
8	chr5:150846511..150848831-chr7:79188913..79190608,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-2	chr7:79100099-79100431	NONHSAT121719
2	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121719
3	lnc-GNAI1-2	chr7:79099907-79099997	NONHSAT121718
4	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121725
5	lnc-GNAI1-2	chr7:79098343-79098762	NONHSAT121725
6	lnc-GNAI1-2	chr7:79100099-79100452	NONHSAT121725
7	lnc-GNAI1-2	chr7:79099743-79099995	ENSG00000234456.2
8	lnc-MAGI2-2	chr7:79173227-79174169	NONHSAT121727
9	lnc-GNAI1-2	chr7:79099910-79099995	ENSG00000234456.2
10	lnc-GNAI1-2	chr7:79100099-79100516	ENSG00000234456.2
11	lnc-GNAI1-2	chr7:79088852-79096786	ENSG00000234456.3
12	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121723
13	lnc-GNAI1-2	chr7:79100099-79100185	NONHSAT121703
14	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121717
15	lnc-GNAI1-2	chr7:79100099-79100170	NONHSAT121723
16	lnc-GNAI1-2	chr7:79100099-79100515	NONHSAT121718
17	lnc-GNAI1-2	chr7:79100099-79100512	ENSG00000234456.2
18	lnc-GNAI1-2	chr7:79100099-79100447	NONHSAT121717
19	lnc-GNAI1-2	chr7:79100099-79100524	ENSG00000234456.2

Variant related genes	Relation type
MAGI2-AS3	TF binding region
ENSG00000226285	TF binding region
MAGI2-AS3	CpG island
ENSG00000226285	CpG island
ENSG00000226285	chromatin interactions

Extended variants
information (count: 3997 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3997 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559417899	chr7:79096813-79096814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554430260	chr7:79096847-79096848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141909402	chr7:79096849-79096850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373480621	chr7:79096923-79096924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564535258	chr7:79096944-79096945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17489727	chr7:79096991-79096992	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs186711319	chr7:79096994-79096995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559433717	chr7:79097014-79097015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528376181	chr7:79097024-79097025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547912635	chr7:79097053-79097054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567697125	chr7:79097064-79097065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369080761	chr7:79097087-79097088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150644715	chr7:79097176-79097177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369945809	chr7:79097192-79097193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530938926	chr7:79097254-79097255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76173745	chr7:79097267-79097268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78841393	chr7:79097268-79097269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139668262	chr7:79097272-79097273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374002299	chr7:79097278-79097279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539650715	chr7:79097294-79097295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143084070	chr7:79097336-79097337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553531278	chr7:79097459-79097460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10238639	chr7:79097463-79097464	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs10252126	chr7:79097483-79097484	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs191565712	chr7:79097522-79097523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575722598	chr7:79097551-79097552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544573360	chr7:79097567-79097568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558286673	chr7:79097568-79097569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374246377	chr7:79097607-79097608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150370861	chr7:79097608-79097609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143600959	chr7:79097628-79097629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375073862	chr7:79097635-79097636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545718923	chr7:79097691-79097692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35905395	chr7:79097774-79097775	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566102741	chr7:79097777-79097778	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs559481790	chr7:79097835-79097836	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs377075133	chr7:79097843-79097844	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs528404644	chr7:79097853-79097854	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542129737	chr7:79097871-79097872	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561615487	chr7:79097914-79097915	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371003057	chr7:79098076-79098077	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs374313954	chr7:79098083-79098084	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs530433950	chr7:79098092-79098093	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs368197291	chr7:79098098-79098099	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs182539694	chr7:79098105-79098106	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs146875340	chr7:79098109-79098110	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563887138	chr7:79098148-79098149	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs533039322	chr7:79098149-79098150	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs117437100	chr7:79098173-79098174	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371693419	chr7:79098183-79098184	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Cancer	20164920	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79084400-79102200	Weak transcription	Left Ventricle	heart
2	chr7:79084600-79101000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:79084800-79100800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr7:79084800-79102800	Weak transcription	HSMM	muscle
5	chr7:79085000-79098600	Weak transcription	Fetal Muscle Leg	muscle
6	chr7:79085000-79099600	Weak transcription	Fetal Stomach	stomach
7	chr7:79085800-79098000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:79086000-79099800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr7:79086600-79099600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:79086600-79100600	Weak transcription	Brain Anterior Caudate	brain
11	chr7:79086600-79101000	Weak transcription	Brain Angular Gyrus	brain
12	chr7:79086600-79101400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:79086600-79104200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr7:79087600-79099800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:79087800-79099800	Weak transcription	Fetal Lung	lung
16	chr7:79088000-79109600	Weak transcription	Aorta	Aorta
17	chr7:79089000-79098800	Weak transcription	Fetal Muscle Trunk	muscle
18	chr7:79089000-79102800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr7:79089200-79098000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:79089200-79100200	Weak transcription	Adipose Nuclei	Adipose
21	chr7:79089200-79109600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:79089400-79101800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:79089800-79099000	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr7:79089800-79101800	Weak transcription	Liver	Liver
25	chr7:79090000-79101000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr7:79090200-79098600	Weak transcription	NHDF-Ad	bronchial
27	chr7:79091800-79101200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:79092000-79101800	Weak transcription	HUVEC	blood vessel
29	chr7:79092000-79103000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr7:79092200-79097800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:79092200-79097800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:79092200-79102200	Weak transcription	Ovary	ovary
33	chr7:79093800-79098000	Weak transcription	Brain Hippocampus Middle	brain
34	chr7:79094200-79097800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:79094200-79099800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:79094200-79099800	Weak transcription	Brain Substantia Nigra	brain
37	chr7:79094400-79099800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:79094600-79096800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:79094800-79097800	Weak transcription	NHLF	lung
40	chr7:79095200-79097400	Weak transcription	Osteobl	bone
41	chr7:79096800-79101200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:79097400-79100400	Strong transcription	Osteobl	bone
43	chr7:79097800-79098000	Enhancers	Brain Cingulate Gyrus	brain
44	chr7:79097800-79098400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr7:79097800-79098400	Strong transcription	NHLF	lung
46	chr7:79097800-79098600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:79097800-79100800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:79098000-79098200	Enhancers	Spleen	Spleen
49	chr7:79098000-79098400	Enhancers	Brain Hippocampus Middle	brain
50	chr7:79098000-79098600	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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