Variant report

Variant	nsv1031761
Chromosome Location	chr7:70125949-70182744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1222)
CpG islands
(count:1100)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70163321-70163538	K562	blood:	n/a	n/a
2	ATF2	chr7:70164867-70165954	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70159737-70160179	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70164947-70166179	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:70133624-70133911	GM12878	blood:	n/a	n/a
6	ATF2	chr7:70161308-70161791	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:70163149-70163641	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:70158188-70158571	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr7:70181519-70181861	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:70145962-70146088	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:70171826-70171998	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr7:70144546-70144968	GM12878	blood:	n/a	n/a
13	BATF	chr7:70175177-70175456	GM12878	blood:	n/a	chr7:70175301-70175311 chr7:70175300-70175311
14	BATF	chr7:70146926-70147314	GM12878	blood:	n/a	n/a
15	BATF	chr7:70144538-70144907	GM12878	blood:	n/a	n/a
16	BATF	chr7:70175130-70175457	GM12878	blood:	n/a	chr7:70175301-70175311 chr7:70175300-70175311 chr7:70175171-70175180
17	BATF	chr7:70128632-70129069	GM12878	blood:	n/a	n/a
18	BATF	chr7:70128646-70129082	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:70165263-70165600	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr7:70128600-70129082	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:70128594-70129058	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:70165146-70165623	H1-hESC	embryonic stem cell:	n/a	n/a
23	BHLHE40	chr7:70146929-70147278	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:70175191-70175547	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:70133463-70133982	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:70158734-70159179	GM12878	blood:	n/a	chr7:70159147-70159163
27	BHLHE40	chr7:70163292-70163553	K562	blood:	n/a	n/a
28	BHLHE40	chr7:70163235-70163633	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:70128509-70129192	GM12878	blood:	n/a	chr7:70128654-70128675
30	BHLHE40	chr7:70160128-70160685	GM12878	blood:	n/a	chr7:70160375-70160391
31	BRCA1	chr7:70162537-70162717	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr7:70165059-70165724	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr7:70160153-70160203	GM12878	blood:	n/a	n/a
34	CEBPB	chr7:70157364-70157603	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:70158581-70158954	MCF-7	breast:	n/a	chr7:70158756-70158767
36	CEBPB	chr7:70175154-70175673	MCF-7	breast:	n/a	n/a
37	CEBPB	chr7:70158563-70158948	H1-hESC	embryonic stem cell:	n/a	chr7:70158756-70158767
38	CEBPB	chr7:70181533-70181881	MCF-7	breast:	n/a	chr7:70181727-70181738
39	CEBPB	chr7:70177945-70178267	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:70158624-70158869	HepG2	liver:	n/a	chr7:70158756-70158767
41	CEBPB	chr7:70181558-70181891	H1-hESC	embryonic stem cell:	n/a	chr7:70181727-70181738
42	CEBPB	chr7:70164569-70164835	A549	lung:	n/a	chr7:70164703-70164714 chr7:70164675-70164688 chr7:70164703-70164716 chr7:70164675-70164686
43	CEBPB	chr7:70142433-70142507	K562	blood:	n/a	n/a
44	CEBPB	chr7:70158582-70158901	A549	lung:	n/a	chr7:70158756-70158767
45	CEBPB	chr7:70158609-70158963	MCF-7	breast:	n/a	chr7:70158756-70158767
46	CEBPB	chr7:70178017-70178283	MCF-7	breast:	n/a	n/a
47	CEBPB	chr7:70158570-70158936	HepG2	liver:	n/a	chr7:70158756-70158767
48	CEBPB	chr7:70163360-70163560	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:70158502-70158961	IMR90	lung:	n/a	chr7:70158756-70158767
50	CEBPB	chr7:70158492-70159079	A549	lung:	n/a	chr7:70158756-70158767

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70139561-70139611	HUVEC	blood vessel:	n/a
2	chr7:70157145-70157195	LNCaP	prostate:	n/a
3	chr7:70139561-70139611	HUVEC	blood vessel:	n/a
4	chr7:70157145-70157195	LNCaP	prostate:	n/a
5	chr7:70157145-70157195	NHDF-neo	bronchial:	n/a
6	chr7:70165515-70165565	BE2_C	brain:	n/a
7	chr7:70139561-70139611	HRE	kidney:	n/a
8	chr7:70158761-70158811	A549	lung:	n/a
9	chr7:70126616-70126666	PANC-1	pancreas:	n/a
10	chr7:70160498-70160548	GM12892	blood:	n/a
11	chr7:70139561-70139611	AG10803	skin:	n/a
12	chr7:70160498-70160548	GM19239	blood:	n/a
13	chr7:70156755-70156805	NT2-D1	testis:	n/a
14	chr7:70160498-70160548	AG04450	lung:	fetal
15	chr7:70157145-70157195	ovcar-3	ovarian:	n/a
16	chr7:70172515-70172565	K562	blood:	n/a
17	chr7:70159330-70159380	Hela-S3	cervix:	n/a
18	chr7:70160734-70160784	SKMC	muscle:	n/a
19	chr7:70159330-70159380	NHBE	bronchial:	n/a
20	chr7:70146354-70146404	NH-A	brain:	n/a
21	chr7:70163455-70163505	AG09319	gingival:	n/a
22	chr7:70159215-70159265	GM12878	blood:	n/a
23	chr7:70160498-70160548	ECC-1	luminal epithelium:	n/a
24	chr7:70163455-70163505	Hela-S3	cervix:	n/a
25	chr7:70132171-70132221	HMEC	breast:	n/a
26	chr7:70165515-70165565	HepG2	liver:	n/a
27	chr7:70159215-70159265	HEK293	kidney:	embryo
28	chr7:70170620-70170670	HCF	heart:	n/a
29	chr7:70159340-70159390	HCF	heart:	n/a
30	chr7:70175567-70175617	AG09319	gingival:	n/a
31	chr7:70159215-70159265	SK-N-SH	brain:	n/a
32	chr7:70132171-70132221	AoSMC	blood vessel:	n/a
33	chr7:70146354-70146404	PFSK-1	brain:	n/a
34	chr7:70159330-70159380	IMR90	lung:	fetal
35	chr7:70160498-70160548	AG09319	gingival:	n/a
36	chr7:70159215-70159265	AG09319	gingival:	n/a
37	chr7:70165515-70165565	Jurkat	blood:	n/a
38	chr7:70160006-70160056	IMR90	lung:	fetal
39	chr7:70159330-70159380	U87	brain:	n/a
40	chr7:70163455-70163505	U87	brain:	n/a
41	chr7:70165515-70165565	GM19239	blood:	n/a
42	chr7:70156755-70156805	NB4	blood:	n/a
43	chr7:70139561-70139611	HCM	heart:	n/a
44	chr7:70146354-70146404	AG04450	lung:	fetal
45	chr7:70156755-70156805	HRCEpiC	kidney:	n/a
46	chr7:70159340-70159390	HUVEC	blood vessel:	n/a
47	chr7:70126616-70126666	SK-N-SH	brain:	n/a
48	chr7:70157145-70157195	GM06990	blood:	n/a
49	chr7:70159330-70159380	ECC-1	luminal epithelium:	n/a
50	chr7:70160734-70160784	AG04449	skin:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70174321..70176691-chr7:70186792..70188789,2	MCF-7	breast:
2	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:
3	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:
4	chr7:70133847..70137058-chr7:70140413..70143195,3	K562	blood:
5	chr7:70182197..70184832-chr7:70191535..70193515,2	MCF-7	breast:
6	chr7:70175580..70177405-chr7:70179545..70181681,2	MCF-7	breast:
7	chr7:70049785..70050737-chr7:70162923..70163511,2	MCF-7	breast:
8	chr7:70175580..70177405-chr7:70179545..70181681,2	MCF-7	breast:
9	chr7:70133847..70137058-chr7:70140413..70143195,3	K562	blood:
10	chr7:69507259..69508393-chr7:70162935..70163782,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WBSCR17-3	chr7:70163555-70164476	NONHSAT121336
2	lnc-WBSCR17-3	chr7:70159859-70160031	NONHSAT121336

No data

Variant related genes	Relation type
AUTS2	TF binding region
AUTS2	CpG island

Extended variants
information (count: 2141 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2141 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566173079	chr7:70125963-70125964	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs190909797	chr7:70125966-70125967	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs141951916	chr7:70126028-70126029	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs576390145	chr7:70126046-70126047	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs543732136	chr7:70126094-70126095	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs4718978	chr7:70126146-70126147	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs746807	chr7:70126193-70126194	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369328312	chr7:70126196-70126197	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs541205789	chr7:70126230-70126231	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559566604	chr7:70126233-70126234	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs736477	chr7:70126273-70126274	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542709738	chr7:70126357-70126358	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146030827	chr7:70126392-70126393	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139949425	chr7:70126394-70126395	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs62456809	chr7:70126440-70126441	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs73178275	chr7:70126471-70126472	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546873030	chr7:70126597-70126598	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532494448	chr7:70126632-70126633	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547602728	chr7:70126649-70126650	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182743337	chr7:70126652-70126653	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536304907	chr7:70126655-70126656	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143401757	chr7:70126663-70126664	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566592270	chr7:70126664-70126665	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150779687	chr7:70126677-70126678	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs13223886	chr7:70126687-70126688	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558710981	chr7:70126695-70126696	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577118281	chr7:70126722-70126723	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs735429	chr7:70126767-70126768	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs574963038	chr7:70126772-70126773	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574713631	chr7:70126783-70126784	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549348134	chr7:70126785-70126786	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561022546	chr7:70126824-70126825	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537460580	chr7:70126835-70126836	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557502900	chr7:70126838-70126839	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567281322	chr7:70126841-70126842	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139140459	chr7:70126855-70126856	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530651596	chr7:70126864-70126865	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543400624	chr7:70126935-70126936	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77642237	chr7:70126940-70126941	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577543506	chr7:70126995-70126996	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs118015584	chr7:70127030-70127031	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532403903	chr7:70127031-70127032	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554436028	chr7:70127032-70127033	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574288927	chr7:70127055-70127056	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185839574	chr7:70127077-70127078	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144946073	chr7:70127078-70127079	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528470078	chr7:70127083-70127084	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529917993	chr7:70127088-70127089	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190167339	chr7:70127107-70127108	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562986263	chr7:70127122-70127123	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	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
T-cell prolymphocytic leukemia	17713554	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70101000-70158200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:70103400-70133600	Weak transcription	Fetal Intestine Small	intestine
3	chr7:70107000-70143800	Weak transcription	Primary B cells from cord blood	blood
4	chr7:70107400-70126200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:70109600-70127000	Weak transcription	Esophagus	oesophagus
6	chr7:70109600-70132600	Weak transcription	Liver	Liver
7	chr7:70110800-70128800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:70111600-70126200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:70111800-70126200	Weak transcription	Brain Hippocampus Middle	brain
10	chr7:70112800-70146000	Weak transcription	Spleen	Spleen
11	chr7:70114000-70128000	Weak transcription	Dnd41	blood
12	chr7:70115200-70126800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr7:70120200-70127400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr7:70120600-70126800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:70120600-70127000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr7:70120600-70133200	Weak transcription	Aorta	Aorta
17	chr7:70120600-70141600	Weak transcription	Brain Anterior Caudate	brain
18	chr7:70120800-70138800	Weak transcription	Right Atrium	heart
19	chr7:70121600-70126200	Enhancers	Fetal Thymus	thymus
20	chr7:70121600-70133200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr7:70121800-70127400	Weak transcription	Fetal Lung	lung
22	chr7:70122800-70127000	Enhancers	Primary T cells fromperipheralblood	blood
23	chr7:70123000-70127000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr7:70123000-70138800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr7:70123200-70133600	Weak transcription	Adipose Nuclei	Adipose
26	chr7:70123400-70131600	Weak transcription	Left Ventricle	heart
27	chr7:70123400-70135000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:70123600-70130600	Weak transcription	Fetal Heart	heart
29	chr7:70123800-70127200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr7:70123800-70146800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:70124000-70126200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr7:70124000-70126400	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr7:70124000-70127200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:70124200-70127000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:70124400-70126400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr7:70124400-70126600	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr7:70124600-70129600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:70124600-70134800	Weak transcription	Thymus	Thymus
39	chr7:70125000-70127000	Weak transcription	Fetal Muscle Leg	muscle
40	chr7:70125400-70126000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr7:70125400-70126200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:70125400-70126200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:70125400-70126400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:70125400-70126400	Strong transcription	Fetal Muscle Trunk	muscle
45	chr7:70125400-70127200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:70125400-70127200	Strong transcription	Fetal Stomach	stomach
47	chr7:70125400-70128000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr7:70125400-70128000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr7:70125600-70126000	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr7:70125600-70126000	Enhancers	Rectal Mucosa Donor 31	rectum

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