Variant report

Variant	nsv538930
Chromosome Location	chr7:70016323-70190353
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2298)
CpG islands
(count:2385)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2298 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

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	ARID3A	chr7:70033765-70034826	K562	blood:	n/a	n/a
3	ARID3A	chr7:70102162-70102182	K562	blood:	n/a	n/a
4	ARID3A	chr7:70036382-70036767	HepG2	liver:	n/a	n/a
5	ATF1	chr7:70033782-70034115	K562	blood:	n/a	n/a
6	ATF1	chr7:70034407-70035107	K562	blood:	n/a	n/a
7	ATF1	chr7:70091841-70091986	K562	blood:	n/a	n/a
8	ATF2	chr7:70163149-70163641	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:70158188-70158571	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:70113044-70113441	GM12878	blood:	n/a	n/a
11	ATF2	chr7:70161308-70161791	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:70164867-70165954	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:70182931-70183279	GM12878	blood:	n/a	n/a
14	ATF2	chr7:70159737-70160179	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr7:70133624-70133911	GM12878	blood:	n/a	n/a
16	ATF2	chr7:70164947-70166179	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr7:70181519-70181861	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:70145962-70146088	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:70061335-70061723	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:70047222-70047546	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:70084144-70084459	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:70171826-70171998	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:70064701-70064711	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:70060789-70060989	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr7:70054021-70054368	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr7:70146926-70147314	GM12878	blood:	n/a	n/a
27	BATF	chr7:70128632-70129069	GM12878	blood:	n/a	n/a
28	BATF	chr7:70113183-70113442	GM12878	blood:	n/a	n/a
29	BATF	chr7:70144546-70144968	GM12878	blood:	n/a	n/a
30	BATF	chr7:70175130-70175457	GM12878	blood:	n/a	chr7:70175301-70175311 chr7:70175300-70175311 chr7:70175171-70175180
31	BATF	chr7:70128646-70129082	GM12878	blood:	n/a	n/a
32	BATF	chr7:70175177-70175456	GM12878	blood:	n/a	chr7:70175301-70175311 chr7:70175300-70175311
33	BATF	chr7:70144538-70144907	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:70165146-70165623	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr7:70128600-70129082	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:70113093-70113397	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:70128594-70129058	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:70165263-70165600	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL11A	chr7:70110801-70111113	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:70033766-70034875	K562	blood:	n/a	n/a
41	BHLHE40	chr7:70158734-70159179	GM12878	blood:	n/a	chr7:70159147-70159163
42	BHLHE40	chr7:70163235-70163633	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:70113074-70113557	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:70079192-70079569	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:70128509-70129192	GM12878	blood:	n/a	chr7:70128654-70128675
46	BHLHE40	chr7:70160128-70160685	GM12878	blood:	n/a	chr7:70160375-70160391
47	BHLHE40	chr7:70146929-70147278	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:70175191-70175547	GM12878	blood:	n/a	n/a
49	BHLHE40	chr7:70110741-70111166	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:70133463-70133982	GM12878	blood:	n/a	n/a

(count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70160006-70160056	AG04449	skin:	fetal
2	chr7:70111180-70111230	HRE	kidney:	n/a
3	chr7:70096458-70096508	HEEpiC	esophagus:	n/a
4	chr7:70139561-70139611	HMEC	breast:	n/a
5	chr7:70060835-70060885	BE2_C	brain:	n/a
6	chr7:70165515-70165565	CMK	blood:	n/a
7	chr7:70160006-70160056	AG04449	skin:	fetal
8	chr7:70111180-70111230	HRE	kidney:	n/a
9	chr7:70096458-70096508	HEEpiC	esophagus:	n/a
10	chr7:70139561-70139611	HMEC	breast:	n/a
11	chr7:70060835-70060885	BE2_C	brain:	n/a
12	chr7:70165515-70165565	CMK	blood:	n/a
13	chr7:70170620-70170670	Hela-S3	cervix:	n/a
14	chr7:70096264-70096314	LNCaP	prostate:	n/a
15	chr7:70055327-70055377	SK-N-MC	brain:	n/a
16	chr7:70096791-70096841	BJ	skin:	n/a
17	chr7:70096791-70096841	AG04449	skin:	fetal
18	chr7:70061455-70061505	Hepatocyte	liver:	n/a
19	chr7:70160498-70160548	PrEC	prostate:	n/a
20	chr7:70146354-70146404	GM12892	blood:	n/a
21	chr7:70170620-70170670	AG04450	lung:	fetal
22	chr7:70061064-70061114	HCM	heart:	n/a
23	chr7:70163455-70163505	CMK	blood:	n/a
24	chr7:70060153-70060203	LNCaP	prostate:	n/a
25	chr7:70172515-70172565	AG09319	gingival:	n/a
26	chr7:70132171-70132221	NHDF-neo	bronchial:	n/a
27	chr7:70132171-70132221	ovcar-3	ovarian:	n/a
28	chr7:70159340-70159390	PANC-1	pancreas:	n/a
29	chr7:70132171-70132221	HEK293	kidney:	embryo
30	chr7:70157145-70157195	Jurkat	blood:	n/a
31	chr7:70160498-70160548	ECC-1	luminal epithelium:	n/a
32	chr7:70172515-70172565	RPTEC	kidney:	n/a
33	chr7:70061616-70061666	NHBE	bronchial:	n/a
34	chr7:70160006-70160056	GM06990	blood:	n/a
35	chr7:70170620-70170670	HRE	kidney:	n/a
36	chr7:70159330-70159380	HRPEpiC	eye:	n/a
37	chr7:70158761-70158811	MCF10A-Er-Src	breast:	n/a
38	chr7:70159340-70159390	HRPEpiC	eye:	n/a
39	chr7:70126616-70126666	IMR90	lung:	fetal
40	chr7:70160734-70160784	BJ	skin:	n/a
41	chr7:70165515-70165565	SK-N-SH	brain:	n/a
42	chr7:70061616-70061666	T-47D	breast:	n/a
43	chr7:70111180-70111230	HUVEC	blood vessel:	n/a
44	chr7:70055327-70055377	U87	brain:	n/a
45	chr7:70160498-70160548	NHBE	bronchial:	n/a
46	chr7:70157145-70157195	HRE	kidney:	n/a
47	chr7:70061064-70061114	GM19239	blood:	n/a
48	chr7:70061508-70061558	BE2_C	brain:	n/a
49	chr7:70158761-70158811	AG04449	skin:	fetal
50	chr7:70126616-70126666	HRCEpiC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70041903..70043590-chr7:70046514..70049488,2	K562	blood:
2	chr7:70116058..70119019-chr7:70120958..70123553,2	K562	blood:
3	chr7:70084622..70086291-chr7:70088234..70089854,2	K562	blood:
4	chr7:70184183..70185798-chr7:70197589..70200298,2	MCF-7	breast:
5	chr7:70084622..70086291-chr7:70088234..70089854,2	K562	blood:
6	chr7:69507259..69508393-chr7:70162935..70163782,5	MCF-7	breast:
7	chr7:70116058..70119019-chr7:70120958..70123553,2	K562	blood:
8	chr7:70029430..70032358-chr7:70034724..70037517,2	K562	blood:
9	chr7:70133847..70137058-chr7:70140413..70143195,3	K562	blood:
10	chr7:70041903..70043590-chr7:70046514..70049488,2	K562	blood:
11	chr7:70069205..70071813-chr7:70077445..70079383,2	K562	blood:
12	chr7:70049785..70050737-chr7:70162923..70163511,2	MCF-7	breast:
13	chr7:70174321..70176691-chr7:70186792..70188789,2	MCF-7	breast:
14	chr7:70175580..70177405-chr7:70179545..70181681,2	MCF-7	breast:
15	chr7:70048823..70050343-chr7:70052305..70054085,2	K562	blood:
16	chr7:70182197..70184832-chr7:70191535..70193515,2	MCF-7	breast:
17	chr7:70029430..70032358-chr7:70034724..70037517,2	K562	blood:
18	chr7:70035377..70037187-chr7:70048714..70051712,2	MCF-7	breast:
19	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:
20	chr7:70048823..70050343-chr7:70052305..70054085,2	K562	blood:
21	chr7:70133847..70137058-chr7:70140413..70143195,3	K562	blood:
22	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:
23	chr7:70049785..70050737-chr7:70162923..70163511,2	MCF-7	breast:
24	chr7:70035377..70037187-chr7:70048714..70051712,2	MCF-7	breast:
25	chr7:70069205..70071813-chr7:70077445..70079383,2	K562	blood:
26	chr7:70092147..70095006-chr7:70098737..70101187,2	K562	blood:
27	chr7:70174321..70176691-chr7:70186792..70188789,2	MCF-7	breast:
28	chr7:70092147..70095006-chr7:70098737..70101187,2	K562	blood:
29	chr7:70175580..70177405-chr7:70179545..70181681,2	MCF-7	breast:

(count:4 , 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
3	lnc-CALN1-4	chr7:70085301-70085806	NONHSAT121334
4	lnc-CALN1-4	chr7:70083180-70083205	NONHSAT121334

No data

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

Extended variants
information (count: 6807 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6807 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548965315	chr7:70016338-70016339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143449371	chr7:70016355-70016356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535734960	chr7:70016372-70016373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550499829	chr7:70016493-70016494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73450557	chr7:70016515-70016516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539273772	chr7:70016644-70016645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568717539	chr7:70016661-70016662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs118042407	chr7:70016678-70016679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7797987	chr7:70016729-70016730	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs151218182	chr7:70016750-70016751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555730809	chr7:70016777-70016778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115152281	chr7:70016781-70016782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115855810	chr7:70016805-70016806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563203189	chr7:70016872-70016873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4718959	chr7:70016901-70016902	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs181353467	chr7:70016925-70016926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556584770	chr7:70016940-70016941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184717473	chr7:70016941-70016942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528194682	chr7:70017076-70017077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs77303187	chr7:70017094-70017095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76421763	chr7:70017098-70017099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139162937	chr7:70017106-70017107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550435873	chr7:70017114-70017115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10486869	chr7:70017184-70017185	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs189999266	chr7:70017217-70017218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539212275	chr7:70017303-70017304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551170058	chr7:70017307-70017308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566804653	chr7:70017340-70017341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554036094	chr7:70017354-70017355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181851280	chr7:70017355-70017356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369010178	chr7:70017365-70017366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373333930	chr7:70017371-70017372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538264906	chr7:70017495-70017496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149930607	chr7:70017521-70017522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs74940756	chr7:70017586-70017587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186423458	chr7:70017591-70017592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545574582	chr7:70017615-70017616	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs62455792	chr7:70017650-70017651	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs114249695	chr7:70017696-70017697	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145787939	chr7:70017799-70017800	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554018081	chr7:70017827-70017828	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572360933	chr7:70017872-70017873	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561656290	chr7:70017877-70017878	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190823192	chr7:70017912-70017913	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543819944	chr7:70017936-70017937	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6946285	chr7:70017937-70017938	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs79763380	chr7:70018013-70018014	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77580084	chr7:70018037-70018038	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74329570	chr7:70018105-70018106	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527522600	chr7:70018112-70018113	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4127 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69996800-70017800	Weak transcription	Aorta	Aorta
2	chr7:70008600-70019600	Weak transcription	Psoas Muscle	Psoas
3	chr7:70011000-70022800	Weak transcription	Primary B cells from peripheral blood	blood
4	chr7:70012600-70036800	Weak transcription	Fetal Stomach	stomach
5	chr7:70012800-70022600	Weak transcription	Primary B cells from cord blood	blood
6	chr7:70015200-70023200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:70016000-70033600	Weak transcription	Ovary	ovary
8	chr7:70016200-70018600	Enhancers	Fetal Brain Male	brain
9	chr7:70016800-70018200	Enhancers	Fetal Brain Female	brain
10	chr7:70016800-70018400	Enhancers	Brain Hippocampus Middle	brain
11	chr7:70017400-70017800	Enhancers	Brain Germinal Matrix	brain
12	chr7:70017400-70019800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:70017600-70018600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
14	chr7:70017800-70018600	Enhancers	Brain Anterior Caudate	brain
15	chr7:70018000-70018600	Enhancers	Brain Cingulate Gyrus	brain
16	chr7:70018000-70018800	Enhancers	Liver	Liver
17	chr7:70018200-70018400	Enhancers	Brain Substantia Nigra	brain
18	chr7:70018200-70018600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr7:70018200-70022200	Weak transcription	Fetal Brain Female	brain
20	chr7:70018400-70018600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:70018400-70018600	Enhancers	Brain Angular Gyrus	brain
22	chr7:70018400-70018600	Enhancers	Gastric	stomach
23	chr7:70018400-70019600	Weak transcription	Brain Substantia Nigra	brain
24	chr7:70018400-70026600	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:70018600-70019800	Weak transcription	Brain Anterior Caudate	brain
26	chr7:70018600-70026600	Weak transcription	Brain Angular Gyrus	brain
27	chr7:70018600-70030200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr7:70018600-70030400	Weak transcription	Gastric	stomach
29	chr7:70018600-70033800	Weak transcription	Fetal Brain Male	brain
30	chr7:70018800-70021800	Weak transcription	Liver	Liver
31	chr7:70019400-70020600	Enhancers	Fetal Muscle Leg	muscle
32	chr7:70019600-70019800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:70019600-70019800	Enhancers	Psoas Muscle	Psoas
34	chr7:70019600-70020000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:70019600-70020000	Enhancers	Brain Substantia Nigra	brain
36	chr7:70019600-70020000	Enhancers	Fetal Muscle Trunk	muscle
37	chr7:70019800-70020000	Enhancers	HSMMtube	muscle
38	chr7:70019800-70020200	Enhancers	Brain Anterior Caudate	brain
39	chr7:70020000-70023000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:70020000-70023200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:70020000-70036600	Weak transcription	Fetal Muscle Trunk	muscle
42	chr7:70020200-70030600	Weak transcription	Brain Anterior Caudate	brain
43	chr7:70020400-70020600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:70020400-70020600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr7:70020400-70023800	Weak transcription	Spleen	Spleen
46	chr7:70020600-70026200	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:70020600-70031000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:70021200-70022400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:70021800-70022600	Enhancers	Liver	Liver
50	chr7:70022200-70023800	Enhancers	Fetal Brain Female	brain

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