Variant report

Variant	nsv529669
Chromosome Location	chr7:69709373-69974708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1272)
CpG islands
(count:550)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1272 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:69897478-69897511	K562	blood:	n/a	n/a
2	ATF1	chr7:69841501-69841890	K562	blood:	n/a	n/a
3	ATF2	chr7:69812779-69813364	GM12878	blood:	n/a	n/a
4	ATF2	chr7:69812755-69813278	GM12878	blood:	n/a	n/a
5	BATF	chr7:69768804-69769091	GM12878	blood:	n/a	n/a
6	BATF	chr7:69768844-69769144	GM12878	blood:	n/a	n/a
7	BATF	chr7:69880623-69881036	GM12878	blood:	n/a	n/a
8	BATF	chr7:69812758-69813280	GM12878	blood:	n/a	n/a
9	BATF	chr7:69880651-69881053	GM12878	blood:	n/a	n/a
10	BATF	chr7:69812869-69813246	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:69812836-69813252	GM12878	blood:	n/a	chr7:69813053-69813062
12	BCL11A	chr7:69960431-69960851	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:69960974-69962359	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:69812866-69813204	GM12878	blood:	n/a	chr7:69813053-69813062
15	BCL11A	chr7:69891444-69891662	GM12878	blood:	n/a	chr7:69891566-69891575
16	BCL3	chr7:69960343-69960674	GM12878	blood:	n/a	n/a
17	BCL3	chr7:69962061-69962442	GM12878	blood:	n/a	n/a
18	BCL3	chr7:69960732-69961220	GM12878	blood:	n/a	n/a
19	BCL3	chr7:69961504-69961824	GM12878	blood:	n/a	n/a
20	BCL3	chr7:69736555-69736900	GM12878	blood:	n/a	n/a
21	BCL3	chr7:69960754-69961310	GM12878	blood:	n/a	n/a
22	BCL3	chr7:69961496-69962445	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:69812703-69813373	GM12878	blood:	n/a	chr7:69813053-69813062
24	BCLAF1	chr7:69812788-69813301	GM12878	blood:	n/a	chr7:69813053-69813062
25	BHLHE40	chr7:69923799-69923846	K562	blood:	n/a	chr7:69923826-69923835
26	BHLHE40	chr7:69960531-69960860	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:69881578-69881956	GM12878	blood:	n/a	chr7:69881704-69881720
28	BRCA1	chr7:69971668-69971768	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:69786019-69786366	HepG2	liver:	n/a	chr7:69786187-69786198
30	CEBPB	chr7:69882085-69882358	H1-hESC	embryonic stem cell:	n/a	chr7:69882271-69882284
31	CEBPB	chr7:69952071-69952283	K562	blood:	n/a	chr7:69952134-69952147
32	CEBPB	chr7:69844364-69844560	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr7:69862784-69863043	HepG2	liver:	n/a	chr7:69862854-69862865
34	CEBPB	chr7:69786049-69786330	H1-hESC	embryonic stem cell:	n/a	chr7:69786187-69786198
35	CEBPB	chr7:69872175-69872224	K562	blood:	n/a	n/a
36	CEBPB	chr7:69731232-69731575	A549	lung:	n/a	chr7:69731363-69731374
37	CEBPB	chr7:69872211-69872402	HepG2	liver:	n/a	chr7:69872257-69872268
38	CEBPB	chr7:69719391-69719575	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:69841594-69841712	K562	blood:	n/a	n/a
40	CEBPB	chr7:69933443-69933814	MCF-7	breast:	n/a	n/a
41	CEBPB	chr7:69951219-69951412	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:69731383-69731696	K562	blood:	n/a	n/a
43	CEBPB	chr7:69776098-69776300	A549	lung:	n/a	n/a
44	CEBPB	chr7:69972978-69973126	K562	blood:	n/a	chr7:69973079-69973088
45	CEBPB	chr7:69933440-69933763	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:69799316-69799332	A549	lung:	n/a	n/a
47	CEBPB	chr7:69786010-69786332	IMR90	lung:	n/a	chr7:69786187-69786198
48	CEBPB	chr7:69731245-69731620	HepG2	liver:	n/a	chr7:69731363-69731374
49	CEBPB	chr7:69786106-69786321	A549	lung:	n/a	chr7:69786187-69786198
50	CEBPB	chr7:69933465-69933727	H1-hESC	embryonic stem cell:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:69858080-69858130	ovcar-3	ovarian:	n/a
2	chr7:69858080-69858130	ovcar-3	ovarian:	n/a
3	chr7:69735590-69735640	ECC-1	luminal epithelium:	n/a
4	chr7:69913915-69913965	IMR90	lung:	fetal
5	chr7:69733045-69733095	SK-N-SH_RA	brain:	n/a
6	chr7:69778639-69778689	T-47D	breast:	n/a
7	chr7:69882555-69882605	GM12878	blood:	n/a
8	chr7:69733045-69733095	BE2_C	brain:	n/a
9	chr7:69735590-69735640	PFSK-1	brain:	n/a
10	chr7:69733045-69733095	Hepatocyte	liver:	n/a
11	chr7:69882555-69882605	HUVEC	blood vessel:	n/a
12	chr7:69733045-69733095	GM12892	blood:	n/a
13	chr7:69858080-69858130	HIPEpiC	eye:	n/a
14	chr7:69923958-69924008	HRE	kidney:	n/a
15	chr7:69858080-69858130	GM19239	blood:	n/a
16	chr7:69923958-69924008	PFSK-1	brain:	n/a
17	chr7:69858080-69858130	LNCaP	prostate:	n/a
18	chr7:69755498-69755548	Jurkat	blood:	n/a
19	chr7:69808286-69808336	AG09309	skin:	n/a
20	chr7:69808286-69808336	A549	lung:	n/a
21	chr7:69858080-69858130	AG04450	lung:	fetal
22	chr7:69808286-69808336	GM19239	blood:	n/a
23	chr7:69808286-69808336	CMK	blood:	n/a
24	chr7:69755498-69755548	HEK293	kidney:	embryo
25	chr7:69808286-69808336	Jurkat	blood:	n/a
26	chr7:69923958-69924008	NB4	blood:	n/a
27	chr7:69733045-69733095	HRCEpiC	kidney:	n/a
28	chr7:69735590-69735640	SK-N-MC	brain:	n/a
29	chr7:69913915-69913965	U87	brain:	n/a
30	chr7:69808286-69808336	ECC-1	luminal epithelium:	n/a
31	chr7:69778639-69778689	GM19239	blood:	n/a
32	chr7:69778639-69778689	PANC-1	pancreas:	n/a
33	chr7:69755498-69755548	LNCaP	prostate:	n/a
34	chr7:69913915-69913965	GM19239	blood:	n/a
35	chr7:69778639-69778689	HUVEC	blood vessel:	n/a
36	chr7:69882555-69882605	LNCaP	prostate:	n/a
37	chr7:69808286-69808336	HEEpiC	esophagus:	n/a
38	chr7:69808286-69808336	HUVEC	blood vessel:	n/a
39	chr7:69735590-69735640	Caco-2	colon:	n/a
40	chr7:69755498-69755548	Hela-S3	cervix:	n/a
41	chr7:69778639-69778689	A549	lung:	n/a
42	chr7:69778639-69778689	GM12891	blood:	n/a
43	chr7:69808286-69808336	MCF10A-Er-Src	breast:	n/a
44	chr7:69882555-69882605	HRE	kidney:	n/a
45	chr7:69733045-69733095	NB4	blood:	n/a
46	chr7:69755498-69755548	A549	lung:	n/a
47	chr7:69755498-69755548	H1-hESC	embryonic stem cell:	embryo
48	chr7:69882555-69882605	H1-hESC	embryonic stem cell:	embryo
49	chr7:69735590-69735640	SAEC	small airway:	n/a
50	chr7:69882555-69882605	HRCEpiC	kidney:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:69923675..69926139-chr7:69934403..69936695,2	K562	blood:
2	chr7:69795306..69797279-chr7:69802181..69805165,2	K562	blood:
3	chr7:69911189..69912929-chr7:69913285..69916011,2	MCF-7	breast:
4	chr7:69716066..69717920-chr7:69722887..69724977,2	K562	blood:
5	chr7:69843540..69845241-chr7:69851441..69854284,2	K562	blood:
6	chr7:69795306..69797279-chr7:69802181..69805165,2	K562	blood:
7	chr7:69716066..69717920-chr7:69722887..69724977,2	K562	blood:
8	chr7:69843540..69845241-chr7:69851441..69854284,2	K562	blood:
9	chr7:69816727..69818493-chr7:69819760..69821575,2	K562	blood:
10	chr7:69926473..69928841-chr7:69935166..69939263,3	K562	blood:
11	chr7:69974438..69975056-chr9:110290515..110291142,2	MCF-7	breast:
12	chr7:69816727..69818493-chr7:69819760..69821575,2	K562	blood:
13	chr7:69962073..69964244-chr7:69965970..69968066,2	K562	blood:
14	chr7:69919039..69921545-chr7:69922833..69924700,2	K562	blood:
15	chr7:69911189..69912929-chr7:69913285..69916011,2	MCF-7	breast:
16	chr7:69919039..69921545-chr7:69922833..69924700,2	K562	blood:
17	chr7:69951787..69954250-chr7:69957841..69960555,2	K562	blood:
18	chr7:69848786..69851251-chr7:69853357..69855930,2	MCF-7	breast:
19	chr7:69848786..69851251-chr7:69853357..69855930,2	MCF-7	breast:
20	chr7:69923675..69926139-chr7:69934403..69936695,2	K562	blood:
21	chr7:69926473..69928841-chr7:69935166..69939263,3	K562	blood:
22	chr7:69951787..69954250-chr7:69957841..69960555,2	K562	blood:
23	chr7:69962073..69964244-chr7:69965970..69968066,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WBSCR17-4	chr7:69961634-69962155	NONHSAT121332
2	lnc-WBSCR17-5	chr7:69781902-69782032	NONHSAT121328
3	lnc-WBSCR17-4	chr7:69960515-69961328	NONHSAT121332
4	lnc-WBSCR17-5	chr7:69900738-69901163	NONHSAT121328

No data

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

Extended variants
information (count: 8787 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:8787 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192499677	chr7:69709389-69709390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141898881	chr7:69709417-69709418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112685113	chr7:69709488-69709489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183650722	chr7:69709496-69709497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528623533	chr7:69709550-69709551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368032453	chr7:69709613-69709614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553462166	chr7:69709736-69709737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568677862	chr7:69709760-69709761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573229758	chr7:69709827-69709828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186827592	chr7:69709833-69709834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76771010	chr7:69709915-69709916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191295005	chr7:69709921-69709922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569407576	chr7:69709923-69709924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536660800	chr7:69709952-69709953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558160793	chr7:69709954-69709955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182182968	chr7:69709974-69709975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143583549	chr7:69710045-69710046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61068581	chr7:69710119-69710120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11979320	chr7:69710120-69710121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11976966	chr7:69710121-69710122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373196236	chr7:69710128-69710129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376035954	chr7:69710130-69710131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375992499	chr7:69710131-69710132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11976295	chr7:69710132-69710133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71077638	chr7:69710150-69710151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35403987	chr7:69710153-69710154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75243690	chr7:69710155-69710156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs57817453	chr7:69710156-69710157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200252798	chr7:69710157-69710158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141683582	chr7:69710159-69710160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55854410	chr7:69710160-69710161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141721834	chr7:69710214-69710215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191747093	chr7:69710325-69710326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574784670	chr7:69710350-69710351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185473693	chr7:69710376-69710377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545116783	chr7:69710408-69710409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150540649	chr7:69710424-69710425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546097135	chr7:69710503-69710504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139535404	chr7:69710516-69710517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142740391	chr7:69710523-69710524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540775484	chr7:69710529-69710530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561991802	chr7:69710553-69710554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369881807	chr7:69710566-69710567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35308787	chr7:69710579-69710580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs550858740	chr7:69710598-69710599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563079802	chr7:69710601-69710602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73171749	chr7:69710610-69710611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551651372	chr7:69710612-69710613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532381443	chr7:69710631-69710632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570161387	chr7:69710835-69710836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Autism	19246517	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1862 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69705600-69713000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:69707000-69724400	Weak transcription	Ovary	ovary
3	chr7:69713000-69716000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:69715000-69716000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:69715200-69715800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
6	chr7:69715400-69716000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:69715600-69715800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:69715600-69716000	ZNF genes & repeats	Fetal Lung	lung
9	chr7:69715800-69721400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:69717600-69721800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr7:69719000-69720000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr7:69719400-69719600	Enhancers	Fetal Brain Female	brain
13	chr7:69719400-69719800	Enhancers	Brain Cingulate Gyrus	brain
14	chr7:69719400-69724400	Weak transcription	Aorta	Aorta
15	chr7:69720600-69721200	Enhancers	Fetal Heart	heart
16	chr7:69721000-69724200	Weak transcription	Fetal Stomach	stomach
17	chr7:69721200-69723000	Weak transcription	Fetal Heart	heart
18	chr7:69721400-69721600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:69722200-69722600	Enhancers	Fetal Brain Male	brain
20	chr7:69722400-69723200	Weak transcription	Fetal Brain Female	brain
21	chr7:69722600-69723000	Weak transcription	Fetal Brain Male	brain
22	chr7:69723000-69723200	Enhancers	Fetal Heart	heart
23	chr7:69723000-69724600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:69723000-69726200	Enhancers	Fetal Brain Male	brain
25	chr7:69723200-69723400	Enhancers	Fetal Brain Female	brain
26	chr7:69723200-69723800	Weak transcription	Fetal Heart	heart
27	chr7:69723200-69724600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:69723200-69725600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:69723400-69724000	Weak transcription	Fetal Brain Female	brain
30	chr7:69723800-69724600	Enhancers	Right Ventricle	heart
31	chr7:69723800-69724800	Enhancers	Colon Smooth Muscle	Colon
32	chr7:69723800-69725000	Enhancers	Fetal Heart	heart
33	chr7:69724000-69724200	Enhancers	Fetal Brain Female	brain
34	chr7:69724000-69724800	Enhancers	NHDF-Ad	bronchial
35	chr7:69724000-69725000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr7:69724000-69725600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:69724200-69724600	Enhancers	Fetal Stomach	stomach
38	chr7:69724200-69731800	Weak transcription	Fetal Brain Female	brain
39	chr7:69724400-69724800	Enhancers	Adipose Nuclei	Adipose
40	chr7:69724400-69724800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr7:69724400-69724800	Enhancers	Esophagus	oesophagus
42	chr7:69724400-69724800	Enhancers	Fetal Lung	lung
43	chr7:69724400-69724800	Enhancers	Left Ventricle	heart
44	chr7:69724400-69724800	Enhancers	Ovary	ovary
45	chr7:69724400-69724800	Enhancers	Rectal Smooth Muscle	rectum
46	chr7:69724400-69724800	Enhancers	Right Atrium	heart
47	chr7:69724400-69724800	Enhancers	Osteobl	bone
48	chr7:69724400-69725200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:69724400-69725200	Enhancers	Fetal Muscle Trunk	muscle
50	chr7:69724400-69725400	Enhancers	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links