Variant report

Variant	nsv869342
Chromosome Location	chr7:69671501-69958576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1188)
CpG islands
(count:612)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1188 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr7:69680455-69680944	GM12878	blood:	n/a	n/a
4	ATF2	chr7:69703053-69703682	GM12878	blood:	n/a	n/a
5	ATF2	chr7:69812779-69813364	GM12878	blood:	n/a	n/a
6	ATF2	chr7:69702998-69703627	GM12878	blood:	n/a	n/a
7	ATF2	chr7:69812755-69813278	GM12878	blood:	n/a	n/a
8	BACH1	chr7:69708411-69708797	H1-hESC	embryonic stem cell:	n/a	chr7:69708581-69708595
9	BATF	chr7:69812869-69813246	GM12878	blood:	n/a	n/a
10	BATF	chr7:69703024-69703532	GM12878	blood:	n/a	n/a
11	BATF	chr7:69812758-69813280	GM12878	blood:	n/a	n/a
12	BATF	chr7:69880651-69881053	GM12878	blood:	n/a	n/a
13	BATF	chr7:69768804-69769091	GM12878	blood:	n/a	n/a
14	BATF	chr7:69703108-69703460	GM12878	blood:	n/a	n/a
15	BATF	chr7:69768844-69769144	GM12878	blood:	n/a	n/a
16	BATF	chr7:69880623-69881036	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:69703134-69703420	GM12878	blood:	n/a	chr7:69703233-69703242
18	BCL11A	chr7:69812866-69813204	GM12878	blood:	n/a	chr7:69813053-69813062
19	BCL11A	chr7:69680508-69680833	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:69891444-69891662	GM12878	blood:	n/a	chr7:69891566-69891575
21	BCL11A	chr7:69703072-69703562	GM12878	blood:	n/a	chr7:69703233-69703242
22	BCL11A	chr7:69812836-69813252	GM12878	blood:	n/a	chr7:69813053-69813062
23	BCL3	chr7:69736555-69736900	GM12878	blood:	n/a	n/a
24	BCL3	chr7:69703113-69703464	GM12878	blood:	n/a	chr7:69703233-69703242
25	BCLAF1	chr7:69703054-69703523	GM12878	blood:	n/a	chr7:69703233-69703242
26	BCLAF1	chr7:69812703-69813373	GM12878	blood:	n/a	chr7:69813053-69813062
27	BCLAF1	chr7:69703014-69703629	GM12878	blood:	n/a	chr7:69703233-69703242
28	BCLAF1	chr7:69812788-69813301	GM12878	blood:	n/a	chr7:69813053-69813062
29	BHLHE40	chr7:69923799-69923846	K562	blood:	n/a	chr7:69923826-69923835
30	BHLHE40	chr7:69881578-69881956	GM12878	blood:	n/a	chr7:69881704-69881720
31	BHLHE40	chr7:69703047-69703613	GM12878	blood:	n/a	n/a
32	CBX3	chr7:69694286-69694496	K562	blood:	n/a	n/a
33	CBX3	chr7:69694236-69694545	K562	blood:	n/a	n/a
34	CEBPB	chr7:69680596-69680895	IMR90	lung:	n/a	chr7:69680752-69680763
35	CEBPB	chr7:69786049-69786330	H1-hESC	embryonic stem cell:	n/a	chr7:69786187-69786198
36	CEBPB	chr7:69799316-69799332	A549	lung:	n/a	n/a
37	CEBPB	chr7:69933443-69933814	MCF-7	breast:	n/a	n/a
38	CEBPB	chr7:69776098-69776300	A549	lung:	n/a	n/a
39	CEBPB	chr7:69719391-69719575	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:69736587-69736799	MCF-7	breast:	n/a	chr7:69736660-69736671
41	CEBPB	chr7:69786019-69786366	HepG2	liver:	n/a	chr7:69786187-69786198
42	CEBPB	chr7:69952071-69952283	K562	blood:	n/a	chr7:69952134-69952147
43	CEBPB	chr7:69672499-69672661	A549	lung:	n/a	n/a
44	CEBPB	chr7:69872175-69872224	K562	blood:	n/a	n/a
45	CEBPB	chr7:69872211-69872402	HepG2	liver:	n/a	chr7:69872257-69872268
46	CEBPB	chr7:69786106-69786321	A549	lung:	n/a	chr7:69786187-69786198
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	chr7:69882085-69882358	H1-hESC	embryonic stem cell:	n/a	chr7:69882271-69882284
50	CEBPB	chr7:69862784-69863043	HepG2	liver:	n/a	chr7:69862854-69862865

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:69882555-69882605	U87	brain:	n/a
2	chr7:69755498-69755548	GM06990	blood:	n/a
3	chr7:69882555-69882605	U87	brain:	n/a
4	chr7:69755498-69755548	GM06990	blood:	n/a
5	chr7:69882555-69882605	HAEpiC	amniotic membrane:	n/a
6	chr7:69778639-69778689	GM19239	blood:	n/a
7	chr7:69913915-69913965	HUVEC	blood vessel:	n/a
8	chr7:69778639-69778689	HEK293	kidney:	embryo
9	chr7:69778639-69778689	NB4	blood:	n/a
10	chr7:69778639-69778689	HUVEC	blood vessel:	n/a
11	chr7:69733045-69733095	HL-60	blood:	n/a
12	chr7:69882555-69882605	NHDF-neo	bronchial:	n/a
13	chr7:69733045-69733095	Hepatocyte	liver:	n/a
14	chr7:69808286-69808336	H1-hESC	embryonic stem cell:	embryo
15	chr7:69913915-69913965	ECC-1	luminal epithelium:	n/a
16	chr7:69923958-69924008	HCPEpiC	choroid plexus:	n/a
17	chr7:69735590-69735640	IMR90	lung:	fetal
18	chr7:69707270-69707320	NHBE	bronchial:	n/a
19	chr7:69778639-69778689	BJ	skin:	n/a
20	chr7:69778639-69778689	NT2-D1	testis:	n/a
21	chr7:69882555-69882605	NH-A	brain:	n/a
22	chr7:69913915-69913965	NH-A	brain:	n/a
23	chr7:69913915-69913965	Caco-2	colon:	n/a
24	chr7:69913915-69913965	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:69882555-69882605	MCF-7	breast:	n/a
26	chr7:69735590-69735640	T-47D	breast:	n/a
27	chr7:69808286-69808336	SKMC	muscle:	n/a
28	chr7:69923958-69924008	HCF	heart:	n/a
29	chr7:69858080-69858130	NB4	blood:	n/a
30	chr7:69913915-69913965	HMEC	breast:	n/a
31	chr7:69913915-69913965	ProgFib	skin:	n/a
32	chr7:69913915-69913965	NT2-D1	testis:	n/a
33	chr7:69923958-69924008	PANC-1	pancreas:	n/a
34	chr7:69735590-69735640	SK-N-MC	brain:	n/a
35	chr7:69755498-69755548	BJ	skin:	n/a
36	chr7:69707270-69707320	AoSMC	blood vessel:	n/a
37	chr7:69707270-69707320	Caco-2	colon:	n/a
38	chr7:69923958-69924008	GM19239	blood:	n/a
39	chr7:69778639-69778689	SK-N-SH_RA	brain:	n/a
40	chr7:69858080-69858130	Hepatocyte	liver:	n/a
41	chr7:69778639-69778689	NHBE	bronchial:	n/a
42	chr7:69882555-69882605	HRE	kidney:	n/a
43	chr7:69913915-69913965	PANC-1	pancreas:	n/a
44	chr7:69858080-69858130	HRPEpiC	eye:	n/a
45	chr7:69735590-69735640	Hepatocyte	liver:	n/a
46	chr7:69707270-69707320	RPTEC	kidney:	n/a
47	chr7:69755498-69755548	AG04449	skin:	fetal
48	chr7:69882555-69882605	NT2-D1	testis:	n/a
49	chr7:69707270-69707320	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:69733045-69733095	A549	lung:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:69681271..69684117-chr7:69686002..69687637,2	K562	blood:
2	chr7:69716066..69717920-chr7:69722887..69724977,2	K562	blood:
3	chr7:69951787..69954250-chr7:69957841..69960555,2	K562	blood:
4	chr7:69795306..69797279-chr7:69802181..69805165,2	K562	blood:
5	chr7:69923675..69926139-chr7:69934403..69936695,2	K562	blood:
6	chr7:69701411..69704010-chr7:69707383..69709265,2	K562	blood:
7	chr7:69681271..69684117-chr7:69686002..69687637,2	K562	blood:
8	chr7:69716066..69717920-chr7:69722887..69724977,2	K562	blood:
9	chr7:69679433..69681013-chr7:69692321..69694747,2	K562	blood:
10	chr7:69926473..69928841-chr7:69935166..69939263,3	K562	blood:
11	chr7:69816727..69818493-chr7:69819760..69821575,2	K562	blood:
12	chr7:69701411..69704010-chr7:69707383..69709265,2	K562	blood:
13	chr7:69843540..69845241-chr7:69851441..69854284,2	K562	blood:
14	chr7:69795306..69797279-chr7:69802181..69805165,2	K562	blood:
15	chr7:69843540..69845241-chr7:69851441..69854284,2	K562	blood:
16	chr7:69919039..69921545-chr7:69922833..69924700,2	K562	blood:
17	chr7:69679433..69681013-chr7:69692321..69694747,2	K562	blood:
18	chr7:69848786..69851251-chr7:69853357..69855930,2	MCF-7	breast:
19	chr7:69926473..69928841-chr7:69935166..69939263,3	K562	blood:
20	chr7:69911189..69912929-chr7:69913285..69916011,2	MCF-7	breast:
21	chr7:69951787..69954250-chr7:69957841..69960555,2	K562	blood:
22	chr7:69848786..69851251-chr7:69853357..69855930,2	MCF-7	breast:
23	chr7:69919039..69921545-chr7:69922833..69924700,2	K562	blood:
24	chr1:12410651..12411212-chr7:69674323..69674880,2	MCF-7	breast:
25	chr7:69923675..69926139-chr7:69934403..69936695,2	K562	blood:
26	chr7:69911189..69912929-chr7:69913285..69916011,2	MCF-7	breast:
27	chr7:69816727..69818493-chr7:69819760..69821575,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WBSCR17-5	chr7:69781902-69782032	NONHSAT121328
2	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: 9363 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:9363 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377359832	chr7:69671505-69671506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188218307	chr7:69671572-69671573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567769253	chr7:69671580-69671581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537903981	chr7:69671593-69671594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556738023	chr7:69671623-69671624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571713120	chr7:69671674-69671675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539206787	chr7:69671736-69671737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554071594	chr7:69671776-69671777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553556603	chr7:69671837-69671838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546760908	chr7:69671925-69671926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572396320	chr7:69672051-69672052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146603548	chr7:69672224-69672225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554897469	chr7:69672238-69672239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141321211	chr7:69672245-69672246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs180740365	chr7:69672340-69672341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562590432	chr7:69672343-69672344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145042137	chr7:69672416-69672417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545224440	chr7:69672418-69672419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573803322	chr7:69672421-69672422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560475097	chr7:69672448-69672449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146796787	chr7:69672454-69672455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549400038	chr7:69672475-69672476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567634892	chr7:69672537-69672538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531846413	chr7:69672653-69672654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117001525	chr7:69672656-69672657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556019229	chr7:69672691-69672692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571691557	chr7:69672730-69672731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576067926	chr7:69672736-69672737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538909209	chr7:69672764-69672765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372652093	chr7:69672787-69672788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553907988	chr7:69672853-69672854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200895186	chr7:69672884-69672885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112094307	chr7:69672923-69672924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566037010	chr7:69672927-69672928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6943630	chr7:69672953-69672954	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs368150530	chr7:69672998-69672999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61267230	chr7:69673020-69673021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185000433	chr7:69673074-69673075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573591893	chr7:69673079-69673080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6967388	chr7:69673080-69673081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544176954	chr7:69673085-69673086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371105239	chr7:69673097-69673098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556035353	chr7:69673123-69673124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189985760	chr7:69673170-69673171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545230934	chr7:69673186-69673187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560341363	chr7:69673190-69673191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572391287	chr7:69673213-69673214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542907014	chr7:69673311-69673312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561219114	chr7:69673401-69673402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564833341	chr7:69673409-69673410	Enhancers 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
Pancreatic cancer	17952125	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

Chromatin state (count:1917 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69655000-69692400	Weak transcription	Primary B cells from cord blood	blood
2	chr7:69670200-69675600	Weak transcription	Psoas Muscle	Psoas
3	chr7:69670800-69671800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:69670800-69672600	Weak transcription	Fetal Intestine Large	intestine
5	chr7:69670800-69674600	Enhancers	Fetal Intestine Small	intestine
6	chr7:69670800-69674800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:69671400-69676600	Weak transcription	Ovary	ovary
8	chr7:69671800-69672200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr7:69672000-69672200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:69672600-69673600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr7:69672600-69674000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr7:69672600-69674600	Enhancers	Fetal Intestine Large	intestine
13	chr7:69672600-69676000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:69673000-69674000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:69673000-69674200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:69673200-69674200	Enhancers	NH-A	brain
17	chr7:69673200-69674200	Enhancers	Osteobl	bone
18	chr7:69673200-69674400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:69673200-69674400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:69673200-69674400	Enhancers	NHEK	skin
21	chr7:69673200-69676200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:69673400-69676200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:69673600-69673800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:69673600-69674000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr7:69673600-69674000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:69673600-69674000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr7:69673600-69674000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr7:69673600-69674000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:69673600-69674200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr7:69673600-69674200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:69673600-69674200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr7:69673600-69674200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr7:69673800-69674200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:69673800-69674200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:69673800-69675200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr7:69674000-69675600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:69674000-69678400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:69674200-69674600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr7:69674200-69675200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr7:69674200-69675600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr7:69674200-69678800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:69674400-69675800	Enhancers	Brain Germinal Matrix	brain
43	chr7:69674600-69675600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:69674600-69679800	Enhancers	Fetal Brain Male	brain
45	chr7:69674800-69676000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:69674800-69676000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:69675000-69676400	Enhancers	Fetal Brain Female	brain
48	chr7:69675200-69675800	Enhancers	Fetal Lung	lung
49	chr7:69675200-69676000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr7:69675200-69676000	Enhancers	HUES64 Cell Line	embryonic stem cell

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