Variant report

Variant	nsv887757
Chromosome Location	chr7:16568529-16615490
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	chr7:16604521-16604844	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:16604359-16604839	K562	blood:	n/a	n/a
3	ARID3A	chr7:16599351-16600031	K562	blood:	n/a	n/a
4	ATF2	chr7:16604579-16604890	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr7:16572571-16572886	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:16604502-16604803	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:16605302-16605435	GM12878	blood:	n/a	chr7:16605353-16605362
8	BHLHE40	chr7:16602847-16603036	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:16602782-16603121	K562	blood:	n/a	n/a
10	BRCA1	chr7:16604574-16604716	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr7:16604506-16605046	HCT-116	colon:	n/a	n/a
12	CEBPB	chr7:16570120-16570445	A549	lung:	n/a	chr7:16570274-16570285
13	CEBPB	chr7:16570134-16570419	HepG2	liver:	n/a	chr7:16570274-16570285
14	CEBPB	chr7:16569407-16569662	IMR90	lung:	n/a	chr7:16569503-16569514
15	CEBPB	chr7:16594155-16594282	K562	blood:	n/a	chr7:16594242-16594253 chr7:16594242-16594253 chr7:16594242-16594255
16	CEBPB	chr7:16604627-16604920	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:16570195-16570423	K562	blood:	n/a	chr7:16570274-16570285
18	CEBPB	chr7:16588291-16588503	HepG2	liver:	n/a	chr7:16588441-16588452
19	CEBPB	chr7:16588282-16588508	A549	lung:	n/a	chr7:16588441-16588452
20	CEBPB	chr7:16599250-16599530	K562	blood:	n/a	n/a
21	CEBPB	chr7:16592806-16593313	HepG2	liver:	n/a	chr7:16592902-16592913
22	CEBPB	chr7:16569415-16569556	H1-hESC	embryonic stem cell:	n/a	chr7:16569503-16569514
23	CEBPB	chr7:16569373-16569665	HepG2	liver:	n/a	chr7:16569503-16569514
24	CEBPB	chr7:16592895-16593290	A549	lung:	n/a	chr7:16592902-16592913
25	CHD2	chr7:16611495-16611668	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr7:16602696-16602704	K562	blood:	n/a	n/a
27	CTCF	chr7:16604940-16605090	AG10803	skin:	n/a	n/a
28	CTCF	chr7:16604958-16605004	Gliobla	brain:	n/a	n/a
29	CTCF	chr7:16604640-16604790	MCF-7	breast:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
30	CTCF	chr7:16604600-16604750	HCPEpiC	choroid plexus:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
31	CTCF	chr7:16604660-16604810	GM12871	blood:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
32	CTCF	chr7:16604591-16604823	GM10266	blood:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
33	CTCF	chr7:16604620-16604770	GM12871	blood:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
34	CTCF	chr7:16605940-16606090	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr7:16604620-16604770	GM12875	blood:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
36	CTCF	chr7:16604025-16605035	A549	lung:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
37	CTCF	chr7:16604140-16604290	NHLF	lung:	n/a	n/a
38	CTCF	chr7:16604700-16604850	GM12866	blood:	n/a	n/a
39	CTCF	chr7:16605240-16605390	AG10803	skin:	n/a	n/a
40	CTCF	chr7:16604620-16604770	MCF-7	breast:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
41	CTCF	chr7:16604472-16604914	GM12878	blood:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
42	CTCF	chr7:16604600-16604750	HPF	lung:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
43	CTCF	chr7:16604620-16604770	HUVEC	blood vessel:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
44	CTCF	chr7:16604500-16604650	HCT-116	colon:	n/a	n/a
45	CTCF	chr7:16604233-16605085	SK-N-SH	brain:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
46	CTCF	chr7:16582100-16582250	Caco-2	colon:	n/a	n/a
47	CTCF	chr7:16605380-16605530	GM12873	blood:	n/a	n/a
48	CTCF	chr7:16604940-16605090	AG04449	skin:	n/a	n/a
49	CTCF	chr7:16604600-16604750	AoAF	blood vessel:	n/a	chr7:16604690-16604706 chr7:16604689-16604707 chr7:16604694-16604702 chr7:16604684-16604705
50	CTCF	chr7:16604200-16604350	HMF	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16605488-16605538	ECC-1	luminal epithelium:	n/a
2	chr7:16570042-16570092	SKMC	muscle:	n/a
3	chr7:16570042-16570092	RPTEC	kidney:	n/a
4	chr7:16570042-16570092	AG09319	gingival:	n/a
5	chr7:16570042-16570092	HMEC	breast:	n/a
6	chr7:16570042-16570092	MCF-7	breast:	n/a
7	chr7:16605488-16605538	HMEC	breast:	n/a
8	chr7:16604349-16604399	HL-60	blood:	n/a
9	chr7:16605488-16605538	HNPCEpiC	eye:	n/a
10	chr7:16604349-16604399	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:16570042-16570092	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:16604349-16604399	MCF10A-Er-Src	breast:	n/a
13	chr7:16605488-16605538	Hepatocyte	liver:	n/a
14	chr7:16570042-16570092	ovcar-3	ovarian:	n/a
15	chr7:16604349-16604399	U87	brain:	n/a
16	chr7:16605488-16605538	NB4	blood:	n/a
17	chr7:16605488-16605538	PANC-1	pancreas:	n/a
18	chr7:16570042-16570092	AG09309	skin:	n/a
19	chr7:16605488-16605538	SK-N-SH	brain:	n/a
20	chr7:16605488-16605538	H1-hESC	embryonic stem cell:	embryo
21	chr7:16605488-16605538	GM06990	blood:	n/a
22	chr7:16570042-16570092	SK-N-MC	brain:	n/a
23	chr7:16605488-16605538	PFSK-1	brain:	n/a
24	chr7:16570042-16570092	GM12891	blood:	n/a
25	chr7:16605488-16605538	CMK	blood:	n/a
26	chr7:16604349-16604399	SKMC	muscle:	n/a
27	chr7:16605488-16605538	IMR90	lung:	fetal
28	chr7:16605488-16605538	PrEC	prostate:	n/a
29	chr7:16570042-16570092	Caco-2	colon:	n/a
30	chr7:16604349-16604399	ProgFib	skin:	n/a
31	chr7:16604349-16604399	HCM	heart:	n/a
32	chr7:16605488-16605538	SK-N-SH_RA	brain:	n/a
33	chr7:16605488-16605538	RPTEC	kidney:	n/a
34	chr7:16605488-16605538	HCPEpiC	choroid plexus:	n/a
35	chr7:16570042-16570092	AG04450	lung:	fetal
36	chr7:16604349-16604399	IMR90	lung:	fetal
37	chr7:16604349-16604399	SK-N-SH_RA	brain:	n/a
38	chr7:16605488-16605538	GM12891	blood:	n/a
39	chr7:16570042-16570092	SK-N-SH	brain:	n/a
40	chr7:16604349-16604399	HCT-116	colon:	n/a
41	chr7:16604349-16604399	HRCEpiC	kidney:	n/a
42	chr7:16605488-16605538	K562	blood:	n/a
43	chr7:16570042-16570092	IMR90	lung:	fetal
44	chr7:16605488-16605538	AG09319	gingival:	n/a
45	chr7:16604349-16604399	GM12891	blood:	n/a
46	chr7:16604349-16604399	HEEpiC	esophagus:	n/a
47	chr7:16605488-16605538	NHDF-neo	bronchial:	n/a
48	chr7:16605488-16605538	LNCaP	prostate:	n/a
49	chr7:16605488-16605538	AG09309	skin:	n/a
50	chr7:16604349-16604399	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:16216050..16218726-chr7:16604270..16606079,2	K562	blood:
2	chr7:16576435..16578704-chr7:16580633..16582179,2	K562	blood:
3	chr7:16297813..16300771-chr7:16597599..16599779,2	K562	blood:
4	chr7:16569319..16572699-chr7:16575594..16578408,3	K562	blood:
5	chr7:16558907..16560805-chr7:16603285..16605880,2	K562	blood:
6	chr7:16470686..16472431-chr7:16604232..16605168,8	MCF-7	breast:
7	chr17:61904198..61906383-chr7:16582501..16585104,2	MCF-7	breast:
8	chr7:16459835..16461646-chr7:16592759..16594715,2	MCF-7	breast:
9	chr7:16571964..16574427-chr7:16575853..16578398,3	K562	blood:
10	chr7:16469862..16472067-chr7:16603591..16606131,2	K562	blood:
11	chr7:16470817..16474361-chr7:16603128..16605805,3	MCF-7	breast:
12	chr7:16597861..16600521-chr7:16618290..16619905,2	K562	blood:
13	chr7:16601048..16602742-chr7:16605165..16606667,2	K562	blood:
14	chr7:16459251..16461047-chr7:16608151..16609870,2	K562	blood:
15	chr7:16471516..16472395-chr7:16604130..16605000,4	MCF-7	breast:
16	chr7:16576435..16578704-chr7:16580633..16582179,2	K562	blood:
17	chr7:16532204..16534776-chr7:16581975..16583734,2	K562	blood:
18	chr7:16460429..16462871-chr7:16594318..16596208,2	K562	blood:
19	chr7:16541764..16543628-chr7:16604079..16606221,2	K562	blood:
20	chr7:16601048..16602742-chr7:16605165..16606667,2	K562	blood:
21	chr7:16117217..16117982-chr7:16604281..16605164,3	K562	blood:
22	chr7:16458453..16461047-chr7:16608151..16609870,3	K562	blood:
23	chr7:16459904..16462016-chr7:16603122..16605308,2	K562	blood:
24	chr7:16600187..16601839-chr7:16604341..16606581,2	K562	blood:
25	chr7:16473484..16474112-chr7:16604373..16605315,2	MCF-7	breast:
26	chr7:16600187..16601839-chr7:16604341..16606581,2	K562	blood:
27	chr7:16567383..16570360-chr7:16572174..16574613,3	K562	blood:
28	chr7:16471505..16472469-chr7:16603743..16605144,6	K562	blood:
29	chr7:16153898..16154837-chr7:16604199..16605221,3	MCF-7	breast:
30	chr7:16117946..16118585-chr7:16603959..16604943,2	MCF-7	breast:
31	chr7:16572386..16575354-chr7:16579474..16582374,2	K562	blood:
32	chr7:16110607..16111591-chr7:16604555..16605101,2	K562	blood:
33	chr7:16571964..16574427-chr7:16575853..16578398,3	K562	blood:
34	chr7:16567461..16570360-chr7:16570875..16573674,2	K562	blood:
35	chr7:16572386..16575354-chr7:16579474..16582374,2	K562	blood:
36	chr7:16160260..16161964-chr7:16601044..16602872,2	K562	blood:
37	chr7:16460502..16462247-chr7:16607695..16610046,2	MCF-7	breast:
38	chr7:16153998..16154693-chr7:16604258..16605163,3	K562	blood:

Variant related genes	Relation type
SOSTDC1	TF binding region
SOSTDC1	CpG island
ENSG00000214960	chromatin interactions
ENSG00000108592	chromatin interactions
ENSG00000171243	chromatin interactions
ENSG00000087191	chromatin interactions

Extended variants
information (count: 1364 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1364 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7794591	chr7:16568529-16568530	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76964181	chr7:16568622-16568623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367721962	chr7:16568643-16568644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538595663	chr7:16568648-16568649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553628676	chr7:16568718-16568719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552644663	chr7:16568790-16568791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552638110	chr7:16568842-16568843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566132426	chr7:16568861-16568862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372007997	chr7:16568890-16568891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75697446	chr7:16568893-16568894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151328154	chr7:16568898-16568899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73295288	chr7:16568907-16568908	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs576216684	chr7:16568940-16568941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368571206	chr7:16568969-16568970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189646688	chr7:16568975-16568976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577306052	chr7:16568997-16568998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541770489	chr7:16569009-16569010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180849321	chr7:16569047-16569048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35345985	chr7:16569069-16569070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530392022	chr7:16569073-16569074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142883647	chr7:16569081-16569082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554971027	chr7:16569092-16569093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116089627	chr7:16569112-16569113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562527014	chr7:16569140-16569141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140597867	chr7:16569160-16569161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76699392	chr7:16569204-16569205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549608560	chr7:16569229-16569230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144628937	chr7:16569238-16569239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138515878	chr7:16569268-16569269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561474010	chr7:16569271-16569272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs386710748	chr7:16569285-16569286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201284565	chr7:16569286-16569287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565659558	chr7:16569294-16569295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536108629	chr7:16569361-16569362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554757093	chr7:16569376-16569377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184295501	chr7:16569440-16569441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188594740	chr7:16569477-16569478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140305803	chr7:16569497-16569498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369662189	chr7:16569511-16569512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577342888	chr7:16569523-16569524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372126303	chr7:16569552-16569553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376714485	chr7:16569605-16569606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77684162	chr7:16569660-16569661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4721512	chr7:16569665-16569666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575088703	chr7:16569696-16569697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181649506	chr7:16569734-16569735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111517826	chr7:16569741-16569742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575729238	chr7:16569742-16569743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550177817	chr7:16569747-16569748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78922498	chr7:16569819-16569820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16567800-16568600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr7:16568200-16568600	Enhancers	K562	blood
3	chr7:16568400-16571000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:16569800-16570000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:16569800-16571400	Enhancers	Fetal Brain Male	brain
6	chr7:16570000-16576600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:16570800-16571800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:16571000-16572000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:16571400-16571800	Weak transcription	Fetal Brain Male	brain
10	chr7:16571400-16574000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:16571600-16572200	Enhancers	Osteobl	bone
12	chr7:16571800-16572400	Enhancers	Fetal Brain Male	brain
13	chr7:16576600-16577000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:16576600-16577000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr7:16581000-16584400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:16582000-16582200	Enhancers	Fetal Intestine Large	intestine
17	chr7:16582200-16583200	Weak transcription	Fetal Intestine Large	intestine
18	chr7:16582200-16583800	Enhancers	Stomach Mucosa	stomach
19	chr7:16583200-16583600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:16583200-16583600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:16583200-16584000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:16583200-16584000	Enhancers	Fetal Intestine Large	intestine
23	chr7:16586600-16586800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr7:16588200-16588400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:16594000-16595000	Enhancers	Fetal Heart	heart
26	chr7:16594200-16594400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:16594400-16595000	Enhancers	K562	blood
28	chr7:16594400-16597600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr7:16594600-16594800	Enhancers	Gastric	stomach
30	chr7:16595000-16596000	Weak transcription	K562	blood
31	chr7:16595000-16598800	Weak transcription	Fetal Heart	heart
32	chr7:16596000-16596600	Enhancers	K562	blood
33	chr7:16596600-16602000	Weak transcription	K562	blood
34	chr7:16598800-16599400	Enhancers	Fetal Heart	heart
35	chr7:16599200-16599400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:16599200-16600600	Enhancers	HUVEC	blood vessel
37	chr7:16599400-16609000	Weak transcription	Fetal Heart	heart
38	chr7:16599800-16600200	Enhancers	Fetal Brain Male	brain
39	chr7:16600600-16603000	Weak transcription	HUVEC	blood vessel
40	chr7:16602000-16602400	Enhancers	K562	blood
41	chr7:16602200-16602400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:16602200-16602600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:16602400-16602600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:16602400-16602800	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr7:16602400-16603800	Active TSS	K562	blood
46	chr7:16602600-16602800	Enhancers	Primary hematopoietic stem cells	blood
47	chr7:16602600-16602800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:16602600-16602800	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr7:16602600-16602800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr7:16602600-16603000	Active TSS	Primary monocytes fromperipheralblood	blood

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