Variant report

Variant	nsv1023105
Chromosome Location	chr7:17702135-17733754
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	chr7:17720492-17720803	K562	blood:	n/a	n/a
2	ARID3A	chr7:17720541-17720883	HepG2	liver:	n/a	n/a
3	ATF1	chr7:17714261-17714461	K562	blood:	n/a	n/a
4	ATF1	chr7:17729747-17729995	K562	blood:	n/a	n/a
5	ATF1	chr7:17724862-17725125	K562	blood:	n/a	n/a
6	BCL3	chr7:17719409-17720099	A549	lung:	n/a	chr7:17719888-17719897 chr7:17719765-17719774
7	BCL3	chr7:17719467-17720248	A549	lung:	n/a	chr7:17719888-17719897 chr7:17719765-17719774
8	BHLHE40	chr7:17729759-17729967	K562	blood:	n/a	n/a
9	BHLHE40	chr7:17719711-17719835	GM12878	blood:	n/a	n/a
10	BRCA1	chr7:17729210-17729955	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr7:17720466-17720857	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:17719700-17720404	A549	lung:	n/a	n/a
13	CEBPB	chr7:17729128-17730076	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:17702684-17703093	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:17713926-17713965	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr7:17719749-17719961	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:17729900-17729901	K562	blood:	n/a	n/a
18	CEBPB	chr7:17713895-17713992	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:17729626-17730082	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:17719497-17720367	A549	lung:	n/a	n/a
21	CEBPB	chr7:17729733-17729807	A549	lung:	n/a	n/a
22	CEBPB	chr7:17719644-17720156	A549	lung:	n/a	n/a
23	CEBPB	chr7:17716968-17717319	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:17713763-17714147	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:17729119-17729470	MCF-7	breast:	n/a	n/a
26	CEBPB	chr7:17719682-17720262	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:17719713-17720056	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr7:17729215-17730058	Hela-S3	cervix:	n/a	n/a
29	CREB1	chr7:17719588-17719931	A549	lung:	n/a	n/a
30	CTCF	chr7:17720600-17720750	GM12874	blood:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
31	CTCF	chr7:17720820-17720970	NHLF	lung:	n/a	n/a
32	CTCF	chr7:17720640-17720790	RPTEC	kidney:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
33	CTCF	chr7:17720465-17720924	K562	blood:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
34	CTCF	chr7:17720457-17720885	A549	lung:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
35	CTCF	chr7:17720598-17720761	GM10248	blood:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
36	CTCF	chr7:17707240-17707390	HEK293	kidney:	n/a	chr7:17707291-17707301
37	CTCF	chr7:17720365-17720909	IMR90	lung:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
38	CTCF	chr7:17720444-17721058	GM12878	blood:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
39	CTCF	chr7:17720900-17721050	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr7:17720593-17720755	A549	lung:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
41	CTCF	chr7:17706872-17706912	Lung_OC	lung:	n/a	n/a
42	CTCF	chr7:17720538-17720813	Lung_OC	lung:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
43	CTCF	chr7:17720936-17720952	GM19240	blood:	n/a	n/a
44	CTCF	chr7:17720640-17720790	HFF	foreskin:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
45	CTCF	chr7:17720620-17720770	AG04449	skin:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
46	CTCF	chr7:17720600-17720750	AG09319	gingival:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
47	CTCF	chr7:17720940-17721090	GM12870	blood:	n/a	n/a
48	CTCF	chr7:17720680-17720830	SK-N-SH_RA	brain:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
49	CTCF	chr7:17720620-17720770	HVMF	connective:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
50	CTCF	chr7:17720434-17720958	MCF-7	breast:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17730027-17730077	NHBE	bronchial:	n/a
2	chr7:17730027-17730077	LNCaP	prostate:	n/a
3	chr7:17704924-17704974	RPTEC	kidney:	n/a
4	chr7:17704924-17704974	PrEC	prostate:	n/a
5	chr7:17704951-17705001	NHBE	bronchial:	n/a
6	chr7:17704951-17705001	HMEC	breast:	n/a
7	chr7:17720468-17720518	NB4	blood:	n/a
8	chr7:17704951-17705001	HRPEpiC	eye:	n/a
9	chr7:17730027-17730077	GM12891	blood:	n/a
10	chr7:17704924-17704974	SKMC	muscle:	n/a
11	chr7:17704951-17705001	NHDF-neo	bronchial:	n/a
12	chr7:17704951-17705001	BE2_C	brain:	n/a
13	chr7:17720468-17720518	K562	blood:	n/a
14	chr7:17704924-17704974	NH-A	brain:	n/a
15	chr7:17704951-17705001	AG09309	skin:	n/a
16	chr7:17720468-17720518	SK-N-SH	brain:	n/a
17	chr7:17720468-17720518	SAEC	small airway:	n/a
18	chr7:17730027-17730077	GM12892	blood:	n/a
19	chr7:17704951-17705001	NB4	blood:	n/a
20	chr7:17702198-17702248	AG04449	skin:	fetal
21	chr7:17720468-17720518	A549	lung:	n/a
22	chr7:17704951-17705001	HCPEpiC	choroid plexus:	n/a
23	chr7:17704924-17704974	HL-60	blood:	n/a
24	chr7:17704951-17705001	Jurkat	blood:	n/a
25	chr7:17704924-17704974	GM12891	blood:	n/a
26	chr7:17704951-17705001	PFSK-1	brain:	n/a
27	chr7:17720468-17720518	Hepatocyte	liver:	n/a
28	chr7:17702198-17702248	CMK	blood:	n/a
29	chr7:17702198-17702248	SK-N-SH_RA	brain:	n/a
30	chr7:17702198-17702248	NB4	blood:	n/a
31	chr7:17702198-17702248	U87	brain:	n/a
32	chr7:17702198-17702248	BJ	skin:	n/a
33	chr7:17730027-17730077	SK-N-SH_RA	brain:	n/a
34	chr7:17704924-17704974	A549	lung:	n/a
35	chr7:17704924-17704974	MCF10A-Er-Src	breast:	n/a
36	chr7:17720468-17720518	HCPEpiC	choroid plexus:	n/a
37	chr7:17702198-17702248	NT2-D1	testis:	n/a
38	chr7:17730027-17730077	SKMC	muscle:	n/a
39	chr7:17704924-17704974	GM12878	blood:	n/a
40	chr7:17702198-17702248	HCT-116	colon:	n/a
41	chr7:17704924-17704974	HUVEC	blood vessel:	n/a
42	chr7:17704924-17704974	Hela-S3	cervix:	n/a
43	chr7:17720468-17720518	AG10803	skin:	n/a
44	chr7:17720468-17720518	GM12891	blood:	n/a
45	chr7:17730027-17730077	BJ	skin:	n/a
46	chr7:17704924-17704974	HNPCEpiC	eye:	n/a
47	chr7:17704924-17704974	NB4	blood:	n/a
48	chr7:17702198-17702248	NHDF-neo	bronchial:	n/a
49	chr7:17704924-17704974	AG10803	skin:	n/a
50	chr7:17704924-17704974	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:17712355..17715598-chr7:17735050..17738524,3	MCF-7	breast:
2	chr7:17702578..17704543-chr7:17713221..17714766,2	MCF-7	breast:
3	chr7:17709533..17711370-chr7:17717501..17719526,2	MCF-7	breast:
4	chr7:17720220..17720870-chr7:20637924..20638671,2	K562	blood:
5	chr7:17702578..17704543-chr7:17713221..17714766,2	MCF-7	breast:
6	chr7:17728037..17729747-chr7:17732682..17734758,2	MCF-7	breast:
7	chr7:17720091..17721114-chr7:17746094..17746756,4	MCF-7	breast:
8	chr7:17728037..17729747-chr7:17732682..17734758,2	MCF-7	breast:
9	chr17:59488041..59490128-chr7:17728518..17731177,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX13-3	chr7:17719080-17719218	NONHSAT119341
2	lnc-AHR-3	chr7:17720085-17720283	XLOC_005999
3	lnc-AHR-3	chr7:17719173-17719246	XLOC_005999

Variant related genes	Relation type
ENSG00000228675	TF binding region
ENSG00000228675	CpG island
ENSG00000187013	chromatin interactions
ENSG00000228675	chromatin interactions
ENSG00000267280	chromatin interactions
SPIN4	miRNA target sites

Extended variants
information (count: 1536 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10488471	chr7:17702135-17702136	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542232284	chr7:17702137-17702138	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs191818818	chr7:17702162-17702163	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs574424720	chr7:17702194-17702195	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs543325864	chr7:17702205-17702206	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs60464669	chr7:17702232-17702233	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs71010262	chr7:17702242-17702243	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs180852236	chr7:17702251-17702252	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs2389829	chr7:17702281-17702282	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs185065191	chr7:17702282-17702283	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs544260518	chr7:17702306-17702307	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs532756160	chr7:17702310-17702311	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs190269000	chr7:17702358-17702359	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs182475276	chr7:17702403-17702404	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs138346333	chr7:17702412-17702413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs548628049	chr7:17702424-17702425	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs556507700	chr7:17702488-17702489	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs369636315	chr7:17702491-17702492	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs199844286	chr7:17702492-17702493	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs567442100	chr7:17702503-17702504	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs538183938	chr7:17702506-17702507	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs187478210	chr7:17702540-17702541	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs571376465	chr7:17702552-17702553	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs75898071	chr7:17702558-17702559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs553417730	chr7:17702565-17702566	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs571844607	chr7:17702581-17702582	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs149609197	chr7:17702591-17702592	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs115726062	chr7:17702622-17702623	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs575958034	chr7:17702654-17702655	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544046036	chr7:17702656-17702657	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs530261543	chr7:17702683-17702684	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs540243541	chr7:17702733-17702734	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs117206008	chr7:17702788-17702789	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs112497590	chr7:17702797-17702798	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577477197	chr7:17702799-17702800	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs76556075	chr7:17702808-17702809	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs559862119	chr7:17702887-17702888	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs74548324	chr7:17702912-17702913	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs191971574	chr7:17702935-17702936	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs551720644	chr7:17702939-17702940	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs563662903	chr7:17702948-17702949	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs2110017	chr7:17702986-17702987	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs550023484	chr7:17702987-17702988	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs143354302	chr7:17703006-17703007	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532160709	chr7:17703018-17703019	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs74806356	chr7:17703026-17703027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs183307260	chr7:17703080-17703081	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs77975978	chr7:17703106-17703107	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs374691577	chr7:17703112-17703113	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs530734036	chr7:17703113-17703114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Sezary syndrome	18413736	CNVD
Autism	22495309	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17699000-17703800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:17699600-17703400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:17699600-17703600	Enhancers	HMEC	breast
4	chr7:17699800-17703600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr7:17699800-17703800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:17700000-17703800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr7:17701000-17703200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr7:17701000-17703600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:17701000-17703600	Enhancers	Osteobl	bone
10	chr7:17701200-17702800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:17701200-17703400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr7:17701200-17703800	Enhancers	NHLF	lung
13	chr7:17701400-17703400	Enhancers	NH-A	brain
14	chr7:17701400-17703600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr7:17701600-17702200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:17701600-17702200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:17701600-17702200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:17701600-17703000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:17701600-17703200	Enhancers	HSMM	muscle
20	chr7:17701600-17703400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:17701800-17702200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr7:17701800-17702200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:17701800-17702200	Enhancers	Stomach Mucosa	stomach
24	chr7:17701800-17702200	Flanking Active TSS	NHDF-Ad	bronchial
25	chr7:17701800-17702600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr7:17701800-17702600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr7:17701800-17702600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:17701800-17702600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:17701800-17702600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:17701800-17702600	Enhancers	Placenta	Placenta
31	chr7:17701800-17702600	Enhancers	Pancreas	Pancrea
32	chr7:17701800-17702800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:17701800-17702800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:17701800-17702800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:17701800-17702800	Enhancers	Esophagus	oesophagus
36	chr7:17701800-17702800	Enhancers	Fetal Muscle Leg	muscle
37	chr7:17701800-17702800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr7:17701800-17702800	Enhancers	Right Atrium	heart
39	chr7:17701800-17702800	Flanking Active TSS	NHEK	skin
40	chr7:17701800-17703000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr7:17701800-17703000	Enhancers	HSMMtube	muscle
42	chr7:17702000-17702600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:17702000-17702800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:17702000-17703200	Enhancers	A549	lung
45	chr7:17702200-17702400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:17702200-17702400	Enhancers	NHDF-Ad	bronchial
47	chr7:17702200-17702600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr7:17702200-17702800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr7:17702200-17703200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:17702400-17702800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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