Variant report

Variant	nsv605934
Chromosome Location	chr7:3687012-3738147
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	BACH1	chr7:3731377-3731827	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:3713169-3713470	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:3721967-3722323	HepG2	liver:	n/a	n/a
4	CEBPB	chr7:3722310-3722477	HepG2	liver:	n/a	chr7:3722426-3722437
5	CEBPB	chr7:3722392-3722443	IMR90	lung:	n/a	chr7:3722426-3722437
6	CEBPB	chr7:3689739-3690076	HepG2	liver:	n/a	chr7:3689906-3689917
7	CEBPB	chr7:3689754-3690077	K562	blood:	n/a	chr7:3689906-3689917
8	CEBPB	chr7:3689750-3690087	Hela-S3	cervix:	n/a	chr7:3689906-3689917
9	CEBPB	chr7:3732825-3733006	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:3722260-3722580	HepG2	liver:	n/a	chr7:3722426-3722437
11	CEBPB	chr7:3735440-3735874	A549	lung:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
12	CEBPB	chr7:3689783-3689977	H1-hESC	embryonic stem cell:	n/a	chr7:3689906-3689917
13	CEBPB	chr7:3689713-3690022	MCF-7	breast:	n/a	chr7:3689906-3689917
14	CEBPB	chr7:3689734-3690090	A549	lung:	n/a	chr7:3689906-3689917
15	CEBPB	chr7:3689730-3690095	IMR90	lung:	n/a	chr7:3689906-3689917
16	CEBPB	chr7:3735419-3735759	H1-hESC	embryonic stem cell:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
17	CEBPB	chr7:3735439-3735877	K562	blood:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
18	CEBPB	chr7:3735387-3735863	HepG2	liver:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
19	CHD2	chr7:3723200-3723390	HepG2	liver:	n/a	n/a
20	CHD2	chr7:3713229-3713285	HepG2	liver:	n/a	n/a
21	CTCF	chr7:3735345-3735557	T-47D	breast:	n/a	chr7:3735433-3735451
22	CTCF	chr7:3688940-3689090	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr7:3713260-3713410	HEEpiC	esophagus:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
24	CTCF	chr7:3735365-3735516	HepG2	liver:	n/a	chr7:3735433-3735451
25	CTCF	chr7:3713266-3713407	A549	lung:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
26	CTCF	chr7:3713260-3713410	GM12864	blood:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
27	CTCF	chr7:3713240-3713390	AG04450	lung:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
28	CTCF	chr7:3713260-3713453	Hela-S3	cervix:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
29	CTCF	chr7:3688964-3689119	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:3713260-3713410	GM12868	blood:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
31	CTCF	chr7:3735400-3735550	GM12864	blood:	n/a	chr7:3735433-3735451
32	CTCF	chr7:3713260-3713410	AG04450	lung:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
33	CTCF	chr7:3688694-3689390	SK-N-SH	brain:	n/a	n/a
34	CTCF	chr7:3713220-3713370	GM12869	blood:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
35	CTCF	chr7:3735380-3735512	GM19239	blood:	n/a	chr7:3735433-3735451
36	CTCF	chr7:3735380-3735530	HRE	kidney:	n/a	chr7:3735433-3735451
37	CTCF	chr7:3735280-3735430	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr7:3735380-3735530	HMF	breast:	n/a	chr7:3735433-3735451
39	CTCF	chr7:3735320-3735470	GM12867	blood:	n/a	chr7:3735433-3735451
40	CTCF	chr7:3733918-3733927	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:3713260-3713410	SK-N-SH_RA	brain:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
42	CTCF	chr7:3713260-3713410	HPAF	blood vessel:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
43	CTCF	chr7:3713300-3713450	GM12866	blood:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
44	CTCF	chr7:3735320-3735470	GM12869	blood:	n/a	chr7:3735433-3735451
45	CTCF	chr7:3688980-3689130	RPTEC	kidney:	n/a	n/a
46	CTCF	chr7:3688920-3689070	NHEK	skin:	n/a	n/a
47	CTCF	chr7:3688960-3689110	NHEK	skin:	n/a	n/a
48	CTCF	chr7:3713280-3713430	SK-N-SH_RA	brain:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
49	CTCF	chr7:3713306-3713441	GM13977	blood:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
50	CTCF	chr7:3688970-3689092	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3713348-3713398	CMK	blood:	n/a
2	chr7:3710628-3710678	AG10803	skin:	n/a
3	chr7:3710628-3710678	HRCEpiC	kidney:	n/a
4	chr7:3713348-3713398	AG09319	gingival:	n/a
5	chr7:3723660-3723710	Caco-2	colon:	n/a
6	chr7:3710628-3710678	SAEC	small airway:	n/a
7	chr7:3727189-3727239	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:3727166-3727216	HRCEpiC	kidney:	n/a
9	chr7:3710628-3710678	RPTEC	kidney:	n/a
10	chr7:3727166-3727216	MCF10A-Er-Src	breast:	n/a
11	chr7:3723660-3723710	NB4	blood:	n/a
12	chr7:3713348-3713398	BE2_C	brain:	n/a
13	chr7:3723660-3723710	HRE	kidney:	n/a
14	chr7:3723660-3723710	U87	brain:	n/a
15	chr7:3727166-3727216	SK-N-SH	brain:	n/a
16	chr7:3710628-3710678	Caco-2	colon:	n/a
17	chr7:3691268-3691318	HIPEpiC	eye:	n/a
18	chr7:3727166-3727216	HUVEC	blood vessel:	n/a
19	chr7:3727189-3727239	BE2_C	brain:	n/a
20	chr7:3723660-3723710	NHBE	bronchial:	n/a
21	chr7:3727189-3727239	AoSMC	blood vessel:	n/a
22	chr7:3727166-3727216	BJ	skin:	n/a
23	chr7:3723660-3723710	ovcar-3	ovarian:	n/a
24	chr7:3691268-3691318	H1-hESC	embryonic stem cell:	embryo
25	chr7:3727189-3727239	H1-hESC	embryonic stem cell:	embryo
26	chr7:3713348-3713398	NT2-D1	testis:	n/a
27	chr7:3727189-3727239	NB4	blood:	n/a
28	chr7:3723660-3723710	AG09309	skin:	n/a
29	chr7:3727166-3727216	AG09319	gingival:	n/a
30	chr7:3710628-3710678	ovcar-3	ovarian:	n/a
31	chr7:3727189-3727239	GM19239	blood:	n/a
32	chr7:3727166-3727216	MCF-7	breast:	n/a
33	chr7:3723660-3723710	BJ	skin:	n/a
34	chr7:3713348-3713398	PrEC	prostate:	n/a
35	chr7:3691268-3691318	AG10803	skin:	n/a
36	chr7:3713348-3713398	GM06990	blood:	n/a
37	chr7:3727166-3727216	U87	brain:	n/a
38	chr7:3727166-3727216	ProgFib	skin:	n/a
39	chr7:3713348-3713398	LNCaP	prostate:	n/a
40	chr7:3713348-3713398	SAEC	small airway:	n/a
41	chr7:3713348-3713398	RPTEC	kidney:	n/a
42	chr7:3710628-3710678	HNPCEpiC	eye:	n/a
43	chr7:3691268-3691318	ECC-1	luminal epithelium:	n/a
44	chr7:3723660-3723710	HUVEC	blood vessel:	n/a
45	chr7:3710628-3710678	SKMC	muscle:	n/a
46	chr7:3691268-3691318	U87	brain:	n/a
47	chr7:3723660-3723710	HepG2	liver:	n/a
48	chr7:3727189-3727239	Jurkat	blood:	n/a
49	chr7:3723660-3723710	NHDF-neo	bronchial:	n/a
50	chr7:3727166-3727216	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:
2	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
3	chr7:3681955..3684927-chr7:3685128..3688064,3	K562	blood:
4	chr7:3522949..3523470-chr7:3687761..3688597,2	MCF-7	breast:
5	chr4:37757943..37758649-chr7:3694176..3695010,2	MCF-7	breast:
6	chr7:3521755..3523053-chr7:3688631..3689551,7	MCF-7	breast:
7	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
8	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
9	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
10	chr7:3734945..3735889-chr7:3936899..3937757,3	MCF-7	breast:
11	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:

Variant related genes	Relation type
ENSG00000236510	TF binding region
ENSG00000236510	CpG island
ENSG00000236510	chromatin interactions

Extended variants
information (count: 3206 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3206 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7793515	chr7:3687012-3687013	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548117872	chr7:3687013-3687014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs55860374	chr7:3687047-3687048	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs567675560	chr7:3687051-3687052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs190333912	chr7:3687067-3687068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550305359	chr7:3687085-3687086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570200879	chr7:3687095-3687096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs6980237	chr7:3687096-3687097	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs558743384	chr7:3687108-3687109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545251276	chr7:3687127-3687128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7793775	chr7:3687132-3687133	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs534932715	chr7:3687139-3687140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7792749	chr7:3687169-3687170	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574384695	chr7:3687178-3687179	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550121808	chr7:3687182-3687183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543054590	chr7:3687189-3687190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376368887	chr7:3687204-3687205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183024987	chr7:3687208-3687209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs114590232	chr7:3687212-3687213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545183405	chr7:3687233-3687234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs61175597	chr7:3687234-3687235	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs527953882	chr7:3687242-3687243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185449402	chr7:3687243-3687244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561083537	chr7:3687253-3687254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374326457	chr7:3687258-3687259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190208648	chr7:3687274-3687275	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs28740932	chr7:3687281-3687282	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569700673	chr7:3687301-3687302	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113948288	chr7:3687306-3687307	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182758625	chr7:3687307-3687308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568419571	chr7:3687308-3687309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs376252398	chr7:3687312-3687313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187475744	chr7:3687345-3687346	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565888227	chr7:3687347-3687348	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs143604180	chr7:3687351-3687352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554840498	chr7:3687352-3687353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568061240	chr7:3687358-3687359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs115237314	chr7:3687364-3687365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556574851	chr7:3687403-3687404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576497887	chr7:3687424-3687425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs111801760	chr7:3687439-3687440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141746477	chr7:3687477-3687478	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572612703	chr7:3687494-3687495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551237798	chr7:3687527-3687528	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1025456	chr7:3687542-3687543	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs561620953	chr7:3687555-3687556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192722113	chr7:3687573-3687574	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs115558126	chr7:3687578-3687579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563686700	chr7:3687579-3687580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555301391	chr7:3687584-3687585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3671000-3695600	Weak transcription	Fetal Intestine Small	intestine
2	chr7:3676200-3688600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:3676600-3687800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:3679800-3690400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:3681200-3695400	Weak transcription	Spleen	Spleen
6	chr7:3682200-3687800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr7:3682400-3687400	Weak transcription	Fetal Stomach	stomach
8	chr7:3683000-3693000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr7:3683200-3695600	Weak transcription	Pancreas	Pancrea
10	chr7:3683400-3688400	Weak transcription	Aorta	Aorta
11	chr7:3683400-3693400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:3683800-3696000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:3687800-3688200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:3687800-3688200	Enhancers	NHDF-Ad	bronchial
15	chr7:3687800-3688400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr7:3688400-3688600	Strong transcription	Aorta	Aorta
17	chr7:3688400-3703200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr7:3688600-3688800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:3688600-3688800	ZNF genes & repeats	Aorta	Aorta
20	chr7:3688800-3703200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:3688800-3728400	Weak transcription	Aorta	Aorta
22	chr7:3690400-3690800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr7:3690800-3691800	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr7:3691800-3692000	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr7:3692000-3692600	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr7:3693400-3694400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:3694400-3705800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:3695400-3695600	Enhancers	Spleen	Spleen
29	chr7:3695400-3695800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr7:3695400-3695800	Enhancers	Stomach Mucosa	stomach
31	chr7:3695600-3695800	Enhancers	Fetal Intestine Small	intestine
32	chr7:3695600-3696000	Enhancers	Pancreas	Pancrea
33	chr7:3695800-3699400	Weak transcription	Stomach Mucosa	stomach
34	chr7:3696000-3707800	Weak transcription	Pancreas	Pancrea
35	chr7:3696800-3697200	Enhancers	Fetal Muscle Trunk	muscle
36	chr7:3696800-3697400	Enhancers	Fetal Muscle Leg	muscle
37	chr7:3696800-3697400	Enhancers	HSMM	muscle
38	chr7:3696800-3697600	Enhancers	HSMMtube	muscle
39	chr7:3697000-3697400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:3699600-3700600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:3700000-3700200	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr7:3700200-3704000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr7:3703000-3704000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr7:3703200-3703400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:3703200-3703800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr7:3703200-3704000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:3703400-3703800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:3703800-3704000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:3704000-3709000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr7:3704000-3723600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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