Variant report

Variant	nsv1028585
Chromosome Location	chr7:3364990-3400105
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:3385311-3385328	K562	blood:	n/a	n/a
2	BACH1	chr7:3370227-3370294	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:3369047-3369093	K562	blood:	n/a	n/a
4	CEBPB	chr7:3393401-3393650	HepG2	liver:	n/a	chr7:3393579-3393590
5	CEBPB	chr7:3393443-3393652	A549	lung:	n/a	chr7:3393579-3393590
6	CTCF	chr7:3395040-3395190	NHEK	skin:	n/a	n/a
7	CTCF	chr7:3398787-3398879	MCF-7	breast:	n/a	n/a
8	CTCF	chr7:3394994-3395106	MCF-7	breast:	n/a	n/a
9	CTCF	chr7:3398734-3398899	HepG2	liver:	n/a	n/a
10	CTCF	chr7:3395220-3395370	NB4	blood:	n/a	n/a
11	CTCF	chr7:3398720-3398870	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:3398740-3398890	HEK293	kidney:	n/a	n/a
13	CTCF	chr7:3398675-3398910	K562	blood:	n/a	n/a
14	CTCF	chr7:3395079-3395151	K562	blood:	n/a	n/a
15	CTCF	chr7:3395100-3395250	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr7:3394980-3395130	GM12870	blood:	n/a	n/a
17	CTCF	chr7:3395012-3395142	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr7:3394960-3395110	HepG2	liver:	n/a	n/a
19	CTCF	chr7:3395002-3395091	Fibrobl	skin:	n/a	n/a
20	CTCF	chr7:3384695-3384722	Lung_OC	lung:	n/a	n/a
21	CTCF	chr7:3398820-3398970	HEK293	kidney:	n/a	n/a
22	CTCF	chr7:3398736-3398878	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:3394940-3395090	GM12873	blood:	n/a	n/a
24	CTCF	chr7:3398674-3398951	K562	blood:	n/a	n/a
25	CTCF	chr7:3395040-3395190	GM12865	blood:	n/a	n/a
26	CTCF	chr7:3395050-3395089	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:3378061-3378112	LNCaP	prostate:	n/a	n/a
28	CTCF	chr7:3394980-3395130	GM12874	blood:	n/a	n/a
29	CTCF	chr7:3398672-3399010	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:3395040-3395190	K562	blood:	n/a	n/a
31	CTCF	chr7:3398787-3398830	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:3395037-3395070	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:3395000-3395150	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr7:3398811-3398884	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:3398610-3399028	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:3395020-3395170	GM12864	blood:	n/a	n/a
37	CTCF	chr7:3395000-3395150	GM12865	blood:	n/a	n/a
38	CTCF	chr7:3395000-3395150	GM12864	blood:	n/a	n/a
39	CTCF	chr7:3395000-3395150	GM12875	blood:	n/a	n/a
40	CTCF	chr7:3398699-3398881	K562	blood:	n/a	n/a
41	CTCF	chr7:3395000-3395150	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:3395020-3395170	HEK293	kidney:	n/a	n/a
43	CTCF	chr7:3395040-3395190	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr7:3398743-3398931	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr7:3395020-3395170	GM12873	blood:	n/a	n/a
46	CTCF	chr7:3398780-3398930	Caco-2	colon:	n/a	n/a
47	CTCF	chr7:3394980-3395130	GM12871	blood:	n/a	n/a
48	CTCF	chr7:3395020-3395170	GM12872	blood:	n/a	n/a
49	CTCF	chr7:3398880-3399030	GM12867	blood:	n/a	n/a
50	CTCF	chr7:3398840-3398990	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3385318-3385368	HRCEpiC	kidney:	n/a
2	chr7:3375859-3375909	AG09319	gingival:	n/a
3	chr7:3385318-3385368	GM12878	blood:	n/a
4	chr7:3385318-3385368	A549	lung:	n/a
5	chr7:3385318-3385368	PrEC	prostate:	n/a
6	chr7:3385318-3385368	MCF-7	breast:	n/a
7	chr7:3375859-3375909	MCF-7	breast:	n/a
8	chr7:3385318-3385368	H1-hESC	embryonic stem cell:	embryo
9	chr7:3385318-3385368	GM12891	blood:	n/a
10	chr7:3375859-3375909	AG09309	skin:	n/a
11	chr7:3375859-3375909	HRE	kidney:	n/a
12	chr7:3375859-3375909	Jurkat	blood:	n/a
13	chr7:3375859-3375909	LNCaP	prostate:	n/a
14	chr7:3375859-3375909	NHBE	bronchial:	n/a
15	chr7:3385318-3385368	CMK	blood:	n/a
16	chr7:3375859-3375909	PrEC	prostate:	n/a
17	chr7:3375859-3375909	GM19239	blood:	n/a
18	chr7:3385318-3385368	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:3375859-3375909	PFSK-1	brain:	n/a
20	chr7:3375859-3375909	AoSMC	blood vessel:	n/a
21	chr7:3385318-3385368	HAEpiC	amniotic membrane:	n/a
22	chr7:3375859-3375909	HUVEC	blood vessel:	n/a
23	chr7:3375859-3375909	GM12891	blood:	n/a
24	chr7:3375859-3375909	SAEC	small airway:	n/a
25	chr7:3375859-3375909	HIPEpiC	eye:	n/a
26	chr7:3375859-3375909	BJ	skin:	n/a
27	chr7:3385318-3385368	HIPEpiC	eye:	n/a
28	chr7:3375859-3375909	GM12892	blood:	n/a
29	chr7:3375859-3375909	ovcar-3	ovarian:	n/a
30	chr7:3375859-3375909	Hepatocyte	liver:	n/a
31	chr7:3375859-3375909	U87	brain:	n/a
32	chr7:3385318-3385368	Jurkat	blood:	n/a
33	chr7:3375859-3375909	HCF	heart:	n/a
34	chr7:3385318-3385368	HRPEpiC	eye:	n/a
35	chr7:3385318-3385368	HEK293	kidney:	embryo
36	chr7:3375859-3375909	AG04450	lung:	fetal
37	chr7:3375859-3375909	AG04449	skin:	fetal
38	chr7:3385318-3385368	AG04449	skin:	fetal
39	chr7:3375859-3375909	RPTEC	kidney:	n/a
40	chr7:3385318-3385368	GM12892	blood:	n/a
41	chr7:3375859-3375909	SK-N-SH	brain:	n/a
42	chr7:3375859-3375909	MCF10A-Er-Src	breast:	n/a
43	chr7:3375859-3375909	HCM	heart:	n/a
44	chr7:3385318-3385368	SAEC	small airway:	n/a
45	chr7:3385318-3385368	NHBE	bronchial:	n/a
46	chr7:3375859-3375909	A549	lung:	n/a
47	chr7:3385318-3385368	U87	brain:	n/a
48	chr7:3375859-3375909	BE2_C	brain:	n/a
49	chr7:3385318-3385368	RPTEC	kidney:	n/a
50	chr7:3375859-3375909	NT2-D1	testis:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3381518..3384288-chr7:3389563..3392329,2	MCF-7	breast:
2	chr7:3385347..3387562-chr7:3388126..3390584,2	K562	blood:
3	chr7:3379742..3382229-chr7:3382243..3386040,3	K562	blood:
4	chr7:3385347..3387289-chr7:3389084..3391687,2	K562	blood:
5	chr7:3388931..3391698-chr7:3393863..3395884,2	K562	blood:
6	chr7:3381518..3384288-chr7:3389563..3392329,2	MCF-7	breast:
7	chr7:3378023..3380579-chr7:3388510..3390019,2	MCF-7	breast:
8	chr7:3385347..3387289-chr7:3389084..3391687,2	K562	blood:
9	chr7:3378023..3380579-chr7:3388510..3390019,2	MCF-7	breast:
10	chr7:3349154..3351811-chr7:3384855..3387148,2	MCF-7	breast:
11	chr7:3398782..3400855-chr7:3415548..3417886,2	MCF-7	breast:
12	chr7:3388931..3391698-chr7:3393863..3395884,2	K562	blood:
13	chr7:3379742..3382229-chr7:3382243..3386040,3	K562	blood:
14	chr7:3390810..3392669-chr7:3397273..3399419,2	MCF-7	breast:
15	chr7:3385347..3387562-chr7:3388126..3390584,2	K562	blood:
16	chr7:3390810..3392669-chr7:3397273..3399419,2	MCF-7	breast:
17	chr7:3354663..3356940-chr7:3364964..3367662,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMZ1-7	chr7:3377521-3378121	NONHSAT118850
2	lnc-AMZ1-7	chr7:3377758-3378233	NONHSAT118851

No data

Variant related genes	Relation type
ENSG00000224593	TF binding region
ENSG00000224593	CpG island

Extended variants
information (count: 1991 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1991 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7798768	chr7:3365055-3365056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549327745	chr7:3365066-3365067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532959006	chr7:3365074-3365075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186135182	chr7:3365155-3365156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569625492	chr7:3365158-3365159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551828110	chr7:3365164-3365165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571865697	chr7:3365172-3365173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190102079	chr7:3365230-3365231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181345633	chr7:3365257-3365258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138865190	chr7:3365265-3365266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185808244	chr7:3365268-3365269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556108187	chr7:3365300-3365301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575998902	chr7:3365302-3365303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545287106	chr7:3365326-3365327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377320575	chr7:3365349-3365350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572020825	chr7:3365381-3365382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540791322	chr7:3365395-3365396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142787428	chr7:3365415-3365416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7780498	chr7:3365441-3365442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs542789537	chr7:3365448-3365449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78206479	chr7:3365504-3365505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182720226	chr7:3365515-3365516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189033307	chr7:3365537-3365538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11312480	chr7:3365540-3365541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551754239	chr7:3365541-3365542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571936824	chr7:3365567-3365568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528014353	chr7:3365571-3365572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7779576	chr7:3365572-3365573	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs567894009	chr7:3365577-3365578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368622723	chr7:3365584-3365585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549659686	chr7:3365612-3365613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147278448	chr7:3365617-3365618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374679624	chr7:3365620-3365621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538217517	chr7:3365663-3365664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191967223	chr7:3365675-3365676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182736493	chr7:3365722-3365723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187460122	chr7:3365768-3365769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140770853	chr7:3365794-3365795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554303449	chr7:3365821-3365822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs117044151	chr7:3365848-3365849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56692246	chr7:3365849-3365850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs59604371	chr7:3365854-3365855	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs576489238	chr7:3365863-3365864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545394263	chr7:3365884-3365885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192224405	chr7:3365888-3365889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527975163	chr7:3365895-3365896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548149302	chr7:3365896-3365897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561465547	chr7:3365936-3365937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530190467	chr7:3365939-3365940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550361584	chr7:3365957-3365958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Urothelial carcinoma	21177765	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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3344600-3366600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:3350200-3366800	Weak transcription	Fetal Brain Male	brain
3	chr7:3358800-3366800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:3359000-3385800	Weak transcription	Pancreas	Pancrea
5	chr7:3363400-3377800	Weak transcription	Aorta	Aorta
6	chr7:3364600-3367800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr7:3366600-3366800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:3366800-3367400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:3366800-3367600	Enhancers	Fetal Brain Male	brain
10	chr7:3366800-3372600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:3367400-3367800	Enhancers	Fetal Heart	heart
12	chr7:3367800-3373000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:3372000-3372800	Enhancers	Colon Smooth Muscle	Colon
14	chr7:3372400-3373200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:3372400-3373200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr7:3372400-3373400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:3372600-3373200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:3372600-3373400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:3372600-3373400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:3372600-3373600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr7:3372600-3374200	Enhancers	Left Ventricle	heart
22	chr7:3373000-3373200	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr7:3373200-3373400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:3373200-3377400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr7:3373400-3375600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:3373400-3378200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:3374000-3374200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:3374200-3375600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:3375400-3376200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr7:3375600-3376000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:3375600-3376000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:3375600-3376000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:3375600-3376000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:3375600-3376200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:3375800-3376200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:3375800-3376200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:3375800-3376600	Enhancers	Esophagus	oesophagus
38	chr7:3376000-3376200	Enhancers	Left Ventricle	heart
39	chr7:3376200-3385800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:3377200-3378200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:3377400-3378400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr7:3377400-3378600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:3377800-3378200	Enhancers	Aorta	Aorta
44	chr7:3378600-3383200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr7:3383200-3384200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:3384200-3389800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr7:3385400-3385800	Enhancers	Brain Anterior Caudate	brain
48	chr7:3385800-3386000	Enhancers	Pancreas	Pancrea
49	chr7:3385800-3386200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:3386000-3388800	Weak transcription	Aorta	Aorta

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