Variant report

Variant	nsv1031116
Chromosome Location	chr7:15428343-15568587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:456)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:15447516-15447947	K562	blood:	n/a	n/a
2	BRCA1	chr7:15511560-15511688	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr7:15447539-15447839	K562	blood:	n/a	n/a
4	CEBPB	chr7:15544100-15544369	A549	lung:	n/a	chr7:15544193-15544204
5	CEBPB	chr7:15483624-15483679	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr7:15466810-15467126	IMR90	lung:	n/a	chr7:15466942-15466953
7	CEBPB	chr7:15468127-15468377	HepG2	liver:	n/a	chr7:15468226-15468237
8	CEBPB	chr7:15435437-15435631	A549	lung:	n/a	n/a
9	CEBPB	chr7:15478355-15478692	A549	lung:	n/a	chr7:15478519-15478530
10	CEBPB	chr7:15435469-15435633	K562	blood:	n/a	n/a
11	CEBPB	chr7:15466804-15467001	K562	blood:	n/a	chr7:15466942-15466953
12	CEBPB	chr7:15435411-15435690	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:15506122-15506411	A549	lung:	n/a	chr7:15506286-15506297
14	CEBPB	chr7:15506113-15506415	IMR90	lung:	n/a	chr7:15506286-15506297
15	CEBPB	chr7:15478389-15478692	HepG2	liver:	n/a	chr7:15478519-15478530
16	CEBPB	chr7:15458749-15459010	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:15483579-15483676	K562	blood:	n/a	chr7:15483605-15483616
18	CEBPB	chr7:15483484-15483779	IMR90	lung:	n/a	chr7:15483605-15483616
19	CEBPB	chr7:15458696-15459049	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:15466850-15467116	HepG2	liver:	n/a	chr7:15466942-15466953
21	CEBPB	chr7:15458726-15459040	A549	lung:	n/a	n/a
22	CEBPB	chr7:15447580-15447867	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:15478370-15478666	IMR90	lung:	n/a	chr7:15478519-15478530
24	CEBPB	chr7:15458723-15459054	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:15506112-15506438	HepG2	liver:	n/a	chr7:15506286-15506297
26	CEBPB	chr7:15483429-15483757	HepG2	liver:	n/a	chr7:15483605-15483616
27	CEBPB	chr7:15515554-15515644	A549	lung:	n/a	n/a
28	CEBPB	chr7:15468148-15468383	IMR90	lung:	n/a	chr7:15468226-15468237
29	CTCF	chr7:15428840-15428990	GM12871	blood:	n/a	n/a
30	CTCF	chr7:15563840-15563990	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr7:15543680-15543830	AG04450	lung:	n/a	chr7:15543711-15543727
32	CTCF	chr7:15428820-15428970	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr7:15428780-15428930	HVMF	connective:	n/a	n/a
34	CTCF	chr7:15543960-15544110	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr7:15543600-15543750	HUVEC	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
36	CTCF	chr7:15519460-15519610	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr7:15543580-15543730	AoAF	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
38	CTCF	chr7:15543480-15543630	NHLF	lung:	n/a	n/a
39	CTCF	chr7:15543620-15543770	HA-sp	spinal cord:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
40	CTCF	chr7:15543600-15543750	AoAF	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
41	CTCF	chr7:15563820-15563970	AG09319	gingival:	n/a	n/a
42	CTCF	chr7:15543672-15543693	Medullo	brain:	n/a	n/a
43	CTCF	chr7:15563760-15563910	HCM	heart:	n/a	n/a
44	CTCF	chr7:15428740-15429011	GM12878	blood:	n/a	n/a
45	CTCF	chr7:15428860-15429010	HFF	foreskin:	n/a	n/a
46	CTCF	chr7:15563780-15563930	AG10803	skin:	n/a	n/a
47	CTCF	chr7:15563860-15564010	AG04449	skin:	n/a	n/a
48	CTCF	chr7:15428760-15428910	GM12875	blood:	n/a	n/a
49	CTCF	chr7:15543640-15543790	HCFaa	heart:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
50	CTCF	chr7:15543620-15543770	HVMF	connective:	n/a	chr7:15543671-15543679 chr7:15543711-15543727

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15436238-15436288	Jurkat	blood:	n/a
2	chr7:15436848-15436898	Hepatocyte	liver:	n/a
3	chr7:15436848-15436898	HRCEpiC	kidney:	n/a
4	chr7:15555129-15555179	ProgFib	skin:	n/a
5	chr7:15436848-15436898	MCF10A-Er-Src	breast:	n/a
6	chr7:15555129-15555179	NB4	blood:	n/a
7	chr7:15555129-15555179	GM06990	blood:	n/a
8	chr7:15436848-15436898	IMR90	lung:	fetal
9	chr7:15436848-15436898	PrEC	prostate:	n/a
10	chr7:15436848-15436898	HCPEpiC	choroid plexus:	n/a
11	chr7:15555129-15555179	AG09309	skin:	n/a
12	chr7:15555129-15555179	NH-A	brain:	n/a
13	chr7:15555129-15555179	AG04449	skin:	fetal
14	chr7:15436848-15436898	SK-N-SH_RA	brain:	n/a
15	chr7:15436848-15436898	AG09309	skin:	n/a
16	chr7:15555129-15555179	PFSK-1	brain:	n/a
17	chr7:15555129-15555179	SKMC	muscle:	n/a
18	chr7:15555129-15555179	NHDF-neo	bronchial:	n/a
19	chr7:15555129-15555179	LNCaP	prostate:	n/a
20	chr7:15436238-15436288	ovcar-3	ovarian:	n/a
21	chr7:15436238-15436288	HIPEpiC	eye:	n/a
22	chr7:15555129-15555179	MCF-7	breast:	n/a
23	chr7:15436848-15436898	U87	brain:	n/a
24	chr7:15436848-15436898	HNPCEpiC	eye:	n/a
25	chr7:15436848-15436898	HEK293	kidney:	embryo
26	chr7:15436848-15436898	HCM	heart:	n/a
27	chr7:15436848-15436898	NHDF-neo	bronchial:	n/a
28	chr7:15436848-15436898	RPTEC	kidney:	n/a
29	chr7:15555129-15555179	HMEC	breast:	n/a
30	chr7:15436238-15436288	HRPEpiC	eye:	n/a
31	chr7:15436238-15436288	GM06990	blood:	n/a
32	chr7:15436238-15436288	Hela-S3	cervix:	n/a
33	chr7:15555129-15555179	Caco-2	colon:	n/a
34	chr7:15436238-15436288	MCF-7	breast:	n/a
35	chr7:15436238-15436288	SKMC	muscle:	n/a
36	chr7:15436848-15436898	Jurkat	blood:	n/a
37	chr7:15436848-15436898	T-47D	breast:	n/a
38	chr7:15436848-15436898	K562	blood:	n/a
39	chr7:15436238-15436288	HNPCEpiC	eye:	n/a
40	chr7:15436848-15436898	H1-hESC	embryonic stem cell:	embryo
41	chr7:15436238-15436288	U87	brain:	n/a
42	chr7:15555129-15555179	HCM	heart:	n/a
43	chr7:15436848-15436898	A549	lung:	n/a
44	chr7:15436238-15436288	LNCaP	prostate:	n/a
45	chr7:15436238-15436288	HEK293	kidney:	embryo
46	chr7:15555129-15555179	A549	lung:	n/a
47	chr7:15436848-15436898	CMK	blood:	n/a
48	chr7:15555129-15555179	Hepatocyte	liver:	n/a
49	chr7:15436848-15436898	HCT-116	colon:	n/a
50	chr7:15555129-15555179	AoSMC	blood vessel:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
2	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
3	chr7:15543347..15544306-chr7:15760242..15761135,3	MCF-7	breast:
4	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEOX2-5	chr7:15494576-15494813	NONHSAT119277
2	lnc-MEOX2-6	chr7:15433738-15433804	NONHSAT119276
3	lnc-MEOX2-6	chr7:15435671-15436219	NONHSAT119276

No data

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

Extended variants
information (count: 5616 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:5616 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529113123	chr7:15428357-15428358	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189031980	chr7:15428361-15428362	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181779623	chr7:15428369-15428370	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185731186	chr7:15428380-15428381	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188978978	chr7:15428387-15428388	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs386710666	chr7:15428399-15428400	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6461171	chr7:15428422-15428423	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs372100757	chr7:15428476-15428477	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7806815	chr7:15428477-15428478	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554928202	chr7:15428480-15428481	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538064111	chr7:15428481-15428482	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556746022	chr7:15428491-15428492	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78352148	chr7:15428494-15428495	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539361340	chr7:15428525-15428526	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557466189	chr7:15428543-15428544	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572881181	chr7:15428560-15428561	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540291172	chr7:15428571-15428572	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555520150	chr7:15428581-15428582	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181068674	chr7:15428615-15428616	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371286291	chr7:15428631-15428632	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116063255	chr7:15428632-15428633	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562735027	chr7:15428658-15428659	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79264542	chr7:15428659-15428660	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6974532	chr7:15428676-15428677	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs560240331	chr7:15428710-15428711	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112540441	chr7:15428711-15428712	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372913482	chr7:15428736-15428737	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557576166	chr7:15428762-15428763	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527687135	chr7:15428765-15428766	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs578096707	chr7:15428853-15428854	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78791212	chr7:15428874-15428875	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4286842	chr7:15428884-15428885	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370441815	chr7:15428897-15428898	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113187272	chr7:15428923-15428924	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76497201	chr7:15428929-15428930	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201549568	chr7:15428931-15428932	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs68008473	chr7:15428932-15428933	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201256003	chr7:15428933-15428934	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10644312	chr7:15428934-15428935	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374504551	chr7:15428935-15428936	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571858143	chr7:15428943-15428944	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563934882	chr7:15428973-15428974	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538918306	chr7:15428988-15428989	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554460265	chr7:15428989-15428990	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74543355	chr7:15429008-15429009	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533794744	chr7:15429055-15429056	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555432956	chr7:15429091-15429092	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573761188	chr7:15429108-15429109	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4639410	chr7:15429109-15429110	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs189971345	chr7:15429126-15429127	Strong 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
Colorectal cancer	16272173	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
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15426600-15430000	Strong transcription	Liver	Liver
2	chr7:15429600-15430400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:15430000-15436400	Weak transcription	Liver	Liver
4	chr7:15435600-15436200	Active TSS	A549	lung
5	chr7:15437000-15437400	Weak transcription	Liver	Liver
6	chr7:15437400-15438200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:15437600-15438000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:15437600-15438000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:15437800-15439600	Enhancers	NHDF-Ad	bronchial
10	chr7:15438000-15442400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:15438200-15442600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr7:15438800-15439800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr7:15438800-15439800	Enhancers	Osteobl	bone
14	chr7:15440000-15440600	Enhancers	Liver	Liver
15	chr7:15440600-15454000	Weak transcription	Liver	Liver
16	chr7:15441400-15441800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:15441800-15442200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:15442000-15442800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:15442200-15443000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr7:15442400-15442800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:15442600-15443000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:15442600-15443000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr7:15443400-15443800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:15443400-15443800	Active TSS	Ovary	ovary
25	chr7:15443600-15444200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:15443800-15447200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:15444200-15447000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:15447000-15448400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr7:15447000-15448400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:15447200-15448600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:15447400-15447800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:15447400-15448400	Enhancers	HUVEC	blood vessel
33	chr7:15454000-15455600	Strong transcription	Liver	Liver
34	chr7:15455000-15455200	ZNF genes & repeats	Aorta	Aorta
35	chr7:15455200-15469800	Weak transcription	Aorta	Aorta
36	chr7:15455600-15456800	Weak transcription	Liver	Liver
37	chr7:15456800-15457400	Genic enhancers	Liver	Liver
38	chr7:15457400-15457600	Enhancers	Liver	Liver
39	chr7:15457600-15461200	Weak transcription	Liver	Liver
40	chr7:15458800-15459400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:15458800-15460400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr7:15459400-15459600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:15459600-15459800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:15459800-15460000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:15460400-15464000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:15461200-15462600	Strong transcription	Liver	Liver
47	chr7:15462600-15466400	Weak transcription	Liver	Liver
48	chr7:15463400-15465000	Enhancers	Osteobl	bone
49	chr7:15463600-15464600	Enhancers	NHDF-Ad	bronchial
50	chr7:15464000-15464600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links