Variant report

Variant	nsv1028314
Chromosome Location	chr7:15336831-15555412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:976)
CpG islands
(count:244)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:15416281-15416587	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:15365751-15365978	HepG2	liver:	n/a	n/a
3	ATF1	chr7:15396881-15397102	K562	blood:	n/a	n/a
4	ATF1	chr7:15365824-15366012	K562	blood:	n/a	n/a
5	ATF1	chr7:15392479-15392850	K562	blood:	n/a	n/a
6	ATF1	chr7:15447516-15447947	K562	blood:	n/a	n/a
7	BACH1	chr7:15365724-15365854	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:15344096-15344290	GM12878	blood:	n/a	chr7:15344230-15344240 chr7:15344229-15344240
9	BRCA1	chr7:15358586-15358654	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr7:15511560-15511688	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr7:15354406-15354606	K562	blood:	n/a	n/a
12	CCNT2	chr7:15392105-15392305	K562	blood:	n/a	chr7:15392156-15392165
13	CEBPB	chr7:15408089-15408100	K562	blood:	n/a	n/a
14	CEBPB	chr7:15344916-15345214	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:15364360-15364438	H1-hESC	embryonic stem cell:	n/a	chr7:15364403-15364414
16	CEBPB	chr7:15348292-15348648	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:15447580-15447867	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:15348308-15348628	A549	lung:	n/a	n/a
19	CEBPB	chr7:15364258-15364551	A549	lung:	n/a	chr7:15364403-15364414
20	CEBPB	chr7:15363362-15363478	A549	lung:	n/a	chr7:15363437-15363448
21	CEBPB	chr7:15506113-15506415	IMR90	lung:	n/a	chr7:15506286-15506297
22	CEBPB	chr7:15458723-15459054	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:15483579-15483676	K562	blood:	n/a	chr7:15483605-15483616
24	CEBPB	chr7:15515554-15515644	A549	lung:	n/a	n/a
25	CEBPB	chr7:15468148-15468383	IMR90	lung:	n/a	chr7:15468226-15468237
26	CEBPB	chr7:15348291-15348635	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:15506112-15506438	HepG2	liver:	n/a	chr7:15506286-15506297
28	CEBPB	chr7:15374252-15374552	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:15466804-15467001	K562	blood:	n/a	chr7:15466942-15466953
30	CEBPB	chr7:15483429-15483757	HepG2	liver:	n/a	chr7:15483605-15483616
31	CEBPB	chr7:15466810-15467126	IMR90	lung:	n/a	chr7:15466942-15466953
32	CEBPB	chr7:15405775-15405910	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:15364285-15364576	HepG2	liver:	n/a	chr7:15364403-15364414
34	CEBPB	chr7:15435411-15435690	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:15478355-15478692	A549	lung:	n/a	chr7:15478519-15478530
36	CEBPB	chr7:15458726-15459040	A549	lung:	n/a	n/a
37	CEBPB	chr7:15359298-15359308	A549	lung:	n/a	n/a
38	CEBPB	chr7:15544100-15544369	A549	lung:	n/a	chr7:15544193-15544204
39	CEBPB	chr7:15447539-15447839	K562	blood:	n/a	n/a
40	CEBPB	chr7:15466850-15467116	HepG2	liver:	n/a	chr7:15466942-15466953
41	CEBPB	chr7:15478370-15478666	IMR90	lung:	n/a	chr7:15478519-15478530
42	CEBPB	chr7:15458749-15459010	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:15374309-15374579	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:15374237-15374521	A549	lung:	n/a	n/a
45	CEBPB	chr7:15483484-15483779	IMR90	lung:	n/a	chr7:15483605-15483616
46	CEBPB	chr7:15363413-15363459	IMR90	lung:	n/a	chr7:15363437-15363448
47	CEBPB	chr7:15364236-15364515	IMR90	lung:	n/a	chr7:15364403-15364414
48	CEBPB	chr7:15435437-15435631	A549	lung:	n/a	n/a
49	CEBPB	chr7:15483624-15483679	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:15506122-15506411	A549	lung:	n/a	chr7:15506286-15506297

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15436238-15436288	AG04450	lung:	fetal
2	chr7:15392612-15392662	HRE	kidney:	n/a
3	chr7:15436238-15436288	HRE	kidney:	n/a
4	chr7:15436848-15436898	SK-N-MC	brain:	n/a
5	chr7:15392612-15392662	RPTEC	kidney:	n/a
6	chr7:15555129-15555179	A549	lung:	n/a
7	chr7:15555129-15555179	H1-hESC	embryonic stem cell:	embryo
8	chr7:15436848-15436898	T-47D	breast:	n/a
9	chr7:15436238-15436288	BE2_C	brain:	n/a
10	chr7:15555129-15555179	Caco-2	colon:	n/a
11	chr7:15555129-15555179	GM12891	blood:	n/a
12	chr7:15436848-15436898	AG04449	skin:	fetal
13	chr7:15392612-15392662	SKMC	muscle:	n/a
14	chr7:15555129-15555179	HepG2	liver:	n/a
15	chr7:15392612-15392662	HMEC	breast:	n/a
16	chr7:15392612-15392662	MCF10A-Er-Src	breast:	n/a
17	chr7:15436238-15436288	U87	brain:	n/a
18	chr7:15555129-15555179	GM19239	blood:	n/a
19	chr7:15555129-15555179	RPTEC	kidney:	n/a
20	chr7:15436848-15436898	GM12891	blood:	n/a
21	chr7:15555129-15555179	GM12892	blood:	n/a
22	chr7:15436848-15436898	HCPEpiC	choroid plexus:	n/a
23	chr7:15436238-15436288	AG09309	skin:	n/a
24	chr7:15436848-15436898	Hepatocyte	liver:	n/a
25	chr7:15436848-15436898	GM12878	blood:	n/a
26	chr7:15392612-15392662	ovcar-3	ovarian:	n/a
27	chr7:15436238-15436288	AG10803	skin:	n/a
28	chr7:15555129-15555179	AG04449	skin:	fetal
29	chr7:15392612-15392662	GM12892	blood:	n/a
30	chr7:15555129-15555179	MCF10A-Er-Src	breast:	n/a
31	chr7:15436848-15436898	RPTEC	kidney:	n/a
32	chr7:15436238-15436288	H1-hESC	embryonic stem cell:	embryo
33	chr7:15392612-15392662	CMK	blood:	n/a
34	chr7:15555129-15555179	HRPEpiC	eye:	n/a
35	chr7:15392612-15392662	HCM	heart:	n/a
36	chr7:15555129-15555179	MCF-7	breast:	n/a
37	chr7:15392612-15392662	SAEC	small airway:	n/a
38	chr7:15555129-15555179	AG09309	skin:	n/a
39	chr7:15436238-15436288	HCT-116	colon:	n/a
40	chr7:15555129-15555179	HEEpiC	esophagus:	n/a
41	chr7:15555129-15555179	PrEC	prostate:	n/a
42	chr7:15436238-15436288	SKMC	muscle:	n/a
43	chr7:15436848-15436898	NH-A	brain:	n/a
44	chr7:15436848-15436898	HL-60	blood:	n/a
45	chr7:15392612-15392662	Jurkat	blood:	n/a
46	chr7:15436848-15436898	HIPEpiC	eye:	n/a
47	chr7:15392612-15392662	AG09309	skin:	n/a
48	chr7:15555129-15555179	HEK293	kidney:	embryo
49	chr7:15436238-15436288	NT2-D1	testis:	n/a
50	chr7:15555129-15555179	NB4	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:15335615..15338376-chr7:15338605..15341131,2	MCF-7	breast:
2	chr7:15344361..15344992-chr7:15760353..15761140,2	MCF-7	breast:
3	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:
4	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
5	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:
6	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
7	chr7:15365462..15366327-chr7:15594881..15595525,2	MCF-7	breast:
8	chr7:15365379..15366315-chr7:15760483..15761223,4	MCF-7	breast:
9	chr7:15344369..15345259-chr7:16109147..16109752,2	MCF-7	breast:
10	chr7:15365412..15365978-chr7:15759570..15760468,2	MCF-7	breast:
11	chr7:15344411..15345401-chr7:15760276..15761708,4	MCF-7	breast:
12	chr7:15543347..15544306-chr7:15760242..15761135,3	MCF-7	breast:
13	chr7:15335615..15338376-chr7:15338605..15341131,2	MCF-7	breast:
14	chr7:15365434..15366404-chr7:16110606..16111525,6	MCF-7	breast:
15	chr7:14757340..14758014-chr7:15344576..15345303,4	MCF-7	breast:
16	chr7:15392439..15394759-chr7:15395448..15398263,2	K562	blood:
17	chr7:15364860..15366538-chr7:15760053..15761291,7	MCF-7	breast:
18	chr7:15344409..15345014-chr7:16111015..16111547,2	MCF-7	breast:
19	chr7:15365402..15367803-chr7:15593636..15595869,2	MCF-7	breast:
20	chr7:15392439..15394759-chr7:15395448..15398263,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 10181 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:10181 , 50 per page) page: 1 2 3 4 5 6 7 ... 204

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10244398	chr7:15336831-15336832	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574805221	chr7:15336849-15336850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142496032	chr7:15336861-15336862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11982393	chr7:15336872-15336873	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs531125273	chr7:15336919-15336920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571067941	chr7:15336977-15336978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367689732	chr7:15336980-15336981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546460505	chr7:15336982-15336983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564754668	chr7:15336996-15336997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144657388	chr7:15336999-15337000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547390528	chr7:15337056-15337057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185203810	chr7:15337060-15337061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188203253	chr7:15337174-15337175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181001863	chr7:15337178-15337179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185677184	chr7:15337199-15337200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536831683	chr7:15337200-15337201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558356645	chr7:15337225-15337226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570382369	chr7:15337240-15337241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534619321	chr7:15337242-15337243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569861147	chr7:15337249-15337250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78867884	chr7:15337255-15337256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372256048	chr7:15337383-15337384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541903761	chr7:15337390-15337391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537634410	chr7:15337395-15337396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138698806	chr7:15337397-15337398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575844104	chr7:15337412-15337413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536045477	chr7:15337430-15337431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73679461	chr7:15337446-15337447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144625293	chr7:15337458-15337459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568218248	chr7:15337462-15337463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540933383	chr7:15337479-15337480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559041261	chr7:15337503-15337504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62450300	chr7:15337514-15337515	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs547908627	chr7:15337568-15337569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6958515	chr7:15337610-15337611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs530538236	chr7:15337675-15337676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76460275	chr7:15337714-15337715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183483306	chr7:15337719-15337720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138695328	chr7:15337722-15337723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534558659	chr7:15337731-15337732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372109617	chr7:15337733-15337734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186806946	chr7:15337751-15337752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568305957	chr7:15337752-15337753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535827018	chr7:15337777-15337778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557104602	chr7:15337785-15337786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374386215	chr7:15337796-15337797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148471125	chr7:15337798-15337799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142444809	chr7:15337812-15337813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539957425	chr7:15337841-15337842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558345693	chr7:15337845-15337846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15335800-15337200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:15336800-15337200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:15337200-15346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:15339800-15340600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:15340000-15340200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:15340000-15340400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:15340600-15343000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:15342400-15343400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:15343000-15343400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:15344200-15344600	Enhancers	NHDF-Ad	bronchial
11	chr7:15344400-15345000	Enhancers	Liver	Liver
12	chr7:15344600-15345000	Weak transcription	NHDF-Ad	bronchial
13	chr7:15345000-15345200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:15345000-15345200	Enhancers	NHDF-Ad	bronchial
15	chr7:15345200-15349400	Weak transcription	NHDF-Ad	bronchial
16	chr7:15345200-15352800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:15346800-15347000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:15347000-15347600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:15347400-15347800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:15347600-15347800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:15348600-15348800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:15348600-15348800	Enhancers	Fetal Muscle Leg	muscle
23	chr7:15349400-15349600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:15349400-15350000	Enhancers	Fetal Brain Male	brain
25	chr7:15349400-15350600	Enhancers	NHDF-Ad	bronchial
26	chr7:15349600-15349800	Enhancers	Fetal Muscle Leg	muscle
27	chr7:15350000-15350400	Weak transcription	Fetal Brain Male	brain
28	chr7:15350400-15350800	Enhancers	Fetal Brain Male	brain
29	chr7:15352400-15353200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:15352800-15353600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:15353000-15353800	Enhancers	Liver	Liver
32	chr7:15355800-15356200	Enhancers	Fetal Intestine Small	intestine
33	chr7:15355800-15356600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:15355800-15357200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:15360600-15361400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:15361000-15361400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:15363000-15363600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:15363200-15363800	Enhancers	Osteobl	bone
39	chr7:15363400-15363600	Active TSS	Fetal Lung	lung
40	chr7:15363400-15363800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:15363400-15363800	Enhancers	NHDF-Ad	bronchial
42	chr7:15363400-15364000	Enhancers	Liver	Liver
43	chr7:15363400-15364000	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr7:15363400-15364000	Enhancers	Brain Substantia Nigra	brain
45	chr7:15363600-15363800	Flanking Active TSS	Fetal Lung	lung
46	chr7:15363800-15364000	Enhancers	Fetal Lung	lung
47	chr7:15363800-15365200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:15363800-15370400	Weak transcription	NHDF-Ad	bronchial
49	chr7:15364000-15365800	Weak transcription	Fetal Lung	lung
50	chr7:15364000-15366000	Weak transcription	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links