Variant report

Variant	nsv606295
Chromosome Location	chr7:15397449-15547950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:479)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:479 , 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	ARID3A	chr7:15416281-15416587	HepG2	liver:	n/a	n/a
2	ATF1	chr7:15447516-15447947	K562	blood:	n/a	n/a
3	BRCA1	chr7:15511560-15511688	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:15506113-15506415	IMR90	lung:	n/a	chr7:15506286-15506297
5	CEBPB	chr7:15435437-15435631	A549	lung:	n/a	n/a
6	CEBPB	chr7:15478389-15478692	HepG2	liver:	n/a	chr7:15478519-15478530
7	CEBPB	chr7:15515554-15515644	A549	lung:	n/a	n/a
8	CEBPB	chr7:15447580-15447867	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:15483484-15483779	IMR90	lung:	n/a	chr7:15483605-15483616
10	CEBPB	chr7:15405781-15406007	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:15458723-15459054	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:15506112-15506438	HepG2	liver:	n/a	chr7:15506286-15506297
13	CEBPB	chr7:15435469-15435633	K562	blood:	n/a	n/a
14	CEBPB	chr7:15483429-15483757	HepG2	liver:	n/a	chr7:15483605-15483616
15	CEBPB	chr7:15405775-15405910	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:15466804-15467001	K562	blood:	n/a	chr7:15466942-15466953
17	CEBPB	chr7:15458726-15459040	A549	lung:	n/a	n/a
18	CEBPB	chr7:15483579-15483676	K562	blood:	n/a	chr7:15483605-15483616
19	CEBPB	chr7:15447539-15447839	K562	blood:	n/a	n/a
20	CEBPB	chr7:15483624-15483679	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:15544100-15544369	A549	lung:	n/a	chr7:15544193-15544204
22	CEBPB	chr7:15468148-15468383	IMR90	lung:	n/a	chr7:15468226-15468237
23	CEBPB	chr7:15415765-15415909	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:15478370-15478666	IMR90	lung:	n/a	chr7:15478519-15478530
25	CEBPB	chr7:15468127-15468377	HepG2	liver:	n/a	chr7:15468226-15468237
26	CEBPB	chr7:15506122-15506411	A549	lung:	n/a	chr7:15506286-15506297
27	CEBPB	chr7:15408089-15408100	K562	blood:	n/a	n/a
28	CEBPB	chr7:15478355-15478692	A549	lung:	n/a	chr7:15478519-15478530
29	CEBPB	chr7:15458749-15459010	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:15466810-15467126	IMR90	lung:	n/a	chr7:15466942-15466953
31	CEBPB	chr7:15426024-15426286	HepG2	liver:	n/a	chr7:15426145-15426154 chr7:15426143-15426154
32	CEBPB	chr7:15435411-15435690	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:15466850-15467116	HepG2	liver:	n/a	chr7:15466942-15466953
34	CEBPB	chr7:15458696-15459049	IMR90	lung:	n/a	n/a
35	CTCF	chr7:15543640-15543790	HPF	lung:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
36	CTCF	chr7:15543660-15543810	HBMEC	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
37	CTCF	chr7:15543600-15543750	AoAF	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
38	CTCF	chr7:15543620-15543770	NHDF-neo	bronchial:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
39	CTCF	chr7:15428760-15428910	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr7:15543608-15543836	HUVEC	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
41	CTCF	chr7:15543500-15543650	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr7:15428780-15428930	AG04449	skin:	n/a	n/a
43	CTCF	chr7:15428740-15428890	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr7:15428820-15428970	AG09309	skin:	n/a	n/a
45	CTCF	chr7:15543672-15543693	Medullo	brain:	n/a	n/a
46	CTCF	chr7:15543480-15543630	NHLF	lung:	n/a	n/a
47	CTCF	chr7:15543960-15544110	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr7:15543540-15543690	NHDF-neo	bronchial:	n/a	chr7:15543671-15543679
49	CTCF	chr7:15428800-15428950	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:15543580-15543730	AoAF	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15436848-15436898	CMK	blood:	n/a
2	chr7:15436238-15436288	T-47D	breast:	n/a
3	chr7:15436238-15436288	AoSMC	blood vessel:	n/a
4	chr7:15436848-15436898	Hela-S3	cervix:	n/a
5	chr7:15436848-15436898	AoSMC	blood vessel:	n/a
6	chr7:15436238-15436288	MCF10A-Er-Src	breast:	n/a
7	chr7:15436238-15436288	HRCEpiC	kidney:	n/a
8	chr7:15436848-15436898	HIPEpiC	eye:	n/a
9	chr7:15436238-15436288	Hela-S3	cervix:	n/a
10	chr7:15436238-15436288	U87	brain:	n/a
11	chr7:15436848-15436898	NHDF-neo	bronchial:	n/a
12	chr7:15436238-15436288	SK-N-SH_RA	brain:	n/a
13	chr7:15436848-15436898	HMEC	breast:	n/a
14	chr7:15436238-15436288	HCPEpiC	choroid plexus:	n/a
15	chr7:15436848-15436898	HepG2	liver:	n/a
16	chr7:15436238-15436288	AG04449	skin:	fetal
17	chr7:15436848-15436898	AG04450	lung:	fetal
18	chr7:15436848-15436898	NT2-D1	testis:	n/a
19	chr7:15436848-15436898	Hepatocyte	liver:	n/a
20	chr7:15436848-15436898	GM06990	blood:	n/a
21	chr7:15436848-15436898	Jurkat	blood:	n/a
22	chr7:15436848-15436898	Caco-2	colon:	n/a
23	chr7:15436238-15436288	HCT-116	colon:	n/a
24	chr7:15436238-15436288	RPTEC	kidney:	n/a
25	chr7:15436848-15436898	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:15436848-15436898	HAEpiC	amniotic membrane:	n/a
27	chr7:15436238-15436288	AG09309	skin:	n/a
28	chr7:15436238-15436288	SAEC	small airway:	n/a
29	chr7:15436848-15436898	HUVEC	blood vessel:	n/a
30	chr7:15436848-15436898	PANC-1	pancreas:	n/a
31	chr7:15436238-15436288	HRPEpiC	eye:	n/a
32	chr7:15436848-15436898	IMR90	lung:	fetal
33	chr7:15436238-15436288	HUVEC	blood vessel:	n/a
34	chr7:15436238-15436288	HEEpiC	esophagus:	n/a
35	chr7:15436238-15436288	PANC-1	pancreas:	n/a
36	chr7:15436238-15436288	HMEC	breast:	n/a
37	chr7:15436238-15436288	LNCaP	prostate:	n/a
38	chr7:15436848-15436898	MCF-7	breast:	n/a
39	chr7:15436848-15436898	GM19239	blood:	n/a
40	chr7:15436238-15436288	SKMC	muscle:	n/a
41	chr7:15436848-15436898	HRE	kidney:	n/a
42	chr7:15436238-15436288	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:15436238-15436288	NH-A	brain:	n/a
44	chr7:15436238-15436288	HL-60	blood:	n/a
45	chr7:15436848-15436898	U87	brain:	n/a
46	chr7:15436848-15436898	SK-N-MC	brain:	n/a
47	chr7:15436848-15436898	BJ	skin:	n/a
48	chr7:15436238-15436288	HEK293	kidney:	embryo
49	chr7:15436238-15436288	CMK	blood:	n/a
50	chr7:15436848-15436898	HRPEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:
2	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:
3	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
4	chr7:15543347..15544306-chr7:15760242..15761135,3	MCF-7	breast:
5	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
6	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	chr7:15435671-15436219	NONHSAT119276
2	lnc-MEOX2-5	chr7:15494576-15494813	NONHSAT119277
3	lnc-MEOX2-6	chr7:15433738-15433804	NONHSAT119276

No data

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

Extended variants
information (count: 6930 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:6930 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6957765	chr7:15397449-15397450	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140345093	chr7:15397451-15397452	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571739878	chr7:15397454-15397455	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538852928	chr7:15397485-15397486	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6957781	chr7:15397487-15397488	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs561580417	chr7:15397501-15397502	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114841425	chr7:15397508-15397509	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145494686	chr7:15397510-15397511	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554913414	chr7:15397559-15397560	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377345606	chr7:15397571-15397572	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573286666	chr7:15397579-15397580	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557933372	chr7:15397605-15397606	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568357145	chr7:15397626-15397627	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578156735	chr7:15397631-15397632	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78185362	chr7:15397632-15397633	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113146184	chr7:15397637-15397638	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6461170	chr7:15397643-15397644	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs10277659	chr7:15397663-15397664	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs544837003	chr7:15397738-15397739	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74984590	chr7:15397747-15397748	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527565653	chr7:15397752-15397753	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114814337	chr7:15397765-15397766	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561197742	chr7:15397785-15397786	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138032422	chr7:15397796-15397797	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550242915	chr7:15397824-15397825	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571639869	chr7:15397839-15397840	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532646565	chr7:15397879-15397880	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547627661	chr7:15397889-15397890	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566283645	chr7:15397898-15397899	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536483866	chr7:15397908-15397909	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554821566	chr7:15397942-15397943	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570063125	chr7:15397951-15397952	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537440047	chr7:15397958-15397959	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576338260	chr7:15397965-15397966	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556136439	chr7:15397978-15397979	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541746328	chr7:15397979-15397980	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149543333	chr7:15397989-15397990	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545113321	chr7:15398018-15398019	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116590855	chr7:15398040-15398041	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572251875	chr7:15398077-15398078	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542868147	chr7:15398078-15398079	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561162597	chr7:15398082-15398083	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531675503	chr7:15398086-15398087	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144108723	chr7:15398087-15398088	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148305177	chr7:15398098-15398099	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532472562	chr7:15398139-15398140	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529006143	chr7:15398141-15398142	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558541659	chr7:15398156-15398157	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373817795	chr7:15398161-15398162	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547884597	chr7:15398177-15398178	Strong transcription Weak transcription	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
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
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15396800-15397600	Enhancers	Fetal Heart	heart
2	chr7:15396800-15397800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr7:15397000-15397800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:15397000-15401000	Strong transcription	Liver	Liver
5	chr7:15397600-15399200	Weak transcription	Fetal Heart	heart
6	chr7:15399200-15400800	Enhancers	Fetal Heart	heart
7	chr7:15401000-15402000	Weak transcription	Liver	Liver
8	chr7:15402000-15402400	Enhancers	Liver	Liver
9	chr7:15402400-15404000	Weak transcription	Liver	Liver
10	chr7:15403800-15413800	Weak transcription	Left Ventricle	heart
11	chr7:15404000-15405200	Strong transcription	Liver	Liver
12	chr7:15405200-15414400	Weak transcription	Liver	Liver
13	chr7:15409800-15410400	Active TSS	Brain Hippocampus Middle	brain
14	chr7:15409800-15410600	Enhancers	Brain Angular Gyrus	brain
15	chr7:15410000-15412800	Weak transcription	Right Atrium	heart
16	chr7:15414400-15414600	Enhancers	Liver	Liver
17	chr7:15414600-15414800	Enhancers	Muscle Satellite Cultured Cells	--
18	chr7:15414600-15415000	Weak transcription	Liver	Liver
19	chr7:15414800-15415800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr7:15415000-15416200	Enhancers	Liver	Liver
21	chr7:15415600-15416400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:15415600-15417200	Enhancers	Osteobl	bone
23	chr7:15415800-15417200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr7:15416200-15417200	Flanking Active TSS	Liver	Liver
25	chr7:15416400-15416800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:15416400-15417000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr7:15416600-15417000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:15417200-15417600	Enhancers	Liver	Liver
29	chr7:15417200-15418400	Weak transcription	Osteobl	bone
30	chr7:15417600-15421000	Weak transcription	Liver	Liver
31	chr7:15418400-15418600	Enhancers	Osteobl	bone
32	chr7:15421000-15423000	Strong transcription	Liver	Liver
33	chr7:15423000-15426600	Weak transcription	Liver	Liver
34	chr7:15426600-15430000	Strong transcription	Liver	Liver
35	chr7:15429600-15430400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:15430000-15436400	Weak transcription	Liver	Liver
37	chr7:15435600-15436200	Active TSS	A549	lung
38	chr7:15437000-15437400	Weak transcription	Liver	Liver
39	chr7:15437400-15438200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr7:15437600-15438000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:15437600-15438000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:15437800-15439600	Enhancers	NHDF-Ad	bronchial
43	chr7:15438000-15442400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:15438200-15442600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr7:15438800-15439800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr7:15438800-15439800	Enhancers	Osteobl	bone
47	chr7:15440000-15440600	Enhancers	Liver	Liver
48	chr7:15440600-15454000	Weak transcription	Liver	Liver
49	chr7:15441400-15441800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:15441800-15442200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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