Variant report

Variant	nsv825378
Chromosome Location	chr10:52855771-52908439
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr10:52873506-52873775	GM12878	blood:	n/a	n/a
2	CEBPB	chr10:52871231-52871495	IMR90	lung:	n/a	n/a
3	CEBPB	chr10:52900251-52900376	HepG2	liver:	n/a	chr10:52900272-52900285 chr10:52900272-52900283
4	CEBPB	chr10:52904000-52904241	K562	blood:	n/a	chr10:52904113-52904124
5	CEBPB	chr10:52907708-52907998	IMR90	lung:	n/a	chr10:52907853-52907864
6	CEBPB	chr10:52901722-52901726	IMR90	lung:	n/a	n/a
7	CEBPB	chr10:52871348-52871451	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr10:52904104-52904170	Hela-S3	cervix:	n/a	chr10:52904113-52904124
9	CEBPB	chr10:52903939-52904300	IMR90	lung:	n/a	chr10:52904113-52904124
10	CEBPB	chr10:52872279-52872452	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:52891321-52891562	IMR90	lung:	n/a	chr10:52891436-52891447
12	CEBPB	chr10:52891349-52891497	HepG2	liver:	n/a	chr10:52891436-52891447
13	CEBPB	chr10:52907731-52907999	HepG2	liver:	n/a	chr10:52907853-52907864
14	CEBPB	chr10:52902042-52902176	A549	lung:	n/a	chr10:52902108-52902121
15	CEBPB	chr10:52897455-52898254	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:52891379-52891579	H1-hESC	embryonic stem cell:	n/a	chr10:52891436-52891447
17	CEBPB	chr10:52903975-52904269	A549	lung:	n/a	chr10:52904113-52904124
18	CEBPB	chr10:52860110-52860230	IMR90	lung:	n/a	chr10:52860125-52860136
19	CEBPB	chr10:52907711-52908017	A549	lung:	n/a	chr10:52907853-52907864
20	CEBPB	chr10:52903985-52904252	H1-hESC	embryonic stem cell:	n/a	chr10:52904113-52904124
21	CEBPB	chr10:52891288-52891607	A549	lung:	n/a	chr10:52891436-52891447
22	CEBPB	chr10:52903944-52904299	HepG2	liver:	n/a	chr10:52904113-52904124
23	CTCF	chr10:52891340-52891490	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr10:52881964-52882017	GM10248	blood:	n/a	n/a
25	CTCF	chr10:52864346-52864373	Gliobla	brain:	n/a	n/a
26	CTCF	chr10:52864351-52864430	LNCaP	prostate:	n/a	n/a
27	CTCF	chr10:52864300-52864450	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr10:52891340-52891490	HEK293	kidney:	n/a	n/a
29	CTCF	chr10:52864360-52864510	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr10:52864100-52864250	HVMF	connective:	n/a	n/a
31	CTCF	chr10:52864333-52864501	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr10:52891320-52891470	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr10:52864140-52864290	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr10:52864080-52864230	HCFaa	heart:	n/a	n/a
35	CTCF	chr10:52864300-52864450	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr10:52864300-52864450	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr10:52864300-52864450	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr10:52891400-52891550	AG10803	skin:	n/a	n/a
39	CTCF	chr10:52906627-52906677	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr10:52891340-52891490	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr10:52889071-52889106	GM20000	blood:	n/a	n/a
42	CTCF	chr10:52891400-52891550	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr10:52891420-52891570	GM12872	blood:	n/a	n/a
44	CTCF	chr10:52871580-52871730	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr10:52864280-52864430	HCT-116	colon:	n/a	n/a
46	CTCF	chr10:52864320-52864470	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:52891380-52891530	HMEC	breast:	n/a	n/a
48	CTCF	chr10:52864352-52864437	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F4	chr10:52899108-52899308	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr10:52893726-52893971	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52898733-52898783	HEEpiC	esophagus:	n/a
2	chr10:52898733-52898783	HPAEpiC	pulmonary alveolar:	n/a
3	chr10:52898733-52898783	PANC-1	pancreas:	n/a
4	chr10:52898733-52898783	HAEpiC	amniotic membrane:	n/a
5	chr10:52898733-52898783	HRCEpiC	kidney:	n/a
6	chr10:52898733-52898783	BJ	skin:	n/a
7	chr10:52898733-52898783	H1-hESC	embryonic stem cell:	embryo
8	chr10:52898733-52898783	SKMC	muscle:	n/a
9	chr10:52898733-52898783	K562	blood:	n/a
10	chr10:52898733-52898783	SAEC	small airway:	n/a
11	chr10:52898733-52898783	GM12891	blood:	n/a
12	chr10:52898733-52898783	HMEC	breast:	n/a
13	chr10:52898733-52898783	T-47D	breast:	n/a
14	chr10:52898733-52898783	HepG2	liver:	n/a
15	chr10:52898733-52898783	BE2_C	brain:	n/a
16	chr10:52898733-52898783	GM19239	blood:	n/a
17	chr10:52898733-52898783	HIPEpiC	eye:	n/a
18	chr10:52898733-52898783	PFSK-1	brain:	n/a
19	chr10:52898733-52898783	A549	lung:	n/a
20	chr10:52898733-52898783	MCF10A-Er-Src	breast:	n/a
21	chr10:52898733-52898783	HCPEpiC	choroid plexus:	n/a
22	chr10:52898733-52898783	AG04450	lung:	fetal
23	chr10:52898733-52898783	ECC-1	luminal epithelium:	n/a
24	chr10:52898733-52898783	RPTEC	kidney:	n/a
25	chr10:52898733-52898783	Caco-2	colon:	n/a
26	chr10:52898733-52898783	AG09309	skin:	n/a
27	chr10:52898733-52898783	HNPCEpiC	eye:	n/a
28	chr10:52898733-52898783	CMK	blood:	n/a
29	chr10:52898733-52898783	AG09319	gingival:	n/a
30	chr10:52898733-52898783	Jurkat	blood:	n/a
31	chr10:52898733-52898783	GM12892	blood:	n/a
32	chr10:52898733-52898783	HL-60	blood:	n/a
33	chr10:52898733-52898783	SK-N-MC	brain:	n/a
34	chr10:52898733-52898783	IMR90	lung:	fetal
35	chr10:52898733-52898783	ovcar-3	ovarian:	n/a
36	chr10:52898733-52898783	HCT-116	colon:	n/a
37	chr10:52898733-52898783	AG04449	skin:	fetal
38	chr10:52898733-52898783	Hepatocyte	liver:	n/a
39	chr10:52898733-52898783	HRE	kidney:	n/a
40	chr10:52898733-52898783	HEK293	kidney:	embryo
41	chr10:52898733-52898783	NHDF-neo	bronchial:	n/a
42	chr10:52898733-52898783	NB4	blood:	n/a
43	chr10:52898733-52898783	U87	brain:	n/a
44	chr10:52898733-52898783	HCF	heart:	n/a
45	chr10:52898733-52898783	HUVEC	blood vessel:	n/a
46	chr10:52898733-52898783	GM06990	blood:	n/a
47	chr10:52898733-52898783	SK-N-SH_RA	brain:	n/a
48	chr10:52898733-52898783	ProgFib	skin:	n/a
49	chr10:52898733-52898783	AG10803	skin:	n/a
50	chr10:52898733-52898783	Hela-S3	cervix:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:52855387..52858289-chr10:52859088..52861078,2	K562	blood:
2	chr10:52855387..52858289-chr10:52859088..52861078,2	K562	blood:
3	chr10:52852996..52855697-chr10:52862209..52864368,2	MCF-7	breast:
4	chr10:52900464..52903171-chr10:52913931..52915447,2	MCF-7	breast:
5	chr10:52860891..52863860-chr11:62621758..62623546,2	K562	blood:

No data

Variant related genes	Relation type
PRKG1	TF binding region
PRKG1	CpG island
ENSG00000168003	chromatin interactions
ENSG00000255717	chromatin interactions

Extended variants
information (count: 1995 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1995 , 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	rs184766759	chr10:52855814-52855815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112473645	chr10:52855828-52855829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544179167	chr10:52855851-52855852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73340468	chr10:52855863-52855864	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs181713816	chr10:52855955-52855956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142602110	chr10:52855986-52855987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560406142	chr10:52855987-52855988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73340469	chr10:52855991-52855992	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185143010	chr10:52855996-52855997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10995617	chr10:52856038-52856039	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529622305	chr10:52856065-52856066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76997869	chr10:52856066-52856067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548682114	chr10:52856088-52856089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568327844	chr10:52856123-52856124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534205218	chr10:52856139-52856140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146899074	chr10:52856155-52856156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7910047	chr10:52856168-52856169	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs540028512	chr10:52856183-52856184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190043583	chr10:52856200-52856201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199899692	chr10:52856207-52856208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370456464	chr10:52856228-52856229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145879709	chr10:52856237-52856238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113637896	chr10:52856241-52856242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574312388	chr10:52856254-52856255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12570681	chr10:52856269-52856270	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs560014900	chr10:52856449-52856450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576769977	chr10:52856456-52856457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545580406	chr10:52856461-52856462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9414815	chr10:52856463-52856464	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs531546253	chr10:52856494-52856495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181102523	chr10:52856529-52856530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562212847	chr10:52856564-52856565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148927639	chr10:52856603-52856604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547809325	chr10:52856656-52856657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186124941	chr10:52856810-52856811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555706551	chr10:52856821-52856822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189040303	chr10:52856844-52856845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75476508	chr10:52856846-52856847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143677591	chr10:52856854-52856855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181956281	chr10:52856881-52856882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536056571	chr10:52856884-52856885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186379697	chr10:52856931-52856932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574524376	chr10:52856936-52856937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112384538	chr10:52856966-52856967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533546017	chr10:52857036-52857037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190827495	chr10:52857064-52857065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2339674	chr10:52857065-52857066	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs371076977	chr10:52857116-52857117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545655919	chr10:52857123-52857124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556046827	chr10:52857134-52857135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52843600-52856200	Weak transcription	Aorta	Aorta
2	chr10:52844000-52877200	Weak transcription	Fetal Stomach	stomach
3	chr10:52850200-52863400	Weak transcription	NHLF	lung
4	chr10:52852400-52856800	Weak transcription	Ovary	ovary
5	chr10:52853000-52871200	Weak transcription	Fetal Muscle Leg	muscle
6	chr10:52853200-52856000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr10:52853200-52856000	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr10:52853200-52856000	Weak transcription	Right Atrium	heart
9	chr10:52853200-52857600	Enhancers	Rectal Smooth Muscle	rectum
10	chr10:52853200-52860000	Weak transcription	Fetal Lung	lung
11	chr10:52853400-52856200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:52853400-52857200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:52853400-52857400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:52853800-52856800	Weak transcription	Left Ventricle	heart
15	chr10:52853800-52858200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr10:52855200-52866200	Weak transcription	Psoas Muscle	Psoas
17	chr10:52855400-52856000	Weak transcription	Colon Smooth Muscle	Colon
18	chr10:52855600-52856800	Enhancers	Fetal Heart	heart
19	chr10:52856000-52856400	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr10:52856000-52856400	Enhancers	Right Atrium	heart
21	chr10:52856000-52856600	Enhancers	Colon Smooth Muscle	Colon
22	chr10:52856000-52859200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr10:52856200-52856600	Enhancers	Stomach Smooth Muscle	stomach
24	chr10:52856200-52858800	Enhancers	Aorta	Aorta
25	chr10:52856400-52861800	Weak transcription	Right Atrium	heart
26	chr10:52856600-52877200	Weak transcription	Colon Smooth Muscle	Colon
27	chr10:52856800-52857400	Enhancers	Left Ventricle	heart
28	chr10:52856800-52857400	Enhancers	Ovary	ovary
29	chr10:52857000-52857400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr10:52857200-52857400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr10:52857200-52858200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr10:52857400-52857800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:52857400-52858600	Weak transcription	Left Ventricle	heart
34	chr10:52857600-52858600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr10:52857600-52877200	Weak transcription	Rectal Smooth Muscle	rectum
36	chr10:52858200-52858800	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr10:52858200-52860200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr10:52858600-52858800	Enhancers	Left Ventricle	heart
39	chr10:52858600-52859600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr10:52858800-52859400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr10:52858800-52866200	Weak transcription	Left Ventricle	heart
42	chr10:52858800-52873000	Weak transcription	Aorta	Aorta
43	chr10:52859400-52863400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr10:52859600-52863200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr10:52859800-52860600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:52860000-52866000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr10:52860200-52860600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr10:52860600-52863400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:52861800-52862600	Enhancers	Right Atrium	heart
50	chr10:52863200-52864400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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