Variant report

Variant	nsv437127
Chromosome Location	chr10:90940003-90968103
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:227)
CpG islands
(count:1100)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:227 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:90962713-90962913	K562	blood:	n/a	n/a
2	ATF2	chr10:90967074-90967622	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr10:90967890-90968348	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:90966612-90967905	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:90961142-90961448	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:90961126-90961416	K562	blood:	n/a	n/a
7	BRCA1	chr10:90940126-90940204	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:90961142-90961395	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:90967011-90967556	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:90967242-90967532	HepG2	liver:	n/a	n/a
11	CEBPB	chr10:90964348-90964494	A549	lung:	n/a	chr10:90964352-90964365
12	CEBPB	chr10:90967911-90968202	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:90964249-90964402	IMR90	lung:	n/a	chr10:90964352-90964365
14	CEBPB	chr10:90967078-90967537	A549	lung:	n/a	n/a
15	CEBPB	chr10:90943379-90943619	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:90940241-90940264	Hela-S3	cervix:	n/a	n/a
17	CHD1	chr10:90967727-90968083	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr10:90967594-90967794	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr10:90966262-90966896	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr10:90966214-90967345	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr10:90967588-90968408	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr10:90963780-90963930	GM12864	blood:	n/a	n/a
23	CTCF	chr10:90966820-90966970	GM12871	blood:	n/a	n/a
24	CTCF	chr10:90966760-90966910	GM12872	blood:	n/a	n/a
25	CTCF	chr10:90966761-90966959	ProgFib	skin:	n/a	n/a
26	CTCF	chr10:90942800-90942950	GM12864	blood:	n/a	n/a
27	CTCF	chr10:90966760-90966910	BJ	skin:	n/a	n/a
28	CTCF	chr10:90966820-90966970	HCM	heart:	n/a	n/a
29	CTCF	chr10:90966780-90966930	AG10803	skin:	n/a	n/a
30	CTCF	chr10:90966820-90966970	GM12864	blood:	n/a	n/a
31	CTCF	chr10:90964440-90964590	BJ	skin:	n/a	n/a
32	CTCF	chr10:90966780-90966930	HFF	foreskin:	n/a	n/a
33	CTCF	chr10:90966720-90966870	HRE	kidney:	n/a	n/a
34	CTCF	chr10:90966840-90966990	GM12872	blood:	n/a	n/a
35	CTCF	chr10:90966773-90966805	GM10248	blood:	n/a	n/a
36	CTCF	chr10:90942799-90942923	Fibrobl	skin:	n/a	n/a
37	CTCF	chr10:90966787-90966939	GM12892	blood:	n/a	n/a
38	CTCF	chr10:90966794-90966894	Fibrobl	skin:	n/a	n/a
39	CTCF	chr10:90966763-90966940	GM19240	blood:	n/a	n/a
40	CTCF	chr10:90966740-90966890	HPF	lung:	n/a	n/a
41	CTCF	chr10:90966700-90966850	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr10:90966700-90966850	AG04449	skin:	n/a	n/a
43	CTCF	chr10:90958850-90958869	GM13976	blood:	n/a	n/a
44	CTCF	chr10:90966780-90966930	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr10:90966800-90966950	AG09319	gingival:	n/a	n/a
46	CTCF	chr10:90966740-90966890	GM12868	blood:	n/a	n/a
47	CTCF	chr10:90966240-90966390	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr10:90966801-90966896	NHEK	skin:	n/a	n/a
49	CTCF	chr10:90966760-90966910	AG10803	skin:	n/a	n/a
50	CTCF	chr10:90959000-90959150	HPF	lung:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90968091-90968141	AoSMC	blood vessel:	n/a
2	chr10:90967918-90967968	H1-hESC	embryonic stem cell:	embryo
3	chr10:90968091-90968141	AoSMC	blood vessel:	n/a
4	chr10:90967918-90967968	H1-hESC	embryonic stem cell:	embryo
5	chr10:90966807-90966857	HL-60	blood:	n/a
6	chr10:90967700-90967750	HMEC	breast:	n/a
7	chr10:90966807-90966857	AG10803	skin:	n/a
8	chr10:90967160-90967210	A549	lung:	n/a
9	chr10:90968091-90968141	HPAEpiC	pulmonary alveolar:	n/a
10	chr10:90966221-90966271	HRPEpiC	eye:	n/a
11	chr10:90967700-90967750	HRCEpiC	kidney:	n/a
12	chr10:90967612-90967662	AoSMC	blood vessel:	n/a
13	chr10:90967052-90967102	AG09319	gingival:	n/a
14	chr10:90967113-90967163	NH-A	brain:	n/a
15	chr10:90967165-90967215	A549	lung:	n/a
16	chr10:90967052-90967102	MCF10A-Er-Src	breast:	n/a
17	chr10:90967700-90967750	SK-N-SH	brain:	n/a
18	chr10:90967612-90967662	AG09309	skin:	n/a
19	chr10:90964806-90964856	HepG2	liver:	n/a
20	chr10:90967612-90967662	HL-60	blood:	n/a
21	chr10:90966524-90966574	HEEpiC	esophagus:	n/a
22	chr10:90967612-90967662	NT2-D1	testis:	n/a
23	chr10:90966807-90966857	AG09309	skin:	n/a
24	chr10:90966701-90966751	HRPEpiC	eye:	n/a
25	chr10:90966221-90966271	HRCEpiC	kidney:	n/a
26	chr10:90967160-90967210	NH-A	brain:	n/a
27	chr10:90967700-90967750	NHBE	bronchial:	n/a
28	chr10:90964806-90964856	HCT-116	colon:	n/a
29	chr10:90967894-90967944	SAEC	small airway:	n/a
30	chr10:90966701-90966751	K562	blood:	n/a
31	chr10:90968091-90968141	HIPEpiC	eye:	n/a
32	chr10:90968091-90968141	HRPEpiC	eye:	n/a
33	chr10:90967896-90967946	ProgFib	skin:	n/a
34	chr10:90966221-90966271	A549	lung:	n/a
35	chr10:90967918-90967968	CMK	blood:	n/a
36	chr10:90968091-90968141	Hepatocyte	liver:	n/a
37	chr10:90967113-90967163	Jurkat	blood:	n/a
38	chr10:90966701-90966751	NB4	blood:	n/a
39	chr10:90966221-90966271	SK-N-MC	brain:	n/a
40	chr10:90967165-90967215	HL-60	blood:	n/a
41	chr10:90967700-90967750	U87	brain:	n/a
42	chr10:90968091-90968141	PFSK-1	brain:	n/a
43	chr10:90966221-90966271	ECC-1	luminal epithelium:	n/a
44	chr10:90967160-90967210	GM19239	blood:	n/a
45	chr10:90967896-90967946	AG09309	skin:	n/a
46	chr10:90966807-90966857	MCF10A-Er-Src	breast:	n/a
47	chr10:90967157-90967207	Hela-S3	cervix:	n/a
48	chr10:90968091-90968141	MCF-7	breast:	n/a
49	chr10:90967233-90967283	Hela-S3	cervix:	n/a
50	chr10:90967165-90967215	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:90807595..90810361-chr10:90944518..90946449,2	MCF-7	breast:

No data

Variant related genes	Relation type
CH25H	TF binding region
CH25H	CpG island

Extended variants
information (count: 678 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2841031	chr10:90940003-90940004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112003789	chr10:90940084-90940085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554334914	chr10:90940085-90940086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551279844	chr10:90940154-90940155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566611443	chr10:90940166-90940167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533853672	chr10:90940176-90940177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12253799	chr10:90940193-90940194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73368245	chr10:90940221-90940222	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567729121	chr10:90940230-90940231	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536178415	chr10:90940250-90940251	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557586730	chr10:90940272-90940273	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150137349	chr10:90940285-90940286	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540070307	chr10:90940288-90940289	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138563248	chr10:90940296-90940297	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184621222	chr10:90940305-90940306	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553352005	chr10:90940310-90940311	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2841029	chr10:90940325-90940326	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs11203014	chr10:90940333-90940334	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189453992	chr10:90940357-90940358	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10887926	chr10:90940358-90940359	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs533076507	chr10:90940381-90940382	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551583878	chr10:90940405-90940406	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369926425	chr10:90940406-90940407	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114582697	chr10:90940413-90940414	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192051857	chr10:90940490-90940491	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371652455	chr10:90940533-90940534	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576531470	chr10:90940576-90940577	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77004054	chr10:90940624-90940625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149297972	chr10:90940632-90940633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs80338499	chr10:90940675-90940676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117779845	chr10:90940676-90940677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10887927	chr10:90940687-90940688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs185466173	chr10:90940709-90940710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189993150	chr10:90940735-90940736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558346162	chr10:90940789-90940790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143274254	chr10:90940798-90940799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181112438	chr10:90940814-90940815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555399246	chr10:90940820-90940821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186395607	chr10:90940913-90940914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113820323	chr10:90940914-90940915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562719885	chr10:90940921-90940922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180985016	chr10:90940926-90940927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544943984	chr10:90940952-90940953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76023004	chr10:90940975-90940976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138899938	chr10:90941012-90941013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549109421	chr10:90941043-90941044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186395923	chr10:90941075-90941076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141935990	chr10:90941078-90941079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191202753	chr10:90941144-90941145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574039969	chr10:90941254-90941255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90936200-90940200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr10:90936200-90942800	Weak transcription	NHDF-Ad	bronchial
3	chr10:90940200-90940600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:90940600-90943000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr10:90942600-90943800	Enhancers	NHLF	lung
6	chr10:90942600-90944000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr10:90942800-90944000	Enhancers	NHDF-Ad	bronchial
8	chr10:90943000-90943800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:90943000-90944200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr10:90943200-90944400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:90943400-90943800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:90943600-90943800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr10:90943600-90944000	Enhancers	HMEC	breast
14	chr10:90943600-90945000	Enhancers	Osteobl	bone
15	chr10:90943800-90944200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr10:90943800-90945400	Weak transcription	NHLF	lung
17	chr10:90944000-90945200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:90944400-90949400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr10:90945200-90945800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr10:90945200-90946000	Enhancers	Stomach Smooth Muscle	stomach
21	chr10:90945400-90945600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr10:90945400-90945800	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr10:90945400-90945800	Enhancers	Hela-S3	cervix
24	chr10:90945400-90946600	Enhancers	Fetal Lung	lung
25	chr10:90945600-90945800	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr10:90945600-90945800	Enhancers	NHLF	lung
27	chr10:90945600-90946000	Enhancers	Colon Smooth Muscle	Colon
28	chr10:90945600-90946000	Bivalent Enhancer	Stomach Mucosa	stomach
29	chr10:90946200-90947200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr10:90946400-90946800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr10:90946400-90947000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr10:90946400-90947000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr10:90955200-90956000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr10:90960800-90962200	Enhancers	NHEK	skin
35	chr10:90961000-90961600	Enhancers	NHDF-Ad	bronchial
36	chr10:90961000-90961800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr10:90961000-90962200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr10:90961000-90962200	Enhancers	NHLF	lung
39	chr10:90961200-90961600	Enhancers	A549	lung
40	chr10:90961200-90962200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:90961400-90962000	Enhancers	Fetal Stomach	stomach
42	chr10:90961400-90962200	Enhancers	HMEC	breast
43	chr10:90961400-90962400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr10:90961600-90961800	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr10:90961600-90962200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr10:90961600-90962400	Enhancers	Esophagus	oesophagus
47	chr10:90961600-90963000	Weak transcription	NHDF-Ad	bronchial
48	chr10:90961800-90963000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:90962200-90963200	Weak transcription	NHLF	lung
50	chr10:90962400-90963400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links