Variant report

Variant	nsv1052613
Chromosome Location	chr10:90500521-90526379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:201)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:201 , 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	ATF2	chr10:90522637-90523078	GM12878	blood:	n/a	n/a
2	ATF2	chr10:90522644-90523045	GM12878	blood:	n/a	n/a
3	ATF2	chr10:90515422-90515874	GM12878	blood:	n/a	n/a
4	BATF	chr10:90522620-90522976	GM12878	blood:	n/a	n/a
5	BATF	chr10:90515512-90515803	GM12878	blood:	n/a	n/a
6	BATF	chr10:90522734-90522932	GM12878	blood:	n/a	n/a
7	BATF	chr10:90515522-90515890	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:90522617-90522933	GM12878	blood:	n/a	n/a
9	BCL3	chr10:90515526-90515892	GM12878	blood:	n/a	n/a
10	BCL3	chr10:90522702-90522971	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:90520657-90520672	GM12878	blood:	n/a	n/a
12	CBX3	chr10:90505376-90505725	HCT-116	colon:	n/a	n/a
13	CEBPB	chr10:90526284-90526472	HepG2	liver:	n/a	chr10:90526369-90526380
14	CEBPB	chr10:90515399-90515928	GM12878	blood:	n/a	n/a
15	CEBPB	chr10:90519354-90519684	HepG2	liver:	n/a	chr10:90519631-90519644
16	CEBPB	chr10:90526302-90526460	H1-hESC	embryonic stem cell:	n/a	chr10:90526369-90526380
17	CEBPB	chr10:90519610-90519695	Hela-S3	cervix:	n/a	chr10:90519631-90519644
18	CHD2	chr10:90503811-90504059	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr10:90503858-90504102	MCF-7	breast:	n/a	n/a
20	CTCF	chr10:90503840-90503990	Caco-2	colon:	n/a	n/a
21	CTCF	chr10:90503900-90504050	RPTEC	kidney:	n/a	n/a
22	CTCF	chr10:90503825-90504052	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr10:90503800-90503950	HCT-116	colon:	n/a	n/a
24	CTCF	chr10:90503817-90504122	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:90503960-90504110	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr10:90503820-90503970	A549	lung:	n/a	n/a
27	CTCF	chr10:90503749-90504223	HCT-116	colon:	n/a	n/a
28	CTCF	chr10:90503820-90503970	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr10:90503880-90504030	GM12874	blood:	n/a	n/a
30	CTCF	chr10:90503820-90503970	HEK293	kidney:	n/a	n/a
31	CTCF	chr10:90503940-90504090	HepG2	liver:	n/a	n/a
32	CTCF	chr10:90503860-90504010	GM12872	blood:	n/a	n/a
33	CTCF	chr10:90503840-90503990	HCT-116	colon:	n/a	n/a
34	CTCF	chr10:90503902-90504021	GM12892	blood:	n/a	n/a
35	CTCF	chr10:90503913-90504027	GM12891	blood:	n/a	n/a
36	CTCF	chr10:90503929-90504064	ProgFib	skin:	n/a	n/a
37	CTCF	chr10:90503840-90503990	GM12867	blood:	n/a	n/a
38	CTCF	chr10:90503880-90504031	A549	lung:	n/a	n/a
39	CTCF	chr10:90504040-90504190	HCT-116	colon:	n/a	n/a
40	CTCF	chr10:90503938-90504035	Gliobla	brain:	n/a	n/a
41	CTCF	chr10:90503900-90504050	HRE	kidney:	n/a	n/a
42	CTCF	chr10:90503761-90504075	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr10:90503840-90503990	HRE	kidney:	n/a	n/a
44	CTCF	chr10:90503824-90504107	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:90503920-90504070	GM12872	blood:	n/a	n/a
46	CTCF	chr10:90503974-90504036	GM19239	blood:	n/a	n/a
47	CTCF	chr10:90503900-90504050	NB4	blood:	n/a	n/a
48	CTCF	chr10:90503653-90504139	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr10:90503852-90504101	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:90503840-90503990	GM12872	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90519680-90519730	GM06990	blood:	n/a
2	chr10:90519680-90519730	ProgFib	skin:	n/a
3	chr10:90519680-90519730	HepG2	liver:	n/a
4	chr10:90519680-90519730	Hepatocyte	liver:	n/a
5	chr10:90519680-90519730	AG09319	gingival:	n/a
6	chr10:90519680-90519730	AG04449	skin:	fetal
7	chr10:90519680-90519730	SK-N-SH_RA	brain:	n/a
8	chr10:90519680-90519730	PrEC	prostate:	n/a
9	chr10:90519680-90519730	BJ	skin:	n/a
10	chr10:90519680-90519730	Caco-2	colon:	n/a
11	chr10:90519680-90519730	GM12891	blood:	n/a
12	chr10:90519680-90519730	ECC-1	luminal epithelium:	n/a
13	chr10:90519680-90519730	PFSK-1	brain:	n/a
14	chr10:90519680-90519730	HRPEpiC	eye:	n/a
15	chr10:90519680-90519730	U87	brain:	n/a
16	chr10:90519680-90519730	H1-hESC	embryonic stem cell:	embryo
17	chr10:90519680-90519730	AoSMC	blood vessel:	n/a
18	chr10:90519680-90519730	SK-N-MC	brain:	n/a
19	chr10:90519680-90519730	HRE	kidney:	n/a
20	chr10:90519680-90519730	RPTEC	kidney:	n/a
21	chr10:90519680-90519730	NB4	blood:	n/a
22	chr10:90519680-90519730	SK-N-SH	brain:	n/a
23	chr10:90519680-90519730	HCPEpiC	choroid plexus:	n/a
24	chr10:90519680-90519730	HIPEpiC	eye:	n/a
25	chr10:90519680-90519730	SKMC	muscle:	n/a
26	chr10:90519680-90519730	BE2_C	brain:	n/a
27	chr10:90519680-90519730	Hela-S3	cervix:	n/a
28	chr10:90519680-90519730	K562	blood:	n/a
29	chr10:90519680-90519730	AG10803	skin:	n/a
30	chr10:90519680-90519730	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:90519680-90519730	IMR90	lung:	fetal
32	chr10:90519680-90519730	PANC-1	pancreas:	n/a
33	chr10:90519680-90519730	NH-A	brain:	n/a
34	chr10:90519680-90519730	NHBE	bronchial:	n/a
35	chr10:90519680-90519730	HCF	heart:	n/a
36	chr10:90519680-90519730	SAEC	small airway:	n/a
37	chr10:90519680-90519730	GM19239	blood:	n/a
38	chr10:90519680-90519730	ovcar-3	ovarian:	n/a
39	chr10:90519680-90519730	HUVEC	blood vessel:	n/a
40	chr10:90519680-90519730	A549	lung:	n/a
41	chr10:90519680-90519730	T-47D	breast:	n/a
42	chr10:90519680-90519730	HMEC	breast:	n/a
43	chr10:90519680-90519730	GM12892	blood:	n/a
44	chr10:90519680-90519730	HNPCEpiC	eye:	n/a
45	chr10:90519680-90519730	NHDF-neo	bronchial:	n/a
46	chr10:90519680-90519730	HCT-116	colon:	n/a
47	chr10:90519680-90519730	AG09309	skin:	n/a
48	chr10:90519680-90519730	NT2-D1	testis:	n/a
49	chr10:90519680-90519730	HL-60	blood:	n/a
50	chr10:90519680-90519730	HEK293	kidney:	embryo

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:90447340..90448268-chr10:90503620..90504424,5	MCF-7	breast:
2	chr10:90515063..90517764-chr10:90518050..90519657,2	MCF-7	breast:
3	chr10:90503565..90504217-chr10:90551517..90552295,3	MCF-7	breast:
4	chr10:90494459..90496110-chr10:90501693..90504577,2	MCF-7	breast:
5	chr10:89619634..89620157-chr10:90503516..90504412,2	MCF-7	breast:
6	chr10:90515063..90517764-chr10:90518050..90519657,2	MCF-7	breast:
7	chr10:90513902..90514787-chr9:127542532..127543165,2	MCF-7	breast:

No data

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

Extended variants
information (count: 987 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs396394	chr10:90500521-90500522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563267203	chr10:90500531-90500532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530574508	chr10:90500533-90500534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567486791	chr10:90500566-90500567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546586714	chr10:90500572-90500573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570351206	chr10:90500595-90500596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17433712	chr10:90500634-90500635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs532378692	chr10:90500649-90500650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546403798	chr10:90500685-90500686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142197202	chr10:90500725-90500726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112965980	chr10:90500726-90500727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117426603	chr10:90500754-90500755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555273372	chr10:90500764-90500765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576811994	chr10:90500770-90500771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537782803	chr10:90500802-90500803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111733558	chr10:90500862-90500863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548162594	chr10:90500928-90500929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577395599	chr10:90500931-90500932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551215455	chr10:90500985-90500986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77263847	chr10:90500997-90500998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76259967	chr10:90500999-90501000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574749488	chr10:90501000-90501001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537427204	chr10:90501132-90501133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7909377	chr10:90501140-90501141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368431728	chr10:90501150-90501151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115718086	chr10:90501158-90501159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552097953	chr10:90501161-90501162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140291148	chr10:90501217-90501218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537214025	chr10:90501238-90501239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149937911	chr10:90501274-90501275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184862736	chr10:90501357-90501358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568085047	chr10:90501393-90501394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375920878	chr10:90501403-90501404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146810575	chr10:90501418-90501419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189745064	chr10:90501510-90501511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs389089	chr10:90501517-90501518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs140577072	chr10:90501573-90501574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181395451	chr10:90501624-90501625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145698876	chr10:90501715-90501716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570991599	chr10:90501739-90501740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534930914	chr10:90501741-90501742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553388245	chr10:90501750-90501751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs427720	chr10:90501795-90501796	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs199645407	chr10:90501797-90501798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541957372	chr10:90501804-90501805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138181961	chr10:90501805-90501806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs386101	chr10:90501833-90501834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545674562	chr10:90501872-90501873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374421005	chr10:90501875-90501876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs417243	chr10:90501882-90501883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

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
Acute lymphoblastic leukemia	21339820	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
Prostate cancer	21147910	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
Bipolar disorder	19114987	CNVD
Sezary syndrome	18413736	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90495600-90514000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:90503600-90503800	Enhancers	Spleen	Spleen
3	chr10:90503600-90504200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr10:90503800-90504200	ZNF genes & repeats	Spleen	Spleen
5	chr10:90503800-90504600	Enhancers	Adipose Nuclei	Adipose
6	chr10:90504200-90504400	Enhancers	Spleen	Spleen
7	chr10:90510600-90510800	Enhancers	NHEK	skin
8	chr10:90511000-90513200	Weak transcription	NHEK	skin
9	chr10:90513000-90515000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:90513200-90514600	Enhancers	NHEK	skin
11	chr10:90513800-90514000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:90513800-90514800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:90513800-90514800	Enhancers	NHDF-Ad	bronchial
14	chr10:90513800-90515000	Enhancers	Osteobl	bone
15	chr10:90513800-90515400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:90513800-90515400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr10:90513800-90515800	Enhancers	HUVEC	blood vessel
18	chr10:90514000-90514200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr10:90514000-90514400	Enhancers	HMEC	breast
20	chr10:90514000-90514400	Enhancers	NHLF	lung
21	chr10:90514000-90514600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr10:90514000-90514600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr10:90514000-90514600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr10:90514000-90514600	Enhancers	HSMM	muscle
25	chr10:90514000-90514800	Enhancers	Hela-S3	cervix
26	chr10:90514000-90515000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr10:90514200-90514600	Enhancers	Primary hematopoietic stem cells	blood
28	chr10:90514200-90514600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr10:90514200-90514800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr10:90514600-90519400	Weak transcription	HSMM	muscle
31	chr10:90514600-90523200	Weak transcription	NHEK	skin
32	chr10:90514800-90523400	Weak transcription	Hela-S3	cervix
33	chr10:90515000-90523200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:90515400-90519000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr10:90515400-90519400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr10:90516600-90517000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr10:90516600-90517200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr10:90516600-90517200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr10:90516600-90517200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr10:90516600-90517200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr10:90516800-90517400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr10:90518400-90519400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr10:90518600-90519000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr10:90518800-90519800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr10:90519000-90519400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr10:90519000-90519400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr10:90519000-90519400	Enhancers	Adipose Nuclei	Adipose
48	chr10:90519000-90521400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr10:90519200-90519600	Enhancers	Brain Substantia Nigra	brain
50	chr10:90519200-90519800	Enhancers	Sigmoid Colon	Sigmoid Colon

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