Variant report

Variant	nsv551878
Chromosome Location	chr10:91922383-91942219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:91927400-91927804	GM12878	blood:	n/a	n/a
2	ATF2	chr10:91927258-91927862	GM12878	blood:	n/a	n/a
3	ATF3	chr10:91939363-91939912	HCT-116	colon:	n/a	n/a
4	BATF	chr10:91927485-91927777	GM12878	blood:	n/a	n/a
5	BATF	chr10:91927387-91927750	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:91927479-91927794	GM12878	blood:	n/a	n/a
7	BCL3	chr10:91927465-91927749	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:91927540-91927714	GM12878	blood:	n/a	n/a
9	CBX3	chr10:91939280-91939970	HCT-116	colon:	n/a	n/a
10	CEBPB	chr10:91939266-91939861	MCF-7	breast:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
11	CEBPB	chr10:91927401-91927883	HCT-116	colon:	n/a	chr10:91927539-91927550
12	CEBPB	chr10:91927610-91927719	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:91939379-91939847	Hela-S3	cervix:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
14	CEBPB	chr10:91939420-91939777	A549	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
15	CEBPB	chr10:91939168-91940050	HCT-116	colon:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
16	CEBPB	chr10:91927487-91927750	Hela-S3	cervix:	n/a	chr10:91927539-91927550
17	CEBPB	chr10:91939218-91940011	HCT-116	colon:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
18	CEBPB	chr10:91939310-91939832	MCF-7	breast:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
19	CEBPB	chr10:91939318-91939779	A549	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
20	CEBPB	chr10:91927556-91927750	IMR90	lung:	n/a	n/a
21	CEBPB	chr10:91939390-91939807	IMR90	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
22	CEBPB	chr10:91939385-91939711	HepG2	liver:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
23	CHD2	chr10:91933751-91933782	GM12878	blood:	n/a	n/a
24	E2F4	chr10:91939550-91939767	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr10:91935261-91935531	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr10:91927511-91927703	GM12878	blood:	n/a	n/a
27	EP300	chr10:91939438-91939767	Hela-S3	cervix:	n/a	chr10:91939554-91939568
28	EP300	chr10:91927508-91927736	GM12878	blood:	n/a	chr10:91927605-91927619 chr10:91927618-91927627
29	EP300	chr10:91927541-91927765	GM12878	blood:	n/a	chr10:91927605-91927619 chr10:91927618-91927627
30	EP300	chr10:91940885-91941512	SK-N-SH_RA	brain:	n/a	chr10:91941395-91941405
31	EP300	chr10:91940855-91941447	SK-N-SH_RA	brain:	n/a	chr10:91941395-91941405
32	FOS	chr10:91934912-91935544	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr10:91939344-91939905	MCF10A-Er-Src	breast:	n/a	chr10:91939625-91939634 chr10:91939609-91939617 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939607-91939619
34	FOS	chr10:91924157-91924357	MCF10A-Er-Src	breast:	n/a	chr10:91924324-91924334 chr10:91924325-91924333 chr10:91924324-91924334 chr10:91924325-91924333 chr10:91924324-91924334 chr10:91924326-91924333
35	FOS	chr10:91939370-91939861	MCF10A-Er-Src	breast:	n/a	chr10:91939625-91939634 chr10:91939609-91939617 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939607-91939619
36	FOS	chr10:91935106-91935516	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr10:91934364-91935553	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr10:91934925-91935540	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr10:91939343-91939840	MCF10A-Er-Src	breast:	n/a	chr10:91939625-91939634 chr10:91939609-91939617 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939607-91939619
40	FOS	chr10:91927392-91927821	MCF10A-Er-Src	breast:	n/a	chr10:91927619-91927628
41	FOS	chr10:91939344-91939853	MCF10A-Er-Src	breast:	n/a	chr10:91939625-91939634 chr10:91939609-91939617 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939608-91939618 chr10:91939607-91939619
42	FOS	chr10:91927333-91927830	MCF10A-Er-Src	breast:	n/a	chr10:91927619-91927628
43	FOS	chr10:91928024-91928392	MCF10A-Er-Src	breast:	n/a	chr10:91928204-91928212 chr10:91928204-91928212 chr10:91928203-91928214 chr10:91928204-91928211
44	FOS	chr10:91928031-91928434	MCF10A-Er-Src	breast:	n/a	chr10:91928204-91928212 chr10:91928204-91928212 chr10:91928203-91928214 chr10:91928204-91928211
45	FOS	chr10:91934316-91934647	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr10:91922434-91922558	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr10:91924275-91924356	MCF10A-Er-Src	breast:	n/a	chr10:91924324-91924334 chr10:91924325-91924333 chr10:91924324-91924334 chr10:91924325-91924333 chr10:91924324-91924334 chr10:91924326-91924333
48	FOS	chr10:91927384-91928372	MCF10A-Er-Src	breast:	n/a	chr10:91928204-91928212 chr10:91927619-91927628 chr10:91928204-91928212 chr10:91928203-91928214 chr10:91928204-91928211
49	FOS	chr10:91927435-91928329	MCF10A-Er-Src	breast:	n/a	chr10:91928204-91928212 chr10:91927619-91927628 chr10:91928204-91928212 chr10:91928203-91928214 chr10:91928204-91928211
50	FOS	chr10:91934327-91934622	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:91931353..91933621-chr10:91948075..91950614,2	K562	blood:
2	chr10:91938353..91941143-chr10:91951885..91953423,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF20B-5	chr10:91923670-91923893	XLOC_008555
2	lnc-PANK1-8	chr10:91923408-91923717	NONHSAT015582
3	lnc-KIF20B-8	chr10:91924526-91924552	NONHSAT015584
4	lnc-KIF20B-8	chr10:91939472-91939926	NONHSAT015584

Variant related genes	Relation type
RN7SKP143	TF binding region

Extended variants
information (count: 829 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7906565	chr10:91922383-91922384	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558936659	chr10:91922385-91922386	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557576351	chr10:91922400-91922401	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573338751	chr10:91922406-91922407	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528030006	chr10:91922416-91922417	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184023468	chr10:91922458-91922459	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7893511	chr10:91922464-91922465	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs553864377	chr10:91922500-91922501	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573756837	chr10:91922537-91922538	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188368995	chr10:91922549-91922550	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74147775	chr10:91922609-91922610	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs148002676	chr10:91922626-91922627	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545334417	chr10:91922634-91922635	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565025358	chr10:91922654-91922655	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112068850	chr10:91922669-91922670	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546298162	chr10:91922678-91922679	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180960386	chr10:91922688-91922689	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186217964	chr10:91922830-91922831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545362558	chr10:91922857-91922858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113839522	chr10:91922960-91922961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565539091	chr10:91922961-91922962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142368336	chr10:91922981-91922982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190690099	chr10:91922985-91922986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116585345	chr10:91923032-91923033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145931230	chr10:91923042-91923043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138760627	chr10:91923045-91923046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141806734	chr10:91923066-91923067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73381500	chr10:91923078-91923079	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570973879	chr10:91923079-91923080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542753528	chr10:91923131-91923132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146272413	chr10:91923143-91923144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532195281	chr10:91923153-91923154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561378936	chr10:91923167-91923168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565214472	chr10:91923172-91923173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139162648	chr10:91923174-91923175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370861518	chr10:91923197-91923198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541287589	chr10:91923213-91923214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375073375	chr10:91923233-91923234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550477708	chr10:91923258-91923259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529993690	chr10:91923283-91923284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373996366	chr10:91923293-91923294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs117970014	chr10:91923324-91923325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569807930	chr10:91923369-91923370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182590649	chr10:91923439-91923440	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs552474460	chr10:91923500-91923501	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs10881759	chr10:91923501-91923502	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186407884	chr10:91923525-91923526	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs116860432	chr10:91923533-91923534	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs149927052	chr10:91923605-91923606	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
50	rs536244361	chr10:91923620-91923621	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91910400-91927200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:91920600-91923200	Enhancers	NHLF	lung
3	chr10:91921600-91923000	Enhancers	Osteobl	bone
4	chr10:91922000-91922400	Weak transcription	NHDF-Ad	bronchial
5	chr10:91922000-91922800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr10:91922200-91922600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:91922200-91923200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr10:91922400-91924000	Enhancers	NHDF-Ad	bronchial
9	chr10:91922400-91927000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:91922600-91923800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr10:91922800-91923000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:91923000-91927000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr10:91923000-91927000	Weak transcription	Osteobl	bone
14	chr10:91923200-91923800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr10:91923200-91923800	Weak transcription	NHLF	lung
16	chr10:91923400-91923800	Enhancers	Esophagus	oesophagus
17	chr10:91923600-91923800	ZNF genes & repeats	Pancreas	Pancrea
18	chr10:91923800-91924400	Enhancers	HMEC	breast
19	chr10:91923800-91924400	Enhancers	NHLF	lung
20	chr10:91923800-91927000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr10:91923800-91935000	Weak transcription	Esophagus	oesophagus
22	chr10:91924000-91930800	Weak transcription	Primary B cells from cord blood	blood
23	chr10:91924400-91927400	Weak transcription	HMEC	breast
24	chr10:91924400-91928000	Weak transcription	NHLF	lung
25	chr10:91926400-91926800	Enhancers	GM12878-XiMat	blood
26	chr10:91926800-91927200	Flanking Active TSS	GM12878-XiMat	blood
27	chr10:91927000-91927400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr10:91927000-91927800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:91927000-91927800	Enhancers	Osteobl	bone
30	chr10:91927000-91928200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr10:91927000-91928200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr10:91927200-91927400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:91927200-91927600	Active TSS	GM12878-XiMat	blood
34	chr10:91927200-91928400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr10:91927400-91928200	Enhancers	HMEC	breast
36	chr10:91927600-91927800	Flanking Active TSS	GM12878-XiMat	blood
37	chr10:91927800-91929200	Enhancers	GM12878-XiMat	blood
38	chr10:91928000-91928200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr10:91928000-91928200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr10:91928000-91928200	Enhancers	NHLF	lung
41	chr10:91928200-91929400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr10:91928200-91933400	Weak transcription	NHLF	lung
43	chr10:91928200-91934800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr10:91928400-91934400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr10:91932400-91933800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr10:91933400-91935400	Enhancers	NHLF	lung
47	chr10:91933600-91936800	Enhancers	HMEC	breast
48	chr10:91933800-91934000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:91933800-91935000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr10:91933800-91935400	Enhancers	Fetal Lung	lung

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