Variant report

Variant	nsv1040910
Chromosome Location	chr10:4554674-4606939
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	ATF3	chr10:4562259-4562601	HCT-116	colon:	n/a	n/a
2	BATF	chr10:4564809-4565232	GM12878	blood:	n/a	n/a
3	BATF	chr10:4564886-4565161	GM12878	blood:	n/a	n/a
4	BATF	chr10:4556707-4556991	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:4564853-4565165	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:4556668-4557002	GM12878	blood:	n/a	chr10:4556876-4556885
7	BHLHE40	chr10:4564876-4565159	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:4599683-4599982	K562	blood:	n/a	n/a
9	CBX3	chr10:4583289-4584004	HCT-116	colon:	n/a	n/a
10	CBX3	chr10:4583123-4584158	HCT-116	colon:	n/a	n/a
11	CEBPB	chr10:4562109-4562666	A549	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
12	CEBPB	chr10:4555268-4555468	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:4554806-4555358	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr10:4575421-4575468	HepG2	liver:	n/a	chr10:4575449-4575460
15	CEBPB	chr10:4575932-4576167	IMR90	lung:	n/a	chr10:4576072-4576083
16	CEBPB	chr10:4583434-4583892	IMR90	lung:	n/a	n/a
17	CEBPB	chr10:4554851-4555290	IMR90	lung:	n/a	n/a
18	CEBPB	chr10:4562195-4562596	A549	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
19	CEBPB	chr10:4589866-4590036	HepG2	liver:	n/a	chr10:4589984-4589995
20	CEBPB	chr10:4562162-4562641	Hela-S3	cervix:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
21	CEBPB	chr10:4562026-4562763	HCT-116	colon:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461 chr10:4562710-4562718
22	CEBPB	chr10:4562180-4562544	K562	blood:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
23	CEBPB	chr10:4562197-4562491	H1-hESC	embryonic stem cell:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
24	CEBPB	chr10:4562072-4562716	HCT-116	colon:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
25	CEBPB	chr10:4589866-4590088	IMR90	lung:	n/a	chr10:4589984-4589995
26	CEBPB	chr10:4583578-4583787	A549	lung:	n/a	n/a
27	CEBPB	chr10:4562195-4562561	HepG2	liver:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
28	CEBPB	chr10:4592915-4592924	A549	lung:	n/a	n/a
29	CEBPB	chr10:4562284-4562540	K562	blood:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
30	CEBPB	chr10:4583235-4584020	HCT-116	colon:	n/a	n/a
31	CEBPB	chr10:4562177-4562613	IMR90	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
32	CEBPB	chr10:4583472-4583889	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr10:4590862-4590896	K562	blood:	n/a	n/a
34	CEBPB	chr10:4562211-4562572	A549	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
35	CHD1	chr10:4554749-4555515	IMR90	lung:	n/a	n/a
36	CTCF	chr10:4555140-4555290	GM06990	blood:	n/a	n/a
37	CTCF	chr10:4583460-4583610	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr10:4583500-4583650	RPTEC	kidney:	n/a	n/a
39	CTCF	chr10:4555140-4555290	HCT-116	colon:	n/a	n/a
40	CTCF	chr10:4583480-4583630	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr10:4555102-4555267	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr10:4555120-4555270	AG09319	gingival:	n/a	n/a
43	CTCF	chr10:4555080-4555347	Gliobla	brain:	n/a	n/a
44	CTCF	chr10:4555013-4555394	IMR90	lung:	n/a	n/a
45	CTCF	chr10:4555034-4555326	T-47D	breast:	n/a	n/a
46	CTCF	chr10:4561935-4561961	GM13976	blood:	n/a	n/a
47	CTCF	chr10:4555080-4555230	NB4	blood:	n/a	n/a
48	CTCF	chr10:4555122-4555333	MCF-7	breast:	n/a	n/a
49	CTCF	chr10:4555140-4555290	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr10:4555120-4555270	HEEpiC	esophagus:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:4599369..4601915-chr10:4639529..4642223,2	K562	blood:
2	chr10:4553609..4555147-chr10:4560263..4562993,2	K562	blood:
3	chr10:4216515..4217122-chr10:4555119..4555688,2	MCF-7	breast:
4	chr10:4571025..4573513-chr10:4576423..4579322,2	K562	blood:
5	chr10:4569855..4572321-chr10:4573462..4575585,2	K562	blood:
6	chr10:4594247..4596024-chr10:4597531..4600000,2	K562	blood:
7	chr10:4554314..4555272-chr10:4813439..4814001,3	MCF-7	breast:
8	chr10:3827049..3829866-chr10:4557123..4559023,2	MCF-7	breast:
9	chr10:4571989..4574751-chr10:4596038..4598866,2	K562	blood:
10	chr10:4554774..4555300-chr10:4623885..4624517,2	MCF-7	breast:
11	chr10:4566048..4568244-chr10:4578718..4581032,2	MCF-7	breast:
12	chr10:4554767..4555670-chr10:4691719..4692590,2	MCF-7	breast:
13	chr10:4555087..4556892-chr10:4807552..4809332,2	MCF-7	breast:
14	chr10:4586883..4588795-chr10:4691830..4693502,2	MCF-7	breast:
15	chr10:4571989..4574751-chr10:4596038..4598866,2	K562	blood:
16	chr10:4553609..4555147-chr10:4560263..4562993,2	K562	blood:
17	chr10:4566048..4568244-chr10:4578718..4581032,2	MCF-7	breast:
18	chr10:4569855..4572321-chr10:4573462..4575585,2	K562	blood:
19	chr10:4582239..4584418-chr10:4702344..4704094,2	MCF-7	breast:
20	chr10:4571025..4573513-chr10:4576423..4579322,2	K562	blood:
21	chr10:4554890..4555444-chr10:4808771..4809867,3	MCF-7	breast:
22	chr10:3826803..3829323-chr10:4602762..4605029,2	MCF-7	breast:
23	chr10:4594247..4596024-chr10:4597531..4600000,2	K562	blood:
24	chr10:4554517..4555692-chr10:4698473..4699407,4	MCF-7	breast:
25	chr10:4554841..4555595-chr10:4693003..4693874,4	MCF-7	breast:
26	chr10:4554964..4555693-chr10:4698445..4699397,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-163P	TF binding region
ENSG00000231298	chromatin interactions
ENSG00000067082	chromatin interactions

Extended variants
information (count: 1971 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1971 , 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	rs11252571	chr10:4554674-4554675	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376714899	chr10:4554686-4554687	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142505241	chr10:4554699-4554700	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs7068271	chr10:4554712-4554713	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147550366	chr10:4554717-4554718	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142075971	chr10:4554722-4554723	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs144271246	chr10:4554730-4554731	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs376702909	chr10:4554776-4554777	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs189789105	chr10:4554788-4554789	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs192898342	chr10:4554818-4554819	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147829880	chr10:4554819-4554820	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200994097	chr10:4554855-4554856	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557712297	chr10:4554871-4554872	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs551325549	chr10:4554886-4554887	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs185173364	chr10:4554899-4554900	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs76801436	chr10:4554926-4554927	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375404287	chr10:4554951-4554952	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201649921	chr10:4554976-4554977	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs140277707	chr10:4555000-4555001	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs55776110	chr10:4555066-4555067	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs17133097	chr10:4555068-4555069	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs527356491	chr10:4555137-4555138	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs150385953	chr10:4555152-4555153	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530599738	chr10:4555161-4555162	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs528716820	chr10:4555171-4555172	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138083876	chr10:4555206-4555207	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371507180	chr10:4555208-4555209	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112579172	chr10:4555241-4555242	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190123323	chr10:4555242-4555243	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375753130	chr10:4555269-4555270	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs17133099	chr10:4555301-4555302	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529047135	chr10:4555304-4555305	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs537792420	chr10:4555326-4555327	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs372191118	chr10:4555333-4555334	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550384948	chr10:4555342-4555343	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs568743311	chr10:4555355-4555356	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539532937	chr10:4555420-4555421	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs148941654	chr10:4555431-4555432	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs566525353	chr10:4555464-4555465	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549667161	chr10:4555485-4555486	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs138175614	chr10:4555498-4555499	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116789829	chr10:4555499-4555500	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574268719	chr10:4555523-4555524	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs79739998	chr10:4555536-4555537	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34654495	chr10:4555555-4555556	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374290009	chr10:4555564-4555565	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs578234716	chr10:4555569-4555570	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs545909663	chr10:4555577-4555578	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538671638	chr10:4555590-4555591	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs557017544	chr10:4555596-4555597	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4541600-4554800	Weak transcription	NHLF	lung
2	chr10:4548600-4554800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:4548800-4555000	Weak transcription	Osteobl	bone
4	chr10:4552000-4556600	Weak transcription	Fetal Thymus	thymus
5	chr10:4552400-4555000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr10:4552800-4555200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr10:4553200-4555400	Enhancers	Fetal Lung	lung
8	chr10:4553200-4558400	Enhancers	NHDF-Ad	bronchial
9	chr10:4553600-4555000	Weak transcription	Colon Smooth Muscle	Colon
10	chr10:4553600-4555800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:4553800-4554800	Weak transcription	NHEK	skin
12	chr10:4553800-4555000	Weak transcription	Fetal Stomach	stomach
13	chr10:4553800-4555200	Weak transcription	Fetal Muscle Leg	muscle
14	chr10:4554000-4555000	Weak transcription	Fetal Kidney	kidney
15	chr10:4554000-4555400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr10:4554200-4557200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:4554600-4555000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr10:4554600-4555600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr10:4554600-4556200	Enhancers	Fetal Heart	heart
20	chr10:4554800-4555000	Enhancers	Adipose Nuclei	Adipose
21	chr10:4554800-4555200	Enhancers	NHLF	lung
22	chr10:4554800-4555400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr10:4554800-4555400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr10:4554800-4555400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr10:4554800-4555400	Enhancers	Rectal Smooth Muscle	rectum
26	chr10:4554800-4555400	Enhancers	HMEC	breast
27	chr10:4554800-4555400	Enhancers	NHEK	skin
28	chr10:4554800-4556600	Enhancers	Left Ventricle	heart
29	chr10:4555000-4555200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr10:4555000-4555200	Enhancers	Stomach Smooth Muscle	stomach
31	chr10:4555000-4555200	Enhancers	HSMM	muscle
32	chr10:4555000-4555400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr10:4555000-4555400	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr10:4555000-4555400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr10:4555000-4555400	Enhancers	Fetal Kidney	kidney
36	chr10:4555000-4555400	Enhancers	Fetal Stomach	stomach
37	chr10:4555000-4555400	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr10:4555000-4555400	Enhancers	A549	lung
39	chr10:4555000-4555400	Enhancers	NH-A	brain
40	chr10:4555000-4555400	Flanking Active TSS	Osteobl	bone
41	chr10:4555000-4556000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr10:4555000-4556400	Enhancers	Colon Smooth Muscle	Colon
43	chr10:4555000-4558400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr10:4555200-4555400	Enhancers	Colonic Mucosa	Colon
45	chr10:4555200-4555400	Enhancers	Fetal Muscle Trunk	muscle
46	chr10:4555200-4555400	Enhancers	Fetal Muscle Leg	muscle
47	chr10:4555200-4555400	Enhancers	Placenta	Placenta
48	chr10:4555200-4555400	Enhancers	Pancreas	Pancrea
49	chr10:4555200-4556400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr10:4555200-4556400	Weak transcription	NHLF	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links