Variant report

Variant	nsv525927
Chromosome Location	chr10:6059898-6078079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:105)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:105 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:6075911-6076305	K562	blood:	n/a	n/a
2	ATF1	chr10:6075942-6076269	K562	blood:	n/a	n/a
3	ATF3	chr10:6075958-6076247	K562	blood:	n/a	n/a
4	BHLHE40	chr10:6061363-6061706	K562	blood:	n/a	n/a
5	BRCA1	chr10:6060651-6061479	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr10:6072111-6072550	K562	blood:	n/a	n/a
7	CBX3	chr10:6072176-6072494	K562	blood:	n/a	n/a
8	CCNT2	chr10:6076005-6076271	K562	blood:	n/a	n/a
9	CEBPB	chr10:6065264-6065464	A549	lung:	n/a	n/a
10	CEBPB	chr10:6061102-6061178	K562	blood:	n/a	n/a
11	CEBPB	chr10:6064831-6065496	K562	blood:	n/a	n/a
12	CEBPB	chr10:6065312-6065488	HepG2	liver:	n/a	n/a
13	CTCF	chr10:6064140-6064290	HEK293	kidney:	n/a	n/a
14	CTCF	chr10:6061020-6061170	GM12873	blood:	n/a	n/a
15	CTCF	chr10:6062020-6062170	GM12871	blood:	n/a	n/a
16	CTCF	chr10:6063440-6063590	K562	blood:	n/a	n/a
17	CTCF	chr10:6063680-6063830	GM12871	blood:	n/a	n/a
18	CTCF	chr10:6065620-6065770	GM12865	blood:	n/a	n/a
19	CTCF	chr10:6067196-6067245	Lung_OC	lung:	n/a	n/a
20	CTCF	chr10:6062040-6062190	GM12868	blood:	n/a	n/a
21	CTCF	chr10:6077060-6077210	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr10:6077340-6077490	GM12866	blood:	n/a	n/a
23	CUX1	chr10:6075553-6076164	K562	blood:	n/a	n/a
24	E2F6	chr10:6061457-6061628	K562	blood:	n/a	n/a
25	EP300	chr10:6075853-6076384	K562	blood:	n/a	n/a
26	EP300	chr10:6077780-6077811	HepG2	liver:	n/a	n/a
27	EP300	chr10:6061257-6061504	K562	blood:	n/a	n/a
28	EP300	chr10:6075821-6076398	K562	blood:	n/a	n/a
29	FOXA1	chr10:6065829-6066250	T-47D	breast:	n/a	n/a
30	FOXA1	chr10:6065849-6066180	T-47D	breast:	n/a	n/a
31	GATA3	chr10:6075797-6075977	SH-SY5Y	brain:	n/a	n/a
32	GTF2F1	chr10:6064884-6064900	K562	blood:	n/a	n/a
33	GTF2F1	chr10:6061195-6061443	K562	blood:	n/a	n/a
34	HCFC1	chr10:6061273-6061364	K562	blood:	n/a	n/a
35	HMGN3	chr10:6061871-6061872	K562	blood:	n/a	n/a
36	HMGN3	chr10:6076014-6076231	K562	blood:	n/a	n/a
37	IRF1	chr10:6073018-6073082	K562	blood:	n/a	n/a
38	JUN	chr10:6075517-6077077	K562	blood:	n/a	n/a
39	JUN	chr10:6075919-6076325	K562	blood:	n/a	n/a
40	JUN	chr10:6075912-6076288	K562	blood:	n/a	n/a
41	JUN	chr10:6075943-6076283	K562	blood:	n/a	n/a
42	JUND	chr10:6075859-6076366	K562	blood:	n/a	n/a
43	KAP1	chr10:6063325-6063790	K562	blood:	n/a	n/a
44	KAP1	chr10:6066091-6066458	K562	blood:	n/a	n/a
45	KAP1	chr10:6067684-6068126	K562	blood:	n/a	n/a
46	KAP1	chr10:6061229-6061895	K562	blood:	n/a	chr10:6061536-6061544
47	KAP1	chr10:6071989-6073345	K562	blood:	n/a	n/a
48	MAFF	chr10:6075902-6076291	K562	blood:	n/a	n/a
49	MAFK	chr10:6065021-6065156	K562	blood:	n/a	n/a
50	MAFK	chr10:6075967-6076204	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:6065835-6065885	PrEC	prostate:	n/a
2	chr10:6065835-6065885	AG04450	lung:	fetal
3	chr10:6065835-6065885	HUVEC	blood vessel:	n/a
4	chr10:6065835-6065885	PANC-1	pancreas:	n/a
5	chr10:6065835-6065885	HRCEpiC	kidney:	n/a
6	chr10:6065835-6065885	SK-N-MC	brain:	n/a
7	chr10:6065835-6065885	HCPEpiC	choroid plexus:	n/a
8	chr10:6065835-6065885	BE2_C	brain:	n/a
9	chr10:6065835-6065885	SAEC	small airway:	n/a
10	chr10:6065835-6065885	AG10803	skin:	n/a
11	chr10:6065835-6065885	NB4	blood:	n/a
12	chr10:6065835-6065885	U87	brain:	n/a
13	chr10:6065835-6065885	AG09309	skin:	n/a
14	chr10:6065835-6065885	GM06990	blood:	n/a
15	chr10:6065835-6065885	Caco-2	colon:	n/a
16	chr10:6065835-6065885	SKMC	muscle:	n/a
17	chr10:6065835-6065885	ProgFib	skin:	n/a
18	chr10:6065835-6065885	CMK	blood:	n/a
19	chr10:6065835-6065885	A549	lung:	n/a
20	chr10:6065835-6065885	ECC-1	luminal epithelium:	n/a
21	chr10:6065835-6065885	AG09319	gingival:	n/a
22	chr10:6065835-6065885	H1-hESC	embryonic stem cell:	embryo
23	chr10:6065835-6065885	IMR90	lung:	fetal
24	chr10:6065835-6065885	HCF	heart:	n/a
25	chr10:6065835-6065885	HL-60	blood:	n/a
26	chr10:6065835-6065885	GM19239	blood:	n/a
27	chr10:6065835-6065885	MCF-7	breast:	n/a
28	chr10:6065835-6065885	NT2-D1	testis:	n/a
29	chr10:6065835-6065885	HPAEpiC	pulmonary alveolar:	n/a
30	chr10:6065835-6065885	K562	blood:	n/a
31	chr10:6065835-6065885	RPTEC	kidney:	n/a
32	chr10:6065835-6065885	HRPEpiC	eye:	n/a
33	chr10:6065835-6065885	BJ	skin:	n/a
34	chr10:6065835-6065885	SK-N-SH_RA	brain:	n/a
35	chr10:6065835-6065885	NHDF-neo	bronchial:	n/a
36	chr10:6065835-6065885	HCM	heart:	n/a
37	chr10:6065835-6065885	SK-N-SH	brain:	n/a
38	chr10:6065835-6065885	AoSMC	blood vessel:	n/a
39	chr10:6065835-6065885	Hepatocyte	liver:	n/a
40	chr10:6065835-6065885	HepG2	liver:	n/a
41	chr10:6065835-6065885	HIPEpiC	eye:	n/a
42	chr10:6065835-6065885	HEEpiC	esophagus:	n/a
43	chr10:6065835-6065885	HRE	kidney:	n/a
44	chr10:6065835-6065885	ovcar-3	ovarian:	n/a
45	chr10:6065835-6065885	AG04449	skin:	fetal
46	chr10:6065835-6065885	GM12892	blood:	n/a
47	chr10:6065835-6065885	Jurkat	blood:	n/a
48	chr10:6065835-6065885	HMEC	breast:	n/a
49	chr10:6065835-6065885	NHBE	bronchial:	n/a
50	chr10:6065835-6065885	MCF10A-Er-Src	breast:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:6051578..6054248-chr10:6061893..6064175,2	K562	blood:
2	chr10:6068386..6070210-chr10:6087289..6089702,2	K562	blood:
3	chr10:6076656..6079069-chr10:6086121..6089076,2	MCF-7	breast:
4	chr10:6076770..6078831-chr10:6080611..6082982,2	MCF-7	breast:
5	chr10:6017825..6020295-chr10:6064566..6066546,2	MCF-7	breast:
6	chr10:5962148..5964571-chr10:6074505..6076333,2	K562	blood:
7	chr10:6068815..6071156-chr10:6071379..6075335,3	K562	blood:
8	chr10:6068815..6071156-chr10:6071379..6075335,3	K562	blood:
9	chr10:6059382..6061395-chr10:6068804..6071571,2	MCF-7	breast:
10	chr10:6065238..6067128-chr10:6067499..6070251,2	MCF-7	breast:
11	chr10:6059382..6061395-chr10:6068804..6071571,2	MCF-7	breast:
12	chr10:6074070..6077031-chr10:6131328..6132999,2	K562	blood:
13	chr10:6056224..6059650-chr10:6062911..6065647,3	MCF-7	breast:
14	chr10:6065213..6067323-chr10:6136961..6139213,2	MCF-7	breast:
15	chr10:6062258..6063971-chr10:6130127..6132844,2	MCF-7	breast:
16	chr10:6059419..6064322-chr10:6065224..6067534,4	K562	blood:
17	chr10:6055685..6057860-chr10:6061812..6063688,2	MCF-7	breast:
18	chr10:6077154..6078797-chr10:6082594..6084607,2	K562	blood:
19	chr10:6059419..6064322-chr10:6065224..6067534,4	K562	blood:
20	chr10:6017486..6019803-chr10:6068609..6071051,2	MCF-7	breast:
21	chr10:6060947..6063701-chr10:6181512..6183483,2	K562	blood:
22	chr10:6070515..6072335-chr10:6076874..6078701,2	K562	blood:
23	chr10:6070515..6072335-chr10:6076874..6078701,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM17-2	chr10:6067941-6068031	ENSG00000229664.1
2	lnc-RBM17-2	chr10:6077903-6078048	ENSG00000229664.1

No data

Variant related genes	Relation type
IL2RA	TF binding region
ENSG00000251922	TF binding region
ENSG00000229664	TF binding region
IL2RA	CpG island
ENSG00000251922	CpG island
ENSG00000229664	CpG island
ENSG00000134460	chromatin interactions
ENSG00000134470	chromatin interactions
ENSG00000134453	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000229664	chromatin interactions
ENSG00000251922	chromatin interactions

Extended variants
information (count: 820 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:820 , 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	rs7899538	chr10:6059898-6059899	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571942858	chr10:6059943-6059944	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112185090	chr10:6059944-6059945	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554056243	chr10:6059946-6059947	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572628967	chr10:6059965-6059966	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12722699	chr10:6060015-6060016	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536344946	chr10:6060022-6060023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140088691	chr10:6060023-6060024	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554680869	chr10:6060033-6060034	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143550766	chr10:6060053-6060054	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113428577	chr10:6060054-6060055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12722698	chr10:6060057-6060058	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs74162100	chr10:6060081-6060082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74162099	chr10:6060085-6060086	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201955877	chr10:6060090-6060091	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373749136	chr10:6060118-6060119	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3215754	chr10:6060172-6060173	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397840138	chr10:6060175-6060176	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570156062	chr10:6060197-6060198	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111378667	chr10:6060199-6060200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74162098	chr10:6060211-6060212	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56032961	chr10:6060234-6060235	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577846037	chr10:6060245-6060246	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79040149	chr10:6060265-6060266	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12722697	chr10:6060290-6060291	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs527525530	chr10:6060315-6060316	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202060940	chr10:6060372-6060373	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369470976	chr10:6060373-6060374	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373369015	chr10:6060394-6060395	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12722589	chr10:6060423-6060424	Enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs12722588	chr10:6060433-6060434	Enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs528048640	chr10:6060462-6060463	Enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538940911	chr10:6060624-6060625	Enhancers Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12722587	chr10:6060630-6060631	Enhancers Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs11256352	chr10:6060631-6060632	Enhancers Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs76140590	chr10:6060639-6060640	Enhancers Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372484011	chr10:6060717-6060718	Enhancers Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs375003561	chr10:6060835-6060836	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs576098233	chr10:6060846-6060847	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs184913967	chr10:6060890-6060891	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs558509477	chr10:6060957-6060958	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs72776071	chr10:6060966-6060967	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs199965784	chr10:6060977-6060978	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs117053021	chr10:6060980-6060981	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs111672227	chr10:6061010-6061011	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs111164953	chr10:6061062-6061063	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs542816766	chr10:6061086-6061087	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs200515389	chr10:6061089-6061090	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561082644	chr10:6061095-6061096	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs372824153	chr10:6061096-6061097	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	22355333	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6056200-6061000	Weak transcription	K562	blood
2	chr10:6056800-6060400	Weak transcription	Primary B cells from peripheral blood	blood
3	chr10:6057000-6066000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr10:6057200-6060600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr10:6057400-6068600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr10:6057600-6060400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr10:6057600-6062800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr10:6057800-6064400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr10:6057800-6069600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr10:6057800-6069800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr10:6058000-6068600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr10:6058400-6060000	Weak transcription	Fetal Thymus	thymus
13	chr10:6058400-6062800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr10:6058600-6063200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr10:6059000-6060600	Enhancers	Duodenum Mucosa	Duodenum
16	chr10:6059000-6060800	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr10:6059200-6060200	Enhancers	Fetal Intestine Small	intestine
18	chr10:6059200-6060400	Enhancers	Colonic Mucosa	Colon
19	chr10:6059200-6060400	Enhancers	Lung	lung
20	chr10:6059200-6060400	Enhancers	Small Intestine	intestine
21	chr10:6059400-6061000	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr10:6059400-6063000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr10:6059400-6068800	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr10:6059800-6060200	Strong transcription	Pancreatic Islets	Pancreatic Islet
25	chr10:6059800-6060600	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr10:6059800-6060800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr10:6059800-6060800	Enhancers	Placenta	Placenta
28	chr10:6059800-6061000	Enhancers	Stomach Mucosa	stomach
29	chr10:6060000-6060200	Enhancers	Fetal Thymus	thymus
30	chr10:6060000-6060400	Enhancers	Stomach Smooth Muscle	stomach
31	chr10:6060000-6060600	Enhancers	Fetal Muscle Leg	muscle
32	chr10:6060000-6060800	Enhancers	Ovary	ovary
33	chr10:6060000-6061200	Enhancers	Spleen	Spleen
34	chr10:6060000-6065600	Weak transcription	Esophagus	oesophagus
35	chr10:6060200-6060600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr10:6060200-6060800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr10:6060200-6060800	Enhancers	Fetal Stomach	stomach
38	chr10:6060200-6060800	Enhancers	Right Atrium	heart
39	chr10:6060200-6061000	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr10:6060400-6061200	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
41	chr10:6060400-6062000	Strong transcription	Primary B cells from peripheral blood	blood
42	chr10:6060400-6063200	Weak transcription	Colonic Mucosa	Colon
43	chr10:6060400-6070000	Weak transcription	Lung	lung
44	chr10:6060600-6060800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:6060600-6060800	Enhancers	Colon Smooth Muscle	Colon
46	chr10:6060600-6061800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr10:6060600-6062200	Weak transcription	Fetal Muscle Leg	muscle
48	chr10:6060600-6063000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr10:6060800-6061800	Weak transcription	Placenta	Placenta
50	chr10:6060800-6064400	Weak transcription	Right Atrium	heart

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