Variant report

Variant	nsv1047226
Chromosome Location	chr10:6651427-6664154
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	chr10:6663485-6663746	K562	blood:	n/a	n/a
2	CEBPB	chr10:6657447-6657691	HepG2	liver:	n/a	n/a
3	E2F4	chr10:6653664-6654135	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F4	chr10:6654393-6654902	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F4	chr10:6652961-6653161	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr10:6651379-6651579	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr10:6651415-6651518	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr10:6654281-6654588	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr10:6661783-6661874	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr10:6663466-6663829	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
11	FOS	chr10:6654272-6654782	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr10:6663485-6663813	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
13	FOS	chr10:6663471-6663830	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
14	FOS	chr10:6654272-6654599	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr10:6654259-6654588	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr10:6663485-6663807	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
17	FOSL2	chr10:6661614-6661969	HepG2	liver:	n/a	n/a
18	FOSL2	chr10:6663419-6663739	SK-N-SH	brain:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
19	GATA3	chr10:6663444-6663521	SH-SY5Y	brain:	n/a	chr10:6663459-6663466 chr10:6663508-6663517 chr10:6663504-6663520 chr10:6663508-6663515 chr10:6663504-6663520 chr10:6663459-6663466 chr10:6663459-6663466 chr10:6663508-6663515 chr10:6663507-6663517 chr10:6663508-6663515 chr10:6663452-6663473
20	JUN	chr10:6663503-6663800	H1-hESC	embryonic stem cell:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
21	JUN	chr10:6663612-6663814	HepG2	liver:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
22	JUND	chr10:6663404-6664010	SK-N-SH	brain:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
23	JUND	chr10:6663460-6663825	H1-hESC	embryonic stem cell:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
24	JUND	chr10:6663504-6663807	K562	blood:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
25	JUND	chr10:6663491-6663795	Hela-S3	cervix:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
26	JUND	chr10:6663493-6663843	HepG2	liver:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
27	KAP1	chr10:6663335-6664022	HEK293	kidney:	n/a	chr10:6663649-6663658
28	KAP1	chr10:6663095-6663993	U2OS	brain:	n/a	chr10:6663649-6663658
29	MAFF	chr10:6657616-6657628	HepG2	liver:	n/a	n/a
30	MAFK	chr10:6657422-6657626	HepG2	liver:	n/a	n/a
31	MAFK	chr10:6652761-6652961	HepG2	liver:	n/a	chr10:6652804-6652824 chr10:6652806-6652822 chr10:6652807-6652821 chr10:6652803-6652818
32	MAFK	chr10:6657451-6657756	HepG2	liver:	n/a	n/a
33	MAFK	chr10:6652715-6652916	HepG2	liver:	n/a	chr10:6652804-6652824 chr10:6652806-6652822 chr10:6652807-6652821 chr10:6652803-6652818
34	MYC	chr10:6654295-6654803	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr10:6656339-6656382	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr10:6663804-6664003	K562	blood:	n/a	n/a
37	POLR2A	chr10:6656347-6656418	K562	blood:	n/a	n/a
38	RCOR1	chr10:6663553-6663753	K562	blood:	n/a	n/a
39	STAT3	chr10:6654390-6654680	MCF10A-Er-Src	breast:	n/a	n/a
40	STAT3	chr10:6654450-6654577	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr10:6663564-6663714	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663656 chr10:6663648-6663657
42	STAT3	chr10:6657958-6658170	MCF10A-Er-Src	breast:	n/a	n/a
43	ZNF384	chr10:6654338-6654482	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:6614415..6616986-chr10:6653036..6655207,2	K562	blood:
2	chr10:6657794..6661242-chr10:6661759..6664532,3	K562	blood:
3	chr10:6622287..6623956-chr10:6655441..6657087,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL137145.1-2	chr10:6657968-6658273	XLOC_008370
2	lnc-AL137145.1-3	chr10:6663672-6663911	XLOC_008371
3	lnc-AL137145.1-3	chr10:6662507-6662895	ucscGeneNc_uc001ijl_2
4	lnc-AL137145.1-3	chr10:6662880-6663135	ENSG00000225948.2
5	lnc-AL137145.1-2	chr10:6657725-6657886	ENSG00000237943.2
6	lnc-AL137145.1-2	chr10:6657388-6657599	XLOC_008370
7	lnc-AL137145.1-3	chr10:6662976-6663135	XLOC_008371
8	lnc-AL137145.1-2	chr10:6657693-6658742	NONHSAT011239
9	lnc-AL137145.1-2	chr10:6657190-6657643	NONHSAT011239
10	lnc-AL137145.1-2	chr10:6657725-6657886	ENSG00000237943.2
11	lnc-AL137145.1-3	chr10:6660597-6660738	XLOC_008371
12	lnc-AL137145.1-2	chr10:6657725-6657912	ENSG00000237943.2
13	lnc-AL137145.1-3	chr10:6662880-6663135	XLOC_008371
14	lnc-AL137145.1-2	chr10:6655593-6655651	ENSG00000237943.2
15	lnc-AL137145.1-2	chr10:6657725-6657810	XLOC_008370
16	lnc-AL137145.1-3	chr10:6663672-6663911	XLOC_008371
17	lnc-AL137145.1-2	chr10:6657481-6657599	ENSG00000237943.2
18	lnc-AL137145.1-3	chr10:6662881-6663135	XLOC_008371
19	lnc-AL137145.1-3	chr10:6663672-6663824	ENSG00000225948.2
20	lnc-AL137145.1-2	chr10:6657968-6658359	ENSG00000237943.2
21	lnc-AL137145.1-2	chr10:6657332-6657409	XLOC_008370
22	lnc-AL137145.1-2	chr10:6657693-6657797	FPKM1_group_2866_transcript_7
23	lnc-AL137145.1-2	chr10:6657725-6657921	ENSG00000237943.2
24	lnc-AL137145.1-3	chr10:6660678-6660738	XLOC_008371
25	lnc-AL137145.1-3	chr10:6660678-6660738	ENSG00000225948.2
26	lnc-AL137145.1-2	chr10:6657190-6657643	FPKM1_group_2866_transcript_7
27	lnc-AL137145.1-2	chr10:6657725-6657886	XLOC_008370
28	lnc-AL137145.1-2	chr10:6657332-6657599	ENSG00000237943.2
29	lnc-AL137145.1-2	chr10:6657968-6658414	ENSG00000237943.2
30	lnc-AL137145.1-3	chr10:6663672-6663824	XLOC_008371

Variant related genes	Relation type
ENSG00000225948	TF binding region
ENSG00000225948	chromatin interactions
ENSG00000237943	chromatin interactions
RNF145	miRNA target sites
DDX6	miRNA target sites
EPHA4	miRNA target sites
TOMM70A	miRNA target sites

Extended variants
information (count: 550 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553587982	chr10:6651455-6651456	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116311196	chr10:6651485-6651486	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143544344	chr10:6651528-6651529	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554376411	chr10:6651545-6651546	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1327249	chr10:6651563-6651564	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs186096838	chr10:6651570-6651571	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562891711	chr10:6651635-6651636	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116185096	chr10:6651637-6651638	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191867552	chr10:6651644-6651645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528968574	chr10:6651674-6651675	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560397121	chr10:6651685-6651686	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184108110	chr10:6651687-6651688	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543163073	chr10:6651748-6651749	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138154491	chr10:6651807-6651808	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141636493	chr10:6651873-6651874	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550150743	chr10:6651878-6651879	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532043734	chr10:6651901-6651902	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10904616	chr10:6651941-6651942	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs188022839	chr10:6651956-6651957	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190543453	chr10:6651964-6651965	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532687436	chr10:6651971-6651972	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147051138	chr10:6652006-6652007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183191144	chr10:6652025-6652026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117765962	chr10:6652029-6652030	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566123075	chr10:6652043-6652044	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187117009	chr10:6652054-6652055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568857087	chr10:6652062-6652063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60192529	chr10:6652066-6652067	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543265222	chr10:6652069-6652070	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558585176	chr10:6652094-6652095	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75374145	chr10:6652143-6652144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545092856	chr10:6652160-6652161	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2478867	chr10:6652162-6652163	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192926264	chr10:6652214-6652215	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138394506	chr10:6652296-6652297	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182466112	chr10:6652307-6652308	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537452421	chr10:6652316-6652317	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531954391	chr10:6652324-6652325	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112302024	chr10:6652357-6652358	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565462898	chr10:6652382-6652383	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532870179	chr10:6652408-6652409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555875803	chr10:6652438-6652439	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534269333	chr10:6652445-6652446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368659748	chr10:6652480-6652481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571491059	chr10:6652514-6652515	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141824712	chr10:6652528-6652529	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569431679	chr10:6652530-6652531	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113161935	chr10:6652559-6652560	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187940842	chr10:6652588-6652589	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs115684656	chr10:6652658-6652659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Mantle cell lymphoma	19029149	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6642800-6651600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:6646600-6652600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr10:6649400-6651600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr10:6649400-6652600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr10:6649400-6653000	Weak transcription	Dnd41	blood
6	chr10:6649800-6651800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr10:6649800-6652200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr10:6649800-6652400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr10:6649800-6652600	Strong transcription	Primary T cells from cord blood	blood
10	chr10:6649800-6652600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr10:6649800-6653000	Weak transcription	Fetal Thymus	thymus
12	chr10:6650000-6651600	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr10:6650000-6651800	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr10:6650000-6652800	Weak transcription	Thymus	Thymus
15	chr10:6650200-6651800	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr10:6650400-6651600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr10:6650600-6652600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr10:6650800-6652400	Weak transcription	NHEK	skin
19	chr10:6650800-6652600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:6651000-6652600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr10:6651000-6652600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr10:6651000-6652800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr10:6651000-6656400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr10:6651200-6651800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr10:6651200-6652400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr10:6651200-6652600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr10:6651200-6661600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr10:6651400-6652000	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr10:6651400-6652800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr10:6651400-6653600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:6651600-6652600	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr10:6651600-6652800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr10:6651600-6654800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr10:6651600-6654800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr10:6651800-6652200	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr10:6651800-6652200	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr10:6651800-6652600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr10:6651800-6655400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr10:6651800-6663200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr10:6652200-6652400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
41	chr10:6652200-6655200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr10:6652200-6655200	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr10:6652400-6653200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr10:6652400-6655000	Enhancers	NHEK	skin
45	chr10:6652400-6655200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr10:6652400-6655400	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr10:6652400-6655400	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr10:6652600-6652800	Weak transcription	Primary T cells from cord blood	blood
49	chr10:6652600-6653400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr10:6652600-6654200	Enhancers	Primary T cells fromperipheralblood	blood

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