Variant report

Variant	nsv829805
Chromosome Location	chr3:177662113-177805003
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:796)
CpG islands
(count:245)
Chromatin interactive
region (count:24)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:177802748-177803132	HepG2	liver:	n/a	n/a
2	ATF1	chr3:177765904-177765980	K562	blood:	n/a	n/a
3	ATF1	chr3:177766537-177767077	K562	blood:	n/a	n/a
4	ATF2	chr3:177719561-177720036	GM12878	blood:	n/a	n/a
5	ATF3	chr3:177766571-177766805	K562	blood:	n/a	n/a
6	BACH1	chr3:177801543-177803106	H1-hESC	embryonic stem cell:	n/a	chr3:177801728-177801742
7	BACH1	chr3:177802023-177802132	K562	blood:	n/a	n/a
8	BATF	chr3:177719639-177719990	GM12878	blood:	n/a	n/a
9	BATF	chr3:177719669-177719992	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:177719612-177719946	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:177684381-177684528	HepG2	liver:	n/a	n/a
12	BRCA1	chr3:177802466-177802927	H1-hESC	embryonic stem cell:	n/a	n/a
13	CCNT2	chr3:177766612-177766809	K562	blood:	n/a	n/a
14	CCNT2	chr3:177800219-177800326	K562	blood:	n/a	n/a
15	CEBPB	chr3:177664375-177665182	Hela-S3	cervix:	n/a	chr3:177664995-177665006 chr3:177664579-177664588 chr3:177664579-177664588 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664551-177664563 chr3:177664995-177665006 chr3:177664993-177665004
16	CEBPB	chr3:177766538-177766885	K562	blood:	n/a	n/a
17	CEBPB	chr3:177762125-177762487	IMR90	lung:	n/a	chr3:177762297-177762308
18	CEBPB	chr3:177762009-177762510	HCT-116	colon:	n/a	chr3:177762297-177762308
19	CEBPB	chr3:177802593-177802942	IMR90	lung:	n/a	n/a
20	CEBPB	chr3:177709192-177709234	HepG2	liver:	n/a	chr3:177709202-177709215
21	CEBPB	chr3:177730213-177730402	K562	blood:	n/a	n/a
22	CEBPB	chr3:177695460-177696133	A549	lung:	n/a	n/a
23	CEBPB	chr3:177663949-177664028	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:177762085-177762539	ECC-1	luminal epithelium:	n/a	chr3:177762297-177762308
25	CEBPB	chr3:177695470-177695978	HCT-116	colon:	n/a	n/a
26	CEBPB	chr3:177664797-177665136	A549	lung:	n/a	chr3:177664995-177665006 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664995-177665006 chr3:177664993-177665004
27	CEBPB	chr3:177730204-177730299	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:177695571-177696022	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:177762117-177762485	A549	lung:	n/a	chr3:177762297-177762308
30	CEBPB	chr3:177762133-177762476	Hela-S3	cervix:	n/a	chr3:177762297-177762308
31	CEBPB	chr3:177774746-177775004	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:177695627-177695962	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:177711874-177711898	K562	blood:	n/a	n/a
34	CEBPB	chr3:177710821-177711139	K562	blood:	n/a	chr3:177710999-177711010 chr3:177710998-177711009
35	CEBPB	chr3:177664724-177665185	A549	lung:	n/a	chr3:177664995-177665006 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664995-177665006 chr3:177664993-177665004
36	CEBPB	chr3:177762121-177762436	A549	lung:	n/a	chr3:177762297-177762308
37	CEBPB	chr3:177687543-177687646	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:177664497-177664566	A549	lung:	n/a	chr3:177664551-177664563
39	CEBPB	chr3:177730265-177730303	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:177762094-177762554	MCF-7	breast:	n/a	chr3:177762297-177762308
41	CEBPB	chr3:177761975-177762513	A549	lung:	n/a	chr3:177762297-177762308
42	CEBPB	chr3:177711800-177711977	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr3:177762156-177762441	K562	blood:	n/a	chr3:177762297-177762308
44	CEBPB	chr3:177664762-177665224	MCF-7	breast:	n/a	chr3:177664995-177665006 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664995-177665006 chr3:177664993-177665004
45	CEBPB	chr3:177762074-177762508	HCT-116	colon:	n/a	chr3:177762297-177762308
46	CEBPB	chr3:177710838-177711139	HepG2	liver:	n/a	chr3:177710999-177711010 chr3:177710998-177711009
47	CEBPB	chr3:177665648-177665684	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr3:177695645-177695997	A549	lung:	n/a	n/a
49	CEBPB	chr3:177762066-177762545	ECC-1	luminal epithelium:	n/a	chr3:177762297-177762308
50	CEBPB	chr3:177710879-177711150	K562	blood:	n/a	chr3:177710999-177711010 chr3:177710998-177711009

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:177778301-177778351	GM12878	blood:	n/a
2	chr3:177778301-177778351	GM12878	blood:	n/a
3	chr3:177700638-177700688	AG04449	skin:	fetal
4	chr3:177696327-177696377	ovcar-3	ovarian:	n/a
5	chr3:177696327-177696377	ProgFib	skin:	n/a
6	chr3:177778301-177778351	A549	lung:	n/a
7	chr3:177696327-177696377	GM19239	blood:	n/a
8	chr3:177696327-177696377	RPTEC	kidney:	n/a
9	chr3:177696327-177696377	PrEC	prostate:	n/a
10	chr3:177700638-177700688	K562	blood:	n/a
11	chr3:177700638-177700688	ovcar-3	ovarian:	n/a
12	chr3:177696327-177696377	MCF10A-Er-Src	breast:	n/a
13	chr3:177778301-177778351	NHBE	bronchial:	n/a
14	chr3:177778301-177778351	HCM	heart:	n/a
15	chr3:177778301-177778351	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:177696327-177696377	Hepatocyte	liver:	n/a
17	chr3:177802381-177802431	K562	blood:	n/a
18	chr3:177696327-177696377	HRE	kidney:	n/a
19	chr3:177802381-177802431	MCF10A-Er-Src	breast:	n/a
20	chr3:177778301-177778351	HRE	kidney:	n/a
21	chr3:177802381-177802431	GM19239	blood:	n/a
22	chr3:177696327-177696377	HRPEpiC	eye:	n/a
23	chr3:177778301-177778351	MCF-7	breast:	n/a
24	chr3:177696327-177696377	AoSMC	blood vessel:	n/a
25	chr3:177700638-177700688	AoSMC	blood vessel:	n/a
26	chr3:177696327-177696377	Caco-2	colon:	n/a
27	chr3:177700638-177700688	SK-N-MC	brain:	n/a
28	chr3:177778301-177778351	IMR90	lung:	fetal
29	chr3:177700638-177700688	NHBE	bronchial:	n/a
30	chr3:177802381-177802431	NT2-D1	testis:	n/a
31	chr3:177802381-177802431	HEEpiC	esophagus:	n/a
32	chr3:177700638-177700688	HCM	heart:	n/a
33	chr3:177700638-177700688	GM12891	blood:	n/a
34	chr3:177696327-177696377	SK-N-MC	brain:	n/a
35	chr3:177802381-177802431	Caco-2	colon:	n/a
36	chr3:177696327-177696377	HEK293	kidney:	embryo
37	chr3:177696327-177696377	HEEpiC	esophagus:	n/a
38	chr3:177778301-177778351	PANC-1	pancreas:	n/a
39	chr3:177700638-177700688	GM06990	blood:	n/a
40	chr3:177700638-177700688	NB4	blood:	n/a
41	chr3:177778301-177778351	NH-A	brain:	n/a
42	chr3:177696327-177696377	HCM	heart:	n/a
43	chr3:177802381-177802431	HAEpiC	amniotic membrane:	n/a
44	chr3:177700638-177700688	HIPEpiC	eye:	n/a
45	chr3:177696327-177696377	BE2_C	brain:	n/a
46	chr3:177700638-177700688	NH-A	brain:	n/a
47	chr3:177700638-177700688	HNPCEpiC	eye:	n/a
48	chr3:177778301-177778351	HUVEC	blood vessel:	n/a
49	chr3:177778301-177778351	H1-hESC	embryonic stem cell:	embryo
50	chr3:177802381-177802431	SAEC	small airway:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:177801343..177802850-chr3:177807715..177810177,2	K562	blood:
2	chr3:177798006..177799686-chr3:177801992..177804180,2	MCF-7	breast:
3	chr3:177534496..177537087-chr3:177660637..177662503,2	MCF-7	breast:
4	chr3:177684306..177686654-chr3:177686995..177689814,2	MCF-7	breast:
5	chr3:177684306..177686654-chr3:177686995..177689814,2	MCF-7	breast:
6	chr3:177746057..177748519-chr3:177753928..177756094,2	MCF-7	breast:
7	chr3:177771468..177773517-chr3:177775171..177778151,2	K562	blood:
8	chr3:177532426..177535224-chr3:177663514..177665237,2	MCF-7	breast:
9	chr3:177709402..177711641-chr3:177711937..177714399,2	K562	blood:
10	chr3:177771468..177773517-chr3:177775171..177778151,2	K562	blood:
11	chr3:177740310..177743198-chr3:177745813..177748789,2	K562	blood:
12	chr3:177756882..177758737-chr3:177759216..177761677,2	MCF-7	breast:
13	chr3:177798084..177799905-chr3:177816555..177819549,2	MCF-7	breast:
14	chr3:177754764..177756707-chr3:177757641..177760042,2	MCF-7	breast:
15	chr3:177746057..177748519-chr3:177753928..177756094,2	MCF-7	breast:
16	chr3:177740310..177743198-chr3:177745813..177748789,2	K562	blood:
17	chr3:177756882..177758737-chr3:177759216..177761677,2	MCF-7	breast:
18	chr3:177798006..177799686-chr3:177801992..177804180,2	MCF-7	breast:
19	chr3:177744544..177746409-chr3:178372546..178374222,2	K562	blood:
20	chr3:177781466..177784342-chr3:177795309..177797884,2	K562	blood:
21	chr3:177781466..177784342-chr3:177795309..177797884,2	K562	blood:
22	chr3:177076309..177079025-chr3:177709045..177711034,2	K562	blood:
23	chr3:177754764..177756707-chr3:177757641..177760042,2	MCF-7	breast:
24	chr3:177709402..177711641-chr3:177711937..177714399,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNMB2-11	chr3:177765543-177765717	l_2533_chr3:177745107-177765717_testes
2	lnc-KCNMB2-10	chr3:177783610-177784110	NONHSAT093364
3	lnc-KCNMB2-10	chr3:177767852-177767894	NONHSAT093364
4	lnc-KCNMB2-11	chr3:177759203-177759422	l_2533_chr3:177745107-177765717_testes
5	lnc-KCNMB2-11	chr3:177745422-177745603	l_2533_chr3:177745107-177765717_testes
6	lnc-KCNMB2-11	chr3:177745108-177745336	l_2533_chr3:177745107-177765717_testes

No data

Variant related genes	Relation type
ENSG00000270321	TF binding region
RNU6-1120P	TF binding region
ENSG00000270321	CpG island
RNU6-1120P	CpG island
ENSG00000231574	chromatin interactions

Extended variants
information (count: 3783 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3783 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553482989	chr3:177662119-177662120	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs576860327	chr3:177662123-177662124	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs141373306	chr3:177662155-177662156	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112418129	chr3:177662185-177662186	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556276299	chr3:177662210-177662211	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2068607	chr3:177662221-177662222	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542109708	chr3:177662229-177662230	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2068608	chr3:177662238-177662239	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369421717	chr3:177662268-177662269	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534907033	chr3:177662287-177662288	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs540623296	chr3:177662291-177662292	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560428131	chr3:177662376-177662377	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs114409145	chr3:177662478-177662479	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs150760083	chr3:177662550-177662551	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs372376367	chr3:177662576-177662577	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs139676086	chr3:177662597-177662598	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs143674010	chr3:177662602-177662603	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182410614	chr3:177662626-177662627	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527834498	chr3:177662633-177662634	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187093336	chr3:177662652-177662653	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77554531	chr3:177662697-177662698	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546982742	chr3:177662745-177662746	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570455079	chr3:177662773-177662774	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539478098	chr3:177662823-177662824	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs556100746	chr3:177662850-177662851	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs576157371	chr3:177662873-177662874	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs189539576	chr3:177662875-177662876	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs79312658	chr3:177662932-177662933	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs147159930	chr3:177662940-177662941	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs540635260	chr3:177662998-177662999	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs369400001	chr3:177663040-177663041	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs563099391	chr3:177663075-177663076	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs372674680	chr3:177663077-177663078	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs560456741	chr3:177663078-177663079	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577284465	chr3:177663090-177663091	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs376902739	chr3:177663123-177663124	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140435029	chr3:177663126-177663127	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs562820682	chr3:177663142-177663143	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529124811	chr3:177663177-177663178	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs149656963	chr3:177663192-177663193	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs559219747	chr3:177663203-177663204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548361898	chr3:177663304-177663305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562088447	chr3:177663350-177663351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182613429	chr3:177663355-177663356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546998713	chr3:177663370-177663371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570393414	chr3:177663416-177663417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189019608	chr3:177663457-177663458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549875270	chr3:177663470-177663471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs193152092	chr3:177663520-177663521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185209126	chr3:177663570-177663571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Cancer	20164920	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1081 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:177653600-177662200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr3:177660800-177662200	Enhancers	Dnd41	blood
3	chr3:177661000-177662200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr3:177661000-177662200	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr3:177661000-177664000	Enhancers	Primary hematopoietic stem cells	blood
6	chr3:177661000-177664000	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr3:177661200-177662200	Enhancers	Primary T cells from cord blood	blood
8	chr3:177661200-177662600	Enhancers	Primary T cells fromperipheralblood	blood
9	chr3:177661200-177662800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr3:177661200-177663400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr3:177661200-177663800	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr3:177661200-177664000	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr3:177661200-177664400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:177661200-177665800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr3:177661400-177663800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr3:177661400-177664000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr3:177661600-177662200	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr3:177661600-177662400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr3:177661800-177662600	Enhancers	Primary B cells from peripheral blood	blood
20	chr3:177661800-177662600	Enhancers	Fetal Thymus	thymus
21	chr3:177661800-177662600	Enhancers	Spleen	Spleen
22	chr3:177661800-177663200	Enhancers	Primary B cells from cord blood	blood
23	chr3:177661800-177663200	Enhancers	Thymus	Thymus
24	chr3:177661800-177663200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr3:177661800-177664000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr3:177662000-177662200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr3:177662000-177662600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr3:177662000-177662800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr3:177662200-177662400	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr3:177662200-177662600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr3:177662200-177662800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr3:177662200-177662800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr3:177662200-177662800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr3:177662200-177662800	Enhancers	Fetal Lung	lung
35	chr3:177662200-177662800	Flanking Active TSS	Dnd41	blood
36	chr3:177662200-177662800	Enhancers	HUVEC	blood vessel
37	chr3:177662200-177663000	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr3:177662200-177663800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr3:177662400-177662600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr3:177662400-177662600	Enhancers	Adipose Nuclei	Adipose
41	chr3:177662600-177662800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:177662600-177663600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr3:177662600-177663800	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr3:177662600-177663800	Weak transcription	Adipose Nuclei	Adipose
45	chr3:177662600-177663800	Weak transcription	Spleen	Spleen
46	chr3:177662600-177664000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr3:177662600-177664200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:177662600-177666400	Weak transcription	Fetal Thymus	thymus
49	chr3:177662800-177663200	Weak transcription	Fetal Lung	lung
50	chr3:177662800-177663800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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