Variant report

Variant	esv2763655
Chromosome Location	chr2:37905976-37933740
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:184)
Chromatin interactive
region (count:12)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37911892-37911895	K562	blood:	n/a	n/a
2	ATF1	chr2:37909689-37909972	K562	blood:	n/a	n/a
3	ATF1	chr2:37910388-37910830	K562	blood:	n/a	n/a
4	CCNT2	chr2:37909833-37910036	K562	blood:	n/a	chr2:37909849-37909869
5	CEBPB	chr2:37908690-37908959	A549	lung:	n/a	chr2:37908841-37908852
6	CEBPB	chr2:37908703-37909025	IMR90	lung:	n/a	chr2:37908841-37908852
7	CEBPB	chr2:37910418-37910696	K562	blood:	n/a	n/a
8	CEBPB	chr2:37925899-37926278	IMR90	lung:	n/a	chr2:37926004-37926021 chr2:37926009-37926020
9	CEBPB	chr2:37928394-37928689	IMR90	lung:	n/a	chr2:37928542-37928553
10	CEBPB	chr2:37928487-37928584	K562	blood:	n/a	chr2:37928542-37928553
11	CEBPB	chr2:37916163-37916740	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:37925954-37926349	Hela-S3	cervix:	n/a	chr2:37926004-37926021 chr2:37926009-37926020
13	CEBPB	chr2:37908668-37909012	HepG2	liver:	n/a	chr2:37908841-37908852
14	CEBPB	chr2:37908762-37908997	Hela-S3	cervix:	n/a	chr2:37908841-37908852
15	CEBPB	chr2:37928474-37928610	HepG2	liver:	n/a	chr2:37928542-37928553
16	CEBPB	chr2:37928502-37928667	Hela-S3	cervix:	n/a	chr2:37928542-37928553
17	CEBPB	chr2:37928450-37928683	A549	lung:	n/a	chr2:37928542-37928553
18	CEBPB	chr2:37919916-37920190	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:37908693-37909016	K562	blood:	n/a	chr2:37908841-37908852
20	CEBPB	chr2:37910357-37910625	K562	blood:	n/a	n/a
21	CEBPB	chr2:37916154-37916564	IMR90	lung:	n/a	n/a
22	CHD2	chr2:37915241-37915444	K562	blood:	n/a	n/a
23	CTCF	chr2:37910101-37910247	K562	blood:	n/a	chr2:37910131-37910149 chr2:37910134-37910143
24	CTCF	chr2:37926880-37927030	RPTEC	kidney:	n/a	n/a
25	CTCF	chr2:37915480-37915630	GM12864	blood:	n/a	n/a
26	CTCF	chr2:37926620-37926770	NHLF	lung:	n/a	n/a
27	CTCF	chr2:37913150-37913209	LNCaP	prostate:	n/a	n/a
28	CTCF	chr2:37926840-37926990	AG04449	skin:	n/a	n/a
29	CTCF	chr2:37908980-37909130	GM12866	blood:	n/a	n/a
30	CTCF	chr2:37926840-37926990	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr2:37926820-37926970	AG04450	lung:	n/a	n/a
32	CTCF	chr2:37927260-37927410	NB4	blood:	n/a	n/a
33	EP300	chr2:37909726-37910045	K562	blood:	n/a	chr2:37909914-37909923
34	EP300	chr2:37910417-37910726	K562	blood:	n/a	n/a
35	EP300	chr2:37906319-37906864	T-47D	breast:	n/a	n/a
36	EP300	chr2:37906338-37906979	MCF-7	breast:	n/a	n/a
37	EP300	chr2:37916190-37916662	ECC-1	luminal epithelium:	n/a	n/a
38	EP300	chr2:37915934-37917235	ECC-1	luminal epithelium:	n/a	n/a
39	EP300	chr2:37906327-37906864	T-47D	breast:	n/a	n/a
40	EP300	chr2:37916302-37916876	T-47D	breast:	n/a	n/a
41	EP300	chr2:37916199-37916632	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr2:37916416-37916682	T-47D	breast:	n/a	n/a
43	EP300	chr2:37925795-37926873	SK-N-SH	brain:	n/a	n/a
44	EP300	chr2:37915899-37917201	SK-N-SH	brain:	n/a	n/a
45	EP300	chr2:37916115-37916647	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr2:37916233-37916569	Hela-S3	cervix:	n/a	n/a
47	EP300	chr2:37925917-37926791	ECC-1	luminal epithelium:	n/a	n/a
48	EP300	chr2:37925811-37926951	SK-N-SH	brain:	n/a	n/a
49	ESR1	chr2:37916334-37916681	ECC-1	luminal epithelium:	n/a	n/a
50	ESR1	chr2:37906371-37906831	T-47D	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37909996-37910046	U87	brain:	n/a
2	chr2:37909996-37910046	U87	brain:	n/a
3	chr2:37927157-37927207	AG04449	skin:	fetal
4	chr2:37909996-37910046	SK-N-MC	brain:	n/a
5	chr2:37917061-37917111	HRPEpiC	eye:	n/a
6	chr2:37917061-37917111	MCF10A-Er-Src	breast:	n/a
7	chr2:37917061-37917111	T-47D	breast:	n/a
8	chr2:37909996-37910046	Caco-2	colon:	n/a
9	chr2:37909996-37910046	NT2-D1	testis:	n/a
10	chr2:37917061-37917111	HCPEpiC	choroid plexus:	n/a
11	chr2:37927157-37927207	HRCEpiC	kidney:	n/a
12	chr2:37909996-37910046	NH-A	brain:	n/a
13	chr2:37917061-37917111	AG09309	skin:	n/a
14	chr2:37927157-37927207	AG10803	skin:	n/a
15	chr2:37909996-37910046	HCM	heart:	n/a
16	chr2:37909996-37910046	MCF-7	breast:	n/a
17	chr2:37927157-37927207	SK-N-SH	brain:	n/a
18	chr2:37927157-37927207	HCPEpiC	choroid plexus:	n/a
19	chr2:37927157-37927207	HMEC	breast:	n/a
20	chr2:37909996-37910046	AoSMC	blood vessel:	n/a
21	chr2:37909996-37910046	SK-N-SH	brain:	n/a
22	chr2:37927157-37927207	NHDF-neo	bronchial:	n/a
23	chr2:37917061-37917111	GM12878	blood:	n/a
24	chr2:37917061-37917111	HRE	kidney:	n/a
25	chr2:37909996-37910046	HEK293	kidney:	embryo
26	chr2:37917061-37917111	NH-A	brain:	n/a
27	chr2:37909996-37910046	AG04450	lung:	fetal
28	chr2:37909996-37910046	Hela-S3	cervix:	n/a
29	chr2:37917061-37917111	HL-60	blood:	n/a
30	chr2:37909996-37910046	HAEpiC	amniotic membrane:	n/a
31	chr2:37927157-37927207	U87	brain:	n/a
32	chr2:37909996-37910046	Jurkat	blood:	n/a
33	chr2:37917061-37917111	SK-N-SH_RA	brain:	n/a
34	chr2:37909996-37910046	CMK	blood:	n/a
35	chr2:37909996-37910046	RPTEC	kidney:	n/a
36	chr2:37917061-37917111	ProgFib	skin:	n/a
37	chr2:37917061-37917111	NB4	blood:	n/a
38	chr2:37909996-37910046	PrEC	prostate:	n/a
39	chr2:37927157-37927207	H1-hESC	embryonic stem cell:	embryo
40	chr2:37927157-37927207	SK-N-MC	brain:	n/a
41	chr2:37909996-37910046	HMEC	breast:	n/a
42	chr2:37909996-37910046	BJ	skin:	n/a
43	chr2:37917061-37917111	GM19239	blood:	n/a
44	chr2:37917061-37917111	K562	blood:	n/a
45	chr2:37927157-37927207	IMR90	lung:	fetal
46	chr2:37917061-37917111	BE2_C	brain:	n/a
47	chr2:37909996-37910046	NB4	blood:	n/a
48	chr2:37927157-37927207	HNPCEpiC	eye:	n/a
49	chr2:37909996-37910046	HNPCEpiC	eye:	n/a
50	chr2:37917061-37917111	A549	lung:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:37900528..37902254-chr2:37903447..37906132,2	MCF-7	breast:
2	chr2:37901542..37903159-chr2:37919185..37920897,2	K562	blood:
3	chr2:37903844..37906735-chr2:37907477..37909784,2	MCF-7	breast:
4	chr2:37903844..37906735-chr2:37907477..37909784,2	MCF-7	breast:
5	chr2:37903809..37907927-chr2:37994371..37997035,4	MCF-7	breast:
6	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
7	chr2:37906138..37908983-chr2:37910229..37911986,2	MCF-7	breast:
8	chr2:37896479..37901472-chr2:37903866..37909932,8	MCF-7	breast:
9	chr2:37897976..37899851-chr2:37913464..37916015,2	MCF-7	breast:
10	chr2:37906138..37908983-chr2:37910229..37911986,2	MCF-7	breast:
11	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
12	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKD3-1	chr2:37909580-37909685	NONHSAT070138
2	lnc-PRKD3-1	chr2:37908256-37908525	NONHSAT070138
3	lnc-PRKD3-1	chr2:37909895-37910045	ucscGeneNc_uc002rqj_1
4	lnc-PRKD3-1	chr2:37906894-37908525	ucscGeneNc_uc002rqj_1
5	lnc-PRKD3-1	chr2:37909580-37909685	ucscGeneNc_uc002rqj_1
6	lnc-PRKD3-1	chr2:37920685-37920906	NONHSAT070140
7	lnc-PRKD3-2	chr2:37911626-37915318	NONHSAT070139
8	lnc-PRKD3-1	chr2:37909895-37910079	NONHSAT070137
9	lnc-PRKD3-1	chr2:37909580-37909685	NONHSAT070137
10	lnc-PRKD3-1	chr2:37906894-37908525	NONHSAT070137
11	lnc-PRKD3-2	chr2:37915960-37915992	NONHSAT070139

No data

Variant related genes	Relation type
CDC42EP3	TF binding region
CDC42EP3	CpG island
ENSG00000163171	chromatin interactions

Extended variants
information (count: 1209 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10490280	chr2:37905976-37905977	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181667434	chr2:37905994-37905995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs72882171	chr2:37906012-37906013	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs56159239	chr2:37906023-37906024	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs374157842	chr2:37906048-37906049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs541912567	chr2:37906070-37906071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560262333	chr2:37906091-37906092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs527660847	chr2:37906105-37906106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564409734	chr2:37906122-37906123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529005868	chr2:37906163-37906164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs543152621	chr2:37906174-37906175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550648488	chr2:37906195-37906196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2072418	chr2:37906216-37906217	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
14	rs564951328	chr2:37906221-37906222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150881987	chr2:37906263-37906264	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138256087	chr2:37906265-37906266	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs72882173	chr2:37906306-37906307	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs184483515	chr2:37906312-37906313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548284055	chr2:37906324-37906325	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530095029	chr2:37906337-37906338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566607091	chr2:37906352-37906353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs533521297	chr2:37906403-37906404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558546733	chr2:37906419-37906420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532026162	chr2:37906428-37906429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114704190	chr2:37906459-37906460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs114274466	chr2:37906470-37906471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs372875947	chr2:37906475-37906476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs574691117	chr2:37906482-37906483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149609391	chr2:37906525-37906526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566136396	chr2:37906593-37906594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs55657376	chr2:37906600-37906601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553814352	chr2:37906606-37906607	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572226637	chr2:37906710-37906711	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567075364	chr2:37906713-37906714	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534472961	chr2:37906715-37906716	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564514538	chr2:37906729-37906730	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs72882174	chr2:37906809-37906810	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs370632339	chr2:37906839-37906840	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562797131	chr2:37906872-37906873	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549175247	chr2:37906873-37906874	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567475444	chr2:37906898-37906899	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs181256923	chr2:37906947-37906948	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs548421835	chr2:37906950-37906951	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs566544857	chr2:37907058-37907059	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs75424275	chr2:37907117-37907118	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs551850625	chr2:37907123-37907124	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs540992826	chr2:37907197-37907198	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs367638372	chr2:37907202-37907203	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs537998772	chr2:37907221-37907222	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs550041421	chr2:37907325-37907326	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37899800-37906800	Weak transcription	Gastric	stomach
2	chr2:37900200-37916000	Weak transcription	Psoas Muscle	Psoas
3	chr2:37900400-37906800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr2:37900400-37910000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:37902400-37910600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr2:37903400-37909600	Weak transcription	K562	blood
7	chr2:37903400-37910000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr2:37903800-37906600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:37903800-37906600	Weak transcription	Stomach Mucosa	stomach
10	chr2:37903800-37910600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:37904000-37906400	Weak transcription	HSMM	muscle
12	chr2:37904000-37911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:37905200-37906800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr2:37905200-37907000	Weak transcription	Lung	lung
15	chr2:37905600-37910000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:37906400-37907000	Enhancers	HSMM	muscle
17	chr2:37906600-37907000	Enhancers	Stomach Mucosa	stomach
18	chr2:37906600-37907200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:37906800-37907200	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr2:37906800-37907400	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr2:37907000-37907200	Enhancers	Lung	lung
22	chr2:37907000-37921000	Weak transcription	Stomach Mucosa	stomach
23	chr2:37907200-37907400	Weak transcription	Gastric	stomach
24	chr2:37907200-37907400	Weak transcription	Lung	lung
25	chr2:37907200-37910200	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr2:37907200-37914200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:37907400-37910200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr2:37908200-37908400	Enhancers	Gastric	stomach
29	chr2:37909600-37910000	Enhancers	K562	blood
30	chr2:37909600-37910200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:37909600-37911400	Enhancers	Fetal Heart	heart
32	chr2:37909600-37911600	Enhancers	Primary T cells fromperipheralblood	blood
33	chr2:37909600-37911800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
34	chr2:37909600-37911800	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr2:37909600-37912000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr2:37909600-37912000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr2:37909800-37910600	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr2:37909800-37911600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr2:37909800-37911800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:37909800-37912000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr2:37909800-37912000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr2:37909800-37912200	Enhancers	Primary T cells from cord blood	blood
43	chr2:37909800-37912200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr2:37909800-37912600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr2:37909800-37912800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr2:37910000-37910200	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr2:37910000-37910400	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr2:37910000-37911000	Flanking Active TSS	K562	blood
49	chr2:37910000-37911600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr2:37910000-37911800	Enhancers	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links