Variant report

Variant	nsv236502
Chromosome Location	chr3:98250046-98254624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:177)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:177 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:98252588-98253414	GM12878	blood:	n/a	n/a
2	ATF2	chr3:98249967-98252577	GM12878	blood:	n/a	n/a
3	ATF2	chr3:98250379-98252988	GM12878	blood:	n/a	n/a
4	BCL3	chr3:98250594-98251898	GM12878	blood:	n/a	n/a
5	BCLAF1	chr3:98249469-98250050	GM12878	blood:	n/a	n/a
6	BCLAF1	chr3:98250486-98252802	GM12878	blood:	n/a	chr3:98250514-98250523
7	BCLAF1	chr3:98253575-98253974	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:98250167-98253505	GM12878	blood:	n/a	chr3:98250514-98250523
9	BHLHE40	chr3:98249324-98251183	GM12878	blood:	n/a	n/a
10	CEBPB	chr3:98250202-98252695	GM12878	blood:	n/a	n/a
11	CHD1	chr3:98246186-98256496	GM12878	blood:	n/a	n/a
12	CHD2	chr3:98250594-98251574	GM12878	blood:	n/a	n/a
13	CREB1	chr3:98250264-98252480	GM12878	blood:	n/a	n/a
14	CTCF	chr3:98251658-98251747	ProgFib	skin:	n/a	n/a
15	CUX1	chr3:98252515-98253058	GM12878	blood:	n/a	n/a
16	CUX1	chr3:98249608-98250960	GM12878	blood:	n/a	n/a
17	CUX1	chr3:98251345-98251830	GM12878	blood:	n/a	n/a
18	CUX1	chr3:98253654-98253894	GM12878	blood:	n/a	n/a
19	EBF1	chr3:98250462-98250778	GM12878	blood:	n/a	n/a
20	EBF1	chr3:98250304-98251523	GM12878	blood:	n/a	n/a
21	EBF1	chr3:98252263-98252507	GM12878	blood:	n/a	n/a
22	EBF1	chr3:98251725-98251966	GM12878	blood:	n/a	n/a
23	ELK1	chr3:98250563-98251398	GM12878	blood:	n/a	n/a
24	EP300	chr3:98250381-98251108	GM12878	blood:	n/a	chr3:98250388-98250398 chr3:98250509-98250523
25	FOXM1	chr3:98250317-98251952	GM12878	blood:	n/a	n/a
26	FOXM1	chr3:98250006-98252764	GM12878	blood:	n/a	n/a
27	GATA3	chr3:98253050-98253240	SH-SY5Y	brain:	n/a	n/a
28	IKZF1	chr3:98250535-98251319	GM12878	blood:	n/a	n/a
29	IRF3	chr3:98250207-98250753	GM12878	blood:	n/a	chr3:98250513-98250522 chr3:98250514-98250524
30	KAT2A	chr3:98250799-98251055	GM12878	blood:	n/a	n/a
31	MAX	chr3:98250540-98252422	GM12878	blood:	n/a	n/a
32	MAZ	chr3:98249802-98252037	GM12878	blood:	n/a	n/a
33	MAZ	chr3:98253869-98253980	GM12878	blood:	n/a	n/a
34	MTA3	chr3:98252898-98253438	GM12878	blood:	n/a	n/a
35	MTA3	chr3:98249535-98254032	GM12878	blood:	n/a	n/a
36	MTA3	chr3:98250511-98252779	GM12878	blood:	n/a	n/a
37	MTA3	chr3:98254427-98256400	GM12878	blood:	n/a	n/a
38	MXI1	chr3:98251776-98252516	GM12878	blood:	n/a	n/a
39	MXI1	chr3:98250141-98251489	GM12878	blood:	n/a	n/a
40	MXI1	chr3:98252966-98253532	GM12878	blood:	n/a	n/a
41	MXI1	chr3:98253793-98254076	GM12878	blood:	n/a	n/a
42	NFATC1	chr3:98253493-98254109	GM12878	blood:	n/a	n/a
43	NFATC1	chr3:98248840-98253424	GM12878	blood:	n/a	n/a
44	NFATC1	chr3:98248493-98253590	GM12878	blood:	n/a	n/a
45	NFE2	chr3:98250888-98251088	GM12878	blood:	n/a	n/a
46	NFE2	chr3:98253236-98253288	GM12878	blood:	n/a	n/a
47	NFIC	chr3:98254503-98256033	GM12878	blood:	n/a	n/a
48	NFIC	chr3:98250026-98256659	GM12878	blood:	n/a	chr3:98252160-98252176 chr3:98250228-98250256 chr3:98250610-98250638 chr3:98252159-98252176
49	NFIC	chr3:98250335-98251055	GM12878	blood:	n/a	chr3:98250610-98250638
50	NFIC	chr3:98251217-98252073	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:98251294-98251344	HEEpiC	esophagus:	n/a
2	chr3:98251294-98251344	AG04449	skin:	fetal
3	chr3:98251294-98251344	GM19239	blood:	n/a
4	chr3:98250723-98250773	PrEC	prostate:	n/a
5	chr3:98251294-98251344	Hepatocyte	liver:	n/a
6	chr3:98251294-98251344	SK-N-SH	brain:	n/a
7	chr3:98251294-98251344	NT2-D1	testis:	n/a
8	chr3:98250723-98250773	GM12878	blood:	n/a
9	chr3:98250382-98250432	HRCEpiC	kidney:	n/a
10	chr3:98250382-98250432	AG09319	gingival:	n/a
11	chr3:98250382-98250432	AG10803	skin:	n/a
12	chr3:98251294-98251344	ECC-1	luminal epithelium:	n/a
13	chr3:98250723-98250773	HL-60	blood:	n/a
14	chr3:98250723-98250773	AG09319	gingival:	n/a
15	chr3:98250382-98250432	PFSK-1	brain:	n/a
16	chr3:98250382-98250432	HepG2	liver:	n/a
17	chr3:98250382-98250432	Hela-S3	cervix:	n/a
18	chr3:98250723-98250773	HRCEpiC	kidney:	n/a
19	chr3:98250723-98250773	NT2-D1	testis:	n/a
20	chr3:98250382-98250432	SK-N-MC	brain:	n/a
21	chr3:98250382-98250432	A549	lung:	n/a
22	chr3:98250382-98250432	HAEpiC	amniotic membrane:	n/a
23	chr3:98250382-98250432	AG04449	skin:	fetal
24	chr3:98251294-98251344	HCF	heart:	n/a
25	chr3:98251294-98251344	GM12892	blood:	n/a
26	chr3:98251294-98251344	AG04450	lung:	fetal
27	chr3:98250382-98250432	HEEpiC	esophagus:	n/a
28	chr3:98250382-98250432	GM12892	blood:	n/a
29	chr3:98250723-98250773	HEK293	kidney:	embryo
30	chr3:98250723-98250773	Hepatocyte	liver:	n/a
31	chr3:98250723-98250773	AG04450	lung:	fetal
32	chr3:98250723-98250773	HNPCEpiC	eye:	n/a
33	chr3:98250723-98250773	HEEpiC	esophagus:	n/a
34	chr3:98250382-98250432	HNPCEpiC	eye:	n/a
35	chr3:98251294-98251344	PANC-1	pancreas:	n/a
36	chr3:98250723-98250773	HCT-116	colon:	n/a
37	chr3:98251294-98251344	T-47D	breast:	n/a
38	chr3:98250723-98250773	AG10803	skin:	n/a
39	chr3:98250382-98250432	BE2_C	brain:	n/a
40	chr3:98250382-98250432	LNCaP	prostate:	n/a
41	chr3:98250382-98250432	NB4	blood:	n/a
42	chr3:98250723-98250773	ECC-1	luminal epithelium:	n/a
43	chr3:98250723-98250773	SK-N-SH_RA	brain:	n/a
44	chr3:98250382-98250432	AG04450	lung:	fetal
45	chr3:98251294-98251344	HCT-116	colon:	n/a
46	chr3:98251294-98251344	CMK	blood:	n/a
47	chr3:98251294-98251344	ovcar-3	ovarian:	n/a
48	chr3:98250723-98250773	Jurkat	blood:	n/a
49	chr3:98250723-98250773	SKMC	muscle:	n/a
50	chr3:98251294-98251344	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:98253977..98257356-chr3:98258364..98261390,4	K562	blood:
2	chr3:98250849..98253211-chr3:98255188..98256757,2	K562	blood:
3	chr3:98245361..98246878-chr3:98252030..98254936,2	K562	blood:

No data

Variant related genes	Relation type
GPR15	TF binding region
GPR15	CpG island

Extended variants
information (count: 195 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:195 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5851123	chr3:98250078-98250079	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs397875850	chr3:98250081-98250082	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs76541666	chr3:98250149-98250150	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs34179940	chr3:98250150-98250151	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs56126006	chr3:98250173-98250174	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs147623467	chr3:98250181-98250182	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs142901579	chr3:98250197-98250198	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs563938074	chr3:98250199-98250200	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs148657909	chr3:98250202-98250203	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs4857399	chr3:98250215-98250216	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
11	rs376890440	chr3:98250382-98250383	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs556278144	chr3:98250410-98250411	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs576444770	chr3:98250453-98250454	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs117204961	chr3:98250505-98250506	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142124631	chr3:98250535-98250536	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs187615152	chr3:98250558-98250559	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs151159854	chr3:98250569-98250570	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs192254861	chr3:98250594-98250595	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs577617028	chr3:98250640-98250641	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs545800355	chr3:98250646-98250647	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs546087326	chr3:98250720-98250721	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs563089947	chr3:98250738-98250739	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs140101017	chr3:98250779-98250780	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs548453533	chr3:98250822-98250823	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369630244	chr3:98250852-98250853	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201851410	chr3:98250861-98250862	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3749260	chr3:98250862-98250863	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
28	rs184408398	chr3:98250875-98250876	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570860091	chr3:98250898-98250899	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539882177	chr3:98250899-98250900	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369731261	chr3:98250908-98250909	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145191023	chr3:98250910-98250911	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199675530	chr3:98250919-98250920	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569843256	chr3:98250923-98250924	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562498362	chr3:98250925-98250926	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145602713	chr3:98250929-98250930	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145928800	chr3:98250950-98250951	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373094519	chr3:98250955-98250956	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376024326	chr3:98250965-98250966	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201534903	chr3:98250971-98250972	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2230344	chr3:98250986-98250987	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs534323108	chr3:98250999-98251000	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114940458	chr3:98251000-98251001	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147957406	chr3:98251038-98251039	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374086937	chr3:98251049-98251050	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145360341	chr3:98251064-98251065	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149131823	chr3:98251071-98251072	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377521784	chr3:98251082-98251083	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs151271302	chr3:98251086-98251087	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569609883	chr3:98251091-98251092	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98242200-98250800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr3:98249200-98250800	Active TSS	GM12878-XiMat	blood
3	chr3:98249200-98250800	Weak transcription	K562	blood
4	chr3:98249200-98251200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr3:98249400-98250200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr3:98249800-98250400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:98250200-98250600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr3:98250200-98256200	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr3:98250400-98251400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr3:98250600-98252400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr3:98250800-98251400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr3:98250800-98251600	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
13	chr3:98250800-98251600	Enhancers	K562	blood
14	chr3:98250800-98252200	Active TSS	Rectal Mucosa Donor 31	rectum
15	chr3:98250800-98252600	Active TSS	Colonic Mucosa	Colon
16	chr3:98250800-98253200	Active TSS	Primary T cells fromperipheralblood	blood
17	chr3:98250800-98253600	Active TSS	Duodenum Mucosa	Duodenum
18	chr3:98251000-98252200	Active TSS	Esophagus	oesophagus
19	chr3:98251000-98252400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr3:98251000-98252400	Active TSS	Sigmoid Colon	Sigmoid Colon
21	chr3:98251200-98251400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:98251200-98251800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:98251200-98252400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr3:98251400-98251800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr3:98251400-98252000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
26	chr3:98251600-98252400	Active TSS	Rectal Smooth Muscle	rectum
27	chr3:98251600-98257400	Active TSS	GM12878-XiMat	blood
28	chr3:98251800-98252000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr3:98251800-98252400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr3:98252000-98252400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
31	chr3:98252000-98252600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr3:98252000-98252600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
33	chr3:98252200-98255200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr3:98252400-98252800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
35	chr3:98252400-98253200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr3:98252400-98253200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr3:98252400-98253200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:98252400-98255000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr3:98252600-98253200	Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr3:98252600-98253400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr3:98252800-98253400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr3:98253200-98253400	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr3:98253200-98253400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr3:98253200-98253800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr3:98253200-98253800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr3:98253200-98257800	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr3:98253400-98253800	Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr3:98253400-98254400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr3:98253400-98255600	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr3:98253400-98257600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links