Variant report

Variant	nsv591270
Chromosome Location	chr3:109462400-109793785
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1156)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1156 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:109525802-109526113	K562	blood:	n/a	n/a
2	ATF3	chr3:109525675-109526362	HCT-116	colon:	n/a	n/a
3	BATF	chr3:109525771-109526057	GM12878	blood:	n/a	chr3:109525937-109525948
4	BATF	chr3:109525796-109526082	GM12878	blood:	n/a	chr3:109525937-109525948
5	BATF	chr3:109523591-109523890	GM12878	blood:	n/a	n/a
6	BATF	chr3:109523569-109523927	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:109523621-109523879	GM12878	blood:	n/a	chr3:109523812-109523821 chr3:109523811-109523820 chr3:109523835-109523844
8	BCL11A	chr3:109479417-109479644	GM12878	blood:	n/a	n/a
9	BCL3	chr3:109645877-109646527	A549	lung:	n/a	n/a
10	BRCA1	chr3:109520687-109520762	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr3:109791375-109791445	GM12878	blood:	n/a	n/a
12	BRCA1	chr3:109550230-109550392	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr3:109645781-109646410	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr3:109525659-109526473	HCT-116	colon:	n/a	n/a
15	CBX3	chr3:109523326-109524153	HCT-116	colon:	n/a	n/a
16	CBX3	chr3:109645702-109646599	HCT-116	colon:	n/a	n/a
17	CBX3	chr3:109645772-109646547	HCT-116	colon:	n/a	n/a
18	CBX3	chr3:109746170-109746640	HCT-116	colon:	n/a	n/a
19	CBX3	chr3:109525677-109526322	HCT-116	colon:	n/a	n/a
20	CBX3	chr3:109609851-109610221	HCT-116	colon:	n/a	n/a
21	CEBPB	chr3:109746303-109746587	A549	lung:	n/a	n/a
22	CEBPB	chr3:109713012-109713264	HepG2	liver:	n/a	chr3:109713148-109713159
23	CEBPB	chr3:109713806-109714074	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:109738325-109738600	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr3:109738237-109738590	A549	lung:	n/a	n/a
26	CEBPB	chr3:109723207-109723552	Hela-S3	cervix:	n/a	chr3:109723414-109723427 chr3:109723416-109723427
27	CEBPB	chr3:109645773-109646686	HCT-116	colon:	n/a	n/a
28	CEBPB	chr3:109549710-109550433	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:109786998-109787264	HepG2	liver:	n/a	chr3:109787158-109787169
30	CEBPB	chr3:109641108-109641558	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:109645998-109646461	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:109658776-109659238	A549	lung:	n/a	chr3:109659035-109659046
33	CEBPB	chr3:109645783-109646595	HCT-116	colon:	n/a	n/a
34	CEBPB	chr3:109658867-109659228	IMR90	lung:	n/a	chr3:109659035-109659046
35	CEBPB	chr3:109713603-109714246	HCT-116	colon:	n/a	n/a
36	CEBPB	chr3:109735063-109735497	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr3:109788690-109789314	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:109523365-109524303	HCT-116	colon:	n/a	chr3:109524031-109524044 chr3:109524032-109524043 chr3:109523391-109523403
39	CEBPB	chr3:109549818-109550425	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:109549963-109550601	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:109658912-109659180	K562	blood:	n/a	chr3:109659035-109659046
42	CEBPB	chr3:109738300-109738547	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:109746103-109746716	HCT-116	colon:	n/a	n/a
44	CEBPB	chr3:109738243-109738606	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:109671813-109672133	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr3:109746219-109746575	HCT-116	colon:	n/a	n/a
47	CEBPB	chr3:109658874-109659211	A549	lung:	n/a	chr3:109659035-109659046
48	CEBPB	chr3:109646013-109646487	IMR90	lung:	n/a	n/a
49	CEBPB	chr3:109645987-109646493	A549	lung:	n/a	n/a
50	CEBPB	chr3:109467570-109467815	A549	lung:	n/a	chr3:109467653-109467664

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:109645423-109645473	AG10803	skin:	n/a
2	chr3:109645423-109645473	AG04450	lung:	fetal
3	chr3:109735618-109735668	GM19239	blood:	n/a
4	chr3:109645423-109645473	H1-hESC	embryonic stem cell:	embryo
5	chr3:109537321-109537371	SK-N-MC	brain:	n/a
6	chr3:109550978-109551028	SAEC	small airway:	n/a
7	chr3:109550978-109551028	Hela-S3	cervix:	n/a
8	chr3:109735618-109735668	HCM	heart:	n/a
9	chr3:109550978-109551028	T-47D	breast:	n/a
10	chr3:109537321-109537371	SK-N-SH	brain:	n/a
11	chr3:109537321-109537371	HMEC	breast:	n/a
12	chr3:109550978-109551028	ProgFib	skin:	n/a
13	chr3:109645423-109645473	NT2-D1	testis:	n/a
14	chr3:109537321-109537371	AoSMC	blood vessel:	n/a
15	chr3:109735618-109735668	HCF	heart:	n/a
16	chr3:109537321-109537371	MCF10A-Er-Src	breast:	n/a
17	chr3:109550978-109551028	PFSK-1	brain:	n/a
18	chr3:109537321-109537371	CMK	blood:	n/a
19	chr3:109735618-109735668	SAEC	small airway:	n/a
20	chr3:109537321-109537371	HCPEpiC	choroid plexus:	n/a
21	chr3:109537321-109537371	AG09319	gingival:	n/a
22	chr3:109550978-109551028	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:109645423-109645473	AoSMC	blood vessel:	n/a
24	chr3:109645423-109645473	PFSK-1	brain:	n/a
25	chr3:109550978-109551028	HNPCEpiC	eye:	n/a
26	chr3:109645423-109645473	HepG2	liver:	n/a
27	chr3:109735618-109735668	GM06990	blood:	n/a
28	chr3:109735618-109735668	A549	lung:	n/a
29	chr3:109645423-109645473	MCF-7	breast:	n/a
30	chr3:109537321-109537371	MCF-7	breast:	n/a
31	chr3:109735618-109735668	Jurkat	blood:	n/a
32	chr3:109550978-109551028	ovcar-3	ovarian:	n/a
33	chr3:109735618-109735668	HepG2	liver:	n/a
34	chr3:109550978-109551028	HAEpiC	amniotic membrane:	n/a
35	chr3:109537321-109537371	NT2-D1	testis:	n/a
36	chr3:109645423-109645473	HRPEpiC	eye:	n/a
37	chr3:109537321-109537371	HL-60	blood:	n/a
38	chr3:109537321-109537371	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:109537321-109537371	HUVEC	blood vessel:	n/a
40	chr3:109537321-109537371	H1-hESC	embryonic stem cell:	embryo
41	chr3:109645423-109645473	SK-N-SH_RA	brain:	n/a
42	chr3:109735618-109735668	HRPEpiC	eye:	n/a
43	chr3:109645423-109645473	GM12878	blood:	n/a
44	chr3:109735618-109735668	AoSMC	blood vessel:	n/a
45	chr3:109550978-109551028	Jurkat	blood:	n/a
46	chr3:109550978-109551028	HIPEpiC	eye:	n/a
47	chr3:109645423-109645473	HMEC	breast:	n/a
48	chr3:109645423-109645473	GM06990	blood:	n/a
49	chr3:109645423-109645473	SK-N-SH	brain:	n/a
50	chr3:109550978-109551028	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:109521488..109524316-chr3:109526133..109527838,2	MCF-7	breast:
2	chr3:109682867..109683387-chr5:36941291..36942072,2	MCF-7	breast:
3	chr3:109581529..109584501-chr3:109598932..109601248,2	K562	blood:
4	chr12:58935829..58938056-chr3:109671221..109673388,2	MCF-7	breast:
5	chr11:63952505..63954555-chr3:109463070..109465225,2	MCF-7	breast:
6	chr3:109359534..109361675-chr3:109706245..109708957,2	MCF-7	breast:
7	chr3:109470837..109472436-chr3:109472571..109474577,2	MCF-7	breast:
8	chr3:109470837..109472436-chr3:109472571..109474577,2	MCF-7	breast:
9	chr3:109762400..109764463-chr3:109767701..109770522,2	K562	blood:
10	chr3:109581529..109584501-chr3:109598932..109601248,2	K562	blood:
11	chr3:109521488..109524316-chr3:109526133..109527838,2	MCF-7	breast:
12	chr3:109641317..109642258-chr6:152662604..152663366,2	MCF-7	breast:
13	chr3:109749391..109751192-chr3:110500927..110502696,2	K562	blood:
14	chr3:109762400..109764463-chr3:109767701..109770522,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPPA4-3	chr3:109696387-109696614	NONHSAT091128
2	lnc-TRAT1-12	chr3:109589133-109590818	ncRnaDb_ncrna_FR244682_1
3	lnc-TRAT1-6	chr3:109529521-109529708	ENSG00000242029
4	lnc-TRAT1-6	chr3:109523629-109523673	ENSG00000242029

No data

Variant related genes	Relation type
ENSG00000214380	TF binding region
ENSG00000243945	TF binding region
ENSG00000214380	CpG island
ENSG00000243945	CpG island
ENSG00000168439	chromatin interactions
ENSG00000258231	chromatin interactions

Extended variants
information (count: 4036 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4036 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530518386	chr3:109463017-109463018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541924111	chr3:109463062-109463063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73853560	chr3:109463080-109463081	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570586187	chr3:109463093-109463094	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532998833	chr3:109463108-109463109	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs13081749	chr3:109463132-109463133	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182384909	chr3:109463148-109463149	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535785824	chr3:109463219-109463220	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142303272	chr3:109463221-109463222	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568466272	chr3:109463246-109463247	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535769163	chr3:109463302-109463303	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147876962	chr3:109463372-109463373	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557188260	chr3:109463386-109463387	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34557596	chr3:109463435-109463436	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs1624474	chr3:109463460-109463461	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs553564338	chr3:109463466-109463467	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564182300	chr3:109463487-109463488	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11922644	chr3:109463506-109463507	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs542163236	chr3:109463524-109463525	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs141537338	chr3:109463569-109463570	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574362173	chr3:109463666-109463667	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs13082356	chr3:109463699-109463700	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs564050281	chr3:109463789-109463790	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533078184	chr3:109463790-109463791	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546464898	chr3:109463807-109463808	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201877616	chr3:109463902-109463903	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373445298	chr3:109463906-109463907	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs386664511	chr3:109463907-109463908	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs75447382	chr3:109463908-109463909	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs74372427	chr3:109463909-109463910	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371987325	chr3:109463910-109463911	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370007736	chr3:109463911-109463912	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560338486	chr3:109463946-109463947	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs529202744	chr3:109463956-109463957	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549305342	chr3:109463978-109463979	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568427702	chr3:109464021-109464022	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537462137	chr3:109464059-109464060	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550979168	chr3:109464099-109464100	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570839842	chr3:109464150-109464151	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562827799	chr3:109464156-109464157	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs533172984	chr3:109464160-109464161	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35804962	chr3:109464167-109464168	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376288501	chr3:109464190-109464191	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551796961	chr3:109464214-109464215	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186725861	chr3:109464222-109464223	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs72944378	chr3:109464351-109464352	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs72944380	chr3:109464391-109464392	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs368931504	chr3:109464392-109464393	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs574866397	chr3:109464399-109464400	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145701981	chr3:109464426-109464427	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:109463000-109463400	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr3:109463200-109463400	Enhancers	Fetal Brain Male	brain
3	chr3:109463200-109463600	Enhancers	Fetal Heart	heart
4	chr3:109463200-109463800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:109464000-109464200	Enhancers	Fetal Brain Male	brain
6	chr3:109472200-109472800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:109472200-109472800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:109472400-109473200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr3:109472400-109473200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:109472600-109473000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr3:109478000-109478200	ZNF genes & repeats	Dnd41	blood
12	chr3:109491800-109493200	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr3:109491800-109493600	Enhancers	Dnd41	blood
14	chr3:109492000-109493000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr3:109492400-109493000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr3:109492400-109493000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr3:109492400-109493600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr3:109492400-109493800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr3:109492600-109493000	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr3:109492600-109493200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr3:109504200-109505600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr3:109520200-109520600	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr3:109520400-109520600	Enhancers	Brain Germinal Matrix	brain
24	chr3:109520600-109521600	Weak transcription	Brain Germinal Matrix	brain
25	chr3:109520600-109523000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr3:109521600-109522000	Enhancers	Brain Germinal Matrix	brain
27	chr3:109522000-109522200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr3:109522200-109522800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr3:109522200-109525400	Enhancers	Primary T cells fromperipheralblood	blood
30	chr3:109522400-109524600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr3:109522800-109525600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr3:109523000-109524200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr3:109523000-109524600	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr3:109523000-109524600	Enhancers	HMEC	breast
35	chr3:109523000-109524800	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr3:109523000-109525200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr3:109523000-109525600	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr3:109523000-109528200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr3:109523000-109528200	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr3:109523400-109524000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr3:109523400-109525200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr3:109523400-109525200	Enhancers	Dnd41	blood
43	chr3:109523400-109527800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr3:109523800-109524200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr3:109523800-109524200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr3:109523800-109528200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr3:109524000-109524200	Enhancers	Primary T cells from cord blood	blood
48	chr3:109524000-109525600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr3:109524200-109524600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:109524200-109524600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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