Variant report

Variant	esv1793984
Chromosome Location	chr2:152138749-152154163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:734)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:152144069-152145119	K562	blood:	n/a	n/a
2	ARID3A	chr2:152148677-152149024	K562	blood:	n/a	n/a
3	ATF1	chr2:152144709-152145319	K562	blood:	n/a	n/a
4	ATF1	chr2:152148713-152148891	K562	blood:	n/a	n/a
5	ATF1	chr2:152144052-152144401	K562	blood:	n/a	n/a
6	ATF1	chr2:152149310-152149311	K562	blood:	n/a	n/a
7	ATF2	chr2:152145671-152147148	GM12878	blood:	n/a	n/a
8	ATF2	chr2:152146027-152146786	GM12878	blood:	n/a	n/a
9	ATF2	chr2:152144596-152145080	GM12878	blood:	n/a	n/a
10	ATF2	chr2:152144635-152145142	GM12878	blood:	n/a	n/a
11	ATF3	chr2:152146235-152146653	K562	blood:	n/a	n/a
12	BACH1	chr2:152146346-152146953	K562	blood:	n/a	n/a
13	BACH1	chr2:152145924-152146143	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr2:152146280-152146808	GM12878	blood:	n/a	n/a
15	BCLAF1	chr2:152144609-152145247	GM12878	blood:	n/a	n/a
16	BCLAF1	chr2:152145708-152147025	GM12878	blood:	n/a	chr2:152146063-152146076 chr2:152146444-152146453 chr2:152146000-152146009
17	BHLHE40	chr2:152144510-152146226	K562	blood:	n/a	chr2:152146057-152146073
18	BHLHE40	chr2:152146442-152146795	K562	blood:	n/a	n/a
19	BHLHE40	chr2:152148836-152148890	K562	blood:	n/a	n/a
20	BHLHE40	chr2:152145785-152146808	GM12878	blood:	n/a	chr2:152146057-152146073
21	BRCA1	chr2:152146349-152146875	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr2:152144386-152145556	K562	blood:	n/a	n/a
23	CBX3	chr2:152144709-152145551	K562	blood:	n/a	n/a
24	CBX3	chr2:152145643-152146858	K562	blood:	n/a	n/a
25	CCNT2	chr2:152145802-152146368	K562	blood:	n/a	n/a
26	CEBPB	chr2:152145261-152145461	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:152149100-152149419	IMR90	lung:	n/a	chr2:152149260-152149277 chr2:152149261-152149274 chr2:152149261-152149272 chr2:152149261-152149274 chr2:152149106-152149117 chr2:152149262-152149273
28	CEBPB	chr2:152146298-152146868	K562	blood:	n/a	n/a
29	CEBPB	chr2:152146459-152147014	A549	lung:	n/a	n/a
30	CEBPB	chr2:152146461-152147006	MCF-7	breast:	n/a	n/a
31	CEBPB	chr2:152146532-152146925	MCF-7	breast:	n/a	n/a
32	CEBPB	chr2:152146497-152146913	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:152145880-152146943	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:152146534-152146922	A549	lung:	n/a	n/a
35	CEBPB	chr2:152149077-152149443	HepG2	liver:	n/a	chr2:152149260-152149277 chr2:152149261-152149274 chr2:152149261-152149272 chr2:152149261-152149274 chr2:152149106-152149117 chr2:152149262-152149273
36	CEBPB	chr2:152149080-152149401	A549	lung:	n/a	chr2:152149260-152149277 chr2:152149261-152149274 chr2:152149261-152149272 chr2:152149261-152149274 chr2:152149106-152149117 chr2:152149262-152149273
37	CEBPB	chr2:152148653-152149456	K562	blood:	n/a	chr2:152149260-152149277 chr2:152149261-152149274 chr2:152149261-152149272 chr2:152149261-152149274 chr2:152149106-152149117 chr2:152149262-152149273
38	CEBPB	chr2:152146470-152146859	K562	blood:	n/a	n/a
39	CEBPB	chr2:152144494-152144823	A549	lung:	n/a	chr2:152144611-152144624
40	CEBPB	chr2:152148641-152148860	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:152144475-152144961	K562	blood:	n/a	chr2:152144611-152144624
42	CHD1	chr2:152144808-152145488	GM12878	blood:	n/a	n/a
43	CHD1	chr2:152145963-152146386	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr2:152145770-152147046	GM12878	blood:	n/a	n/a
45	CHD2	chr2:152146094-152146388	HepG2	liver:	n/a	n/a
46	CHD2	chr2:152146211-152146397	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr2:152143974-152144095	GM12878	blood:	n/a	n/a
48	CHD2	chr2:152144728-152145323	K562	blood:	n/a	n/a
49	CHD2	chr2:152145721-152146819	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr2:152145809-152146384	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152153974-152154024	AG09309	skin:	n/a
2	chr2:152146125-152146175	NH-A	brain:	n/a
3	chr2:152153974-152154024	AG09309	skin:	n/a
4	chr2:152146125-152146175	NH-A	brain:	n/a
5	chr2:152146478-152146528	AG10803	skin:	n/a
6	chr2:152146944-152146994	SK-N-SH_RA	brain:	n/a
7	chr2:152148585-152148635	PFSK-1	brain:	n/a
8	chr2:152146944-152146994	T-47D	breast:	n/a
9	chr2:152145900-152145950	HEEpiC	esophagus:	n/a
10	chr2:152146478-152146528	HRPEpiC	eye:	n/a
11	chr2:152145110-152145160	K562	blood:	n/a
12	chr2:152146125-152146175	GM12892	blood:	n/a
13	chr2:152145110-152145160	AG04450	lung:	fetal
14	chr2:152146295-152146345	BJ	skin:	n/a
15	chr2:152146478-152146528	ProgFib	skin:	n/a
16	chr2:152148585-152148635	IMR90	lung:	fetal
17	chr2:152145110-152145160	HMEC	breast:	n/a
18	chr2:152148585-152148635	GM06990	blood:	n/a
19	chr2:152146478-152146528	HIPEpiC	eye:	n/a
20	chr2:152145110-152145160	SK-N-SH	brain:	n/a
21	chr2:152146944-152146994	PFSK-1	brain:	n/a
22	chr2:152148585-152148635	HEK293	kidney:	embryo
23	chr2:152146318-152146368	NB4	blood:	n/a
24	chr2:152153974-152154024	HCT-116	colon:	n/a
25	chr2:152148585-152148635	HAEpiC	amniotic membrane:	n/a
26	chr2:152146944-152146994	MCF-7	breast:	n/a
27	chr2:152148585-152148635	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:152146478-152146528	HMEC	breast:	n/a
29	chr2:152146318-152146368	HCT-116	colon:	n/a
30	chr2:152148585-152148635	GM12892	blood:	n/a
31	chr2:152146702-152146752	LNCaP	prostate:	n/a
32	chr2:152146478-152146528	PrEC	prostate:	n/a
33	chr2:152146478-152146528	U87	brain:	n/a
34	chr2:152146295-152146345	PFSK-1	brain:	n/a
35	chr2:152145110-152145160	AoSMC	blood vessel:	n/a
36	chr2:152146702-152146752	AG04449	skin:	fetal
37	chr2:152146944-152146994	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:152146125-152146175	AG04450	lung:	fetal
39	chr2:152153974-152154024	AG10803	skin:	n/a
40	chr2:152146702-152146752	BE2_C	brain:	n/a
41	chr2:152146702-152146752	AG09319	gingival:	n/a
42	chr2:152146295-152146345	Hela-S3	cervix:	n/a
43	chr2:152152581-152152631	NHBE	bronchial:	n/a
44	chr2:152148585-152148635	GM12878	blood:	n/a
45	chr2:152145870-152145920	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:152145110-152145160	HRPEpiC	eye:	n/a
47	chr2:152146295-152146345	HRCEpiC	kidney:	n/a
48	chr2:152152581-152152631	PANC-1	pancreas:	n/a
49	chr2:152146125-152146175	MCF-7	breast:	n/a
50	chr2:152146702-152146752	ProgFib	skin:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:152153051..152154778-chr2:152157552..152159537,2	K562	blood:
2	chr2:152145849..152146532-chr2:152266419..152266964,2	MCF-7	breast:
3	chr2:152116868..152120610-chr2:152144685..152147660,4	MCF-7	breast:
4	chr2:152145011..152148288-chr2:152265460..152267609,4	MCF-7	breast:
5	chr2:152117973..152120026-chr2:152143620..152147532,3	K562	blood:
6	chr2:152117804..152120182-chr2:152144785..152147621,2	MCF-7	breast:
7	chr2:152140110..152142929-chr2:152143341..152145563,3	MCF-7	breast:
8	chr2:152144662..152146339-chr2:152277949..152280941,2	MCF-7	breast:
9	chr2:152115426..152120009-chr2:152142898..152146726,5	K562	blood:
10	chr2:152117595..152119182-chr2:152147828..152150131,2	K562	blood:
11	chr2:152137402..152140288-chr2:152140945..152142513,2	K562	blood:
12	chr2:152144705..152147509-chr2:152152105..152154406,3	MCF-7	breast:
13	chr2:152144796..152146879-chr2:152152335..152156277,3	MCF-7	breast:
14	chr2:152143136..152144934-chr2:152266709..152268489,3	K562	blood:
15	chr2:152143066..152145503-chr2:152272183..152273824,2	MCF-7	breast:
16	chr2:152144813..152149803-chr2:152261382..152268379,11	K562	blood:
17	chr2:152132818..152134386-chr2:152140305..152143217,3	K562	blood:
18	chr2:152132701..152134318-chr2:152139892..152142395,2	K562	blood:
19	chr2:152103117..152105386-chr2:152140432..152142822,2	K562	blood:
20	chr2:152136387..152138845-chr2:152146543..152148937,2	MCF-7	breast:
21	chr2:152146753..152148649-chr2:152552733..152554484,2	MCF-7	breast:
22	chr15:41088570..41089090-chr2:152145307..152145896,2	HCT-116	colon:
23	chr2:152124835..152127070-chr2:152140941..152143645,2	K562	blood:
24	chr2:152137402..152140288-chr2:152140945..152142513,2	K562	blood:
25	chr2:152154122..152156029-chr2:152157946..152160743,2	MCF-7	breast:
26	chr2:152153051..152155912-chr2:152157552..152160474,3	K562	blood:
27	chr2:152140110..152142929-chr2:152143341..152145563,3	MCF-7	breast:
28	chr2:152124159..152126726-chr2:152137023..152139855,2	K562	blood:
29	chr2:152145323..152148173-chr2:152152991..152155246,2	K562	blood:
30	chr2:152144798..152147073-chr2:152265350..152268359,5	MCF-7	breast:
31	chr2:152142404..152144724-chr2:152266453..152268489,2	K562	blood:
32	chr2:152023638..152026454-chr2:152144557..152146089,2	K562	blood:
33	chr2:152151929..152153728-chr2:152266086..152267793,2	MCF-7	breast:
34	chr2:152146182..152146803-chr2:152266084..152266913,2	MCF-7	breast:
35	chr2:152149114..152151846-chr2:152155576..152158199,2	K562	blood:
36	chr2:152147623..152151846-chr2:152155576..152159756,4	K562	blood:
37	chr2:152114819..152117297-chr2:152137988..152139768,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM43-3	chr2:152139285-152139468	NONHSAT074950
2	lnc-RBM43-3	chr2:152146107-152146377	NONHSAT074950

No data

Variant related genes	Relation type
NMI	TF binding region
NMI	CpG island
ENSG00000080345	chromatin interactions
ENSG00000184898	chromatin interactions
ENSG00000123609	chromatin interactions

Extended variants
information (count: 666 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3771887	chr2:152138749-152138750	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563822770	chr2:152138769-152138770	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs3771888	chr2:152138789-152138790	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs182923275	chr2:152138800-152138801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529002426	chr2:152138880-152138881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549144709	chr2:152138889-152138890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17191185	chr2:152138902-152138903	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs534953552	chr2:152138917-152138918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558191670	chr2:152138932-152138933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571573641	chr2:152138933-152138934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12328054	chr2:152138948-152138949	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs187543799	chr2:152138964-152138965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143777582	chr2:152139008-152139009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6751802	chr2:152139022-152139023	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs113371672	chr2:152139035-152139036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112293167	chr2:152139066-152139067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56358898	chr2:152139074-152139075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141013586	chr2:152139097-152139098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564226517	chr2:152139101-152139102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577525099	chr2:152139106-152139107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543047491	chr2:152139145-152139146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12328560	chr2:152139211-152139212	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs138815408	chr2:152139227-152139228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548685808	chr2:152139233-152139234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559494483	chr2:152139254-152139255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10169816	chr2:152139271-152139272	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs142639684	chr2:152139294-152139295	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs571836396	chr2:152139340-152139341	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs545834118	chr2:152139364-152139365	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs148602363	chr2:152139415-152139416	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs1048135	chr2:152139416-152139417	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs550676026	chr2:152139425-152139426	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs370311968	chr2:152139474-152139475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10182245	chr2:152139493-152139494	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs41268705	chr2:152139507-152139508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192358660	chr2:152139513-152139514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534820681	chr2:152139519-152139520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373867316	chr2:152139530-152139531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557979267	chr2:152139567-152139568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577837972	chr2:152139594-152139595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543735635	chr2:152139613-152139614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs55744578	chr2:152139655-152139656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559020331	chr2:152139657-152139658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563104688	chr2:152139679-152139680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34703117	chr2:152139685-152139686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10187344	chr2:152139686-152139687	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs559034082	chr2:152139694-152139695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531122957	chr2:152139718-152139719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111349037	chr2:152139736-152139737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12617669	chr2:152139787-152139788	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:50)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152118600-152142800	Weak transcription	Small Intestine	intestine
2	chr2:152118800-152144000	Weak transcription	Stomach Mucosa	stomach
3	chr2:152118800-152144200	Weak transcription	Psoas Muscle	Psoas
4	chr2:152119000-152145000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:152119000-152145200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr2:152119000-152145200	Weak transcription	NHEK	skin
7	chr2:152119000-152145800	Weak transcription	HSMM	muscle
8	chr2:152119400-152142800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr2:152119400-152144400	Weak transcription	A549	lung
10	chr2:152119400-152144800	Weak transcription	Brain Substantia Nigra	brain
11	chr2:152119400-152145200	Weak transcription	Brain Hippocampus Middle	brain
12	chr2:152121200-152145000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:152121200-152145400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:152124600-152139200	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr2:152125200-152145400	Weak transcription	Aorta	Aorta
16	chr2:152125800-152139200	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr2:152125800-152145200	Weak transcription	Right Ventricle	heart
18	chr2:152126000-152139200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr2:152126200-152139200	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr2:152126200-152139200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:152126200-152139200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr2:152126200-152139400	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr2:152126200-152139400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr2:152126200-152139400	Strong transcription	Placenta	Placenta
25	chr2:152126200-152139800	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr2:152126200-152141200	Strong transcription	Dnd41	blood
27	chr2:152126400-152139200	Strong transcription	Primary T cells from cord blood	blood
28	chr2:152126400-152139200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr2:152126400-152139200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr2:152126400-152139200	Strong transcription	Adipose Nuclei	Adipose
31	chr2:152126400-152139400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr2:152126400-152139400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr2:152126400-152139400	Strong transcription	Liver	Liver
34	chr2:152126400-152139400	Strong transcription	Duodenum Mucosa	Duodenum
35	chr2:152126400-152139400	Strong transcription	Fetal Thymus	thymus
36	chr2:152126400-152139600	Strong transcription	Primary B cells from peripheral blood	blood
37	chr2:152126400-152139600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr2:152126800-152139400	Strong transcription	Primary B cells from cord blood	blood
39	chr2:152126800-152145200	Weak transcription	HMEC	breast
40	chr2:152126800-152145600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr2:152127000-152145400	Weak transcription	Fetal Muscle Trunk	muscle
42	chr2:152128000-152144600	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr2:152128400-152145200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr2:152128600-152145200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:152130200-152145600	Weak transcription	Fetal Kidney	kidney
46	chr2:152130600-152144600	Weak transcription	Fetal Lung	lung
47	chr2:152131600-152139200	Strong transcription	Rectal Mucosa Donor 29	rectum
48	chr2:152131800-152139200	Strong transcription	Primary hematopoietic stem cells	blood
49	chr2:152133600-152139200	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr2:152134400-152138800	Weak transcription	Fetal Muscle Leg	muscle

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