Variant report

Variant	nsv875294
Chromosome Location	chr2:153607506-153733325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:183)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:153668506-153668637	K562	blood:	n/a	n/a
2	ARID3A	chr2:153717957-153718191	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:153731287-153731310	K562	blood:	n/a	n/a
4	BACH1	chr2:153703429-153703896	H1-hESC	embryonic stem cell:	n/a	chr2:153703724-153703738
5	BACH1	chr2:153617958-153617967	K562	blood:	n/a	n/a
6	BATF	chr2:153707072-153707272	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:153611663-153611866	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:153718002-153718019	K562	blood:	n/a	n/a
9	CBX3	chr2:153717900-153718268	K562	blood:	n/a	n/a
10	CBX3	chr2:153717874-153718228	K562	blood:	n/a	n/a
11	CBX3	chr2:153668508-153668785	K562	blood:	n/a	n/a
12	CEBPB	chr2:153622073-153622423	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:153608431-153608727	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:153622083-153622316	K562	blood:	n/a	n/a
15	CEBPB	chr2:153622114-153622394	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:153624376-153624658	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:153727380-153727489	HepG2	liver:	n/a	chr2:153727422-153727439
18	CEBPB	chr2:153618531-153619185	IMR90	lung:	n/a	chr2:153619016-153619033
19	CEBPB	chr2:153622082-153622419	K562	blood:	n/a	n/a
20	CEBPB	chr2:153608470-153608672	A549	lung:	n/a	n/a
21	CEBPB	chr2:153656811-153656840	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:153622105-153622322	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:153723904-153723916	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:153682553-153682764	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:153732868-153733178	A549	lung:	n/a	n/a
26	CEBPB	chr2:153622220-153622300	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:153608511-153608611	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:153608400-153608748	HepG2	liver:	n/a	n/a
29	CHD2	chr2:153611770-153611850	GM12878	blood:	n/a	n/a
30	CTCF	chr2:153717892-153718210	MCF-7	breast:	n/a	n/a
31	CTCF	chr2:153717877-153718214	GM12878	blood:	n/a	n/a
32	CTCF	chr2:153611618-153611774	GM19240	blood:	n/a	n/a
33	CTCF	chr2:153611620-153611770	HEK293	kidney:	n/a	n/a
34	CTCF	chr2:153611530-153611859	A549	lung:	n/a	n/a
35	CTCF	chr2:153717960-153718110	GM12866	blood:	n/a	n/a
36	CTCF	chr2:153717980-153718130	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr2:153611620-153611770	HCM	heart:	n/a	n/a
38	CTCF	chr2:153611720-153611870	HCT-116	colon:	n/a	n/a
39	CTCF	chr2:153611640-153611790	GM12874	blood:	n/a	n/a
40	CTCF	chr2:153611600-153611750	GM12869	blood:	n/a	n/a
41	CTCF	chr2:153718000-153718150	HCM	heart:	n/a	n/a
42	CTCF	chr2:153611640-153611790	SAEC	small airway:	n/a	n/a
43	CTCF	chr2:153611660-153611810	GM12864	blood:	n/a	n/a
44	CTCF	chr2:153718022-153718124	GM12891	blood:	n/a	n/a
45	CTCF	chr2:153717952-153718131	GM10248	blood:	n/a	n/a
46	CTCF	chr2:153718000-153718150	GM12873	blood:	n/a	n/a
47	CTCF	chr2:153611600-153611750	HCM	heart:	n/a	n/a
48	CTCF	chr2:153611644-153611769	GM10248	blood:	n/a	n/a
49	CTCF	chr2:153611600-153611750	GM12864	blood:	n/a	n/a
50	CTCF	chr2:153611620-153611770	GM12873	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	chr2:153682841-153682891	U87	brain:	n/a
2	chr2:153618725-153618775	HEEpiC	esophagus:	n/a
3	chr2:153618725-153618775	SK-N-MC	brain:	n/a
4	chr2:153732388-153732438	HAEpiC	amniotic membrane:	n/a
5	chr2:153682841-153682891	T-47D	breast:	n/a
6	chr2:153732388-153732438	AG04450	lung:	fetal
7	chr2:153682841-153682891	HRCEpiC	kidney:	n/a
8	chr2:153682841-153682891	BJ	skin:	n/a
9	chr2:153732388-153732438	Jurkat	blood:	n/a
10	chr2:153732388-153732438	GM06990	blood:	n/a
11	chr2:153732388-153732438	T-47D	breast:	n/a
12	chr2:153682841-153682891	H1-hESC	embryonic stem cell:	embryo
13	chr2:153618725-153618775	HRPEpiC	eye:	n/a
14	chr2:153618725-153618775	NT2-D1	testis:	n/a
15	chr2:153682841-153682891	SK-N-SH	brain:	n/a
16	chr2:153732388-153732438	NHDF-neo	bronchial:	n/a
17	chr2:153682841-153682891	PFSK-1	brain:	n/a
18	chr2:153618725-153618775	RPTEC	kidney:	n/a
19	chr2:153682841-153682891	SAEC	small airway:	n/a
20	chr2:153618725-153618775	HCT-116	colon:	n/a
21	chr2:153682841-153682891	HIPEpiC	eye:	n/a
22	chr2:153732388-153732438	AoSMC	blood vessel:	n/a
23	chr2:153618725-153618775	NB4	blood:	n/a
24	chr2:153732388-153732438	HRCEpiC	kidney:	n/a
25	chr2:153732388-153732438	AG10803	skin:	n/a
26	chr2:153682841-153682891	HCF	heart:	n/a
27	chr2:153732388-153732438	ProgFib	skin:	n/a
28	chr2:153618725-153618775	A549	lung:	n/a
29	chr2:153618725-153618775	HepG2	liver:	n/a
30	chr2:153682841-153682891	AoSMC	blood vessel:	n/a
31	chr2:153618725-153618775	Hepatocyte	liver:	n/a
32	chr2:153618725-153618775	NH-A	brain:	n/a
33	chr2:153682841-153682891	NT2-D1	testis:	n/a
34	chr2:153682841-153682891	HMEC	breast:	n/a
35	chr2:153618725-153618775	NHBE	bronchial:	n/a
36	chr2:153618725-153618775	HEK293	kidney:	embryo
37	chr2:153682841-153682891	HUVEC	blood vessel:	n/a
38	chr2:153618725-153618775	BE2_C	brain:	n/a
39	chr2:153732388-153732438	AG09319	gingival:	n/a
40	chr2:153732388-153732438	H1-hESC	embryonic stem cell:	embryo
41	chr2:153682841-153682891	Hela-S3	cervix:	n/a
42	chr2:153618725-153618775	AG04449	skin:	fetal
43	chr2:153682841-153682891	HEEpiC	esophagus:	n/a
44	chr2:153682841-153682891	Hepatocyte	liver:	n/a
45	chr2:153732388-153732438	HNPCEpiC	eye:	n/a
46	chr2:153618725-153618775	Jurkat	blood:	n/a
47	chr2:153618725-153618775	Caco-2	colon:	n/a
48	chr2:153682841-153682891	PANC-1	pancreas:	n/a
49	chr2:153732388-153732438	SK-N-SH_RA	brain:	n/a
50	chr2:153732388-153732438	MCF10A-Er-Src	breast:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:153618496..153621083-chr2:153625320..153627724,2	K562	blood:
2	chr2:153717735..153718254-chr2:154375545..154376170,2	MCF-7	breast:
3	chr2:153601362..153603681-chr2:153610761..153612819,4	K562	blood:
4	chr2:153707340..153709817-chr2:153711548..153713253,2	MCF-7	breast:
5	chr2:153612625..153615210-chr2:153618975..153622018,4	K562	blood:
6	chr2:153600659..153603319-chr2:153618153..153620356,2	MCF-7	breast:
7	chr2:153622504..153625105-chr2:153625415..153627400,2	K562	blood:
8	chr2:153575605..153578815-chr2:153624118..153627025,3	K562	blood:
9	chr2:153572925..153575286-chr2:153613633..153616476,2	K562	blood:
10	chr2:153615552..153617292-chr2:153619332..153620895,2	MCF-7	breast:
11	chr2:153717664..153718501-chr2:154375747..154376336,2	MCF-7	breast:
12	chr2:153712317..153713926-chr2:153715979..153717562,2	K562	blood:
13	chr2:153573784..153577602-chr2:153618161..153622533,3	K562	blood:
14	chr2:153615552..153617292-chr2:153619332..153620895,2	MCF-7	breast:
15	chr2:153717618..153718133-chr2:154334966..154335590,2	MCF-7	breast:
16	chr2:153618898..153620403-chr2:153623294..153625594,2	K562	blood:
17	chr2:153599292..153601773-chr2:153604538..153608666,3	K562	blood:
18	chr2:153717536..153718371-chr2:154148277..154149253,2	MCF-7	breast:
19	chr2:153622504..153625105-chr2:153625415..153627400,2	K562	blood:
20	chr2:153559758..153562464-chr2:153616501..153619452,2	K562	blood:
21	chr2:153707340..153709817-chr2:153711548..153713253,2	MCF-7	breast:
22	chr2:153605163..153608137-chr2:153613624..153617167,3	K562	blood:
23	chr2:153712317..153713926-chr2:153715979..153717562,2	K562	blood:
24	chr2:153605163..153608137-chr2:153613624..153617167,3	K562	blood:
25	chr2:153574234..153576272-chr2:153605870..153607963,2	K562	blood:
26	chr2:153612625..153615210-chr2:153618975..153622018,4	K562	blood:
27	chr2:153618898..153620403-chr2:153623294..153625594,2	K562	blood:
28	chr2:153618496..153621083-chr2:153625320..153627724,2	K562	blood:
29	chr2:153717488..153718201-chr2:154019699..154020209,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL6IP6-2	chr2:153616261-153617109	NONHSAT074992

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ARL6IP6	hsa-let-7a-5p	chr2:153617490-153617511
2	ARL6IP6	hsa-let-7a-5p	chr2:153616601-153616607
3	ARL6IP6	hsa-miR-181a-5p	chr2:153617638-153617660

Variant related genes	Relation type
UBQLN4P2	TF binding region
ENSG00000234932	TF binding region
UBQLN4P2	CpG island
ENSG00000234932	CpG island
ENSG00000177917	chromatin interactions
ENSG00000196504	chromatin interactions
ENSG00000177519	chromatin interactions

Extended variants
information (count: 3033 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3033 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16831740	chr2:153607506-153607507	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567301023	chr2:153607621-153607622	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs535864165	chr2:153607668-153607669	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs565626006	chr2:153607696-153607697	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553665728	chr2:153607699-153607700	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs202178750	chr2:153607715-153607716	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs547682579	chr2:153607718-153607719	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs555703387	chr2:153607720-153607721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548546179	chr2:153607721-153607722	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs59436061	chr2:153607723-153607724	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76178261	chr2:153607731-153607732	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs184154610	chr2:153607757-153607758	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558740068	chr2:153607763-153607764	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575390477	chr2:153607820-153607821	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs74586745	chr2:153607841-153607842	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544391076	chr2:153607849-153607850	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554761735	chr2:153607853-153607854	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs115524728	chr2:153607897-153607898	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs529319199	chr2:153607898-153607899	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540247588	chr2:153607902-153607903	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551087816	chr2:153607953-153607954	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551064276	chr2:153607958-153607959	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs141970058	chr2:153607962-153607963	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528411937	chr2:153607994-153607995	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs367874823	chr2:153608012-153608013	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs545283954	chr2:153608040-153608041	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs565076724	chr2:153608066-153608067	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs111757510	chr2:153608068-153608069	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs550694344	chr2:153608081-153608082	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs560807500	chr2:153608085-153608086	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs187540234	chr2:153608096-153608097	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs546209211	chr2:153608127-153608128	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs566094557	chr2:153608138-153608139	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs34585982	chr2:153608153-153608154	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs555044148	chr2:153608221-153608222	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs150245337	chr2:153608275-153608276	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs113238298	chr2:153608314-153608315	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs192629301	chr2:153608330-153608331	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs367610190	chr2:153608339-153608340	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs538046424	chr2:153608343-153608344	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs139095959	chr2:153608360-153608361	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs143136872	chr2:153608397-153608398	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs62181163	chr2:153608405-153608406	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs554218033	chr2:153608477-153608478	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs114990168	chr2:153608498-153608499	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs376094638	chr2:153608570-153608571	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs565170264	chr2:153608632-153608633	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147452216	chr2:153608644-153608645	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544057089	chr2:153608690-153608691	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186870279	chr2:153608698-153608699	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:153575800-153611600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:153575800-153611600	Weak transcription	Esophagus	oesophagus
3	chr2:153575800-153621400	Weak transcription	Pancreas	Pancrea
4	chr2:153576000-153615800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr2:153577200-153617600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr2:153577600-153617800	Weak transcription	NHLF	lung
7	chr2:153582000-153610600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:153583000-153611600	Weak transcription	Lung	lung
9	chr2:153587400-153608800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr2:153587400-153610600	Weak transcription	Small Intestine	intestine
11	chr2:153587600-153618000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:153587600-153621600	Weak transcription	NHEK	skin
13	chr2:153588000-153617800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr2:153588200-153618600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr2:153588600-153619400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr2:153589400-153613600	Weak transcription	Brain Angular Gyrus	brain
17	chr2:153590200-153616800	Weak transcription	Right Ventricle	heart
18	chr2:153590400-153620400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:153591000-153611800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:153592200-153618800	Weak transcription	HSMMtube	muscle
21	chr2:153593200-153618800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr2:153593200-153628400	Weak transcription	Fetal Kidney	kidney
23	chr2:153593600-153617000	Weak transcription	Brain Anterior Caudate	brain
24	chr2:153593600-153618600	Weak transcription	Osteobl	bone
25	chr2:153593600-153621800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr2:153593800-153608000	Weak transcription	HSMM	muscle
27	chr2:153593800-153613400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr2:153593800-153617600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr2:153593800-153617600	Weak transcription	NH-A	brain
30	chr2:153593800-153620000	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:153593800-153621400	Weak transcription	HMEC	breast
32	chr2:153593800-153621600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr2:153594200-153613400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:153594400-153615000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:153595200-153607600	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr2:153595200-153608600	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr2:153595200-153608600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:153595200-153608800	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr2:153595200-153608800	Weak transcription	Spleen	Spleen
40	chr2:153595200-153616800	Weak transcription	Colonic Mucosa	Colon
41	chr2:153595200-153618000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:153595200-153618000	Weak transcription	Brain Hippocampus Middle	brain
43	chr2:153595200-153621800	Weak transcription	Aorta	Aorta
44	chr2:153595200-153622000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr2:153595400-153613400	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr2:153595400-153618400	Weak transcription	Left Ventricle	heart
47	chr2:153595400-153621600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr2:153595600-153609000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr2:153595600-153613600	Weak transcription	Gastric	stomach
50	chr2:153596000-153608800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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