Variant report

Variant	nsv821631
Chromosome Location	chr2:211528918-211658981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:211551150-211551337	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:211537752-211538123	HepG2	liver:	n/a	n/a
3	BACH1	chr2:211554831-211554832	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:211586881-211587076	GM12878	blood:	n/a	n/a
5	BRCA1	chr2:211619752-211619828	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr2:211583593-211583625	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:211652767-211653045	A549	lung:	n/a	chr2:211652876-211652887
8	CEBPB	chr2:211536549-211536844	HepG2	liver:	n/a	chr2:211536688-211536699
9	CEBPB	chr2:211581774-211581974	A549	lung:	n/a	chr2:211581849-211581860 chr2:211581847-211581858 chr2:211581847-211581860
10	CEBPB	chr2:211654929-211655153	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:211612614-211612796	A549	lung:	n/a	chr2:211612721-211612732 chr2:211612720-211612733 chr2:211612679-211612690
12	CEBPB	chr2:211536528-211536844	A549	lung:	n/a	chr2:211536688-211536699
13	CEBPB	chr2:211615583-211615910	HepG2	liver:	n/a	chr2:211615752-211615763 chr2:211615754-211615763 chr2:211615753-211615764
14	CEBPB	chr2:211581704-211582010	IMR90	lung:	n/a	chr2:211581849-211581860 chr2:211581847-211581858 chr2:211581847-211581860
15	CEBPB	chr2:211540927-211541100	A549	lung:	n/a	n/a
16	CEBPB	chr2:211586997-211587345	HepG2	liver:	n/a	chr2:211587116-211587133
17	CEBPB	chr2:211615678-211615913	IMR90	lung:	n/a	chr2:211615752-211615763 chr2:211615754-211615763 chr2:211615753-211615764
18	CEBPB	chr2:211587160-211587375	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:211652744-211653060	HepG2	liver:	n/a	chr2:211652876-211652887
20	CEBPB	chr2:211588286-211588498	IMR90	lung:	n/a	chr2:211588368-211588377 chr2:211588368-211588377 chr2:211588366-211588377 chr2:211588368-211588377 chr2:211588368-211588377
21	CEBPB	chr2:211612560-211612867	HepG2	liver:	n/a	chr2:211612721-211612732 chr2:211612720-211612733 chr2:211612679-211612690
22	CEBPB	chr2:211581688-211581975	HepG2	liver:	n/a	chr2:211581849-211581860 chr2:211581847-211581858 chr2:211581847-211581860
23	CHD1	chr2:211557890-211557907	GM12878	blood:	n/a	n/a
24	CHD1	chr2:211548349-211548351	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr2:211654359-211654361	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr2:211627512-211627921	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr2:211577960-211578110	GM12864	blood:	n/a	n/a
28	CTCF	chr2:211567420-211567570	GM06990	blood:	n/a	n/a
29	CTCF	chr2:211577940-211578090	GM12873	blood:	n/a	n/a
30	CTCF	chr2:211528126-211528946	SK-N-SH	brain:	n/a	n/a
31	CTCF	chr2:211577920-211578070	GM12874	blood:	n/a	n/a
32	CTCF	chr2:211577960-211578110	HepG2	liver:	n/a	n/a
33	CTCF	chr2:211652135-211652178	GM13976	blood:	n/a	n/a
34	CTCF	chr2:211578018-211578075	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:211635663-211635715	GM13976	blood:	n/a	n/a
36	CTCF	chr2:211578020-211578170	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr2:211577980-211578130	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr2:211633180-211633330	WI-38	lung:	n/a	n/a
39	CTCF	chr2:211604551-211604617	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr2:211578024-211578039	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr2:211577940-211578090	GM12867	blood:	n/a	n/a
42	CTCF	chr2:211577940-211578090	GM12875	blood:	n/a	n/a
43	CTCF	chr2:211577960-211578110	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr2:211604820-211604970	GM12875	blood:	n/a	n/a
45	CTCF	chr2:211578040-211578190	GM12872	blood:	n/a	n/a
46	CTCF	chr2:211578013-211578059	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:211577900-211578050	BE2_C	brain:	n/a	n/a
48	CTCF	chr2:211578000-211578150	GM12872	blood:	n/a	n/a
49	CTCF	chr2:211631135-211631140	GM13976	blood:	n/a	n/a
50	CTCF	chr2:211577980-211578130	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:211583084-211583134	NHBE	bronchial:	n/a
2	chr2:211583084-211583134	HRCEpiC	kidney:	n/a
3	chr2:211633248-211633298	T-47D	breast:	n/a
4	chr2:211633248-211633298	NB4	blood:	n/a
5	chr2:211633248-211633298	GM12891	blood:	n/a
6	chr2:211633248-211633298	K562	blood:	n/a
7	chr2:211539520-211539570	SK-N-SH_RA	brain:	n/a
8	chr2:211583084-211583134	HIPEpiC	eye:	n/a
9	chr2:211539520-211539570	HepG2	liver:	n/a
10	chr2:211633248-211633298	NT2-D1	testis:	n/a
11	chr2:211583084-211583134	SK-N-SH	brain:	n/a
12	chr2:211633248-211633298	ovcar-3	ovarian:	n/a
13	chr2:211633248-211633298	ECC-1	luminal epithelium:	n/a
14	chr2:211539520-211539570	HCF	heart:	n/a
15	chr2:211539520-211539570	T-47D	breast:	n/a
16	chr2:211633248-211633298	AG04449	skin:	fetal
17	chr2:211633248-211633298	BJ	skin:	n/a
18	chr2:211633248-211633298	Caco-2	colon:	n/a
19	chr2:211539520-211539570	HCM	heart:	n/a
20	chr2:211539520-211539570	HCPEpiC	choroid plexus:	n/a
21	chr2:211583084-211583134	K562	blood:	n/a
22	chr2:211539520-211539570	SKMC	muscle:	n/a
23	chr2:211633248-211633298	HepG2	liver:	n/a
24	chr2:211539520-211539570	U87	brain:	n/a
25	chr2:211633248-211633298	HL-60	blood:	n/a
26	chr2:211583084-211583134	SK-N-SH_RA	brain:	n/a
27	chr2:211633248-211633298	BE2_C	brain:	n/a
28	chr2:211633248-211633298	HNPCEpiC	eye:	n/a
29	chr2:211583084-211583134	H1-hESC	embryonic stem cell:	embryo
30	chr2:211583084-211583134	HCPEpiC	choroid plexus:	n/a
31	chr2:211539520-211539570	CMK	blood:	n/a
32	chr2:211633248-211633298	SAEC	small airway:	n/a
33	chr2:211539520-211539570	HL-60	blood:	n/a
34	chr2:211583084-211583134	A549	lung:	n/a
35	chr2:211633248-211633298	HCT-116	colon:	n/a
36	chr2:211583084-211583134	Hepatocyte	liver:	n/a
37	chr2:211633248-211633298	AG09319	gingival:	n/a
38	chr2:211539520-211539570	Caco-2	colon:	n/a
39	chr2:211583084-211583134	HRPEpiC	eye:	n/a
40	chr2:211583084-211583134	HRE	kidney:	n/a
41	chr2:211583084-211583134	IMR90	lung:	fetal
42	chr2:211539520-211539570	HMEC	breast:	n/a
43	chr2:211539520-211539570	SK-N-SH	brain:	n/a
44	chr2:211539520-211539570	K562	blood:	n/a
45	chr2:211539520-211539570	HEEpiC	esophagus:	n/a
46	chr2:211583084-211583134	HNPCEpiC	eye:	n/a
47	chr2:211583084-211583134	MCF10A-Er-Src	breast:	n/a
48	chr2:211633248-211633298	HRCEpiC	kidney:	n/a
49	chr2:211539520-211539570	HRE	kidney:	n/a
50	chr2:211583084-211583134	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:211644357..211645963-chr2:211649245..211651246,2	K562	blood:
2	chr2:211593761..211595532-chr2:211597006..211598681,2	K562	blood:
3	chr2:211644357..211645963-chr2:211649245..211651246,2	K562	blood:
4	chr2:211593761..211595532-chr2:211597006..211598681,2	K562	blood:

Variant related genes	Relation type
CPS1	TF binding region
CPS1	CpG island

Extended variants
information (count: 2447 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2447 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144506682	chr2:211528981-211528982	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377077562	chr2:211529038-211529039	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139229378	chr2:211529079-211529080	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143979614	chr2:211529081-211529082	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12990908	chr2:211529121-211529122	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs561828433	chr2:211529124-211529125	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527347831	chr2:211529139-211529140	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547414272	chr2:211529144-211529145	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191607626	chr2:211529152-211529153	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533087320	chr2:211529211-211529212	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4673542	chr2:211529217-211529218	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs142220703	chr2:211529224-211529225	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548859459	chr2:211529227-211529228	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182790493	chr2:211529238-211529239	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577446626	chr2:211529255-211529256	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538566607	chr2:211529264-211529265	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534024735	chr2:211529282-211529283	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556473792	chr2:211529290-211529291	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116573496	chr2:211529322-211529323	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151187298	chr2:211529328-211529329	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539814268	chr2:211529329-211529330	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140323502	chr2:211529334-211529335	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376661529	chr2:211529345-211529346	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114159907	chr2:211529368-211529369	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4233981	chr2:211529378-211529379	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs373025890	chr2:211529394-211529395	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555676757	chr2:211529400-211529401	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150357933	chr2:211529408-211529409	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377187443	chr2:211529479-211529480	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186691146	chr2:211529515-211529516	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545847540	chr2:211529519-211529520	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573118450	chr2:211529527-211529528	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73984682	chr2:211529540-211529541	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532782526	chr2:211529553-211529554	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184787155	chr2:211529555-211529556	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565701888	chr2:211529588-211529589	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147899513	chr2:211529594-211529595	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549202623	chr2:211529603-211529604	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531490987	chr2:211529605-211529606	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565720873	chr2:211529657-211529658	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527812839	chr2:211529722-211529723	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141690236	chr2:211529725-211529726	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570924181	chr2:211529743-211529744	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368931959	chr2:211529766-211529767	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556547167	chr2:211529770-211529771	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570408142	chr2:211529786-211529787	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35170724	chr2:211529802-211529803	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543739755	chr2:211529806-211529807	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535762070	chr2:211529810-211529811	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12997383	chr2:211529850-211529851	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211498200-211529000	Strong transcription	Hela-S3	cervix
2	chr2:211501000-211540600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:211525800-211530000	Genic enhancers	Liver	Liver
4	chr2:211526200-211537600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:211526400-211540400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:211527600-211538800	Weak transcription	Fetal Intestine Small	intestine
7	chr2:211527800-211530000	Strong transcription	Duodenum Mucosa	Duodenum
8	chr2:211527800-211530000	Strong transcription	Fetal Intestine Large	intestine
9	chr2:211528400-211529000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:211528600-211529000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:211528600-211529000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr2:211528600-211529000	Enhancers	Adipose Nuclei	Adipose
13	chr2:211528600-211529000	Enhancers	Brain Angular Gyrus	brain
14	chr2:211528600-211529000	Flanking Active TSS	Brain Cingulate Gyrus	brain
15	chr2:211528600-211529000	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr2:211528600-211529000	Enhancers	Brain Substantia Nigra	brain
17	chr2:211528600-211529200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:211528800-211542400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:211529000-211529200	Enhancers	Brain Hippocampus Middle	brain
20	chr2:211529000-211532000	Weak transcription	Hela-S3	cervix
21	chr2:211529200-211535800	Weak transcription	Brain Hippocampus Middle	brain
22	chr2:211530000-211532000	Weak transcription	Liver	Liver
23	chr2:211530000-211532400	Weak transcription	Fetal Intestine Large	intestine
24	chr2:211530000-211533000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr2:211532000-211539000	Strong transcription	Hela-S3	cervix
26	chr2:211532000-211547000	Strong transcription	Liver	Liver
27	chr2:211532200-211532600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr2:211532400-211547200	Strong transcription	Fetal Intestine Large	intestine
29	chr2:211533000-211547000	Strong transcription	Duodenum Mucosa	Duodenum
30	chr2:211535400-211536600	Enhancers	Brain Angular Gyrus	brain
31	chr2:211535600-211535800	Enhancers	Brain Anterior Caudate	brain
32	chr2:211535800-211536000	Flanking Active TSS	Brain Anterior Caudate	brain
33	chr2:211535800-211536200	Active TSS	Brain Hippocampus Middle	brain
34	chr2:211535800-211537000	Enhancers	Brain Substantia Nigra	brain
35	chr2:211536000-211536200	Active TSS	Brain Anterior Caudate	brain
36	chr2:211536200-211536600	Enhancers	Brain Anterior Caudate	brain
37	chr2:211536200-211536600	Enhancers	Brain Cingulate Gyrus	brain
38	chr2:211536200-211537600	Enhancers	Brain Hippocampus Middle	brain
39	chr2:211537400-211538400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr2:211537400-211538400	Enhancers	HepG2	liver
41	chr2:211537600-211538200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr2:211537600-211538400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:211537600-211538400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:211538000-211538200	Enhancers	Pancreas	Pancrea
45	chr2:211538400-211540400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:211538400-211541000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:211538800-211539000	Strong transcription	Fetal Intestine Small	intestine
48	chr2:211539000-211539800	Weak transcription	Hela-S3	cervix
49	chr2:211539000-211542600	Weak transcription	Fetal Intestine Small	intestine
50	chr2:211539800-211545400	Strong transcription	Hela-S3	cervix

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