Variant report

Variant	nsv523114
Chromosome Location	chr1:220486349-220500958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:220486334-220486396	K562	blood:	n/a	n/a
2	BHLHE40	chr1:220495373-220495390	K562	blood:	n/a	n/a
3	CEBPB	chr1:220491114-220491314	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:220491119-220491179	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:220490593-220490793	HepG2	liver:	n/a	n/a
6	CTCF	chr1:220495169-220495527	K562	blood:	n/a	n/a
7	CTCF	chr1:220495288-220495383	A549	lung:	n/a	n/a
8	CTCF	chr1:220495356-220495366	GM19238	blood:	n/a	n/a
9	CTCF	chr1:220495154-220495540	MCF-7	breast:	n/a	n/a
10	CTCF	chr1:220495269-220495428	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr1:220495340-220495490	Caco-2	colon:	n/a	n/a
12	CTCF	chr1:220500673-220500699	HepG2	liver:	n/a	n/a
13	CTCF	chr1:220495260-220495410	K562	blood:	n/a	n/a
14	CTCF	chr1:220495261-220495416	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:220495255-220495393	HepG2	liver:	n/a	n/a
16	CTCF	chr1:220495312-220495372	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:220500575-220500868	HCT-116	colon:	n/a	n/a
18	CTCF	chr1:220489400-220489550	GM12878	blood:	n/a	n/a
19	CTCF	chr1:220495330-220495407	GM12892	blood:	n/a	n/a
20	CTCF	chr1:220495360-220495510	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:220495214-220495489	K562	blood:	n/a	n/a
22	CTCF	chr1:220495320-220495470	GM12864	blood:	n/a	n/a
23	CTCF	chr1:220500660-220500810	Caco-2	colon:	n/a	n/a
24	CTCF	chr1:220495200-220495350	GM12872	blood:	n/a	n/a
25	CTCF	chr1:220495256-220495459	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:220495279-220495403	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:220500620-220500770	AG09319	gingival:	n/a	n/a
28	CTCF	chr1:220495280-220495430	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr1:220495328-220495347	GM12891	blood:	n/a	n/a
30	CTCF	chr1:220495300-220495450	HepG2	liver:	n/a	n/a
31	CTCF	chr1:220495260-220495424	K562	blood:	n/a	n/a
32	CTCF	chr1:220495331-220495357	GM19239	blood:	n/a	n/a
33	CTCF	chr1:220495258-220495435	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:220486846-220487121	K562	blood:	n/a	n/a
35	CTCF	chr1:220495250-220495451	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:220495143-220495598	K562	blood:	n/a	n/a
37	CTCF	chr1:220495234-220495398	GM12878	blood:	n/a	n/a
38	E2F4	chr1:220492194-220492295	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr1:220488199-220488393	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr1:220498678-220498745	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:220488480-220488727	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:220488442-220488795	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr1:220489326-220489459	MCF10A-Er-Src	breast:	n/a	chr1:220489337-220489348 chr1:220489334-220489345 chr1:220489336-220489344
44	FOS	chr1:220499953-220500339	MCF10A-Er-Src	breast:	n/a	chr1:220500179-220500189 chr1:220500181-220500188 chr1:220500180-220500188 chr1:220500178-220500190 chr1:220500180-220500189
45	FOS	chr1:220498781-220499384	MCF10A-Er-Src	breast:	n/a	chr1:220499123-220499131 chr1:220499123-220499131 chr1:220499124-220499131
46	FOS	chr1:220498730-220499422	MCF10A-Er-Src	breast:	n/a	chr1:220499123-220499131 chr1:220499123-220499131 chr1:220499124-220499131
47	FOS	chr1:220488408-220488941	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:220498873-220499360	MCF10A-Er-Src	breast:	n/a	chr1:220499123-220499131 chr1:220499123-220499131 chr1:220499124-220499131
49	FOS	chr1:220499991-220500358	MCF10A-Er-Src	breast:	n/a	chr1:220500179-220500189 chr1:220500181-220500188 chr1:220500180-220500188 chr1:220500178-220500190 chr1:220500180-220500189
50	FOS	chr1:220499935-220500359	MCF10A-Er-Src	breast:	n/a	chr1:220500179-220500189 chr1:220500181-220500188 chr1:220500180-220500188 chr1:220500178-220500190 chr1:220500180-220500189

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:220500857-220500907	MCF10A-Er-Src	breast:	n/a
2	chr1:220500857-220500907	SAEC	small airway:	n/a
3	chr1:220500857-220500907	HRE	kidney:	n/a
4	chr1:220500857-220500907	LNCaP	prostate:	n/a
5	chr1:220500857-220500907	ProgFib	skin:	n/a
6	chr1:220500857-220500907	AG04449	skin:	fetal
7	chr1:220500857-220500907	SKMC	muscle:	n/a
8	chr1:220500857-220500907	Hela-S3	cervix:	n/a
9	chr1:220500857-220500907	A549	lung:	n/a
10	chr1:220500857-220500907	RPTEC	kidney:	n/a
11	chr1:220500857-220500907	HAEpiC	amniotic membrane:	n/a
12	chr1:220500857-220500907	HCM	heart:	n/a
13	chr1:220500857-220500907	Hepatocyte	liver:	n/a
14	chr1:220500857-220500907	PrEC	prostate:	n/a
15	chr1:220500857-220500907	AG10803	skin:	n/a
16	chr1:220500857-220500907	SK-N-MC	brain:	n/a
17	chr1:220500857-220500907	HEEpiC	esophagus:	n/a
18	chr1:220500857-220500907	SK-N-SH_RA	brain:	n/a
19	chr1:220500857-220500907	HMEC	breast:	n/a
20	chr1:220500857-220500907	GM06990	blood:	n/a
21	chr1:220500857-220500907	H1-hESC	embryonic stem cell:	embryo
22	chr1:220500857-220500907	PFSK-1	brain:	n/a
23	chr1:220500857-220500907	BJ	skin:	n/a
24	chr1:220500857-220500907	HCF	heart:	n/a
25	chr1:220500857-220500907	HEK293	kidney:	embryo
26	chr1:220500857-220500907	AoSMC	blood vessel:	n/a
27	chr1:220500857-220500907	Jurkat	blood:	n/a
28	chr1:220500857-220500907	SK-N-SH	brain:	n/a
29	chr1:220500857-220500907	NHDF-neo	bronchial:	n/a
30	chr1:220500857-220500907	ovcar-3	ovarian:	n/a
31	chr1:220500857-220500907	NB4	blood:	n/a
32	chr1:220500857-220500907	AG09319	gingival:	n/a
33	chr1:220500857-220500907	CMK	blood:	n/a
34	chr1:220500857-220500907	U87	brain:	n/a
35	chr1:220500857-220500907	GM12892	blood:	n/a
36	chr1:220500857-220500907	BE2_C	brain:	n/a
37	chr1:220500857-220500907	HRPEpiC	eye:	n/a
38	chr1:220500857-220500907	K562	blood:	n/a
39	chr1:220500857-220500907	Caco-2	colon:	n/a
40	chr1:220500857-220500907	HIPEpiC	eye:	n/a
41	chr1:220500857-220500907	HNPCEpiC	eye:	n/a
42	chr1:220500857-220500907	HCT-116	colon:	n/a
43	chr1:220500857-220500907	MCF-7	breast:	n/a
44	chr1:220500857-220500907	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:220500857-220500907	GM19239	blood:	n/a
46	chr1:220500857-220500907	IMR90	lung:	fetal
47	chr1:220500857-220500907	HCPEpiC	choroid plexus:	n/a
48	chr1:220500857-220500907	HepG2	liver:	n/a
49	chr1:220500857-220500907	NH-A	brain:	n/a
50	chr1:220500857-220500907	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:220492579..220494999-chr1:220497676..220499408,2	MCF-7	breast:
2	chr1:220491693..220493296-chr1:220495769..220497470,2	K562	blood:
3	chr1:220469373..220470129-chr1:220494958..220495790,3	MCF-7	breast:
4	chr1:220485586..220488205-chr1:220491001..220493113,2	MCF-7	breast:
5	chr1:220492579..220494999-chr1:220497676..220499408,2	MCF-7	breast:
6	chr1:220490409..220493296-chr1:220495769..220497672,3	K562	blood:
7	chr1:220469913..220472006-chr1:220498061..220500308,2	MCF-7	breast:
8	chr1:220485586..220488205-chr1:220491001..220493113,2	MCF-7	breast:
9	chr1:220491693..220493296-chr1:220495769..220497470,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000232883	TF binding region
XRCC6P3	TF binding region
ENSG00000232883	CpG island
XRCC6P3	CpG island
ENSG00000232883	chromatin interactions

Extended variants
information (count: 708 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4272630	chr1:220486349-220486350	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188071998	chr1:220486374-220486375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568282711	chr1:220486388-220486389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141297431	chr1:220486435-220486436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554389030	chr1:220486444-220486445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570845536	chr1:220486447-220486448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186979269	chr1:220486476-220486477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4460644	chr1:220486482-220486483	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369237823	chr1:220486538-220486539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556573479	chr1:220486563-220486564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572003117	chr1:220486628-220486629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192728134	chr1:220486658-220486659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542109794	chr1:220486739-220486740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555708006	chr1:220486742-220486743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572224698	chr1:220486747-220486748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145031263	chr1:220486762-220486763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564346914	chr1:220486763-220486764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532871786	chr1:220486765-220486766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71167224	chr1:220486773-220486774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369541937	chr1:220486782-220486783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575102135	chr1:220486783-220486784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12124538	chr1:220486796-220486797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9793772	chr1:220486799-220486800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs528876560	chr1:220486802-220486803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9793779	chr1:220486925-220486926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs147920124	chr1:220486932-220486933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376009197	chr1:220486941-220486942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113561692	chr1:220486942-220486943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200204299	chr1:220486944-220486945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367920380	chr1:220486945-220486946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141929947	chr1:220486946-220486947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61397452	chr1:220486954-220486955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs202118139	chr1:220486955-220486956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547657603	chr1:220486956-220486957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571050634	chr1:220486964-220486965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138874554	chr1:220486988-220486989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556708111	chr1:220487073-220487074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570024225	chr1:220487080-220487081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535852910	chr1:220487097-220487098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555844693	chr1:220487163-220487164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115137322	chr1:220487187-220487188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541351787	chr1:220487375-220487376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557647680	chr1:220487421-220487422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187587490	chr1:220487459-220487460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12044104	chr1:220487499-220487500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574739232	chr1:220487516-220487517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148160538	chr1:220487537-220487538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192261022	chr1:220487605-220487606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556964175	chr1:220487609-220487610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369534128	chr1:220487611-220487612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220486000-220486600	Enhancers	Fetal Lung	lung
2	chr1:220486200-220488600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:220487000-220488400	Enhancers	Right Ventricle	heart
4	chr1:220487200-220487400	Enhancers	Right Atrium	heart
5	chr1:220487400-220495400	Weak transcription	Right Atrium	heart
6	chr1:220487800-220489600	Enhancers	Fetal Heart	heart
7	chr1:220488200-220488800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:220488200-220490800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:220488400-220488800	Enhancers	Left Ventricle	heart
10	chr1:220488400-220490200	Enhancers	Adipose Nuclei	Adipose
11	chr1:220488400-220490200	Weak transcription	Right Ventricle	heart
12	chr1:220488600-220489400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr1:220488800-220489600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:220488800-220491800	Weak transcription	Left Ventricle	heart
15	chr1:220489000-220489600	Enhancers	NHDF-Ad	bronchial
16	chr1:220489600-220491200	Weak transcription	Fetal Heart	heart
17	chr1:220490200-220490600	Enhancers	Right Ventricle	heart
18	chr1:220490200-220492400	Weak transcription	Adipose Nuclei	Adipose
19	chr1:220490600-220491600	Weak transcription	Right Ventricle	heart
20	chr1:220490800-220491200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:220491200-220491400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:220491200-220493000	Enhancers	Fetal Heart	heart
23	chr1:220491400-220492400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:220491600-220492000	Enhancers	HSMMtube	muscle
25	chr1:220491800-220492000	Enhancers	Fetal Muscle Leg	muscle
26	chr1:220491800-220492000	Enhancers	Left Ventricle	heart
27	chr1:220491800-220492000	Enhancers	Right Ventricle	heart
28	chr1:220491800-220492200	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr1:220492400-220492600	Enhancers	Adipose Nuclei	Adipose
30	chr1:220492400-220493200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:220493000-220499600	Weak transcription	Fetal Heart	heart
32	chr1:220495000-220495600	Enhancers	GM12878-XiMat	blood
33	chr1:220495600-220495800	Weak transcription	Right Atrium	heart
34	chr1:220495600-220498800	Weak transcription	GM12878-XiMat	blood
35	chr1:220498400-220498800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr1:220498400-220498800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr1:220498400-220499000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr1:220498400-220499000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:220498400-220500200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:220498800-220499000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:220498800-220499000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:220498800-220499000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:220498800-220499000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:220498800-220499200	Enhancers	Esophagus	oesophagus
45	chr1:220498800-220500000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr1:220498800-220500000	Enhancers	HSMMtube	muscle
47	chr1:220498800-220500200	Enhancers	GM12878-XiMat	blood
48	chr1:220498800-220503000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:220499000-220500000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr1:220499000-220500200	Enhancers	NH-A	brain

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