Variant report

Variant	esv3344055
Chromosome Location	chr1:175873040-175887908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:175880278-175880656	HCT-116	colon:	n/a	n/a
2	CBX3	chr1:175880242-175880616	HCT-116	colon:	n/a	n/a
3	CEBPB	chr1:175880486-175880535	K562	blood:	n/a	n/a
4	CEBPB	chr1:175887373-175888012	IMR90	lung:	n/a	n/a
5	EP300	chr1:175887540-175887911	H1-hESC	embryonic stem cell:	n/a	n/a
6	FOXA1	chr1:175875651-175875823	T-47D	breast:	n/a	n/a
7	FOXA1	chr1:175882340-175882657	T-47D	breast:	n/a	n/a
8	GATA3	chr1:175886765-175886827	SH-SY5Y	brain:	n/a	n/a
9	GATA3	chr1:175877302-175877760	T-47D	breast:	n/a	n/a
10	HDAC2	chr1:175887339-175888048	H1-hESC	embryonic stem cell:	n/a	n/a
11	HDAC2	chr1:175887674-175887902	H1-hESC	embryonic stem cell:	n/a	n/a
12	IRF1	chr1:175875523-175875524	K562	blood:	n/a	n/a
13	IRF1	chr1:175875935-175875954	K562	blood:	n/a	n/a
14	JUND	chr1:175877262-175877812	T-47D	breast:	n/a	n/a
15	KAP1	chr1:175880177-175880754	K562	blood:	n/a	n/a
16	KAP1	chr1:175880116-175880827	HEK293	kidney:	n/a	n/a
17	KAP1	chr1:175880209-175880716	U2OS	brain:	n/a	n/a
18	MAFF	chr1:175883264-175883630	HepG2	liver:	n/a	chr1:175883441-175883455 chr1:175883442-175883460
19	MAFF	chr1:175883265-175883614	K562	blood:	n/a	chr1:175883441-175883455 chr1:175883442-175883460
20	MAFK	chr1:175883273-175883630	K562	blood:	n/a	chr1:175883441-175883455 chr1:175883438-175883458 chr1:175883443-175883458 chr1:175883440-175883456
21	MAFK	chr1:175874878-175875055	HepG2	liver:	n/a	chr1:175874889-175874905 chr1:175874889-175874900 chr1:175874890-175874901 chr1:175874889-175874900
22	MAFK	chr1:175883316-175883604	Hela-S3	cervix:	n/a	chr1:175883441-175883455 chr1:175883438-175883458 chr1:175883443-175883458 chr1:175883440-175883456
23	MAFK	chr1:175874963-175875028	HepG2	liver:	n/a	n/a
24	MAFK	chr1:175883279-175883580	H1-hESC	embryonic stem cell:	n/a	chr1:175883441-175883455 chr1:175883438-175883458 chr1:175883443-175883458 chr1:175883440-175883456
25	MAFK	chr1:175883231-175883634	IMR90	lung:	n/a	chr1:175883441-175883455 chr1:175883438-175883458 chr1:175883443-175883458 chr1:175883440-175883456
26	MAFK	chr1:175883268-175883622	HepG2	liver:	n/a	chr1:175883441-175883455 chr1:175883438-175883458 chr1:175883443-175883458 chr1:175883440-175883456
27	MAFK	chr1:175883261-175883632	HepG2	liver:	n/a	chr1:175883441-175883455 chr1:175883438-175883458 chr1:175883443-175883458 chr1:175883440-175883456
28	MYC	chr1:175879509-175879633	MCF-7	breast:	n/a	n/a
29	NANOG	chr1:175887511-175887713	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr1:175879459-175879631	Gliobla	brain:	n/a	n/a
31	POLR2A	chr1:175883153-175883218	ProgFib	skin:	n/a	n/a
32	POLR2A	chr1:175880001-175880182	ProgFib	skin:	n/a	n/a
33	POLR2A	chr1:175879523-175879723	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr1:175883072-175883135	ProgFib	skin:	n/a	n/a
35	POLR2A	chr1:175887613-175887934	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr1:175883739-175883811	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr1:175879641-175879645	Gliobla	brain:	n/a	n/a
38	POLR2A	chr1:175887534-175887710	MCF10A-Er-Src	breast:	n/a	n/a
39	SETDB1	chr1:175880101-175880899	U2OS	brain:	n/a	n/a
40	STAT3	chr1:175874246-175874286	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr1:175882629-175882663	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr1:175873206-175873463	MCF10A-Er-Src	breast:	n/a	n/a
43	TCF12	chr1:175887535-175887796	H1-hESC	embryonic stem cell:	n/a	n/a
44	TEAD4	chr1:175887614-175888019	H1-hESC	embryonic stem cell:	n/a	n/a
45	USF1	chr1:175882854-175883267	H1-hESC	embryonic stem cell:	n/a	n/a
46	USF1	chr1:175882947-175883343	H1-hESC	embryonic stem cell:	n/a	n/a
47	USF1	chr1:175880310-175880726	HCT-116	colon:	n/a	n/a
48	USF2	chr1:175880230-175880309	H1-hESC	embryonic stem cell:	n/a	n/a
49	USF2	chr1:175879591-175879647	HepG2	liver:	n/a	n/a
50	USF2	chr1:175882912-175883268	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:175886537-175886587	HCM	heart:	n/a
2	chr1:175886537-175886587	HRPEpiC	eye:	n/a
3	chr1:175886537-175886587	NT2-D1	testis:	n/a
4	chr1:175886537-175886587	HNPCEpiC	eye:	n/a
5	chr1:175886537-175886587	SK-N-SH_RA	brain:	n/a
6	chr1:175886537-175886587	RPTEC	kidney:	n/a
7	chr1:175886537-175886587	AoSMC	blood vessel:	n/a
8	chr1:175886537-175886587	AG09309	skin:	n/a
9	chr1:175886537-175886587	Hela-S3	cervix:	n/a
10	chr1:175886537-175886587	HEK293	kidney:	embryo
11	chr1:175886537-175886587	T-47D	breast:	n/a
12	chr1:175886537-175886587	A549	lung:	n/a
13	chr1:175886537-175886587	GM06990	blood:	n/a
14	chr1:175886537-175886587	SK-N-SH	brain:	n/a
15	chr1:175886537-175886587	NHDF-neo	bronchial:	n/a
16	chr1:175886537-175886587	NH-A	brain:	n/a
17	chr1:175886537-175886587	AG09319	gingival:	n/a
18	chr1:175886537-175886587	NHBE	bronchial:	n/a
19	chr1:175886537-175886587	AG10803	skin:	n/a
20	chr1:175886537-175886587	SK-N-MC	brain:	n/a
21	chr1:175886537-175886587	ovcar-3	ovarian:	n/a
22	chr1:175886537-175886587	AG04450	lung:	fetal
23	chr1:175886537-175886587	HUVEC	blood vessel:	n/a
24	chr1:175886537-175886587	BJ	skin:	n/a
25	chr1:175886537-175886587	HRE	kidney:	n/a
26	chr1:175886537-175886587	HRCEpiC	kidney:	n/a
27	chr1:175886537-175886587	HMEC	breast:	n/a
28	chr1:175886537-175886587	CMK	blood:	n/a
29	chr1:175886537-175886587	SKMC	muscle:	n/a
30	chr1:175886537-175886587	LNCaP	prostate:	n/a
31	chr1:175886537-175886587	GM12892	blood:	n/a
32	chr1:175886537-175886587	Caco-2	colon:	n/a
33	chr1:175886537-175886587	HL-60	blood:	n/a
34	chr1:175886537-175886587	Hepatocyte	liver:	n/a
35	chr1:175886537-175886587	HCT-116	colon:	n/a
36	chr1:175886537-175886587	HIPEpiC	eye:	n/a
37	chr1:175886537-175886587	HCF	heart:	n/a
38	chr1:175886537-175886587	Jurkat	blood:	n/a
39	chr1:175886537-175886587	PFSK-1	brain:	n/a
40	chr1:175886537-175886587	SAEC	small airway:	n/a
41	chr1:175886537-175886587	BE2_C	brain:	n/a
42	chr1:175886537-175886587	ECC-1	luminal epithelium:	n/a
43	chr1:175886537-175886587	HCPEpiC	choroid plexus:	n/a
44	chr1:175886537-175886587	HAEpiC	amniotic membrane:	n/a
45	chr1:175886537-175886587	MCF-7	breast:	n/a
46	chr1:175886537-175886587	GM19239	blood:	n/a
47	chr1:175886537-175886587	HEEpiC	esophagus:	n/a
48	chr1:175886537-175886587	HepG2	liver:	n/a
49	chr1:175886537-175886587	MCF10A-Er-Src	breast:	n/a
50	chr1:175886537-175886587	GM12891	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:175880486..175882098-chr1:175883160..175885443,2	K562	blood:
2	chr1:175882539..175884540-chr1:175888670..175890175,2	K562	blood:
3	chr1:175881029..175882738-chr1:175891650..175894034,2	K562	blood:
4	chr1:175873582..175875624-chr1:176663065..176665878,2	K562	blood:
5	chr1:175867730..175870144-chr1:175872565..175874152,2	K562	blood:
6	chr1:175880486..175882098-chr1:175883160..175885443,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFWD2-1	chr1:175877683-175877906	XLOC_001099
2	lnc-RFWD2-4	chr1:175886432-175887024	NONHSAT007762
3	lnc-RFWD2-1	chr1:175873898-175874272	XLOC_001099

No data

Variant related genes	Relation type
ENSG00000230777	TF binding region
ENSG00000230777	CpG island
ENSG00000227740	chromatin interactions
CDKN1A	miRNA target sites

Extended variants
information (count: 539 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547511643	chr1:175873040-175873041	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530080852	chr1:175873085-175873086	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141684751	chr1:175873088-175873089	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563752899	chr1:175873105-175873106	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190061155	chr1:175873251-175873252	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200093574	chr1:175873305-175873306	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12752542	chr1:175873370-175873371	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs571334193	chr1:175873372-175873373	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527616715	chr1:175873399-175873400	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547257424	chr1:175873414-175873415	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150551812	chr1:175873446-175873447	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555994754	chr1:175873499-175873500	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182237965	chr1:175873508-175873509	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79449858	chr1:175873556-175873557	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12405136	chr1:175873561-175873562	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs535671869	chr1:175873592-175873593	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376717204	chr1:175873665-175873666	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7514816	chr1:175873840-175873841	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555273457	chr1:175873854-175873855	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574885871	chr1:175873893-175873894	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs16849351	chr1:175873952-175873953	Enhancers Weak transcription Bivalent Enhancer Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs187448055	chr1:175873958-175873959	Enhancers Weak transcription Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs532684360	chr1:175873988-175873989	Enhancers Weak transcription Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs545968028	chr1:175874002-175874003	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs571156352	chr1:175874031-175874032	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs193278107	chr1:175874049-175874050	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs527457825	chr1:175874066-175874067	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs555579817	chr1:175874105-175874106	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs567183242	chr1:175874134-175874135	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs113507067	chr1:175874136-175874137	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs10494494	chr1:175874139-175874140	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs183705230	chr1:175874140-175874141	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs541308643	chr1:175874141-175874142	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs75163737	chr1:175874163-175874164	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs372798750	chr1:175874179-175874180	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs12035001	chr1:175874206-175874207	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs538759079	chr1:175874207-175874208	Bivalent Enhancer Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs558334708	chr1:175874302-175874303	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147426206	chr1:175874311-175874312	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28636481	chr1:175874319-175874320	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76788540	chr1:175874328-175874329	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369124776	chr1:175874330-175874331	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72713227	chr1:175874348-175874349	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs575246810	chr1:175874350-175874351	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577575924	chr1:175874368-175874369	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12740514	chr1:175874395-175874396	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188994189	chr1:175874398-175874399	Bivalent Enhancer Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557361825	chr1:175874419-175874420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577131216	chr1:175874468-175874469	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546302125	chr1:175874470-175874471	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175855200-175879400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:175855400-175879400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:175857200-175875800	Weak transcription	Brain Germinal Matrix	brain
4	chr1:175857600-175879400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:175858200-175879400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr1:175858800-175876800	Weak transcription	HSMM	muscle
7	chr1:175858800-175879400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr1:175858800-175879400	Weak transcription	HSMMtube	muscle
9	chr1:175859200-175879400	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:175862400-175879400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:175863200-175906400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:175863400-175879400	Weak transcription	Primary T cells from cord blood	blood
13	chr1:175864800-175878000	Weak transcription	Fetal Brain Female	brain
14	chr1:175865200-175879400	Weak transcription	Fetal Lung	lung
15	chr1:175865400-175879400	Weak transcription	Fetal Stomach	stomach
16	chr1:175866600-175876200	Weak transcription	Ovary	ovary
17	chr1:175868200-175877000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:175869600-175879400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:175870000-175873200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:175870000-175879400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr1:175870200-175879400	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr1:175870600-175874400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:175871400-175878400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:175871400-175879600	Weak transcription	Psoas Muscle	Psoas
25	chr1:175871600-175875000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:175871800-175879400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:175871800-175879400	Weak transcription	Aorta	Aorta
28	chr1:175871800-175879400	Weak transcription	Pancreas	Pancrea
29	chr1:175872000-175876800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr1:175872400-175873400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:175872400-175874000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:175872600-175873400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
33	chr1:175872800-175879400	Weak transcription	Left Ventricle	heart
34	chr1:175873000-175873200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr1:175873200-175873400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
36	chr1:175873200-175875000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:175873400-175875000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:175873800-175874000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
39	chr1:175874000-175874400	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:175874000-175879400	Weak transcription	Lung	lung
41	chr1:175874400-175876200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:175874400-175945600	Weak transcription	A549	lung
43	chr1:175874600-175874800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
44	chr1:175874800-175875000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr1:175874800-175875000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
46	chr1:175875000-175875400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:175875000-175876600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:175875000-175882800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:175875400-175875800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:175875600-175875800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell

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