Variant report

Variant	esv1817255
Chromosome Location	chr1:171170733-171185865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:171182396-171182642	IMR90	lung:	n/a	n/a
2	CEBPB	chr1:171179528-171179841	MCF-7	breast:	n/a	n/a
3	CEBPB	chr1:171176111-171176340	HepG2	liver:	n/a	chr1:171176174-171176185
4	CTCF	chr1:171183280-171183499	MCF-7	breast:	n/a	n/a
5	CTCF	chr1:171183340-171183490	MCF-7	breast:	n/a	n/a
6	CTCF	chr1:171183340-171183490	HEK293	kidney:	n/a	n/a
7	CTCF	chr1:171183300-171183450	HMF	breast:	n/a	n/a
8	CTCF	chr1:171183400-171183550	RPTEC	kidney:	n/a	n/a
9	CTCF	chr1:171183415-171183424	A549	lung:	n/a	n/a
10	CTCF	chr1:171183458-171183466	ProgFib	skin:	n/a	n/a
11	CTCF	chr1:171183220-171183370	RPTEC	kidney:	n/a	n/a
12	CTCF	chr1:171183360-171183510	BE2_C	brain:	n/a	n/a
13	CTCF	chr1:171183320-171183470	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:171183384-171183397	GM12878	blood:	n/a	n/a
15	CTCF	chr1:171183391-171183404	A549	lung:	n/a	n/a
16	CTCF	chr1:171183324-171183454	HepG2	liver:	n/a	n/a
17	CTCF	chr1:171183300-171183450	GM12864	blood:	n/a	n/a
18	CTCF	chr1:171183410-171183422	GM13977	blood:	n/a	n/a
19	CTCF	chr1:171183332-171183485	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:171183280-171183430	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr1:171183220-171183370	NHEK	skin:	n/a	n/a
22	CTCF	chr1:171183340-171183490	GM06990	blood:	n/a	n/a
23	CTCF	chr1:171183240-171183390	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr1:171183340-171183490	AG10803	skin:	n/a	n/a
25	CTCF	chr1:171183240-171183390	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr1:171183143-171183491	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:171183348-171183448	NHEK	skin:	n/a	n/a
28	CTCF	chr1:171183345-171183349	Medullo	brain:	n/a	n/a
29	CTCF	chr1:171183300-171183450	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr1:171183316-171183448	GM12878	blood:	n/a	n/a
31	CTCF	chr1:171183293-171183479	Gliobla	brain:	n/a	n/a
32	CTCF	chr1:171183346-171183453	ProgFib	skin:	n/a	n/a
33	CTCF	chr1:171183328-171183436	K562	blood:	n/a	n/a
34	CTCF	chr1:171183357-171183431	Fibrobl	skin:	n/a	n/a
35	CTCF	chr1:171183340-171183490	HCT-116	colon:	n/a	n/a
36	CTCF	chr1:171183320-171183470	GM12873	blood:	n/a	n/a
37	CTCF	chr1:171183300-171183450	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr1:171183337-171183436	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr1:171183173-171183617	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:171183240-171183390	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr1:171183300-171183450	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr1:171183300-171183450	RPTEC	kidney:	n/a	n/a
43	CTCF	chr1:171183279-171183447	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr1:171183266-171183518	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:171183356-171183403	Medullo	brain:	n/a	n/a
46	CTCF	chr1:171183343-171183483	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:171183360-171183460	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:171183356-171183410	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr1:171183360-171183510	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr1:171183340-171183490	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:171179875-171179925	AG09319	gingival:	n/a
2	chr1:171179875-171179925	Caco-2	colon:	n/a
3	chr1:171179875-171179925	GM06990	blood:	n/a
4	chr1:171179875-171179925	HepG2	liver:	n/a
5	chr1:171179875-171179925	AG10803	skin:	n/a
6	chr1:171179875-171179925	PANC-1	pancreas:	n/a
7	chr1:171179875-171179925	SAEC	small airway:	n/a
8	chr1:171179875-171179925	GM19239	blood:	n/a
9	chr1:171179875-171179925	PFSK-1	brain:	n/a
10	chr1:171179875-171179925	K562	blood:	n/a
11	chr1:171179875-171179925	HRCEpiC	kidney:	n/a
12	chr1:171179875-171179925	HEK293	kidney:	embryo
13	chr1:171179875-171179925	HEEpiC	esophagus:	n/a
14	chr1:171179875-171179925	HMEC	breast:	n/a
15	chr1:171179875-171179925	HCF	heart:	n/a
16	chr1:171179875-171179925	NH-A	brain:	n/a
17	chr1:171179875-171179925	MCF10A-Er-Src	breast:	n/a
18	chr1:171179875-171179925	PrEC	prostate:	n/a
19	chr1:171179875-171179925	H1-hESC	embryonic stem cell:	embryo
20	chr1:171179875-171179925	HUVEC	blood vessel:	n/a
21	chr1:171179875-171179925	HRE	kidney:	n/a
22	chr1:171179875-171179925	HNPCEpiC	eye:	n/a
23	chr1:171179875-171179925	Hela-S3	cervix:	n/a
24	chr1:171179875-171179925	NHDF-neo	bronchial:	n/a
25	chr1:171179875-171179925	HAEpiC	amniotic membrane:	n/a
26	chr1:171179875-171179925	Jurkat	blood:	n/a
27	chr1:171179875-171179925	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:171179875-171179925	HL-60	blood:	n/a
29	chr1:171179875-171179925	MCF-7	breast:	n/a
30	chr1:171179875-171179925	NB4	blood:	n/a
31	chr1:171179875-171179925	ovcar-3	ovarian:	n/a
32	chr1:171179875-171179925	CMK	blood:	n/a
33	chr1:171179875-171179925	T-47D	breast:	n/a
34	chr1:171179875-171179925	GM12892	blood:	n/a
35	chr1:171179875-171179925	HCPEpiC	choroid plexus:	n/a
36	chr1:171179875-171179925	BJ	skin:	n/a
37	chr1:171179875-171179925	AG04450	lung:	fetal
38	chr1:171179875-171179925	HCM	heart:	n/a
39	chr1:171179875-171179925	NHBE	bronchial:	n/a
40	chr1:171179875-171179925	HCT-116	colon:	n/a
41	chr1:171179875-171179925	HIPEpiC	eye:	n/a
42	chr1:171179875-171179925	GM12891	blood:	n/a
43	chr1:171179875-171179925	BE2_C	brain:	n/a
44	chr1:171179875-171179925	NT2-D1	testis:	n/a
45	chr1:171179875-171179925	ProgFib	skin:	n/a
46	chr1:171179875-171179925	SK-N-SH	brain:	n/a
47	chr1:171179875-171179925	SK-N-MC	brain:	n/a
48	chr1:171179875-171179925	AG04449	skin:	fetal
49	chr1:171179875-171179925	SK-N-SH_RA	brain:	n/a
50	chr1:171179875-171179925	HRPEpiC	eye:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:171177619..171179300-chr1:171182219..171184780,2	K562	blood:
2	chr1:171180730..171183096-chr4:189101938..189104230,2	MCF-7	breast:
3	chr1:171182864..171185763-chr1:171186408..171189341,2	MCF-7	breast:
4	chr1:171177619..171179300-chr1:171182219..171184780,2	K562	blood:
5	chr1:171161907..171164775-chr1:171168366..171171218,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOC-1	chr1:171173030-171173127	ENSG00000225243.1
2	lnc-MYOC-1	chr1:171173030-171173127	ENSG00000225243.1

No data

Variant related genes	Relation type
FMO2	TF binding region
FMO2	CpG island

Extended variants
information (count: 571 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4916183	chr1:171170733-171170734	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182180941	chr1:171170734-171170735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563818840	chr1:171170736-171170737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140700968	chr1:171170764-171170765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545793079	chr1:171170774-171170775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145903760	chr1:171170817-171170818	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4916243	chr1:171170852-171170853	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs187152914	chr1:171170890-171170891	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191596012	chr1:171170895-171170896	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28369884	chr1:171170908-171170909	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs550363509	chr1:171170911-171170912	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568937525	chr1:171170943-171170944	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28369885	chr1:171170963-171170964	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557830510	chr1:171170969-171170970	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs386636737	chr1:171170971-171170972	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12735631	chr1:171170972-171170973	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74989447	chr1:171170976-171170977	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28735332	chr1:171170978-171170979	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs397793012	chr1:171170981-171170982	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28369886	chr1:171171002-171171003	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182434932	chr1:171171050-171171051	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12691472	chr1:171171055-171171056	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs557126835	chr1:171171088-171171089	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs28369887	chr1:171171170-171171171	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs545782825	chr1:171171205-171171206	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564172231	chr1:171171206-171171207	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369556645	chr1:171171331-171171332	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540537311	chr1:171171379-171171380	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141363710	chr1:171171471-171171472	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566500803	chr1:171171489-171171490	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535138281	chr1:171171491-171171492	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28369888	chr1:171171493-171171494	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376092944	chr1:171171720-171171721	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188439898	chr1:171171754-171171755	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150218125	chr1:171171766-171171767	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28369889	chr1:171171771-171171772	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs571747104	chr1:171171795-171171796	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551375711	chr1:171171818-171171819	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552847611	chr1:171171866-171171867	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566450398	chr1:171171889-171171890	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574585566	chr1:171171954-171171955	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs555443887	chr1:171171964-171171965	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs193029909	chr1:171171977-171171978	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575809598	chr1:171171978-171171979	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs28369890	chr1:171171982-171171983	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs114867280	chr1:171172096-171172097	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs537638482	chr1:171172115-171172116	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs556363831	chr1:171172120-171172121	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs575318241	chr1:171172132-171172133	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs7527478	chr1:171172147-171172148	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:92)

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
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	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
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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171156600-171177200	Weak transcription	Esophagus	oesophagus
2	chr1:171156600-171179600	Weak transcription	NHLF	lung
3	chr1:171156800-171179600	Weak transcription	Right Ventricle	heart
4	chr1:171161000-171171800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr1:171165600-171173400	Strong transcription	Left Ventricle	heart
6	chr1:171165800-171174400	Weak transcription	Stomach Mucosa	stomach
7	chr1:171166000-171174600	Weak transcription	Pancreas	Pancrea
8	chr1:171166000-171178000	Weak transcription	Psoas Muscle	Psoas
9	chr1:171166000-171184000	Weak transcription	Gastric	stomach
10	chr1:171166600-171175400	Strong transcription	Adipose Nuclei	Adipose
11	chr1:171167200-171187800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr1:171168400-171171800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:171169200-171176200	Weak transcription	Lung	lung
14	chr1:171169800-171189800	Weak transcription	Right Atrium	heart
15	chr1:171170000-171173800	Strong transcription	Aorta	Aorta
16	chr1:171170200-171173400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:171170200-171174600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:171170400-171171200	Weak transcription	Fetal Lung	lung
19	chr1:171170800-171171000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:171170800-171171400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:171170800-171171600	Enhancers	HMEC	breast
22	chr1:171171200-171172200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:171171200-171174000	Strong transcription	Fetal Lung	lung
24	chr1:171171400-171179400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr1:171172200-171178600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:171172800-171173600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:171173400-171173800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:171173400-171174200	Weak transcription	Left Ventricle	heart
29	chr1:171173600-171179000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:171173800-171174600	Weak transcription	Aorta	Aorta
31	chr1:171173800-171175400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:171174000-171177000	Weak transcription	Fetal Lung	lung
33	chr1:171174200-171178600	Strong transcription	Left Ventricle	heart
34	chr1:171174400-171177400	Enhancers	Stomach Mucosa	stomach
35	chr1:171174600-171174800	Enhancers	Pancreas	Pancrea
36	chr1:171174600-171175600	Enhancers	Duodenum Mucosa	Duodenum
37	chr1:171174600-171178200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr1:171174600-171178200	Strong transcription	Aorta	Aorta
39	chr1:171175400-171175600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:171175400-171176800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:171175400-171177200	Genic enhancers	Adipose Nuclei	Adipose
42	chr1:171175600-171176800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:171175600-171177200	Enhancers	Fetal Intestine Large	intestine
44	chr1:171175600-171179000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr1:171176200-171176400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:171176200-171176400	ZNF genes & repeats	Lung	lung
47	chr1:171176200-171176800	Enhancers	Osteobl	bone
48	chr1:171176200-171177400	Enhancers	Fetal Intestine Small	intestine
49	chr1:171176400-171176600	Weak transcription	Lung	lung
50	chr1:171176800-171177200	Enhancers	Liver	Liver

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