Variant report

Variant	esv1792733
Chromosome Location	chr1:168526394-168544716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:316)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:168543576-168543663	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:168543585-168543670	K562	blood:	n/a	n/a
3	ATF1	chr1:168532008-168532100	K562	blood:	n/a	n/a
4	ATF1	chr1:168539928-168540010	K562	blood:	n/a	n/a
5	BATF	chr1:168541966-168542286	GM12878	blood:	n/a	n/a
6	BATF	chr1:168541992-168542278	GM12878	blood:	n/a	n/a
7	BATF	chr1:168531233-168531559	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:168542032-168542239	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:168526869-168527242	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:168528417-168528523	GM12878	blood:	n/a	n/a
11	CEBPB	chr1:168543465-168543821	Hela-S3	cervix:	n/a	chr1:168543617-168543628
12	CEBPB	chr1:168540762-168540867	K562	blood:	n/a	n/a
13	CEBPB	chr1:168543552-168543714	MCF-7	breast:	n/a	chr1:168543617-168543628
14	CEBPB	chr1:168543483-168543773	HepG2	liver:	n/a	chr1:168543617-168543628
15	CEBPB	chr1:168538595-168539018	MCF-7	breast:	n/a	chr1:168538833-168538846 chr1:168538834-168538845 chr1:168538833-168538844
16	CEBPB	chr1:168543468-168543694	IMR90	lung:	n/a	chr1:168543617-168543628
17	CEBPB	chr1:168543469-168543784	A549	lung:	n/a	chr1:168543617-168543628
18	CEBPB	chr1:168543413-168543733	A549	lung:	n/a	chr1:168543617-168543628
19	CEBPB	chr1:168526554-168526915	A549	lung:	n/a	chr1:168526711-168526724 chr1:168526711-168526722
20	CEBPB	chr1:168543368-168543720	MCF-7	breast:	n/a	chr1:168543617-168543628
21	CEBPB	chr1:168526557-168527225	Hela-S3	cervix:	n/a	chr1:168526711-168526724 chr1:168526711-168526722
22	CEBPB	chr1:168543492-168543698	H1-hESC	embryonic stem cell:	n/a	chr1:168543617-168543628
23	CEBPB	chr1:168543357-168543865	K562	blood:	n/a	chr1:168543617-168543628
24	CEBPB	chr1:168538659-168538974	HepG2	liver:	n/a	chr1:168538833-168538846 chr1:168538834-168538845 chr1:168538833-168538844
25	CEBPB	chr1:168538724-168538888	A549	lung:	n/a	chr1:168538833-168538846 chr1:168538834-168538845 chr1:168538833-168538844
26	CEBPB	chr1:168526630-168527186	A549	lung:	n/a	chr1:168526711-168526724 chr1:168526711-168526722
27	CEBPB	chr1:168543459-168543808	K562	blood:	n/a	chr1:168543617-168543628
28	CEBPB	chr1:168526647-168527121	HepG2	liver:	n/a	chr1:168526711-168526724 chr1:168526711-168526722
29	CEBPB	chr1:168543493-168543716	K562	blood:	n/a	chr1:168543617-168543628
30	CEBPD	chr1:168543461-168543805	K562	blood:	n/a	n/a
31	CHD2	chr1:168526842-168527326	GM12878	blood:	n/a	n/a
32	CTCF	chr1:168543540-168543690	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr1:168543620-168543770	GM12866	blood:	n/a	n/a
34	CTCF	chr1:168543600-168543750	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr1:168543588-168543808	GM10248	blood:	n/a	n/a
36	CTCF	chr1:168543540-168543690	GM12866	blood:	n/a	n/a
37	CTCF	chr1:168543596-168543718	T-47D	breast:	n/a	n/a
38	CTCF	chr1:168543629-168543806	GM20000	blood:	n/a	n/a
39	CTCF	chr1:168543979-168544010	GM12878	blood:	n/a	n/a
40	CTCF	chr1:168543520-168543670	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr1:168544180-168544330	GM12872	blood:	n/a	n/a
42	CTCF	chr1:168543600-168543750	HPF	lung:	n/a	n/a
43	CTCF	chr1:168543500-168543650	HAc	cerebellar:	n/a	n/a
44	CTCF	chr1:168544220-168544370	GM12873	blood:	n/a	n/a
45	CTCF	chr1:168543574-168543786	A549	lung:	n/a	n/a
46	CTCF	chr1:168543482-168543724	HepG2	liver:	n/a	n/a
47	CTCF	chr1:168543637-168543744	GM13976	blood:	n/a	n/a
48	CTCF	chr1:168543826-168543828	LNCaP	prostate:	n/a	n/a
49	CTCF	chr1:168543599-168543814	A549	lung:	n/a	n/a
50	CTCF	chr1:168543540-168543690	HVMF	connective:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168544539-168544589	NHDF-neo	bronchial:	n/a
2	chr1:168544539-168544589	PFSK-1	brain:	n/a
3	chr1:168544539-168544589	ProgFib	skin:	n/a
4	chr1:168544539-168544589	AG04449	skin:	fetal
5	chr1:168544539-168544589	HCT-116	colon:	n/a
6	chr1:168544539-168544589	NHBE	bronchial:	n/a
7	chr1:168544539-168544589	MCF-7	breast:	n/a
8	chr1:168544539-168544589	GM12878	blood:	n/a
9	chr1:168544539-168544589	Caco-2	colon:	n/a
10	chr1:168544539-168544589	Hepatocyte	liver:	n/a
11	chr1:168544539-168544589	Hela-S3	cervix:	n/a
12	chr1:168544539-168544589	HepG2	liver:	n/a
13	chr1:168544539-168544589	SK-N-SH	brain:	n/a
14	chr1:168544539-168544589	GM06990	blood:	n/a
15	chr1:168544539-168544589	GM12892	blood:	n/a
16	chr1:168544539-168544589	H1-hESC	embryonic stem cell:	embryo
17	chr1:168544539-168544589	SKMC	muscle:	n/a
18	chr1:168544539-168544589	AG04450	lung:	fetal
19	chr1:168544539-168544589	SAEC	small airway:	n/a
20	chr1:168544539-168544589	BJ	skin:	n/a
21	chr1:168544539-168544589	HIPEpiC	eye:	n/a
22	chr1:168544539-168544589	HUVEC	blood vessel:	n/a
23	chr1:168544539-168544589	AG10803	skin:	n/a
24	chr1:168544539-168544589	AG09309	skin:	n/a
25	chr1:168544539-168544589	HRPEpiC	eye:	n/a
26	chr1:168544539-168544589	HAEpiC	amniotic membrane:	n/a
27	chr1:168544539-168544589	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:168544539-168544589	PANC-1	pancreas:	n/a
29	chr1:168544539-168544589	LNCaP	prostate:	n/a
30	chr1:168544539-168544589	RPTEC	kidney:	n/a
31	chr1:168544539-168544589	HL-60	blood:	n/a
32	chr1:168544539-168544589	MCF10A-Er-Src	breast:	n/a
33	chr1:168544539-168544589	U87	brain:	n/a
34	chr1:168544539-168544589	K562	blood:	n/a
35	chr1:168544539-168544589	HMEC	breast:	n/a
36	chr1:168544539-168544589	HRE	kidney:	n/a
37	chr1:168544539-168544589	HCM	heart:	n/a
38	chr1:168544539-168544589	ovcar-3	ovarian:	n/a
39	chr1:168544539-168544589	IMR90	lung:	fetal
40	chr1:168544539-168544589	CMK	blood:	n/a
41	chr1:168544539-168544589	NT2-D1	testis:	n/a
42	chr1:168544539-168544589	BE2_C	brain:	n/a
43	chr1:168544539-168544589	ECC-1	luminal epithelium:	n/a
44	chr1:168544539-168544589	GM19239	blood:	n/a
45	chr1:168544539-168544589	HCPEpiC	choroid plexus:	n/a
46	chr1:168544539-168544589	HEEpiC	esophagus:	n/a
47	chr1:168544539-168544589	PrEC	prostate:	n/a
48	chr1:168544539-168544589	AoSMC	blood vessel:	n/a
49	chr1:168544539-168544589	SK-N-SH_RA	brain:	n/a
50	chr1:168544539-168544589	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:168408738..168409696-chr1:168543083..168544145,4	MCF-7	breast:
2	chr1:168530651..168532220-chr1:168536771..168538342,2	K562	blood:
3	chr1:168421956..168424286-chr1:168536137..168537722,2	K562	blood:
4	chr1:168538915..168539776-chr8:141248331..141249019,2	MCF-7	breast:
5	chr1:168409048..168409630-chr1:168543648..168544296,2	K562	blood:
6	chr1:168535665..168537230-chr1:168537379..168540147,2	MCF-7	breast:
7	chr1:168521001..168522517-chr1:168539526..168541091,2	K562	blood:
8	chr1:168535665..168537230-chr1:168537379..168540147,2	MCF-7	breast:
9	chr1:168530651..168532220-chr1:168536771..168538342,2	K562	blood:

No data

Variant related genes	Relation type
XCL1	TF binding region
XCL1	CpG island
ENSG00000167632	chromatin interactions

Extended variants
information (count: 717 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:717 , 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	rs1933105	chr1:168526394-168526395	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184566985	chr1:168526502-168526503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189082436	chr1:168526523-168526524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567422130	chr1:168526571-168526572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192135980	chr1:168526589-168526590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1024177	chr1:168526715-168526716	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528086084	chr1:168526734-168526735	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs74120941	chr1:168526735-168526736	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs184679893	chr1:168526754-168526755	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78086842	chr1:168526791-168526792	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535545742	chr1:168526865-168526866	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551164671	chr1:168526867-168526868	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142058973	chr1:168526877-168526878	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189544261	chr1:168526896-168526897	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138518263	chr1:168526949-168526950	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539675723	chr1:168527049-168527050	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs560112354	chr1:168527072-168527073	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs558426112	chr1:168527088-168527089	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs377552035	chr1:168527097-168527098	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs527268798	chr1:168527153-168527154	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs115302462	chr1:168527170-168527171	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs181554702	chr1:168527172-168527173	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs563393201	chr1:168527181-168527182	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs74120943	chr1:168527183-168527184	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs3929671	chr1:168527215-168527216	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs3929672	chr1:168527217-168527218	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs12757136	chr1:168527225-168527226	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs12757138	chr1:168527227-168527228	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs61047461	chr1:168527231-168527232	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs540953741	chr1:168527333-168527334	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs573769179	chr1:168527357-168527358	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs544315572	chr1:168527370-168527371	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs562676509	chr1:168527379-168527380	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs140314561	chr1:168527387-168527388	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs545725114	chr1:168527470-168527471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116401866	chr1:168527483-168527484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184456393	chr1:168527514-168527515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188964999	chr1:168527600-168527601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529566773	chr1:168527603-168527604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181653776	chr1:168527635-168527636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550677054	chr1:168527639-168527640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551208134	chr1:168527682-168527683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532437749	chr1:168527703-168527704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535968704	chr1:168527713-168527714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533564275	chr1:168527725-168527726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186304996	chr1:168527732-168527733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567108673	chr1:168527740-168527741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552098022	chr1:168527745-168527746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534244707	chr1:168527752-168527753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192308666	chr1:168527762-168527763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

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
Lung cancer	18438408	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
Breast cancer	21509527	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
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168522000-168527400	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr1:168523000-168526400	Enhancers	Primary T cells fromperipheralblood	blood
3	chr1:168523000-168527200	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr1:168523000-168527600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr1:168524800-168526800	Weak transcription	A549	lung
6	chr1:168525400-168526600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:168525400-168526600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr1:168525400-168526800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr1:168525400-168527600	Enhancers	HepG2	liver
10	chr1:168526000-168526600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:168526000-168526800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:168526000-168527400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr1:168526200-168526400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:168526200-168527000	Enhancers	Muscle Satellite Cultured Cells	--
15	chr1:168526200-168527000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:168526200-168527000	Enhancers	HMEC	breast
17	chr1:168526200-168527600	Enhancers	Hela-S3	cervix
18	chr1:168526600-168526800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:168526600-168526800	Enhancers	Osteobl	bone
20	chr1:168526600-168527400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:168526600-168527400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr1:168526600-168527600	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr1:168526800-168527000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:168526800-168527000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:168526800-168527000	Enhancers	A549	lung
26	chr1:168526800-168527000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr1:168526800-168527000	Flanking Active TSS	NHDF-Ad	bronchial
28	chr1:168526800-168527200	Enhancers	Gastric	stomach
29	chr1:168526800-168527400	Flanking Active TSS	Osteobl	bone
30	chr1:168526800-168527600	Enhancers	HSMM	muscle
31	chr1:168527000-168527200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:168527000-168527200	Enhancers	Placenta Amnion	Placenta Amnion
33	chr1:168527000-168527200	Enhancers	NHDF-Ad	bronchial
34	chr1:168527000-168527400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:168527200-168527400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:168527400-168527600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:168527400-168527800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr1:168527400-168527800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:168527400-168534600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:168527600-168538000	Weak transcription	HepG2	liver
41	chr1:168534400-168536800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr1:168534600-168534800	Enhancers	Small Intestine	intestine
43	chr1:168534600-168535000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:168534600-168535200	Enhancers	Primary hematopoietic stem cells	blood
45	chr1:168534600-168536600	Enhancers	Duodenum Mucosa	Duodenum
46	chr1:168534600-168536800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr1:168534800-168535800	Weak transcription	Small Intestine	intestine
48	chr1:168535000-168535400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:168535200-168536200	Weak transcription	Primary hematopoietic stem cells	blood
50	chr1:168535400-168536600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links