Variant report

Variant	nsv1009493
Chromosome Location	chr1:179110523-179121079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:62)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179120877-179121723	HepG2	liver:	n/a	n/a
2	BHLHE40	chr1:179121057-179121117	GM12878	blood:	n/a	n/a
3	BRCA1	chr1:179111943-179112801	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr1:179111882-179112853	HCT-116	colon:	n/a	n/a
5	CBX3	chr1:179111987-179112814	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:179113813-179114058	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:179111010-179111408	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:179112025-179112877	HCT-116	colon:	n/a	n/a
9	CEBPB	chr1:179112005-179112813	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:179112039-179112841	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:179120941-179121587	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:179120993-179121398	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:179112036-179112895	A549	lung:	n/a	n/a
14	CEBPB	chr1:179111947-179112920	HCT-116	colon:	n/a	n/a
15	CEBPB	chr1:179121056-179121372	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:179120901-179121555	A549	lung:	n/a	n/a
17	CEBPB	chr1:179112120-179112789	A549	lung:	n/a	n/a
18	CEBPB	chr1:179110994-179111335	IMR90	lung:	n/a	n/a
19	CTCF	chr1:179115825-179115946	Medullo	brain:	n/a	n/a
20	CTCF	chr1:179112222-179112284	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr1:179113408-179113450	GM13977	blood:	n/a	n/a
22	CUX1	chr1:179112315-179112395	K562	blood:	n/a	n/a
23	E2F4	chr1:179111033-179111679	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr1:179112041-179112799	MCF10A-Er-Src	breast:	n/a	n/a
25	EGR1	chr1:179111036-179111290	K562	blood:	n/a	chr1:179111206-179111228
26	EGR1	chr1:179111995-179112606	HCT-116	colon:	n/a	n/a
27	EGR1	chr1:179111905-179112690	HCT-116	colon:	n/a	n/a
28	EP300	chr1:179111811-179112984	SK-N-SH	brain:	n/a	chr1:179112220-179112229
29	EP300	chr1:179111966-179112925	A549	lung:	n/a	chr1:179112220-179112229
30	EP300	chr1:179120906-179121631	A549	lung:	n/a	n/a
31	EP300	chr1:179110851-179111552	Hela-S3	cervix:	n/a	chr1:179111459-179111473
32	EP300	chr1:179111989-179112933	SK-N-SH	brain:	n/a	chr1:179112220-179112229
33	EP300	chr1:179111994-179112859	A549	lung:	n/a	chr1:179112220-179112229
34	EP300	chr1:179112006-179112841	Hela-S3	cervix:	n/a	chr1:179112220-179112229
35	EP300	chr1:179120867-179121531	HepG2	liver:	n/a	n/a
36	EP300	chr1:179120923-179121559	HepG2	liver:	n/a	n/a
37	EP300	chr1:179121010-179121411	HepG2	liver:	n/a	n/a
38	EP300	chr1:179112051-179112404	SK-N-SH_RA	brain:	n/a	chr1:179112220-179112229
39	EP300	chr1:179111047-179111323	SK-N-SH_RA	brain:	n/a	n/a
40	FOS	chr1:179113756-179114143	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:179112042-179112829	Hela-S3	cervix:	n/a	chr1:179112382-179112393
42	FOS	chr1:179111855-179112883	MCF10A-Er-Src	breast:	n/a	chr1:179112382-179112393
43	FOS	chr1:179113727-179114178	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr1:179110931-179111504	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:179113786-179114123	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:179110915-179111491	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr1:179111830-179112882	MCF10A-Er-Src	breast:	n/a	chr1:179112382-179112393
48	FOS	chr1:179113705-179114201	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:179111988-179112835	HUVEC	blood vessel:	n/a	chr1:179112382-179112393
50	FOS	chr1:179110651-179111399	HUVEC	blood vessel:	n/a	chr1:179110819-179110828

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179112077-179112127	T-47D	breast:	n/a
2	chr1:179112077-179112127	T-47D	breast:	n/a
3	chr1:179112077-179112127	Caco-2	colon:	n/a
4	chr1:179112077-179112127	NB4	blood:	n/a
5	chr1:179112077-179112127	AG09319	gingival:	n/a
6	chr1:179112077-179112127	MCF10A-Er-Src	breast:	n/a
7	chr1:179112077-179112127	Hepatocyte	liver:	n/a
8	chr1:179112077-179112127	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:179112077-179112127	AG10803	skin:	n/a
10	chr1:179112077-179112127	HRCEpiC	kidney:	n/a
11	chr1:179112077-179112127	Hela-S3	cervix:	n/a
12	chr1:179112077-179112127	K562	blood:	n/a
13	chr1:179112077-179112127	HMEC	breast:	n/a
14	chr1:179112077-179112127	A549	lung:	n/a
15	chr1:179112077-179112127	HCF	heart:	n/a
16	chr1:179112077-179112127	HCT-116	colon:	n/a
17	chr1:179112077-179112127	GM12892	blood:	n/a
18	chr1:179112077-179112127	HCM	heart:	n/a
19	chr1:179112077-179112127	H1-hESC	embryonic stem cell:	embryo
20	chr1:179112077-179112127	MCF-7	breast:	n/a
21	chr1:179112077-179112127	SK-N-SH	brain:	n/a
22	chr1:179112077-179112127	ECC-1	luminal epithelium:	n/a
23	chr1:179112077-179112127	IMR90	lung:	fetal
24	chr1:179112077-179112127	GM12891	blood:	n/a
25	chr1:179112077-179112127	SAEC	small airway:	n/a
26	chr1:179112077-179112127	Jurkat	blood:	n/a
27	chr1:179112077-179112127	AoSMC	blood vessel:	n/a
28	chr1:179112077-179112127	PrEC	prostate:	n/a
29	chr1:179112077-179112127	SK-N-SH_RA	brain:	n/a
30	chr1:179112077-179112127	NHBE	bronchial:	n/a
31	chr1:179112077-179112127	NH-A	brain:	n/a
32	chr1:179112077-179112127	U87	brain:	n/a
33	chr1:179112077-179112127	BE2_C	brain:	n/a
34	chr1:179112077-179112127	AG09309	skin:	n/a
35	chr1:179112077-179112127	HCPEpiC	choroid plexus:	n/a
36	chr1:179112077-179112127	GM19239	blood:	n/a
37	chr1:179112077-179112127	HL-60	blood:	n/a
38	chr1:179112077-179112127	AG04449	skin:	fetal
39	chr1:179112077-179112127	HRE	kidney:	n/a
40	chr1:179112077-179112127	HepG2	liver:	n/a
41	chr1:179112077-179112127	HAEpiC	amniotic membrane:	n/a
42	chr1:179112077-179112127	HNPCEpiC	eye:	n/a
43	chr1:179112077-179112127	ProgFib	skin:	n/a
44	chr1:179112077-179112127	BJ	skin:	n/a
45	chr1:179112077-179112127	RPTEC	kidney:	n/a
46	chr1:179112077-179112127	SKMC	muscle:	n/a
47	chr1:179112077-179112127	HUVEC	blood vessel:	n/a
48	chr1:179112077-179112127	GM06990	blood:	n/a
49	chr1:179112077-179112127	HIPEpiC	eye:	n/a
50	chr1:179112077-179112127	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:179108694..179110499-chr1:179120494..179123045,2	MCF-7	breast:
2	chr1:179091554..179094304-chr1:179109132..179111261,2	MCF-7	breast:
3	chr1:179110656..179113275-chr1:179262488..179264481,2	K562	blood:

No data

Variant related genes	Relation type
ABL2	TF binding region
ABL2	CpG island
ENSG00000057252	chromatin interactions

Extended variants
information (count: 381 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549412087	chr1:179110611-179110612	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs76460460	chr1:179110641-179110642	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs538339934	chr1:179110685-179110686	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35893274	chr1:179110718-179110719	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545783034	chr1:179110758-179110759	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs147278917	chr1:179110770-179110771	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577808052	chr1:179110808-179110809	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565606557	chr1:179110827-179110828	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533815228	chr1:179110867-179110868	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375497113	chr1:179110870-179110871	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553622044	chr1:179111002-179111003	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs115487603	chr1:179111003-179111004	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531089946	chr1:179111023-179111024	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs562511139	chr1:179111056-179111057	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2636276	chr1:179111060-179111061	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs545131670	chr1:179111107-179111108	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564504693	chr1:179111198-179111199	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs377597890	chr1:179111217-179111218	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533593635	chr1:179111234-179111235	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547234485	chr1:179111261-179111262	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs28914507	chr1:179111262-179111263	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561332068	chr1:179111303-179111304	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs140769019	chr1:179111325-179111326	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs529622755	chr1:179111329-179111330	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549061126	chr1:179111375-179111376	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569279991	chr1:179111378-179111379	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs558117735	chr1:179111408-179111409	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs28914506	chr1:179111409-179111410	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551879686	chr1:179111416-179111417	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs28914505	chr1:179111423-179111424	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377766523	chr1:179111462-179111463	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200197661	chr1:179111463-179111464	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144830051	chr1:179111479-179111480	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs28914504	chr1:179111490-179111491	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs546709391	chr1:179111645-179111646	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs202245102	chr1:179111649-179111650	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs148597281	chr1:179111758-179111759	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536195765	chr1:179111825-179111826	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs60189973	chr1:179111827-179111828	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560587562	chr1:179111831-179111832	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77938858	chr1:179111850-179111851	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565479490	chr1:179111877-179111878	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs648727	chr1:179111950-179111951	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs648741	chr1:179111954-179111955	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs669864	chr1:179111972-179111973	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376770494	chr1:179112077-179112078	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370969107	chr1:179112084-179112085	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558591074	chr1:179112087-179112088	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556966283	chr1:179112091-179112092	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566591407	chr1:179112093-179112094	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179063200-179112000	Weak transcription	Fetal Kidney	kidney
2	chr1:179087800-179113000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:179093400-179117200	Weak transcription	Fetal Stomach	stomach
4	chr1:179098200-179112000	Weak transcription	Lung	lung
5	chr1:179099200-179114800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr1:179099400-179112000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:179099400-179112000	Weak transcription	Left Ventricle	heart
8	chr1:179099600-179110600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr1:179099600-179110800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:179099600-179116800	Weak transcription	Thymus	Thymus
11	chr1:179099600-179119400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr1:179099600-179122600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr1:179099800-179111800	Weak transcription	HepG2	liver
14	chr1:179100000-179121000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr1:179100600-179110800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr1:179100600-179112000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:179100600-179117200	Weak transcription	Fetal Intestine Small	intestine
18	chr1:179107200-179110800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr1:179107200-179112000	Weak transcription	Brain Substantia Nigra	brain
20	chr1:179107400-179111000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr1:179107600-179111800	Weak transcription	Fetal Muscle Leg	muscle
22	chr1:179107600-179112000	Weak transcription	Fetal Lung	lung
23	chr1:179107600-179112000	Weak transcription	Placenta	Placenta
24	chr1:179107600-179119800	Weak transcription	Liver	Liver
25	chr1:179108200-179113200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr1:179109000-179110800	Weak transcription	Brain Hippocampus Middle	brain
27	chr1:179109400-179110800	Weak transcription	Right Atrium	heart
28	chr1:179109400-179110800	Enhancers	Hela-S3	cervix
29	chr1:179109400-179112000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr1:179109400-179112000	Weak transcription	Pancreas	Pancrea
31	chr1:179109400-179112400	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr1:179109400-179112400	Active TSS	Psoas Muscle	Psoas
33	chr1:179109600-179110800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr1:179109600-179110800	Weak transcription	A549	lung
35	chr1:179109600-179112600	Active TSS	NHDF-Ad	bronchial
36	chr1:179109800-179110600	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr1:179109800-179112400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr1:179109800-179112400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr1:179109800-179112800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:179110000-179110600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:179110000-179110800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:179110000-179111000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:179110000-179111000	Enhancers	Primary B cells from cord blood	blood
44	chr1:179110000-179112000	Weak transcription	Small Intestine	intestine
45	chr1:179110000-179112200	Active TSS	HSMM	muscle
46	chr1:179110000-179112400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:179110000-179112400	Active TSS	Muscle Satellite Cultured Cells	--
48	chr1:179110000-179112400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr1:179110000-179112400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:179110000-179112600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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