Variant report

Variant	esv3453132
Chromosome Location	chr1:179327629-179332727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:41)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:41 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179332575-179332913	K562	blood:	n/a	n/a
2	ATF1	chr1:179332419-179332755	K562	blood:	n/a	n/a
3	BHLHE40	chr1:179332521-179332721	K562	blood:	n/a	n/a
4	CEBPB	chr1:179329778-179330058	HepG2	liver:	n/a	chr1:179329888-179329901
5	CTCF	chr1:179327970-179328026	Lung_OC	lung:	n/a	n/a
6	EP300	chr1:179332413-179332796	K562	blood:	n/a	n/a
7	GATA2	chr1:179332443-179332967	HUVEC	blood vessel:	n/a	n/a
8	IRF1	chr1:179332206-179332336	K562	blood:	n/a	n/a
9	JUND	chr1:179332429-179332803	K562	blood:	n/a	n/a
10	MAFK	chr1:179332585-179332723	K562	blood:	n/a	n/a
11	MAX	chr1:179332569-179332802	K562	blood:	n/a	n/a
12	MAZ	chr1:179332508-179332725	K562	blood:	n/a	n/a
13	MYC	chr1:179332290-179332626	K562	blood:	n/a	n/a
14	NR2F2	chr1:179332430-179332775	K562	blood:	n/a	n/a
15	POLR2A	chr1:179328508-179328541	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr1:179330444-179330568	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr1:179327769-179327884	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr1:179328573-179328894	K562	blood:	n/a	n/a
19	POLR2A	chr1:179329337-179329567	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr1:179328588-179329025	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr1:179331037-179331459	K562	blood:	n/a	n/a
22	POLR2A	chr1:179328356-179328630	HepG2	liver:	n/a	n/a
23	POLR2A	chr1:179329086-179329302	HepG2	liver:	n/a	n/a
24	POLR2A	chr1:179332035-179332135	K562	blood:	n/a	n/a
25	POLR2A	chr1:179329529-179329556	HepG2	liver:	n/a	n/a
26	POLR2A	chr1:179329353-179329476	GM12878	blood:	n/a	n/a
27	POLR2A	chr1:179327415-179327763	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr1:179332512-179332817	K562	blood:	n/a	n/a
29	POLR2A	chr1:179325503-179327637	K562	blood:	n/a	n/a
30	POLR2A	chr1:179328666-179328733	HepG2	liver:	n/a	n/a
31	POLR2A	chr1:179329333-179329473	HepG2	liver:	n/a	n/a
32	POLR2A	chr1:179327924-179328083	K562	blood:	n/a	n/a
33	RCOR1	chr1:179332489-179332789	K562	blood:	n/a	n/a
34	TAL1	chr1:179332539-179332698	K562	blood:	n/a	n/a
35	TBL1XR1	chr1:179332656-179332683	K562	blood:	n/a	n/a
36	TBP	chr1:179332442-179332627	K562	blood:	n/a	n/a
37	TEAD4	chr1:179332346-179332885	K562	blood:	n/a	n/a
38	UBTF	chr1:179332626-179332761	K562	blood:	n/a	n/a
39	YY1	chr1:179332410-179332785	K562	blood:	n/a	n/a
40	ZNF143	chr1:179332474-179332617	K562	blood:	n/a	n/a
41	ZNF384	chr1:179331552-179331704	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179332148-179332198	PFSK-1	brain:	n/a
2	chr1:179332148-179332198	NHDF-neo	bronchial:	n/a
3	chr1:179332148-179332198	H1-hESC	embryonic stem cell:	embryo
4	chr1:179332148-179332198	GM12891	blood:	n/a
5	chr1:179332148-179332198	GM19239	blood:	n/a
6	chr1:179332148-179332198	Hepatocyte	liver:	n/a
7	chr1:179332148-179332198	GM12892	blood:	n/a
8	chr1:179332148-179332198	SK-N-SH	brain:	n/a
9	chr1:179332148-179332198	HIPEpiC	eye:	n/a
10	chr1:179332148-179332198	HRE	kidney:	n/a
11	chr1:179332148-179332198	NH-A	brain:	n/a
12	chr1:179332148-179332198	PANC-1	pancreas:	n/a
13	chr1:179332148-179332198	HCT-116	colon:	n/a
14	chr1:179332148-179332198	AG09309	skin:	n/a
15	chr1:179332148-179332198	ProgFib	skin:	n/a
16	chr1:179332148-179332198	HRCEpiC	kidney:	n/a
17	chr1:179332148-179332198	U87	brain:	n/a
18	chr1:179332148-179332198	HCF	heart:	n/a
19	chr1:179332148-179332198	CMK	blood:	n/a
20	chr1:179332148-179332198	SAEC	small airway:	n/a
21	chr1:179332148-179332198	RPTEC	kidney:	n/a
22	chr1:179332148-179332198	T-47D	breast:	n/a
23	chr1:179332148-179332198	HAEpiC	amniotic membrane:	n/a
24	chr1:179332148-179332198	IMR90	lung:	fetal
25	chr1:179332148-179332198	AG04450	lung:	fetal
26	chr1:179332148-179332198	SK-N-MC	brain:	n/a
27	chr1:179332148-179332198	LNCaP	prostate:	n/a
28	chr1:179332148-179332198	AG04449	skin:	fetal
29	chr1:179332148-179332198	A549	lung:	n/a
30	chr1:179332148-179332198	NB4	blood:	n/a
31	chr1:179332148-179332198	Caco-2	colon:	n/a
32	chr1:179332148-179332198	HUVEC	blood vessel:	n/a
33	chr1:179332148-179332198	HNPCEpiC	eye:	n/a
34	chr1:179332148-179332198	HCM	heart:	n/a
35	chr1:179332148-179332198	BJ	skin:	n/a
36	chr1:179332148-179332198	SKMC	muscle:	n/a
37	chr1:179332148-179332198	HRPEpiC	eye:	n/a
38	chr1:179332148-179332198	K562	blood:	n/a
39	chr1:179332148-179332198	HepG2	liver:	n/a
40	chr1:179332148-179332198	MCF10A-Er-Src	breast:	n/a
41	chr1:179332148-179332198	NT2-D1	testis:	n/a
42	chr1:179332148-179332198	ovcar-3	ovarian:	n/a
43	chr1:179332148-179332198	HEEpiC	esophagus:	n/a
44	chr1:179332148-179332198	HEK293	kidney:	embryo
45	chr1:179332148-179332198	BE2_C	brain:	n/a
46	chr1:179332148-179332198	AG10803	skin:	n/a
47	chr1:179332148-179332198	AoSMC	blood vessel:	n/a
48	chr1:179332148-179332198	HMEC	breast:	n/a
49	chr1:179332148-179332198	SK-N-SH_RA	brain:	n/a
50	chr1:179332148-179332198	NHBE	bronchial:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179049229..179051266-chr1:179328606..179330148,2	MCF-7	breast:
2	chr1:179303201..179305368-chr1:179327214..179329206,2	MCF-7	breast:
3	chr1:179324764..179330437-chr1:179332106..179336685,6	K562	blood:
4	chr1:179315802..179317742-chr1:179327309..179329268,2	K562	blood:
5	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
6	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
7	chr1:179317813..179320620-chr1:179325439..179328200,3	MCF-7	breast:
8	chr1:179048972..179052099-chr1:179331450..179336701,5	MCF-7	breast:
9	chr1:179330939..179332441-chr1:179334465..179336040,2	MCF-7	breast:
10	chr1:179319158..179320695-chr1:179327831..179330357,2	K562	blood:
11	chr1:179329907..179332888-chr1:179333300..179336235,2	MCF-7	breast:
12	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:

No data

Variant related genes	Relation type
RN7SL374P	TF binding region
AXDND1	TF binding region
RN7SL374P	CpG island
AXDND1	CpG island
ENSG00000186283	chromatin interactions
ENSG00000263633	chromatin interactions
ENSG00000162779	chromatin interactions

Extended variants
information (count: 200 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:200 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369658610	chr1:179327651-179327652	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs531082085	chr1:179327731-179327732	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs541819800	chr1:179327833-179327834	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546102820	chr1:179327839-179327840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs28626318	chr1:179327890-179327891	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs530955132	chr1:179327900-179327901	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs557169557	chr1:179327957-179327958	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12117333	chr1:179327958-179327959	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs148300321	chr1:179327966-179327967	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546940084	chr1:179327973-179327974	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376706541	chr1:179327974-179327975	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533205898	chr1:179327999-179328000	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs140426423	chr1:179328031-179328032	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187407780	chr1:179328044-179328045	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs75666748	chr1:179328058-179328059	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs374437534	chr1:179328063-179328064	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs377407193	chr1:179328083-179328084	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192252660	chr1:179328106-179328107	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184738300	chr1:179328110-179328111	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs370155719	chr1:179328160-179328161	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539615414	chr1:179328177-179328178	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs544635448	chr1:179328184-179328185	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs374038473	chr1:179328185-179328186	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs188813110	chr1:179328191-179328192	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542506855	chr1:179328192-179328193	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564858252	chr1:179328200-179328201	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs533428342	chr1:179328223-179328224	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555519284	chr1:179328227-179328228	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs575579214	chr1:179328233-179328234	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544748904	chr1:179328244-179328245	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs12144580	chr1:179328245-179328246	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs113023562	chr1:179328256-179328257	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533179369	chr1:179328416-179328417	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540386275	chr1:179328431-179328432	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs367848651	chr1:179328439-179328440	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs560397632	chr1:179328472-179328473	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs569901669	chr1:179328529-179328530	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs61824395	chr1:179328547-179328548	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs147302756	chr1:179328583-179328584	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs568794105	chr1:179328623-179328624	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs139214056	chr1:179328637-179328638	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs370230007	chr1:179328769-179328770	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs376581656	chr1:179328785-179328786	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs551082275	chr1:179328799-179328800	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs143318758	chr1:179328827-179328828	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs192691953	chr1:179328832-179328833	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs553338409	chr1:179328903-179328904	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs375335574	chr1:179328908-179328909	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs567045877	chr1:179328909-179328910	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs151227352	chr1:179328977-179328978	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179264800-179334200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:179292400-179328000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:179296800-179327800	Weak transcription	Colonic Mucosa	Colon
4	chr1:179300400-179334600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr1:179305600-179334200	Weak transcription	Pancreas	Pancrea
6	chr1:179312600-179334400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:179314800-179327800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr1:179314800-179334400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr1:179315000-179334400	Weak transcription	Brain Substantia Nigra	brain
10	chr1:179315000-179334400	Weak transcription	Left Ventricle	heart
11	chr1:179315400-179334400	Weak transcription	Fetal Kidney	kidney
12	chr1:179315600-179334400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr1:179315800-179334200	Weak transcription	Fetal Thymus	thymus
14	chr1:179316000-179334000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr1:179316000-179334200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr1:179316000-179334400	Weak transcription	Fetal Brain Female	brain
17	chr1:179316000-179334400	Weak transcription	Ovary	ovary
18	chr1:179316400-179332800	Weak transcription	Fetal Intestine Small	intestine
19	chr1:179317600-179334400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:179317800-179327800	Weak transcription	NHEK	skin
21	chr1:179319200-179334400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr1:179319800-179334000	Weak transcription	HepG2	liver
23	chr1:179319800-179334200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr1:179320000-179334600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:179320800-179334000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr1:179320800-179334200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr1:179320800-179334400	Weak transcription	Fetal Lung	lung
28	chr1:179321000-179334200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:179321200-179334400	Weak transcription	Fetal Stomach	stomach
30	chr1:179321200-179334400	Weak transcription	Lung	lung
31	chr1:179322400-179334200	Weak transcription	Primary B cells from cord blood	blood
32	chr1:179323000-179330600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr1:179323000-179333400	Weak transcription	Placenta	Placenta
34	chr1:179323000-179334200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr1:179323000-179334200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:179323000-179334200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr1:179323000-179334400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr1:179323000-179334400	Weak transcription	Primary hematopoietic stem cells	blood
39	chr1:179323000-179334400	Weak transcription	NH-A	brain
40	chr1:179323000-179334400	Weak transcription	Osteobl	bone
41	chr1:179323200-179330200	Weak transcription	Brain Anterior Caudate	brain
42	chr1:179323200-179330600	Weak transcription	HMEC	breast
43	chr1:179323200-179334200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr1:179323200-179334200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr1:179323200-179334200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr1:179323200-179334200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:179323200-179334200	Weak transcription	A549	lung
48	chr1:179323200-179334400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:179323200-179334400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr1:179323200-179334400	Weak transcription	Brain Cingulate Gyrus	brain

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