Variant report

Variant	nsv528675
Chromosome Location	chr1:174195629-174219398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174199624-174199775	K562	blood:	n/a	n/a
2	ARID3A	chr1:174208511-174209005	HepG2	liver:	n/a	n/a
3	ATF1	chr1:174199566-174199927	K562	blood:	n/a	n/a
4	ATF1	chr1:174201924-174202155	K562	blood:	n/a	n/a
5	BHLHE40	chr1:174201914-174202107	K562	blood:	n/a	n/a
6	BHLHE40	chr1:174199609-174199894	K562	blood:	n/a	n/a
7	CBX3	chr1:174201841-174202179	K562	blood:	n/a	n/a
8	CEBPD	chr1:174199485-174200047	K562	blood:	n/a	n/a
9	CEBPD	chr1:174199513-174200039	K562	blood:	n/a	n/a
10	CUX1	chr1:174199753-174199826	K562	blood:	n/a	n/a
11	CUX1	chr1:174211252-174211261	K562	blood:	n/a	n/a
12	ELF1	chr1:174201963-174202363	K562	blood:	n/a	chr1:174202192-174202205
13	EP300	chr1:174199553-174199899	K562	blood:	n/a	n/a
14	FOS	chr1:174196600-174196652	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr1:174196563-174196658	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr1:174196567-174196685	MCF10A-Er-Src	breast:	n/a	n/a
17	FOXA1	chr1:174208651-174209038	HepG2	liver:	n/a	n/a
18	FOXA1	chr1:174208348-174208551	T-47D	breast:	n/a	n/a
19	FOXA1	chr1:174208610-174209120	HepG2	liver:	n/a	n/a
20	FOXA1	chr1:174208328-174208605	T-47D	breast:	n/a	n/a
21	FOXA2	chr1:174207726-174208304	A549	lung:	n/a	n/a
22	FOXA2	chr1:174208364-174209319	HepG2	liver:	n/a	n/a
23	FOXA2	chr1:174208743-174209006	HepG2	liver:	n/a	n/a
24	FOXA2	chr1:174207584-174208614	A549	lung:	n/a	n/a
25	GATA1	chr1:174199532-174199965	PBDE	blood:	n/a	n/a
26	GATA2	chr1:174199462-174199997	K562	blood:	n/a	n/a
27	GATA2	chr1:174199515-174199949	K562	blood:	n/a	n/a
28	GATA3	chr1:174215309-174215342	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr1:174210952-174211130	SH-SY5Y	brain:	n/a	n/a
30	IRF1	chr1:174199592-174199961	K562	blood:	n/a	n/a
31	IRF1	chr1:174199596-174199729	K562	blood:	n/a	n/a
32	JUND	chr1:174199582-174199898	K562	blood:	n/a	n/a
33	MAFF	chr1:174208771-174208924	K562	blood:	n/a	chr1:174208878-174208896
34	MAFF	chr1:174208708-174209056	HepG2	liver:	n/a	chr1:174208878-174208896
35	MAFK	chr1:174208738-174209007	IMR90	lung:	n/a	chr1:174208880-174208895
36	MAFK	chr1:174208717-174209072	HepG2	liver:	n/a	chr1:174208880-174208895
37	MAFK	chr1:174199764-174199892	K562	blood:	n/a	n/a
38	MAFK	chr1:174208719-174209063	HepG2	liver:	n/a	chr1:174208880-174208895
39	MAZ	chr1:174199742-174199772	K562	blood:	n/a	n/a
40	MYC	chr1:174208038-174208081	MCF-7	breast:	n/a	n/a
41	MYC	chr1:174208012-174208073	MCF-7	breast:	n/a	n/a
42	NFATC1	chr1:174216642-174217080	GM12878	blood:	n/a	n/a
43	NFIC	chr1:174208636-174209054	HepG2	liver:	n/a	n/a
44	NR2F2	chr1:174201751-174202213	K562	blood:	n/a	n/a
45	NR2F2	chr1:174199471-174200007	K562	blood:	n/a	n/a
46	PML	chr1:174199531-174199938	K562	blood:	n/a	n/a
47	PML	chr1:174199445-174200003	K562	blood:	n/a	n/a
48	POLR2A	chr1:174218328-174218523	GM12878	blood:	n/a	n/a
49	POLR2A	chr1:174207996-174208097	A549	lung:	n/a	n/a
50	POLR2A	chr1:174208136-174208426	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174208162-174208212	SK-N-SH	brain:	n/a
2	chr1:174208162-174208212	T-47D	breast:	n/a
3	chr1:174208162-174208212	A549	lung:	n/a
4	chr1:174208162-174208212	HUVEC	blood vessel:	n/a
5	chr1:174208162-174208212	NHBE	bronchial:	n/a
6	chr1:174208162-174208212	AoSMC	blood vessel:	n/a
7	chr1:174208162-174208212	H1-hESC	embryonic stem cell:	embryo
8	chr1:174208162-174208212	GM12892	blood:	n/a
9	chr1:174208162-174208212	Caco-2	colon:	n/a
10	chr1:174208162-174208212	HNPCEpiC	eye:	n/a
11	chr1:174208162-174208212	BE2_C	brain:	n/a
12	chr1:174208162-174208212	Hela-S3	cervix:	n/a
13	chr1:174208162-174208212	BJ	skin:	n/a
14	chr1:174208162-174208212	NT2-D1	testis:	n/a
15	chr1:174208162-174208212	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:174208162-174208212	HCF	heart:	n/a
17	chr1:174208162-174208212	AG09309	skin:	n/a
18	chr1:174208162-174208212	U87	brain:	n/a
19	chr1:174208162-174208212	IMR90	lung:	fetal
20	chr1:174208162-174208212	PFSK-1	brain:	n/a
21	chr1:174208162-174208212	HEEpiC	esophagus:	n/a
22	chr1:174208162-174208212	ProgFib	skin:	n/a
23	chr1:174208162-174208212	Hepatocyte	liver:	n/a
24	chr1:174208162-174208212	AG04449	skin:	fetal
25	chr1:174208162-174208212	ECC-1	luminal epithelium:	n/a
26	chr1:174208162-174208212	PANC-1	pancreas:	n/a
27	chr1:174208162-174208212	CMK	blood:	n/a
28	chr1:174208162-174208212	NB4	blood:	n/a
29	chr1:174208162-174208212	HEK293	kidney:	embryo
30	chr1:174208162-174208212	HAEpiC	amniotic membrane:	n/a
31	chr1:174208162-174208212	AG09319	gingival:	n/a
32	chr1:174208162-174208212	GM12878	blood:	n/a
33	chr1:174208162-174208212	K562	blood:	n/a
34	chr1:174208162-174208212	SAEC	small airway:	n/a
35	chr1:174208162-174208212	ovcar-3	ovarian:	n/a
36	chr1:174208162-174208212	RPTEC	kidney:	n/a
37	chr1:174208162-174208212	HepG2	liver:	n/a
38	chr1:174208162-174208212	HRPEpiC	eye:	n/a
39	chr1:174208162-174208212	HCT-116	colon:	n/a
40	chr1:174208162-174208212	SK-N-MC	brain:	n/a
41	chr1:174208162-174208212	MCF10A-Er-Src	breast:	n/a
42	chr1:174208162-174208212	HL-60	blood:	n/a
43	chr1:174208162-174208212	GM06990	blood:	n/a
44	chr1:174208162-174208212	SK-N-SH_RA	brain:	n/a
45	chr1:174208162-174208212	HCPEpiC	choroid plexus:	n/a
46	chr1:174208162-174208212	SKMC	muscle:	n/a
47	chr1:174208162-174208212	PrEC	prostate:	n/a
48	chr1:174208162-174208212	Jurkat	blood:	n/a
49	chr1:174208162-174208212	HIPEpiC	eye:	n/a
50	chr1:174208162-174208212	GM12891	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:174189286..174192266-chr1:174192457..174196292,4	K562	blood:
2	chr1:173989061..173991259-chr1:174208907..174211636,3	MCF-7	breast:
3	chr1:174185151..174188008-chr1:174194442..174198142,3	K562	blood:
4	chr1:174186060..174188372-chr1:174193893..174195942,2	K562	blood:
5	chr1:174215485..174217028-chr1:174218870..174220698,2	MCF-7	breast:
6	chr1:174208904..174211373-chr1:174212924..174214774,3	MCF-7	breast:
7	chr1:174217947..174220664-chr1:174222845..174224894,3	K562	blood:
8	chr1:174207103..174211366-chr1:174211395..174216784,8	MCF-7	breast:
9	chr1:174193716..174196579-chr1:174196717..174200011,3	MCF-7	breast:
10	chr1:174208598..174210493-chr1:174218021..174220094,2	MCF-7	breast:
11	chr1:174148713..174151052-chr1:174207157..174208937,2	MCF-7	breast:
12	chr1:174215485..174217028-chr1:174218870..174220698,2	MCF-7	breast:
13	chr1:174188949..174191911-chr1:174193700..174196292,5	K562	blood:
14	chr1:174208904..174211373-chr1:174212924..174214774,3	MCF-7	breast:
15	chr1:174209547..174211969-chr1:174214945..174217167,2	MCF-7	breast:
16	chr1:174208598..174210493-chr1:174218021..174220094,2	MCF-7	breast:
17	chr1:174209681..174211217-chr1:174211648..174214510,2	K562	blood:
18	chr1:173834767..173837428-chr1:174208360..174210582,3	MCF-7	breast:
19	chr1:174214049..174216342-chr7:121419636..121421271,2	MCF-7	breast:
20	chr1:174207103..174211366-chr1:174211395..174216784,8	MCF-7	breast:
21	chr1:174193716..174196579-chr1:174196717..174200011,3	MCF-7	breast:
22	chr1:173923747..173925915-chr1:174209553..174212014,2	MCF-7	breast:
23	chr1:174209547..174211969-chr1:174214945..174217167,2	MCF-7	breast:
24	chr1:174209681..174211217-chr1:174211648..174214510,2	K562	blood:

No data

Variant related genes	Relation type
RABGAP1L	TF binding region
RABGAP1L	CpG island
ENSG00000234741	chromatin interactions
ENSG00000208317	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000152061	chromatin interactions

Extended variants
information (count: 767 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:767 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6682607	chr1:174195629-174195630	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562355263	chr1:174195641-174195642	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565679131	chr1:174195659-174195660	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142074316	chr1:174195660-174195661	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146870004	chr1:174195680-174195681	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77569928	chr1:174195769-174195770	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs113257446	chr1:174195783-174195784	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561165849	chr1:174195787-174195788	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564866036	chr1:174195799-174195800	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183217322	chr1:174195845-174195846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs74128323	chr1:174195874-174195875	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs12081355	chr1:174195887-174195888	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541650308	chr1:174195888-174195889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147723001	chr1:174195910-174195911	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs74348266	chr1:174195920-174195921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550258816	chr1:174195921-174195922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187863503	chr1:174195927-174195928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368542977	chr1:174195928-174195929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539284535	chr1:174195943-174195944	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs576780032	chr1:174196008-174196009	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs12081445	chr1:174196061-174196062	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs114764687	chr1:174196077-174196078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200254376	chr1:174196083-174196084	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs111334561	chr1:174196088-174196089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534979606	chr1:174196120-174196121	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560532218	chr1:174196184-174196185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192022108	chr1:174196187-174196188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35013443	chr1:174196242-174196243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs28399009	chr1:174196249-174196250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554548440	chr1:174196338-174196339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78840146	chr1:174196354-174196355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397981984	chr1:174196355-174196356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536238572	chr1:174196402-174196403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555889199	chr1:174196407-174196408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575712058	chr1:174196433-174196434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370985007	chr1:174196483-174196484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367667874	chr1:174196541-174196542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572324417	chr1:174196572-174196573	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs532451079	chr1:174196613-174196614	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs540919425	chr1:174196634-174196635	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs140673284	chr1:174196660-174196661	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs35261457	chr1:174196663-174196664	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs541057823	chr1:174196691-174196692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550195470	chr1:174196693-174196694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35661393	chr1:174196712-174196713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185036164	chr1:174196720-174196721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532618338	chr1:174196738-174196739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552827851	chr1:174196829-174196830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566094149	chr1:174196843-174196844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188744152	chr1:174196890-174196891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
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
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
Invasive pancreatic ductal carcinoma	16982739	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
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174174200-174200200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:174175400-174200200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr1:174176000-174222400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr1:174176800-174222400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:174177200-174212000	Weak transcription	Lung	lung
6	chr1:174178600-174212200	Weak transcription	Psoas Muscle	Psoas
7	chr1:174186600-174216600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:174186800-174200400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:174186800-174200600	Weak transcription	Fetal Stomach	stomach
10	chr1:174186800-174200600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr1:174186800-174208000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr1:174186800-174212800	Weak transcription	Fetal Heart	heart
13	chr1:174186800-174213200	Weak transcription	Ovary	ovary
14	chr1:174186800-174217000	Weak transcription	Brain Angular Gyrus	brain
15	chr1:174186800-174232000	Weak transcription	HSMMtube	muscle
16	chr1:174187000-174199600	Weak transcription	A549	lung
17	chr1:174187000-174217000	Weak transcription	Pancreas	Pancrea
18	chr1:174187400-174200400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr1:174187400-174208000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr1:174187600-174199800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr1:174188400-174202000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:174188600-174202000	Weak transcription	Fetal Muscle Leg	muscle
23	chr1:174188600-174213400	Weak transcription	Spleen	Spleen
24	chr1:174189000-174232000	Weak transcription	HSMM	muscle
25	chr1:174189200-174200200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:174189200-174216800	Weak transcription	Small Intestine	intestine
27	chr1:174189400-174203200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr1:174189400-174203400	Weak transcription	Brain Hippocampus Middle	brain
29	chr1:174189600-174203200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:174189600-174215400	Weak transcription	NH-A	brain
31	chr1:174190200-174204200	Weak transcription	Brain Germinal Matrix	brain
32	chr1:174190600-174200400	Weak transcription	NHDF-Ad	bronchial
33	chr1:174191000-174215600	Weak transcription	Fetal Brain Male	brain
34	chr1:174191400-174215400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:174191400-174232000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:174191600-174198600	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr1:174191600-174199600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr1:174191600-174200200	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr1:174191600-174200200	Weak transcription	Fetal Intestine Large	intestine
40	chr1:174191600-174200400	Weak transcription	Fetal Muscle Trunk	muscle
41	chr1:174191600-174200400	Weak transcription	Left Ventricle	heart
42	chr1:174191600-174200600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr1:174191600-174200600	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr1:174191600-174200600	Weak transcription	Aorta	Aorta
45	chr1:174191600-174208600	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr1:174191600-174213400	Weak transcription	Thymus	Thymus
47	chr1:174191600-174232200	Weak transcription	Brain Substantia Nigra	brain
48	chr1:174191800-174199400	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr1:174191800-174199600	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr1:174191800-174199800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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