Variant report

Variant	nsv872836
Chromosome Location	chr1:194032486-194130204
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:505)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:194087000-194087095	HepG2	liver:	n/a	n/a
2	BACH1	chr1:194086865-194087088	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr1:194086860-194086904	K562	blood:	n/a	n/a
4	BRCA1	chr1:194078223-194078228	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:194039336-194039635	HepG2	liver:	n/a	chr1:194039488-194039499
6	CEBPB	chr1:194039459-194039507	K562	blood:	n/a	chr1:194039488-194039499
7	CEBPB	chr1:194048359-194048574	A549	lung:	n/a	n/a
8	CEBPB	chr1:194129231-194129530	MCF-7	breast:	n/a	n/a
9	CEBPB	chr1:194080724-194080877	A549	lung:	n/a	n/a
10	CEBPB	chr1:194042787-194042929	A549	lung:	n/a	chr1:194042802-194042813
11	CEBPB	chr1:194039336-194039667	IMR90	lung:	n/a	chr1:194039488-194039499
12	CEBPB	chr1:194042667-194042867	HepG2	liver:	n/a	chr1:194042802-194042813
13	CEBPB	chr1:194074827-194075027	A549	lung:	n/a	n/a
14	CEBPB	chr1:194039387-194039642	A549	lung:	n/a	chr1:194039488-194039499
15	CTCF	chr1:194129140-194129290	Caco-2	colon:	n/a	chr1:194129261-194129279 chr1:194129263-194129284 chr1:194129264-194129277 chr1:194129262-194129278
16	CTCF	chr1:194086860-194087010	GM12865	blood:	n/a	n/a
17	CTCF	chr1:194071903-194071948	GM19240	blood:	n/a	n/a
18	CTCF	chr1:194086860-194087010	GM12873	blood:	n/a	n/a
19	CTCF	chr1:194125394-194125473	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr1:194086800-194086950	A549	lung:	n/a	n/a
21	CTCF	chr1:194071800-194072066	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:194086808-194087079	K562	blood:	n/a	n/a
23	CTCF	chr1:194086780-194086930	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr1:194071860-194072010	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr1:194129200-194129350	NHEK	skin:	n/a	chr1:194129261-194129279 chr1:194129263-194129284 chr1:194129264-194129277 chr1:194129262-194129278
26	CTCF	chr1:194086835-194087013	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:194086860-194087010	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr1:194086860-194087010	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr1:194071880-194072030	BJ	skin:	n/a	n/a
30	CTCF	chr1:194129240-194129390	MCF-7	breast:	n/a	chr1:194129261-194129279 chr1:194129263-194129284 chr1:194129264-194129277 chr1:194129262-194129278
31	CTCF	chr1:194071900-194072050	HEK293	kidney:	n/a	n/a
32	CTCF	chr1:194086820-194086970	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr1:194087000-194087150	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:194129120-194129270	HCM	heart:	n/a	n/a
35	CTCF	chr1:194071880-194072030	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr1:194086760-194086910	HEK293	kidney:	n/a	n/a
37	CTCF	chr1:194086780-194086930	HCT-116	colon:	n/a	n/a
38	CTCF	chr1:194071860-194072010	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr1:194086911-194086923	GM12878	blood:	n/a	n/a
40	CTCF	chr1:194086940-194087090	BE2_C	brain:	n/a	n/a
41	CTCF	chr1:194071888-194072036	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:194071800-194071950	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:194071840-194071990	AG04449	skin:	n/a	n/a
44	CTCF	chr1:194129180-194129330	SK-N-SH_RA	brain:	n/a	chr1:194129261-194129279 chr1:194129263-194129284 chr1:194129264-194129277 chr1:194129262-194129278
45	CTCF	chr1:194129180-194129330	Hela-S3	cervix:	n/a	chr1:194129261-194129279 chr1:194129263-194129284 chr1:194129264-194129277 chr1:194129262-194129278
46	CTCF	chr1:194086740-194086890	GM12874	blood:	n/a	n/a
47	CTCF	chr1:194129199-194129385	MCF-7	breast:	n/a	chr1:194129261-194129279 chr1:194129263-194129284 chr1:194129264-194129277 chr1:194129262-194129278
48	CTCF	chr1:194071900-194072050	A549	lung:	n/a	n/a
49	CTCF	chr1:194087000-194087150	BE2_C	brain:	n/a	n/a
50	CTCF	chr1:194126308-194126369	GM20000	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:194087394-194087444	ovcar-3	ovarian:	n/a
2	chr1:194087394-194087444	SKMC	muscle:	n/a
3	chr1:194087394-194087444	HepG2	liver:	n/a
4	chr1:194087368-194087418	HCT-116	colon:	n/a
5	chr1:194087394-194087444	PrEC	prostate:	n/a
6	chr1:194087394-194087444	HCF	heart:	n/a
7	chr1:194087394-194087444	GM19239	blood:	n/a
8	chr1:194087394-194087444	AG04449	skin:	fetal
9	chr1:194087368-194087418	HCM	heart:	n/a
10	chr1:194087368-194087418	Caco-2	colon:	n/a
11	chr1:194087368-194087418	MCF-7	breast:	n/a
12	chr1:194087368-194087418	Jurkat	blood:	n/a
13	chr1:194087368-194087418	NHBE	bronchial:	n/a
14	chr1:194087368-194087418	SK-N-MC	brain:	n/a
15	chr1:194087394-194087444	K562	blood:	n/a
16	chr1:194087368-194087418	HNPCEpiC	eye:	n/a
17	chr1:194087368-194087418	SAEC	small airway:	n/a
18	chr1:194087368-194087418	ProgFib	skin:	n/a
19	chr1:194087394-194087444	HMEC	breast:	n/a
20	chr1:194087394-194087444	HCT-116	colon:	n/a
21	chr1:194087368-194087418	HCPEpiC	choroid plexus:	n/a
22	chr1:194087368-194087418	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:194087394-194087444	Caco-2	colon:	n/a
24	chr1:194087368-194087418	AG04449	skin:	fetal
25	chr1:194087394-194087444	NH-A	brain:	n/a
26	chr1:194087368-194087418	HEK293	kidney:	embryo
27	chr1:194087368-194087418	RPTEC	kidney:	n/a
28	chr1:194087394-194087444	SK-N-SH	brain:	n/a
29	chr1:194087394-194087444	U87	brain:	n/a
30	chr1:194087394-194087444	Hepatocyte	liver:	n/a
31	chr1:194087368-194087418	HAEpiC	amniotic membrane:	n/a
32	chr1:194087394-194087444	GM06990	blood:	n/a
33	chr1:194087394-194087444	ProgFib	skin:	n/a
34	chr1:194087368-194087418	Hepatocyte	liver:	n/a
35	chr1:194087368-194087418	SKMC	muscle:	n/a
36	chr1:194087394-194087444	NB4	blood:	n/a
37	chr1:194087368-194087418	HRCEpiC	kidney:	n/a
38	chr1:194087368-194087418	HCF	heart:	n/a
39	chr1:194087368-194087418	CMK	blood:	n/a
40	chr1:194087368-194087418	IMR90	lung:	fetal
41	chr1:194087394-194087444	NHBE	bronchial:	n/a
42	chr1:194087394-194087444	PANC-1	pancreas:	n/a
43	chr1:194087394-194087444	T-47D	breast:	n/a
44	chr1:194087368-194087418	AG04450	lung:	fetal
45	chr1:194087394-194087444	HEK293	kidney:	embryo
46	chr1:194087368-194087418	NH-A	brain:	n/a
47	chr1:194087394-194087444	HUVEC	blood vessel:	n/a
48	chr1:194087368-194087418	HUVEC	blood vessel:	n/a
49	chr1:194087368-194087418	GM06990	blood:	n/a
50	chr1:194087394-194087444	AG10803	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:194088100..194089633-chr1:194091869..194093663,2	K562	blood:
2	chr1:194070430..194072677-chr1:194322592..194324190,2	K562	blood:
3	chr1:194030362..194032550-chr1:194034091..194036103,2	MCF-7	breast:
4	chr1:194088100..194089633-chr1:194091869..194093663,2	K562	blood:
5	chr1:194073743..194077900-chr1:194079205..194082721,3	MCF-7	breast:
6	chr1:194129570..194131258-chr1:194135186..194137115,2	K562	blood:
7	chr1:194128967..194129865-chr1:194264643..194265551,3	MCF-7	breast:
8	chr1:194030362..194032550-chr1:194034091..194036103,2	MCF-7	breast:
9	chr1:194034954..194036751-chr1:194037029..194038550,2	MCF-7	breast:
10	chr1:194073743..194077900-chr1:194079205..194082721,3	MCF-7	breast:
11	chr1:194072910..194073570-chr1:194264512..194265049,2	MCF-7	breast:
12	chr1:194026694..194028807-chr1:194030753..194032744,2	K562	blood:
13	chr1:194034954..194036751-chr1:194037029..194038550,2	MCF-7	breast:
14	chr1:194128824..194129656-chr1:194264555..194265184,3	MCF-7	breast:
15	chr1:194040189..194042332-chr11:65188813..65191352,2	MCF-7	breast:
16	chr1:194071422..194072384-chr1:194264231..194265518,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC73-3	chr1:194118603-194118986	ENSG00000227240.1

No data

Variant related genes	Relation type
ENSG00000227240	TF binding region
ENSG00000227240	CpG island
ENSG00000245532	chromatin interactions

Extended variants
information (count: 1276 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1276 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10429908	chr1:194032486-194032487	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567622096	chr1:194032503-194032504	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs536165304	chr1:194032522-194032523	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs144516244	chr1:194032573-194032574	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs151127274	chr1:194032577-194032578	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs567847892	chr1:194032584-194032585	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529847139	chr1:194032601-194032602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554894143	chr1:194032610-194032611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369321423	chr1:194032629-194032630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564991606	chr1:194032632-194032633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188740893	chr1:194032647-194032648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534736169	chr1:194032668-194032669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77968124	chr1:194032674-194032675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138527935	chr1:194032675-194032676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577764379	chr1:194032676-194032677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576599447	chr1:194032694-194032695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555064240	chr1:194032698-194032699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139982388	chr1:194032717-194032718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559151846	chr1:194032741-194032742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192698784	chr1:194032845-194032846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548481155	chr1:194032860-194032861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375261270	chr1:194032862-194032863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75035426	chr1:194032874-194032875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369723090	chr1:194032883-194032884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117349146	chr1:194032928-194032929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs5779711	chr1:194032944-194032945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3063301	chr1:194032945-194032946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374105625	chr1:194032946-194032947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397814848	chr1:194032947-194032948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111644851	chr1:194032948-194032949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552328556	chr1:194032958-194032959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184495828	chr1:194033003-194033004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373920552	chr1:194033004-194033005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535147960	chr1:194033044-194033045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190538473	chr1:194033139-194033140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77701451	chr1:194033154-194033155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568683159	chr1:194033171-194033172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535732152	chr1:194033242-194033243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557639945	chr1:194033246-194033247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376080446	chr1:194033253-194033254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181978667	chr1:194033258-194033259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540674247	chr1:194033298-194033299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558166814	chr1:194033365-194033366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145803920	chr1:194033419-194033420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559290739	chr1:194033433-194033434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540748508	chr1:194033443-194033444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141660786	chr1:194033534-194033535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1966754	chr1:194033550-194033551	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs541705374	chr1:194033577-194033578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147054199	chr1:194033593-194033594	Weak transcription	n/a	n/a	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
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	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
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194030600-194037200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:194032000-194032600	Flanking Active TSS	HUVEC	blood vessel
3	chr1:194032200-194043000	Weak transcription	Right Atrium	heart
4	chr1:194032400-194037600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr1:194032600-194032800	Enhancers	HUVEC	blood vessel
6	chr1:194032800-194033600	Weak transcription	HUVEC	blood vessel
7	chr1:194033600-194033800	Enhancers	HUVEC	blood vessel
8	chr1:194033800-194040400	Weak transcription	HUVEC	blood vessel
9	chr1:194037000-194037200	Weak transcription	Fetal Heart	heart
10	chr1:194037000-194037200	Enhancers	Left Ventricle	heart
11	chr1:194037000-194037400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:194037000-194038800	Enhancers	Ovary	ovary
13	chr1:194037200-194037800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr1:194037200-194039600	Enhancers	Fetal Heart	heart
15	chr1:194037400-194037600	Enhancers	Colon Smooth Muscle	Colon
16	chr1:194037400-194038600	Weak transcription	Left Ventricle	heart
17	chr1:194037600-194038600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr1:194037600-194038600	Weak transcription	Colon Smooth Muscle	Colon
19	chr1:194037600-194038800	Enhancers	Adipose Nuclei	Adipose
20	chr1:194037800-194042400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr1:194038000-194040800	Enhancers	Fetal Brain Male	brain
22	chr1:194038400-194039400	Enhancers	Rectal Smooth Muscle	rectum
23	chr1:194038600-194038800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:194038600-194039000	Enhancers	Aorta	Aorta
25	chr1:194038600-194039000	Enhancers	Left Ventricle	heart
26	chr1:194038600-194039200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr1:194038600-194039200	Enhancers	Stomach Smooth Muscle	stomach
28	chr1:194038600-194039400	Enhancers	Colon Smooth Muscle	Colon
29	chr1:194038600-194042000	Enhancers	Brain Germinal Matrix	brain
30	chr1:194038800-194039000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:194039200-194040200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr1:194039400-194042800	Weak transcription	Colon Smooth Muscle	Colon
33	chr1:194039400-194045200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr1:194039600-194043000	Weak transcription	Fetal Heart	heart
35	chr1:194039800-194040600	Enhancers	Fetal Brain Female	brain
36	chr1:194040400-194041200	Enhancers	HUVEC	blood vessel
37	chr1:194042400-194044000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr1:194042800-194045800	Enhancers	Colon Smooth Muscle	Colon
39	chr1:194043000-194043200	Enhancers	Right Atrium	heart
40	chr1:194043000-194043400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:194043000-194043800	Enhancers	Fetal Heart	heart
42	chr1:194043800-194054000	Weak transcription	Fetal Heart	heart
43	chr1:194044400-194046800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr1:194045000-194046000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:194045200-194045600	Enhancers	Rectal Smooth Muscle	rectum
46	chr1:194045200-194045800	Enhancers	Fetal Thymus	thymus
47	chr1:194045400-194045800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:194045800-194046400	Weak transcription	Colon Smooth Muscle	Colon
49	chr1:194052400-194053400	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr1:194053600-194054000	Enhancers	Colon Smooth Muscle	Colon

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