Variant report

Variant	nsv872984
Chromosome Location	chr1:196694094-196705167
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:105)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:105 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:196701740-196701890	HA-sp	spinal cord:	n/a	n/a
2	CTCF	chr1:196701800-196701950	HRPEpiC	eye:	n/a	n/a
3	CTCF	chr1:196701735-196701952	MCF-7	breast:	n/a	n/a
4	CTCF	chr1:196701800-196701950	GM12869	blood:	n/a	n/a
5	CTCF	chr1:196701760-196701910	NHLF	lung:	n/a	n/a
6	CTCF	chr1:196701760-196701910	AG04450	lung:	n/a	n/a
7	CTCF	chr1:196701840-196701990	HFF-Myc	foreskin:	n/a	n/a
8	CTCF	chr1:196701780-196701930	AoAF	blood vessel:	n/a	n/a
9	CTCF	chr1:196701824-196701892	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr1:196701820-196701970	HCFaa	heart:	n/a	n/a
11	CTCF	chr1:196701803-196701895	Gliobla	brain:	n/a	n/a
12	CTCF	chr1:196701780-196701930	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr1:196701680-196701830	HFF-Myc	foreskin:	n/a	n/a
14	CTCF	chr1:196701780-196701930	BE2_C	brain:	n/a	n/a
15	CTCF	chr1:196701780-196701930	GM12871	blood:	n/a	n/a
16	CTCF	chr1:196702080-196702230	RPTEC	kidney:	n/a	n/a
17	CTCF	chr1:196701561-196702035	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:196701760-196701910	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr1:196701800-196701950	A549	lung:	n/a	n/a
20	CTCF	chr1:196701640-196701790	HCM	heart:	n/a	n/a
21	CTCF	chr1:196701700-196701850	GM12864	blood:	n/a	n/a
22	CTCF	chr1:196701740-196701890	GM12873	blood:	n/a	n/a
23	CTCF	chr1:196701760-196701910	BJ	skin:	n/a	n/a
24	CTCF	chr1:196701780-196701930	SAEC	small airway:	n/a	n/a
25	CTCF	chr1:196701780-196701930	AG10803	skin:	n/a	n/a
26	CTCF	chr1:196701940-196702090	AG09319	gingival:	n/a	n/a
27	CTCF	chr1:196701740-196701890	HCT-116	colon:	n/a	n/a
28	CTCF	chr1:196701720-196701870	HVMF	connective:	n/a	n/a
29	CTCF	chr1:196701792-196701901	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr1:196701740-196701890	GM12868	blood:	n/a	n/a
31	CTCF	chr1:196701804-196701913	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:196701780-196701930	AG04449	skin:	n/a	n/a
33	CTCF	chr1:196701747-196701939	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:196701820-196701970	RPTEC	kidney:	n/a	n/a
35	CTCF	chr1:196701840-196701990	NB4	blood:	n/a	n/a
36	CTCF	chr1:196701680-196701830	HRE	kidney:	n/a	n/a
37	CTCF	chr1:196701794-196701900	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:196701760-196701910	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr1:196701820-196701970	HPF	lung:	n/a	n/a
40	CTCF	chr1:196701740-196701890	HMF	breast:	n/a	n/a
41	CTCF	chr1:196701720-196701870	Caco-2	colon:	n/a	n/a
42	CTCF	chr1:196701800-196701950	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:196701760-196701910	HAc	cerebellar:	n/a	n/a
44	CTCF	chr1:196701800-196701950	AG09309	skin:	n/a	n/a
45	CTCF	chr1:196701798-196701806	LNCaP	prostate:	n/a	n/a
46	CTCF	chr1:196701807-196701882	LNCaP	prostate:	n/a	n/a
47	CTCF	chr1:196701717-196701912	HepG2	liver:	n/a	n/a
48	CTCF	chr1:196701640-196701790	NHEK	skin:	n/a	n/a
49	CTCF	chr1:196701740-196701890	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr1:196701780-196701930	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:196702931-196702981	SAEC	small airway:	n/a
2	chr1:196702931-196702981	SK-N-SH	brain:	n/a
3	chr1:196702931-196702981	GM19239	blood:	n/a
4	chr1:196702931-196702981	HCF	heart:	n/a
5	chr1:196702931-196702981	HEEpiC	esophagus:	n/a
6	chr1:196702931-196702981	U87	brain:	n/a
7	chr1:196702931-196702981	CMK	blood:	n/a
8	chr1:196702931-196702981	HRE	kidney:	n/a
9	chr1:196702931-196702981	HNPCEpiC	eye:	n/a
10	chr1:196702931-196702981	AG09309	skin:	n/a
11	chr1:196702931-196702981	MCF10A-Er-Src	breast:	n/a
12	chr1:196702931-196702981	AG04449	skin:	fetal
13	chr1:196702931-196702981	HUVEC	blood vessel:	n/a
14	chr1:196702931-196702981	AG04450	lung:	fetal
15	chr1:196702931-196702981	Jurkat	blood:	n/a
16	chr1:196702931-196702981	HCPEpiC	choroid plexus:	n/a
17	chr1:196702931-196702981	K562	blood:	n/a
18	chr1:196702931-196702981	NB4	blood:	n/a
19	chr1:196702931-196702981	NT2-D1	testis:	n/a
20	chr1:196702931-196702981	ECC-1	luminal epithelium:	n/a
21	chr1:196702931-196702981	ProgFib	skin:	n/a
22	chr1:196702931-196702981	HMEC	breast:	n/a
23	chr1:196702931-196702981	IMR90	lung:	fetal
24	chr1:196702931-196702981	Caco-2	colon:	n/a
25	chr1:196702931-196702981	AoSMC	blood vessel:	n/a
26	chr1:196702931-196702981	NHDF-neo	bronchial:	n/a
27	chr1:196702931-196702981	GM12878	blood:	n/a
28	chr1:196702931-196702981	ovcar-3	ovarian:	n/a
29	chr1:196702931-196702981	HCM	heart:	n/a
30	chr1:196702931-196702981	HRPEpiC	eye:	n/a
31	chr1:196702931-196702981	Hepatocyte	liver:	n/a
32	chr1:196702931-196702981	AG10803	skin:	n/a
33	chr1:196702931-196702981	MCF-7	breast:	n/a
34	chr1:196702931-196702981	Hela-S3	cervix:	n/a
35	chr1:196702931-196702981	SK-N-MC	brain:	n/a
36	chr1:196702931-196702981	HIPEpiC	eye:	n/a
37	chr1:196702931-196702981	NHBE	bronchial:	n/a
38	chr1:196702931-196702981	SK-N-SH_RA	brain:	n/a
39	chr1:196702931-196702981	PrEC	prostate:	n/a
40	chr1:196702931-196702981	NH-A	brain:	n/a
41	chr1:196702931-196702981	GM06990	blood:	n/a
42	chr1:196702931-196702981	AG09319	gingival:	n/a
43	chr1:196702931-196702981	HCT-116	colon:	n/a
44	chr1:196702931-196702981	SKMC	muscle:	n/a
45	chr1:196702931-196702981	BJ	skin:	n/a
46	chr1:196702931-196702981	PANC-1	pancreas:	n/a
47	chr1:196702931-196702981	HepG2	liver:	n/a
48	chr1:196702931-196702981	GM12891	blood:	n/a
49	chr1:196702931-196702981	RPTEC	kidney:	n/a
50	chr1:196702931-196702981	HPAEpiC	pulmonary alveolar:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:196697444..196700419-chr1:196700685..196703503,2	K562	blood:
2	chr1:196692213..196693146-chr1:196701336..196702240,4	MCF-7	breast:
3	chr1:196629812..196630524-chr1:196701384..196702319,3	MCF-7	breast:
4	chr1:196700723..196702673-chr1:196877017..196878794,2	K562	blood:
5	chr1:196701976..196704900-chr1:197163664..197165558,2	K562	blood:
6	chr1:196697444..196700419-chr1:196700685..196703503,2	K562	blood:

No data

Variant related genes	Relation type
CFH	TF binding region
CFH	CpG island

Extended variants
information (count: 448 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34436878	chr1:196694094-196694095	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113111123	chr1:196694146-196694147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs55773353	chr1:196694187-196694188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56225627	chr1:196694212-196694213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111869506	chr1:196694238-196694239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144976181	chr1:196694261-196694262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76405615	chr1:196694262-196694263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141021080	chr1:196694284-196694285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532344479	chr1:196694289-196694290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201411537	chr1:196694290-196694291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144696019	chr1:196694298-196694299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138890387	chr1:196694299-196694300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200921441	chr1:196694375-196694376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200141451	chr1:196694378-196694379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148165372	chr1:196694379-196694380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368206533	chr1:196694402-196694403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145770949	chr1:196694414-196694415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150694809	chr1:196694427-196694428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372064485	chr1:196694447-196694448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186916601	chr1:196694471-196694472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369313875	chr1:196694478-196694479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554671084	chr1:196694506-196694507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569503244	chr1:196694507-196694508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529924768	chr1:196694523-196694524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537058072	chr1:196694541-196694542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116355899	chr1:196694614-196694615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577163159	chr1:196694633-196694634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541203392	chr1:196694667-196694668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28442192	chr1:196694695-196694696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544820055	chr1:196694701-196694702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575001225	chr1:196694771-196694772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541913858	chr1:196694772-196694773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556763075	chr1:196694824-196694825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563814945	chr1:196694841-196694842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190374308	chr1:196694880-196694881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546226319	chr1:196694888-196694889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565155374	chr1:196694890-196694891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182616029	chr1:196694904-196694905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374591449	chr1:196694921-196694922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550053203	chr1:196694931-196694932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559560469	chr1:196695006-196695007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529901656	chr1:196695037-196695038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547935097	chr1:196695075-196695076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139612353	chr1:196695079-196695080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569988864	chr1:196695099-196695100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545117613	chr1:196695146-196695147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3766405	chr1:196695161-196695162	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs35479160	chr1:196695176-196695177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551780440	chr1:196695246-196695247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34763899	chr1:196695247-196695248	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

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
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
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196648400-196706200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:196649600-196707200	Weak transcription	Osteobl	bone
3	chr1:196671400-196695600	Weak transcription	HSMM	muscle
4	chr1:196674000-196706600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr1:196676000-196700600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:196678600-196707000	Weak transcription	HSMMtube	muscle
7	chr1:196685600-196706800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:196685800-196697400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:196689400-196697800	Strong transcription	Liver	Liver
10	chr1:196690800-196701800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr1:196690800-196707200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:196691200-196718400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr1:196692800-196697400	Weak transcription	Right Ventricle	heart
14	chr1:196693000-196707800	Weak transcription	Lung	lung
15	chr1:196693200-196698800	Weak transcription	Gastric	stomach
16	chr1:196693200-196707800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:196693600-196700200	Weak transcription	Dnd41	blood
18	chr1:196693600-196706000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr1:196693600-196707000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:196693600-196707000	Weak transcription	Fetal Muscle Trunk	muscle
21	chr1:196693800-196695800	Weak transcription	Ovary	ovary
22	chr1:196693800-196701800	Weak transcription	Fetal Muscle Leg	muscle
23	chr1:196694400-196706600	Weak transcription	Psoas Muscle	Psoas
24	chr1:196695600-196698400	Strong transcription	HSMM	muscle
25	chr1:196695600-196707600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:196695800-196697600	Strong transcription	Ovary	ovary
27	chr1:196697400-196699200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:196697600-196701600	Weak transcription	Ovary	ovary
29	chr1:196697800-196699400	Genic enhancers	Liver	Liver
30	chr1:196698400-196701800	Weak transcription	HSMM	muscle
31	chr1:196699200-196701800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:196699200-196707200	Weak transcription	Adipose Nuclei	Adipose
33	chr1:196699400-196700400	Strong transcription	Liver	Liver
34	chr1:196700200-196705400	Strong transcription	Dnd41	blood
35	chr1:196700400-196704600	Genic enhancers	Liver	Liver
36	chr1:196700600-196703800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:196701200-196707000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr1:196701600-196703800	Strong transcription	Ovary	ovary
39	chr1:196701800-196702000	Enhancers	Colon Smooth Muscle	Colon
40	chr1:196701800-196702200	Strong transcription	Primary hematopoietic stem cells	blood
41	chr1:196701800-196702400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:196701800-196702600	Strong transcription	HSMM	muscle
43	chr1:196701800-196703800	Strong transcription	Fetal Muscle Leg	muscle
44	chr1:196701800-196707000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:196702000-196702200	Flanking Active TSS	Colon Smooth Muscle	Colon
46	chr1:196702000-196702200	Enhancers	Rectal Smooth Muscle	rectum
47	chr1:196702200-196702600	Flanking Active TSS	Rectal Smooth Muscle	rectum
48	chr1:196702200-196702800	Active TSS	Colon Smooth Muscle	Colon
49	chr1:196702200-196702800	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr1:196702200-196707200	Weak transcription	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links