Variant report

Variant	nsv872987
Chromosome Location	chr1:196697288-196707336
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:107)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:107 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:196701720-196701870	WERI-Rb-1	eye:	n/a	n/a
2	CTCF	chr1:196701760-196701910	AG04449	skin:	n/a	n/a
3	CTCF	chr1:196701860-196702010	K562	blood:	n/a	n/a
4	CTCF	chr1:196701740-196701890	GM12868	blood:	n/a	n/a
5	CTCF	chr1:196701780-196701930	SAEC	small airway:	n/a	n/a
6	CTCF	chr1:196701747-196701939	MCF-7	breast:	n/a	n/a
7	CTCF	chr1:196701800-196701950	GM12874	blood:	n/a	n/a
8	CTCF	chr1:196701780-196701930	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr1:196701780-196701930	MCF-7	breast:	n/a	n/a
10	CTCF	chr1:196701800-196701950	GM12866	blood:	n/a	n/a
11	CTCF	chr1:196701740-196701890	NHDF-neo	bronchial:	n/a	n/a
12	CTCF	chr1:196701720-196701870	HRE	kidney:	n/a	n/a
13	CTCF	chr1:196701804-196701908	Fibrobl	skin:	n/a	n/a
14	CTCF	chr1:196701640-196701790	HCM	heart:	n/a	n/a
15	CTCF	chr1:196701800-196701950	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr1:196701700-196701850	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr1:196701800-196701950	GM12869	blood:	n/a	n/a
18	CTCF	chr1:196701700-196701850	GM12865	blood:	n/a	n/a
19	CTCF	chr1:196701780-196701930	GM12871	blood:	n/a	n/a
20	CTCF	chr1:196701747-196701950	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:196701800-196701950	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:196701682-196702003	HepG2	liver:	n/a	n/a
23	CTCF	chr1:196701780-196701930	AG09319	gingival:	n/a	n/a
24	CTCF	chr1:196701760-196701910	NHLF	lung:	n/a	n/a
25	CTCF	chr1:196701720-196701870	GM06990	blood:	n/a	n/a
26	CTCF	chr1:196701720-196701870	Caco-2	colon:	n/a	n/a
27	CTCF	chr1:196701820-196701970	HPF	lung:	n/a	n/a
28	CTCF	chr1:196701620-196701770	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr1:196701760-196701910	HepG2	liver:	n/a	n/a
30	CTCF	chr1:196701680-196701830	HRE	kidney:	n/a	n/a
31	CTCF	chr1:196701800-196701950	HCT-116	colon:	n/a	n/a
32	CTCF	chr1:196701780-196701930	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr1:196701780-196701930	BE2_C	brain:	n/a	n/a
34	CTCF	chr1:196701800-196701950	A549	lung:	n/a	n/a
35	CTCF	chr1:196701780-196701930	AG10803	skin:	n/a	n/a
36	CTCF	chr1:196701800-196701950	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr1:196701814-196701893	ProgFib	skin:	n/a	n/a
38	CTCF	chr1:196701720-196701870	GM12865	blood:	n/a	n/a
39	CTCF	chr1:196701740-196701890	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr1:196701760-196701910	BJ	skin:	n/a	n/a
41	CTCF	chr1:196703560-196703710	HPF	lung:	n/a	n/a
42	CTCF	chr1:196701780-196701930	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr1:196701780-196701930	RPTEC	kidney:	n/a	n/a
44	CTCF	chr1:196701760-196701910	AG04450	lung:	n/a	n/a
45	CTCF	chr1:196701753-196701910	HepG2	liver:	n/a	n/a
46	CTCF	chr1:196701820-196701970	RPTEC	kidney:	n/a	n/a
47	CTCF	chr1:196701803-196701895	Gliobla	brain:	n/a	n/a
48	CTCF	chr1:196701804-196701913	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:196701717-196701912	HepG2	liver:	n/a	n/a
50	CTCF	chr1:196701880-196702030	Hela-S3	cervix:	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	Hepatocyte	liver:	n/a
2	chr1:196702931-196702981	PrEC	prostate:	n/a
3	chr1:196702931-196702981	HepG2	liver:	n/a
4	chr1:196702931-196702981	HL-60	blood:	n/a
5	chr1:196702931-196702981	GM06990	blood:	n/a
6	chr1:196702931-196702981	AoSMC	blood vessel:	n/a
7	chr1:196702931-196702981	GM12878	blood:	n/a
8	chr1:196702931-196702981	BJ	skin:	n/a
9	chr1:196702931-196702981	HRE	kidney:	n/a
10	chr1:196702931-196702981	HRCEpiC	kidney:	n/a
11	chr1:196702931-196702981	SK-N-SH_RA	brain:	n/a
12	chr1:196702931-196702981	K562	blood:	n/a
13	chr1:196702931-196702981	Hela-S3	cervix:	n/a
14	chr1:196702931-196702981	A549	lung:	n/a
15	chr1:196702931-196702981	HUVEC	blood vessel:	n/a
16	chr1:196702931-196702981	GM19239	blood:	n/a
17	chr1:196702931-196702981	AG04449	skin:	fetal
18	chr1:196702931-196702981	AG09309	skin:	n/a
19	chr1:196702931-196702981	HCPEpiC	choroid plexus:	n/a
20	chr1:196702931-196702981	HCM	heart:	n/a
21	chr1:196702931-196702981	NT2-D1	testis:	n/a
22	chr1:196702931-196702981	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:196702931-196702981	AG09319	gingival:	n/a
24	chr1:196702931-196702981	SK-N-MC	brain:	n/a
25	chr1:196702931-196702981	IMR90	lung:	fetal
26	chr1:196702931-196702981	H1-hESC	embryonic stem cell:	embryo
27	chr1:196702931-196702981	U87	brain:	n/a
28	chr1:196702931-196702981	MCF-7	breast:	n/a
29	chr1:196702931-196702981	MCF10A-Er-Src	breast:	n/a
30	chr1:196702931-196702981	HEK293	kidney:	embryo
31	chr1:196702931-196702981	HCF	heart:	n/a
32	chr1:196702931-196702981	HRPEpiC	eye:	n/a
33	chr1:196702931-196702981	Jurkat	blood:	n/a
34	chr1:196702931-196702981	ProgFib	skin:	n/a
35	chr1:196702931-196702981	SAEC	small airway:	n/a
36	chr1:196702931-196702981	LNCaP	prostate:	n/a
37	chr1:196702931-196702981	SKMC	muscle:	n/a
38	chr1:196702931-196702981	AG10803	skin:	n/a
39	chr1:196702931-196702981	HMEC	breast:	n/a
40	chr1:196702931-196702981	ovcar-3	ovarian:	n/a
41	chr1:196702931-196702981	HEEpiC	esophagus:	n/a
42	chr1:196702931-196702981	RPTEC	kidney:	n/a
43	chr1:196702931-196702981	NHBE	bronchial:	n/a
44	chr1:196702931-196702981	GM12892	blood:	n/a
45	chr1:196702931-196702981	PFSK-1	brain:	n/a
46	chr1:196702931-196702981	Caco-2	colon:	n/a
47	chr1:196702931-196702981	HAEpiC	amniotic membrane:	n/a
48	chr1:196702931-196702981	NHDF-neo	bronchial:	n/a
49	chr1:196702931-196702981	SK-N-SH	brain:	n/a
50	chr1:196702931-196702981	BE2_C	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:196706600..196708493-chr1:196711945..196714734,2	K562	blood:
2	chr1:196697444..196700419-chr1:196700685..196703503,2	K562	blood:
3	chr1:196692213..196693146-chr1:196701336..196702240,4	MCF-7	breast:
4	chr1:196697444..196700419-chr1:196700685..196703503,2	K562	blood:
5	chr1:196701976..196704900-chr1:197163664..197165558,2	K562	blood:
6	chr1:196700723..196702673-chr1:196877017..196878794,2	K562	blood:
7	chr1:196629812..196630524-chr1:196701384..196702319,3	MCF-7	breast:

No data

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

Extended variants
information (count: 407 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:407 , 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	rs1329429	chr1:196697288-196697289	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575087674	chr1:196697298-196697299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560513295	chr1:196697318-196697319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545641799	chr1:196697319-196697320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543703511	chr1:196697344-196697345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563817440	chr1:196697353-196697354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528207494	chr1:196697354-196697355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188634176	chr1:196697424-196697425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373044714	chr1:196697486-196697487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377521002	chr1:196697495-196697496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528884855	chr1:196697501-196697502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551215138	chr1:196697534-196697535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374704701	chr1:196697553-196697554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1060821	chr1:196697578-196697579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148445529	chr1:196697599-196697600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs55931547	chr1:196697631-196697632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374526857	chr1:196697644-196697645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569488635	chr1:196697652-196697653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs55871663	chr1:196697672-196697673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367587413	chr1:196697682-196697683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371381987	chr1:196697685-196697686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200739652	chr1:196697700-196697701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552029607	chr1:196697740-196697741	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566952664	chr1:196697748-196697749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111492337	chr1:196697753-196697754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181049216	chr1:196697841-196697842	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374176162	chr1:196697845-196697846	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549229012	chr1:196697862-196697863	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112137282	chr1:196697863-196697864	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs66528938	chr1:196697864-196697865	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537895985	chr1:196697865-196697866	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200057268	chr1:196697867-196697868	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71927401	chr1:196697875-196697876	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34018998	chr1:196697886-196697887	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113641435	chr1:196697889-196697890	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150910598	chr1:196697899-196697900	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551712748	chr1:196697968-196697969	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575188506	chr1:196698000-196698001	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184358533	chr1:196698029-196698030	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557496547	chr1:196698037-196698038	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77302817	chr1:196698083-196698084	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200707080	chr1:196698086-196698087	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190510734	chr1:196698119-196698120	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182460635	chr1:196698126-196698127	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139401651	chr1:196698145-196698146	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564821001	chr1:196698165-196698166	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373871611	chr1:196698190-196698191	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543916762	chr1:196698215-196698216	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563152695	chr1:196698223-196698224	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145035620	chr1:196698243-196698244	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	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:95 , 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	chr1:196674000-196706600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr1:196676000-196700600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:196678600-196707000	Weak transcription	HSMMtube	muscle
6	chr1:196685600-196706800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:196685800-196697400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:196689400-196697800	Strong transcription	Liver	Liver
9	chr1:196690800-196701800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:196690800-196707200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr1:196691200-196718400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr1:196692800-196697400	Weak transcription	Right Ventricle	heart
13	chr1:196693000-196707800	Weak transcription	Lung	lung
14	chr1:196693200-196698800	Weak transcription	Gastric	stomach
15	chr1:196693200-196707800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:196693600-196700200	Weak transcription	Dnd41	blood
17	chr1:196693600-196706000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr1:196693600-196707000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:196693600-196707000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr1:196693800-196701800	Weak transcription	Fetal Muscle Leg	muscle
21	chr1:196694400-196706600	Weak transcription	Psoas Muscle	Psoas
22	chr1:196695600-196698400	Strong transcription	HSMM	muscle
23	chr1:196695600-196707600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr1:196695800-196697600	Strong transcription	Ovary	ovary
25	chr1:196697400-196699200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:196697600-196701600	Weak transcription	Ovary	ovary
27	chr1:196697800-196699400	Genic enhancers	Liver	Liver
28	chr1:196698400-196701800	Weak transcription	HSMM	muscle
29	chr1:196699200-196701800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:196699200-196707200	Weak transcription	Adipose Nuclei	Adipose
31	chr1:196699400-196700400	Strong transcription	Liver	Liver
32	chr1:196700200-196705400	Strong transcription	Dnd41	blood
33	chr1:196700400-196704600	Genic enhancers	Liver	Liver
34	chr1:196700600-196703800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:196701200-196707000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:196701600-196703800	Strong transcription	Ovary	ovary
37	chr1:196701800-196702000	Enhancers	Colon Smooth Muscle	Colon
38	chr1:196701800-196702200	Strong transcription	Primary hematopoietic stem cells	blood
39	chr1:196701800-196702400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:196701800-196702600	Strong transcription	HSMM	muscle
41	chr1:196701800-196703800	Strong transcription	Fetal Muscle Leg	muscle
42	chr1:196701800-196707000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:196702000-196702200	Flanking Active TSS	Colon Smooth Muscle	Colon
44	chr1:196702000-196702200	Enhancers	Rectal Smooth Muscle	rectum
45	chr1:196702200-196702600	Flanking Active TSS	Rectal Smooth Muscle	rectum
46	chr1:196702200-196702800	Active TSS	Colon Smooth Muscle	Colon
47	chr1:196702200-196702800	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr1:196702200-196707200	Weak transcription	Primary hematopoietic stem cells	blood
49	chr1:196702400-196702800	Active TSS	Stomach Smooth Muscle	stomach
50	chr1:196702400-196706000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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