Variant report

Variant	nsv1001013
Chromosome Location	chr1:169913597-169960549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:169955146-169955152	K562	blood:	n/a	n/a
2	CEBPB	chr1:169920105-169920380	A549	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
3	CEBPB	chr1:169920089-169920421	IMR90	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
4	CEBPB	chr1:169915356-169915820	Hela-S3	cervix:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
5	CEBPB	chr1:169915309-169915804	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
6	CEBPB	chr1:169953474-169953649	K562	blood:	n/a	n/a
7	CEBPB	chr1:169953584-169953585	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:169953500-169953638	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:169915401-169915893	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
10	CEBPB	chr1:169920135-169920408	HepG2	liver:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
11	CEBPB	chr1:169920115-169920364	K562	blood:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
12	CEBPB	chr1:169915475-169915783	IMR90	lung:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
13	CTCF	chr1:169914627-169914631	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:169914555-169914672	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:169944840-169944990	AG09319	gingival:	n/a	n/a
16	CTCF	chr1:169951340-169951490	HepG2	liver:	n/a	chr1:169951427-169951440
17	CTCF	chr1:169932721-169932758	GM19240	blood:	n/a	n/a
18	CTCF	chr1:169914572-169914617	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:169926841-169926902	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr1:169914619-169914624	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:169914599-169914659	Fibrobl	skin:	n/a	n/a
22	CTCF	chr1:169959221-169959279	GM13977	blood:	n/a	n/a
23	CUX1	chr1:169943514-169943612	K562	blood:	n/a	n/a
24	CUX1	chr1:169943282-169943471	GM12878	blood:	n/a	n/a
25	CUX1	chr1:169958684-169958851	GM12878	blood:	n/a	n/a
26	EP300	chr1:169955476-169955581	K562	blood:	n/a	n/a
27	EP300	chr1:169958639-169959100	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr1:169937046-169937893	SK-N-SH	brain:	n/a	n/a
29	EP300	chr1:169958852-169959130	SK-N-SH_RA	brain:	n/a	chr1:169959115-169959124
30	EP300	chr1:169937342-169937642	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr1:169922354-169922368	K562	blood:	n/a	n/a
32	EP300	chr1:169937349-169937727	SK-N-SH_RA	brain:	n/a	n/a
33	FOS	chr1:169915443-169915573	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:169959136-169959311	MCF10A-Er-Src	breast:	n/a	chr1:169959191-169959199 chr1:169959190-169959200
35	GATA2	chr1:169937314-169937695	SH-SY5Y	brain:	n/a	n/a
36	GATA2	chr1:169928101-169928458	SH-SY5Y	brain:	n/a	chr1:169928371-169928381 chr1:169928243-169928255
37	GATA3	chr1:169955632-169955693	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr1:169929536-169929591	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr1:169915380-169915864	MCF-7	breast:	n/a	chr1:169915612-169915628
40	GATA3	chr1:169936518-169936617	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr1:169918154-169918674	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr1:169937216-169937729	SK-N-SH	brain:	n/a	chr1:169937265-169937275
43	GATA3	chr1:169915098-169916052	MCF-7	breast:	n/a	chr1:169916004-169916015 chr1:169915612-169915628
44	GATA3	chr1:169928128-169928498	SH-SY5Y	brain:	n/a	chr1:169928371-169928381 chr1:169928243-169928255
45	GATA3	chr1:169937235-169937683	SH-SY5Y	brain:	n/a	chr1:169937265-169937275
46	GATA3	chr1:169955318-169955736	MCF-7	breast:	n/a	n/a
47	GATA3	chr1:169918241-169918770	SK-N-SH	brain:	n/a	n/a
48	IRF1	chr1:169957131-169957132	K562	blood:	n/a	n/a
49	JUN	chr1:169922440-169922488	K562	blood:	n/a	n/a
50	JUN	chr1:169956469-169956692	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:169953487..169956228-chr1:169957640..169960024,2	MCF-7	breast:
2	chr1:169861655..169864221-chr1:169940931..169943553,2	MCF-7	breast:
3	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
4	chr1:169927495..169930307-chr1:170507858..170509808,2	K562	blood:
5	chr1:169863023..169865011-chr1:169913232..169916470,3	MCF-7	breast:
6	chr1:169942236..169943172-chrX:26753938..26754794,2	MCF-7	breast:
7	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
8	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
9	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
10	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
11	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCYL3-1	chr1:169927085-169927387	NONHSAT007483

Variant related genes	Relation type
MRPS10P1	TF binding region
RN7SL269P	TF binding region
ENSG00000235378	chromatin interactions
ENSG00000120370	chromatin interactions
ENSG00000000457	chromatin interactions

Extended variants
information (count: 1626 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1626 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565397	chr1:169913597-169913598	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538343008	chr1:169913639-169913640	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527737763	chr1:169913650-169913651	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549155394	chr1:169913662-169913663	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs374963440	chr1:169913698-169913699	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567640670	chr1:169913727-169913728	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs146269608	chr1:169913736-169913737	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550440032	chr1:169913856-169913857	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs76004681	chr1:169913861-169913862	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs79725244	chr1:169913866-169913867	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs478709	chr1:169913878-169913879	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139418106	chr1:169913891-169913892	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs76741109	chr1:169913931-169913932	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537469374	chr1:169913932-169913933	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190965669	chr1:169913936-169913937	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374173222	chr1:169913937-169913938	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537811438	chr1:169913946-169913947	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149497395	chr1:169913997-169913998	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs578239022	chr1:169914032-169914033	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545617858	chr1:169914050-169914051	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555662532	chr1:169914072-169914073	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572487217	chr1:169914116-169914117	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144058520	chr1:169914145-169914146	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148629690	chr1:169914184-169914185	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574202523	chr1:169914194-169914195	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549732480	chr1:169914197-169914198	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs142108022	chr1:169914221-169914222	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182398303	chr1:169914222-169914223	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs56802002	chr1:169914245-169914246	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs147805818	chr1:169914249-169914250	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376693804	chr1:169914252-169914253	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544547821	chr1:169914266-169914267	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200701449	chr1:169914288-169914289	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533687654	chr1:169914290-169914291	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549082103	chr1:169914295-169914296	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371560164	chr1:169914323-169914324	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2093050	chr1:169914343-169914344	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs373399020	chr1:169914395-169914396	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs61806095	chr1:169914421-169914422	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs113186750	chr1:169914435-169914436	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186669186	chr1:169914442-169914443	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565263785	chr1:169914481-169914482	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572577529	chr1:169914528-169914529	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs139453964	chr1:169914539-169914540	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs561450877	chr1:169914596-169914597	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145071523	chr1:169914634-169914635	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559972182	chr1:169914679-169914680	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs147946410	chr1:169914693-169914694	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564936523	chr1:169914699-169914700	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371567896	chr1:169914722-169914723	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Glioblastoma multiforme	21080181	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
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
Breast cancer	21509527	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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169878400-169946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr1:169886600-169915600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr1:169904000-169929800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:169904000-169934800	Weak transcription	Fetal Heart	heart
5	chr1:169904000-169949800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:169904000-170010400	Weak transcription	Aorta	Aorta
7	chr1:169905200-169915400	Weak transcription	GM12878-XiMat	blood
8	chr1:169909200-169946000	Weak transcription	Primary T cells from cord blood	blood
9	chr1:169910400-169946200	Weak transcription	Primary B cells from cord blood	blood
10	chr1:169911200-169914800	Weak transcription	Gastric	stomach
11	chr1:169911200-169948800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:169911400-169914400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr1:169911400-169923000	Weak transcription	Liver	Liver
14	chr1:169911400-169946200	Weak transcription	Dnd41	blood
15	chr1:169911400-169948600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr1:169911600-169918400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:169911600-169927000	Weak transcription	Fetal Intestine Large	intestine
18	chr1:169911600-169945800	Weak transcription	Fetal Muscle Leg	muscle
19	chr1:169911800-169914400	Weak transcription	Brain Substantia Nigra	brain
20	chr1:169911800-169914800	Weak transcription	Fetal Lung	lung
21	chr1:169911800-169946400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr1:169911800-169949600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:169911800-169951200	Weak transcription	Brain Hippocampus Middle	brain
24	chr1:169911800-169968400	Weak transcription	Psoas Muscle	Psoas
25	chr1:169912000-169913800	Weak transcription	Hela-S3	cervix
26	chr1:169912000-169914400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:169912000-169918600	Weak transcription	NHLF	lung
28	chr1:169912000-169922400	Weak transcription	HSMM	muscle
29	chr1:169912000-169946200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr1:169912000-169953600	Weak transcription	Rectal Smooth Muscle	rectum
31	chr1:169912000-169966000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:169912000-169968600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr1:169912400-169918000	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr1:169912400-169918200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:169912400-169950400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr1:169912600-169914400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:169912600-169915200	Weak transcription	Right Atrium	heart
38	chr1:169912600-169915400	Weak transcription	Right Ventricle	heart
39	chr1:169912600-169918800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:169912800-169967200	Weak transcription	NHDF-Ad	bronchial
41	chr1:169913000-169913600	Genic enhancers	Fetal Muscle Trunk	muscle
42	chr1:169913000-169913800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:169913000-169913800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:169913000-169914000	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr1:169913000-169914200	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr1:169913000-169914400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:169913000-169914600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:169913000-169914600	Strong transcription	Fetal Stomach	stomach
49	chr1:169913000-169914800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr1:169913000-169914800	Strong transcription	Left Ventricle	heart

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