Variant report

Variant	nsv946456
Chromosome Location	chr1:160812650-160824679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:160814615-160814939	K562	blood:	n/a	n/a
2	CEBPB	chr1:160821111-160821348	HepG2	liver:	n/a	chr1:160821206-160821217
3	CEBPB	chr1:160821090-160821316	A549	lung:	n/a	chr1:160821206-160821217
4	CEBPB	chr1:160814697-160814992	K562	blood:	n/a	n/a
5	CEBPB	chr1:160814682-160814857	K562	blood:	n/a	n/a
6	CEBPB	chr1:160814676-160815007	K562	blood:	n/a	n/a
7	EBF1	chr1:160820443-160820595	GM12878	blood:	n/a	n/a
8	EBF1	chr1:160824654-160824903	GM12878	blood:	n/a	n/a
9	EP300	chr1:160814697-160815031	K562	blood:	n/a	n/a
10	FOS	chr1:160814640-160814993	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr1:160814753-160814985	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr1:160814658-160814993	MCF10A-Er-Src	breast:	n/a	n/a
13	GATA1	chr1:160815045-160815579	K562	blood:	n/a	n/a
14	JUND	chr1:160814627-160814958	K562	blood:	n/a	n/a
15	MAX	chr1:160815230-160815272	NB4	blood:	n/a	n/a
16	MYC	chr1:160814712-160814956	NB4	blood:	n/a	n/a
17	MYC	chr1:160823604-160823767	MCF10A-Er-Src	breast:	n/a	n/a
18	PAX5	chr1:160814642-160814934	GM12878	blood:	n/a	n/a
19	POLR2A	chr1:160818030-160818866	K562	blood:	n/a	n/a
20	POLR2A	chr1:160824024-160824579	K562	blood:	n/a	n/a
21	POLR2A	chr1:160822353-160822762	K562	blood:	n/a	n/a
22	POLR2A	chr1:160824149-160824256	K562	blood:	n/a	n/a
23	POLR2A	chr1:160812622-160813364	K562	blood:	n/a	n/a
24	POLR2A	chr1:160814478-160814762	K562	blood:	n/a	n/a
25	POLR2A	chr1:160820423-160820753	K562	blood:	n/a	n/a
26	POLR2A	chr1:160816638-160817799	K562	blood:	n/a	n/a
27	POLR2A	chr1:160815546-160815689	K562	blood:	n/a	n/a
28	POLR2A	chr1:160819937-160820095	K562	blood:	n/a	n/a
29	POLR2A	chr1:160823567-160823695	K562	blood:	n/a	n/a
30	POLR2A	chr1:160815964-160816155	K562	blood:	n/a	n/a
31	POLR2A	chr1:160819351-160819474	K562	blood:	n/a	n/a
32	RCOR1	chr1:160814569-160814960	K562	blood:	n/a	n/a
33	SETDB1	chr1:160814773-160815164	U2OS	brain:	n/a	n/a
34	STAT3	chr1:160821543-160821635	MCF10A-Er-Src	breast:	n/a	n/a
35	STAT3	chr1:160822867-160823025	MCF10A-Er-Src	breast:	n/a	n/a
36	STAT3	chr1:160818179-160818213	MCF10A-Er-Src	breast:	n/a	n/a
37	STAT3	chr1:160817190-160817736	MCF10A-Er-Src	breast:	n/a	n/a
38	TEAD4	chr1:160814644-160814950	K562	blood:	n/a	n/a
39	TEAD4	chr1:160815052-160815455	K562	blood:	n/a	n/a
40	TEAD4	chr1:160814294-160815018	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:160824025-160824075	HL-60	blood:	n/a
2	chr1:160824025-160824075	HEEpiC	esophagus:	n/a
3	chr1:160824025-160824075	NB4	blood:	n/a
4	chr1:160824025-160824075	H1-hESC	embryonic stem cell:	embryo
5	chr1:160824025-160824075	HMEC	breast:	n/a
6	chr1:160824025-160824075	GM19239	blood:	n/a
7	chr1:160824025-160824075	Caco-2	colon:	n/a
8	chr1:160824025-160824075	Jurkat	blood:	n/a
9	chr1:160824025-160824075	AG04449	skin:	fetal
10	chr1:160824025-160824075	CMK	blood:	n/a
11	chr1:160824025-160824075	SK-N-MC	brain:	n/a
12	chr1:160824025-160824075	SK-N-SH	brain:	n/a
13	chr1:160824025-160824075	IMR90	lung:	fetal
14	chr1:160824025-160824075	BJ	skin:	n/a
15	chr1:160824025-160824075	ECC-1	luminal epithelium:	n/a
16	chr1:160824025-160824075	NHDF-neo	bronchial:	n/a
17	chr1:160824025-160824075	ovcar-3	ovarian:	n/a
18	chr1:160824025-160824075	HepG2	liver:	n/a
19	chr1:160824025-160824075	HCPEpiC	choroid plexus:	n/a
20	chr1:160824025-160824075	GM12892	blood:	n/a
21	chr1:160824025-160824075	MCF10A-Er-Src	breast:	n/a
22	chr1:160824025-160824075	HCT-116	colon:	n/a
23	chr1:160824025-160824075	Hepatocyte	liver:	n/a
24	chr1:160824025-160824075	GM12878	blood:	n/a
25	chr1:160824025-160824075	A549	lung:	n/a
26	chr1:160824025-160824075	HCM	heart:	n/a
27	chr1:160824025-160824075	AG10803	skin:	n/a
28	chr1:160824025-160824075	AG09319	gingival:	n/a
29	chr1:160824025-160824075	HRCEpiC	kidney:	n/a
30	chr1:160824025-160824075	ProgFib	skin:	n/a
31	chr1:160824025-160824075	K562	blood:	n/a
32	chr1:160824025-160824075	PFSK-1	brain:	n/a
33	chr1:160824025-160824075	T-47D	breast:	n/a
34	chr1:160824025-160824075	HRPEpiC	eye:	n/a
35	chr1:160824025-160824075	PANC-1	pancreas:	n/a
36	chr1:160824025-160824075	U87	brain:	n/a
37	chr1:160824025-160824075	LNCaP	prostate:	n/a
38	chr1:160824025-160824075	SKMC	muscle:	n/a
39	chr1:160824025-160824075	HAEpiC	amniotic membrane:	n/a
40	chr1:160824025-160824075	HRE	kidney:	n/a
41	chr1:160824025-160824075	NH-A	brain:	n/a
42	chr1:160824025-160824075	AG09309	skin:	n/a
43	chr1:160824025-160824075	HCF	heart:	n/a
44	chr1:160824025-160824075	SAEC	small airway:	n/a
45	chr1:160824025-160824075	HUVEC	blood vessel:	n/a
46	chr1:160824025-160824075	HIPEpiC	eye:	n/a
47	chr1:160824025-160824075	GM12891	blood:	n/a
48	chr1:160824025-160824075	NHBE	bronchial:	n/a
49	chr1:160824025-160824075	HNPCEpiC	eye:	n/a
50	chr1:160824025-160824075	HEK293	kidney:	embryo

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:160815023..160816835-chr1:160823211..160824951,2	K562	blood:
2	chr1:160805876..160808335-chr1:160811999..160814822,2	K562	blood:
3	chr1:160808897..160810604-chr1:160813448..160815134,2	MCF-7	breast:
4	chr1:160811365..160813058-chr1:160817059..160818706,2	K562	blood:
5	chr1:160805876..160809429-chr1:160811999..160815816,3	K562	blood:
6	chr1:160812347..160814026-chr1:160815697..160817940,2	K562	blood:
7	chr1:160815023..160816835-chr1:160823211..160824951,2	K562	blood:
8	chr1:160822600..160825606-chr1:160827669..160829423,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000226003	TF binding region
CD244	TF binding region
ENSG00000226003	CpG island
CD244	CpG island
ENSG00000122223	chromatin interactions
ENSG00000226003	chromatin interactions

Extended variants
information (count: 471 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562122566	chr1:160812655-160812656	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs527860544	chr1:160812657-160812658	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs547700121	chr1:160812727-160812728	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs189821260	chr1:160812738-160812739	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs12732471	chr1:160812758-160812759	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs570770414	chr1:160812762-160812763	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs182268944	chr1:160812787-160812788	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs12733846	chr1:160812809-160812810	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs79375199	chr1:160812810-160812811	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs144959889	chr1:160812811-160812812	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs12732625	chr1:160812822-160812823	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs12732638	chr1:160812838-160812839	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs537526704	chr1:160812841-160812842	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs554777120	chr1:160812852-160812853	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs12732788	chr1:160812883-160812884	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs12734044	chr1:160812900-160812901	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs186531482	chr1:160813012-160813013	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370615180	chr1:160813017-160813018	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs533936919	chr1:160813018-160813019	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs146788516	chr1:160813027-160813028	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs577159785	chr1:160813058-160813059	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs116691952	chr1:160813060-160813061	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs534303780	chr1:160813112-160813113	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs564047592	chr1:160813124-160813125	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs140696682	chr1:160813132-160813133	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs541983386	chr1:160813187-160813188	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs367550539	chr1:160813198-160813199	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs551386882	chr1:160813223-160813224	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113354301	chr1:160813232-160813233	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs571178885	chr1:160813262-160813263	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs73021982	chr1:160813263-160813264	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145918515	chr1:160813276-160813277	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138411835	chr1:160813312-160813313	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs369928019	chr1:160813352-160813353	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs190134442	chr1:160813354-160813355	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs1412848	chr1:160813380-160813381	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs6696695	chr1:160813408-160813409	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs537819419	chr1:160813456-160813457	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536890534	chr1:160813466-160813467	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375440678	chr1:160813509-160813510	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs60533943	chr1:160813558-160813559	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533977489	chr1:160813573-160813574	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs183064497	chr1:160813595-160813596	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577246818	chr1:160813655-160813656	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539725612	chr1:160813676-160813677	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs377416200	chr1:160813678-160813679	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs188552490	chr1:160813680-160813681	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs553691194	chr1:160813694-160813695	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs193084653	chr1:160813704-160813705	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112317658	chr1:160813715-160813716	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	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
Bladder cancer	21909424	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160809000-160812800	Enhancers	Thymus	Thymus
2	chr1:160809000-160813600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:160809000-160813600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:160809000-160814200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr1:160809000-160814400	Weak transcription	Spleen	Spleen
6	chr1:160809200-160814400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr1:160809200-160814800	Weak transcription	Primary B cells from cord blood	blood
8	chr1:160810200-160814800	Weak transcription	Dnd41	blood
9	chr1:160810200-160815000	Weak transcription	Primary T cells from cord blood	blood
10	chr1:160810600-160813000	Enhancers	Fetal Thymus	thymus
11	chr1:160810600-160814400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr1:160811400-160820200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:160811600-160813000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr1:160811800-160814200	Weak transcription	Fetal Intestine Small	intestine
15	chr1:160811800-160814400	Weak transcription	Fetal Intestine Large	intestine
16	chr1:160811800-160815000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:160811800-160824600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr1:160812000-160813000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr1:160812200-160814400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr1:160812400-160814200	Weak transcription	Left Ventricle	heart
21	chr1:160812400-160814400	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr1:160812400-160816600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr1:160812600-160812800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:160812600-160814400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr1:160812600-160814400	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr1:160812600-160816000	Weak transcription	Fetal Heart	heart
27	chr1:160812600-160816800	Enhancers	Primary hematopoietic stem cells	blood
28	chr1:160812800-160816800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr1:160812800-160824200	Weak transcription	Thymus	Thymus
30	chr1:160813000-160813400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr1:160813000-160813400	Enhancers	Rectal Smooth Muscle	rectum
32	chr1:160813400-160813800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:160813400-160815400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr1:160813600-160813800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:160813600-160813800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:160813800-160814400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:160813800-160814400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:160813800-160814400	Enhancers	HMEC	breast
39	chr1:160814200-160814400	Enhancers	Fetal Intestine Small	intestine
40	chr1:160814200-160814400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr1:160814200-160814600	Enhancers	K562	blood
42	chr1:160814200-160815400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr1:160814400-160814600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:160814400-160814600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:160814400-160814600	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr1:160814400-160814600	Enhancers	Left Ventricle	heart
47	chr1:160814400-160814600	Enhancers	Right Ventricle	heart
48	chr1:160814400-160814600	Enhancers	Spleen	Spleen
49	chr1:160814400-160814800	Enhancers	Fetal Intestine Large	intestine
50	chr1:160814400-160815000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links