Variant report

Variant	nsv945428
Chromosome Location	chr1:246680046-246691781
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:123)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:246690039-246690639	K562	blood:	n/a	n/a
2	CBX3	chr1:246690693-246691006	K562	blood:	n/a	n/a
3	CTCF	chr1:246685009-246685072	LNCaP	prostate:	n/a	n/a
4	CTCF	chr1:246683706-246683740	GM10266	blood:	n/a	n/a
5	CTCF	chr1:246690380-246690530	GM12864	blood:	n/a	n/a
6	EBF1	chr1:246690767-246690995	GM12878	blood:	n/a	n/a
7	ELF1	chr1:246690711-246691053	K562	blood:	n/a	chr1:246690869-246690881 chr1:246690850-246690863
8	ELF1	chr1:246690537-246691003	GM12878	blood:	n/a	chr1:246690869-246690881 chr1:246690850-246690863
9	MAX	chr1:246690184-246690488	K562	blood:	n/a	n/a
10	MAX	chr1:246690717-246691337	NB4	blood:	n/a	chr1:246691192-246691203 chr1:246690872-246690882
11	POLR2A	chr1:246691374-246691413	GM12878	blood:	n/a	n/a
12	POLR2A	chr1:246690629-246691190	GM12892	blood:	n/a	n/a
13	POLR2A	chr1:246690614-246691272	HL-60	blood:	n/a	n/a
14	POLR2A	chr1:246690835-246691011	GM12878	blood:	n/a	n/a
15	POLR2A	chr1:246690757-246691054	GM12878	blood:	n/a	n/a
16	POLR2A	chr1:246691419-246691432	GM12878	blood:	n/a	n/a
17	RUNX3	chr1:246690645-246691040	GM12878	blood:	n/a	n/a
18	RUNX3	chr1:246690665-246691021	GM12878	blood:	n/a	n/a
19	SETDB1	chr1:246679814-246680908	K562	blood:	n/a	n/a
20	SPI1	chr1:246690753-246690945	K562	blood:	n/a	n/a
21	SPI1	chr1:246690774-246690903	GM12878	blood:	n/a	n/a
22	SPI1	chr1:246690599-246691134	HL-60	blood:	n/a	chr1:246690621-246690634 chr1:246691061-246691074
23	SPI1	chr1:246690676-246690930	GM12878	blood:	n/a	n/a
24	SPI1	chr1:246690661-246691085	HL-60	blood:	n/a	chr1:246691061-246691074
25	SPI1	chr1:246690734-246690935	GM12891	blood:	n/a	n/a
26	USF1	chr1:246689757-246689967	HepG2	liver:	n/a	chr1:246689884-246689895
27	USF1	chr1:246689703-246689959	K562	blood:	n/a	chr1:246689884-246689895
28	USF2	chr1:246689878-246689970	HepG2	liver:	n/a	n/a
29	YY1	chr1:246690018-246690179	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246684329-246684379	HMEC	breast:	n/a
2	chr1:246684329-246684379	HMEC	breast:	n/a
3	chr1:246684329-246684379	AG09309	skin:	n/a
4	chr1:246684329-246684379	AG04449	skin:	fetal
5	chr1:246684329-246684379	T-47D	breast:	n/a
6	chr1:246684113-246684163	RPTEC	kidney:	n/a
7	chr1:246684113-246684163	HCM	heart:	n/a
8	chr1:246684113-246684163	HEEpiC	esophagus:	n/a
9	chr1:246684329-246684379	Hela-S3	cervix:	n/a
10	chr1:246684329-246684379	HAEpiC	amniotic membrane:	n/a
11	chr1:246684113-246684163	AG04449	skin:	fetal
12	chr1:246684329-246684379	GM12892	blood:	n/a
13	chr1:246684113-246684163	Jurkat	blood:	n/a
14	chr1:246684113-246684163	AoSMC	blood vessel:	n/a
15	chr1:246684113-246684163	LNCaP	prostate:	n/a
16	chr1:246684113-246684163	HIPEpiC	eye:	n/a
17	chr1:246684113-246684163	HAEpiC	amniotic membrane:	n/a
18	chr1:246684113-246684163	PFSK-1	brain:	n/a
19	chr1:246684329-246684379	HRE	kidney:	n/a
20	chr1:246684113-246684163	Hepatocyte	liver:	n/a
21	chr1:246684329-246684379	Hepatocyte	liver:	n/a
22	chr1:246684113-246684163	GM12891	blood:	n/a
23	chr1:246684113-246684163	HNPCEpiC	eye:	n/a
24	chr1:246684329-246684379	HIPEpiC	eye:	n/a
25	chr1:246684329-246684379	BJ	skin:	n/a
26	chr1:246684329-246684379	HNPCEpiC	eye:	n/a
27	chr1:246684329-246684379	Caco-2	colon:	n/a
28	chr1:246684113-246684163	BE2_C	brain:	n/a
29	chr1:246684113-246684163	ovcar-3	ovarian:	n/a
30	chr1:246684329-246684379	HCT-116	colon:	n/a
31	chr1:246684329-246684379	BE2_C	brain:	n/a
32	chr1:246684113-246684163	SK-N-SH	brain:	n/a
33	chr1:246684329-246684379	HEK293	kidney:	embryo
34	chr1:246684113-246684163	HEK293	kidney:	embryo
35	chr1:246684113-246684163	GM06990	blood:	n/a
36	chr1:246684113-246684163	H1-hESC	embryonic stem cell:	embryo
37	chr1:246684113-246684163	PANC-1	pancreas:	n/a
38	chr1:246684329-246684379	AG09319	gingival:	n/a
39	chr1:246684329-246684379	AG04450	lung:	fetal
40	chr1:246684113-246684163	GM19239	blood:	n/a
41	chr1:246684329-246684379	MCF-7	breast:	n/a
42	chr1:246684113-246684163	HCPEpiC	choroid plexus:	n/a
43	chr1:246684329-246684379	ECC-1	luminal epithelium:	n/a
44	chr1:246684113-246684163	NH-A	brain:	n/a
45	chr1:246684329-246684379	NT2-D1	testis:	n/a
46	chr1:246684329-246684379	ovcar-3	ovarian:	n/a
47	chr1:246684113-246684163	HUVEC	blood vessel:	n/a
48	chr1:246684329-246684379	AoSMC	blood vessel:	n/a
49	chr1:246684113-246684163	BJ	skin:	n/a
50	chr1:246684329-246684379	HCM	heart:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246679194..246683104-chr1:246689621..246693878,4	K562	blood:
2	chr1:246680075..246681714-chr1:246684033..246686969,2	K562	blood:
3	chr1:246685591..246688881-chr1:246727054..246730014,3	K562	blood:
4	chr1:246671783..246672632-chr1:246690944..246691587,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNST-2	chr1:246691213-246691457	NONHSAT010708
2	lnc-CNST-2	chr1:246690332-246690503	NONHSAT010708

No data

Variant related genes	Relation type
ENSG00000227728	TF binding region
ENSG00000242042	TF binding region
ENSG00000230813	TF binding region
ENSG00000227728	CpG island
ENSG00000242042	CpG island
ENSG00000230813	CpG island
ENSG00000230813	chromatin interactions
ENSG00000162852	chromatin interactions
ENSG00000229112	chromatin interactions
ENSG00000162851	chromatin interactions
ENSG00000227728	chromatin interactions

Extended variants
information (count: 506 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143604743	chr1:246680063-246680064	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181222587	chr1:246680068-246680069	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs539930442	chr1:246680076-246680077	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs550046419	chr1:246680079-246680080	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs151240128	chr1:246680096-246680097	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535509846	chr1:246680149-246680150	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs555681464	chr1:246680181-246680182	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs546807168	chr1:246680182-246680183	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs534779877	chr1:246680187-246680188	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs557995877	chr1:246680189-246680190	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs577803152	chr1:246680196-246680197	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs561732048	chr1:246680205-246680206	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs140604634	chr1:246680214-246680215	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs57970491	chr1:246680221-246680222	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs573566375	chr1:246680224-246680225	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs542274245	chr1:246680231-246680232	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs562018467	chr1:246680253-246680254	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs527982678	chr1:246680257-246680258	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs562784985	chr1:246680271-246680272	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs10924762	chr1:246680283-246680284	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs564329917	chr1:246680335-246680336	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs533406367	chr1:246680369-246680370	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs550226059	chr1:246680374-246680375	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs115783761	chr1:246680378-246680379	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs186666503	chr1:246680408-246680409	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs566189835	chr1:246680468-246680469	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs371594319	chr1:246680506-246680507	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs375501175	chr1:246680538-246680539	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs60153804	chr1:246680615-246680616	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77669359	chr1:246680699-246680700	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs374768725	chr1:246680702-246680703	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs534908941	chr1:246680715-246680716	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs558133414	chr1:246680773-246680774	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs4654278	chr1:246680787-246680788	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs150471583	chr1:246680788-246680789	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs556983904	chr1:246680805-246680806	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs189665137	chr1:246680820-246680821	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs542171220	chr1:246680825-246680826	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs112064909	chr1:246680831-246680832	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs12753237	chr1:246680836-246680837	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs142583989	chr1:246680876-246680877	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs564652528	chr1:246680882-246680883	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs41303143	chr1:246680886-246680887	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543667613	chr1:246680902-246680903	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs563771665	chr1:246680907-246680908	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs138759669	chr1:246680939-246680940	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs549541539	chr1:246680959-246680960	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs372889434	chr1:246680977-246680978	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556133295	chr1:246680984-246680985	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs566079036	chr1:246680993-246680994	ZNF genes & repeats Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	19805367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246680200-246682400	Weak transcription	Right Atrium	heart
2	chr1:246680600-246683000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:246681600-246681800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:246685400-246685600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:246685600-246687600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:246686200-246686400	Bivalent Enhancer	HepG2	liver
7	chr1:246687400-246687600	Bivalent Enhancer	HepG2	liver
8	chr1:246687600-246687800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:246687800-246689800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:246689800-246690000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:246689800-246690000	Enhancers	Esophagus	oesophagus
12	chr1:246689800-246690400	Active TSS	HepG2	liver
13	chr1:246690000-246690800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:246690000-246692600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr1:246690200-246690400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
16	chr1:246690400-246690600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
17	chr1:246690400-246690600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr1:246690400-246690600	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr1:246690400-246690800	Flanking Active TSS	HepG2	liver
20	chr1:246690400-246691000	Enhancers	Gastric	stomach
21	chr1:246690400-246691200	Enhancers	Lung	lung
22	chr1:246690400-246691400	ZNF genes & repeats	GM12878-XiMat	blood
23	chr1:246690400-246691600	Enhancers	Primary T cells fromperipheralblood	blood
24	chr1:246690400-246691600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:246690400-246691600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:246690400-246691800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
27	chr1:246690400-246693000	Enhancers	HMEC	breast
28	chr1:246690600-246690800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr1:246690600-246691000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr1:246690600-246691200	Enhancers	Primary B cells from peripheral blood	blood
31	chr1:246690600-246691200	Enhancers	Stomach Mucosa	stomach
32	chr1:246690600-246691400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:246690600-246691400	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr1:246690600-246691400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:246690600-246691400	Enhancers	Esophagus	oesophagus
36	chr1:246690600-246691400	Enhancers	Spleen	Spleen
37	chr1:246690600-246691400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr1:246690600-246691600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr1:246690800-246691000	Active TSS	HepG2	liver
40	chr1:246690800-246691200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:246690800-246691200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr1:246690800-246691200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr1:246690800-246691200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:246690800-246691200	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr1:246690800-246691400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:246690800-246691400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr1:246690800-246691400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr1:246691000-246691400	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr1:246691000-246691400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr1:246691000-246691400	Flanking Bivalent TSS/Enh	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links