Variant report

Variant	nsv549586
Chromosome Location	chr1:247336193-247340784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:247339076-247339083	K562	blood:	n/a	n/a
2	BHLHE40	chr1:247336352-247336802	GM12878	blood:	n/a	n/a
3	CCNT2	chr1:247339059-247339140	K562	blood:	n/a	n/a
4	CEBPB	chr1:247338712-247339142	K562	blood:	n/a	chr1:247338910-247338921
5	CEBPB	chr1:247338788-247339084	HepG2	liver:	n/a	chr1:247338910-247338921
6	CEBPB	chr1:247338782-247338995	Hela-S3	cervix:	n/a	chr1:247338910-247338921
7	CEBPB	chr1:247336561-247336893	A549	lung:	n/a	n/a
8	CEBPB	chr1:247338812-247339073	IMR90	lung:	n/a	chr1:247338910-247338921
9	CEBPB	chr1:247338751-247339126	K562	blood:	n/a	chr1:247338910-247338921
10	CEBPB	chr1:247338815-247339099	A549	lung:	n/a	chr1:247338910-247338921
11	CUX1	chr1:247336842-247336926	K562	blood:	n/a	n/a
12	EBF1	chr1:247336298-247336500	GM12878	blood:	n/a	n/a
13	EP300	chr1:247338890-247339050	K562	blood:	n/a	n/a
14	GATA3	chr1:247339164-247339262	SH-SY5Y	brain:	n/a	chr1:247339174-247339195 chr1:247339182-247339199 chr1:247339181-247339188 chr1:247339181-247339188 chr1:247339177-247339193 chr1:247339181-247339188 chr1:247339180-247339190
15	MAX	chr1:247336553-247337043	K562	blood:	n/a	chr1:247336961-247336971
16	MAX	chr1:247336286-247337178	NB4	blood:	n/a	chr1:247336961-247336971
17	MYC	chr1:247338948-247338955	K562	blood:	n/a	n/a
18	MYC	chr1:247336268-247337107	NB4	blood:	n/a	chr1:247336961-247336971
19	POLR2A	chr1:247339918-247340012	MCF-7	breast:	n/a	n/a
20	POLR2A	chr1:247337062-247337222	ProgFib	skin:	n/a	n/a
21	POLR2A	chr1:247337543-247337603	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr1:247336170-247337069	HL-60	blood:	n/a	n/a
23	POLR2A	chr1:247337135-247337211	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr1:247337386-247337782	H1-neurons	neurons:	n/a	n/a
25	POLR2A	chr1:247336818-247337223	HepG2	liver:	n/a	n/a
26	POLR2A	chr1:247338205-247338243	MCF10A-Er-Src	breast:	n/a	n/a
27	RCOR1	chr1:247338942-247339142	K562	blood:	n/a	n/a
28	RUNX3	chr1:247336232-247336526	GM12878	blood:	n/a	n/a
29	RUNX3	chr1:247336229-247336647	GM12878	blood:	n/a	n/a
30	SPI1	chr1:247338882-247339113	K562	blood:	n/a	chr1:247339004-247339017
31	SPI1	chr1:247338726-247339213	HL-60	blood:	n/a	chr1:247339004-247339017
32	SPI1	chr1:247338827-247339124	HL-60	blood:	n/a	chr1:247339004-247339017
33	STAT3	chr1:247336751-247336940	MCF10A-Er-Src	breast:	n/a	n/a
34	STAT3	chr1:247338344-247338437	MCF10A-Er-Src	breast:	n/a	n/a
35	STAT3	chr1:247336206-247336326	MCF10A-Er-Src	breast:	n/a	n/a
36	STAT3	chr1:247336585-247336602	MCF10A-Er-Src	breast:	n/a	n/a
37	TEAD4	chr1:247338730-247339180	K562	blood:	n/a	n/a
38	ZMIZ1	chr1:247339002-247339176	K562	blood:	n/a	n/a
39	ZNF384	chr1:247337554-247337879	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:247336686-247336736	PANC-1	pancreas:	n/a
2	chr1:247336686-247336736	AG09319	gingival:	n/a
3	chr1:247338637-247338687	HRPEpiC	eye:	n/a
4	chr1:247338637-247338687	NH-A	brain:	n/a
5	chr1:247336686-247336736	RPTEC	kidney:	n/a
6	chr1:247336686-247336736	GM12892	blood:	n/a
7	chr1:247336686-247336736	MCF10A-Er-Src	breast:	n/a
8	chr1:247338637-247338687	PrEC	prostate:	n/a
9	chr1:247336686-247336736	HRPEpiC	eye:	n/a
10	chr1:247338637-247338687	HCPEpiC	choroid plexus:	n/a
11	chr1:247336686-247336736	LNCaP	prostate:	n/a
12	chr1:247336686-247336736	U87	brain:	n/a
13	chr1:247338637-247338687	GM12891	blood:	n/a
14	chr1:247338637-247338687	HIPEpiC	eye:	n/a
15	chr1:247338637-247338687	GM19239	blood:	n/a
16	chr1:247336686-247336736	NB4	blood:	n/a
17	chr1:247336686-247336736	A549	lung:	n/a
18	chr1:247338637-247338687	HRE	kidney:	n/a
19	chr1:247338637-247338687	BE2_C	brain:	n/a
20	chr1:247336686-247336736	SAEC	small airway:	n/a
21	chr1:247338637-247338687	MCF10A-Er-Src	breast:	n/a
22	chr1:247338637-247338687	AG10803	skin:	n/a
23	chr1:247338637-247338687	AG04449	skin:	fetal
24	chr1:247338637-247338687	BJ	skin:	n/a
25	chr1:247338637-247338687	Hepatocyte	liver:	n/a
26	chr1:247336686-247336736	NT2-D1	testis:	n/a
27	chr1:247338637-247338687	SK-N-SH_RA	brain:	n/a
28	chr1:247338637-247338687	NHBE	bronchial:	n/a
29	chr1:247336686-247336736	CMK	blood:	n/a
30	chr1:247336686-247336736	HCT-116	colon:	n/a
31	chr1:247338637-247338687	H1-hESC	embryonic stem cell:	embryo
32	chr1:247336686-247336736	NHBE	bronchial:	n/a
33	chr1:247338637-247338687	HCF	heart:	n/a
34	chr1:247338637-247338687	SAEC	small airway:	n/a
35	chr1:247336686-247336736	AG04449	skin:	fetal
36	chr1:247338637-247338687	SKMC	muscle:	n/a
37	chr1:247336686-247336736	PFSK-1	brain:	n/a
38	chr1:247336686-247336736	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:247338637-247338687	PFSK-1	brain:	n/a
40	chr1:247336686-247336736	HUVEC	blood vessel:	n/a
41	chr1:247338637-247338687	AoSMC	blood vessel:	n/a
42	chr1:247338637-247338687	AG09309	skin:	n/a
43	chr1:247336686-247336736	GM06990	blood:	n/a
44	chr1:247336686-247336736	AoSMC	blood vessel:	n/a
45	chr1:247336686-247336736	AG10803	skin:	n/a
46	chr1:247336686-247336736	PrEC	prostate:	n/a
47	chr1:247336686-247336736	HepG2	liver:	n/a
48	chr1:247338637-247338687	PANC-1	pancreas:	n/a
49	chr1:247338637-247338687	HepG2	liver:	n/a
50	chr1:247336686-247336736	NH-A	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:247093657..247095310-chr1:247336196..247337981,2	K562	blood:
2	chr1:247334201..247339672-chr1:247340521..247343576,5	K562	blood:
3	chr1:247334201..247338259-chr1:247340322..247342599,5	K562	blood:
4	chr1:247339167..247342052-chr1:247346290..247348151,2	MCF-7	breast:
5	chr1:247336789..247339124-chr1:247364118..247365695,2	K562	blood:
6	chr1:247340563..247342412-chr1:247369147..247370920,2	K562	blood:
7	chr1:247338400..247340247-chr1:247370932..247373277,2	K562	blood:
8	chr1:247340250..247344678-chr1:247346787..247348448,4	K562	blood:
9	chr1:247339304..247343861-chr1:247346826..247352020,6	K562	blood:
10	chr1:247266149..247268665-chr1:247339211..247341763,2	K562	blood:
11	chr1:247093657..247096650-chr1:247335096..247337981,2	K562	blood:
12	chr1:247339304..247341719-chr1:247348819..247353321,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF124-3	chr1:247337904-247338553	NONHSAT010759
2	lnc-NLRP3-7	chr1:247336346-247336681	NONHSAT010757
3	lnc-NLRP3-7	chr1:247336678-247337751	NONHSAT010758
4	lnc-NLRP3-6	chr1:247338558-247338827	NONHSAT010760
5	lnc-ZNF124-3	chr1:247338766-247338870	NONHSAT010759
6	lnc-NLRP3-8	chr1:247335968-247336278	NONHSAT010756

No data

Variant related genes	Relation type
ENSG00000224014	TF binding region
ZNF124	TF binding region
ENSG00000224014	CpG island
ZNF124	CpG island
ENSG00000196418	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000188295	chromatin interactions
ENSG00000215795	chromatin interactions
ENSG00000224014	chromatin interactions
ENSG00000227671	chromatin interactions
ENSG00000263568	chromatin interactions
ENSG00000259865	chromatin interactions

Extended variants
information (count: 254 )
Associated
traits (count: 30 )

Variant overlapped rSNPs/rCNVs (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28879193	chr1:247336193-247336194	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571515894	chr1:247336226-247336227	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs78449047	chr1:247336310-247336311	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs116496298	chr1:247336326-247336327	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs567502551	chr1:247336370-247336371	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs536439497	chr1:247336421-247336422	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs114588504	chr1:247336449-247336450	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs572894442	chr1:247336481-247336482	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs544735419	chr1:247336495-247336496	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs558542676	chr1:247336510-247336511	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs574868270	chr1:247336552-247336553	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs543737060	chr1:247336576-247336577	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs5782419	chr1:247336579-247336580	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs201946572	chr1:247336580-247336581	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs563626226	chr1:247336604-247336605	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs149714308	chr1:247336606-247336607	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs543205037	chr1:247336610-247336611	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs74781810	chr1:247336687-247336688	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs1609840	chr1:247336726-247336727	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs144534544	chr1:247336815-247336816	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs78090905	chr1:247336819-247336820	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs555981014	chr1:247336829-247336830	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs527720952	chr1:247336918-247336919	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs530910971	chr1:247336952-247336953	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs567972463	chr1:247336971-247336972	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs561465482	chr1:247336981-247336982	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs202136562	chr1:247336992-247336993	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs114552817	chr1:247337025-247337026	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs536502784	chr1:247337034-247337035	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs553139058	chr1:247337041-247337042	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs566511803	chr1:247337045-247337046	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs148748484	chr1:247337050-247337051	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs377397965	chr1:247337062-247337063	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs535364197	chr1:247337075-247337076	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs142305518	chr1:247337081-247337082	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs10924931	chr1:247337159-247337160	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs571992909	chr1:247337187-247337188	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs369601160	chr1:247337223-247337224	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs543797559	chr1:247337233-247337234	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs376123259	chr1:247337236-247337237	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs375389108	chr1:247337255-247337256	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs557279188	chr1:247337267-247337268	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs573999488	chr1:247337392-247337393	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs2201596	chr1:247337412-247337413	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183040411	chr1:247337414-247337415	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs115456175	chr1:247337437-247337438	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs114486492	chr1:247337444-247337445	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs111952821	chr1:247337450-247337451	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs10924932	chr1:247337461-247337462	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs530970949	chr1:247337464-247337465	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:30)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20435627	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	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

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247327800-247336800	Weak transcription	HSMM	muscle
2	chr1:247331400-247336200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr1:247331800-247347400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:247332800-247338800	Weak transcription	K562	blood
5	chr1:247332800-247346400	Weak transcription	Pancreas	Pancrea
6	chr1:247333000-247345800	Weak transcription	Ovary	ovary
7	chr1:247335600-247336200	Enhancers	Primary B cells from peripheral blood	blood
8	chr1:247335600-247336200	Enhancers	Primary T cells fromperipheralblood	blood
9	chr1:247335600-247336200	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr1:247335600-247336200	Enhancers	Dnd41	blood
11	chr1:247335600-247336400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr1:247335600-247336800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:247335600-247336800	Enhancers	Fetal Thymus	thymus
14	chr1:247335600-247337000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr1:247335600-247337200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr1:247335600-247337200	Enhancers	Primary B cells from cord blood	blood
17	chr1:247335600-247337600	Enhancers	Primary hematopoietic stem cells	blood
18	chr1:247335600-247337600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:247335600-247337800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:247336000-247336800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr1:247336000-247336800	Enhancers	Adipose Nuclei	Adipose
22	chr1:247336000-247336800	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr1:247336000-247336800	Bivalent Enhancer	HepG2	liver
24	chr1:247336000-247336800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr1:247336000-247337000	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr1:247336200-247336400	Enhancers	Duodenum Mucosa	Duodenum
27	chr1:247336200-247346200	Weak transcription	Dnd41	blood
28	chr1:247336800-247337600	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr1:247336800-247337600	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr1:247336800-247337800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:247337200-247338000	Weak transcription	Primary B cells from cord blood	blood
32	chr1:247337200-247338400	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr1:247338000-247338600	ZNF genes & repeats	Primary B cells from cord blood	blood
34	chr1:247338400-247339200	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr1:247338600-247339000	Strong transcription	Primary B cells from cord blood	blood
36	chr1:247338800-247339200	Enhancers	K562	blood
37	chr1:247339000-247342800	Weak transcription	Primary B cells from cord blood	blood
38	chr1:247339800-247340200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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