Variant report

Variant	nsv524498
Chromosome Location	chr1:246576661-246618880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:490)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246614048-246614417	K562	blood:	n/a	chr1:246614110-246614126
2	ARID3A	chr1:246587912-246588291	K562	blood:	n/a	n/a
3	ARID3A	chr1:246614088-246614383	HepG2	liver:	n/a	chr1:246614110-246614126
4	ARID3A	chr1:246591789-246592119	K562	blood:	n/a	n/a
5	ATF1	chr1:246589653-246589853	K562	blood:	n/a	n/a
6	ATF1	chr1:246591887-246592268	K562	blood:	n/a	n/a
7	ATF1	chr1:246588435-246588914	K562	blood:	n/a	n/a
8	ATF2	chr1:246598868-246599249	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:246591894-246592194	K562	blood:	n/a	n/a
10	BACH1	chr1:246606450-246606451	K562	blood:	n/a	n/a
11	BATF	chr1:246591880-246592213	GM12878	blood:	n/a	n/a
12	BATF	chr1:246591816-246592158	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:246591893-246592220	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:246591909-246592164	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:246580932-246580933	K562	blood:	n/a	n/a
16	BHLHE40	chr1:246591822-246592280	K562	blood:	n/a	n/a
17	BHLHE40	chr1:246588462-246588796	K562	blood:	n/a	n/a
18	BRCA1	chr1:246598938-246599254	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr1:246582052-246582537	K562	blood:	n/a	n/a
20	CBX3	chr1:246611654-246611998	K562	blood:	n/a	n/a
21	CBX3	chr1:246581941-246582555	K562	blood:	n/a	n/a
22	CBX3	chr1:246580386-246580871	K562	blood:	n/a	n/a
23	CBX3	chr1:246591771-246592290	K562	blood:	n/a	n/a
24	CBX3	chr1:246576729-246577165	K562	blood:	n/a	n/a
25	CBX3	chr1:246591794-246592269	K562	blood:	n/a	n/a
26	CBX3	chr1:246588426-246589002	K562	blood:	n/a	n/a
27	CCNT2	chr1:246588441-246589002	K562	blood:	n/a	n/a
28	CEBPB	chr1:246591895-246592281	K562	blood:	n/a	n/a
29	CEBPB	chr1:246598404-246598904	A549	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
30	CEBPB	chr1:246614101-246614437	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:246598491-246599425	Hela-S3	cervix:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
32	CEBPB	chr1:246598418-246598737	HepG2	liver:	n/a	chr1:246598665-246598678
33	CEBPB	chr1:246614170-246614380	A549	lung:	n/a	n/a
34	CEBPB	chr1:246598435-246599408	H1-hESC	embryonic stem cell:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
35	CEBPB	chr1:246591815-246592267	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:246598407-246599012	IMR90	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
37	CEBPB	chr1:246588404-246588847	K562	blood:	n/a	n/a
38	CEBPB	chr1:246598407-246598920	K562	blood:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
39	CEBPB	chr1:246591783-246592270	K562	blood:	n/a	n/a
40	CEBPD	chr1:246588359-246589002	K562	blood:	n/a	n/a
41	CEBPD	chr1:246588409-246588903	K562	blood:	n/a	n/a
42	CEBPD	chr1:246591700-246592270	K562	blood:	n/a	n/a
43	CHD2	chr1:246598938-246599346	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr1:246576797-246577088	K562	blood:	n/a	n/a
45	CHD2	chr1:246591932-246592102	K562	blood:	n/a	n/a
46	CTCF	chr1:246614140-246614290	HFF-Myc	foreskin:	n/a	chr1:246614241-246614262 chr1:246614247-246614263 chr1:246614246-246614264 chr1:246614253-246614260
47	CTCF	chr1:246614140-246614290	GM12868	blood:	n/a	chr1:246614241-246614262 chr1:246614247-246614263 chr1:246614246-246614264 chr1:246614253-246614260
48	CTCF	chr1:246614039-246614427	ECC-1	luminal epithelium:	n/a	chr1:246614241-246614262 chr1:246614247-246614263 chr1:246614246-246614264 chr1:246614253-246614260
49	CTCF	chr1:246581582-246581754	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:246614160-246614310	GM12870	blood:	n/a	chr1:246614241-246614262 chr1:246614247-246614263 chr1:246614246-246614264 chr1:246614253-246614260

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246582116-246582166	PANC-1	pancreas:	n/a
2	chr1:246581705-246581755	HRPEpiC	eye:	n/a
3	chr1:246582116-246582166	PANC-1	pancreas:	n/a
4	chr1:246581705-246581755	HRPEpiC	eye:	n/a
5	chr1:246580717-246580767	NHDF-neo	bronchial:	n/a
6	chr1:246582116-246582166	T-47D	breast:	n/a
7	chr1:246592123-246592173	BJ	skin:	n/a
8	chr1:246599230-246599280	SK-N-MC	brain:	n/a
9	chr1:246580717-246580767	HCT-116	colon:	n/a
10	chr1:246582071-246582121	U87	brain:	n/a
11	chr1:246580717-246580767	PANC-1	pancreas:	n/a
12	chr1:246599230-246599280	HRCEpiC	kidney:	n/a
13	chr1:246582035-246582085	HAEpiC	amniotic membrane:	n/a
14	chr1:246581705-246581755	BJ	skin:	n/a
15	chr1:246580717-246580767	HIPEpiC	eye:	n/a
16	chr1:246592123-246592173	K562	blood:	n/a
17	chr1:246582071-246582121	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:246592123-246592173	PrEC	prostate:	n/a
19	chr1:246592123-246592173	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:246580717-246580767	NH-A	brain:	n/a
21	chr1:246582071-246582121	BE2_C	brain:	n/a
22	chr1:246582035-246582085	HCF	heart:	n/a
23	chr1:246581705-246581755	Jurkat	blood:	n/a
24	chr1:246581705-246581755	GM12878	blood:	n/a
25	chr1:246613311-246613361	AG09319	gingival:	n/a
26	chr1:246613311-246613361	NHDF-neo	bronchial:	n/a
27	chr1:246581705-246581755	PrEC	prostate:	n/a
28	chr1:246581705-246581755	Hepatocyte	liver:	n/a
29	chr1:246582116-246582166	MCF10A-Er-Src	breast:	n/a
30	chr1:246599230-246599280	MCF-7	breast:	n/a
31	chr1:246599230-246599280	SKMC	muscle:	n/a
32	chr1:246581705-246581755	H1-hESC	embryonic stem cell:	embryo
33	chr1:246582116-246582166	LNCaP	prostate:	n/a
34	chr1:246582071-246582121	PANC-1	pancreas:	n/a
35	chr1:246582035-246582085	AG09319	gingival:	n/a
36	chr1:246582071-246582121	K562	blood:	n/a
37	chr1:246599230-246599280	HAEpiC	amniotic membrane:	n/a
38	chr1:246592123-246592173	NH-A	brain:	n/a
39	chr1:246613311-246613361	NT2-D1	testis:	n/a
40	chr1:246580717-246580767	GM06990	blood:	n/a
41	chr1:246580717-246580767	Jurkat	blood:	n/a
42	chr1:246582035-246582085	HRCEpiC	kidney:	n/a
43	chr1:246582071-246582121	HIPEpiC	eye:	n/a
44	chr1:246592123-246592173	AG09309	skin:	n/a
45	chr1:246581705-246581755	MCF-7	breast:	n/a
46	chr1:246582035-246582085	AG10803	skin:	n/a
47	chr1:246592123-246592173	Caco-2	colon:	n/a
48	chr1:246599230-246599280	NH-A	brain:	n/a
49	chr1:246582035-246582085	NHBE	bronchial:	n/a
50	chr1:246582116-246582166	HNPCEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246280440..246281134-chr1:246613800..246614445,2	MCF-7	breast:
2	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
3	chr1:246587797..246590207-chr1:246590613..246593809,3	K562	blood:
4	chr1:246601270..246602898-chr1:246608886..246610495,2	K562	blood:
5	chr1:246175245..246176233-chr1:246613342..246615151,4	MCF-7	breast:
6	chr1:246444872..246446533-chr1:246597803..246600502,2	MCF-7	breast:
7	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:
8	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
9	chr1:246579015..246582043-chr1:246583981..246587038,3	K562	blood:
10	chr1:246175508..246176198-chr1:246613763..246614605,2	K562	blood:
11	chr1:246601270..246602898-chr1:246608886..246610495,2	K562	blood:
12	chr1:246600615..246602867-chr1:246611265..246613184,2	K562	blood:
13	chr1:246174027..246176471-chr1:246609850..246611898,2	K562	blood:
14	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
15	chr1:246618350..246620200-chr1:246622120..246624573,2	K562	blood:
16	chr1:246576999..246579498-chr1:246580594..246582855,2	K562	blood:
17	chr1:246600615..246602867-chr1:246611265..246613184,2	K562	blood:
18	chr1:246606314..246608137-chr1:246622294..246625192,2	K562	blood:
19	chr1:246582285..246585491-chr1:246585683..246590369,6	K562	blood:
20	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:

No data

Variant related genes	Relation type
SMYD3	TF binding region
ENSG00000207326	TF binding region
SMYD3	CpG island
ENSG00000207326	CpG island
ENSG00000207326	chromatin interactions
ENSG00000185420	chromatin interactions

Extended variants
information (count: 1580 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1580 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4654110	chr1:246576661-246576662	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562552278	chr1:246576675-246576676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531563981	chr1:246576694-246576695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541979568	chr1:246576706-246576707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562188383	chr1:246576719-246576720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529263033	chr1:246576737-246576738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548115616	chr1:246576741-246576742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540298678	chr1:246576744-246576745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554291248	chr1:246576803-246576804	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs566012609	chr1:246576804-246576805	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs187266053	chr1:246576831-246576832	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs533266526	chr1:246576887-246576888	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs550057219	chr1:246576915-246576916	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs76918010	chr1:246576927-246576928	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs145698936	chr1:246576941-246576942	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs191846328	chr1:246576961-246576962	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs555208971	chr1:246576999-246577000	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183653117	chr1:246577005-246577006	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534175685	chr1:246577142-246577143	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187617150	chr1:246577235-246577236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565022897	chr1:246577237-246577238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs533383894	chr1:246577253-246577254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551579860	chr1:246577356-246577357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs374606997	chr1:246577364-246577365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138358138	chr1:246577398-246577399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs537158610	chr1:246577592-246577593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs539761038	chr1:246577596-246577597	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141298077	chr1:246577627-246577628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576054866	chr1:246577646-246577647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145017801	chr1:246577651-246577652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs193253199	chr1:246577718-246577719	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs572495915	chr1:246577729-246577730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548794262	chr1:246577739-246577740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567298665	chr1:246577781-246577782	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs371064057	chr1:246577797-246577798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185726525	chr1:246577813-246577814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544484874	chr1:246577837-246577838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376882946	chr1:246577845-246577846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs12082021	chr1:246577853-246577854	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs550130095	chr1:246577884-246577885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563562695	chr1:246577886-246577887	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs57946769	chr1:246577924-246577925	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35633135	chr1:246577925-246577926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77318145	chr1:246577962-246577963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs578009062	chr1:246577975-246577976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs367920220	chr1:246578007-246578008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs74985478	chr1:246578008-246578009	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs79041610	chr1:246578018-246578019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs76540934	chr1:246578019-246578020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74840785	chr1:246578022-246578023	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246554600-246594800	Weak transcription	Right Ventricle	heart
2	chr1:246557200-246590800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:246560200-246580600	Weak transcription	Primary T cells from cord blood	blood
4	chr1:246560400-246580200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:246564600-246578400	Weak transcription	Osteobl	bone
6	chr1:246568000-246578400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:246571000-246580400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:246573000-246576800	Weak transcription	Aorta	Aorta
9	chr1:246575800-246580200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:246576400-246588600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr1:246576600-246577400	Enhancers	K562	blood
12	chr1:246576800-246577200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:246576800-246577200	ZNF genes & repeats	Aorta	Aorta
14	chr1:246577000-246577200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:246577000-246577200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:246577200-246588600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr1:246577200-246588600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr1:246577200-246588600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:246577400-246577600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr1:246578400-246578800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:246578400-246578800	Flanking Active TSS	Osteobl	bone
22	chr1:246578600-246580200	Enhancers	NHDF-Ad	bronchial
23	chr1:246578800-246579600	Active TSS	Osteobl	bone
24	chr1:246578800-246579800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:246578800-246584000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:246579000-246585000	Weak transcription	Ovary	ovary
27	chr1:246579200-246580600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr1:246579200-246580800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr1:246579200-246582000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:246579400-246580000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:246579400-246581200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:246579600-246579800	Flanking Active TSS	Osteobl	bone
33	chr1:246579600-246580200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:246579600-246584200	Weak transcription	Pancreas	Pancrea
35	chr1:246579600-246584800	Weak transcription	Primary B cells from peripheral blood	blood
36	chr1:246579800-246580000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:246579800-246580000	Enhancers	NHEK	skin
38	chr1:246579800-246580000	Active TSS	Osteobl	bone
39	chr1:246580000-246580200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:246580000-246580400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:246580000-246580400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:246580000-246581000	Flanking Active TSS	Osteobl	bone
43	chr1:246580000-246581400	Enhancers	Brain Substantia Nigra	brain
44	chr1:246580000-246581400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr1:246580000-246581800	ZNF genes & repeats	NHEK	skin
46	chr1:246580000-246592000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr1:246580200-246580400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:246580200-246581000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:246580200-246581000	Flanking Active TSS	NHDF-Ad	bronchial
50	chr1:246580200-246581200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin

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