Variant report

Variant	nsv1002980
Chromosome Location	chr1:246569732-246635324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:636)
CpG islands
(count:671)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246614088-246614383	HepG2	liver:	n/a	chr1:246614110-246614126
2	ARID3A	chr1:246591789-246592119	K562	blood:	n/a	n/a
3	ARID3A	chr1:246614048-246614417	K562	blood:	n/a	chr1:246614110-246614126
4	ARID3A	chr1:246587912-246588291	K562	blood:	n/a	n/a
5	ATF1	chr1:246591887-246592268	K562	blood:	n/a	n/a
6	ATF1	chr1:246589653-246589853	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	chr1:246591816-246592158	GM12878	blood:	n/a	n/a
12	BATF	chr1:246591880-246592213	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:246591909-246592164	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:246591893-246592220	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:246580932-246580933	K562	blood:	n/a	n/a
16	BHLHE40	chr1:246588462-246588796	K562	blood:	n/a	n/a
17	BHLHE40	chr1:246591822-246592280	K562	blood:	n/a	n/a
18	BRCA1	chr1:246598938-246599254	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr1:246622436-246622858	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr1:246611654-246611998	K562	blood:	n/a	n/a
21	CBX3	chr1:246588426-246589002	K562	blood:	n/a	n/a
22	CBX3	chr1:246591794-246592269	K562	blood:	n/a	n/a
23	CBX3	chr1:246591771-246592290	K562	blood:	n/a	n/a
24	CBX3	chr1:246582052-246582537	K562	blood:	n/a	n/a
25	CBX3	chr1:246580386-246580871	K562	blood:	n/a	n/a
26	CBX3	chr1:246576729-246577165	K562	blood:	n/a	n/a
27	CBX3	chr1:246581941-246582555	K562	blood:	n/a	n/a
28	CCNT2	chr1:246588441-246589002	K562	blood:	n/a	n/a
29	CEBPB	chr1:246633988-246634252	Hela-S3	cervix:	n/a	chr1:246634078-246634089
30	CEBPB	chr1:246588404-246588847	K562	blood:	n/a	n/a
31	CEBPB	chr1:246598404-246598904	A549	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
32	CEBPB	chr1:246633942-246634262	K562	blood:	n/a	chr1:246634078-246634089
33	CEBPB	chr1:246598407-246598920	K562	blood:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
34	CEBPB	chr1:246591895-246592281	K562	blood:	n/a	n/a
35	CEBPB	chr1:246598407-246599012	IMR90	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
36	CEBPB	chr1:246624833-246625067	HepG2	liver:	n/a	chr1:246624986-246624997
37	CEBPB	chr1:246614170-246614380	A549	lung:	n/a	n/a
38	CEBPB	chr1:246614101-246614437	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:246598435-246599408	H1-hESC	embryonic stem cell:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
40	CEBPB	chr1:246624876-246625076	K562	blood:	n/a	chr1:246624986-246624997
41	CEBPB	chr1:246591815-246592267	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:246598418-246598737	HepG2	liver:	n/a	chr1:246598665-246598678
43	CEBPB	chr1:246633921-246634267	IMR90	lung:	n/a	chr1:246634078-246634089
44	CEBPB	chr1:246633927-246634250	A549	lung:	n/a	chr1:246634078-246634089
45	CEBPB	chr1:246598491-246599425	Hela-S3	cervix:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
46	CEBPB	chr1:246633906-246634251	HepG2	liver:	n/a	chr1:246634078-246634089
47	CEBPB	chr1:246591783-246592270	K562	blood:	n/a	n/a
48	CEBPB	chr1:246624890-246625084	HepG2	liver:	n/a	chr1:246624986-246624997
49	CEBPB	chr1:246624828-246625147	IMR90	lung:	n/a	chr1:246624986-246624997
50	CEBPD	chr1:246588409-246588903	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246580717-246580767	Caco-2	colon:	n/a
2	chr1:246582116-246582166	HCF	heart:	n/a
3	chr1:246613311-246613361	SAEC	small airway:	n/a
4	chr1:246622633-246622683	AoSMC	blood vessel:	n/a
5	chr1:246581705-246581755	MCF10A-Er-Src	breast:	n/a
6	chr1:246582035-246582085	NB4	blood:	n/a
7	chr1:246582071-246582121	ECC-1	luminal epithelium:	n/a
8	chr1:246622662-246622712	GM12878	blood:	n/a
9	chr1:246599230-246599280	GM12891	blood:	n/a
10	chr1:246622633-246622683	HMEC	breast:	n/a
11	chr1:246622633-246622683	AG04449	skin:	fetal
12	chr1:246599230-246599280	HMEC	breast:	n/a
13	chr1:246599230-246599280	Hela-S3	cervix:	n/a
14	chr1:246599230-246599280	GM19239	blood:	n/a
15	chr1:246581705-246581755	NHBE	bronchial:	n/a
16	chr1:246581705-246581755	AG04450	lung:	fetal
17	chr1:246582116-246582166	NHDF-neo	bronchial:	n/a
18	chr1:246613311-246613361	LNCaP	prostate:	n/a
19	chr1:246622483-246622533	Hepatocyte	liver:	n/a
20	chr1:246582035-246582085	PANC-1	pancreas:	n/a
21	chr1:246581705-246581755	HRPEpiC	eye:	n/a
22	chr1:246622483-246622533	A549	lung:	n/a
23	chr1:246599230-246599280	AoSMC	blood vessel:	n/a
24	chr1:246581705-246581755	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:246599230-246599280	CMK	blood:	n/a
26	chr1:246613311-246613361	Hela-S3	cervix:	n/a
27	chr1:246592123-246592173	ovcar-3	ovarian:	n/a
28	chr1:246622662-246622712	CMK	blood:	n/a
29	chr1:246581705-246581755	NB4	blood:	n/a
30	chr1:246622633-246622683	HRE	kidney:	n/a
31	chr1:246582071-246582121	MCF10A-Er-Src	breast:	n/a
32	chr1:246622662-246622712	AG04449	skin:	fetal
33	chr1:246581705-246581755	U87	brain:	n/a
34	chr1:246592123-246592173	AG04449	skin:	fetal
35	chr1:246622662-246622712	A549	lung:	n/a
36	chr1:246582116-246582166	HEEpiC	esophagus:	n/a
37	chr1:246582116-246582166	AG09309	skin:	n/a
38	chr1:246581705-246581755	Caco-2	colon:	n/a
39	chr1:246622633-246622683	AG09309	skin:	n/a
40	chr1:246599230-246599280	NHBE	bronchial:	n/a
41	chr1:246582116-246582166	SK-N-SH	brain:	n/a
42	chr1:246581705-246581755	HCPEpiC	choroid plexus:	n/a
43	chr1:246580717-246580767	HUVEC	blood vessel:	n/a
44	chr1:246592123-246592173	H1-hESC	embryonic stem cell:	embryo
45	chr1:246592123-246592173	HIPEpiC	eye:	n/a
46	chr1:246592123-246592173	GM19239	blood:	n/a
47	chr1:246622483-246622533	SAEC	small airway:	n/a
48	chr1:246580717-246580767	NHDF-neo	bronchial:	n/a
49	chr1:246581705-246581755	K562	blood:	n/a
50	chr1:246592123-246592173	HCF	heart:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246576999..246579498-chr1:246580594..246582855,2	K562	blood:
2	chr1:246174027..246176471-chr1:246609850..246611898,2	K562	blood:
3	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:
4	chr1:246601270..246602898-chr1:246608886..246610495,2	K562	blood:
5	chr1:246606314..246608137-chr1:246622294..246625192,2	K562	blood:
6	chr1:246606314..246608137-chr1:246622294..246625192,2	K562	blood:
7	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
8	chr1:246582285..246585491-chr1:246585683..246590369,6	K562	blood:
9	chr1:246618350..246620200-chr1:246622120..246624573,2	K562	blood:
10	chr1:246175245..246176233-chr1:246613342..246615151,4	MCF-7	breast:
11	chr1:246579015..246582043-chr1:246583981..246587038,3	K562	blood:
12	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:
13	chr1:246444872..246446533-chr1:246597803..246600502,2	MCF-7	breast:
14	chr1:246600615..246602867-chr1:246611265..246613184,2	K562	blood:
15	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
16	chr1:246175508..246176198-chr1:246613763..246614605,2	K562	blood:
17	chr1:246618350..246620200-chr1:246622120..246624573,2	K562	blood:
18	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
19	chr1:246601270..246602898-chr1:246608886..246610495,2	K562	blood:
20	chr1:246280440..246281134-chr1:246613800..246614445,2	MCF-7	breast:
21	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
22	chr1:246587797..246590207-chr1:246590613..246593809,3	K562	blood:
23	chr1:246600615..246602867-chr1:246611265..246613184,2	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: 2507 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11805778	chr1:246569758-246569759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182081194	chr1:246569779-246569780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186843392	chr1:246569877-246569878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113165876	chr1:246569884-246569885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560885813	chr1:246569922-246569923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141456613	chr1:246569935-246569936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6672203	chr1:246569963-246569964	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs111981143	chr1:246570000-246570001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562544771	chr1:246570001-246570002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146312337	chr1:246570007-246570008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550515605	chr1:246570020-246570021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548441585	chr1:246570054-246570055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548291340	chr1:246570058-246570059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191275769	chr1:246570063-246570064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116540869	chr1:246570116-246570117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547272381	chr1:246570117-246570118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570767091	chr1:246570127-246570128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181297910	chr1:246570132-246570133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536295851	chr1:246570143-246570144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552800566	chr1:246570148-246570149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372434798	chr1:246570155-246570156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6682121	chr1:246570169-246570170	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs139476700	chr1:246570173-246570174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534251274	chr1:246570187-246570188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538891618	chr1:246570199-246570200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570302020	chr1:246570204-246570205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115582629	chr1:246570222-246570223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540861573	chr1:246570242-246570243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560529432	chr1:246570256-246570257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577319702	chr1:246570268-246570269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111561613	chr1:246570278-246570279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185076331	chr1:246570367-246570368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189883502	chr1:246570386-246570387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570812526	chr1:246570414-246570415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183188483	chr1:246570419-246570420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145001587	chr1:246570435-246570436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373005739	chr1:246570436-246570437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6666645	chr1:246570448-246570449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs527776472	chr1:246570451-246570452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556803660	chr1:246570490-246570491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192037649	chr1:246570512-246570513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539594440	chr1:246570514-246570515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574978159	chr1:246570519-246570520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550118003	chr1:246570528-246570529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76642375	chr1:246570586-246570587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535487248	chr1:246570642-246570643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555390222	chr1:246570693-246570694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76622204	chr1:246570721-246570722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534430273	chr1:246570726-246570727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557800879	chr1:246570747-246570748	Weak transcription	n/a	n/a	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:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr1:246575400-246575600	ZNF genes & repeats	Dnd41	blood
10	chr1:246575800-246580200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:246576400-246588600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:246576600-246577400	Enhancers	K562	blood
13	chr1:246576800-246577200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:246576800-246577200	ZNF genes & repeats	Aorta	Aorta
15	chr1:246577000-246577200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:246577000-246577200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:246577200-246588600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr1:246577200-246588600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr1:246577200-246588600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:246577400-246577600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr1:246578400-246578800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:246578400-246578800	Flanking Active TSS	Osteobl	bone
23	chr1:246578600-246580200	Enhancers	NHDF-Ad	bronchial
24	chr1:246578800-246579600	Active TSS	Osteobl	bone
25	chr1:246578800-246579800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:246578800-246584000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr1:246579000-246585000	Weak transcription	Ovary	ovary
28	chr1:246579200-246580600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr1:246579200-246580800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr1:246579200-246582000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr1:246579400-246580000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:246579400-246581200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:246579600-246579800	Flanking Active TSS	Osteobl	bone
34	chr1:246579600-246580200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:246579600-246584200	Weak transcription	Pancreas	Pancrea
36	chr1:246579600-246584800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr1:246579800-246580000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:246579800-246580000	Enhancers	NHEK	skin
39	chr1:246579800-246580000	Active TSS	Osteobl	bone
40	chr1:246580000-246580200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:246580000-246580400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:246580000-246580400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:246580000-246581000	Flanking Active TSS	Osteobl	bone
44	chr1:246580000-246581400	Enhancers	Brain Substantia Nigra	brain
45	chr1:246580000-246581400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr1:246580000-246581800	ZNF genes & repeats	NHEK	skin
47	chr1:246580000-246592000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr1:246580200-246580400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:246580200-246581000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:246580200-246581000	Flanking Active TSS	NHDF-Ad	bronchial

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