Variant report

Variant	nsv527673
Chromosome Location	chr1:58526235-58531627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:123)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr1:58531305-58531353	GM12878	blood:	n/a	n/a
2	CEBPB	chr1:58531472-58531540	HepG2	liver:	n/a	n/a
3	CTCF	chr1:58531372-58531518	GM10266	blood:	n/a	n/a
4	CTCF	chr1:58531296-58531566	GM12891	blood:	n/a	n/a
5	CTCF	chr1:58531340-58531490	GM12869	blood:	n/a	n/a
6	CTCF	chr1:58531360-58531510	GM12875	blood:	n/a	n/a
7	CTCF	chr1:58531360-58531510	HMEC	breast:	n/a	n/a
8	CTCF	chr1:58531322-58531565	GM12892	blood:	n/a	n/a
9	CTCF	chr1:58531340-58531490	HepG2	liver:	n/a	n/a
10	CTCF	chr1:58531340-58531490	GM12872	blood:	n/a	n/a
11	CTCF	chr1:58531380-58531521	A549	lung:	n/a	n/a
12	CTCF	chr1:58530040-58530190	HepG2	liver:	n/a	n/a
13	CTCF	chr1:58531440-58531590	HepG2	liver:	n/a	n/a
14	CTCF	chr1:58531300-58531450	GM12873	blood:	n/a	n/a
15	CTCF	chr1:58531253-58531564	HepG2	liver:	n/a	n/a
16	CTCF	chr1:58531319-58531541	GM12878	blood:	n/a	n/a
17	CTCF	chr1:58531320-58531470	GM12866	blood:	n/a	n/a
18	CTCF	chr1:58531360-58531510	HEK293	kidney:	n/a	n/a
19	CTCF	chr1:58531360-58531510	GM12874	blood:	n/a	n/a
20	CTCF	chr1:58531340-58531490	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:58531396-58531445	GM20000	blood:	n/a	n/a
22	CTCF	chr1:58531440-58531590	GM12872	blood:	n/a	n/a
23	CTCF	chr1:58531322-58531527	HepG2	liver:	n/a	n/a
24	CTCF	chr1:58531400-58531550	GM12874	blood:	n/a	n/a
25	CTCF	chr1:58531340-58531490	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr1:58531320-58531470	GM12868	blood:	n/a	n/a
27	CTCF	chr1:58531364-58531469	GM10248	blood:	n/a	n/a
28	CTCF	chr1:58531520-58531670	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr1:58531360-58531510	GM12864	blood:	n/a	n/a
30	CTCF	chr1:58531347-58531516	K562	blood:	n/a	n/a
31	CTCF	chr1:58531349-58531519	Gliobla	brain:	n/a	n/a
32	CTCF	chr1:58530180-58530330	GM12872	blood:	n/a	n/a
33	CTCF	chr1:58531420-58531570	HEK293	kidney:	n/a	n/a
34	CTCF	chr1:58531340-58531490	GM12865	blood:	n/a	n/a
35	CTCF	chr1:58531218-58531616	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr1:58531360-58531510	Caco-2	colon:	n/a	n/a
37	CTCF	chr1:58531440-58531590	HMEC	breast:	n/a	n/a
38	CTCF	chr1:58531400-58531550	GM12869	blood:	n/a	n/a
39	CTCF	chr1:58531400-58531550	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr1:58530112-58530254	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr1:58531360-58531510	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr1:58531304-58531572	GM19239	blood:	n/a	n/a
43	CTCF	chr1:58531400-58531550	BE2_C	brain:	n/a	n/a
44	CTCF	chr1:58531380-58531530	GM12870	blood:	n/a	n/a
45	CTCF	chr1:58531350-58531505	LNCaP	prostate:	n/a	n/a
46	CTCF	chr1:58531380-58531530	GM12873	blood:	n/a	n/a
47	CTCF	chr1:58531372-58531491	GM13977	blood:	n/a	n/a
48	CTCF	chr1:58531340-58531490	GM06990	blood:	n/a	n/a
49	CTCF	chr1:58531360-58531510	GM12878	blood:	n/a	n/a
50	CTCF	chr1:58531352-58531521	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58530146-58530196	SK-N-SH_RA	brain:	n/a
2	chr1:58530146-58530196	HepG2	liver:	n/a
3	chr1:58530146-58530196	RPTEC	kidney:	n/a
4	chr1:58530146-58530196	MCF-7	breast:	n/a
5	chr1:58530146-58530196	HUVEC	blood vessel:	n/a
6	chr1:58530146-58530196	Caco-2	colon:	n/a
7	chr1:58530146-58530196	BE2_C	brain:	n/a
8	chr1:58530146-58530196	SK-N-MC	brain:	n/a
9	chr1:58530146-58530196	LNCaP	prostate:	n/a
10	chr1:58530146-58530196	HL-60	blood:	n/a
11	chr1:58530146-58530196	NHBE	bronchial:	n/a
12	chr1:58530146-58530196	ECC-1	luminal epithelium:	n/a
13	chr1:58530146-58530196	HCT-116	colon:	n/a
14	chr1:58530146-58530196	AG09319	gingival:	n/a
15	chr1:58530146-58530196	AG09309	skin:	n/a
16	chr1:58530146-58530196	HCM	heart:	n/a
17	chr1:58530146-58530196	CMK	blood:	n/a
18	chr1:58530146-58530196	NT2-D1	testis:	n/a
19	chr1:58530146-58530196	SK-N-SH	brain:	n/a
20	chr1:58530146-58530196	NHDF-neo	bronchial:	n/a
21	chr1:58530146-58530196	K562	blood:	n/a
22	chr1:58530146-58530196	Jurkat	blood:	n/a
23	chr1:58530146-58530196	GM12892	blood:	n/a
24	chr1:58530146-58530196	PrEC	prostate:	n/a
25	chr1:58530146-58530196	Hela-S3	cervix:	n/a
26	chr1:58530146-58530196	SKMC	muscle:	n/a
27	chr1:58530146-58530196	SAEC	small airway:	n/a
28	chr1:58530146-58530196	HAEpiC	amniotic membrane:	n/a
29	chr1:58530146-58530196	HRPEpiC	eye:	n/a
30	chr1:58530146-58530196	NH-A	brain:	n/a
31	chr1:58530146-58530196	GM19239	blood:	n/a
32	chr1:58530146-58530196	PANC-1	pancreas:	n/a
33	chr1:58530146-58530196	ProgFib	skin:	n/a
34	chr1:58530146-58530196	GM12878	blood:	n/a
35	chr1:58530146-58530196	AG04450	lung:	fetal
36	chr1:58530146-58530196	IMR90	lung:	fetal
37	chr1:58530146-58530196	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:58530146-58530196	HCPEpiC	choroid plexus:	n/a
39	chr1:58530146-58530196	AG10803	skin:	n/a
40	chr1:58530146-58530196	HNPCEpiC	eye:	n/a
41	chr1:58530146-58530196	A549	lung:	n/a
42	chr1:58530146-58530196	HRCEpiC	kidney:	n/a
43	chr1:58530146-58530196	BJ	skin:	n/a
44	chr1:58530146-58530196	T-47D	breast:	n/a
45	chr1:58530146-58530196	HEEpiC	esophagus:	n/a
46	chr1:58530146-58530196	MCF10A-Er-Src	breast:	n/a
47	chr1:58530146-58530196	HIPEpiC	eye:	n/a
48	chr1:58530146-58530196	AG04449	skin:	fetal
49	chr1:58530146-58530196	GM12891	blood:	n/a
50	chr1:58530146-58530196	Hepatocyte	liver:	n/a

No data

Variant related genes	Relation type
RPS26P15	TF binding region
RPS26P15	CpG island

Extended variants
information (count: 218 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:218 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10443242	chr1:58526235-58526236	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2764677	chr1:58526257-58526258	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs374866464	chr1:58526300-58526301	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs192977509	chr1:58526305-58526306	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs386631526	chr1:58526346-58526347	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs10443244	chr1:58526347-58526348	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs17116782	chr1:58526382-58526383	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530165750	chr1:58526415-58526416	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs10443245	chr1:58526416-58526417	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs10443246	chr1:58526421-58526422	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546298522	chr1:58526459-58526460	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs561864006	chr1:58526462-58526463	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538459623	chr1:58526470-58526471	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs552039620	chr1:58526472-58526473	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs368557314	chr1:58526475-58526476	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs184831319	chr1:58526532-58526533	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs370229909	chr1:58526533-58526534	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs374244044	chr1:58526537-58526538	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs537381314	chr1:58526579-58526580	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533838299	chr1:58526653-58526654	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs553931921	chr1:58526677-58526678	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs573441958	chr1:58526690-58526691	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs528881038	chr1:58526696-58526697	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs565574722	chr1:58526702-58526703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2025616	chr1:58526746-58526747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs376613309	chr1:58526754-58526755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11207162	chr1:58526758-58526759	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs530061537	chr1:58526772-58526773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72906523	chr1:58526826-58526827	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs144104738	chr1:58526835-58526836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577768975	chr1:58526837-58526838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2025617	chr1:58526854-58526855	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs552002761	chr1:58526859-58526860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568804761	chr1:58526910-58526911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376921685	chr1:58526941-58526942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2025618	chr1:58526964-58526965	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548191531	chr1:58526965-58526966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568021951	chr1:58526968-58526969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557273798	chr1:58527019-58527020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190121282	chr1:58527071-58527072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192096573	chr1:58527085-58527086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370965583	chr1:58527091-58527092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533569416	chr1:58527112-58527113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184551592	chr1:58527175-58527176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577058765	chr1:58527315-58527316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539225677	chr1:58527377-58527378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559153882	chr1:58527406-58527407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs5774394	chr1:58527438-58527439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397708710	chr1:58527439-58527440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201700263	chr1:58527456-58527457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58524600-58526800	Enhancers	Fetal Brain Male	brain
2	chr1:58525200-58526600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:58525200-58526800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr1:58525400-58526400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:58525400-58526800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:58525600-58526600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:58525600-58526800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:58525800-58526600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr1:58525800-58529800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:58525800-58531600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr1:58526000-58526600	Weak transcription	Fetal Brain Female	brain
12	chr1:58526000-58530000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr1:58526400-58527200	Enhancers	Adipose Nuclei	Adipose
14	chr1:58526400-58529800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:58526600-58527400	Enhancers	Fetal Brain Female	brain
16	chr1:58526600-58530000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:58526600-58531200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr1:58526800-58528200	Weak transcription	Fetal Brain Male	brain
19	chr1:58526800-58531400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:58527400-58530200	Weak transcription	Fetal Brain Female	brain
21	chr1:58528000-58529200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:58528000-58529400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr1:58528000-58529400	Enhancers	HMEC	breast
24	chr1:58528000-58529400	Enhancers	NHEK	skin
25	chr1:58528000-58529600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:58528200-58528400	Enhancers	Fetal Brain Male	brain
27	chr1:58528200-58529200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:58528400-58529000	Weak transcription	Fetal Brain Male	brain
29	chr1:58528600-58529000	Enhancers	Hela-S3	cervix
30	chr1:58529000-58530400	Enhancers	Fetal Brain Male	brain
31	chr1:58529400-58531400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:58529600-58531400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:58529800-58530000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr1:58529800-58530200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr1:58529800-58530400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:58530000-58530400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr1:58530000-58530400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:58530000-58530600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr1:58530000-58532600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:58530200-58530400	Enhancers	Fetal Brain Female	brain
41	chr1:58530400-58531200	Weak transcription	Fetal Brain Female	brain
42	chr1:58530400-58531400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:58530400-58532800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr1:58530600-58531000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr1:58531000-58531600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:58531200-58532600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:58531200-58532800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr1:58531400-58531600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:58531400-58531800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:58531400-58531800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links