Variant report

Variant	nsv1008205
Chromosome Location	chr1:58349005-58375261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:46)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:46 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr1:58359457-58359471	GM12878	blood:	n/a	n/a
2	CTCF	chr1:58364260-58364410	WERI-Rb-1	eye:	n/a	n/a
3	CTCF	chr1:58364318-58364439	Medullo	brain:	n/a	n/a
4	CTCF	chr1:58371320-58371470	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr1:58364300-58364450	HRPEpiC	eye:	n/a	n/a
6	E2F6	chr1:58372733-58373287	H1-hESC	embryonic stem cell:	n/a	n/a
7	EBF1	chr1:58365979-58366282	GM12878	blood:	n/a	chr1:58366137-58366150 chr1:58366139-58366148 chr1:58366139-58366149 chr1:58366139-58366148
8	EP300	chr1:58374273-58374593	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr1:58374310-58374641	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr1:58348694-58349472	SK-N-SH_RA	brain:	n/a	chr1:58349340-58349354
11	EP300	chr1:58348667-58349295	SK-N-SH_RA	brain:	n/a	n/a
12	FAM48A	chr1:58356319-58356432	GM12878	blood:	n/a	n/a
13	FOS	chr1:58360063-58360299	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr1:58360020-58360290	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr1:58356493-58356497	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr1:58355463-58355546	MCF10A-Er-Src	breast:	n/a	n/a
17	GATA3	chr1:58362499-58362540	SH-SY5Y	brain:	n/a	n/a
18	JUND	chr1:58356287-58356484	HepG2	liver:	n/a	chr1:58356392-58356403
19	KAP1	chr1:58353596-58354205	HEK293	kidney:	n/a	n/a
20	KAP1	chr1:58353527-58354198	U2OS	brain:	n/a	n/a
21	MAX	chr1:58360186-58360386	H1-hESC	embryonic stem cell:	n/a	n/a
22	MYC	chr1:58360091-58360307	MCF10A-Er-Src	breast:	n/a	n/a
23	MYC	chr1:58360091-58360497	MCF10A-Er-Src	breast:	n/a	chr1:58360453-58360462
24	POLR2A	chr1:58360365-58360431	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr1:58360245-58360391	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr1:58352525-58352680	GM12878	blood:	n/a	n/a
27	POLR2A	chr1:58364105-58364189	GM12878	blood:	n/a	n/a
28	POLR2A	chr1:58369295-58369461	GM12878	blood:	n/a	n/a
29	RAD21	chr1:58374224-58374594	SK-N-SH_RA	brain:	n/a	n/a
30	REST	chr1:58374086-58374598	PFSK-1	brain:	n/a	n/a
31	REST	chr1:58374068-58374480	PFSK-1	brain:	n/a	n/a
32	SPI1	chr1:58359982-58360302	HL-60	blood:	n/a	n/a
33	SPI1	chr1:58359909-58360329	HL-60	blood:	n/a	n/a
34	STAT3	chr1:58363114-58363264	MCF10A-Er-Src	breast:	n/a	n/a
35	STAT3	chr1:58374056-58374147	MCF10A-Er-Src	breast:	n/a	chr1:58374108-58374116
36	STAT3	chr1:58369720-58369775	MCF10A-Er-Src	breast:	n/a	chr1:58369723-58369730
37	TCF7L2	chr1:58353622-58354046	HEK293	kidney:	n/a	n/a
38	TEAD4	chr1:58371418-58371706	H1-hESC	embryonic stem cell:	n/a	n/a
39	TEAD4	chr1:58363232-58363531	H1-hESC	embryonic stem cell:	n/a	n/a
40	TEAD4	chr1:58363151-58363573	H1-hESC	embryonic stem cell:	n/a	n/a
41	UBTF	chr1:58374469-58374539	K562	blood:	n/a	n/a
42	USF2	chr1:58350363-58350552	HepG2	liver:	n/a	n/a
43	WRNIP1	chr1:58360476-58360550	GM12878	blood:	n/a	n/a
44	YY1	chr1:58374348-58374675	SK-N-SH_RA	brain:	n/a	n/a
45	YY1	chr1:58374231-58374763	SK-N-SH_RA	brain:	n/a	n/a
46	ZNF263	chr1:58373785-58374362	HEK293-T-REx	kidney:	n/a	chr1:58374139-58374148

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58353581-58353631	PrEC	prostate:	n/a
2	chr1:58353581-58353631	ECC-1	luminal epithelium:	n/a
3	chr1:58353581-58353631	GM19239	blood:	n/a
4	chr1:58353581-58353631	AoSMC	blood vessel:	n/a
5	chr1:58353581-58353631	Hela-S3	cervix:	n/a
6	chr1:58353581-58353631	NH-A	brain:	n/a
7	chr1:58353581-58353631	SK-N-MC	brain:	n/a
8	chr1:58353581-58353631	T-47D	breast:	n/a
9	chr1:58353581-58353631	HCF	heart:	n/a
10	chr1:58353581-58353631	MCF-7	breast:	n/a
11	chr1:58353581-58353631	SKMC	muscle:	n/a
12	chr1:58353581-58353631	HRPEpiC	eye:	n/a
13	chr1:58353581-58353631	SK-N-SH_RA	brain:	n/a
14	chr1:58353581-58353631	GM06990	blood:	n/a
15	chr1:58353581-58353631	Caco-2	colon:	n/a
16	chr1:58353581-58353631	ovcar-3	ovarian:	n/a
17	chr1:58353581-58353631	AG09309	skin:	n/a
18	chr1:58353581-58353631	NB4	blood:	n/a
19	chr1:58353581-58353631	HCPEpiC	choroid plexus:	n/a
20	chr1:58353581-58353631	GM12878	blood:	n/a
21	chr1:58353581-58353631	PFSK-1	brain:	n/a
22	chr1:58353581-58353631	BJ	skin:	n/a
23	chr1:58353581-58353631	GM12892	blood:	n/a
24	chr1:58353581-58353631	AG04450	lung:	fetal
25	chr1:58353581-58353631	K562	blood:	n/a
26	chr1:58353581-58353631	H1-hESC	embryonic stem cell:	embryo
27	chr1:58353581-58353631	HepG2	liver:	n/a
28	chr1:58353581-58353631	HUVEC	blood vessel:	n/a
29	chr1:58353581-58353631	Jurkat	blood:	n/a
30	chr1:58353581-58353631	RPTEC	kidney:	n/a
31	chr1:58353581-58353631	HCT-116	colon:	n/a
32	chr1:58353581-58353631	GM12891	blood:	n/a
33	chr1:58353581-58353631	PANC-1	pancreas:	n/a
34	chr1:58353581-58353631	ProgFib	skin:	n/a
35	chr1:58353581-58353631	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:58353581-58353631	HEEpiC	esophagus:	n/a
37	chr1:58353581-58353631	NT2-D1	testis:	n/a
38	chr1:58353581-58353631	AG10803	skin:	n/a
39	chr1:58353581-58353631	IMR90	lung:	fetal
40	chr1:58353581-58353631	HIPEpiC	eye:	n/a
41	chr1:58353581-58353631	A549	lung:	n/a
42	chr1:58353581-58353631	HAEpiC	amniotic membrane:	n/a
43	chr1:58353581-58353631	HRE	kidney:	n/a
44	chr1:58353581-58353631	Hepatocyte	liver:	n/a
45	chr1:58353581-58353631	NHDF-neo	bronchial:	n/a
46	chr1:58353581-58353631	SAEC	small airway:	n/a
47	chr1:58353581-58353631	HL-60	blood:	n/a
48	chr1:58353581-58353631	AG09319	gingival:	n/a
49	chr1:58353581-58353631	HEK293	kidney:	embryo
50	chr1:58353581-58353631	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:58358016..58360181-chr1:58361121..58362700,2	MCF-7	breast:
2	chr1:58362313..58365047-chr1:58367118..58369976,3	K562	blood:
3	chr1:58362313..58363892-chr1:58368338..58369976,2	K562	blood:
4	chr1:58362313..58363892-chr1:58368338..58369976,2	K562	blood:
5	chr1:58358016..58360181-chr1:58361121..58362700,2	MCF-7	breast:
6	chr1:58362313..58365047-chr1:58367118..58369976,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OMA1-4	chr1:58349671-58349757	NONHSAT003479

No data

Variant related genes	Relation type
DAB1	TF binding region
DAB1	CpG island

Extended variants
information (count: 1027 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1027 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1202824	chr1:58349005-58349006	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574758346	chr1:58349006-58349007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193252289	chr1:58349039-58349040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560649648	chr1:58349044-58349045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146948863	chr1:58349062-58349063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552328653	chr1:58349120-58349121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562993423	chr1:58349136-58349137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542553904	chr1:58349139-58349140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557259940	chr1:58349140-58349141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531843694	chr1:58349167-58349168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548360771	chr1:58349185-58349186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568286225	chr1:58349293-58349294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35767358	chr1:58349297-58349298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115165275	chr1:58349358-58349359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547656162	chr1:58349400-58349401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570700348	chr1:58349432-58349433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143190087	chr1:58349448-58349449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115879857	chr1:58349468-58349469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569371879	chr1:58349480-58349481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535191257	chr1:58349497-58349498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554713704	chr1:58349523-58349524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148583445	chr1:58349534-58349535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540458579	chr1:58349637-58349638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141978330	chr1:58349698-58349699	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs113400719	chr1:58349715-58349716	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs150693967	chr1:58349719-58349720	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs562746370	chr1:58349728-58349729	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs531804065	chr1:58349763-58349764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184022707	chr1:58349808-58349809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562201504	chr1:58349912-58349913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187815365	chr1:58349952-58349953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547324320	chr1:58350034-58350035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527679951	chr1:58350042-58350043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556269473	chr1:58350048-58350049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570679685	chr1:58350057-58350058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139673521	chr1:58350112-58350113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149780738	chr1:58350144-58350145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71642142	chr1:58350196-58350197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528434012	chr1:58350198-58350199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116078217	chr1:58350239-58350240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555029558	chr1:58350279-58350280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191145028	chr1:58350287-58350288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565477514	chr1:58350294-58350295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183700680	chr1:58350296-58350297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201557425	chr1:58350322-58350323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375871505	chr1:58350344-58350345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1202825	chr1:58350364-58350365	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146809552	chr1:58350399-58350400	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373564366	chr1:58350421-58350422	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs529943137	chr1:58350523-58350524	Enhancers Weak transcription	TF binding region	1 gene(s)	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
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58346000-58349600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:58346800-58349400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:58346800-58350000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:58347400-58349600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr1:58347800-58359600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:58348200-58353400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:58348800-58349800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:58349000-58349600	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr1:58349400-58355600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:58349600-58350600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:58349600-58355400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:58350000-58353400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:58350600-58373800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:58353200-58354400	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr1:58353400-58354000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr1:58353400-58354800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:58353600-58353800	Enhancers	NH-A	brain
18	chr1:58353600-58354000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr1:58353600-58354200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr1:58353600-58354200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:58353600-58359800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr1:58353800-58354000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr1:58353800-58354000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:58353800-58354200	Enhancers	Fetal Intestine Small	intestine
25	chr1:58353800-58354800	Weak transcription	NH-A	brain
26	chr1:58353800-58355400	Enhancers	Fetal Intestine Large	intestine
27	chr1:58354000-58354200	Enhancers	HMEC	breast
28	chr1:58354000-58355200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:58354000-58358200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr1:58354000-58358400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr1:58354200-58355200	Weak transcription	HMEC	breast
32	chr1:58354200-58358200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr1:58354200-58358600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:58354400-58358200	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr1:58354800-58356000	Enhancers	NH-A	brain
36	chr1:58354800-58359800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:58355000-58355400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:58355000-58356200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr1:58355200-58356000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:58355200-58356000	Enhancers	HMEC	breast
41	chr1:58355400-58356400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr1:58355600-58356000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:58355600-58356000	Enhancers	NHEK	skin
44	chr1:58355600-58356200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:58355800-58356000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:58355800-58356000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:58356000-58358400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:58356000-58358400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:58356000-58358600	Weak transcription	HMEC	breast
50	chr1:58356000-58358600	Weak transcription	NHEK	skin

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