Variant report

Variant	nsv871943
Chromosome Location	chr1:57784144-57855876
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:489)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:57850364-57850571	HepG2	liver:	n/a	chr1:57850477-57850488
2	CEBPB	chr1:57850432-57850554	A549	lung:	n/a	chr1:57850477-57850488
3	CEBPB	chr1:57801786-57801796	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:57790959-57791153	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:57784917-57785205	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:57790923-57791211	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:57810407-57810538	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:57849385-57849579	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:57790819-57791252	HepG2	liver:	n/a	n/a
10	CTCF	chr1:57806460-57806610	HMEC	breast:	n/a	n/a
11	CTCF	chr1:57788880-57789030	HEEpiC	esophagus:	n/a	n/a
12	CTCF	chr1:57806463-57806550	NHEK	skin:	n/a	n/a
13	CTCF	chr1:57843575-57843798	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:57788900-57789050	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr1:57788905-57789017	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:57833931-57833934	Fibrobl	skin:	n/a	n/a
17	CTCF	chr1:57815267-57815548	K562	blood:	n/a	n/a
18	CTCF	chr1:57815376-57815469	HepG2	liver:	n/a	n/a
19	CTCF	chr1:57833869-57833923	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr1:57843443-57843821	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:57843620-57843770	Caco-2	colon:	n/a	n/a
22	CTCF	chr1:57806380-57806530	GM12874	blood:	n/a	n/a
23	CTCF	chr1:57788940-57789090	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr1:57833840-57833990	HepG2	liver:	n/a	n/a
25	CTCF	chr1:57815365-57815471	LNCaP	prostate:	n/a	n/a
26	CTCF	chr1:57806398-57806555	LNCaP	prostate:	n/a	n/a
27	CTCF	chr1:57832940-57833090	Caco-2	colon:	n/a	n/a
28	CTCF	chr1:57806420-57806570	NHEK	skin:	n/a	n/a
29	CTCF	chr1:57806360-57806510	SAEC	small airway:	n/a	n/a
30	CTCF	chr1:57843428-57843788	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:57806390-57806626	K562	blood:	n/a	n/a
32	CTCF	chr1:57788820-57788970	HEK293	kidney:	n/a	n/a
33	CTCF	chr1:57806340-57806490	HepG2	liver:	n/a	n/a
34	CTCF	chr1:57843520-57843670	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr1:57843621-57843675	K562	blood:	n/a	n/a
36	CTCF	chr1:57806420-57806570	SAEC	small airway:	n/a	n/a
37	CTCF	chr1:57788969-57789029	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:57806437-57806572	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:57806440-57806590	HMEC	breast:	n/a	n/a
40	CTCF	chr1:57806420-57806570	HRE	kidney:	n/a	n/a
41	CTCF	chr1:57788936-57789003	NHEK	skin:	n/a	n/a
42	CTCF	chr1:57843560-57843710	HEK293	kidney:	n/a	n/a
43	CTCF	chr1:57806340-57806490	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr1:57806457-57806465	K562	blood:	n/a	n/a
45	CTCF	chr1:57806340-57806490	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr1:57788960-57789110	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:57843520-57843670	K562	blood:	n/a	n/a
48	CTCF	chr1:57806420-57806570	Caco-2	colon:	n/a	n/a
49	CTCF	chr1:57788918-57788994	HepG2	liver:	n/a	n/a
50	CTCF	chr1:57788960-57789110	HMF	breast:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:57816236-57816286	Caco-2	colon:	n/a
2	chr1:57816236-57816286	Caco-2	colon:	n/a
3	chr1:57822544-57822594	NHBE	bronchial:	n/a
4	chr1:57790248-57790298	AG10803	skin:	n/a
5	chr1:57790248-57790298	HMEC	breast:	n/a
6	chr1:57816236-57816286	HUVEC	blood vessel:	n/a
7	chr1:57802279-57802329	HEEpiC	esophagus:	n/a
8	chr1:57836927-57836977	HRE	kidney:	n/a
9	chr1:57816236-57816286	HMEC	breast:	n/a
10	chr1:57816236-57816286	AG10803	skin:	n/a
11	chr1:57819219-57819269	HEK293	kidney:	embryo
12	chr1:57785036-57785086	T-47D	breast:	n/a
13	chr1:57790248-57790298	HepG2	liver:	n/a
14	chr1:57809419-57809469	Jurkat	blood:	n/a
15	chr1:57809419-57809469	NH-A	brain:	n/a
16	chr1:57822544-57822594	HIPEpiC	eye:	n/a
17	chr1:57819219-57819269	MCF-7	breast:	n/a
18	chr1:57802279-57802329	HMEC	breast:	n/a
19	chr1:57802279-57802329	AG09319	gingival:	n/a
20	chr1:57809419-57809469	AG04449	skin:	fetal
21	chr1:57790248-57790298	HEEpiC	esophagus:	n/a
22	chr1:57836927-57836977	NT2-D1	testis:	n/a
23	chr1:57790248-57790298	NHBE	bronchial:	n/a
24	chr1:57819219-57819269	ECC-1	luminal epithelium:	n/a
25	chr1:57819219-57819269	AG04450	lung:	fetal
26	chr1:57816236-57816286	ProgFib	skin:	n/a
27	chr1:57819219-57819269	SAEC	small airway:	n/a
28	chr1:57816236-57816286	RPTEC	kidney:	n/a
29	chr1:57790248-57790298	HCM	heart:	n/a
30	chr1:57809419-57809469	BE2_C	brain:	n/a
31	chr1:57836927-57836977	HCM	heart:	n/a
32	chr1:57802279-57802329	ovcar-3	ovarian:	n/a
33	chr1:57822544-57822594	MCF-7	breast:	n/a
34	chr1:57809419-57809469	AG09319	gingival:	n/a
35	chr1:57790248-57790298	AoSMC	blood vessel:	n/a
36	chr1:57785036-57785086	HepG2	liver:	n/a
37	chr1:57816236-57816286	NB4	blood:	n/a
38	chr1:57836927-57836977	HMEC	breast:	n/a
39	chr1:57809419-57809469	HepG2	liver:	n/a
40	chr1:57816236-57816286	SK-N-SH_RA	brain:	n/a
41	chr1:57802279-57802329	HUVEC	blood vessel:	n/a
42	chr1:57785036-57785086	H1-hESC	embryonic stem cell:	embryo
43	chr1:57809419-57809469	AG09309	skin:	n/a
44	chr1:57816236-57816286	Hela-S3	cervix:	n/a
45	chr1:57816236-57816286	HIPEpiC	eye:	n/a
46	chr1:57836927-57836977	SK-N-MC	brain:	n/a
47	chr1:57822544-57822594	NH-A	brain:	n/a
48	chr1:57809419-57809469	PANC-1	pancreas:	n/a
49	chr1:57836927-57836977	Jurkat	blood:	n/a
50	chr1:57819219-57819269	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:57798562..57800179-chr1:57803164..57805312,2	K562	blood:
2	chr1:57798562..57800179-chr1:57803164..57805312,2	K562	blood:
3	chr1:57797489..57800179-chr1:57802405..57805312,2	K562	blood:
4	chr1:57793484..57795323-chr1:57799611..57801917,2	K562	blood:
5	chr1:57793484..57795323-chr1:57799611..57801917,2	K562	blood:
6	chr1:57797489..57800179-chr1:57802405..57805312,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8A-3	chr1:57852562-57853122	ENSG00000227935
2	lnc-C8A-3	chr1:57852248-57852394	ENSG00000227935

No data

Variant related genes	Relation type
ENSG00000227935	TF binding region
ENSG00000227935	CpG island

Extended variants
information (count: 2867 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2867 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs746937	chr1:57784144-57784145	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144808829	chr1:57784177-57784178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556797045	chr1:57784196-57784197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183716441	chr1:57784213-57784214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542854559	chr1:57784225-57784226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs55727998	chr1:57784237-57784238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188477821	chr1:57784255-57784256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539917883	chr1:57784274-57784275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148160531	chr1:57784311-57784312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143094882	chr1:57784317-57784318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146157025	chr1:57784338-57784339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140001852	chr1:57784342-57784343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181429411	chr1:57784393-57784394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140099133	chr1:57784402-57784403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576903553	chr1:57784403-57784404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201205725	chr1:57784404-57784405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533148481	chr1:57784424-57784425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373435399	chr1:57784425-57784426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562133799	chr1:57784426-57784427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201415053	chr1:57784427-57784428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529554498	chr1:57784434-57784435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374845	chr1:57784445-57784446	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs80305863	chr1:57784492-57784493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77213812	chr1:57784499-57784500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534476186	chr1:57784500-57784501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189997305	chr1:57784511-57784512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74074918	chr1:57784550-57784551	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs536602270	chr1:57784607-57784608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556538046	chr1:57784638-57784639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115510744	chr1:57784639-57784640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs94216	chr1:57784669-57784670	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182226398	chr1:57784699-57784700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186507429	chr1:57784724-57784725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150849312	chr1:57784763-57784764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76002459	chr1:57784766-57784767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533366764	chr1:57784781-57784782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543881693	chr1:57784785-57784786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563661828	chr1:57784838-57784839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529626207	chr1:57784860-57784861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139332290	chr1:57784897-57784898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115493640	chr1:57784898-57784899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528643023	chr1:57784903-57784904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551065796	chr1:57784941-57784942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4557995	chr1:57784965-57784966	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs149925724	chr1:57784987-57784988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs439378	chr1:57784989-57784990	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs401065	chr1:57785043-57785044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs390203	chr1:57785048-57785049	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs552960373	chr1:57785049-57785050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77576034	chr1:57785054-57785055	Weak transcription Enhancers	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
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57773200-57790200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:57776600-57790200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:57779800-57784800	Weak transcription	Fetal Intestine Large	intestine
4	chr1:57779800-57784800	Weak transcription	Fetal Intestine Small	intestine
5	chr1:57780400-57784600	Weak transcription	Brain Angular Gyrus	brain
6	chr1:57780400-57787000	Weak transcription	Fetal Brain Male	brain
7	chr1:57782000-57784600	Weak transcription	Fetal Brain Female	brain
8	chr1:57784000-57785000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:57784000-57785400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:57784600-57784800	Enhancers	Brain Angular Gyrus	brain
11	chr1:57784600-57785000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:57784600-57785200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:57784600-57785200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:57784600-57785200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:57784600-57785200	Enhancers	Fetal Muscle Leg	muscle
16	chr1:57784600-57785400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:57784600-57785400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:57784600-57785400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:57784600-57785400	Enhancers	Fetal Brain Female	brain
20	chr1:57784600-57785600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr1:57784600-57785600	Enhancers	Hela-S3	cervix
22	chr1:57784600-57785800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr1:57784600-57785800	Enhancers	Fetal Lung	lung
24	chr1:57784600-57786000	Enhancers	Duodenum Mucosa	Duodenum
25	chr1:57784800-57785200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:57784800-57785200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:57784800-57785200	Enhancers	HMEC	breast
28	chr1:57784800-57785400	Enhancers	NHEK	skin
29	chr1:57784800-57785600	Weak transcription	Brain Angular Gyrus	brain
30	chr1:57784800-57785600	Enhancers	Fetal Stomach	stomach
31	chr1:57784800-57786000	Enhancers	Fetal Intestine Large	intestine
32	chr1:57784800-57786000	Enhancers	Fetal Intestine Small	intestine
33	chr1:57785000-57785400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:57785200-57790000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr1:57785200-57793800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:57785400-57790400	Weak transcription	Fetal Brain Female	brain
37	chr1:57785600-57785800	Enhancers	Brain Angular Gyrus	brain
38	chr1:57786000-57787000	Weak transcription	Fetal Intestine Large	intestine
39	chr1:57786000-57789800	Weak transcription	Fetal Intestine Small	intestine
40	chr1:57786000-57790200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr1:57787000-57787200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:57787000-57787200	Enhancers	Fetal Brain Male	brain
43	chr1:57787000-57787600	Enhancers	Fetal Intestine Large	intestine
44	chr1:57787200-57793800	Weak transcription	Fetal Brain Male	brain
45	chr1:57787400-57787600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr1:57787600-57789800	Weak transcription	Fetal Intestine Large	intestine
47	chr1:57789800-57790400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:57789800-57792400	Enhancers	Fetal Intestine Small	intestine
49	chr1:57789800-57792600	Enhancers	Fetal Intestine Large	intestine
50	chr1:57790000-57790800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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