Variant report

Variant	nsv523574
Chromosome Location	chr1:58018103-58087789
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:58063178-58063197	K562	blood:	n/a	n/a
2	BHLHE40	chr1:58086631-58086962	HepG2	liver:	n/a	n/a
3	CEBPB	chr1:58057416-58057954	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:58082341-58082590	HepG2	liver:	n/a	chr1:58082424-58082435 chr1:58082394-58082407
5	CEBPB	chr1:58087547-58087831	HepG2	liver:	n/a	chr1:58087680-58087691 chr1:58087679-58087692 chr1:58087678-58087695
6	CEBPB	chr1:58058579-58058899	HepG2	liver:	n/a	chr1:58058738-58058749
7	CEBPB	chr1:58058603-58058831	A549	lung:	n/a	chr1:58058738-58058749
8	CEBPB	chr1:58058628-58058865	K562	blood:	n/a	chr1:58058738-58058749
9	CEBPB	chr1:58082349-58082548	A549	lung:	n/a	chr1:58082424-58082435 chr1:58082394-58082407
10	CEBPB	chr1:58057433-58057791	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:58058567-58058891	IMR90	lung:	n/a	chr1:58058738-58058749
12	CEBPB	chr1:58057454-58057785	HepG2	liver:	n/a	n/a
13	CTBP2	chr1:58065752-58066522	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:58049651-58049679	GM13977	blood:	n/a	n/a
15	CTCF	chr1:58086439-58086516	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:58023983-58024048	LNCaP	prostate:	n/a	n/a
17	CTCF	chr1:58086460-58086610	HEK293	kidney:	n/a	n/a
18	CTCF	chr1:58056108-58056145	GM10266	blood:	n/a	n/a
19	CTCF	chr1:58039720-58039870	GM12866	blood:	n/a	n/a
20	CTCF	chr1:58086360-58086510	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr1:58079120-58079270	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr1:58073500-58073650	GM12865	blood:	n/a	n/a
23	CTCF	chr1:58034856-58034980	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr1:58034861-58034980	GM10248	blood:	n/a	n/a
25	CTCF	chr1:58026804-58026845	LNCaP	prostate:	n/a	n/a
26	CTCF	chr1:58024340-58024490	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr1:58028420-58028465	GM13976	blood:	n/a	n/a
28	EP300	chr1:58086232-58086558	SK-N-SH_RA	brain:	n/a	chr1:58086477-58086493
29	EP300	chr1:58052376-58052911	SK-N-SH	brain:	n/a	chr1:58052487-58052501 chr1:58052481-58052495 chr1:58052412-58052426
30	FAM48A	chr1:58073611-58073720	GM12878	blood:	n/a	n/a
31	FOS	chr1:58020474-58020549	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:58057632-58057842	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:58067323-58067448	MCF10A-Er-Src	breast:	n/a	chr1:58067387-58067397 chr1:58067388-58067395 chr1:58067387-58067396 chr1:58067386-58067398 chr1:58067388-58067397
34	FOS	chr1:58081412-58082186	HUVEC	blood vessel:	n/a	n/a
35	FOXA1	chr1:58086606-58086886	HepG2	liver:	n/a	n/a
36	FOXA1	chr1:58042504-58042784	HepG2	liver:	n/a	chr1:58042668-58042683
37	FOXA2	chr1:58042519-58042766	HepG2	liver:	n/a	n/a
38	FOXA2	chr1:58029216-58029616	A549	lung:	n/a	n/a
39	FOXP2	chr1:58057443-58057967	SK-N-MC	brain:	n/a	n/a
40	GATA2	chr1:58052596-58052844	SH-SY5Y	brain:	n/a	n/a
41	GATA2	chr1:58044030-58044251	SH-SY5Y	brain:	n/a	n/a
42	GATA2	chr1:58086131-58086580	SH-SY5Y	brain:	n/a	chr1:58086270-58086291 chr1:58086275-58086285 chr1:58086277-58086284 chr1:58086277-58086284 chr1:58086277-58086284
43	GATA3	chr1:58052250-58053052	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr1:58052547-58053131	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr1:58087637-58087813	SH-SY5Y	brain:	n/a	chr1:58087687-58087708
46	GATA3	chr1:58052261-58053048	SK-N-SH	brain:	n/a	n/a
47	GTF2F1	chr1:58065475-58065485	H1-hESC	embryonic stem cell:	n/a	n/a
48	GTF2F1	chr1:58066291-58066405	H1-hESC	embryonic stem cell:	n/a	n/a
49	HDAC2	chr1:58066082-58066562	H1-hESC	embryonic stem cell:	n/a	chr1:58066325-58066339
50	JUN	chr1:58056678-58057037	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58063953-58064003	A549	lung:	n/a
2	chr1:58018699-58018749	HCPEpiC	choroid plexus:	n/a
3	chr1:58018699-58018749	Jurkat	blood:	n/a
4	chr1:58018699-58018749	A549	lung:	n/a
5	chr1:58063953-58064003	T-47D	breast:	n/a
6	chr1:58018699-58018749	HPAEpiC	pulmonary alveolar:	n/a
7	chr1:58018699-58018749	HRPEpiC	eye:	n/a
8	chr1:58018699-58018749	NHBE	bronchial:	n/a
9	chr1:58063953-58064003	PrEC	prostate:	n/a
10	chr1:58018699-58018749	K562	blood:	n/a
11	chr1:58018699-58018749	HMEC	breast:	n/a
12	chr1:58018699-58018749	AG04449	skin:	fetal
13	chr1:58018699-58018749	HEK293	kidney:	embryo
14	chr1:58018699-58018749	GM19239	blood:	n/a
15	chr1:58018699-58018749	BE2_C	brain:	n/a
16	chr1:58018699-58018749	SK-N-SH_RA	brain:	n/a
17	chr1:58018699-58018749	GM12878	blood:	n/a
18	chr1:58018699-58018749	HCF	heart:	n/a
19	chr1:58063953-58064003	HUVEC	blood vessel:	n/a
20	chr1:58018699-58018749	H1-hESC	embryonic stem cell:	embryo
21	chr1:58063953-58064003	SAEC	small airway:	n/a
22	chr1:58018699-58018749	Hepatocyte	liver:	n/a
23	chr1:58018699-58018749	GM12891	blood:	n/a
24	chr1:58063953-58064003	HCPEpiC	choroid plexus:	n/a
25	chr1:58063953-58064003	LNCaP	prostate:	n/a
26	chr1:58063953-58064003	SK-N-SH	brain:	n/a
27	chr1:58018699-58018749	HepG2	liver:	n/a
28	chr1:58063953-58064003	MCF-7	breast:	n/a
29	chr1:58063953-58064003	HCT-116	colon:	n/a
30	chr1:58063953-58064003	Jurkat	blood:	n/a
31	chr1:58063953-58064003	HAEpiC	amniotic membrane:	n/a
32	chr1:58018699-58018749	HCM	heart:	n/a
33	chr1:58063953-58064003	HCF	heart:	n/a
34	chr1:58063953-58064003	Hela-S3	cervix:	n/a
35	chr1:58018699-58018749	CMK	blood:	n/a
36	chr1:58063953-58064003	CMK	blood:	n/a
37	chr1:58063953-58064003	SK-N-SH_RA	brain:	n/a
38	chr1:58063953-58064003	GM19239	blood:	n/a
39	chr1:58018699-58018749	SK-N-MC	brain:	n/a
40	chr1:58063953-58064003	HCM	heart:	n/a
41	chr1:58018699-58018749	RPTEC	kidney:	n/a
42	chr1:58063953-58064003	GM12878	blood:	n/a
43	chr1:58063953-58064003	AG04449	skin:	fetal
44	chr1:58018699-58018749	SAEC	small airway:	n/a
45	chr1:58063953-58064003	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:58063953-58064003	SKMC	muscle:	n/a
47	chr1:58063953-58064003	NHBE	bronchial:	n/a
48	chr1:58063953-58064003	NHDF-neo	bronchial:	n/a
49	chr1:58063953-58064003	HEK293	kidney:	embryo
50	chr1:58018699-58018749	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:58083604..58085124-chr19:54704799..54707163,2	K562	blood:
2	chr1:57972252..57973978-chr1:58083473..58085053,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8B-3	chr1:58071519-58071878	NONHSAT003477

Variant related genes	Relation type
RPS20P5	TF binding region
RPS20P5	CpG island
ENSG00000170889	chromatin interactions

Extended variants
information (count: 2164 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2164 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1341319	chr1:58018103-58018104	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377643586	chr1:58018144-58018145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566716015	chr1:58018167-58018168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532196724	chr1:58018168-58018169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551883759	chr1:58018170-58018171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187916310	chr1:58018177-58018178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191422420	chr1:58018187-58018188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557092213	chr1:58018193-58018194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567281749	chr1:58018245-58018246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138483284	chr1:58018246-58018247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183953821	chr1:58018266-58018267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374568025	chr1:58018305-58018306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373114433	chr1:58018310-58018311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572694994	chr1:58018312-58018313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573143476	chr1:58018330-58018331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545258009	chr1:58018379-58018380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4475776	chr1:58018447-58018448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17115991	chr1:58018456-58018457	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575268126	chr1:58018472-58018473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544263508	chr1:58018478-58018479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189793899	chr1:58018492-58018493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192762529	chr1:58018575-58018576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184972158	chr1:58018578-58018579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17115993	chr1:58018588-58018589	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532362923	chr1:58018626-58018627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189858046	chr1:58018645-58018646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181573521	chr1:58018688-58018689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530918777	chr1:58018737-58018738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371707475	chr1:58018764-58018765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571640752	chr1:58018776-58018777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72914825	chr1:58018790-58018791	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs567370138	chr1:58018816-58018817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536237294	chr1:58018818-58018819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553288712	chr1:58018824-58018825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567033242	chr1:58018869-58018870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539294134	chr1:58018870-58018871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144084105	chr1:58018888-58018889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575744227	chr1:58018902-58018903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537587374	chr1:58018918-58018919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186067200	chr1:58018949-58018950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574517701	chr1:58018953-58018954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573556961	chr1:58018967-58018968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535482527	chr1:58018977-58018978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7413600	chr1:58019001-58019002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7417730	chr1:58019011-58019012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7417766	chr1:58019021-58019022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7417767	chr1:58019025-58019026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs28397657	chr1:58019033-58019034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368467261	chr1:58019037-58019038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7417768	chr1:58019040-58019041	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

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
Developmental delay	21147756	CNVD

Chromatin state (count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58015800-58018800	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr1:58015800-58020200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:58016800-58018200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:58017200-58019400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:58017600-58020000	Weak transcription	Stomach Mucosa	stomach
6	chr1:58017800-58019400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:58017800-58019400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr1:58017800-58019800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr1:58018000-58019200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr1:58018000-58019400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr1:58018200-58019400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:58018800-58019200	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr1:58019200-58019600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr1:58019200-58020200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr1:58019400-58019600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:58019400-58020000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:58019400-58020000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr1:58019400-58020000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr1:58019400-58020000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:58019400-58020200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr1:58019600-58019800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr1:58019800-58020200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:58020000-58020400	Enhancers	Stomach Mucosa	stomach
24	chr1:58020200-58024000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:58024000-58024200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:58037000-58039200	Weak transcription	Stomach Mucosa	stomach
27	chr1:58037400-58038200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr1:58038200-58042000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:58039200-58046800	Enhancers	Stomach Mucosa	stomach
30	chr1:58040600-58040800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:58041000-58042000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:58041400-58041600	Enhancers	Small Intestine	intestine
33	chr1:58041600-58042600	Weak transcription	Small Intestine	intestine
34	chr1:58042000-58042800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:58042000-58043000	Enhancers	Fetal Intestine Small	intestine
36	chr1:58042000-58044200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:58042000-58044800	Enhancers	Duodenum Mucosa	Duodenum
38	chr1:58042200-58042600	Enhancers	Fetal Intestine Large	intestine
39	chr1:58042600-58043400	Enhancers	Small Intestine	intestine
40	chr1:58042600-58043600	Weak transcription	Fetal Intestine Large	intestine
41	chr1:58042800-58051600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr1:58043000-58043800	Weak transcription	Fetal Intestine Small	intestine
43	chr1:58043800-58044000	Enhancers	Fetal Intestine Large	intestine
44	chr1:58043800-58044200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr1:58043800-58044800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:58044000-58044200	Enhancers	Fetal Intestine Small	intestine
47	chr1:58044200-58045000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:58044400-58044800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr1:58044400-58045200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr1:58046800-58049200	Weak transcription	Stomach Mucosa	stomach

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