Variant report

Variant	nsv546852
Chromosome Location	chr1:95122518-95142843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:95134884-95134905	K562	blood:	n/a	n/a
2	ATF2	chr1:95126491-95127014	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:95123440-95123857	HCT-116	colon:	n/a	n/a
4	ATF3	chr1:95123472-95123678	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr1:95123460-95124186	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:95127192-95127290	K562	blood:	n/a	n/a
7	CEBPB	chr1:95123360-95123910	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:95126571-95127497	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:95123438-95124284	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
12	CEBPB	chr1:95127135-95127409	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:95132331-95132574	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:95123481-95123658	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:95123420-95123775	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:95123371-95123906	HCT-116	colon:	n/a	n/a
17	CEBPB	chr1:95123365-95124075	HCT-116	colon:	n/a	n/a
18	CHD2	chr1:95123457-95123663	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr1:95123362-95124002	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr1:95127052-95127160	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr1:95126260-95126410	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr1:95123720-95123870	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr1:95123800-95123950	AoAF	blood vessel:	n/a	n/a
25	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F6	chr1:95123421-95123759	H1-hESC	embryonic stem cell:	n/a	n/a
27	EGR1	chr1:95122454-95122959	HCT-116	colon:	n/a	chr1:95122617-95122630
28	EGR1	chr1:95122555-95122784	K562	blood:	n/a	chr1:95122617-95122630
29	EGR1	chr1:95122613-95122811	K562	blood:	n/a	chr1:95122617-95122630
30	EP300	chr1:95130100-95130300	Hela-S3	cervix:	n/a	n/a
31	EP300	chr1:95134844-95134975	K562	blood:	n/a	n/a
32	EP300	chr1:95123394-95123974	Hela-S3	cervix:	n/a	n/a
33	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
37	FOXA1	chr1:95131200-95131489	HepG2	liver:	n/a	chr1:95131350-95131365
38	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
39	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
41	GTF2F1	chr1:95126707-95126950	H1-hESC	embryonic stem cell:	n/a	n/a
42	GTF2F1	chr1:95123377-95124094	Hela-S3	cervix:	n/a	n/a
43	HDAC2	chr1:95132354-95132585	H1-hESC	embryonic stem cell:	n/a	n/a
44	HDAC2	chr1:95126394-95126878	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUND	chr1:95126541-95126955	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr1:95123521-95123706	H1-hESC	embryonic stem cell:	n/a	n/a
47	JUND	chr1:95123383-95124175	Hela-S3	cervix:	n/a	n/a
48	MAFF	chr1:95134814-95135118	K562	blood:	n/a	n/a
49	MAFF	chr1:95142674-95143010	HepG2	liver:	n/a	chr1:95142838-95142856
50	MAFF	chr1:95142755-95142907	K562	blood:	n/a	chr1:95142838-95142856

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95141800-95141850	PANC-1	pancreas:	n/a
2	chr1:95141800-95141850	AoSMC	blood vessel:	n/a
3	chr1:95133907-95133957	GM12878	blood:	n/a
4	chr1:95133907-95133957	Caco-2	colon:	n/a
5	chr1:95133907-95133957	GM19239	blood:	n/a
6	chr1:95133907-95133957	SK-N-SH_RA	brain:	n/a
7	chr1:95141800-95141850	IMR90	lung:	fetal
8	chr1:95141800-95141850	SAEC	small airway:	n/a
9	chr1:95133907-95133957	BJ	skin:	n/a
10	chr1:95141800-95141850	AG04449	skin:	fetal
11	chr1:95133907-95133957	PFSK-1	brain:	n/a
12	chr1:95133907-95133957	AoSMC	blood vessel:	n/a
13	chr1:95133907-95133957	HepG2	liver:	n/a
14	chr1:95141800-95141850	MCF-7	breast:	n/a
15	chr1:95141800-95141850	Caco-2	colon:	n/a
16	chr1:95133907-95133957	CMK	blood:	n/a
17	chr1:95141800-95141850	U87	brain:	n/a
18	chr1:95141800-95141850	HL-60	blood:	n/a
19	chr1:95133907-95133957	ECC-1	luminal epithelium:	n/a
20	chr1:95141800-95141850	A549	lung:	n/a
21	chr1:95133907-95133957	AG10803	skin:	n/a
22	chr1:95141800-95141850	HCPEpiC	choroid plexus:	n/a
23	chr1:95133907-95133957	HUVEC	blood vessel:	n/a
24	chr1:95141800-95141850	NT2-D1	testis:	n/a
25	chr1:95133907-95133957	AG09319	gingival:	n/a
26	chr1:95141800-95141850	SK-N-SH_RA	brain:	n/a
27	chr1:95133907-95133957	Hepatocyte	liver:	n/a
28	chr1:95141800-95141850	LNCaP	prostate:	n/a
29	chr1:95141800-95141850	HRE	kidney:	n/a
30	chr1:95133907-95133957	GM06990	blood:	n/a
31	chr1:95141800-95141850	GM06990	blood:	n/a
32	chr1:95133907-95133957	AG04449	skin:	fetal
33	chr1:95141800-95141850	HAEpiC	amniotic membrane:	n/a
34	chr1:95133907-95133957	HEEpiC	esophagus:	n/a
35	chr1:95141800-95141850	K562	blood:	n/a
36	chr1:95133907-95133957	Jurkat	blood:	n/a
37	chr1:95141800-95141850	AG09309	skin:	n/a
38	chr1:95133907-95133957	HRE	kidney:	n/a
39	chr1:95141800-95141850	NB4	blood:	n/a
40	chr1:95133907-95133957	HAEpiC	amniotic membrane:	n/a
41	chr1:95133907-95133957	H1-hESC	embryonic stem cell:	embryo
42	chr1:95133907-95133957	HRPEpiC	eye:	n/a
43	chr1:95133907-95133957	A549	lung:	n/a
44	chr1:95133907-95133957	LNCaP	prostate:	n/a
45	chr1:95141800-95141850	NH-A	brain:	n/a
46	chr1:95133907-95133957	BE2_C	brain:	n/a
47	chr1:95133907-95133957	HNPCEpiC	eye:	n/a
48	chr1:95141800-95141850	T-47D	breast:	n/a
49	chr1:95133907-95133957	HL-60	blood:	n/a
50	chr1:95133907-95133957	HPAEpiC	pulmonary alveolar:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
2	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
3	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
4	chr1:95130856..95133124-chr1:95137358..95139966,2	K562	blood:
5	chr1:95115535..95119175-chr1:95123580..95126438,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-2	chr1:95123530-95123608	NONHSAT004607
2	lnc-F3-2	chr1:95138492-95138827	NONHSAT004609
3	lnc-CNN3-3	chr1:95138685-95138827	ENSG00000224081.2
4	lnc-F3-2	chr1:95138492-95138827	NONHSAT004608
5	lnc-CNN3-3	chr1:95123089-95123611	ENSG00000224081.2
6	lnc-CNN3-3	chr1:95138453-95138827	ENSG00000224081.2
7	lnc-CNN3-3	chr1:95123762-95123806	ENSG00000224081.2
8	lnc-CNN3-3	chr1:95123481-95123611	ENSG00000224081.2

No data

Variant related genes	Relation type
LINC01057	TF binding region
PGBD4P7	TF binding region
LINC01057	CpG island
PGBD4P7	CpG island
ENSG00000244433	chromatin interactions
ENSG00000232857	chromatin interactions

Extended variants
information (count: 715 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17111996	chr1:95122518-95122519	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566583829	chr1:95122529-95122530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569122193	chr1:95122548-95122549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1772914	chr1:95122565-95122566	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs572332225	chr1:95122611-95122612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189330414	chr1:95122638-95122639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534435646	chr1:95122726-95122727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192472892	chr1:95122749-95122750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567954315	chr1:95122798-95122799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536519881	chr1:95122851-95122852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372808001	chr1:95122905-95122906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574919338	chr1:95122922-95122923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376016725	chr1:95122948-95122949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369561317	chr1:95122952-95122953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148296343	chr1:95122972-95122973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557615662	chr1:95122988-95122989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557469619	chr1:95123008-95123009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142950062	chr1:95123055-95123056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184795626	chr1:95123057-95123058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146134992	chr1:95123061-95123062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141526301	chr1:95123082-95123083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529202542	chr1:95123087-95123088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11584894	chr1:95123150-95123151	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs562750923	chr1:95123153-95123154	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs376513010	chr1:95123154-95123155	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs557470135	chr1:95123176-95123177	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs531786742	chr1:95123190-95123191	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs551791954	chr1:95123196-95123197	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs565389570	chr1:95123199-95123200	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs371420008	chr1:95123337-95123338	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs527740189	chr1:95123375-95123376	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs145445481	chr1:95123403-95123404	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs148406861	chr1:95123411-95123412	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs536830912	chr1:95123465-95123466	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs142528638	chr1:95123474-95123475	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs147635679	chr1:95123536-95123537	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs537454667	chr1:95123546-95123547	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs374713357	chr1:95123555-95123556	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs557283344	chr1:95123557-95123558	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs142314247	chr1:95123559-95123560	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs577740888	chr1:95123571-95123572	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs539990040	chr1:95123601-95123602	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs533617364	chr1:95123655-95123656	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553815036	chr1:95123708-95123709	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374899462	chr1:95123737-95123738	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs6667206	chr1:95123749-95123750	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs188867656	chr1:95123779-95123780	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs562813199	chr1:95123810-95123811	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573450187	chr1:95123820-95123821	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs145934287	chr1:95123855-95123856	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
Papillary thyroid carcinoma	21436994	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
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
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95114600-95123400	Weak transcription	NHDF-Ad	bronchial
2	chr1:95114600-95124000	Weak transcription	Small Intestine	intestine
3	chr1:95114600-95126600	Weak transcription	Esophagus	oesophagus
4	chr1:95114800-95123800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:95119000-95125000	Enhancers	Fetal Heart	heart
6	chr1:95119400-95123400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:95119400-95123400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:95119400-95123400	Weak transcription	Lung	lung
9	chr1:95119600-95123400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:95119600-95123400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:95119600-95125200	Enhancers	Hela-S3	cervix
12	chr1:95119600-95126400	Weak transcription	Left Ventricle	heart
13	chr1:95119800-95122600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:95119800-95123400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:95119800-95123400	Weak transcription	Aorta	Aorta
16	chr1:95119800-95123400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr1:95119800-95123400	Weak transcription	Right Atrium	heart
18	chr1:95120000-95123400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:95120000-95123400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:95120000-95123400	Weak transcription	Gastric	stomach
21	chr1:95120000-95123400	Weak transcription	Stomach Mucosa	stomach
22	chr1:95120000-95123600	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr1:95120000-95123800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr1:95120000-95126000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:95120000-95126600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:95120000-95126600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:95120200-95122800	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr1:95120400-95123400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:95120400-95123400	Weak transcription	A549	lung
30	chr1:95120400-95123600	Weak transcription	Colon Smooth Muscle	Colon
31	chr1:95120600-95123400	Weak transcription	Duodenum Mucosa	Duodenum
32	chr1:95120600-95123600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr1:95120600-95123600	Weak transcription	NHLF	lung
34	chr1:95120800-95122600	Weak transcription	NHEK	skin
35	chr1:95120800-95123400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:95120800-95123400	Weak transcription	Fetal Intestine Large	intestine
37	chr1:95120800-95123400	Weak transcription	Ovary	ovary
38	chr1:95120800-95123400	Weak transcription	HepG2	liver
39	chr1:95120800-95126400	Weak transcription	Pancreas	Pancrea
40	chr1:95121000-95122600	Weak transcription	HMEC	breast
41	chr1:95121000-95123400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:95121000-95126400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr1:95121200-95122600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:95121200-95122600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:95121600-95126200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:95122200-95123400	Weak transcription	Fetal Intestine Small	intestine
47	chr1:95122200-95124000	Enhancers	Placenta Amnion	Placenta Amnion
48	chr1:95122400-95122800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:95122400-95123000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:95122400-95123600	Enhancers	HUES6 Cell Line	embryonic stem cell

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