Variant report

Variant	esv3431786
Chromosome Location	chr1:119977797-120005821
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	BACH1	chr1:119991492-119991514	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr1:119985662-119985676	K562	blood:	n/a	n/a
3	BHLHE40	chr1:119999982-120000347	GM12878	blood:	n/a	n/a
4	CEBPB	chr1:119989437-119989685	IMR90	lung:	n/a	chr1:119989575-119989586 chr1:119989575-119989588 chr1:119989577-119989588 chr1:119989650-119989662
5	CEBPB	chr1:119989454-119989731	K562	blood:	n/a	chr1:119989575-119989586 chr1:119989575-119989588 chr1:119989577-119989588 chr1:119989650-119989662
6	CEBPB	chr1:119989509-119989688	HepG2	liver:	n/a	chr1:119989575-119989586 chr1:119989575-119989588 chr1:119989577-119989588 chr1:119989650-119989662
7	CTCF	chr1:119990860-119991010	HUVEC	blood vessel:	n/a	chr1:119990868-119990889
8	CTCF	chr1:119990864-119990982	GM19239	blood:	n/a	chr1:119990868-119990889
9	CTCF	chr1:119991200-119991350	HVMF	connective:	n/a	n/a
10	CTCF	chr1:119992705-119992871	GM12892	blood:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
11	CTCF	chr1:119992740-119992890	Hela-S3	cervix:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
12	CTCF	chr1:119990809-119991057	MCF-7	breast:	n/a	chr1:119990868-119990889
13	CTCF	chr1:119992744-119992746	ProgFib	skin:	n/a	n/a
14	CTCF	chr1:119990900-119991050	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:119990920-119991070	GM12873	blood:	n/a	n/a
16	CTCF	chr1:119990880-119991030	HCM	heart:	n/a	n/a
17	CTCF	chr1:119990880-119991030	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr1:119992700-119992850	GM12874	blood:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
19	CTCF	chr1:119990865-119991086	K562	blood:	n/a	chr1:119990868-119990889
20	CTCF	chr1:119992690-119992839	LNCaP	prostate:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
21	CTCF	chr1:119992673-119992894	H1-hESC	embryonic stem cell:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
22	CTCF	chr1:119990820-119990970	GM12867	blood:	n/a	chr1:119990868-119990889
23	CTCF	chr1:119992680-119992830	AG09309	skin:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
24	CTCF	chr1:119990828-119991022	Fibrobl	skin:	n/a	chr1:119990868-119990889
25	CTCF	chr1:119992760-119992910	GM12872	blood:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
26	CTCF	chr1:119990840-119991035	GM19238	blood:	n/a	chr1:119990868-119990889
27	CTCF	chr1:119990856-119991015	A549	lung:	n/a	chr1:119990868-119990889
28	CTCF	chr1:119990816-119991035	Gliobla	brain:	n/a	chr1:119990868-119990889
29	CTCF	chr1:119980940-119981090	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr1:119990900-119991050	K562	blood:	n/a	n/a
31	CTCF	chr1:119992701-119992880	GM12878	blood:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
32	CTCF	chr1:119992686-119992885	MCF-7	breast:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
33	CTCF	chr1:119992720-119992870	Caco-2	colon:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
34	CTCF	chr1:119990817-119991045	MCF-7	breast:	n/a	chr1:119990868-119990889
35	CTCF	chr1:119992680-119992830	HEEpiC	esophagus:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
36	CTCF	chr1:119990900-119991050	AG10803	skin:	n/a	n/a
37	CTCF	chr1:119990860-119991010	GM12871	blood:	n/a	chr1:119990868-119990889
38	CTCF	chr1:119990820-119990970	HRPEpiC	eye:	n/a	chr1:119990868-119990889
39	CTCF	chr1:119992620-119992770	GM12866	blood:	n/a	chr1:119992667-119992685
40	CTCF	chr1:119992800-119992950	AG10803	skin:	n/a	n/a
41	CTCF	chr1:119990780-119990930	GM12868	blood:	n/a	chr1:119990868-119990889
42	CTCF	chr1:119990813-119991046	HepG2	liver:	n/a	chr1:119990868-119990889
43	CTCF	chr1:119992668-119992893	MCF-7	breast:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
44	CTCF	chr1:119990840-119990990	GM12865	blood:	n/a	chr1:119990868-119990889
45	CTCF	chr1:119990820-119990970	AG09319	gingival:	n/a	chr1:119990868-119990889
46	CTCF	chr1:119992720-119992870	HMF	breast:	n/a	chr1:119992787-119992800 chr1:119992786-119992807
47	CTCF	chr1:119990900-119991050	HAc	cerebellar:	n/a	n/a
48	CTCF	chr1:119992641-119992867	HepG2	liver:	n/a	chr1:119992667-119992685 chr1:119992787-119992800 chr1:119992786-119992807
49	CTCF	chr1:119990900-119991050	GM12864	blood:	n/a	n/a
50	CTCF	chr1:119990824-119991167	MCF-7	breast:	n/a	chr1:119990868-119990889

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:119981031-119981081	Hepatocyte	liver:	n/a
2	chr1:119981031-119981081	Jurkat	blood:	n/a
3	chr1:119982100-119982150	Hela-S3	cervix:	n/a
4	chr1:119981031-119981081	Hela-S3	cervix:	n/a
5	chr1:119982100-119982150	GM12878	blood:	n/a
6	chr1:119982100-119982150	HAEpiC	amniotic membrane:	n/a
7	chr1:119981031-119981081	HCF	heart:	n/a
8	chr1:119981031-119981081	ovcar-3	ovarian:	n/a
9	chr1:119981031-119981081	A549	lung:	n/a
10	chr1:119982100-119982150	HMEC	breast:	n/a
11	chr1:119982100-119982150	HCT-116	colon:	n/a
12	chr1:119981031-119981081	HMEC	breast:	n/a
13	chr1:119981031-119981081	HCT-116	colon:	n/a
14	chr1:119982100-119982150	PrEC	prostate:	n/a
15	chr1:119982100-119982150	Hepatocyte	liver:	n/a
16	chr1:119982100-119982150	NHBE	bronchial:	n/a
17	chr1:119982100-119982150	Jurkat	blood:	n/a
18	chr1:119981031-119981081	T-47D	breast:	n/a
19	chr1:119981031-119981081	GM12878	blood:	n/a
20	chr1:119981031-119981081	SK-N-SH	brain:	n/a
21	chr1:119981031-119981081	LNCaP	prostate:	n/a
22	chr1:119981031-119981081	NH-A	brain:	n/a
23	chr1:119982100-119982150	U87	brain:	n/a
24	chr1:119982100-119982150	GM12892	blood:	n/a
25	chr1:119982100-119982150	SK-N-SH_RA	brain:	n/a
26	chr1:119982100-119982150	ProgFib	skin:	n/a
27	chr1:119982100-119982150	NT2-D1	testis:	n/a
28	chr1:119982100-119982150	PFSK-1	brain:	n/a
29	chr1:119981031-119981081	AG09319	gingival:	n/a
30	chr1:119982100-119982150	HEEpiC	esophagus:	n/a
31	chr1:119981031-119981081	AG09309	skin:	n/a
32	chr1:119982100-119982150	HRPEpiC	eye:	n/a
33	chr1:119982100-119982150	SAEC	small airway:	n/a
34	chr1:119981031-119981081	ECC-1	luminal epithelium:	n/a
35	chr1:119981031-119981081	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:119982100-119982150	IMR90	lung:	fetal
37	chr1:119982100-119982150	HCM	heart:	n/a
38	chr1:119981031-119981081	HRPEpiC	eye:	n/a
39	chr1:119982100-119982150	HNPCEpiC	eye:	n/a
40	chr1:119981031-119981081	HNPCEpiC	eye:	n/a
41	chr1:119982100-119982150	Caco-2	colon:	n/a
42	chr1:119982100-119982150	AG09319	gingival:	n/a
43	chr1:119982100-119982150	HRE	kidney:	n/a
44	chr1:119982100-119982150	AoSMC	blood vessel:	n/a
45	chr1:119982100-119982150	AG09309	skin:	n/a
46	chr1:119981031-119981081	PFSK-1	brain:	n/a
47	chr1:119981031-119981081	H1-hESC	embryonic stem cell:	embryo
48	chr1:119982100-119982150	CMK	blood:	n/a
49	chr1:119981031-119981081	RPTEC	kidney:	n/a
50	chr1:119981031-119981081	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:119975044..119977179-chr1:119989940..119992153,2	MCF-7	breast:
2	chr1:119971252..119974055-chr1:119989493..119992356,2	MCF-7	breast:
3	chr1:119993879..119996617-chr1:119997198..119998785,2	K562	blood:
4	chr1:119915031..119915964-chr1:119992237..119993475,3	MCF-7	breast:
5	chr1:119993879..119996617-chr1:119997198..119998785,2	K562	blood:
6	chr1:119992181..119992827-chr1:120018455..120019108,2	MCF-7	breast:

Variant related genes	Relation type
HSD3BP1	TF binding region
HSD3BP2	TF binding region
GAPDHP23	TF binding region
ENSG00000232780	TF binding region
HSD3BP1	CpG island
HSD3BP2	CpG island
GAPDHP23	CpG island
ENSG00000232780	CpG island

Extended variants
information (count: 1043 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1043 , 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	rs587774893	chr1:119977797-119977798	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs1417609	chr1:119977806-119977807	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs141176666	chr1:119977821-119977822	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs1417608	chr1:119977833-119977834	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs587677897	chr1:119977834-119977835	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs587707588	chr1:119977965-119977966	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs587612105	chr1:119978007-119978008	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs146929013	chr1:119978031-119978032	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs151018821	chr1:119978032-119978033	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs587624537	chr1:119978079-119978080	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs183053333	chr1:119978093-119978094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140871045	chr1:119978124-119978125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370823406	chr1:119978187-119978188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587672579	chr1:119978252-119978253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587616056	chr1:119978270-119978271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372881654	chr1:119978281-119978282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587748401	chr1:119978283-119978284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587629779	chr1:119978322-119978323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370847177	chr1:119978332-119978333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587774929	chr1:119978344-119978345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587662303	chr1:119978351-119978352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188386656	chr1:119978374-119978375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587772671	chr1:119978381-119978382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587649326	chr1:119978432-119978433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs57778712	chr1:119978459-119978460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs377200367	chr1:119978484-119978485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370116390	chr1:119978510-119978511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7555375	chr1:119978577-119978578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs201035410	chr1:119978590-119978591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587706093	chr1:119978636-119978637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191576078	chr1:119978657-119978658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374349460	chr1:119978665-119978666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587661283	chr1:119978721-119978722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183827933	chr1:119978741-119978742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587596554	chr1:119978750-119978751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34324308	chr1:119978763-119978764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188620612	chr1:119978778-119978779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587731281	chr1:119978829-119978830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587623033	chr1:119978860-119978861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201771031	chr1:119978861-119978862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587766558	chr1:119978868-119978869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587641656	chr1:119978901-119978902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587721699	chr1:119978923-119978924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1417607	chr1:119978924-119978925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs587658406	chr1:119978927-119978928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587632504	chr1:119979023-119979024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115533796	chr1:119979030-119979031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138598020	chr1:119979061-119979062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587641360	chr1:119979083-119979084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12402935	chr1:119979121-119979122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:119974600-119980800	Weak transcription	Fetal Intestine Small	intestine
2	chr1:119975200-119980600	Weak transcription	Fetal Intestine Large	intestine
3	chr1:119977400-119977800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:119977400-119978200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:119977400-119978200	Enhancers	HMEC	breast
6	chr1:119977600-119978000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:119977600-119978000	Enhancers	NHDF-Ad	bronchial
8	chr1:119977600-119978200	Enhancers	NHEK	skin
9	chr1:119978000-119979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:119979400-119979600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:119979400-119979600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:119980400-119981000	Enhancers	Adipose Nuclei	Adipose
13	chr1:119980600-119986800	Enhancers	Fetal Intestine Large	intestine
14	chr1:119980800-119982000	Enhancers	Fetal Intestine Small	intestine
15	chr1:119981000-119981600	Weak transcription	Adipose Nuclei	Adipose
16	chr1:119981600-119981800	Enhancers	Adipose Nuclei	Adipose
17	chr1:119981800-119982800	Enhancers	Liver	Liver
18	chr1:119982000-119984400	Weak transcription	Fetal Intestine Small	intestine
19	chr1:119983200-119983600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:119983400-119983800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr1:119983400-119983800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr1:119983400-119984000	Enhancers	Fetal Lung	lung
23	chr1:119983400-119984200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:119983600-119984200	Enhancers	Ovary	ovary
25	chr1:119983800-119993200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr1:119984200-119988800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:119984400-119986400	Enhancers	Fetal Intestine Small	intestine
28	chr1:119985200-119985800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:119985200-119985800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:119985200-119985800	Enhancers	Pancreas	Pancrea
31	chr1:119985200-119985800	Enhancers	NHEK	skin
32	chr1:119986200-119995800	Weak transcription	Right Atrium	heart
33	chr1:119986400-119988400	Weak transcription	Fetal Intestine Small	intestine
34	chr1:119986800-119987600	Weak transcription	Fetal Intestine Large	intestine
35	chr1:119987600-119990400	Enhancers	Fetal Intestine Large	intestine
36	chr1:119988400-119989800	Enhancers	Fetal Intestine Small	intestine
37	chr1:119988800-119989000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:119989000-119989400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:119989000-119991400	Enhancers	Liver	Liver
40	chr1:119989800-119993800	Weak transcription	Fetal Intestine Small	intestine
41	chr1:119990400-119993200	Weak transcription	Fetal Intestine Large	intestine
42	chr1:119991200-119991400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:119991400-119992800	Weak transcription	Liver	Liver
44	chr1:119991600-119992600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:119992600-119993000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:119992800-119993000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:119992800-119993400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:119992800-119993600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:119992800-119995600	Enhancers	Liver	Liver
50	chr1:119993000-119993400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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