Variant report

Variant	nsv822963
Chromosome Location	chr5:1884480-1885198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTBP2	chr5:1882832-1885692	H1-hESC	embryonic stem cell:	n/a	n/a
2	EGR1	chr5:1884700-1884966	H1-hESC	embryonic stem cell:	n/a	n/a
3	FOS	chr5:1884338-1884711	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr5:1884302-1884787	MCF10A-Er-Src	breast:	n/a	n/a
5	FOS	chr5:1884358-1884637	MCF10A-Er-Src	breast:	n/a	n/a
6	HDAC2	chr5:1883649-1884545	MCF-7	breast:	n/a	chr5:1884495-1884514
7	MAX	chr5:1881356-1884611	HCT-116	colon:	n/a	chr5:1882349-1882358 chr5:1882349-1882358 chr5:1882351-1882360 chr5:1884034-1884044 chr5:1882349-1882358
8	MYC	chr5:1884255-1884801	MCF10A-Er-Src	breast:	n/a	n/a
9	MYC	chr5:1883027-1884765	MCF10A-Er-Src	breast:	n/a	chr5:1884034-1884044
10	POLR2A	chr5:1882409-1891588	MCF10A-Er-Src	breast:	n/a	n/a
11	POLR2A	chr5:1882926-1884900	H1-neurons	neurons:	n/a	n/a
12	POLR2A	chr5:1881481-1891348	MCF10A-Er-Src	breast:	n/a	n/a
13	POLR2A	chr5:1884107-1884856	H1-neurons	neurons:	n/a	n/a
14	SP1	chr5:1884691-1885071	H1-hESC	embryonic stem cell:	n/a	n/a
15	STAT3	chr5:1885079-1885337	MCF10A-Er-Src	breast:	n/a	n/a
16	STAT3	chr5:1884291-1884601	MCF10A-Er-Src	breast:	n/a	n/a
17	STAT3	chr5:1884348-1884553	MCF10A-Er-Src	breast:	n/a	n/a
18	STAT3	chr5:1884353-1884557	MCF10A-Er-Src	breast:	n/a	n/a
19	SUZ12	chr5:1885091-1887033	H1-hESC	embryonic stem cell:	n/a	n/a
20	SUZ12	chr5:1884073-1884494	H1-hESC	embryonic stem cell:	n/a	n/a
21	SUZ12	chr5:1882701-1884720	NT2-D1	testis:	n/a	n/a
22	ZNF143	chr5:1884757-1885262	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:1885174-1885224	GM06990	blood:	n/a
2	chr5:1885174-1885224	NH-A	brain:	n/a
3	chr5:1884513-1884563	ovcar-3	ovarian:	n/a
4	chr5:1884513-1884563	AG04449	skin:	fetal
5	chr5:1884513-1884563	BJ	skin:	n/a
6	chr5:1885174-1885224	HCT-116	colon:	n/a
7	chr5:1884513-1884563	PANC-1	pancreas:	n/a
8	chr5:1884513-1884563	NT2-D1	testis:	n/a
9	chr5:1884513-1884563	GM12891	blood:	n/a
10	chr5:1885174-1885224	NT2-D1	testis:	n/a
11	chr5:1885174-1885224	BE2_C	brain:	n/a
12	chr5:1884513-1884563	HUVEC	blood vessel:	n/a
13	chr5:1884513-1884563	IMR90	lung:	fetal
14	chr5:1884513-1884563	HCPEpiC	choroid plexus:	n/a
15	chr5:1884513-1884563	SKMC	muscle:	n/a
16	chr5:1885174-1885224	HUVEC	blood vessel:	n/a
17	chr5:1884513-1884563	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:1884513-1884563	NHBE	bronchial:	n/a
19	chr5:1885174-1885224	Caco-2	colon:	n/a
20	chr5:1884513-1884563	GM12892	blood:	n/a
21	chr5:1885174-1885224	CMK	blood:	n/a
22	chr5:1885174-1885224	HRCEpiC	kidney:	n/a
23	chr5:1885174-1885224	GM12891	blood:	n/a
24	chr5:1885174-1885224	RPTEC	kidney:	n/a
25	chr5:1885174-1885224	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:1885174-1885224	NHBE	bronchial:	n/a
27	chr5:1884513-1884563	CMK	blood:	n/a
28	chr5:1884513-1884563	HRE	kidney:	n/a
29	chr5:1884513-1884563	Hela-S3	cervix:	n/a
30	chr5:1884513-1884563	HIPEpiC	eye:	n/a
31	chr5:1884513-1884563	GM06990	blood:	n/a
32	chr5:1885174-1885224	HCM	heart:	n/a
33	chr5:1885174-1885224	HEK293	kidney:	embryo
34	chr5:1884513-1884563	HepG2	liver:	n/a
35	chr5:1885174-1885224	SK-N-SH_RA	brain:	n/a
36	chr5:1885174-1885224	HMEC	breast:	n/a
37	chr5:1885174-1885224	HCPEpiC	choroid plexus:	n/a
38	chr5:1884513-1884563	T-47D	breast:	n/a
39	chr5:1885174-1885224	T-47D	breast:	n/a
40	chr5:1885174-1885224	GM12892	blood:	n/a
41	chr5:1884513-1884563	HL-60	blood:	n/a
42	chr5:1884513-1884563	HRCEpiC	kidney:	n/a
43	chr5:1885174-1885224	SAEC	small airway:	n/a
44	chr5:1884513-1884563	SK-N-SH_RA	brain:	n/a
45	chr5:1885174-1885224	NB4	blood:	n/a
46	chr5:1884513-1884563	HNPCEpiC	eye:	n/a
47	chr5:1884513-1884563	MCF10A-Er-Src	breast:	n/a
48	chr5:1884513-1884563	AG10803	skin:	n/a
49	chr5:1885174-1885224	K562	blood:	n/a
50	chr5:1885174-1885224	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:1881475..1885354-chr5:1933918..1938503,4	MCF-7	breast:
2	chr5:1793765..1806799-chr5:1879445..1889322,45	MCF-7	breast:
3	chr5:1796457..1805482-chr5:1878036..1885786,21	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFS6-2	chr5:1884594-1884804	NONHSAT100075

No data

Variant related genes	Relation type
ENSG00000249326	TF binding region
IRX4	TF binding region
ENSG00000249326	CpG island
IRX4	CpG island
ENSG00000248994	chromatin interactions
ENSG00000171421	chromatin interactions
ENSG00000145494	chromatin interactions

Extended variants
information (count: 26 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563492309	chr5:1884532-1884533	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs140979757	chr5:1884603-1884604	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs113785908	chr5:1884606-1884607	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs547068412	chr5:1884617-1884618	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
5	rs72706718	chr5:1884638-1884639	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs191412813	chr5:1884676-1884677	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs546592984	chr5:1884718-1884719	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs568778734	chr5:1884729-1884730	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs536136412	chr5:1884802-1884803	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs111302613	chr5:1884803-1884804	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs569410466	chr5:1884828-1884829	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs539580619	chr5:1884923-1884924	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs557843157	chr5:1884926-1884927	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs200737902	chr5:1884932-1884933	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs572971582	chr5:1884990-1884991	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs533933444	chr5:1884991-1884992	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs555303269	chr5:1885005-1885006	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs59156267	chr5:1885034-1885035	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs372644932	chr5:1885064-1885065	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs563369084	chr5:1885102-1885103	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs71602763	chr5:1885111-1885112	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs398050302	chr5:1885114-1885115	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs532863877	chr5:1885127-1885128	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs575381305	chr5:1885143-1885144	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs115543324	chr5:1885174-1885175	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs116333777	chr5:1885175-1885176	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16608533	CNVD
Cervical cancer	16585170	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	17925434	CNVD
Ovarian cancer	20844748	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	21829676	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	19181860	CNVD
prenatal diagnosis	20453657	CNVD
Developmental delay	19490664	CNVD
Human papillomavirus	17975027	CNVD
Acute monocytic leukemia	16498392	CNVD
Gastric cancer	16891809	CNVD
Intracranial aneurysm	16715129	CNVD
Emphysema	19352772	CNVD
Chordoma	18071362	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21509527	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Oral cancer	22144094	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Schizophrenia	23813976	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1879800-1885200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr5:1880800-1887800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
3	chr5:1881200-1885200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
4	chr5:1881400-1886800	Bivalent Enhancer	Fetal Stomach	stomach
5	chr5:1881600-1884600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:1881600-1885600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
7	chr5:1882200-1884600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
8	chr5:1882400-1884600	Bivalent Enhancer	Lung	lung
9	chr5:1882400-1884800	Bivalent Enhancer	Spleen	Spleen
10	chr5:1882400-1885400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
11	chr5:1882400-1887600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:1882400-1887600	Active TSS	NHEK	skin
13	chr5:1882400-1887800	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr5:1882600-1884600	Active TSS	Left Ventricle	heart
15	chr5:1882600-1885000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:1882800-1885000	Bivalent/Poised TSS	Esophagus	oesophagus
17	chr5:1883000-1884600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
18	chr5:1883000-1884600	Active TSS	Right Ventricle	heart
19	chr5:1883000-1884800	Active TSS	Fetal Heart	heart
20	chr5:1883000-1885200	Active TSS	HMEC	breast
21	chr5:1883400-1884600	Bivalent Enhancer	Liver	Liver
22	chr5:1883600-1886800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:1883800-1884600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:1883800-1884600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
25	chr5:1883800-1884800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:1883800-1885000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:1883800-1885400	Bivalent Enhancer	Brain Hippocampus Middle	brain
28	chr5:1884000-1884800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
29	chr5:1884000-1884800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:1884000-1884800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:1884000-1884800	Bivalent Enhancer	Brain Germinal Matrix	brain
32	chr5:1884000-1885000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr5:1884000-1885000	Bivalent Enhancer	Fetal Brain Female	brain
34	chr5:1884200-1884600	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr5:1884200-1884600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
36	chr5:1884200-1884600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr5:1884200-1884600	Bivalent Enhancer	Fetal Muscle Leg	muscle
38	chr5:1884200-1884800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
39	chr5:1884200-1884800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
40	chr5:1884200-1884800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
41	chr5:1884200-1884800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr5:1884200-1885400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr5:1884200-1885400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chr5:1884200-1885600	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:1884200-1898200	Weak transcription	Gastric	stomach
46	chr5:1884400-1884600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
47	chr5:1884400-1884600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr5:1884400-1884600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
49	chr5:1884400-1884600	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
50	chr5:1884400-1884600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum

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