Variant report

Variant	nsv9173
Chromosome Location	chr14:104334250-104336486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:104334912-104335177	HepG2	liver:	n/a	n/a
2	CTCF	chr14:104335060-104335210	NHEK	skin:	n/a	n/a
3	CTCF	chr14:104334980-104335130	HEEpiC	esophagus:	n/a	n/a
4	CTCF	chr14:104335020-104335170	HepG2	liver:	n/a	n/a
5	CTCF	chr14:104335000-104335150	HMEC	breast:	n/a	n/a
6	E2F4	chr14:104334867-104335221	MCF10A-Er-Src	breast:	n/a	n/a
7	EBF1	chr14:104336319-104336543	GM12878	blood:	n/a	chr14:104336457-104336467
8	EP300	chr14:104334413-104334439	GM12878	blood:	n/a	n/a
9	EP300	chr14:104333581-104334419	ECC-1	luminal epithelium:	n/a	n/a
10	FOS	chr14:104334783-104335274	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr14:104334895-104335182	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr14:104334774-104335274	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr14:104334826-104335286	MCF10A-Er-Src	breast:	n/a	n/a
14	MAX	chr14:104333706-104334323	ECC-1	luminal epithelium:	n/a	n/a
15	MAX	chr14:104333631-104334414	ECC-1	luminal epithelium:	n/a	n/a
16	MYC	chr14:104334872-104335263	MCF10A-Er-Src	breast:	n/a	n/a
17	MYC	chr14:104334783-104335251	MCF10A-Er-Src	breast:	n/a	n/a
18	NFIC	chr14:104333581-104334439	ECC-1	luminal epithelium:	n/a	n/a
19	NFIC	chr14:104336304-104336913	ECC-1	luminal epithelium:	n/a	n/a
20	NFIC	chr14:104333700-104334413	ECC-1	luminal epithelium:	n/a	n/a
21	POLR2A	chr14:104336032-104336707	HepG2	liver:	n/a	n/a
22	POLR2A	chr14:104333477-104334661	HepG2	liver:	n/a	n/a
23	POLR2A	chr14:104334737-104337508	HepG2	liver:	n/a	n/a
24	POLR2A	chr14:104333866-104334273	HepG2	liver:	n/a	n/a
25	POLR2A	chr14:104333587-104335203	HepG2	liver:	n/a	n/a
26	POLR2A	chr14:104334703-104334730	HepG2	liver:	n/a	n/a
27	POLR2A	chr14:104335837-104336813	HepG2	liver:	n/a	n/a
28	POLR2A	chr14:104334932-104335186	MCF10A-Er-Src	breast:	n/a	n/a
29	STAT3	chr14:104334870-104335191	MCF10A-Er-Src	breast:	n/a	n/a
30	STAT3	chr14:104334914-104335188	MCF10A-Er-Src	breast:	n/a	n/a
31	STAT3	chr14:104334846-104335219	MCF10A-Er-Src	breast:	n/a	n/a
32	TCF12	chr14:104333604-104334433	ECC-1	luminal epithelium:	n/a	n/a
33	TCF12	chr14:104333627-104334448	ECC-1	luminal epithelium:	n/a	n/a
34	ZNF143	chr14:104335970-104335987	K562	blood:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104336130..104339253-chr14:104343612..104346035,4	MCF-7	breast:
2	chr14:104330031..104331593-chr14:104332707..104335169,2	MCF-7	breast:
3	chr14:104322796..104324811-chr14:104333710..104335450,2	K562	blood:
4	chr14:104332802..104335861-chr14:104354361..104356131,3	MCF-7	breast:
5	chr14:104308064..104309884-chr14:104336014..104338785,2	MCF-7	breast:
6	chr14:104327639..104330027-chr14:104333927..104335918,2	MCF-7	breast:
7	chr14:104333923..104335751-chr14:104336446..104338911,2	MCF-7	breast:
8	chr14:104335495..104338152-chr14:104341158..104343164,2	MCF-7	breast:
9	chr14:104312089..104314904-chr14:104334479..104336712,3	MCF-7	breast:
10	chr14:104333923..104335751-chr14:104336446..104338911,2	MCF-7	breast:
11	chr14:104324206..104326944-chr14:104336332..104338348,2	MCF-7	breast:
12	chr14:104332785..104335222-chr14:104358563..104360147,2	MCF-7	breast:
13	chr14:104335008..104337928-chr14:104351341..104353510,3	MCF-7	breast:
14	chr14:104320014..104324951-chr14:104331915..104336985,8	MCF-7	breast:
15	chr14:104313742..104315578-chr14:104335128..104336698,2	MCF-7	breast:
16	chr14:104333964..104338190-chr14:104344769..104347298,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R13B-1	chr14:104335739-104335925	NONHSAT040223
2	lnc-PPP1R13B-1	chr14:104336208-104336349	ENSG00000258534
3	lnc-PPP1R13B-1	chr14:104336208-104336349	NONHSAT040223

No data

Variant related genes	Relation type
ENSG00000258914	TF binding region
ENSG00000088808	chromatin interactions
ENSG00000258534	chromatin interactions
ENSG00000258914	chromatin interactions
ENSG00000258735	chromatin interactions

Extended variants
information (count: 138 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:138 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35382778	chr14:104334263-104334264	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs567233656	chr14:104334279-104334280	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs111699240	chr14:104334289-104334290	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs73350566	chr14:104334311-104334312	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566445770	chr14:104334403-104334404	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs145256071	chr14:104334406-104334407	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184612693	chr14:104334414-104334415	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs369984890	chr14:104334439-104334440	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558372339	chr14:104334454-104334455	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372994774	chr14:104334500-104334501	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs150549620	chr14:104334501-104334502	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs139564957	chr14:104334539-104334540	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs149705618	chr14:104334576-104334577	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs145501237	chr14:104334611-104334612	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs140252984	chr14:104334660-104334661	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs559752788	chr14:104334682-104334683	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs377190220	chr14:104334730-104334731	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs189130988	chr14:104334740-104334741	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs564723665	chr14:104334763-104334764	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs11849080	chr14:104334801-104334802	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs143971839	chr14:104334817-104334818	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs74086476	chr14:104334820-104334821	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549682828	chr14:104334833-104334834	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs61995845	chr14:104334917-104334918	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
25	rs61995846	chr14:104334932-104334933	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs146178629	chr14:104334942-104334943	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs566501202	chr14:104334943-104334944	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs183983323	chr14:104334952-104334953	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs140692960	chr14:104334973-104334974	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs571213180	chr14:104334981-104334982	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs571841068	chr14:104335011-104335012	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs537657648	chr14:104335036-104335037	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs74086477	chr14:104335054-104335055	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs531501217	chr14:104335060-104335061	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs76410794	chr14:104335124-104335125	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs537263961	chr14:104335170-104335171	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs12435813	chr14:104335175-104335176	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs527750637	chr14:104335177-104335178	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs553084728	chr14:104335179-104335180	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs115548956	chr14:104335210-104335211	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs6576009	chr14:104335229-104335230	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs189110154	chr14:104335234-104335235	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs575064927	chr14:104335236-104335237	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs143769872	chr14:104335250-104335251	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs561180746	chr14:104335267-104335268	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs117519854	chr14:104335279-104335280	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs77968020	chr14:104335290-104335291	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs67283123	chr14:104335303-104335304	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535454455	chr14:104335356-104335357	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs148150434	chr14:104335377-104335378	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104323600-104336000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr14:104323600-104337600	Weak transcription	Fetal Intestine Small	intestine
3	chr14:104326600-104336400	Weak transcription	Right Atrium	heart
4	chr14:104328200-104336000	Weak transcription	Spleen	Spleen
5	chr14:104329400-104338000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr14:104332200-104337200	Enhancers	Pancreas	Pancrea
7	chr14:104332800-104334400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr14:104333200-104337200	Enhancers	Right Ventricle	heart
9	chr14:104333400-104335200	Enhancers	Gastric	stomach
10	chr14:104333400-104337200	Enhancers	Esophagus	oesophagus
11	chr14:104333600-104334400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:104333600-104334400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:104333600-104334400	Enhancers	Brain Anterior Caudate	brain
14	chr14:104333600-104334600	Enhancers	Brain Substantia Nigra	brain
15	chr14:104333600-104334600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr14:104333600-104334600	Enhancers	Fetal Muscle Leg	muscle
17	chr14:104333600-104334600	Enhancers	Fetal Stomach	stomach
18	chr14:104333600-104334600	Enhancers	Left Ventricle	heart
19	chr14:104333600-104334600	Enhancers	Hela-S3	cervix
20	chr14:104333600-104334600	Flanking Active TSS	HepG2	liver
21	chr14:104333600-104334800	Enhancers	Fetal Heart	heart
22	chr14:104333600-104334800	Enhancers	Stomach Mucosa	stomach
23	chr14:104333600-104335000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr14:104333600-104335400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:104333600-104335600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr14:104333600-104335600	Enhancers	HMEC	breast
27	chr14:104333800-104334400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr14:104333800-104334400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr14:104333800-104334400	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr14:104333800-104334400	Enhancers	Liver	Liver
31	chr14:104333800-104334400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr14:104333800-104334400	Enhancers	A549	lung
33	chr14:104333800-104334600	Enhancers	Brain Angular Gyrus	brain
34	chr14:104333800-104334600	Enhancers	Brain Hippocampus Middle	brain
35	chr14:104333800-104334600	Enhancers	Rectal Smooth Muscle	rectum
36	chr14:104333800-104334800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:104333800-104334800	Enhancers	Brain Cingulate Gyrus	brain
38	chr14:104333800-104334800	Enhancers	Fetal Muscle Trunk	muscle
39	chr14:104333800-104338400	Enhancers	Placenta	Placenta
40	chr14:104334000-104334400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr14:104334000-104334400	Flanking Active TSS	Stomach Smooth Muscle	stomach
42	chr14:104334000-104334600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr14:104334000-104337800	Weak transcription	Colonic Mucosa	Colon
44	chr14:104334000-104338400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr14:104334200-104334400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr14:104334200-104334400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr14:104334200-104334600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr14:104334200-104334600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr14:104334200-104334600	Enhancers	Lung	lung
50	chr14:104334200-104334800	Enhancers	Colon Smooth Muscle	Colon

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