Variant report

Variant	esv3397950
Chromosome Location	chr14:105686557-105689055
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:307)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr14:105686569-105687846	SK-N-SH	brain:	n/a	chr14:105687171-105687187
2	GATA2	chr14:105687150-105687567	SH-SY5Y	brain:	n/a	n/a
3	GATA3	chr14:105688491-105688761	SH-SY5Y	brain:	n/a	n/a
4	MXI1	chr14:105686937-105687823	SK-N-SH	brain:	n/a	n/a
5	POLR2A	chr14:105687281-105687313	Gliobla	brain:	n/a	n/a
6	REST	chr14:105687081-105687587	SK-N-SH	brain:	n/a	chr14:105687141-105687161 chr14:105687141-105687161

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105688421-105688471	HRE	kidney:	n/a
2	chr14:105688129-105688179	A549	lung:	n/a
3	chr14:105688421-105688471	HRE	kidney:	n/a
4	chr14:105688129-105688179	A549	lung:	n/a
5	chr14:105688375-105688425	HMEC	breast:	n/a
6	chr14:105688375-105688425	K562	blood:	n/a
7	chr14:105688421-105688471	LNCaP	prostate:	n/a
8	chr14:105688412-105688462	SAEC	small airway:	n/a
9	chr14:105688412-105688462	SK-N-SH_RA	brain:	n/a
10	chr14:105688412-105688462	HEEpiC	esophagus:	n/a
11	chr14:105688914-105688964	Jurkat	blood:	n/a
12	chr14:105688421-105688471	Caco-2	colon:	n/a
13	chr14:105688375-105688425	HEEpiC	esophagus:	n/a
14	chr14:105688914-105688964	CMK	blood:	n/a
15	chr14:105688129-105688179	GM19239	blood:	n/a
16	chr14:105688412-105688462	K562	blood:	n/a
17	chr14:105688421-105688471	HUVEC	blood vessel:	n/a
18	chr14:105688914-105688964	HL-60	blood:	n/a
19	chr14:105688914-105688964	AG04449	skin:	fetal
20	chr14:105688412-105688462	GM12878	blood:	n/a
21	chr14:105688412-105688462	BJ	skin:	n/a
22	chr14:105688375-105688425	SK-N-SH_RA	brain:	n/a
23	chr14:105688421-105688471	HAEpiC	amniotic membrane:	n/a
24	chr14:105688412-105688462	HIPEpiC	eye:	n/a
25	chr14:105688375-105688425	SK-N-SH	brain:	n/a
26	chr14:105688914-105688964	GM19239	blood:	n/a
27	chr14:105688914-105688964	Hepatocyte	liver:	n/a
28	chr14:105688421-105688471	SK-N-MC	brain:	n/a
29	chr14:105688129-105688179	ovcar-3	ovarian:	n/a
30	chr14:105688375-105688425	PFSK-1	brain:	n/a
31	chr14:105688421-105688471	PFSK-1	brain:	n/a
32	chr14:105688375-105688425	A549	lung:	n/a
33	chr14:105688375-105688425	BJ	skin:	n/a
34	chr14:105688375-105688425	CMK	blood:	n/a
35	chr14:105688914-105688964	ProgFib	skin:	n/a
36	chr14:105688914-105688964	HEK293	kidney:	embryo
37	chr14:105688375-105688425	AG04450	lung:	fetal
38	chr14:105688129-105688179	HCM	heart:	n/a
39	chr14:105688914-105688964	NB4	blood:	n/a
40	chr14:105688375-105688425	HUVEC	blood vessel:	n/a
41	chr14:105688412-105688462	T-47D	breast:	n/a
42	chr14:105688412-105688462	BE2_C	brain:	n/a
43	chr14:105688375-105688425	HCM	heart:	n/a
44	chr14:105688412-105688462	HRPEpiC	eye:	n/a
45	chr14:105688375-105688425	AG04449	skin:	fetal
46	chr14:105688421-105688471	Hela-S3	cervix:	n/a
47	chr14:105688421-105688471	ovcar-3	ovarian:	n/a
48	chr14:105688129-105688179	BE2_C	brain:	n/a
49	chr14:105688129-105688179	AG04450	lung:	fetal
50	chr14:105688914-105688964	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:105687326..105689962-chr14:105713390..105716265,3	MCF-7	breast:
2	chr14:105678829..105680411-chr14:105684341..105687261,3	MCF-7	breast:

No data

Variant related genes	Relation type
BRF1	TF binding region
BRF1	CpG island
ENSG00000185024	chromatin interactions
ENSG00000184887	chromatin interactions

Extended variants
information (count: 131 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:131 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8005486	chr14:105686570-105686571	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587719523	chr14:105686607-105686608	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs144122079	chr14:105686613-105686614	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587772085	chr14:105686629-105686630	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs373487592	chr14:105686630-105686631	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs587705756	chr14:105686636-105686637	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs149226803	chr14:105686665-105686666	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs368055093	chr14:105686669-105686670	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs189208744	chr14:105686692-105686693	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs587637367	chr14:105686694-105686695	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs587725286	chr14:105686701-105686702	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs587604773	chr14:105686773-105686774	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs148460013	chr14:105686776-105686777	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs587704346	chr14:105686794-105686795	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs587673222	chr14:105686806-105686807	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs8005029	chr14:105686852-105686853	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs587660660	chr14:105686887-105686888	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs79241600	chr14:105686901-105686902	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587615951	chr14:105686982-105686983	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs587668034	chr14:105686987-105686988	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs145221459	chr14:105686994-105686995	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs180738523	chr14:105687060-105687061	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10400745	chr14:105687108-105687109	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs587772751	chr14:105687115-105687116	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs587653953	chr14:105687150-105687151	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs587688470	chr14:105687161-105687162	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs111266432	chr14:105687162-105687163	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs11621385	chr14:105687199-105687200	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs587709961	chr14:105687207-105687208	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs587751484	chr14:105687238-105687239	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs587649162	chr14:105687243-105687244	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587706175	chr14:105687248-105687249	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs587663299	chr14:105687284-105687285	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs587607986	chr14:105687329-105687330	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs587655350	chr14:105687339-105687340	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs587719165	chr14:105687360-105687361	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs587597911	chr14:105687373-105687374	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs587664715	chr14:105687388-105687389	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs587766324	chr14:105687399-105687400	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs78453771	chr14:105687413-105687414	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs12147166	chr14:105687426-105687427	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs587698862	chr14:105687455-105687456	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs373401722	chr14:105687485-105687486	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs186463888	chr14:105687525-105687526	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs587634048	chr14:105687534-105687535	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs10400759	chr14:105687536-105687537	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs587747794	chr14:105687560-105687561	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs371106189	chr14:105687592-105687593	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs587692396	chr14:105687617-105687618	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs587751843	chr14:105687629-105687630	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105668200-105687200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr14:105668600-105714200	Weak transcription	HUVEC	blood vessel
3	chr14:105669800-105691200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr14:105669800-105713800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr14:105671400-105697000	Weak transcription	Small Intestine	intestine
6	chr14:105671600-105689400	Weak transcription	NHEK	skin
7	chr14:105672200-105694200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:105672400-105687000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr14:105672400-105713200	Weak transcription	Osteobl	bone
10	chr14:105672600-105695600	Weak transcription	HMEC	breast
11	chr14:105673400-105690000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr14:105673600-105687400	Weak transcription	HepG2	liver
13	chr14:105673600-105713600	Weak transcription	Stomach Mucosa	stomach
14	chr14:105673800-105689800	Weak transcription	Hela-S3	cervix
15	chr14:105674000-105696000	Strong transcription	Fetal Stomach	stomach
16	chr14:105674000-105698600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr14:105674200-105687000	Weak transcription	Right Atrium	heart
18	chr14:105674200-105687200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr14:105674200-105695800	Strong transcription	Fetal Intestine Small	intestine
20	chr14:105674800-105687600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr14:105674800-105689600	Weak transcription	K562	blood
22	chr14:105674800-105694200	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr14:105674800-105695400	Strong transcription	Fetal Brain Female	brain
24	chr14:105674800-105696000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr14:105675200-105687000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr14:105675200-105695800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr14:105675400-105687000	Strong transcription	Gastric	stomach
28	chr14:105675400-105687000	Strong transcription	Stomach Smooth Muscle	stomach
29	chr14:105675400-105687200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr14:105675400-105688400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr14:105675400-105693400	Strong transcription	Duodenum Mucosa	Duodenum
32	chr14:105675400-105693800	Strong transcription	Primary T cells from cord blood	blood
33	chr14:105675400-105694200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:105675400-105694400	Strong transcription	Brain Germinal Matrix	brain
35	chr14:105675400-105695800	Strong transcription	Dnd41	blood
36	chr14:105675600-105695400	Strong transcription	Thymus	Thymus
37	chr14:105675600-105695600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr14:105675800-105690400	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr14:105675800-105693200	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr14:105676800-105713800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr14:105677400-105686600	Genic enhancers	Spleen	Spleen
42	chr14:105678400-105688800	Strong transcription	Aorta	Aorta
43	chr14:105678400-105690200	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr14:105679800-105714000	Weak transcription	NHDF-Ad	bronchial
45	chr14:105680400-105687200	Strong transcription	A549	lung
46	chr14:105680600-105688400	Strong transcription	Brain Hippocampus Middle	brain
47	chr14:105680600-105714000	Weak transcription	Psoas Muscle	Psoas
48	chr14:105681400-105687800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr14:105681400-105687800	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr14:105681400-105688000	Strong transcription	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links