Variant report

Variant	esv3350859
Chromosome Location	chr14:105249685-105252976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:105252720-105252870	HBMEC	blood vessel:	n/a	chr14:105252831-105252840
2	CTCF	chr14:105252700-105252850	HMEC	breast:	n/a	chr14:105252831-105252840
3	CTCF	chr14:105252791-105252825	Spleen_OC	spleen:	n/a	n/a
4	CTCF	chr14:105252660-105252810	HL-60	blood:	n/a	n/a
5	CTCF	chr14:105252773-105252890	Lung_OC	lung:	n/a	chr14:105252831-105252840
6	CTCF	chr14:105251327-105251394	Lung_OC	lung:	n/a	n/a
7	CTCF	chr14:105252720-105252870	SAEC	small airway:	n/a	chr14:105252831-105252840
8	CTCF	chr14:105252700-105252850	HBMEC	blood vessel:	n/a	chr14:105252831-105252840
9	CTCF	chr14:105252720-105252870	NHEK	skin:	n/a	chr14:105252831-105252840
10	GABPA	chr14:105252453-105252896	HL-60	blood:	n/a	chr14:105252552-105252561
11	MYC	chr14:105252666-105252792	MCF-7	breast:	n/a	n/a
12	MYC	chr14:105250738-105250796	H1-hESC	embryonic stem cell:	n/a	n/a
13	NFIC	chr14:105250436-105250904	ECC-1	luminal epithelium:	n/a	n/a
14	NFIC	chr14:105251004-105251665	ECC-1	luminal epithelium:	n/a	n/a
15	NFIC	chr14:105251004-105251674	ECC-1	luminal epithelium:	n/a	n/a
16	POLR2A	chr14:105250213-105250961	GM12878	blood:	n/a	n/a
17	POLR2A	chr14:105250459-105250821	GM12892	blood:	n/a	n/a
18	POLR2A	chr14:105249660-105249803	GM12878	blood:	n/a	n/a
19	POLR2A	chr14:105252665-105252733	K562	blood:	n/a	n/a
20	POLR2A	chr14:105250684-105250698	MCF-7	breast:	n/a	n/a
21	POLR2A	chr14:105252821-105252836	HepG2	liver:	n/a	n/a
22	POLR2A	chr14:105251015-105251231	K562	blood:	n/a	n/a
23	POLR2A	chr14:105251349-105251479	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr14:105251208-105251347	HepG2	liver:	n/a	n/a
25	POLR2A	chr14:105250521-105250527	MCF-7	breast:	n/a	n/a
26	POLR2A	chr14:105250510-105250542	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr14:105250493-105250862	GM12878	blood:	n/a	n/a
28	POLR2A	chr14:105251280-105251560	K562	blood:	n/a	n/a
29	POLR2A	chr14:105250351-105250391	MCF-7	breast:	n/a	n/a
30	POLR2A	chr14:105251799-105251848	HepG2	liver:	n/a	n/a
31	POLR2A	chr14:105249867-105250867	GM12892	blood:	n/a	n/a
32	POLR2A	chr14:105251276-105251321	MCF-7	breast:	n/a	n/a
33	POLR2A	chr14:105252036-105252180	MCF-7	breast:	n/a	n/a
34	POLR2A	chr14:105251172-105251178	MCF-7	breast:	n/a	n/a
35	POLR2A	chr14:105250410-105250514	MCF-7	breast:	n/a	n/a
36	POLR2A	chr14:105250558-105250643	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr14:105249429-105250018	MCF-7	breast:	n/a	n/a
38	POLR2A	chr14:105250765-105251146	HepG2	liver:	n/a	n/a
39	POLR2A	chr14:105252478-105252869	GM12878	blood:	n/a	n/a
40	POLR2A	chr14:105250643-105250700	K562	blood:	n/a	n/a
41	POLR2A	chr14:105251864-105251934	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:105250965-105251166	MCF-7	breast:	n/a	n/a
43	POLR2A	chr14:105249510-105249861	GM12878	blood:	n/a	n/a
44	POLR2A	chr14:105252859-105252867	HepG2	liver:	n/a	n/a
45	POLR2A	chr14:105250027-105250919	HepG2	liver:	n/a	n/a
46	POLR2A	chr14:105250597-105250847	GM12878	blood:	n/a	n/a
47	POLR2A	chr14:105251980-105253963	HL-60	blood:	n/a	n/a
48	POLR2A	chr14:105252614-105253196	MCF-7	breast:	n/a	n/a
49	POLR2A	chr14:105252349-105253037	HL-60	blood:	n/a	n/a
50	POLR2A	chr14:105249949-105250019	HUVEC	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105251402-105251452	AG09319	gingival:	n/a
2	chr14:105251610-105251660	GM12891	blood:	n/a
3	chr14:105251610-105251660	PANC-1	pancreas:	n/a
4	chr14:105251402-105251452	NB4	blood:	n/a
5	chr14:105251188-105251238	AG04450	lung:	fetal
6	chr14:105251188-105251238	SK-N-SH	brain:	n/a
7	chr14:105251188-105251238	NH-A	brain:	n/a
8	chr14:105251610-105251660	HL-60	blood:	n/a
9	chr14:105251610-105251660	HEK293	kidney:	embryo
10	chr14:105251188-105251238	HEEpiC	esophagus:	n/a
11	chr14:105251610-105251660	HEEpiC	esophagus:	n/a
12	chr14:105251188-105251238	GM12878	blood:	n/a
13	chr14:105251610-105251660	AG04450	lung:	fetal
14	chr14:105251610-105251660	A549	lung:	n/a
15	chr14:105251610-105251660	IMR90	lung:	fetal
16	chr14:105251188-105251238	GM12891	blood:	n/a
17	chr14:105251188-105251238	LNCaP	prostate:	n/a
18	chr14:105251402-105251452	HUVEC	blood vessel:	n/a
19	chr14:105251610-105251660	HRPEpiC	eye:	n/a
20	chr14:105251188-105251238	AG09319	gingival:	n/a
21	chr14:105251188-105251238	U87	brain:	n/a
22	chr14:105251188-105251238	PANC-1	pancreas:	n/a
23	chr14:105251402-105251452	HEEpiC	esophagus:	n/a
24	chr14:105251610-105251660	Hela-S3	cervix:	n/a
25	chr14:105251610-105251660	Hepatocyte	liver:	n/a
26	chr14:105251610-105251660	H1-hESC	embryonic stem cell:	embryo
27	chr14:105251188-105251238	SK-N-MC	brain:	n/a
28	chr14:105251610-105251660	HRE	kidney:	n/a
29	chr14:105251610-105251660	GM19239	blood:	n/a
30	chr14:105251610-105251660	GM12892	blood:	n/a
31	chr14:105251188-105251238	HCF	heart:	n/a
32	chr14:105251610-105251660	AG10803	skin:	n/a
33	chr14:105251188-105251238	HUVEC	blood vessel:	n/a
34	chr14:105251610-105251660	Jurkat	blood:	n/a
35	chr14:105251402-105251452	HMEC	breast:	n/a
36	chr14:105251402-105251452	CMK	blood:	n/a
37	chr14:105251402-105251452	BE2_C	brain:	n/a
38	chr14:105251402-105251452	LNCaP	prostate:	n/a
39	chr14:105251188-105251238	NHDF-neo	bronchial:	n/a
40	chr14:105251188-105251238	MCF10A-Er-Src	breast:	n/a
41	chr14:105251402-105251452	HCT-116	colon:	n/a
42	chr14:105251188-105251238	H1-hESC	embryonic stem cell:	embryo
43	chr14:105251188-105251238	HIPEpiC	eye:	n/a
44	chr14:105251188-105251238	NT2-D1	testis:	n/a
45	chr14:105251610-105251660	LNCaP	prostate:	n/a
46	chr14:105251188-105251238	ProgFib	skin:	n/a
47	chr14:105251402-105251452	PANC-1	pancreas:	n/a
48	chr14:105251402-105251452	PrEC	prostate:	n/a
49	chr14:105251402-105251452	Caco-2	colon:	n/a
50	chr14:105251188-105251238	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:105250763..105252757-chr14:105330393..105333309,2	K562	blood:
2	chr14:105246961..105249735-chr14:105330074..105332395,2	MCF-7	breast:

No data

Variant related genes	Relation type
AKT1	TF binding region
AKT1	CpG island
ENSG00000099814	chromatin interactions

Extended variants
information (count: 136 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551930341	chr14:105249712-105249713	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs571795662	chr14:105249714-105249715	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376017339	chr14:105249760-105249761	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs111684231	chr14:105249931-105249932	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537545135	chr14:105249962-105249963	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116684055	chr14:105249988-105249989	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142065631	chr14:105249989-105249990	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571431325	chr14:105250017-105250018	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs367883437	chr14:105250019-105250020	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2498789	chr14:105250045-105250046	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552967868	chr14:105250053-105250054	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572789384	chr14:105250061-105250062	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182486805	chr14:105250099-105250100	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188455638	chr14:105250131-105250132	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575387152	chr14:105250158-105250159	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544403535	chr14:105250159-105250160	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560917853	chr14:105250213-105250214	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374668787	chr14:105250223-105250224	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs61759796	chr14:105250229-105250230	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546584997	chr14:105250246-105250247	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560219741	chr14:105250259-105250260	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192682199	chr14:105250297-105250298	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551828444	chr14:105250299-105250300	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571919277	chr14:105250304-105250305	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs5811153	chr14:105250370-105250371	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34907636	chr14:105250372-105250373	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs61417473	chr14:105250375-105250376	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537200802	chr14:105250386-105250387	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550781846	chr14:105250419-105250420	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs567386077	chr14:105250426-105250427	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs113750262	chr14:105250439-105250440	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs367784990	chr14:105250450-105250451	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs575052198	chr14:105250576-105250577	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs61759795	chr14:105250644-105250645	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs61759794	chr14:105250655-105250656	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs544004241	chr14:105250699-105250700	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs61759793	chr14:105250724-105250725	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs556663702	chr14:105250738-105250739	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs558612575	chr14:105250745-105250746	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs144187261	chr14:105250750-105250751	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs554388361	chr14:105250768-105250769	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558533234	chr14:105250790-105250791	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573785599	chr14:105250795-105250796	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs184690341	chr14:105250807-105250808	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs148686406	chr14:105250824-105250825	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375949641	chr14:105250847-105250848	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561082543	chr14:105250903-105250904	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs145970556	chr14:105250925-105250926	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188457850	chr14:105250940-105250941	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs61759792	chr14:105250952-105250953	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
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
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
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
Breast cancer	21364760	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105221600-105253800	Weak transcription	Psoas Muscle	Psoas
2	chr14:105235400-105251400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr14:105235400-105252600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr14:105235400-105259200	Strong transcription	NHLF	lung
5	chr14:105235400-105259400	Weak transcription	Right Atrium	heart
6	chr14:105235600-105252600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr14:105235600-105255600	Strong transcription	Dnd41	blood
8	chr14:105235600-105257600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:105238000-105250600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr14:105238000-105254000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr14:105238000-105257400	Weak transcription	NH-A	brain
12	chr14:105238200-105250200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:105238200-105258800	Strong transcription	Fetal Intestine Large	intestine
14	chr14:105238200-105259800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr14:105238400-105250600	Strong transcription	Liver	Liver
16	chr14:105238600-105250600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr14:105238600-105259600	Strong transcription	Fetal Intestine Small	intestine
18	chr14:105238800-105251200	Weak transcription	Stomach Mucosa	stomach
19	chr14:105238800-105258000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:105238800-105258600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr14:105239000-105251800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr14:105239000-105253800	Weak transcription	Hela-S3	cervix
23	chr14:105239000-105256800	Weak transcription	NHDF-Ad	bronchial
24	chr14:105239200-105251000	Weak transcription	Primary hematopoietic stem cells	blood
25	chr14:105239400-105255600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr14:105239600-105250600	Strong transcription	Lung	lung
27	chr14:105239600-105250600	Strong transcription	Spleen	Spleen
28	chr14:105239600-105252600	Weak transcription	HSMMtube	muscle
29	chr14:105239800-105253600	Weak transcription	Osteobl	bone
30	chr14:105239800-105256800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr14:105239800-105256800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr14:105240000-105259800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr14:105240200-105253200	Weak transcription	Primary B cells from cord blood	blood
34	chr14:105240800-105252200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr14:105241800-105252400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr14:105242200-105250600	Weak transcription	Brain Anterior Caudate	brain
37	chr14:105242200-105252000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr14:105242200-105255600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr14:105242400-105254000	Weak transcription	HepG2	liver
40	chr14:105242400-105256200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr14:105242800-105259800	Weak transcription	K562	blood
42	chr14:105243000-105255800	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr14:105243200-105250800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr14:105243200-105256000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr14:105243400-105253600	Weak transcription	Brain Cingulate Gyrus	brain
46	chr14:105243400-105253600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr14:105243400-105258800	Weak transcription	HUVEC	blood vessel
48	chr14:105243400-105259800	Weak transcription	Aorta	Aorta
49	chr14:105243600-105251200	Weak transcription	Rectal Smooth Muscle	rectum
50	chr14:105243600-105252000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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