Variant report

Variant	nsv902467
Chromosome Location	chr14:105709106-105719306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:1101)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:105714406-105715709	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr14:105714554-105714894	GM12878	blood:	n/a	chr14:105714818-105714831
3	BHLHE40	chr14:105714708-105714897	GM12878	blood:	n/a	chr14:105714722-105714738
4	BRCA1	chr14:105714576-105714669	GM12878	blood:	n/a	n/a
5	BRCA1	chr14:105714311-105714507	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:105711936-105712063	K562	blood:	n/a	chr14:105711997-105712008
7	CEBPB	chr14:105711878-105712144	HepG2	liver:	n/a	chr14:105711997-105712008
8	CHD1	chr14:105714496-105714696	GM12878	blood:	n/a	n/a
9	CHD2	chr14:105714688-105714896	Hela-S3	cervix:	n/a	chr14:105714767-105714777
10	CHD2	chr14:105714441-105714842	H1-hESC	embryonic stem cell:	n/a	chr14:105714767-105714777
11	CREB1	chr14:105714486-105715078	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr14:105714431-105715408	A549	lung:	n/a	n/a
13	CREB1	chr14:105714545-105715112	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr14:105714633-105714984	A549	lung:	n/a	n/a
15	CREB1	chr14:105714484-105715182	GM12878	blood:	n/a	n/a
16	CREB1	chr14:105714614-105715071	ECC-1	luminal epithelium:	n/a	n/a
17	CTCF	chr14:105714580-105714730	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr14:105715380-105715530	GM12864	blood:	n/a	n/a
19	CTCF	chr14:105714974-105715078	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr14:105714746-105714889	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr14:105715320-105715470	GM12867	blood:	n/a	n/a
22	CTCF	chr14:105714918-105715111	MCF-7	breast:	n/a	n/a
23	CTCF	chr14:105714860-105715010	GM12864	blood:	n/a	n/a
24	CTCF	chr14:105714800-105714950	SAEC	small airway:	n/a	n/a
25	CTCF	chr14:105714776-105715121	GM12878	blood:	n/a	n/a
26	CTCF	chr14:105714820-105714970	GM12875	blood:	n/a	n/a
27	CTCF	chr14:105714867-105714993	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr14:105714880-105715030	GM12871	blood:	n/a	n/a
29	CTCF	chr14:105714912-105715061	GM10266	blood:	n/a	n/a
30	CTCF	chr14:105714900-105715050	GM12865	blood:	n/a	n/a
31	CTCF	chr14:105714940-105715032	GM10248	blood:	n/a	n/a
32	CTCF	chr14:105714820-105714970	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr14:105714820-105714970	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr14:105714640-105714790	GM12867	blood:	n/a	n/a
35	CTCF	chr14:105714967-105715020	Lung_OC	lung:	n/a	n/a
36	CTCF	chr14:105714860-105715010	GM12872	blood:	n/a	n/a
37	CTCF	chr14:105714940-105715090	GM12873	blood:	n/a	n/a
38	CTCF	chr14:105714920-105715070	GM12869	blood:	n/a	n/a
39	CTCF	chr14:105714880-105715030	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr14:105714920-105715070	GM12874	blood:	n/a	n/a
41	CTCF	chr14:105715520-105715670	AG04449	skin:	n/a	n/a
42	CTCF	chr14:105714600-105714750	GM12874	blood:	n/a	n/a
43	CTCF	chr14:105714890-105714893	GM10266	blood:	n/a	n/a
44	CTCF	chr14:105715520-105715670	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr14:105714940-105715090	HEK293	kidney:	n/a	n/a
46	CTCF	chr14:105714928-105715101	GM12891	blood:	n/a	n/a
47	CTCF	chr14:105714900-105715050	GM12870	blood:	n/a	n/a
48	CTCF	chr14:105714900-105715050	GM12871	blood:	n/a	n/a
49	CTCF	chr14:105714940-105715090	GM12865	blood:	n/a	n/a
50	CTCF	chr14:105714900-105715050	GM12868	blood:	n/a	n/a

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105714589-105714639	MCF10A-Er-Src	breast:	n/a
2	chr14:105714153-105714203	AG09319	gingival:	n/a
3	chr14:105718851-105718901	K562	blood:	n/a
4	chr14:105714589-105714639	MCF10A-Er-Src	breast:	n/a
5	chr14:105714153-105714203	AG09319	gingival:	n/a
6	chr14:105718851-105718901	K562	blood:	n/a
7	chr14:105718851-105718901	HCPEpiC	choroid plexus:	n/a
8	chr14:105714843-105714893	HNPCEpiC	eye:	n/a
9	chr14:105714400-105714450	HIPEpiC	eye:	n/a
10	chr14:105710500-105710550	HCPEpiC	choroid plexus:	n/a
11	chr14:105715741-105715791	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:105715926-105715976	LNCaP	prostate:	n/a
13	chr14:105714379-105714429	H1-hESC	embryonic stem cell:	embryo
14	chr14:105716052-105716102	ovcar-3	ovarian:	n/a
15	chr14:105714846-105714896	NHBE	bronchial:	n/a
16	chr14:105714153-105714203	HRCEpiC	kidney:	n/a
17	chr14:105714589-105714639	H1-hESC	embryonic stem cell:	embryo
18	chr14:105714274-105714324	NHDF-neo	bronchial:	n/a
19	chr14:105714274-105714324	H1-hESC	embryonic stem cell:	embryo
20	chr14:105714846-105714896	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:105715926-105715976	Hepatocyte	liver:	n/a
22	chr14:105714274-105714324	T-47D	breast:	n/a
23	chr14:105715464-105715514	CMK	blood:	n/a
24	chr14:105714404-105714454	LNCaP	prostate:	n/a
25	chr14:105714843-105714893	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:105718851-105718901	AG04450	lung:	fetal
27	chr14:105714843-105714893	AG04450	lung:	fetal
28	chr14:105714274-105714324	Jurkat	blood:	n/a
29	chr14:105715741-105715791	NHBE	bronchial:	n/a
30	chr14:105715025-105715075	SK-N-SH_RA	brain:	n/a
31	chr14:105714833-105714883	T-47D	breast:	n/a
32	chr14:105717038-105717088	AG09309	skin:	n/a
33	chr14:105714274-105714324	HRCEpiC	kidney:	n/a
34	chr14:105715025-105715075	MCF-7	breast:	n/a
35	chr14:105713866-105713916	LNCaP	prostate:	n/a
36	chr14:105714400-105714450	GM06990	blood:	n/a
37	chr14:105714274-105714324	NH-A	brain:	n/a
38	chr14:105718851-105718901	NT2-D1	testis:	n/a
39	chr14:105714843-105714893	HEEpiC	esophagus:	n/a
40	chr14:105714843-105714893	AG09319	gingival:	n/a
41	chr14:105714400-105714450	HCPEpiC	choroid plexus:	n/a
42	chr14:105714274-105714324	K562	blood:	n/a
43	chr14:105718851-105718901	BJ	skin:	n/a
44	chr14:105715025-105715075	Hepatocyte	liver:	n/a
45	chr14:105714843-105714893	K562	blood:	n/a
46	chr14:105714833-105714883	HAEpiC	amniotic membrane:	n/a
47	chr14:105718851-105718901	HAEpiC	amniotic membrane:	n/a
48	chr14:105715926-105715976	NH-A	brain:	n/a
49	chr14:105715464-105715514	GM19239	blood:	n/a
50	chr14:105717038-105717088	GM06990	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105687326..105689962-chr14:105713390..105716265,3	MCF-7	breast:
2	chr14:105717901..105719933-chr14:105721820..105724297,3	MCF-7	breast:
3	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:
4	chr14:105717742..105719473-chr14:105729003..105731764,2	MCF-7	breast:
5	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:
6	chr11:62358871..62359665-chr14:105714579..105715245,2	Hela-S3	cervix:
7	chr14:105718161..105724247-chr14:105765636..105769156,6	MCF-7	breast:
8	chr14:105706521..105709177-chr14:105712711..105714374,2	MCF-7	breast:
9	chr14:105709578..105712149-chr14:105714194..105716568,3	MCF-7	breast:
10	chr14:105706521..105709177-chr14:105712711..105714374,2	MCF-7	breast:
11	chr14:105713833..105716142-chr14:105716723..105718932,2	K562	blood:
12	chr14:105717555..105718335-chr3:138200943..138201661,2	MCF-7	breast:
13	chr14:105718698..105721537-chr14:105739124..105741867,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-2	chr14:105717014-105717436	NONHSAT040340

No data

Variant related genes	Relation type
BRF1	TF binding region
BTBD6	TF binding region
BRF1	CpG island
BTBD6	CpG island
ENSG00000184887	chromatin interactions
ENSG00000255508	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000149016	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000185024	chromatin interactions

Extended variants
information (count: 490 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10162524	chr14:105709106-105709107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184494133	chr14:105709183-105709184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200589011	chr14:105709191-105709192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189799867	chr14:105709226-105709227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587685698	chr14:105709243-105709244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs367618382	chr14:105709245-105709246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587600638	chr14:105709251-105709252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587658626	chr14:105709258-105709259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587711880	chr14:105709266-105709267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370431252	chr14:105709270-105709271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373840428	chr14:105709274-105709275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs137929966	chr14:105709313-105709314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181402084	chr14:105709352-105709353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587694748	chr14:105709368-105709369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587750254	chr14:105709390-105709391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587649913	chr14:105709399-105709400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587682816	chr14:105709411-105709412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587743663	chr14:105709475-105709476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113453968	chr14:105709527-105709528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368594428	chr14:105709565-105709566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60736240	chr14:105709582-105709583	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs367604541	chr14:105709583-105709584	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs28513571	chr14:105709592-105709593	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs28588570	chr14:105709606-105709607	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs28454985	chr14:105709611-105709612	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs374355364	chr14:105709622-105709623	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375399380	chr14:105709625-105709626	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs587632835	chr14:105709657-105709658	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs149448745	chr14:105709658-105709659	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs185984766	chr14:105709664-105709665	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs189245864	chr14:105709679-105709680	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587708805	chr14:105709748-105709749	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs587697732	chr14:105709749-105709750	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs117427573	chr14:105709787-105709788	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs587630818	chr14:105709800-105709801	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587718758	chr14:105709801-105709802	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs367697069	chr14:105709803-105709804	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs10137807	chr14:105709805-105709806	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs200320625	chr14:105709811-105709812	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs587672926	chr14:105709829-105709830	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs143836775	chr14:105709837-105709838	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372596306	chr14:105709888-105709889	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148160690	chr14:105709894-105709895	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs79805330	chr14:105709938-105709939	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs78147862	chr14:105709939-105709940	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78390437	chr14:105709949-105709950	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs75858185	chr14:105709950-105709951	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs144043138	chr14:105709953-105709954	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs587601004	chr14:105709958-105709959	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs587672164	chr14:105709979-105709980	Weak transcription Strong transcription	Chromatin interactive region	2 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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105668600-105714200	Weak transcription	HUVEC	blood vessel
2	chr14:105669800-105713800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr14:105672400-105713200	Weak transcription	Osteobl	bone
4	chr14:105673600-105713600	Weak transcription	Stomach Mucosa	stomach
5	chr14:105676800-105713800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr14:105679800-105714000	Weak transcription	NHDF-Ad	bronchial
7	chr14:105680600-105714000	Weak transcription	Psoas Muscle	Psoas
8	chr14:105681400-105714000	Weak transcription	HSMMtube	muscle
9	chr14:105681400-105714200	Weak transcription	HSMM	muscle
10	chr14:105687200-105714000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr14:105687400-105714200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr14:105688400-105712000	Weak transcription	HepG2	liver
13	chr14:105688800-105713800	Weak transcription	NH-A	brain
14	chr14:105689800-105714000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr14:105690000-105710600	Weak transcription	Primary B cells from cord blood	blood
16	chr14:105690200-105713800	Weak transcription	NHEK	skin
17	chr14:105690400-105714000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr14:105690400-105721400	Weak transcription	K562	blood
19	chr14:105691600-105714000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr14:105693000-105710200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr14:105693000-105713600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr14:105693200-105713400	Weak transcription	GM12878-XiMat	blood
23	chr14:105693200-105713400	Weak transcription	Hela-S3	cervix
24	chr14:105693200-105713800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr14:105693200-105714000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr14:105693400-105714000	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr14:105693600-105713200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr14:105693600-105713800	Weak transcription	Colon Smooth Muscle	Colon
29	chr14:105694000-105714200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr14:105694200-105713600	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr14:105694200-105714200	Weak transcription	Primary T cells from cord blood	blood
32	chr14:105695600-105710200	Weak transcription	Fetal Lung	lung
33	chr14:105695600-105711800	Weak transcription	Liver	Liver
34	chr14:105703800-105714200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr14:105706000-105711800	Weak transcription	Fetal Brain Male	brain
36	chr14:105706200-105713200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr14:105707200-105710800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr14:105707200-105711000	Strong transcription	Fetal Intestine Small	intestine
39	chr14:105707200-105711000	Strong transcription	Fetal Stomach	stomach
40	chr14:105707200-105713800	Weak transcription	Fetal Thymus	thymus
41	chr14:105707200-105714000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr14:105707400-105709200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr14:105707400-105711000	Strong transcription	Fetal Muscle Leg	muscle
44	chr14:105707400-105711600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr14:105707400-105713400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:105707600-105714000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:105707800-105714000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr14:105708000-105713400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr14:105708200-105714000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr14:105708400-105710200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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