Variant report

Variant	esv3378814
Chromosome Location	chr14:105680407-105684005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr14:105681677-105681921	GM12878	blood:	n/a	n/a
2	BCL3	chr14:105681691-105682038	GM12878	blood:	n/a	n/a
3	CTCF	chr14:105682427-105682438	GM19239	blood:	n/a	n/a
4	CTCF	chr14:105681814-105681928	GM19239	blood:	n/a	n/a
5	CTCF	chr14:105682196-105682303	NHEK	skin:	n/a	n/a
6	CTCF	chr14:105682880-105683030	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr14:105681240-105681390	GM12866	blood:	n/a	n/a
8	CTCF	chr14:105681929-105681938	GM19239	blood:	n/a	n/a
9	CTCF	chr14:105682002-105682424	GM19239	blood:	n/a	n/a
10	MYC	chr14:105682074-105682420	MCF-7	breast:	n/a	n/a
11	MYC	chr14:105681832-105681914	MCF-7	breast:	n/a	n/a
12	MYC	chr14:105682224-105682336	MCF-7	breast:	n/a	n/a
13	MYC	chr14:105681997-105682160	GM12878	blood:	n/a	n/a
14	MYC	chr14:105682068-105682073	MCF-7	breast:	n/a	n/a
15	MYC	chr14:105682252-105682258	H1-hESC	embryonic stem cell:	n/a	n/a
16	MYC	chr14:105682117-105682391	MCF-7	breast:	n/a	n/a
17	NR2C2	chr14:105681533-105682317	GM12878	blood:	n/a	n/a
18	POLR2A	chr14:105682016-105682222	GM12878	blood:	n/a	n/a
19	POLR2A	chr14:105683209-105683240	HepG2	liver:	n/a	n/a
20	POLR2A	chr14:105682750-105682910	GM12878	blood:	n/a	n/a
21	POLR2A	chr14:105682004-105682364	A549	lung:	n/a	n/a
22	POLR2A	chr14:105681999-105682439	MCF-7	breast:	n/a	n/a
23	POLR2A	chr14:105681645-105682622	HepG2	liver:	n/a	n/a
24	POLR2A	chr14:105682064-105682109	GM12878	blood:	n/a	n/a
25	POLR2A	chr14:105681980-105681988	MCF-7	breast:	n/a	n/a
26	POLR2A	chr14:105682077-105682211	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr14:105682102-105682342	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr14:105682702-105682705	GM12878	blood:	n/a	n/a
29	POLR2A	chr14:105681628-105682498	GM12878	blood:	n/a	n/a
30	POLR2A	chr14:105682215-105682370	Gliobla	brain:	n/a	n/a
31	POLR2A	chr14:105681568-105682552	GM12892	blood:	n/a	n/a
32	POLR2A	chr14:105682105-105682351	A549	lung:	n/a	n/a
33	POLR2A	chr14:105682397-105682460	K562	blood:	n/a	n/a
34	POLR2A	chr14:105681807-105681949	MCF-7	breast:	n/a	n/a
35	POLR2A	chr14:105682243-105682309	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr14:105682303-105682311	GM12878	blood:	n/a	n/a
37	POLR2A	chr14:105682139-105682294	GM12878	blood:	n/a	n/a
38	POLR2A	chr14:105681764-105682381	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr14:105681782-105681856	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr14:105681688-105681760	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr14:105682337-105682466	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr14:105681787-105681858	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr14:105682117-105682198	Gliobla	brain:	n/a	n/a
44	POLR2A	chr14:105682086-105682434	MCF-7	breast:	n/a	n/a
45	POLR2A	chr14:105682010-105682358	A549	lung:	n/a	n/a
46	POLR2A	chr14:105681989-105682064	MCF-7	breast:	n/a	n/a
47	STAT5A	chr14:105681454-105682289	K562	blood:	n/a	n/a
48	STAT5A	chr14:105681465-105681957	GM12878	blood:	n/a	n/a
49	SUZ12	chr14:105681486-105682524	H1-hESC	embryonic stem cell:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105684005-105684055	RPTEC	kidney:	n/a
2	chr14:105683361-105683411	HNPCEpiC	eye:	n/a
3	chr14:105681416-105681466	AG09309	skin:	n/a
4	chr14:105683798-105683848	HCT-116	colon:	n/a
5	chr14:105683361-105683411	A549	lung:	n/a
6	chr14:105683798-105683848	HUVEC	blood vessel:	n/a
7	chr14:105683798-105683848	BE2_C	brain:	n/a
8	chr14:105683361-105683411	HIPEpiC	eye:	n/a
9	chr14:105683361-105683411	K562	blood:	n/a
10	chr14:105681416-105681466	HMEC	breast:	n/a
11	chr14:105681416-105681466	SK-N-MC	brain:	n/a
12	chr14:105683925-105683975	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:105683798-105683848	PANC-1	pancreas:	n/a
14	chr14:105683925-105683975	HRE	kidney:	n/a
15	chr14:105683798-105683848	Hela-S3	cervix:	n/a
16	chr14:105683798-105683848	K562	blood:	n/a
17	chr14:105683798-105683848	NB4	blood:	n/a
18	chr14:105681416-105681466	GM12891	blood:	n/a
19	chr14:105684005-105684055	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:105683361-105683411	H1-hESC	embryonic stem cell:	embryo
21	chr14:105683925-105683975	SK-N-SH_RA	brain:	n/a
22	chr14:105683798-105683848	HNPCEpiC	eye:	n/a
23	chr14:105684005-105684055	GM19239	blood:	n/a
24	chr14:105683798-105683848	HIPEpiC	eye:	n/a
25	chr14:105684005-105684055	NHBE	bronchial:	n/a
26	chr14:105681416-105681466	AoSMC	blood vessel:	n/a
27	chr14:105683925-105683975	A549	lung:	n/a
28	chr14:105683798-105683848	GM06990	blood:	n/a
29	chr14:105681416-105681466	PrEC	prostate:	n/a
30	chr14:105683925-105683975	HCT-116	colon:	n/a
31	chr14:105681416-105681466	HL-60	blood:	n/a
32	chr14:105683798-105683848	T-47D	breast:	n/a
33	chr14:105684005-105684055	HCM	heart:	n/a
34	chr14:105683798-105683848	SK-N-MC	brain:	n/a
35	chr14:105683361-105683411	GM12878	blood:	n/a
36	chr14:105684005-105684055	HRPEpiC	eye:	n/a
37	chr14:105683798-105683848	AG09319	gingival:	n/a
38	chr14:105683925-105683975	GM12891	blood:	n/a
39	chr14:105681416-105681466	LNCaP	prostate:	n/a
40	chr14:105684005-105684055	AG04450	lung:	fetal
41	chr14:105681416-105681466	NT2-D1	testis:	n/a
42	chr14:105684005-105684055	AG04449	skin:	fetal
43	chr14:105684005-105684055	HMEC	breast:	n/a
44	chr14:105683361-105683411	GM06990	blood:	n/a
45	chr14:105683798-105683848	HAEpiC	amniotic membrane:	n/a
46	chr14:105683361-105683411	U87	brain:	n/a
47	chr14:105681416-105681466	MCF-7	breast:	n/a
48	chr14:105683361-105683411	NHDF-neo	bronchial:	n/a
49	chr14:105683925-105683975	SKMC	muscle:	n/a
50	chr14:105683361-105683411	NHBE	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105681198..105683564-chr14:105712338..105715416,3	MCF-7	breast:
2	chr14:105680829..105682565-chr14:105686561..105688543,2	MCF-7	breast:
3	chr14:105671389..105673472-chr14:105681134..105682646,2	K562	blood:
4	chr14:105678829..105680411-chr14:105684341..105687261,3	MCF-7	breast:
5	chr14:105682211..105684471-chr14:105686659..105689301,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-3	chr14:105681490-105682260	NONHSAT040337
2	lnc-BTBD6-3	chr14:105682370-105682401	NONHSAT040337

No data

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

Extended variants
information (count: 234 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:234 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77208236	chr14:105680410-105680411	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs7147888	chr14:105680414-105680415	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs117780681	chr14:105680432-105680433	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185486538	chr14:105680441-105680442	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147563940	chr14:105680451-105680452	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141934770	chr14:105680455-105680456	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190011669	chr14:105680459-105680460	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35736913	chr14:105680474-105680475	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs181407261	chr14:105680475-105680476	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587643561	chr14:105680518-105680519	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587672569	chr14:105680538-105680539	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370472942	chr14:105680541-105680542	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374902999	chr14:105680573-105680574	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs587773534	chr14:105680623-105680624	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587656209	chr14:105680663-105680664	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587737748	chr14:105680669-105680670	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587596589	chr14:105680675-105680676	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587644330	chr14:105680691-105680692	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587719745	chr14:105680694-105680695	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587602631	chr14:105680701-105680702	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587674509	chr14:105680720-105680721	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34448993	chr14:105680769-105680770	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs147118704	chr14:105680773-105680774	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587609738	chr14:105680785-105680786	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184770098	chr14:105680788-105680789	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189232751	chr14:105680826-105680827	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77506769	chr14:105680838-105680839	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587694664	chr14:105680857-105680858	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200301308	chr14:105680863-105680864	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587726040	chr14:105680866-105680867	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587629981	chr14:105680881-105680882	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34491320	chr14:105680884-105680885	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587626059	chr14:105680913-105680914	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs587702854	chr14:105680930-105680931	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587773767	chr14:105680944-105680945	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs587657986	chr14:105680949-105680950	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587715484	chr14:105680969-105680970	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113210876	chr14:105681061-105681062	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141059672	chr14:105681086-105681087	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587639038	chr14:105681095-105681096	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369425093	chr14:105681145-105681146	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587725105	chr14:105681149-105681150	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs180965036	chr14:105681168-105681169	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587658454	chr14:105681176-105681177	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185912416	chr14:105681177-105681178	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs191607947	chr14:105681270-105681271	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs74092222	chr14:105681285-105681286	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs587740953	chr14:105681309-105681310	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs138847182	chr14:105681313-105681314	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs587663755	chr14:105681359-105681360	Weak transcription Enhancers Strong transcription Genic 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:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105663800-105681600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr14:105668200-105687200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr14:105668600-105683000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr14:105668600-105714200	Weak transcription	HUVEC	blood vessel
5	chr14:105668800-105683000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr14:105669800-105681600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr14:105669800-105683400	Weak transcription	Fetal Thymus	thymus
8	chr14:105669800-105684800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr14:105669800-105691200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr14:105669800-105713800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:105671000-105681400	Weak transcription	Fetal Kidney	kidney
12	chr14:105671000-105682000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr14:105671400-105697000	Weak transcription	Small Intestine	intestine
14	chr14:105671600-105683000	Weak transcription	Colon Smooth Muscle	Colon
15	chr14:105671600-105689400	Weak transcription	NHEK	skin
16	chr14:105671800-105681800	Weak transcription	Fetal Brain Male	brain
17	chr14:105672200-105694200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:105672400-105681600	Weak transcription	Fetal Lung	lung
19	chr14:105672400-105683200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr14:105672400-105687000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr14:105672400-105713200	Weak transcription	Osteobl	bone
22	chr14:105672600-105681800	Weak transcription	Brain Angular Gyrus	brain
23	chr14:105672600-105695600	Weak transcription	HMEC	breast
24	chr14:105673400-105690000	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr14:105673600-105687400	Weak transcription	HepG2	liver
26	chr14:105673600-105713600	Weak transcription	Stomach Mucosa	stomach
27	chr14:105673800-105684800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:105673800-105689800	Weak transcription	Hela-S3	cervix
29	chr14:105674000-105696000	Strong transcription	Fetal Stomach	stomach
30	chr14:105674000-105698600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:105674200-105681400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:105674200-105685600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:105674200-105687000	Weak transcription	Right Atrium	heart
34	chr14:105674200-105687200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr14:105674200-105695800	Strong transcription	Fetal Intestine Small	intestine
36	chr14:105674400-105683600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr14:105674800-105687600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr14:105674800-105689600	Weak transcription	K562	blood
39	chr14:105674800-105694200	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr14:105674800-105695400	Strong transcription	Fetal Brain Female	brain
41	chr14:105674800-105696000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:105675000-105681200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:105675200-105681400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr14:105675200-105687000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr14:105675200-105695800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:105675400-105680800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
47	chr14:105675400-105681200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr14:105675400-105681200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr14:105675400-105681600	Strong transcription	Lung	lung
50	chr14:105675400-105681800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links