Variant report

Variant	nsv974312
Chromosome Location	chr14:21652582-21678548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:806)
CpG islands
(count:367)
Chromatin interactive
region (count:21)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:21653751-21653965	K562	blood:	n/a	n/a
2	ATF2	chr14:21671164-21671970	GM12878	blood:	n/a	n/a
3	ATF2	chr14:21674092-21674706	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr14:21673281-21674952	GM12878	blood:	n/a	n/a
5	ATF2	chr14:21669277-21669678	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr14:21671705-21673219	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr14:21672214-21673111	GM12878	blood:	n/a	n/a
8	BCL3	chr14:21665003-21666748	A549	lung:	n/a	n/a
9	BCL3	chr14:21670042-21670347	GM12878	blood:	n/a	n/a
10	BCL3	chr14:21667303-21667605	GM12878	blood:	n/a	n/a
11	BCL3	chr14:21663286-21664632	A549	lung:	n/a	n/a
12	BCL3	chr14:21673287-21673627	GM12878	blood:	n/a	n/a
13	BCL3	chr14:21666904-21669895	A549	lung:	n/a	n/a
14	BCL3	chr14:21673671-21674743	GM12878	blood:	n/a	n/a
15	BCL3	chr14:21667620-21668187	A549	lung:	n/a	n/a
16	BCL3	chr14:21668935-21669706	GM12878	blood:	n/a	n/a
17	BCL3	chr14:21669980-21671752	A549	lung:	n/a	n/a
18	BCL3	chr14:21664965-21666757	A549	lung:	n/a	n/a
19	BCL3	chr14:21670476-21673261	GM12878	blood:	n/a	chr14:21672778-21672787
20	BCLAF1	chr14:21674052-21674559	GM12878	blood:	n/a	n/a
21	BCLAF1	chr14:21671128-21675456	GM12878	blood:	n/a	chr14:21672778-21672787
22	BHLHE40	chr14:21660193-21660398	K562	blood:	n/a	n/a
23	BRCA1	chr14:21663745-21663770	HepG2	liver:	n/a	n/a
24	CCNT2	chr14:21674840-21675631	K562	blood:	n/a	n/a
25	CCNT2	chr14:21676495-21676698	K562	blood:	n/a	n/a
26	CCNT2	chr14:21674265-21674637	K562	blood:	n/a	n/a
27	CCNT2	chr14:21660109-21660405	K562	blood:	n/a	n/a
28	CEBPB	chr14:21665611-21665883	K562	blood:	n/a	n/a
29	CEBPB	chr14:21665568-21665898	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:21665558-21665907	A549	lung:	n/a	n/a
31	CEBPB	chr14:21665566-21665906	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:21660939-21661110	H1-hESC	embryonic stem cell:	n/a	chr14:21661097-21661108
33	CEBPB	chr14:21668250-21668441	HepG2	liver:	n/a	chr14:21668348-21668359
34	CEBPB	chr14:21660054-21660282	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr14:21659973-21660136	K562	blood:	n/a	n/a
36	CEBPB	chr14:21665624-21665765	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:21661038-21661205	K562	blood:	n/a	chr14:21661097-21661108
38	CEBPB	chr14:21660945-21661264	IMR90	lung:	n/a	chr14:21661097-21661108
39	CEBPB	chr14:21668282-21668680	IMR90	lung:	n/a	chr14:21668348-21668359
40	CEBPB	chr14:21665552-21665908	IMR90	lung:	n/a	n/a
41	CEBPB	chr14:21660061-21660213	HepG2	liver:	n/a	n/a
42	CEBPB	chr14:21665417-21665925	A549	lung:	n/a	n/a
43	CEBPB	chr14:21660914-21661269	HepG2	liver:	n/a	chr14:21661097-21661108
44	CHD1	chr14:21659958-21660255	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr14:21671544-21671872	K562	blood:	n/a	n/a
46	CHD2	chr14:21660230-21660286	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr14:21671796-21671930	HepG2	liver:	n/a	n/a
48	CHD2	chr14:21672290-21672387	K562	blood:	n/a	n/a
49	CHD2	chr14:21660291-21660470	HepG2	liver:	n/a	n/a
50	CREB1	chr14:21671427-21673664	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21656260-21656310	GM12892	blood:	n/a
2	chr14:21656260-21656310	GM12892	blood:	n/a
3	chr14:21660372-21660422	HCPEpiC	choroid plexus:	n/a
4	chr14:21673796-21673846	AG09319	gingival:	n/a
5	chr14:21676297-21676347	AG09309	skin:	n/a
6	chr14:21660372-21660422	GM12878	blood:	n/a
7	chr14:21656260-21656310	HRPEpiC	eye:	n/a
8	chr14:21657028-21657078	PANC-1	pancreas:	n/a
9	chr14:21673796-21673846	SK-N-MC	brain:	n/a
10	chr14:21673796-21673846	SK-N-SH_RA	brain:	n/a
11	chr14:21673796-21673846	GM19239	blood:	n/a
12	chr14:21673491-21673541	PFSK-1	brain:	n/a
13	chr14:21657028-21657078	GM12878	blood:	n/a
14	chr14:21657028-21657078	Hepatocyte	liver:	n/a
15	chr14:21656260-21656310	LNCaP	prostate:	n/a
16	chr14:21676297-21676347	AG10803	skin:	n/a
17	chr14:21673491-21673541	H1-hESC	embryonic stem cell:	embryo
18	chr14:21673796-21673846	U87	brain:	n/a
19	chr14:21656260-21656310	HIPEpiC	eye:	n/a
20	chr14:21673796-21673846	HCM	heart:	n/a
21	chr14:21673796-21673846	AG09309	skin:	n/a
22	chr14:21676297-21676347	HUVEC	blood vessel:	n/a
23	chr14:21656260-21656310	NHBE	bronchial:	n/a
24	chr14:21676297-21676347	SKMC	muscle:	n/a
25	chr14:21676297-21676347	HEK293	kidney:	embryo
26	chr14:21673796-21673846	SK-N-SH	brain:	n/a
27	chr14:21673491-21673541	HCM	heart:	n/a
28	chr14:21673796-21673846	RPTEC	kidney:	n/a
29	chr14:21657028-21657078	SK-N-SH_RA	brain:	n/a
30	chr14:21657028-21657078	SKMC	muscle:	n/a
31	chr14:21673796-21673846	Jurkat	blood:	n/a
32	chr14:21676297-21676347	T-47D	breast:	n/a
33	chr14:21656260-21656310	SAEC	small airway:	n/a
34	chr14:21676297-21676347	HCF	heart:	n/a
35	chr14:21657028-21657078	PrEC	prostate:	n/a
36	chr14:21657028-21657078	HCF	heart:	n/a
37	chr14:21656260-21656310	HL-60	blood:	n/a
38	chr14:21676297-21676347	AG04449	skin:	fetal
39	chr14:21676297-21676347	Hepatocyte	liver:	n/a
40	chr14:21673491-21673541	AG10803	skin:	n/a
41	chr14:21673796-21673846	HNPCEpiC	eye:	n/a
42	chr14:21657028-21657078	U87	brain:	n/a
43	chr14:21673491-21673541	HCT-116	colon:	n/a
44	chr14:21657028-21657078	ProgFib	skin:	n/a
45	chr14:21673491-21673541	HAEpiC	amniotic membrane:	n/a
46	chr14:21676297-21676347	NB4	blood:	n/a
47	chr14:21676297-21676347	U87	brain:	n/a
48	chr14:21676297-21676347	AoSMC	blood vessel:	n/a
49	chr14:21676297-21676347	IMR90	lung:	fetal
50	chr14:21673491-21673541	GM12878	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21667683..21669653-chr14:21671055..21672975,3	K562	blood:
2	chr14:21676404..21679681-chr14:21680227..21682594,3	K562	blood:
3	chr14:21670255..21673011-chr14:21674256..21675777,2	K562	blood:
4	chr14:21659338..21661906-chr14:21661938..21664120,2	MCF-7	breast:
5	chr14:21521893..21523709-chr14:21667067..21669493,2	K562	blood:
6	chr14:21538648..21540908-chr14:21670664..21672653,2	K562	blood:
7	chr14:21659836..21662080-chr14:21664452..21667045,3	MCF-7	breast:
8	chr14:21649811..21651897-chr14:21658475..21660736,2	MCF-7	breast:
9	chr14:21673262..21673938-chr2:85132255..85133130,2	NB4	blood:
10	chr14:21671465..21674942-chr14:21676988..21681110,7	MCF-7	breast:
11	chr14:21670001..21672457-chr14:21706378..21709017,2	K562	blood:
12	chr14:21671465..21674942-chr14:21676988..21681110,7	MCF-7	breast:
13	chr14:21659338..21661906-chr14:21661938..21664120,2	MCF-7	breast:
14	chr14:21667683..21669653-chr14:21671055..21672975,3	K562	blood:
15	chr14:21651029..21652913-chr14:21654690..21656270,2	K562	blood:
16	chr14:21667283..21669208-chr14:21670633..21672838,2	MCF-7	breast:
17	chr14:21667283..21669208-chr14:21670633..21672838,2	MCF-7	breast:
18	chr14:21678499..21681454-chr14:21736107..21737906,2	MCF-7	breast:
19	chr14:21659836..21662080-chr14:21664452..21667045,3	MCF-7	breast:
20	chr14:21651029..21652913-chr14:21654690..21656270,2	K562	blood:
21	chr14:21678068..21679716-chr14:21682875..21685617,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPC-1	chr14:21674770-21675059	NONHSAT035664
2	lnc-HNRNPC-1	chr14:21674770-21675059	ENSG00000258441
3	lnc-RPGRIP1-2	chr14:21668434-21668954	ENSG00000247386
4	lnc-RPGRIP1-2	chr14:21669731-21672514	ENSG00000247386
5	lnc-HNRNPC-1	chr14:21668240-21672514	NONHSAT035665
6	lnc-HNRNPC-1	chr14:21674770-21675059	ENSG00000251466
7	lnc-HNRNPC-1	chr14:21668238-21670092	NONHSAT035664
8	lnc-HNRNPC-1	chr14:21668238-21673662	ENSG00000258441
9	lnc-HNRNPC-1	chr14:21668620-21670092	ENSG00000258441
10	lnc-HNRNPC-2	chr14:21652500-21653118	NONHSAT035662
11	lnc-HNRNPC-1	chr14:21668621-21670092	ENSG00000251466

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HNRNPC	hsa-miR-142-3p	chr14:21678022-21678046

Variant related genes	Relation type
LINC00641	TF binding region
ENSG00000258906	TF binding region
LINC00641	CpG island
ENSG00000258906	CpG island
ENSG00000092199	chromatin interactions
ENSG00000258441	chromatin interactions
ENSG00000034510	chromatin interactions
ENSG00000165795	chromatin interactions
MTA2	miRNA target sites
RUNX2	miRNA target sites
STK4	miRNA target sites
GFPT2	miRNA target sites

Extended variants
information (count: 1094 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1094 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148273002	chr14:21652607-21652608	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs546680978	chr14:21652620-21652621	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs182583371	chr14:21652649-21652650	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs538427902	chr14:21652740-21652741	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs552377369	chr14:21652785-21652786	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs569042491	chr14:21652793-21652794	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs12436835	chr14:21652837-21652838	Flanking Active TSS Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs77980562	chr14:21652838-21652839	Flanking Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs12431416	chr14:21652897-21652898	Flanking Active TSS Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs12434234	chr14:21652934-21652935	Flanking Active TSS Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553937967	chr14:21652935-21652936	Flanking Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs548830406	chr14:21652948-21652949	Flanking Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs117490583	chr14:21653003-21653004	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs186563492	chr14:21653091-21653092	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs576663331	chr14:21653096-21653097	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
16	rs542497389	chr14:21653115-21653116	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
17	rs562380047	chr14:21653133-21653134	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs77213511	chr14:21653147-21653148	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs559186048	chr14:21653171-21653172	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs546640382	chr14:21653188-21653189	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs559970758	chr14:21653205-21653206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532270104	chr14:21653215-21653216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552075338	chr14:21653220-21653221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192330194	chr14:21653240-21653241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537652332	chr14:21653242-21653243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548040429	chr14:21653292-21653293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73575703	chr14:21653325-21653326	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs141134293	chr14:21653355-21653356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs118124541	chr14:21653359-21653360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554163996	chr14:21653374-21653375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147355914	chr14:21653401-21653402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139540859	chr14:21653428-21653429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185523550	chr14:21653438-21653439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576672139	chr14:21653449-21653450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553821871	chr14:21653493-21653494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114369913	chr14:21653500-21653501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188732171	chr14:21653544-21653545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200823512	chr14:21653598-21653599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs36098578	chr14:21653600-21653601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12434619	chr14:21653649-21653650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570045038	chr14:21653666-21653667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376674862	chr14:21653667-21653668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57894855	chr14:21653688-21653689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560136572	chr14:21653747-21653748	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs532105024	chr14:21653775-21653776	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs542241367	chr14:21653806-21653807	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368039992	chr14:21653807-21653808	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs28733840	chr14:21653842-21653843	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs543097219	chr14:21653864-21653865	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs562452894	chr14:21653915-21653916	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21651200-21659600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr14:21651800-21652800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:21652000-21654200	Enhancers	Fetal Brain Male	brain
4	chr14:21652800-21653000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr14:21652800-21653200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:21653000-21653600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr14:21653000-21654200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr14:21653200-21654000	Enhancers	Small Intestine	intestine
9	chr14:21653200-21654200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:21653200-21654200	Enhancers	Fetal Lung	lung
11	chr14:21653200-21654800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:21653400-21654200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr14:21653600-21654200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr14:21653800-21654000	Enhancers	Lung	lung
15	chr14:21653800-21654200	Enhancers	Primary hematopoietic stem cells	blood
16	chr14:21654200-21659200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:21654200-21659400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr14:21654200-21659400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr14:21654800-21659400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:21656200-21656400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr14:21656200-21656400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr14:21656200-21656400	Bivalent Enhancer	Lung	lung
23	chr14:21656200-21660000	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr14:21656400-21656600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:21656400-21660000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr14:21656800-21659600	Weak transcription	Lung	lung
27	chr14:21657400-21658000	Enhancers	HepG2	liver
28	chr14:21658000-21659200	Weak transcription	HepG2	liver
29	chr14:21659200-21659400	Enhancers	Dnd41	blood
30	chr14:21659200-21659400	Enhancers	HepG2	liver
31	chr14:21659200-21659600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr14:21659200-21659800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr14:21659200-21659800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr14:21659200-21660000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr14:21659200-21660000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:21659200-21660000	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr14:21659200-21660000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
38	chr14:21659200-21660200	Enhancers	Fetal Thymus	thymus
39	chr14:21659400-21659600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:21659400-21659600	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr14:21659400-21659600	Enhancers	Hela-S3	cervix
42	chr14:21659400-21659800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr14:21659400-21659800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr14:21659400-21659800	Enhancers	Primary T cells from cord blood	blood
45	chr14:21659400-21659800	Enhancers	Primary T cells fromperipheralblood	blood
46	chr14:21659400-21659800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr14:21659400-21659800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr14:21659400-21659800	Enhancers	Brain Angular Gyrus	brain
49	chr14:21659400-21659800	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr14:21659400-21659800	Enhancers	K562	blood

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