Variant report

Variant	nsv932194
Chromosome Location	chr14:39173578-39411337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1157)
CpG islands
(count:183)
Chromatin interactive
region (count:45)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:39337705-39338397	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:39324637-39325034	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:39350421-39350651	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:39353442-39353584	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:39336756-39337350	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:39191075-39191411	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:39352251-39352701	HepG2	liver:	n/a	chr14:39352333-39352349
8	BACH1	chr14:39193066-39193072	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:39378402-39378716	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:39401603-39401789	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr14:39377237-39377526	GM12878	blood:	n/a	n/a
12	BHLHE40	chr14:39324868-39325068	HepG2	liver:	n/a	n/a
13	BRCA1	chr14:39321919-39321965	GM12878	blood:	n/a	n/a
14	BRCA1	chr14:39247661-39247666	GM12878	blood:	n/a	n/a
15	BRCA1	chr14:39336676-39337062	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:39308735-39309404	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr14:39258149-39258462	HepG2	liver:	n/a	chr14:39258283-39258294
18	CEBPB	chr14:39347306-39347486	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:39261058-39261258	HepG2	liver:	n/a	chr14:39261104-39261117 chr14:39261105-39261116
20	CEBPB	chr14:39310365-39310688	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:39310341-39310683	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:39258136-39258446	IMR90	lung:	n/a	chr14:39258283-39258294
23	CEBPB	chr14:39260985-39261342	H1-hESC	embryonic stem cell:	n/a	chr14:39261104-39261117 chr14:39261105-39261116
24	CEBPB	chr14:39324839-39325134	HepG2	liver:	n/a	chr14:39324998-39325009
25	CEBPB	chr14:39259898-39259942	HepG2	liver:	n/a	chr14:39259913-39259926
26	CEBPB	chr14:39397314-39397701	MCF-7	breast:	n/a	chr14:39397513-39397524
27	CEBPB	chr14:39376341-39376661	HepG2	liver:	n/a	chr14:39376550-39376563 chr14:39376467-39376476 chr14:39376467-39376478 chr14:39376467-39376478 chr14:39376488-39376499 chr14:39376465-39376476 chr14:39376467-39376476 chr14:39376465-39376478 chr14:39376487-39376504 chr14:39376467-39376476 chr14:39376467-39376476
28	CEBPB	chr14:39397346-39397680	K562	blood:	n/a	chr14:39397513-39397524
29	CEBPB	chr14:39376355-39376611	A549	lung:	n/a	chr14:39376550-39376563 chr14:39376467-39376476 chr14:39376467-39376478 chr14:39376467-39376478 chr14:39376488-39376499 chr14:39376465-39376476 chr14:39376467-39376476 chr14:39376465-39376478 chr14:39376487-39376504 chr14:39376467-39376476 chr14:39376467-39376476
30	CEBPB	chr14:39309020-39309318	ECC-1	luminal epithelium:	n/a	chr14:39309136-39309147
31	CEBPB	chr14:39308777-39310096	Hela-S3	cervix:	n/a	chr14:39309136-39309147
32	CEBPB	chr14:39258148-39258411	K562	blood:	n/a	chr14:39258283-39258294
33	CEBPB	chr14:39257566-39257629	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:39361291-39361420	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:39308980-39309305	HepG2	liver:	n/a	chr14:39309136-39309147
36	CEBPB	chr14:39176051-39176254	HepG2	liver:	n/a	chr14:39176157-39176168 chr14:39176157-39176170
37	CEBPB	chr14:39350450-39350598	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:39397351-39397676	HepG2	liver:	n/a	chr14:39397513-39397524
39	CEBPB	chr14:39347803-39348002	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:39309002-39309208	A549	lung:	n/a	chr14:39309136-39309147
41	CEBPB	chr14:39309520-39309747	HepG2	liver:	n/a	n/a
42	CEBPB	chr14:39180257-39180308	HepG2	liver:	n/a	chr14:39180263-39180274
43	CEBPB	chr14:39260262-39260316	A549	lung:	n/a	n/a
44	CEBPB	chr14:39310368-39310591	A549	lung:	n/a	n/a
45	CEBPB	chr14:39309022-39309361	MCF-7	breast:	n/a	chr14:39309136-39309147
46	CEBPB	chr14:39324868-39325090	HepG2	liver:	n/a	chr14:39324998-39325009
47	CEBPB	chr14:39228767-39228863	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:39347368-39347566	A549	lung:	n/a	n/a
49	CHD1	chr14:39336674-39337209	IMR90	lung:	n/a	n/a
50	CHD2	chr14:39261150-39261334	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:39308079-39308129	HCM	heart:	n/a
2	chr14:39308079-39308129	ECC-1	luminal epithelium:	n/a
3	chr14:39308079-39308129	HRCEpiC	kidney:	n/a
4	chr14:39307962-39308012	HRE	kidney:	n/a
5	chr14:39308881-39308931	NHDF-neo	bronchial:	n/a
6	chr14:39308079-39308129	HCF	heart:	n/a
7	chr14:39308079-39308129	HepG2	liver:	n/a
8	chr14:39308079-39308129	Jurkat	blood:	n/a
9	chr14:39307962-39308012	SK-N-MC	brain:	n/a
10	chr14:39308079-39308129	H1-hESC	embryonic stem cell:	embryo
11	chr14:39307962-39308012	AoSMC	blood vessel:	n/a
12	chr14:39308079-39308129	NT2-D1	testis:	n/a
13	chr14:39308881-39308931	AG09319	gingival:	n/a
14	chr14:39308079-39308129	ProgFib	skin:	n/a
15	chr14:39308079-39308129	AG09309	skin:	n/a
16	chr14:39307962-39308012	U87	brain:	n/a
17	chr14:39308079-39308129	GM06990	blood:	n/a
18	chr14:39308881-39308931	NT2-D1	testis:	n/a
19	chr14:39308881-39308931	HepG2	liver:	n/a
20	chr14:39307962-39308012	HCT-116	colon:	n/a
21	chr14:39307962-39308012	GM19239	blood:	n/a
22	chr14:39308079-39308129	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:39308881-39308931	PANC-1	pancreas:	n/a
24	chr14:39308079-39308129	RPTEC	kidney:	n/a
25	chr14:39307962-39308012	GM06990	blood:	n/a
26	chr14:39308881-39308931	AG04450	lung:	fetal
27	chr14:39308881-39308931	K562	blood:	n/a
28	chr14:39307962-39308012	Caco-2	colon:	n/a
29	chr14:39308881-39308931	ECC-1	luminal epithelium:	n/a
30	chr14:39308079-39308129	GM19239	blood:	n/a
31	chr14:39308881-39308931	HCT-116	colon:	n/a
32	chr14:39308881-39308931	BE2_C	brain:	n/a
33	chr14:39308079-39308129	HL-60	blood:	n/a
34	chr14:39308881-39308931	MCF10A-Er-Src	breast:	n/a
35	chr14:39308881-39308931	IMR90	lung:	fetal
36	chr14:39308881-39308931	SK-N-SH_RA	brain:	n/a
37	chr14:39308079-39308129	GM12891	blood:	n/a
38	chr14:39308881-39308931	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:39308881-39308931	SKMC	muscle:	n/a
40	chr14:39307962-39308012	LNCaP	prostate:	n/a
41	chr14:39307962-39308012	BJ	skin:	n/a
42	chr14:39307962-39308012	ProgFib	skin:	n/a
43	chr14:39307962-39308012	NHBE	bronchial:	n/a
44	chr14:39308079-39308129	PFSK-1	brain:	n/a
45	chr14:39308881-39308931	T-47D	breast:	n/a
46	chr14:39308881-39308931	HIPEpiC	eye:	n/a
47	chr14:39308881-39308931	BJ	skin:	n/a
48	chr14:39308079-39308129	NHDF-neo	bronchial:	n/a
49	chr14:39308881-39308931	HUVEC	blood vessel:	n/a
50	chr14:39308079-39308129	SK-N-MC	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:39269261..39271872-chr14:39273107..39275037,2	K562	blood:
2	chr14:39074220..39075249-chr14:39336439..39337107,3	MCF-7	breast:
3	chr14:39341664..39344220-chr14:39347442..39349909,2	MCF-7	breast:
4	chr14:39190911..39191748-chr14:39503600..39504605,4	MCF-7	breast:
5	chr14:39344148..39344668-chr2:36899113..36899743,2	MCF-7	breast:
6	chr14:39190836..39192002-chr14:39336266..39337492,9	MCF-7	breast:
7	chr14:39336463..39337323-chr14:39484303..39484820,2	MCF-7	breast:
8	chr14:39299667..39302667-chr17:41399639..41402216,3	K562	blood:
9	chr14:39324002..39326709-chr14:39331497..39334526,3	K562	blood:
10	chr14:39191195..39191809-chr14:39336434..39337274,3	MCF-7	breast:
11	chr14:39288692..39291150-chr14:39292998..39295978,2	K562	blood:
12	chr14:39214251..39216737-chr14:39221189..39223720,2	MCF-7	breast:
13	chr14:39190760..39191270-chr14:39336463..39337395,3	K562	blood:
14	chr14:39244076..39244917-chr2:3391368..3392121,2	MCF-7	breast:
15	chr14:39345165..39347327-chr14:39348361..39351300,3	MCF-7	breast:
16	chr14:38372704..38373564-chr14:39336508..39337178,3	K562	blood:
17	chr14:39301147..39302647-chr17:41466196..41467820,2	MCF-7	breast:
18	chr14:39301167..39302667-chr17:41380615..41383519,2	K562	blood:
19	chr14:39324002..39326709-chr14:39331497..39334526,3	K562	blood:
20	chr14:39380747..39381570-chr14:39484361..39485038,2	K562	blood:
21	chr14:21571639..21574238-chr14:39269844..39272001,2	MCF-7	breast:
22	chr14:39190797..39191604-chr14:39484170..39485007,2	MCF-7	breast:
23	chr14:39269261..39271872-chr14:39273107..39275037,2	K562	blood:
24	chr14:39301612..39303299-chr14:39311657..39313476,2	MCF-7	breast:
25	chr14:39299647..39301167-chr17:41400823..41402637,2	MCF-7	breast:
26	chr14:39301612..39303299-chr14:39311657..39313476,2	MCF-7	breast:
27	chr14:39214251..39216737-chr14:39221189..39223720,2	MCF-7	breast:
28	chr14:39284637..39287612-chr14:39288269..39291004,2	K562	blood:
29	chr14:39333342..39335144-chr14:39336605..39338510,2	K562	blood:
30	chr14:39345165..39347327-chr14:39348361..39351300,3	MCF-7	breast:
31	chr14:39341664..39344220-chr14:39347442..39349909,2	MCF-7	breast:
32	chr14:39410789..39411608-chr14:39483894..39485313,6	MCF-7	breast:
33	chr14:39190836..39192002-chr14:39336266..39337492,9	MCF-7	breast:
34	chr14:39116309..39118781-chr14:39205092..39207512,2	MCF-7	breast:
35	chr14:39223383..39224246-chr6:89075754..89076656,2	MCF-7	breast:
36	chr14:39074390..39075072-chr14:39192252..39192857,2	MCF-7	breast:
37	chr14:39288692..39291150-chr14:39292998..39295978,2	K562	blood:
38	chr14:39284637..39287612-chr14:39288269..39291004,2	K562	blood:
39	chr14:39299667..39301167-chr17:41380346..41382223,2	K562	blood:
40	chr14:39366197..39366930-chr7:100486909..100487549,2	MCF-7	breast:
41	chr14:39333342..39335144-chr14:39336605..39338510,2	K562	blood:
42	chr14:39190717..39191738-chr14:39484001..39485313,7	MCF-7	breast:
43	chr14:39191195..39191809-chr14:39336434..39337274,3	MCF-7	breast:
44	chr14:39409994..39412907-chr14:39426330..39428595,2	MCF-7	breast:
45	chr14:39190760..39191270-chr14:39336463..39337395,3	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GEMIN2-2	chr14:39377287-39377321	XLOC_010810
2	lnc-SEC23A-1	chr14:39410558-39410577	ENSG00000259070.1
3	lnc-SEC23A-1	chr14:39308050-39308408	ENSG00000259070.1
4	lnc-SEC23A-1	chr14:39308093-39308408	ENSG00000259070.1
5	lnc-SEC23A-1	chr14:39410724-39410899	ENSG00000259070.1
6	lnc-SEC23A-1	chr14:39410724-39410899	ENSG00000259070.1
7	lnc-GEMIN2-9	chr14:39304593-39304992	NONHSAT036499

No data

Variant related genes	Relation type
LINC00639	TF binding region
KRT8P1	TF binding region
ENSG00000258680	TF binding region
LINC00639	CpG island
KRT8P1	CpG island
ENSG00000258680	CpG island
ENSG00000176125	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000271468	chromatin interactions
ENSG00000171853	chromatin interactions
ENSG00000165804	chromatin interactions
HUWE1	miRNA target sites

Extended variants
information (count: 7185 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:7185 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561179514	chr14:39173615-39173616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574785921	chr14:39173623-39173624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543494343	chr14:39173648-39173649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563340141	chr14:39173659-39173660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551983652	chr14:39173724-39173725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567648025	chr14:39173747-39173748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532700166	chr14:39173776-39173777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552417148	chr14:39173819-39173820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538207516	chr14:39173820-39173821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559543264	chr14:39173835-39173836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183302102	chr14:39173838-39173839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567086944	chr14:39173839-39173840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149641185	chr14:39173866-39173867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527860979	chr14:39173878-39173879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568101407	chr14:39173927-39173928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188080862	chr14:39173939-39173940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556616959	chr14:39174003-39174004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369764316	chr14:39174004-39174005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143417284	chr14:39174006-39174007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577962849	chr14:39174012-39174013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200887398	chr14:39174032-39174033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114876725	chr14:39174045-39174046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372827839	chr14:39174204-39174205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs8007332	chr14:39174214-39174215	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553279473	chr14:39174215-39174216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566664463	chr14:39174236-39174237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535256119	chr14:39174251-39174252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148296303	chr14:39174304-39174305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574884129	chr14:39174331-39174332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141983848	chr14:39174377-39174378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369853566	chr14:39174379-39174380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11845026	chr14:39174391-39174392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189816129	chr14:39174396-39174397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182119192	chr14:39174400-39174401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11844961	chr14:39174420-39174421	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187875632	chr14:39174442-39174443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192608969	chr14:39174487-39174488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373667649	chr14:39174536-39174537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117875162	chr14:39174555-39174556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139633058	chr14:39174590-39174591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556280740	chr14:39174602-39174603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141703363	chr14:39174625-39174626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532912198	chr14:39174655-39174656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546925907	chr14:39174671-39174672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566693913	chr14:39174674-39174675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535739307	chr14:39174675-39174676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555302427	chr14:39174707-39174708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568998813	chr14:39174711-39174712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12586775	chr14:39174715-39174716	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs150773207	chr14:39174758-39174759	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39173400-39173600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr14:39173600-39175800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr14:39175800-39181400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr14:39179800-39180400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr14:39179800-39180800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr14:39181400-39181800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr14:39181800-39185800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr14:39184800-39186200	Weak transcription	Brain Substantia Nigra	brain
9	chr14:39185800-39186200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:39185800-39186800	Enhancers	Brain Hippocampus Middle	brain
11	chr14:39185800-39186800	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr14:39185800-39186800	Enhancers	Hela-S3	cervix
13	chr14:39185800-39187600	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr14:39185800-39188400	Enhancers	Brain Cingulate Gyrus	brain
15	chr14:39186000-39186400	Enhancers	Primary B cells from peripheral blood	blood
16	chr14:39186000-39186400	Enhancers	HSMMtube	muscle
17	chr14:39186000-39186800	Enhancers	Primary B cells from cord blood	blood
18	chr14:39186000-39186800	Enhancers	Brain Angular Gyrus	brain
19	chr14:39186200-39186800	Enhancers	Brain Substantia Nigra	brain
20	chr14:39186400-39186600	Enhancers	Brain Anterior Caudate	brain
21	chr14:39186600-39197000	Weak transcription	Brain Anterior Caudate	brain
22	chr14:39186800-39187800	Weak transcription	Brain Substantia Nigra	brain
23	chr14:39186800-39188000	Weak transcription	Brain Hippocampus Middle	brain
24	chr14:39186800-39191000	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr14:39186800-39197400	Weak transcription	Brain Angular Gyrus	brain
26	chr14:39187600-39197000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr14:39187800-39188200	Enhancers	Adipose Nuclei	Adipose
28	chr14:39187800-39188200	Enhancers	Brain Substantia Nigra	brain
29	chr14:39187800-39188600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr14:39188000-39188400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr14:39188000-39188400	Enhancers	Brain Hippocampus Middle	brain
32	chr14:39188200-39197000	Weak transcription	Brain Substantia Nigra	brain
33	chr14:39188400-39196200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr14:39188400-39197000	Weak transcription	Brain Hippocampus Middle	brain
35	chr14:39188600-39190800	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr14:39189400-39189600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr14:39190800-39191200	Enhancers	HUVEC	blood vessel
38	chr14:39190800-39191800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr14:39191000-39192000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr14:39192000-39193000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr14:39193000-39193200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr14:39193000-39193400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr14:39193400-39194000	Enhancers	Fetal Kidney	kidney
44	chr14:39194000-39201400	Weak transcription	Fetal Kidney	kidney
45	chr14:39196200-39196400	Enhancers	Brain Cingulate Gyrus	brain
46	chr14:39196200-39197400	Enhancers	Fetal Muscle Trunk	muscle
47	chr14:39196200-39197800	Enhancers	Fetal Muscle Leg	muscle
48	chr14:39196400-39196800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:39196400-39196800	Weak transcription	Brain Cingulate Gyrus	brain
50	chr14:39196800-39197400	Enhancers	Brain Cingulate Gyrus	brain

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