Variant report

Variant	nsv976811
Chromosome Location	chr14:24421381-24470070
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1216)
CpG islands
(count:2079)
Chromatin interactive
region (count:11)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1216 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24443416-24443612	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24422800-24422908	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:24423178-24423574	HepG2	liver:	n/a	n/a
4	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
5	ATF3	chr14:24423153-24423533	A549	lung:	n/a	n/a
6	BACH1	chr14:24439122-24439137	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr14:24423720-24424085	GM12878	blood:	n/a	n/a
9	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
10	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
11	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
12	BCL11A	chr14:24423865-24424037	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:24423190-24423452	GM12878	blood:	n/a	n/a
14	BCL3	chr14:24422958-24423594	A549	lung:	n/a	n/a
15	BCLAF1	chr14:24422706-24423635	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
17	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
18	BHLHE40	chr14:24423117-24423544	K562	blood:	n/a	n/a
19	BHLHE40	chr14:24422878-24423495	HepG2	liver:	n/a	n/a
20	BHLHE40	chr14:24422805-24422983	GM12878	blood:	n/a	n/a
21	BHLHE40	chr14:24422789-24422794	K562	blood:	n/a	n/a
22	BRCA1	chr14:24422911-24423016	HepG2	liver:	n/a	n/a
23	BRCA1	chr14:24423250-24423488	HepG2	liver:	n/a	n/a
24	BRCA1	chr14:24423242-24423570	Hela-S3	cervix:	n/a	n/a
25	CCNT2	chr14:24422729-24423159	K562	blood:	n/a	chr14:24422739-24422748
26	CEBPB	chr14:24423214-24423650	Hela-S3	cervix:	n/a	chr14:24423462-24423473
27	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
28	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
29	CEBPB	chr14:24423287-24423491	K562	blood:	n/a	chr14:24423462-24423473
30	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
31	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:24423302-24423566	IMR90	lung:	n/a	chr14:24423462-24423473
33	CEBPB	chr14:24422846-24423653	HepG2	liver:	n/a	chr14:24423462-24423473
34	CEBPB	chr14:24423255-24423518	HepG2	liver:	n/a	chr14:24423462-24423473
35	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
36	CEBPB	chr14:24423347-24423547	K562	blood:	n/a	chr14:24423462-24423473
37	CEBPB	chr14:24423180-24423697	A549	lung:	n/a	chr14:24423462-24423473
38	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
39	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
40	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
41	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
42	CEBPB	chr14:24423252-24423596	HepG2	liver:	n/a	chr14:24423462-24423473
43	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
44	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
45	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
46	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
47	CEBPD	chr14:24423163-24423525	HepG2	liver:	n/a	n/a
48	CEBPD	chr14:24422642-24423596	HepG2	liver:	n/a	n/a
49	CEBPD	chr14:24422665-24423162	HepG2	liver:	n/a	n/a
50	CEBPD	chr14:24439025-24439361	HepG2	liver:	n/a	n/a

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24422837-24422887	ECC-1	luminal epithelium:	n/a
2	chr14:24438909-24438959	BJ	skin:	n/a
3	chr14:24458299-24458349	AG10803	skin:	n/a
4	chr14:24423140-24423190	HCF	heart:	n/a
5	chr14:24424191-24424241	AG10803	skin:	n/a
6	chr14:24422837-24422887	ECC-1	luminal epithelium:	n/a
7	chr14:24438909-24438959	BJ	skin:	n/a
8	chr14:24458299-24458349	AG10803	skin:	n/a
9	chr14:24423140-24423190	HCF	heart:	n/a
10	chr14:24424191-24424241	AG10803	skin:	n/a
11	chr14:24423140-24423190	ProgFib	skin:	n/a
12	chr14:24458208-24458258	HL-60	blood:	n/a
13	chr14:24458004-24458054	HEEpiC	esophagus:	n/a
14	chr14:24458014-24458064	HAEpiC	amniotic membrane:	n/a
15	chr14:24422368-24422418	RPTEC	kidney:	n/a
16	chr14:24458345-24458395	LNCaP	prostate:	n/a
17	chr14:24435159-24435209	RPTEC	kidney:	n/a
18	chr14:24423199-24423249	GM12892	blood:	n/a
19	chr14:24439430-24439480	SKMC	muscle:	n/a
20	chr14:24457915-24457965	SAEC	small airway:	n/a
21	chr14:24423483-24423533	NT2-D1	testis:	n/a
22	chr14:24422368-24422418	AG10803	skin:	n/a
23	chr14:24439157-24439207	Hela-S3	cervix:	n/a
24	chr14:24457509-24457559	H1-hESC	embryonic stem cell:	embryo
25	chr14:24458099-24458149	PFSK-1	brain:	n/a
26	chr14:24422419-24422469	HCF	heart:	n/a
27	chr14:24454443-24454493	SK-N-SH	brain:	n/a
28	chr14:24423031-24423081	GM12892	blood:	n/a
29	chr14:24422928-24422978	AoSMC	blood vessel:	n/a
30	chr14:24457915-24457965	AG09309	skin:	n/a
31	chr14:24424191-24424241	T-47D	breast:	n/a
32	chr14:24425012-24425062	T-47D	breast:	n/a
33	chr14:24458299-24458349	HCM	heart:	n/a
34	chr14:24457915-24457965	SK-N-SH	brain:	n/a
35	chr14:24422872-24422922	MCF-7	breast:	n/a
36	chr14:24424191-24424241	AG09319	gingival:	n/a
37	chr14:24458345-24458395	NT2-D1	testis:	n/a
38	chr14:24438909-24438959	NHDF-neo	bronchial:	n/a
39	chr14:24422368-24422418	SK-N-MC	brain:	n/a
40	chr14:24439157-24439207	AoSMC	blood vessel:	n/a
41	chr14:24454443-24454493	HEK293	kidney:	embryo
42	chr14:24423199-24423249	HL-60	blood:	n/a
43	chr14:24422916-24422966	AoSMC	blood vessel:	n/a
44	chr14:24439157-24439207	Hepatocyte	liver:	n/a
45	chr14:24422956-24423006	MCF10A-Er-Src	breast:	n/a
46	chr14:24423864-24423914	Hela-S3	cervix:	n/a
47	chr14:24457915-24457965	HepG2	liver:	n/a
48	chr14:24439157-24439207	HEEpiC	esophagus:	n/a
49	chr14:24439157-24439207	HIPEpiC	eye:	n/a
50	chr14:24422956-24423006	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:
2	chr14:24099084..24100809-chr14:24421080..24423663,2	MCF-7	breast:
3	chr14:24197895..24200996-chr14:24421897..24424681,3	MCF-7	breast:
4	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
5	chr14:24398247..24400471-chr14:24419661..24421717,2	MCF-7	breast:
6	chr1:186344468..186345047-chr14:24423051..24423847,2	MCF-7	breast:
7	chr14:24421589..24424746-chr14:24425153..24428957,4	MCF-7	breast:
8	chr14:24036767..24038500-chr14:24420729..24424068,4	MCF-7	breast:
9	chr14:24421741..24423927-chr14:24582561..24584260,2	K562	blood:
10	chr14:24422551..24423442-chr5:180229136..180229785,2	HCT-116	colon:
11	chr14:24422915..24424427-chr14:24563237..24565374,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24423334-24423406	NR_023923
2	lnc-NRL-1	chr14:24422199-24422628	ENSG00000215256.3
3	lnc-NRL-1	chr14:24422518-24422578	ENSG00000215256.3
4	lnc-NRL-1	chr14:24422783-24423406	NR_023921
5	lnc-NRL-1	chr14:24422983-24423242	NR_023923
6	lnc-NRL-1	chr14:24422983-24423406	ENSG00000215256.3
7	lnc-NRL-1	chr14:24422783-24423331	ENSG00000215256.3
8	lnc-NRL-1	chr14:24422983-24423061	ENSG00000215256.3
9	lnc-NRL-1	chr14:24423957-24424298	NONHSAT035953
10	lnc-NRL-1	chr14:24423334-24423392	NONHSAT035952
11	lnc-NRL-1	chr14:24422783-24423392	NONHSAT035954
12	lnc-NRL-1	chr14:24422983-24423242	ENSG00000215256.3
13	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3
14	lnc-NRL-1	chr14:24422983-24423242	NONHSAT035952
15	lnc-NRL-1	chr14:24423334-24423375	ENSG00000215256.3

No data

Variant related genes	Relation type
DHRS4	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	TF binding region
DHRS4	CpG island
DHRS4L2	CpG island
DHRS4-AS1	CpG island
ENSG00000225766	chromatin interactions
ENSG00000213983	chromatin interactions
ENSG00000047410	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000157181	chromatin interactions
ENSG00000100867	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000187630	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000258464	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000129535	chromatin interactions

Extended variants
information (count: 2542 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2542 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10149094	chr14:24421381-24421382	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564800574	chr14:24421403-24421404	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575182905	chr14:24421404-24421405	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs10137992	chr14:24421472-24421473	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs563699934	chr14:24421475-24421476	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs529313163	chr14:24421480-24421481	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs148235317	chr14:24421483-24421484	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs112055567	chr14:24421510-24421511	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs541384361	chr14:24421521-24421522	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs10149300	chr14:24421575-24421576	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369630171	chr14:24421586-24421587	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs150783616	chr14:24421595-24421596	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs541308150	chr14:24421610-24421611	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs2011934	chr14:24421617-24421618	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs527565012	chr14:24421641-24421642	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs74036728	chr14:24421664-24421665	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs74036729	chr14:24421676-24421677	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs147132946	chr14:24421685-24421686	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs1815263	chr14:24421709-24421710	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs2332118	chr14:24421713-24421714	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs369436734	chr14:24421722-24421723	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs367760070	chr14:24421723-24421724	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs386775659	chr14:24421734-24421735	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs3049828	chr14:24421738-24421739	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs113274437	chr14:24421740-24421741	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
26	rs57684448	chr14:24421741-24421742	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs552852191	chr14:24421742-24421743	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs397832930	chr14:24421750-24421751	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs150051563	chr14:24421754-24421755	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs2332145	chr14:24421834-24421835	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs17099424	chr14:24421841-24421842	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs112725630	chr14:24421874-24421875	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
33	rs573959664	chr14:24421894-24421895	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs542679651	chr14:24421902-24421903	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs4048597	chr14:24421907-24421908	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs4048598	chr14:24421917-24421918	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs4048599	chr14:24421921-24421922	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs2332123	chr14:24421923-24421924	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs2332124	chr14:24421937-24421938	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs551959937	chr14:24421957-24421958	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs4048601	chr14:24421969-24421970	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs4048602	chr14:24421974-24421975	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs374743294	chr14:24421975-24421976	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs112507497	chr14:24422002-24422003	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs551233622	chr14:24422012-24422013	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs142400275	chr14:24422016-24422017	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	mRNA abundance
47	rs4048603	chr14:24422030-24422031	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs546285074	chr14:24422035-24422036	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs566181873	chr14:24422044-24422045	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs529840492	chr14:24422082-24422083	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24405600-24422400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr14:24405800-24421400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr14:24405800-24422400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr14:24407400-24422400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr14:24407600-24422200	Weak transcription	Primary B cells from cord blood	blood
6	chr14:24407800-24422400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr14:24410600-24421800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr14:24410800-24421800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr14:24410800-24422000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr14:24410800-24422400	Weak transcription	Aorta	Aorta
11	chr14:24412200-24422400	Weak transcription	Esophagus	oesophagus
12	chr14:24413600-24421400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr14:24419200-24422200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:24420200-24421400	Enhancers	Pancreas	Pancrea
15	chr14:24420400-24422000	Weak transcription	NHEK	skin
16	chr14:24420400-24422200	Weak transcription	Primary T cells from cord blood	blood
17	chr14:24420400-24422200	Weak transcription	HSMM	muscle
18	chr14:24420400-24422400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr14:24420400-24422400	Enhancers	Placenta	Placenta
20	chr14:24420600-24421400	Enhancers	Ovary	ovary
21	chr14:24420600-24421800	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr14:24420800-24421400	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr14:24420800-24421400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr14:24420800-24421400	Enhancers	Fetal Thymus	thymus
25	chr14:24420800-24421400	Enhancers	Lung	lung
26	chr14:24420800-24421400	Enhancers	Psoas Muscle	Psoas
27	chr14:24420800-24421400	Enhancers	Right Atrium	heart
28	chr14:24420800-24421600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr14:24420800-24421600	Enhancers	Fetal Stomach	stomach
30	chr14:24420800-24421600	Enhancers	Spleen	Spleen
31	chr14:24420800-24421800	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr14:24420800-24422200	Enhancers	Brain Cingulate Gyrus	brain
33	chr14:24420800-24422400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr14:24420800-24422400	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr14:24421000-24421400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:24421000-24421400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr14:24421000-24421400	Flanking Active TSS	Brain Angular Gyrus	brain
38	chr14:24421000-24421400	Flanking Active TSS	Brain Anterior Caudate	brain
39	chr14:24421000-24421400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr14:24421000-24421400	Enhancers	Fetal Brain Male	brain
41	chr14:24421000-24421400	Enhancers	Gastric	stomach
42	chr14:24421000-24421600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr14:24421000-24421600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr14:24421000-24421600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr14:24421000-24421600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:24421000-24421600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr14:24421000-24421600	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr14:24421000-24421600	Enhancers	Fetal Muscle Trunk	muscle
49	chr14:24421000-24421600	Enhancers	Left Ventricle	heart
50	chr14:24421000-24421800	Enhancers	Fetal Lung	lung

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