Variant report

Variant	nsv564171
Chromosome Location	chr14:31068090-31149630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1583)
CpG islands
(count:610)
Chromatin interactive
region (count:84)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1583 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31125378-31125782	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31126878-31127122	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:31126872-31127129	K562	blood:	n/a	n/a
4	ARID3A	chr14:31091375-31091649	K562	blood:	n/a	n/a
5	ARID3A	chr14:31091039-31091830	HepG2	liver:	n/a	n/a
6	ATF1	chr14:31091142-31091915	K562	blood:	n/a	n/a
7	ATF1	chr14:31086813-31086906	K562	blood:	n/a	n/a
8	ATF2	chr14:31091040-31091625	GM12878	blood:	n/a	n/a
9	ATF2	chr14:31089323-31089846	GM12878	blood:	n/a	n/a
10	ATF2	chr14:31089253-31089845	GM12878	blood:	n/a	n/a
11	ATF2	chr14:31090646-31091953	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr14:31090487-31092090	GM12878	blood:	n/a	n/a
13	ATF2	chr14:31090789-31091861	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr14:31089374-31089710	GM12878	blood:	n/a	chr14:31089538-31089549
15	BATF	chr14:31089440-31089721	GM12878	blood:	n/a	chr14:31089538-31089549
16	BATF	chr14:31091307-31091645	GM12878	blood:	n/a	n/a
17	BCL11A	chr14:31089486-31089678	GM12878	blood:	n/a	chr14:31089537-31089546 chr14:31089538-31089547
18	BCL11A	chr14:31089353-31089762	GM12878	blood:	n/a	chr14:31089537-31089546 chr14:31089538-31089547
19	BCL3	chr14:31090411-31092048	A549	lung:	n/a	n/a
20	BCL3	chr14:31091078-31091714	K562	blood:	n/a	n/a
21	BCL3	chr14:31090258-31092000	A549	lung:	n/a	n/a
22	BCL3	chr14:31091163-31091727	K562	blood:	n/a	n/a
23	BCL3	chr14:31090423-31091866	GM12878	blood:	n/a	n/a
24	BCLAF1	chr14:31090542-31092119	GM12878	blood:	n/a	n/a
25	BCLAF1	chr14:31090531-31092159	GM12878	blood:	n/a	n/a
26	BHLHE40	chr14:31090224-31090793	GM12878	blood:	n/a	n/a
27	BHLHE40	chr14:31090789-31091935	HepG2	liver:	n/a	n/a
28	BHLHE40	chr14:31091222-31091896	K562	blood:	n/a	n/a
29	BHLHE40	chr14:31091018-31092097	GM12878	blood:	n/a	n/a
30	BHLHE40	chr14:31080081-31080524	K562	blood:	n/a	n/a
31	BHLHE40	chr14:31090397-31090990	K562	blood:	n/a	n/a
32	BRCA1	chr14:31090846-31091826	HepG2	liver:	n/a	n/a
33	BRCA1	chr14:31091261-31092022	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr14:31091051-31091729	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr14:31091217-31091620	GM12878	blood:	n/a	n/a
36	BRCA1	chr14:31125461-31125683	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr14:31090973-31091893	HCT-116	colon:	n/a	n/a
38	CBX3	chr14:31091027-31091605	K562	blood:	n/a	n/a
39	CCNT2	chr14:31090625-31091970	K562	blood:	n/a	chr14:31091729-31091738
40	CEBPB	chr14:31126382-31126619	HepG2	liver:	n/a	chr14:31126518-31126531 chr14:31126470-31126481
41	CEBPB	chr14:31076440-31076640	A549	lung:	n/a	chr14:31076513-31076524
42	CEBPB	chr14:31125388-31125798	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr14:31072645-31072993	IMR90	lung:	n/a	n/a
44	CEBPB	chr14:31091313-31091598	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:31125420-31125819	IMR90	lung:	n/a	n/a
46	CEBPB	chr14:31098538-31099086	A549	lung:	n/a	chr14:31098839-31098850
47	CEBPB	chr14:31121249-31121532	K562	blood:	n/a	n/a
48	CEBPB	chr14:31076468-31076665	HepG2	liver:	n/a	chr14:31076513-31076524
49	CEBPB	chr14:31089969-31090265	IMR90	lung:	n/a	chr14:31090137-31090148
50	CEBPB	chr14:31125412-31125923	HepG2	liver:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31090974-31091024	GM12892	blood:	n/a
2	chr14:31091672-31091722	NH-A	brain:	n/a
3	chr14:31091426-31091476	ProgFib	skin:	n/a
4	chr14:31090880-31090930	NHDF-neo	bronchial:	n/a
5	chr14:31091339-31091389	Jurkat	blood:	n/a
6	chr14:31091651-31091701	BE2_C	brain:	n/a
7	chr14:31091339-31091389	BJ	skin:	n/a
8	chr14:31091651-31091701	Hela-S3	cervix:	n/a
9	chr14:31091012-31091062	NH-A	brain:	n/a
10	chr14:31086887-31086937	BJ	skin:	n/a
11	chr14:31091426-31091476	GM06990	blood:	n/a
12	chr14:31091672-31091722	ECC-1	luminal epithelium:	n/a
13	chr14:31091339-31091389	Caco-2	colon:	n/a
14	chr14:31091426-31091476	PFSK-1	brain:	n/a
15	chr14:31090535-31090585	HUVEC	blood vessel:	n/a
16	chr14:31090880-31090930	GM12892	blood:	n/a
17	chr14:31091392-31091442	AG09319	gingival:	n/a
18	chr14:31090535-31090585	GM12892	blood:	n/a
19	chr14:31091651-31091701	HRCEpiC	kidney:	n/a
20	chr14:31091012-31091062	Caco-2	colon:	n/a
21	chr14:31091672-31091722	BE2_C	brain:	n/a
22	chr14:31090974-31091024	NHDF-neo	bronchial:	n/a
23	chr14:31091392-31091442	IMR90	lung:	fetal
24	chr14:31091392-31091442	HEK293	kidney:	embryo
25	chr14:31090535-31090585	HMEC	breast:	n/a
26	chr14:31091672-31091722	HCPEpiC	choroid plexus:	n/a
27	chr14:31090535-31090585	ProgFib	skin:	n/a
28	chr14:31091392-31091442	HMEC	breast:	n/a
29	chr14:31091426-31091476	HIPEpiC	eye:	n/a
30	chr14:31090880-31090930	HAEpiC	amniotic membrane:	n/a
31	chr14:31091012-31091062	AoSMC	blood vessel:	n/a
32	chr14:31091392-31091442	HRPEpiC	eye:	n/a
33	chr14:31091392-31091442	HEEpiC	esophagus:	n/a
34	chr14:31091012-31091062	HRE	kidney:	n/a
35	chr14:31091339-31091389	HMEC	breast:	n/a
36	chr14:31091426-31091476	GM19239	blood:	n/a
37	chr14:31091339-31091389	H1-hESC	embryonic stem cell:	embryo
38	chr14:31091426-31091476	BE2_C	brain:	n/a
39	chr14:31091339-31091389	NH-A	brain:	n/a
40	chr14:31086887-31086937	HRCEpiC	kidney:	n/a
41	chr14:31091672-31091722	HUVEC	blood vessel:	n/a
42	chr14:31090974-31091024	NHBE	bronchial:	n/a
43	chr14:31090974-31091024	HepG2	liver:	n/a
44	chr14:31091339-31091389	K562	blood:	n/a
45	chr14:31091651-31091701	GM19239	blood:	n/a
46	chr14:31086887-31086937	SAEC	small airway:	n/a
47	chr14:31090535-31090585	Hepatocyte	liver:	n/a
48	chr14:31091012-31091062	RPTEC	kidney:	n/a
49	chr14:31091426-31091476	AG04449	skin:	fetal
50	chr14:31091392-31091442	MCF-7	breast:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:31091484..31091986-chr6:27114657..27115436,2	Hela-S3	cervix:
2	chr14:31062088..31063595-chr14:31068760..31070343,2	MCF-7	breast:
3	chr14:31092450..31095337-chr14:31106738..31109368,2	K562	blood:
4	chr14:31090029..31096005-chr14:31342159..31346650,8	K562	blood:
5	chr14:31091399..31091961-chr15:67834767..67835630,2	Hela-S3	cervix:
6	chr14:31121612..31124772-chr14:31129285..31132285,3	K562	blood:
7	chr14:31078979..31080673-chr14:31091206..31092941,2	MCF-7	breast:
8	chr14:31067916..31070610-chr14:31073012..31074923,2	MCF-7	breast:
9	chr14:31098733..31102116-chr14:31103840..31105961,3	MCF-7	breast:
10	chr14:31089949..31092197-chr14:31126575..31129516,2	K562	blood:
11	chr14:31122938..31124536-chr14:31343628..31346007,2	K562	blood:
12	chr14:31102024..31103662-chr14:31107714..31110233,2	MCF-7	breast:
13	chr14:31028766..31030922-chr14:31085217..31087715,2	MCF-7	breast:
14	chr14:31075132..31078327-chr14:31090098..31093775,4	MCF-7	breast:
15	chr14:31071248..31073927-chr14:31089916..31091588,2	MCF-7	breast:
16	chr14:31069035..31071443-chr14:31073257..31074780,2	K562	blood:
17	chr14:31090926..31091428-chr4:40057983..40058796,2	NB4	blood:
18	chr14:31069035..31071443-chr14:31073257..31074780,2	K562	blood:
19	chr14:31070404..31072787-chr14:31077582..31080526,2	K562	blood:
20	chr14:31125505..31127901-chr14:31342669..31344938,2	MCF-7	breast:
21	chr14:31106497..31108478-chr14:31110822..31112690,2	K562	blood:
22	chr14:31071248..31073927-chr14:31089916..31091588,2	MCF-7	breast:
23	chr14:31092884..31094625-chr14:31094770..31097263,2	MCF-7	breast:
24	chr14:31067708..31069634-chr14:31090291..31092583,3	MCF-7	breast:
25	chr14:31104327..31107315-chr14:31142719..31144888,2	K562	blood:
26	chr14:31026939..31029879-chr14:31115213..31118106,2	K562	blood:
27	chr14:31139778..31142183-chr14:31146346..31148580,3	K562	blood:
28	chr14:31139778..31141334-chr14:31146346..31148580,2	K562	blood:
29	chr14:31091067..31091965-chr17:34900623..34901463,3	Hela-S3	cervix:
30	chr14:31090421..31092379-chr14:31107832..31110754,2	MCF-7	breast:
31	chr14:31077974..31078580-chr14:31550888..31551785,2	K562	blood:
32	chr14:31069776..31071443-chr14:31072053..31074757,2	K562	blood:
33	chr14:31121612..31124772-chr14:31129285..31132285,3	K562	blood:
34	chr14:31126822..31127443-chr14:31225811..31226448,2	MCF-7	breast:
35	chr14:31139778..31142183-chr14:31146346..31148580,3	K562	blood:
36	chr14:31100141..31102895-chr14:31109728..31111873,2	K562	blood:
37	chr14:31065524..31068364-chr14:31100216..31102324,3	K562	blood:
38	chr14:31109175..31111007-chr14:31121039..31122781,2	K562	blood:
39	chr14:31074562..31083390-chr14:31084587..31093565,15	K562	blood:
40	chr14:31078979..31080673-chr14:31091206..31092941,2	MCF-7	breast:
41	chr1:153935357..153936246-chr14:31091282..31091843,2	Hela-S3	cervix:
42	chr14:31083098..31087151-chr14:31087433..31093138,6	MCF-7	breast:
43	chr14:31091111..31091770-chr2:85198621..85199391,2	Hela-S3	cervix:
44	chr14:31125303..31125862-chr14:31225605..31226401,2	MCF-7	breast:
45	chr14:31080176..31082868-chr14:31086897..31089129,2	MCF-7	breast:
46	chr14:31027121..31031753-chr14:31090278..31094067,6	K562	blood:
47	chr14:31083262..31084954-chr14:31090297..31092479,2	MCF-7	breast:
48	chr14:31090963..31091593-chr2:148777702..148778439,2	Hela-S3	cervix:
49	chr14:31067708..31069634-chr14:31090291..31092583,3	MCF-7	breast:
50	chr14:31126959..31127930-chr14:31220934..31221847,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-G2E3-4	chr14:31144190-31144537	NONHSAT036241
2	lnc-SCFD1-1	chr14:31084555-31084745	NONHSAT036236
3	lnc-SCFD1-1	chr14:31080508-31081585	NONHSAT036236
4	lnc-G2E3-4	chr14:31143130-31143203	NONHSAT036241
5	lnc-SCFD1-1	chr14:31085484-31087438	NONHSAT036236
6	lnc-G2E3-4	chr14:31142479-31142553	NONHSAT036241

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	G2E3	hsa-miR-335-5p	chr14:31086790-31086797
2	G2E3	hsa-miR-186-5p	chr14:31088629-31088650
3	G2E3	hsa-miR-186-5p	chr14:31088319-31088326
4	G2E3	hsa-miR-215-5p	chr14:31087931-31087952
5	G2E3	hsa-miR-186-5p	chr14:31088304-31088326
6	G2E3	hsa-miR-186-5p	chr14:31085766-31085772
7	G2E3	hsa-miR-335-5p	chr14:31086775-31086797
8	G2E3	hsa-miR-192-5p	chr14:31087931-31087952

Variant related genes	Relation type
G2E3	TF binding region
SCFD1	TF binding region
G2E3	CpG island
SCFD1	CpG island
ENSG00000184825	chromatin interactions
ENSG00000137764	chromatin interactions
ENSG00000005955	chromatin interactions
ENSG00000111540	chromatin interactions
ENSG00000258648	chromatin interactions
ENSG00000115947	chromatin interactions
ENSG00000064102	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000176407	chromatin interactions
ENSG00000092140	chromatin interactions
ENSG00000257636	chromatin interactions
ENSG00000129493	chromatin interactions
ENSG00000100473	chromatin interactions
ENSG00000078177	chromatin interactions
ENSG00000092108	chromatin interactions
ENSG00000270964	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000111790	chromatin interactions

Extended variants
information (count: 2973 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2973 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs229261	chr14:31068090-31068091	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376971485	chr14:31068116-31068117	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371381534	chr14:31068145-31068146	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535318887	chr14:31068166-31068167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs374552919	chr14:31068277-31068278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553651877	chr14:31068311-31068312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191290134	chr14:31068331-31068332	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536016573	chr14:31068332-31068333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs170665	chr14:31068345-31068346	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs570889211	chr14:31068387-31068388	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs76536965	chr14:31068431-31068432	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200707201	chr14:31068439-31068440	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183525153	chr14:31068442-31068443	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113211755	chr14:31068453-31068454	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553484596	chr14:31068475-31068476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545907093	chr14:31068484-31068485	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558118875	chr14:31068524-31068525	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577106669	chr14:31068528-31068529	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139240788	chr14:31068558-31068559	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187068445	chr14:31068606-31068607	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529852708	chr14:31068624-31068625	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541596428	chr14:31068636-31068637	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs10152074	chr14:31068637-31068638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191613666	chr14:31068671-31068672	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185271454	chr14:31068713-31068714	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551925871	chr14:31068724-31068725	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570426059	chr14:31068725-31068726	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10152019	chr14:31068758-31068759	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs144065087	chr14:31068774-31068775	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547327356	chr14:31068796-31068797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs568736484	chr14:31068817-31068818	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs535738844	chr14:31068961-31068962	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs536080371	chr14:31068964-31068965	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201630875	chr14:31068966-31068967	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556573144	chr14:31068986-31068987	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577533483	chr14:31068995-31068996	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569289548	chr14:31069002-31069003	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs80176698	chr14:31069073-31069074	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs448175	chr14:31069204-31069205	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs573197122	chr14:31069313-31069314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115405832	chr14:31069331-31069332	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs17096939	chr14:31069354-31069355	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs374676857	chr14:31069427-31069428	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs111583823	chr14:31069451-31069452	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs533122666	chr14:31069498-31069499	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs190220451	chr14:31069503-31069504	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560268037	chr14:31069522-31069523	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142200360	chr14:31069546-31069547	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs151227732	chr14:31069547-31069548	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs572857565	chr14:31069566-31069567	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
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
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
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
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2741 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31029000-31071800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:31029200-31071800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:31033800-31070000	Weak transcription	Lung	lung
4	chr14:31040200-31069800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr14:31043000-31079600	Weak transcription	Gastric	stomach
6	chr14:31043000-31090600	Weak transcription	Small Intestine	intestine
7	chr14:31045000-31070000	Weak transcription	Aorta	Aorta
8	chr14:31046800-31069800	Weak transcription	Fetal Kidney	kidney
9	chr14:31047000-31069800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:31047000-31079600	Weak transcription	Pancreas	Pancrea
11	chr14:31049600-31079600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr14:31050200-31079800	Weak transcription	Brain Angular Gyrus	brain
13	chr14:31051800-31079600	Weak transcription	Fetal Brain Male	brain
14	chr14:31052000-31077400	Weak transcription	Psoas Muscle	Psoas
15	chr14:31053600-31079800	Weak transcription	Brain Substantia Nigra	brain
16	chr14:31053800-31070200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr14:31053800-31090600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr14:31054200-31090400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr14:31054800-31072000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr14:31054800-31087200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:31055000-31086800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr14:31055400-31069800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:31055400-31070000	Weak transcription	Colonic Mucosa	Colon
24	chr14:31055600-31088000	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr14:31057200-31071800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr14:31057400-31077600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr14:31057800-31079800	Weak transcription	Brain Cingulate Gyrus	brain
28	chr14:31058400-31080000	Weak transcription	Fetal Heart	heart
29	chr14:31058800-31069800	Weak transcription	Spleen	Spleen
30	chr14:31058800-31074800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr14:31059200-31069400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr14:31059600-31069200	Weak transcription	NHEK	skin
33	chr14:31059600-31069400	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr14:31059800-31069400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr14:31059800-31080000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr14:31060000-31070000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr14:31061000-31069400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr14:31061000-31071800	Weak transcription	NHLF	lung
39	chr14:31061400-31070200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr14:31061600-31090400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr14:31062200-31069000	Weak transcription	Fetal Lung	lung
42	chr14:31063000-31069600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr14:31064200-31078200	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr14:31064400-31087800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr14:31064600-31073800	Strong transcription	Primary B cells from cord blood	blood
46	chr14:31064800-31078000	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr14:31064800-31086600	Strong transcription	Dnd41	blood
48	chr14:31064800-31087800	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr14:31065000-31068400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:31065000-31075000	Strong transcription	Primary T cells fromperipheralblood	blood

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