Variant report

Variant	nsv1044090
Chromosome Location	chr14:71496198-71780026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2776)
CpG islands
(count:1220)
Chromatin interactive
region (count:102)
LncRNA
region (count:52)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2776 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:71610207-71610661	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:71596906-71597822	K562	blood:	n/a	n/a
3	ARID3A	chr14:71583321-71583963	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:71584599-71585049	HepG2	liver:	n/a	n/a
5	ATF1	chr14:71727998-71728254	K562	blood:	n/a	n/a
6	ATF1	chr14:71610189-71610768	K562	blood:	n/a	n/a
7	ATF1	chr14:71695576-71695749	K562	blood:	n/a	n/a
8	ATF1	chr14:71597363-71597860	K562	blood:	n/a	n/a
9	ATF1	chr14:71698554-71698831	K562	blood:	n/a	n/a
10	ATF1	chr14:71609002-71609339	K562	blood:	n/a	n/a
11	ATF2	chr14:71733644-71734392	GM12878	blood:	n/a	n/a
12	ATF2	chr14:71733590-71734374	GM12878	blood:	n/a	n/a
13	ATF2	chr14:71757731-71758278	GM12878	blood:	n/a	n/a
14	ATF3	chr14:71610318-71610639	K562	blood:	n/a	n/a
15	ATF3	chr14:71648413-71648601	K562	blood:	n/a	n/a
16	BACH1	chr14:71688475-71688837	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr14:71688589-71688804	K562	blood:	n/a	n/a
18	BATF	chr14:71678810-71679025	GM12878	blood:	n/a	n/a
19	BATF	chr14:71733636-71734280	GM12878	blood:	n/a	n/a
20	BATF	chr14:71609226-71609612	GM12878	blood:	n/a	n/a
21	BATF	chr14:71678844-71679079	GM12878	blood:	n/a	n/a
22	BATF	chr14:71733698-71734249	GM12878	blood:	n/a	n/a
23	BATF	chr14:71757764-71758214	GM12878	blood:	n/a	chr14:71757976-71757986 chr14:71757975-71757986
24	BCL11A	chr14:71733704-71734153	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:71597411-71597742	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:71733677-71734278	GM12878	blood:	n/a	n/a
27	BCL3	chr14:71756209-71756577	GM12878	blood:	n/a	chr14:71756475-71756484
28	BCL3	chr14:71733638-71734245	GM12878	blood:	n/a	n/a
29	BCLAF1	chr14:71609019-71609668	GM12878	blood:	n/a	chr14:71609253-71609262
30	BHLHE40	chr14:71632108-71632438	K562	blood:	n/a	n/a
31	BHLHE40	chr14:71597583-71597614	GM12878	blood:	n/a	n/a
32	BHLHE40	chr14:71647954-71648314	K562	blood:	n/a	n/a
33	BHLHE40	chr14:71695422-71695622	GM12878	blood:	n/a	chr14:71695534-71695555
34	BHLHE40	chr14:71665607-71665710	K562	blood:	n/a	n/a
35	BHLHE40	chr14:71696913-71697064	GM12878	blood:	n/a	n/a
36	BHLHE40	chr14:71609976-71610290	HepG2	liver:	n/a	n/a
37	BHLHE40	chr14:71709161-71709452	K562	blood:	n/a	chr14:71709302-71709323 chr14:71709307-71709316
38	BHLHE40	chr14:71706924-71707203	HepG2	liver:	n/a	n/a
39	BHLHE40	chr14:71716749-71716966	K562	blood:	n/a	n/a
40	BHLHE40	chr14:71695388-71695788	HepG2	liver:	n/a	chr14:71695534-71695555
41	BHLHE40	chr14:71610027-71610482	K562	blood:	n/a	n/a
42	BHLHE40	chr14:71597213-71597764	K562	blood:	n/a	n/a
43	BRCA1	chr14:71541284-71541304	GM12878	blood:	n/a	n/a
44	BRCA1	chr14:71501498-71501685	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr14:71605864-71605925	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr14:71545338-71545530	K562	blood:	n/a	n/a
47	CCNT2	chr14:71597368-71597644	K562	blood:	n/a	n/a
48	CEBPB	chr14:71705937-71706035	K562	blood:	n/a	chr14:71705988-71705999
49	CEBPB	chr14:71712003-71712298	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:71511088-71511415	A549	lung:	n/a	chr14:71511242-71511253

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:71722116-71722166	PANC-1	pancreas:	n/a
2	chr14:71609158-71609208	Hela-S3	cervix:	n/a
3	chr14:71598219-71598269	HCT-116	colon:	n/a
4	chr14:71609158-71609208	IMR90	lung:	fetal
5	chr14:71606274-71606324	HL-60	blood:	n/a
6	chr14:71694874-71694924	RPTEC	kidney:	n/a
7	chr14:71527576-71527626	HRE	kidney:	n/a
8	chr14:71577479-71577529	NHBE	bronchial:	n/a
9	chr14:71635288-71635338	MCF10A-Er-Src	breast:	n/a
10	chr14:71515513-71515563	ProgFib	skin:	n/a
11	chr14:71712645-71712695	NHBE	bronchial:	n/a
12	chr14:71605994-71606044	NHBE	bronchial:	n/a
13	chr14:71687739-71687789	GM06990	blood:	n/a
14	chr14:71687739-71687789	AG09319	gingival:	n/a
15	chr14:71632612-71632662	HL-60	blood:	n/a
16	chr14:71581031-71581081	AoSMC	blood vessel:	n/a
17	chr14:71577479-71577529	U87	brain:	n/a
18	chr14:71694874-71694924	PANC-1	pancreas:	n/a
19	chr14:71635288-71635338	HCPEpiC	choroid plexus:	n/a
20	chr14:71598219-71598269	PFSK-1	brain:	n/a
21	chr14:71515513-71515563	HepG2	liver:	n/a
22	chr14:71687739-71687789	SK-N-SH	brain:	n/a
23	chr14:71660200-71660250	HRPEpiC	eye:	n/a
24	chr14:71515513-71515563	A549	lung:	n/a
25	chr14:71694874-71694924	GM19239	blood:	n/a
26	chr14:71712645-71712695	ovcar-3	ovarian:	n/a
27	chr14:71527576-71527626	GM12892	blood:	n/a
28	chr14:71687739-71687789	K562	blood:	n/a
29	chr14:71598219-71598269	SK-N-SH_RA	brain:	n/a
30	chr14:71581031-71581081	MCF-7	breast:	n/a
31	chr14:71585510-71585560	SK-N-SH_RA	brain:	n/a
32	chr14:71609158-71609208	ovcar-3	ovarian:	n/a
33	chr14:71635288-71635338	ovcar-3	ovarian:	n/a
34	chr14:71722116-71722166	HCT-116	colon:	n/a
35	chr14:71605994-71606044	A549	lung:	n/a
36	chr14:71555837-71555887	NH-A	brain:	n/a
37	chr14:71605994-71606044	HEK293	kidney:	embryo
38	chr14:71606506-71606556	SAEC	small airway:	n/a
39	chr14:71758942-71758992	PFSK-1	brain:	n/a
40	chr14:71660200-71660250	Jurkat	blood:	n/a
41	chr14:71577479-71577529	Jurkat	blood:	n/a
42	chr14:71632612-71632662	A549	lung:	n/a
43	chr14:71712645-71712695	SKMC	muscle:	n/a
44	chr14:71687739-71687789	HEEpiC	esophagus:	n/a
45	chr14:71609158-71609208	SK-N-SH_RA	brain:	n/a
46	chr14:71660200-71660250	PANC-1	pancreas:	n/a
47	chr14:71660200-71660250	SKMC	muscle:	n/a
48	chr14:71758942-71758992	CMK	blood:	n/a
49	chr14:71660200-71660250	K562	blood:	n/a
50	chr14:71758942-71758992	NT2-D1	testis:	n/a

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:71570724..71571280-chr14:72321914..72322593,2	K562	blood:
2	chr14:71775069..71776742-chr14:71785163..71787953,2	MCF-7	breast:
3	chr14:71662526..71664078-chr14:71674837..71676717,2	K562	blood:
4	chr14:71640952..71644715-chr14:71785827..71788552,4	MCF-7	breast:
5	chr14:71775609..71778063-chr14:71785888..71789597,3	MCF-7	breast:
6	chr14:71771730..71773986-chr14:71778512..71780433,2	MCF-7	breast:
7	chr14:71582880..71584385-chr14:71586431..71588999,2	MCF-7	breast:
8	chr14:71576010..71578175-chr14:71578987..71581734,2	K562	blood:
9	chr14:71652798..71655797-chr14:71786372..71789241,2	MCF-7	breast:
10	chr14:71580577..71583944-chr14:71584359..71586589,3	K562	blood:
11	chr14:71633131..71633707-chr14:71787970..71788477,2	MCF-7	breast:
12	chr14:71610357..71611926-chr14:71786839..71789393,2	MCF-7	breast:
13	chr14:71536680..71538584-chr14:71630559..71632306,2	MCF-7	breast:
14	chr14:71653618..71655729-chr14:71657519..71659044,2	MCF-7	breast:
15	chr14:71570510..71571060-chr14:71673984..71674688,2	K562	blood:
16	chr14:71604769..71607668-chr14:71786929..71789620,2	MCF-7	breast:
17	chr14:71629289..71631183-chr14:71936634..71939360,2	MCF-7	breast:
18	chr14:71741562..71743432-chr14:71786529..71788512,2	MCF-7	breast:
19	chr14:71708680..71711261-chr14:71786150..71788899,2	MCF-7	breast:
20	chr14:71511687..71514106-chr14:71519945..71521504,2	MCF-7	breast:
21	chr14:71710210..71712589-chr14:71742927..71745344,2	MCF-7	breast:
22	chr14:71700024..71702819-chr14:71710024..71711999,2	MCF-7	breast:
23	chr14:71673720..71675748-chr14:71787192..71788845,2	MCF-7	breast:
24	chr14:71630664..71636301-chr14:71785635..71788811,7	MCF-7	breast:
25	chr14:71521439..71523990-chr14:71537038..71539301,2	MCF-7	breast:
26	chr14:71631309..71633976-chr14:71786806..71788570,3	MCF-7	breast:
27	chr14:71749102..71753074-chr14:71759195..71761901,3	MCF-7	breast:
28	chr14:71731979..71733968-chr14:71736696..71738464,2	MCF-7	breast:
29	chr14:71779441..71781507-chr14:71786096..71788865,2	MCF-7	breast:
30	chr14:71722316..71725212-chr14:71787395..71789447,2	MCF-7	breast:
31	chr14:71570776..71571452-chr14:72219467..72220345,2	MCF-7	breast:
32	chr14:71700024..71702819-chr14:71710024..71711999,2	MCF-7	breast:
33	chr14:71673509..71676275-chr14:71679068..71681548,4	MCF-7	breast:
34	chr14:71641459..71643782-chr14:71787456..71790205,2	MCF-7	breast:
35	chr14:71604707..71606600-chr14:72213499..72215384,2	MCF-7	breast:
36	chr14:71582880..71584385-chr14:71586431..71588999,2	MCF-7	breast:
37	chr14:71710210..71712589-chr14:71742927..71745344,2	MCF-7	breast:
38	chr14:71775177..71777237-chr14:71783119..71784623,2	MCF-7	breast:
39	chr14:71570663..71571191-chr14:72219553..72220390,2	MCF-7	breast:
40	chr14:71605592..71606386-chr14:71869586..71870379,2	MCF-7	breast:
41	chr14:71749102..71753074-chr14:71759195..71761901,3	MCF-7	breast:
42	chr14:71605403..71606379-chr14:72219242..72220271,11	MCF-7	breast:
43	chr14:71605800..71606303-chr14:71871146..71871852,2	K562	blood:
44	chr14:71511687..71514106-chr14:71519945..71521504,2	MCF-7	breast:
45	chr14:71540159..71540880-chr9:91932962..91933924,2	NB4	blood:
46	chr14:71768291..71772700-chr14:71783468..71788933,6	MCF-7	breast:
47	chr14:71715549..71717674-chr14:71721103..71723805,2	MCF-7	breast:
48	chr14:71605408..71606120-chr14:72322432..72323318,2	K562	blood:
49	chr14:71576318..71579821-chr14:71580472..71584172,4	MCF-7	breast:
50	chr14:71772110..71773635-chr14:71786502..71788506,2	K562	blood:

(count:52 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP3K9-3	chr14:71761980-71762173	ENSG00000259146.1
2	lnc-MAP3K9-7	chr14:71498403-71498687	NONHSAT037603
3	lnc-MAP3K9-3	chr14:71777275-71777449	XLOC_011064
4	lnc-MAP3K9-3	chr14:71761980-71762173	XLOC_011064
5	lnc-SIPA1L1-1	chr14:71761989-71762475	NONHSAT037621
6	lnc-MAP3K9-3	chr14:71777797-71778093	NONHSAT037628
7	lnc-MAP3K9-9	chr14:71552199-71552550	NONHSAT037605
8	lnc-MAP3K9-3	chr14:71773887-71774080	ENSG00000259146.1
9	lnc-SIPA1L1-1	chr14:71760761-71760926	NONHSAT037621
10	lnc-MAP3K9-3	chr14:71760754-71760997	ENSG00000259146.1
11	lnc-MAP3K9-3	chr14:71777275-71778093	XLOC_011064
12	lnc-MAP3K9-3	chr14:71761980-71762173	XLOC_011064
13	lnc-MAP3K9-3	chr14:71777929-71778076	ENSG00000259146.1
14	lnc-MAP3K9-3	chr14:71759518-71759619	XLOC_011064
15	lnc-MAP3K9-1	chr14:71647679-71647919	XLOC_011063
16	lnc-MAP3K9-10	chr14:71607842-71609970	ENSG00000269927.1
17	lnc-SIPA1L1-4	chr14:71685817-71689441	ENSG00000269945.1
18	lnc-MAP3K9-3	chr14:71761980-71762173	XLOC_011064
19	lnc-MAP3K9-3	chr14:71761980-71762173	XLOC_011064
20	lnc-MAP3K9-3	chr14:71759472-71759619	XLOC_011064
21	lnc-PCNX-1	chr14:71648173-71648823	ENSG00000259907.1
22	lnc-MAP3K9-3	chr14:71761980-71762173	XLOC_011064
23	lnc-MAP3K9-3	chr14:71761920-71762173	XLOC_011064
24	lnc-SIPA1L1-1	chr14:71761992-71762290	XLOC_010868
25	lnc-SIPA1L1-1	chr14:71760231-71761127	NONHSAT037616
26	lnc-SIPA1L1-1	chr14:71764774-71764863	XLOC_010868
27	lnc-MAP3K9-3	chr14:71760646-71760934	XLOC_011064
28	lnc-MAP3K9-3	chr14:71777275-71777286	XLOC_011064
29	lnc-SIPA1L1-1	chr14:71759472-71759942	NONHSAT037616
30	lnc-MAP3K9-3	chr14:71773895-71774080	XLOC_011064
31	lnc-PCNX-1	chr14:71648069-71648822	NONHSAT037608
32	lnc-MAP3K9-3	chr14:71761979-71762509	XLOC_011064
33	lnc-MAP3K9-3	chr14:71760771-71760873	XLOC_011064
34	lnc-PCNX-3	chr14:71679350-71679659	ENSG00000258517
35	lnc-MAP3K9-1	chr14:71648070-71648822	XLOC_011063
36	lnc-MAP3K9-3	chr14:71760863-71760873	XLOC_011064
37	lnc-MAP3K9-3	chr14:71777275-71777436	XLOC_011064
38	lnc-MAP3K9-3	chr14:71759442-71759619	ENSG00000259146.1
39	lnc-MAP3K9-3	chr14:71777275-71777328	XLOC_011064
40	lnc-MAP3K9-3	chr14:71761980-71762173	XLOC_011064
41	lnc-MAP3K9-3	chr14:71760684-71760997	XLOC_011064
42	lnc-PCNX-3	chr14:71684523-71684933	ENSG00000258517
43	lnc-MAP3K9-3	chr14:71777275-71777396	ENSG00000259146.1
44	lnc-MAP3K9-3	chr14:71759472-71759619	XLOC_011064
45	lnc-MAP3K9-3	chr14:71759435-71759615	ENSG00000259146.1
46	lnc-MAP3K9-3	chr14:71761980-71762079	ENSG00000259146.1
47	lnc-MAP3K9-8	chr14:71511092-71511357	NONHSAT037604
48	lnc-MAP3K9-3	chr14:71777715-71778093	XLOC_011064
49	lnc-PCNX-1	chr14:71647678-71647919	NONHSAT037608
50	lnc-MAP3K9-3	chr14:71777275-71777358	XLOC_011064

No data

Variant related genes	Relation type
ENSG00000267901	TF binding region
ENSG00000269945	TF binding region
ENSG00000269927	TF binding region
PCNX	TF binding region
ENSG00000258930	TF binding region
ENSG00000259907	TF binding region
PTTG4P	TF binding region
ENSG00000258517	TF binding region
ENSG00000259146	TF binding region
ENSG00000258966	TF binding region
ENSG00000267901	CpG island
ENSG00000269945	CpG island
ENSG00000269927	CpG island
PCNX	CpG island
ENSG00000258930	CpG island
ENSG00000259907	CpG island
PTTG4P	CpG island
ENSG00000258517	CpG island
ENSG00000259146	CpG island
ENSG00000258966	CpG island
ENSG00000197555	chromatin interactions
ENSG00000258517	chromatin interactions
ENSG00000258930	chromatin interactions
ENSG00000100731	chromatin interactions
ENSG00000259907	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000259146	chromatin interactions
ENSG00000080815	chromatin interactions
ZNF451	miRNA target sites
FAM76A	miRNA target sites
PGGT1B	miRNA target sites
HELZ	miRNA target sites
HELLS	miRNA target sites
AKAP12	miRNA target sites
ABCA5	miRNA target sites
E2F3	miRNA target sites
WDR37	miRNA target sites

Extended variants
information (count: 10157 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:10157 , 50 per page) page: 1 2 3 4 5 6 7 ... 204

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143398931	chr14:71496290-71496291	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183289345	chr14:71496306-71496307	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538353361	chr14:71496330-71496331	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556595270	chr14:71496336-71496337	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568737110	chr14:71496350-71496351	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536415169	chr14:71496369-71496370	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533130072	chr14:71496376-71496377	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2240536	chr14:71496409-71496410	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs74851379	chr14:71496410-71496411	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534756276	chr14:71496436-71496437	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs72724347	chr14:71496445-71496446	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553395501	chr14:71496501-71496502	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578041914	chr14:71496507-71496508	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545539867	chr14:71496612-71496613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563735921	chr14:71496784-71496785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575782141	chr14:71496803-71496804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543184541	chr14:71496830-71496831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561470696	chr14:71496839-71496840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528769182	chr14:71496856-71496857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28534442	chr14:71496875-71496876	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs116025395	chr14:71496877-71496878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141574926	chr14:71496889-71496890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550278476	chr14:71496898-71496899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568921239	chr14:71496909-71496910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376329794	chr14:71496925-71496926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7152781	chr14:71496986-71496987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548362420	chr14:71497049-71497050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567179522	chr14:71497058-71497059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372189846	chr14:71497186-71497187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559878149	chr14:71497195-71497196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376158899	chr14:71497205-71497206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534090183	chr14:71497237-71497238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558863168	chr14:71497261-71497262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112201936	chr14:71497266-71497267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539019155	chr14:71497274-71497275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369603716	chr14:71497311-71497312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145948801	chr14:71497313-71497314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575687178	chr14:71497339-71497340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369404788	chr14:71497391-71497392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542890012	chr14:71497444-71497445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189078283	chr14:71497501-71497502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545844426	chr14:71497545-71497546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551526402	chr14:71497554-71497555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549770184	chr14:71497611-71497612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564516198	chr14:71497614-71497615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs17108907	chr14:71497627-71497628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
47	rs192636036	chr14:71497673-71497674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17108910	chr14:71497699-71497700	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs552622511	chr14:71497720-71497721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532016921	chr14:71497743-71497744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:4698 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71426000-71508800	Weak transcription	Psoas Muscle	Psoas
2	chr14:71438600-71502800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:71439600-71502800	Weak transcription	Small Intestine	intestine
4	chr14:71445200-71496200	Weak transcription	Fetal Brain Male	brain
5	chr14:71445200-71497800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr14:71445200-71502800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:71445200-71510800	Weak transcription	Colonic Mucosa	Colon
8	chr14:71445400-71498000	Weak transcription	Brain Hippocampus Middle	brain
9	chr14:71445400-71502800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr14:71455600-71497400	Weak transcription	Right Ventricle	heart
11	chr14:71462600-71497200	Weak transcription	Esophagus	oesophagus
12	chr14:71462800-71497200	Weak transcription	Pancreas	Pancrea
13	chr14:71469600-71506200	Weak transcription	Fetal Heart	heart
14	chr14:71471200-71497800	Weak transcription	Gastric	stomach
15	chr14:71471600-71497200	Weak transcription	Aorta	Aorta
16	chr14:71473000-71497800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:71476000-71503200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr14:71477200-71503600	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr14:71480800-71496200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr14:71480800-71496800	Weak transcription	Thymus	Thymus
21	chr14:71480800-71497000	Weak transcription	Fetal Stomach	stomach
22	chr14:71480800-71497600	Weak transcription	Fetal Brain Female	brain
23	chr14:71480800-71498000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr14:71481000-71497800	Weak transcription	Brain Angular Gyrus	brain
25	chr14:71481000-71498000	Weak transcription	Brain Anterior Caudate	brain
26	chr14:71483000-71502800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr14:71483800-71506200	Weak transcription	Brain Substantia Nigra	brain
28	chr14:71485000-71503600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:71486200-71496400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr14:71486400-71496200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr14:71486400-71496800	Weak transcription	Brain Cingulate Gyrus	brain
32	chr14:71486400-71497200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr14:71486600-71496400	Weak transcription	Fetal Muscle Trunk	muscle
34	chr14:71486800-71496200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:71486800-71496400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr14:71486800-71497000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr14:71486800-71497000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr14:71486800-71497000	Weak transcription	Brain Germinal Matrix	brain
39	chr14:71486800-71497000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr14:71486800-71497000	Weak transcription	Fetal Intestine Small	intestine
41	chr14:71486800-71497000	Weak transcription	Fetal Muscle Leg	muscle
42	chr14:71486800-71497000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr14:71486800-71497200	Weak transcription	Ovary	ovary
44	chr14:71486800-71497600	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr14:71486800-71497600	Weak transcription	Lung	lung
46	chr14:71486800-71497600	Weak transcription	Spleen	Spleen
47	chr14:71486800-71497800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr14:71486800-71498000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr14:71486800-71498000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr14:71486800-71502600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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