Variant report

Variant	esv3442210
Chromosome Location	chr14:96878392-97038700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1912)
CpG islands
(count:1711)
Chromatin interactive
region (count:133)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1912 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:96975227-96975533	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:96881799-96882325	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:96928525-96928975	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:96978913-96979336	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:96890757-96891051	K562	blood:	n/a	n/a
6	ARID3A	chr14:96967807-96968858	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:96973384-96973459	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:96890740-96891102	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:96935021-96935515	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:97030779-97030978	HepG2	liver:	n/a	n/a
11	ATF1	chr14:97026028-97026228	K562	blood:	n/a	n/a
12	ATF1	chr14:96882739-96882993	K562	blood:	n/a	n/a
13	ATF1	chr14:96968320-96968900	K562	blood:	n/a	chr14:96968699-96968713
14	ATF1	chr14:96908946-96909216	K562	blood:	n/a	n/a
15	ATF2	chr14:96968160-96968794	H1-hESC	embryonic stem cell:	n/a	chr14:96968699-96968713
16	ATF2	chr14:96968335-96968901	GM12878	blood:	n/a	chr14:96968699-96968713
17	ATF3	chr14:96928471-96929081	HepG2	liver:	n/a	n/a
18	ATF3	chr14:96928566-96928897	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr14:96908976-96909063	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr14:96969149-96969219	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr14:96968150-96968670	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr14:96968226-96968972	K562	blood:	n/a	n/a
23	BACH1	chr14:97027940-97027967	K562	blood:	n/a	n/a
24	BATF	chr14:96888556-96888713	GM12878	blood:	n/a	n/a
25	BATF	chr14:96963428-96963708	GM12878	blood:	n/a	n/a
26	BATF	chr14:96888445-96888712	GM12878	blood:	n/a	n/a
27	BCL3	chr14:96968052-96968938	A549	lung:	n/a	chr14:96968870-96968883 chr14:96968878-96968887 chr14:96968874-96968887 chr14:96968873-96968886 chr14:96968303-96968316 chr14:96968351-96968364 chr14:96968433-96968442
28	BCL3	chr14:96949985-96950252	GM12878	blood:	n/a	n/a
29	BCLAF1	chr14:96968123-96968997	GM12878	blood:	n/a	chr14:96968870-96968883 chr14:96968878-96968887 chr14:96968874-96968887 chr14:96968873-96968886 chr14:96968303-96968316 chr14:96968351-96968364 chr14:96968433-96968442
30	BCLAF1	chr14:96967906-96968878	GM12878	blood:	n/a	chr14:96968303-96968316 chr14:96968351-96968364 chr14:96968433-96968442
31	BCLAF1	chr14:96890757-96891003	GM12878	blood:	n/a	n/a
32	BCLAF1	chr14:96968913-96969704	GM12878	blood:	n/a	chr14:96969176-96969185
33	BHLHE40	chr14:96975224-96975384	HepG2	liver:	n/a	n/a
34	BHLHE40	chr14:96968130-96969386	GM12878	blood:	n/a	chr14:96969150-96969166 chr14:96969158-96969174
35	BHLHE40	chr14:96967868-96969564	K562	blood:	n/a	chr14:96969150-96969166 chr14:96969158-96969174
36	BHLHE40	chr14:96928490-96928949	HepG2	liver:	n/a	n/a
37	BHLHE40	chr14:96890822-96891035	K562	blood:	n/a	n/a
38	BHLHE40	chr14:96968192-96969199	HepG2	liver:	n/a	chr14:96969150-96969166 chr14:96969158-96969174
39	BHLHE40	chr14:96912602-96913014	K562	blood:	n/a	n/a
40	BHLHE40	chr14:96975974-96976436	GM12878	blood:	n/a	n/a
41	BHLHE40	chr14:96890785-96891084	GM12878	blood:	n/a	n/a
42	BRCA1	chr14:96968825-96969250	GM12878	blood:	n/a	n/a
43	BRCA1	chr14:96967961-96968840	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr14:96968499-96968717	HepG2	liver:	n/a	n/a
45	BRCA1	chr14:96968258-96968734	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr14:96890817-96890939	GM12878	blood:	n/a	n/a
47	CBX3	chr14:96968233-96968902	K562	blood:	n/a	n/a
48	CCNT2	chr14:96968151-96969594	K562	blood:	n/a	chr14:96969136-96969145
49	CCNT2	chr14:97033729-97033854	K562	blood:	n/a	n/a
50	CCNT2	chr14:96890506-96890725	K562	blood:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:96890445-96890495	PrEC	prostate:	n/a
2	chr14:96968625-96968675	HRE	kidney:	n/a
3	chr14:96968050-96968100	AG04450	lung:	fetal
4	chr14:96890445-96890495	PrEC	prostate:	n/a
5	chr14:96968625-96968675	HRE	kidney:	n/a
6	chr14:96968050-96968100	AG04450	lung:	fetal
7	chr14:96978537-96978587	HEK293	kidney:	embryo
8	chr14:96890632-96890682	HEEpiC	esophagus:	n/a
9	chr14:97037846-97037896	SAEC	small airway:	n/a
10	chr14:96969303-96969353	Hepatocyte	liver:	n/a
11	chr14:96968737-96968787	H1-hESC	embryonic stem cell:	embryo
12	chr14:96893892-96893942	HRPEpiC	eye:	n/a
13	chr14:96969303-96969353	AG09319	gingival:	n/a
14	chr14:96890120-96890170	HepG2	liver:	n/a
15	chr14:96968481-96968531	SKMC	muscle:	n/a
16	chr14:96978537-96978587	LNCaP	prostate:	n/a
17	chr14:96965678-96965728	NHDF-neo	bronchial:	n/a
18	chr14:96978537-96978587	HRCEpiC	kidney:	n/a
19	chr14:96967897-96967947	GM12891	blood:	n/a
20	chr14:96968745-96968795	ProgFib	skin:	n/a
21	chr14:96968510-96968560	A549	lung:	n/a
22	chr14:96968510-96968560	AG09309	skin:	n/a
23	chr14:96978537-96978587	RPTEC	kidney:	n/a
24	chr14:96890449-96890499	SAEC	small airway:	n/a
25	chr14:96968050-96968100	HNPCEpiC	eye:	n/a
26	chr14:96967798-96967848	LNCaP	prostate:	n/a
27	chr14:96969243-96969293	GM12878	blood:	n/a
28	chr14:96970127-96970177	HCM	heart:	n/a
29	chr14:96969303-96969353	K562	blood:	n/a
30	chr14:96968745-96968795	Caco-2	colon:	n/a
31	chr14:96968481-96968531	SAEC	small airway:	n/a
32	chr14:97031960-97032010	BE2_C	brain:	n/a
33	chr14:96968640-96968690	HRE	kidney:	n/a
34	chr14:96955063-96955113	AG09319	gingival:	n/a
35	chr14:96890632-96890682	SK-N-MC	brain:	n/a
36	chr14:96969243-96969293	BE2_C	brain:	n/a
37	chr14:96968737-96968787	NT2-D1	testis:	n/a
38	chr14:96890961-96891011	BE2_C	brain:	n/a
39	chr14:96890632-96890682	ProgFib	skin:	n/a
40	chr14:96968640-96968690	NHDF-neo	bronchial:	n/a
41	chr14:96890120-96890170	HCPEpiC	choroid plexus:	n/a
42	chr14:96969243-96969293	Jurkat	blood:	n/a
43	chr14:97019527-97019577	NT2-D1	testis:	n/a
44	chr14:96968640-96968690	AG10803	skin:	n/a
45	chr14:96967825-96967875	PANC-1	pancreas:	n/a
46	chr14:97037846-97037896	NB4	blood:	n/a
47	chr14:96890961-96891011	GM06990	blood:	n/a
48	chr14:96968625-96968675	MCF10A-Er-Src	breast:	n/a
49	chr14:96890961-96891011	ECC-1	luminal epithelium:	n/a
50	chr14:96967798-96967848	K562	blood:	n/a

(count:133 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:96967059..96968706-chr14:97003755..97006595,2	K562	blood:
2	chr14:96916306..96917840-chr14:96922779..96924408,2	MCF-7	breast:
3	chr14:96980482..96982184-chr14:96985254..96987490,2	K562	blood:
4	chr14:96950411..96952541-chr14:96959008..96961670,2	MCF-7	breast:
5	chr14:97030602..97033303-chr14:97033642..97035609,3	K562	blood:
6	chr14:97006749..97008466-chr14:97026369..97029131,2	MCF-7	breast:
7	chr14:96968705..96971658-chr14:97028687..97030507,2	MCF-7	breast:
8	chr14:96967942..96968907-chr16:2014395..2014982,2	Hela-S3	cervix:
9	chr14:96967004..96969133-chr14:97009562..97011863,2	MCF-7	breast:
10	chr14:96968663..96969298-chrX:53710499..53711222,2	HCT-116	colon:
11	chr14:97037640..97039282-chr14:97177961..97179544,2	MCF-7	breast:
12	chr14:96992168..96995386-chr14:96999762..97002036,3	MCF-7	breast:
13	chr14:96968408..96969093-chr7:39989276..39989838,2	Hela-S3	cervix:
14	chr14:96947839..96950152-chr14:96988315..96991118,2	K562	blood:
15	chr14:96903862..96905382-chr4:37697642..37700393,2	K562	blood:
16	chr14:97018033..97019612-chr14:97020291..97022357,2	K562	blood:
17	chr14:96968426..96968992-chr19:9731602..9732102,2	NB4	blood:
18	chr14:96956955..96959176-chr14:96966805..96969527,2	K562	blood:
19	chr14:97033169..97036076-chr14:97041923..97044671,2	MCF-7	breast:
20	chr14:96876815..96879566-chr14:96880954..96883744,3	K562	blood:
21	chr14:96909028..96911274-chr14:96967250..96968928,2	MCF-7	breast:
22	chr14:96977217..96979586-chr14:96982926..96984761,2	MCF-7	breast:
23	chr14:96980357..96982346-chr14:96989639..96991890,2	MCF-7	breast:
24	chr14:96965294..96968379-chr14:96992362..96994561,3	MCF-7	breast:
25	chr14:96966203..96970615-chr14:96984362..96986675,5	MCF-7	breast:
26	chr14:96967194..96972735-chr14:96975570..96985371,13	K562	blood:
27	chr14:96948001..96951041-chr14:96966273..96969529,4	MCF-7	breast:
28	chr14:96928829..96930351-chr14:96930416..96933252,2	MCF-7	breast:
29	chr14:96968318..96970026-chr14:96990174..96992851,2	K562	blood:
30	chr14:97007480..97011210-chr14:97011511..97014615,3	K562	blood:
31	chr14:97018033..97019612-chr14:97020291..97022357,2	K562	blood:
32	chr1:46216043..46216614-chr14:96968529..96969256,2	Hela-S3	cervix:
33	chr14:96968120..96968788-chr17:80250092..80250824,2	Hela-S3	cervix:
34	chr14:96889980..96892782-chr14:96967434..96969470,2	MCF-7	breast:
35	chr14:96944597..96947618-chr14:96962282..96964814,3	MCF-7	breast:
36	chr14:97032756..97036569-chr14:97036806..97040099,4	K562	blood:
37	chr14:96759438..96761870-chr14:96967375..96970054,2	MCF-7	breast:
38	chr14:96968950..96970471-chr14:97010412..97012390,2	MCF-7	breast:
39	chr14:96985630..96987652-chr14:97013134..97015914,2	MCF-7	breast:
40	chr14:97023617..97026546-chr14:97637896..97640052,3	K562	blood:
41	chr14:96968041..96970064-chr14:96987625..96989616,3	MCF-7	breast:
42	chr14:96968572..96970585-chr14:96987828..96990250,2	K562	blood:
43	chr14:96913037..96914989-chr14:96966222..96968484,2	MCF-7	breast:
44	chr14:96973732..96976070-chr14:96984297..96985956,2	K562	blood:
45	chr14:96826635..96830412-chr14:96966894..96969371,6	K562	blood:
46	chr14:96856973..96858498-chr14:96967462..96970110,2	K562	blood:
47	chr14:96951595..96958320-chr14:96966555..96970647,8	MCF-7	breast:
48	chr14:96935260..96938071-chr14:96944532..96946257,2	MCF-7	breast:
49	chr14:96889980..96892782-chr14:96967434..96969470,2	MCF-7	breast:
50	chr14:97006749..97008466-chr14:97026369..97029131,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG2B-2	chr14:96967985-96968630	NONHSAT039531
2	lnc-ATG2B-1	chr14:96932561-96932661	ENSG00000258530.1
3	lnc-PAPOLA-2	chr14:96999722-97000248	ucscGeneNc_uc001yfu_2
4	lnc-ATG2B-7	chr14:96949043-96949280	uc_381_-
5	lnc-PAPOLA-3	chr14:96949043-96949280	uc_381_+
6	lnc-ATG2B-6	chr14:96922913-96923378	NONHSAT039527
7	lnc-AK7-5	chr14:97031292-97031443	NONHSAT039542
8	lnc-PAPOLA-2	chr14:96997894-96998422	ucscGeneNc_uc001yfu_2
9	lnc-PAPOLA-2	chr14:96994960-96995017	ucscGeneNc_uc001yfu_2
10	lnc-ATG2B-2	chr14:96967028-96968641	NONHSAT039529
11	lnc-ATG2B-2	chr14:96967147-96968658	ENSG00000260806.1
12	lnc-ATG2B-1	chr14:96939596-96940208	ENSG00000258530.1
13	lnc-AK7-5	chr14:97028795-97029230	NONHSAT039542

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PAPOLA	hsa-miR-155-5p	chr14:96998551-96998571
2	PAPOLA	hsa-miR-155-5p	chr14:97031585-97031607
3	PAPOLA	hsa-miR-93-5p	chr14:97031736-97031760
4	PAPOLA	hsa-miR-93-5p	chr14:97031753-97031759
5	PAPOLA	hsa-miR-320a	chr14:97031785-97031808

Variant related genes	Relation type
PAPOLA	TF binding region
RPL23AP10	TF binding region
ENSG00000260806	TF binding region
AK7	TF binding region
PEBP1P1	TF binding region
PAPOLA	CpG island
RPL23AP10	CpG island
ENSG00000260806	CpG island
AK7	CpG island
PEBP1P1	CpG island
ENSG00000086758	chromatin interactions
ENSG00000173207	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000105323	chromatin interactions
ENSG00000228265	chromatin interactions
ENSG00000001630	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000265692	chromatin interactions
ENSG00000066739	chromatin interactions
ENSG00000259059	chromatin interactions
ENSG00000134248	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000167930	chromatin interactions
ENSG00000260806	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000100744	chromatin interactions
ENSG00000170315	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000188693	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000122034	chromatin interactions
ENSG00000238776	chromatin interactions
ENSG00000197429	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000145740	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000100697	chromatin interactions
ENSG00000124207	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000168395	chromatin interactions
ENSG00000171469	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000267106	chromatin interactions
ENSG00000235706	chromatin interactions
ENSG00000140057	chromatin interactions
ENSG00000240051	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000224699	chromatin interactions
ENSG00000125970	chromatin interactions
ENSG00000229980	chromatin interactions

Extended variants
information (count: 5784 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:5784 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117943019	chr14:96878414-96878415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs556943470	chr14:96878430-96878431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572441408	chr14:96878434-96878435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531609722	chr14:96878480-96878481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548205836	chr14:96878491-96878492	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77697567	chr14:96878530-96878531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114121917	chr14:96878550-96878551	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs200828872	chr14:96878563-96878564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs34331496	chr14:96878564-96878565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs398026276	chr14:96878582-96878583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs533535535	chr14:96878588-96878589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs192631986	chr14:96878596-96878597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544042013	chr14:96878620-96878621	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547259250	chr14:96878651-96878652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562370949	chr14:96878713-96878714	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529579954	chr14:96878714-96878715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548097954	chr14:96878763-96878764	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565523564	chr14:96878785-96878786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372599929	chr14:96878808-96878809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375356088	chr14:96878817-96878818	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532802259	chr14:96878852-96878853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551055674	chr14:96878862-96878863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs151108543	chr14:96878864-96878865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs536807557	chr14:96878930-96878931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184774781	chr14:96878937-96878938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141051615	chr14:96878994-96878995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534600724	chr14:96879003-96879004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs4905488	chr14:96879029-96879030	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs78001820	chr14:96879070-96879071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs546223081	chr14:96879071-96879072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576250058	chr14:96879104-96879105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs558244027	chr14:96879132-96879133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576627477	chr14:96879148-96879149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138539712	chr14:96879184-96879185	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141225920	chr14:96879233-96879234	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574210314	chr14:96879259-96879260	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146941805	chr14:96879340-96879341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536111438	chr14:96879360-96879361	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189635273	chr14:96879378-96879379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs75869016	chr14:96879400-96879401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550969851	chr14:96879440-96879441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563008848	chr14:96879443-96879444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530503119	chr14:96879457-96879458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs137917768	chr14:96879467-96879468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs74614718	chr14:96879489-96879490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143372359	chr14:96879560-96879561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192549415	chr14:96879566-96879567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs144168974	chr14:96879584-96879585	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs148264497	chr14:96879607-96879608	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558207018	chr14:96879618-96879619	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3080 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:96859000-96890400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:96866000-96886400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:96867600-96879600	Weak transcription	Brain Anterior Caudate	brain
4	chr14:96867600-96881600	Weak transcription	Brain Substantia Nigra	brain
5	chr14:96876400-96890000	Weak transcription	Pancreas	Pancrea
6	chr14:96876600-96879600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:96877000-96878800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr14:96878000-96878400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr14:96878200-96878400	Enhancers	Hela-S3	cervix
10	chr14:96878200-96878400	Enhancers	HepG2	liver
11	chr14:96878400-96879000	Weak transcription	HepG2	liver
12	chr14:96878800-96879600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr14:96879600-96880000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:96879600-96880000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr14:96879600-96880000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr14:96879600-96881000	Strong transcription	Brain Anterior Caudate	brain
17	chr14:96880000-96880600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr14:96881000-96890200	Weak transcription	Brain Anterior Caudate	brain
19	chr14:96882400-96884000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:96882600-96884000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:96882800-96883400	Weak transcription	HepG2	liver
22	chr14:96883200-96884200	Enhancers	Liver	Liver
23	chr14:96883600-96883800	Enhancers	HepG2	liver
24	chr14:96884000-96887400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr14:96884000-96888600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:96884200-96890200	Weak transcription	Liver	Liver
27	chr14:96886400-96886600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr14:96886600-96887000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr14:96886600-96889400	Weak transcription	Brain Hippocampus Middle	brain
30	chr14:96887200-96888400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr14:96887400-96888200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr14:96887600-96887800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr14:96887800-96890400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr14:96887800-96890800	Enhancers	Fetal Heart	heart
35	chr14:96888200-96888600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:96888400-96890000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr14:96888600-96889800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:96888600-96890000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:96889000-96889400	Weak transcription	Brain Substantia Nigra	brain
40	chr14:96889200-96889400	Enhancers	Brain Cingulate Gyrus	brain
41	chr14:96889200-96890200	Enhancers	Brain Angular Gyrus	brain
42	chr14:96889200-96890200	Enhancers	Brain Germinal Matrix	brain
43	chr14:96889200-96890200	Enhancers	Fetal Intestine Large	intestine
44	chr14:96889400-96889600	Enhancers	Brain Substantia Nigra	brain
45	chr14:96889400-96889600	Enhancers	Fetal Kidney	kidney
46	chr14:96889400-96890000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr14:96889400-96890000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr14:96889400-96890000	Active TSS	Spleen	Spleen
49	chr14:96889400-96890200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr14:96889400-96890200	Enhancers	Brain Hippocampus Middle	brain

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