Variant report

Variant	nsv832804
Chromosome Location	chr14:56083850-56277632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2059)
CpG islands
(count:1468)
Chromatin interactive
region (count:99)
LncRNA
region (count:55)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2059 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:56269777-56270150	K562	blood:	n/a	n/a
2	ARID3A	chr14:56263450-56263638	K562	blood:	n/a	n/a
3	ARID3A	chr14:56269808-56270347	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:56266440-56266575	K562	blood:	n/a	n/a
5	ATF1	chr14:56273773-56274242	K562	blood:	n/a	n/a
6	ATF1	chr14:56247898-56248141	K562	blood:	n/a	n/a
7	ATF1	chr14:56269833-56270095	K562	blood:	n/a	n/a
8	ATF2	chr14:56131774-56132158	GM12878	blood:	n/a	n/a
9	ATF3	chr14:56269770-56270084	K562	blood:	n/a	n/a
10	ATF3	chr14:56165795-56166334	A549	lung:	n/a	n/a
11	ATF3	chr14:56269705-56270171	A549	lung:	n/a	n/a
12	BACH1	chr14:56174241-56174259	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:56269838-56270128	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr14:56131780-56132130	GM12878	blood:	n/a	chr14:56131921-56131930
15	BATF	chr14:56131730-56132108	GM12878	blood:	n/a	chr14:56131921-56131930
16	BCL11A	chr14:56131816-56132106	GM12878	blood:	n/a	n/a
17	BCL11A	chr14:56168405-56168683	GM12878	blood:	n/a	n/a
18	BCL11A	chr14:56168319-56168740	GM12878	blood:	n/a	n/a
19	BCL3	chr14:56219701-56220211	A549	lung:	n/a	n/a
20	BCL3	chr14:56269695-56270227	A549	lung:	n/a	n/a
21	BCL3	chr14:56165683-56166291	A549	lung:	n/a	n/a
22	BCL3	chr14:56219661-56220203	A549	lung:	n/a	n/a
23	BHLHE40	chr14:56273738-56274250	K562	blood:	n/a	n/a
24	BHLHE40	chr14:56229831-56229884	A549	lung:	n/a	n/a
25	BHLHE40	chr14:56274015-56274204	GM12878	blood:	n/a	n/a
26	BHLHE40	chr14:56272034-56272312	HepG2	liver:	n/a	n/a
27	BHLHE40	chr14:56271998-56272245	K562	blood:	n/a	n/a
28	BHLHE40	chr14:56263316-56263590	K562	blood:	n/a	n/a
29	BHLHE40	chr14:56266279-56266500	K562	blood:	n/a	n/a
30	BHLHE40	chr14:56229447-56229780	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:56131219-56131251	HepG2	liver:	n/a	n/a
32	BRCA1	chr14:56273645-56274482	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr14:56113291-56113333	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr14:56269601-56270259	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr14:56188055-56188395	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr14:56246845-56247541	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr14:56263500-56263523	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr14:56113304-56113504	GM12878	blood:	n/a	n/a
39	BRCA1	chr14:56246068-56246093	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr14:56269582-56269918	K562	blood:	n/a	n/a
41	CBX3	chr14:56269598-56271060	HCT-116	colon:	n/a	n/a
42	CBX3	chr14:56087085-56087293	K562	blood:	n/a	n/a
43	CBX3	chr14:56086998-56087381	K562	blood:	n/a	n/a
44	CBX3	chr14:56269448-56271180	HCT-116	colon:	n/a	n/a
45	CCNT2	chr14:56273825-56274155	K562	blood:	n/a	n/a
46	CEBPB	chr14:56257520-56258686	Hela-S3	cervix:	n/a	chr14:56258134-56258151
47	CEBPB	chr14:56219573-56220424	MCF-7	breast:	n/a	n/a
48	CEBPB	chr14:56143716-56143976	A549	lung:	n/a	chr14:56143854-56143863 chr14:56143853-56143864 chr14:56143852-56143863 chr14:56143852-56143865
49	CEBPB	chr14:56216172-56216500	HepG2	liver:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
50	CEBPB	chr14:56180227-56180573	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56157197-56157247	CMK	blood:	n/a
2	chr14:56232985-56233035	HL-60	blood:	n/a
3	chr14:56207327-56207377	HL-60	blood:	n/a
4	chr14:56228816-56228866	HRE	kidney:	n/a
5	chr14:56157197-56157247	CMK	blood:	n/a
6	chr14:56232985-56233035	HL-60	blood:	n/a
7	chr14:56207327-56207377	HL-60	blood:	n/a
8	chr14:56228816-56228866	HRE	kidney:	n/a
9	chr14:56229661-56229711	Caco-2	colon:	n/a
10	chr14:56233068-56233118	GM12878	blood:	n/a
11	chr14:56225464-56225514	HMEC	breast:	n/a
12	chr14:56231604-56231654	Jurkat	blood:	n/a
13	chr14:56207327-56207377	BE2_C	brain:	n/a
14	chr14:56257750-56257800	GM12892	blood:	n/a
15	chr14:56264651-56264701	BJ	skin:	n/a
16	chr14:56247892-56247942	GM12891	blood:	n/a
17	chr14:56264651-56264701	A549	lung:	n/a
18	chr14:56233178-56233228	SAEC	small airway:	n/a
19	chr14:56232985-56233035	NT2-D1	testis:	n/a
20	chr14:56228816-56228866	GM12891	blood:	n/a
21	chr14:56232813-56232863	AoSMC	blood vessel:	n/a
22	chr14:56231604-56231654	MCF10A-Er-Src	breast:	n/a
23	chr14:56232985-56233035	AoSMC	blood vessel:	n/a
24	chr14:56236843-56236893	HepG2	liver:	n/a
25	chr14:56236843-56236893	PFSK-1	brain:	n/a
26	chr14:56232813-56232863	LNCaP	prostate:	n/a
27	chr14:56232921-56232971	Hepatocyte	liver:	n/a
28	chr14:56216951-56217001	BE2_C	brain:	n/a
29	chr14:56151250-56151300	K562	blood:	n/a
30	chr14:56232985-56233035	HNPCEpiC	eye:	n/a
31	chr14:56157197-56157247	NHDF-neo	bronchial:	n/a
32	chr14:56232650-56232700	HCPEpiC	choroid plexus:	n/a
33	chr14:56233068-56233118	Jurkat	blood:	n/a
34	chr14:56225464-56225514	HCPEpiC	choroid plexus:	n/a
35	chr14:56232650-56232700	Hela-S3	cervix:	n/a
36	chr14:56264651-56264701	NHDF-neo	bronchial:	n/a
37	chr14:56233163-56233213	HRCEpiC	kidney:	n/a
38	chr14:56207327-56207377	HEK293	kidney:	embryo
39	chr14:56232650-56232700	Jurkat	blood:	n/a
40	chr14:56225464-56225514	A549	lung:	n/a
41	chr14:56229661-56229711	SK-N-MC	brain:	n/a
42	chr14:56257750-56257800	LNCaP	prostate:	n/a
43	chr14:56264651-56264701	IMR90	lung:	fetal
44	chr14:56232813-56232863	HMEC	breast:	n/a
45	chr14:56232813-56232863	Hela-S3	cervix:	n/a
46	chr14:56216951-56217001	H1-hESC	embryonic stem cell:	embryo
47	chr14:56236843-56236893	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:56231604-56231654	GM12892	blood:	n/a
49	chr14:56264322-56264372	HRE	kidney:	n/a
50	chr14:56236843-56236893	T-47D	breast:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:56136295..56138118-chr14:56139376..56142156,3	K562	blood:
2	chr14:56256977..56259600-chr14:56273193..56275837,3	K562	blood:
3	chr14:56096758..56098924-chr14:56100584..56102581,2	K562	blood:
4	chr14:56145481..56148002-chr14:56152406..56155008,3	K562	blood:
5	chr14:56178438..56180249-chr14:56182200..56183742,2	K562	blood:
6	chr14:56209789..56211421-chr14:56215723..56218469,2	MCF-7	breast:
7	chr14:56118646..56123000-chr14:56124614..56127350,4	MCF-7	breast:
8	chr14:56172874..56174577-chr14:56174772..56176710,2	MCF-7	breast:
9	chr14:56219849..56221518-chr14:56225046..56227362,2	MCF-7	breast:
10	chr14:56110772..56112668-chr14:56115971..56118185,2	K562	blood:
11	chr14:56135952..56138303-chr14:56139128..56140660,2	MCF-7	breast:
12	chr14:56221789..56224702-chr14:56769776..56771612,2	K562	blood:
13	chr14:56090621..56092571-chr14:56092593..56095117,2	K562	blood:
14	chr14:56273918..56276327-chr14:56286651..56288892,2	MCF-7	breast:
15	chr14:56207089..56208058-chr14:56265155..56265723,2	MCF-7	breast:
16	chr14:56093158..56095942-chr14:56099777..56101884,2	MCF-7	breast:
17	chr14:56248252..56249940-chr14:56263162..56264665,2	MCF-7	breast:
18	chr14:56198273..56199200-chr14:56551636..56552463,2	MCF-7	breast:
19	chr14:56133519..56136072-chr14:56136743..56138846,2	MCF-7	breast:
20	chr14:56226675..56229343-chr14:56231799..56234788,2	K562	blood:
21	chr14:56120266..56122635-chr14:56124757..56126273,2	K562	blood:
22	chr14:56089891..56092554-chr14:56094348..56096423,2	MCF-7	breast:
23	chr14:56269404..56272163-chr14:56272459..56274714,3	MCF-7	breast:
24	chr14:56136295..56138118-chr14:56139376..56142156,3	K562	blood:
25	chr14:55890007..55892259-chr14:56172820..56174391,2	K562	blood:
26	chr14:56101889..56105853-chr14:56107857..56111727,3	K562	blood:
27	chr14:56174160..56174699-chr14:56889058..56890030,2	K562	blood:
28	chr14:56102256..56103857-chr14:56152714..56154637,2	K562	blood:
29	chr14:56149406..56151839-chr14:56154721..56157088,2	K562	blood:
30	chr14:56046049..56048917-chr14:56082832..56086431,3	MCF-7	breast:
31	chr14:56264106..56265769-chr14:56291458..56293554,2	MCF-7	breast:
32	chr14:56264314..56267640-chr14:56270614..56273646,3	K562	blood:
33	chr14:56207915..56209917-chr14:56216169..56218035,2	MCF-7	breast:
34	chr14:56219849..56221518-chr14:56225046..56227362,2	MCF-7	breast:
35	chr14:56133519..56136072-chr14:56136743..56138846,2	MCF-7	breast:
36	chr14:56224023..56226441-chr14:56261049..56262918,2	MCF-7	breast:
37	chr14:56209875..56212045-chr14:56256095..56258296,2	MCF-7	breast:
38	chr14:56145095..56147248-chr14:56151830..56154443,3	K562	blood:
39	chr14:56266308..56267973-chr14:56270310..56271812,2	MCF-7	breast:
40	chr14:56245870..56248010-chr14:56260063..56261577,2	K562	blood:
41	chr14:55904850..55905413-chr14:56172276..56173086,2	MCF-7	breast:
42	chr14:55737454..55740283-chr14:56178729..56181502,2	MCF-7	breast:
43	chr14:56090621..56092571-chr14:56092593..56095117,2	K562	blood:
44	chr14:56178438..56180249-chr14:56182200..56183742,2	K562	blood:
45	chr14:56220561..56223458-chr14:56223829..56226647,2	K562	blood:
46	chr14:56045529..56047420-chr14:56089416..56091183,2	MCF-7	breast:
47	chr14:56238761..56241278-chr14:56243560..56245184,2	MCF-7	breast:
48	chr14:56263621..56267640-chr14:56269558..56273646,4	K562	blood:
49	chr14:56110772..56112668-chr14:56115971..56118185,2	K562	blood:
50	chr14:56256977..56259600-chr14:56273193..56275837,3	K562	blood:

(count:55 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KTN1-AS1-1	chr14:56260086-56260174	XLOC_011037
2	lnc-FBXO34-2	chr14:56118608-56118645	NONHSAT037017
3	lnc-KTN1-AS1-1	chr14:56260086-56260178	NONHSAT037025
4	lnc-FBXO34-2	chr14:56138580-56138595	NONHSAT037020
5	lnc-KTN1-AS1-1	chr14:56261002-56261063	ENSG00000258791.2
6	lnc-KTN1-AS1-1	chr14:56254645-56255094	ENSG00000258791.2
7	lnc-KTN1-2	chr14:56221453-56222019	NONHSAT037023
8	lnc-KTN1-AS1-1	chr14:56263323-56263406	ENSG00000258791.2
9	lnc-FBXO34-2	chr14:56119568-56119658	NONHSAT037017
10	lnc-KTN1-AS1-1	chr14:56248785-56249492	ENSG00000258791.2
11	lnc-FBXO34-2	chr14:56117353-56117355	NONHSAT037017
12	lnc-KTN1-AS1-1	chr14:56249144-56249698	ENSG00000258791.2
13	lnc-FBXO34-2	chr14:56119735-56119803	NONHSAT037017
14	lnc-KTN1-AS1-1	chr14:56247854-56249698	XLOC_011037
15	lnc-KTN1-AS1-1	chr14:56263321-56263406	ENSG00000258791.2
16	lnc-KTN1-AS1-1	chr14:56259443-56260174	ENSG00000258791.2
17	lnc-FBXO34-2	chr14:56085742-56087778	ucscGeneNc_uc001xci_2
18	lnc-KTN1-AS1-1	chr14:56261002-56261063	NONHSAT037026
19	lnc-KTN1-AS1-1	chr14:56263321-56263406	ENSG00000258791.3
20	lnc-FBXO34-2	chr14:56125264-56125332	NONHSAT037019
21	lnc-KTN1-AS1-1	chr14:56248785-56249492	ENSG00000258791.3
22	lnc-KTN1-1	chr14:56238349-56238423	ENSG00000258784.1
23	lnc-KTN1-AS1-1	chr14:56247432-56247714	NONHSAT037025
24	lnc-FBXO34-2	chr14:56139348-56139419	NONHSAT037020
25	lnc-KTN1-AS1-1	chr14:56249127-56249299	ENSG00000258791.2
26	lnc-KTN1-AS1-1	chr14:56263265-56263417	NONHSAT037025
27	lnc-KTN1-AS1-1	chr14:56247800-56248072	NONHSAT037025
28	lnc-FBXO34-2	chr14:56120277-56120314	NONHSAT037017
29	lnc-KTN1-1	chr14:56239474-56239567	ENSG00000258784.1
30	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.2
31	lnc-KTN1-AS1-1	chr14:56263321-56263374	ENSG00000258791.2
32	lnc-KTN1-AS1-1	chr14:56259764-56259828	NONHSAT037025
33	lnc-KTN1-AS1-1	chr14:56261002-56261063	ENSG00000258791.2
34	lnc-KTN1-AS1-1	chr14:56260015-56260078	ENSG00000258791.2
35	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.2
36	lnc-KTN1-1	chr14:56214926-56215000	ENSG00000258784.1
37	lnc-KTN1-AS1-1	chr14:56247853-56249698	NONHSAT037027
38	lnc-KTN1-AS1-1	chr14:56260086-56260174	NONHSAT037026
39	lnc-FBXO34-2	chr14:56139647-56141022	NONHSAT037020
40	lnc-KTN1-AS1-1	chr14:56263321-56263392	NONHSAT037027
41	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.2
42	lnc-KTN1-AS1-1	chr14:56260086-56260174	NONHSAT037027
43	lnc-KTN1-AS1-1	chr14:56263321-56263392	XLOC_011037
44	lnc-KTN1-AS1-1	chr14:56247853-56249698	NONHSAT037026
45	lnc-KTN1-1	chr14:56239707-56239921	ENSG00000258784.1
46	lnc-KTN1-AS1-1	chr14:56261002-56261063	ENSG00000258791.2
47	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.3
48	lnc-FBXO34-2	chr14:56122818-56122850	NONHSAT037019
49	lnc-KTN1-AS1-1	chr14:56263321-56263357	ENSG00000258791.2
50	lnc-KTN1-AS1-1	chr14:56247864-56248070	ENSG00000258791.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KTN1	hsa-miR-34a-5p	chr14:56151185-56151206

Variant related genes	Relation type
ENSG00000200742	TF binding region
LINC00520	TF binding region
ENSG00000258784	TF binding region
KTN1	TF binding region
RPL13AP3	TF binding region
ENSG00000200742	CpG island
LINC00520	CpG island
ENSG00000258784	CpG island
KTN1	CpG island
RPL13AP3	CpG island
ENSG00000177350	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000070269	chromatin interactions
ENSG00000186615	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000258791	chromatin interactions
ENSG00000258413	chromatin interactions

Extended variants
information (count: 7930 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:7930 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183956131	chr14:56083853-56083854	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs543360137	chr14:56083883-56083884	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs201437187	chr14:56083900-56083901	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs75114515	chr14:56083910-56083911	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs76142514	chr14:56083917-56083918	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374875590	chr14:56083926-56083927	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs571371316	chr14:56083951-56083952	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139276362	chr14:56083957-56083958	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs547052816	chr14:56083973-56083974	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540986710	chr14:56084012-56084013	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559070775	chr14:56084023-56084024	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs529767568	chr14:56084055-56084056	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs564231358	chr14:56084063-56084064	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547879321	chr14:56084074-56084075	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569956772	chr14:56084108-56084109	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs186609734	chr14:56084122-56084123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs552600839	chr14:56084205-56084206	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571100151	chr14:56084271-56084272	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs534726417	chr14:56084283-56084284	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs192548952	chr14:56084353-56084354	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185417948	chr14:56084418-56084419	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536322249	chr14:56084480-56084481	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535992778	chr14:56084504-56084505	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs141726419	chr14:56084506-56084507	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190321326	chr14:56084534-56084535	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs537220559	chr14:56084597-56084598	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs558593029	chr14:56084606-56084607	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs577103235	chr14:56084609-56084610	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576885861	chr14:56084620-56084621	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs371780822	chr14:56084635-56084636	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs539484339	chr14:56084640-56084641	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150328744	chr14:56084650-56084651	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs114044861	chr14:56084652-56084653	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375347305	chr14:56084684-56084685	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs192960670	chr14:56084687-56084688	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs185227628	chr14:56084690-56084691	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs137964512	chr14:56084714-56084715	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369421121	chr14:56084768-56084769	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs372749909	chr14:56084787-56084788	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200175290	chr14:56084790-56084791	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146224815	chr14:56084812-56084813	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs139072949	chr14:56084820-56084821	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs376987068	chr14:56084840-56084841	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs149871368	chr14:56084850-56084851	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373477959	chr14:56084860-56084861	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs373633201	chr14:56084886-56084887	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538787767	chr14:56084916-56084917	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs149459695	chr14:56084981-56084982	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370485045	chr14:56085051-56085052	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188707557	chr14:56085107-56085108	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3421 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56048400-56086000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:56061000-56085400	Weak transcription	Fetal Kidney	kidney
3	chr14:56061000-56085400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr14:56066600-56086200	Weak transcription	Fetal Intestine Small	intestine
5	chr14:56066600-56086200	Weak transcription	Gastric	stomach
6	chr14:56066800-56086200	Weak transcription	Fetal Stomach	stomach
7	chr14:56068600-56086200	Weak transcription	Spleen	Spleen
8	chr14:56068600-56086600	Weak transcription	Lung	lung
9	chr14:56069600-56086800	Weak transcription	Pancreas	Pancrea
10	chr14:56070400-56086200	Weak transcription	Aorta	Aorta
11	chr14:56070800-56085000	Weak transcription	Colon Smooth Muscle	Colon
12	chr14:56071000-56086000	Weak transcription	Thymus	Thymus
13	chr14:56071800-56086200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr14:56072400-56086200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:56074600-56084600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr14:56074600-56086000	Weak transcription	Brain Angular Gyrus	brain
17	chr14:56076200-56086000	Weak transcription	Small Intestine	intestine
18	chr14:56076400-56085800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr14:56076600-56085800	Weak transcription	Ovary	ovary
20	chr14:56076600-56086000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:56076600-56086200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr14:56077000-56085000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:56077000-56085000	Weak transcription	Right Ventricle	heart
24	chr14:56077000-56085600	Weak transcription	Brain Substantia Nigra	brain
25	chr14:56077000-56085800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr14:56077000-56086000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr14:56077000-56086200	Weak transcription	NHLF	lung
28	chr14:56077200-56084400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr14:56077800-56087800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr14:56077800-56092000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:56078200-56086000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:56078600-56084200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:56078600-56084600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:56078600-56085400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr14:56078600-56148600	Weak transcription	Stomach Mucosa	stomach
36	chr14:56078800-56095400	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr14:56079000-56085800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr14:56079000-56085800	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr14:56079000-56086000	Strong transcription	Primary B cells from cord blood	blood
40	chr14:56079000-56086000	Strong transcription	Primary B cells from peripheral blood	blood
41	chr14:56079000-56086800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr14:56079000-56086800	Strong transcription	Fetal Intestine Large	intestine
43	chr14:56079000-56089000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:56079000-56091000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr14:56079200-56084200	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr14:56079200-56084600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:56079200-56085200	Strong transcription	Dnd41	blood
48	chr14:56079200-56095200	Strong transcription	Primary T cells from cord blood	blood
49	chr14:56079400-56084600	Weak transcription	Brain Germinal Matrix	brain
50	chr14:56079400-56085600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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