Variant report

Variant	esv1820504
Chromosome Location	chr18:9614250-9621841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:521)
CpG islands
(count:305)
Chromatin interactive
region (count:28)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:9616059-9616297	K562	blood:	n/a	n/a
2	ARID3A	chr18:9616735-9617052	K562	blood:	n/a	n/a
3	ARID3A	chr18:9615316-9615343	K562	blood:	n/a	n/a
4	BACH1	chr18:9615794-9615952	K562	blood:	n/a	n/a
5	BACH1	chr18:9614924-9615365	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:9616289-9616297	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr18:9616006-9616377	GM12878	blood:	n/a	chr18:9616049-9616058
8	BCLAF1	chr18:9614980-9615345	GM12878	blood:	n/a	n/a
9	BCLAF1	chr18:9613533-9614307	GM12878	blood:	n/a	chr18:9613942-9613955
10	BHLHE40	chr18:9615193-9615231	GM12878	blood:	n/a	n/a
11	BHLHE40	chr18:9615211-9615252	K562	blood:	n/a	n/a
12	BHLHE40	chr18:9614571-9614942	GM12878	blood:	n/a	chr18:9614847-9614863 chr18:9614823-9614839
13	BRCA1	chr18:9615220-9615258	HepG2	liver:	n/a	n/a
14	CBX3	chr18:9615013-9615553	K562	blood:	n/a	n/a
15	CCNT2	chr18:9613769-9615322	K562	blood:	n/a	chr18:9615058-9615067 chr18:9615031-9615040
16	CEBPB	chr18:9616794-9616914	K562	blood:	n/a	n/a
17	CEBPB	chr18:9619942-9620341	A549	lung:	n/a	chr18:9620226-9620237
18	CEBPB	chr18:9620157-9620320	MCF-7	breast:	n/a	chr18:9620226-9620237
19	CEBPB	chr18:9619999-9620321	A549	lung:	n/a	chr18:9620226-9620237
20	CEBPB	chr18:9619429-9620429	IMR90	lung:	n/a	chr18:9620226-9620237
21	CEBPB	chr18:9620050-9620426	HepG2	liver:	n/a	chr18:9620226-9620237
22	CEBPB	chr18:9620049-9620386	K562	blood:	n/a	chr18:9620226-9620237
23	CEBPB	chr18:9614962-9614975	HepG2	liver:	n/a	n/a
24	CEBPB	chr18:9614898-9615080	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr18:9619958-9620303	K562	blood:	n/a	chr18:9620226-9620237
26	CEBPB	chr18:9620166-9620279	HepG2	liver:	n/a	chr18:9620226-9620237
27	CEBPB	chr18:9620096-9620314	H1-hESC	embryonic stem cell:	n/a	chr18:9620226-9620237
28	CEBPB	chr18:9616225-9616335	K562	blood:	n/a	n/a
29	CEBPB	chr18:9620051-9620417	A549	lung:	n/a	chr18:9620226-9620237
30	CEBPB	chr18:9620110-9620316	K562	blood:	n/a	chr18:9620226-9620237
31	CEBPB	chr18:9620049-9620425	Hela-S3	cervix:	n/a	chr18:9620226-9620237
32	CEBPD	chr18:9614302-9615025	HepG2	liver:	n/a	n/a
33	CHD1	chr18:9614808-9615019	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr18:9613825-9614260	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr18:9615158-9615326	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr18:9613665-9614293	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr18:9614524-9615426	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr18:9614986-9615168	GM12878	blood:	n/a	n/a
39	CHD2	chr18:9613860-9614298	HepG2	liver:	n/a	n/a
40	CHD2	chr18:9614528-9614562	HepG2	liver:	n/a	n/a
41	CREB1	chr18:9614691-9615008	A549	lung:	n/a	n/a
42	CTCF	chr18:9614160-9614310	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr18:9614219-9614263	Fibrobl	skin:	n/a	n/a
44	CTCF	chr18:9614564-9614580	GM12878	blood:	n/a	n/a
45	CTCF	chr18:9613847-9614354	K562	blood:	n/a	chr18:9614097-9614110
46	CTCF	chr18:9614140-9614290	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr18:9614140-9614290	NHEK	skin:	n/a	n/a
48	CTCF	chr18:9614160-9614310	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr18:9615279-9615293	GM12878	blood:	n/a	n/a
50	CTCF	chr18:9615200-9615350	AG10803	skin:	n/a	chr18:9615277-9615286 chr18:9615277-9615290

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:9615155-9615205	HCF	heart:	n/a
2	chr18:9614450-9614500	HCT-116	colon:	n/a
3	chr18:9615209-9615259	MCF-7	breast:	n/a
4	chr18:9615155-9615205	GM12891	blood:	n/a
5	chr18:9614206-9614256	K562	blood:	n/a
6	chr18:9614450-9614500	HEEpiC	esophagus:	n/a
7	chr18:9615155-9615205	SK-N-SH	brain:	n/a
8	chr18:9615093-9615143	AG10803	skin:	n/a
9	chr18:9614206-9614256	BE2_C	brain:	n/a
10	chr18:9615209-9615259	AoSMC	blood vessel:	n/a
11	chr18:9614450-9614500	GM19239	blood:	n/a
12	chr18:9614450-9614500	CMK	blood:	n/a
13	chr18:9615209-9615259	BE2_C	brain:	n/a
14	chr18:9615093-9615143	CMK	blood:	n/a
15	chr18:9614450-9614500	IMR90	lung:	fetal
16	chr18:9614206-9614256	U87	brain:	n/a
17	chr18:9615209-9615259	K562	blood:	n/a
18	chr18:9614206-9614256	NB4	blood:	n/a
19	chr18:9614206-9614256	HRCEpiC	kidney:	n/a
20	chr18:9614206-9614256	GM06990	blood:	n/a
21	chr18:9615155-9615205	HCPEpiC	choroid plexus:	n/a
22	chr18:9614206-9614256	LNCaP	prostate:	n/a
23	chr18:9615155-9615205	U87	brain:	n/a
24	chr18:9614450-9614500	ProgFib	skin:	n/a
25	chr18:9614450-9614500	HPAEpiC	pulmonary alveolar:	n/a
26	chr18:9615209-9615259	U87	brain:	n/a
27	chr18:9615155-9615205	NHBE	bronchial:	n/a
28	chr18:9614206-9614256	HUVEC	blood vessel:	n/a
29	chr18:9615209-9615259	NHDF-neo	bronchial:	n/a
30	chr18:9615155-9615205	HMEC	breast:	n/a
31	chr18:9614206-9614256	SK-N-SH	brain:	n/a
32	chr18:9614450-9614500	NB4	blood:	n/a
33	chr18:9615093-9615143	LNCaP	prostate:	n/a
34	chr18:9615209-9615259	ovcar-3	ovarian:	n/a
35	chr18:9615093-9615143	Jurkat	blood:	n/a
36	chr18:9615155-9615205	MCF10A-Er-Src	breast:	n/a
37	chr18:9615209-9615259	GM12878	blood:	n/a
38	chr18:9615093-9615143	PANC-1	pancreas:	n/a
39	chr18:9615093-9615143	AG04450	lung:	fetal
40	chr18:9615093-9615143	BE2_C	brain:	n/a
41	chr18:9615093-9615143	HepG2	liver:	n/a
42	chr18:9615209-9615259	Caco-2	colon:	n/a
43	chr18:9615155-9615205	HUVEC	blood vessel:	n/a
44	chr18:9614450-9614500	AoSMC	blood vessel:	n/a
45	chr18:9615209-9615259	Hela-S3	cervix:	n/a
46	chr18:9614450-9614500	K562	blood:	n/a
47	chr18:9615209-9615259	SKMC	muscle:	n/a
48	chr18:9614450-9614500	HRPEpiC	eye:	n/a
49	chr18:9615209-9615259	SK-N-MC	brain:	n/a
50	chr18:9614450-9614500	HCF	heart:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:9614482..9616420-chr18:9617986..9621274,5	K562	blood:
2	chr17:57970172..57971882-chr18:9614484..9616129,2	MCF-7	breast:
3	chr18:9612136..9615353-chr18:9912435..9915971,5	MCF-7	breast:
4	chr18:9584254..9588034-chr18:9613364..9615601,3	MCF-7	breast:
5	chr15:66994774..66995660-chr18:9613961..9614955,2	Hela-S3	cervix:
6	chr18:9614922..9615897-chrX:48815132..48816087,2	Hela-S3	cervix:
7	chr18:9569658..9574401-chr18:9612462..9616455,5	K562	blood:
8	chr18:9613016..9616228-chr18:9911513..9913644,4	K562	blood:
9	chr18:9612893..9615735-chr18:9913834..9918265,4	K562	blood:
10	chr18:9616424..9618415-chr18:9912586..9915951,3	MCF-7	breast:
11	chr18:9614482..9616420-chr18:9617986..9621274,5	K562	blood:
12	chr18:9613570..9616156-chr18:9878427..9881071,2	K562	blood:
13	chr18:9611182..9615699-chr18:9705314..9711194,13	MCF-7	breast:
14	chr18:9615287..9617165-chr18:9631128..9633561,2	K562	blood:
15	chr18:9614624..9617257-chr18:9707449..9709089,2	K562	blood:
16	chr18:9613045..9616469-chr18:9913547..9915707,4	K562	blood:
17	chr18:9593651..9596050-chr18:9613258..9616024,2	MCF-7	breast:
18	chr18:9614430..9615143-chr19:1249294..1250146,2	Hela-S3	cervix:
19	chr18:9615576..9617257-chr18:9706860..9708949,2	K562	blood:
20	chr18:9614449..9616140-chr18:9677968..9679576,2	K562	blood:
21	chr18:9615456..9617526-chr18:9895448..9898198,2	K562	blood:
22	chr18:9612628..9617891-chr18:9619605..9623342,5	MCF-7	breast:
23	chr18:9613618..9614587-chr22:31686737..31687476,2	Hela-S3	cervix:
24	chr18:9612544..9617098-chr18:9708301..9712595,6	MCF-7	breast:
25	chr1:28974882..28975858-chr18:9614139..9614753,2	Hela-S3	cervix:
26	chr18:9594858..9597558-chr18:9614248..9616397,2	MCF-7	breast:
27	chr18:9596087..9600746-chr18:9613522..9617540,6	MCF-7	breast:
28	chr18:9474922..9476536-chr18:9613527..9616238,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RALBP1-2	chr18:9615262-9615333	ENSG00000263627.1
2	lnc-RALBP1-2	chr18:9619193-9619364	NONHSAT057230
3	lnc-RALBP1-2	chr18:9614694-9615333	NONHSAT057230
4	lnc-RALBP1-2	chr18:9615186-9616194	NONHSAT057231
5	lnc-RALBP1-2	chr18:9619193-9619361	ENSG00000263627.1
6	lnc-RALBP1-2	chr18:9617146-9617283	NONHSAT057230
7	lnc-PIEZO2-14	chr18:9614224-9614272	NONHSAT057228
8	lnc-RALBP1-2	chr18:9617146-9617283	ENSG00000263627.1

No data

Variant related genes	Relation type
ENSG00000263627	TF binding region
RNU6-903P	TF binding region
PPP4R1	TF binding region
ENSG00000263627	CpG island
RNU6-903P	CpG island
PPP4R1	CpG island
ENSG00000168461	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000266541	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000154845	chromatin interactions
ENSG00000264644	chromatin interactions
ENSG00000265564	chromatin interactions
ENSG00000263627	chromatin interactions
ENSG00000100100	chromatin interactions
ENSG00000272799	chromatin interactions
ENSG00000068308	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000212572	chromatin interactions
ENSG00000137834	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000101558	chromatin interactions

Extended variants
information (count: 274 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368991458	chr18:9614298-9614299	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs28461902	chr18:9614332-9614333	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs532576735	chr18:9614333-9614334	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs199537124	chr18:9614594-9614595	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
5	rs545123424	chr18:9614707-9614708	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
6	rs77036092	chr18:9614730-9614731	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
7	rs143264046	chr18:9614885-9614886	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
8	rs527335206	chr18:9614887-9614888	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
9	rs184540458	chr18:9614970-9614971	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
10	rs566883915	chr18:9614982-9614983	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
11	rs531515644	chr18:9615034-9615035	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
12	rs549776851	chr18:9615105-9615106	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
13	rs62088910	chr18:9615145-9615146	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538437872	chr18:9615163-9615164	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
15	rs554282552	chr18:9615169-9615170	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
16	rs576648325	chr18:9615181-9615182	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
17	rs566175065	chr18:9615215-9615216	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
18	rs536696744	chr18:9615243-9615244	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
19	rs555011764	chr18:9615249-9615250	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
20	rs118132050	chr18:9615303-9615304	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
21	rs554822906	chr18:9615308-9615309	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
22	rs565493673	chr18:9615386-9615387	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
23	rs544157534	chr18:9615462-9615463	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
24	rs188897682	chr18:9615508-9615509	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
25	rs577408018	chr18:9615596-9615597	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
26	rs72951459	chr18:9615610-9615611	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
27	rs62088911	chr18:9615667-9615668	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs571819201	chr18:9615668-9615669	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
29	rs368473975	chr18:9615674-9615675	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
30	rs542279246	chr18:9615776-9615777	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
31	rs560570204	chr18:9615791-9615792	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
32	rs531183872	chr18:9615801-9615802	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
33	rs141503493	chr18:9615807-9615808	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
34	rs565023500	chr18:9615846-9615847	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
35	rs8090926	chr18:9615851-9615852	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536687109	chr18:9615944-9615945	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
37	rs376820166	chr18:9615991-9615992	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
38	rs181321122	chr18:9616008-9616009	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
39	rs184633053	chr18:9616046-9616047	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
40	rs570100072	chr18:9616094-9616095	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
41	rs537041930	chr18:9616202-9616203	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs559252054	chr18:9616233-9616234	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs35547777	chr18:9616250-9616251	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs397691340	chr18:9616263-9616264	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs376756697	chr18:9616264-9616265	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs377378789	chr18:9616265-9616266	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs577473427	chr18:9616275-9616276	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs189757175	chr18:9616305-9616306	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs535285378	chr18:9616351-9616352	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs145408172	chr18:9616422-9616423	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9612000-9615000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr18:9612200-9615200	Active TSS	NHLF	lung
3	chr18:9612400-9614800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr18:9612400-9615200	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr18:9612400-9615200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr18:9612400-9615200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr18:9612400-9615400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr18:9612400-9615800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr18:9612600-9615200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr18:9612600-9615200	Active TSS	HMEC	breast
11	chr18:9612600-9615400	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr18:9612600-9615400	Active TSS	Ovary	ovary
13	chr18:9612600-9615600	Active TSS	Right Ventricle	heart
14	chr18:9612600-9615800	Active TSS	Aorta	Aorta
15	chr18:9612800-9615000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr18:9612800-9615200	Active TSS	Fetal Muscle Leg	muscle
17	chr18:9612800-9615200	Active TSS	HSMM	muscle
18	chr18:9612800-9615200	Active TSS	HSMMtube	muscle
19	chr18:9612800-9615200	Active TSS	NHDF-Ad	bronchial
20	chr18:9612800-9615400	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr18:9612800-9615400	Active TSS	A549	lung
22	chr18:9612800-9615600	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr18:9613000-9615200	Active TSS	H1 Cell Line	embryonic stem cell
24	chr18:9613000-9615200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr18:9613000-9615200	Active TSS	Fetal Stomach	stomach
26	chr18:9613000-9615400	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr18:9613000-9615600	Active TSS	Fetal Brain Female	brain
28	chr18:9613200-9615000	Active TSS	K562	blood
29	chr18:9613200-9615200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr18:9613200-9615200	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr18:9613200-9615200	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr18:9613200-9615200	Active TSS	Brain Cingulate Gyrus	brain
33	chr18:9613200-9615200	Active TSS	Brain Hippocampus Middle	brain
34	chr18:9613200-9615200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr18:9613200-9615200	Active TSS	Brain Substantia Nigra	brain
36	chr18:9613200-9615200	Active TSS	Colonic Mucosa	Colon
37	chr18:9613200-9615200	Active TSS	Fetal Intestine Small	intestine
38	chr18:9613200-9615200	Active TSS	Placenta	Placenta
39	chr18:9613200-9615200	Active TSS	Fetal Thymus	thymus
40	chr18:9613200-9615200	Active TSS	Stomach Smooth Muscle	stomach
41	chr18:9613200-9615200	Active TSS	NHEK	skin
42	chr18:9613200-9615400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr18:9613200-9615400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr18:9613200-9615400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr18:9613200-9615400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr18:9613200-9615400	Active TSS	Colon Smooth Muscle	Colon
47	chr18:9613200-9615400	Active TSS	Fetal Intestine Large	intestine
48	chr18:9613200-9615600	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr18:9613400-9615000	Active TSS	Muscle Satellite Cultured Cells	--
50	chr18:9613400-9615000	Active TSS	Fetal Muscle Trunk	muscle

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