Variant report

Variant	nsv1056541
Chromosome Location	chr18:11336695-11558542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2005)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:90)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2005 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:11519203-11519408	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:11500265-11501942	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:11512685-11512993	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:11493958-11494614	HepG2	liver:	n/a	chr18:11494545-11494561
5	ARID3A	chr18:11497589-11497898	HepG2	liver:	n/a	n/a
6	ATF2	chr18:11511354-11511912	GM12878	blood:	n/a	n/a
7	ATF2	chr18:11511325-11511711	GM12878	blood:	n/a	n/a
8	ATF3	chr18:11519178-11519339	K562	blood:	n/a	n/a
9	ATF3	chr18:11519029-11519344	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr18:11361870-11362230	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:11388405-11388414	K562	blood:	n/a	n/a
12	BACH1	chr18:11361885-11362210	K562	blood:	n/a	n/a
13	BACH1	chr18:11468208-11468461	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr18:11387929-11388160	GM12878	blood:	n/a	n/a
15	BATF	chr18:11437092-11437379	GM12878	blood:	n/a	n/a
16	BATF	chr18:11500458-11500756	GM12878	blood:	n/a	n/a
17	BATF	chr18:11367921-11368318	GM12878	blood:	n/a	n/a
18	BATF	chr18:11367943-11368357	GM12878	blood:	n/a	n/a
19	BCL11A	chr18:11367995-11368321	GM12878	blood:	n/a	n/a
20	BCL11A	chr18:11367993-11368334	GM12878	blood:	n/a	n/a
21	BCLAF1	chr18:11419356-11419720	GM12878	blood:	n/a	n/a
22	BHLHE40	chr18:11532341-11532541	HepG2	liver:	n/a	n/a
23	BHLHE40	chr18:11511453-11512073	GM12878	blood:	n/a	n/a
24	BHLHE40	chr18:11391796-11391825	K562	blood:	n/a	n/a
25	BHLHE40	chr18:11553397-11553707	GM12878	blood:	n/a	n/a
26	BHLHE40	chr18:11519095-11519341	K562	blood:	n/a	n/a
27	BHLHE40	chr18:11533514-11533708	K562	blood:	n/a	n/a
28	BHLHE40	chr18:11405971-11406112	K562	blood:	n/a	chr18:11405985-11406006 chr18:11405992-11406001 chr18:11405989-11406002 chr18:11405991-11406000 chr18:11405991-11406000 chr18:11405990-11405999
29	BHLHE40	chr18:11500447-11501074	HepG2	liver:	n/a	n/a
30	BRCA1	chr18:11496621-11496902	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr18:11464371-11464386	HepG2	liver:	n/a	n/a
32	BRCA1	chr18:11500467-11500505	HepG2	liver:	n/a	n/a
33	BRCA1	chr18:11500423-11500877	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr18:11366509-11366746	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr18:11553368-11553604	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr18:11506874-11507253	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr18:11488272-11488735	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr18:11360926-11360964	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr18:11388046-11388227	HepG2	liver:	n/a	n/a
40	BRCA1	chr18:11519100-11519333	H1-hESC	embryonic stem cell:	n/a	n/a
41	CBX3	chr18:11544142-11544394	K562	blood:	n/a	n/a
42	CBX3	chr18:11544082-11544485	HCT-116	colon:	n/a	n/a
43	CBX3	chr18:11544140-11544504	HCT-116	colon:	n/a	n/a
44	CBX3	chr18:11500325-11500942	HCT-116	colon:	n/a	n/a
45	CBX3	chr18:11544117-11544406	K562	blood:	n/a	n/a
46	CBX3	chr18:11500362-11500760	HCT-116	colon:	n/a	n/a
47	CEBPB	chr18:11355770-11355997	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr18:11497638-11497869	HepG2	liver:	n/a	n/a
49	CEBPB	chr18:11471736-11472072	Hela-S3	cervix:	n/a	chr18:11471865-11471878 chr18:11471865-11471876 chr18:11471865-11471878 chr18:11471865-11471876
50	CEBPB	chr18:11512219-11512921	Hela-S3	cervix:	n/a	chr18:11512377-11512388

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11519034-11519084	AG04449	skin:	fetal
2	chr18:11519034-11519084	LNCaP	prostate:	n/a
3	chr18:11519034-11519084	NHDF-neo	bronchial:	n/a
4	chr18:11519034-11519084	MCF-7	breast:	n/a
5	chr18:11519034-11519084	HepG2	liver:	n/a
6	chr18:11519034-11519084	NHBE	bronchial:	n/a
7	chr18:11519034-11519084	IMR90	lung:	fetal
8	chr18:11519034-11519084	HUVEC	blood vessel:	n/a
9	chr18:11519034-11519084	ECC-1	luminal epithelium:	n/a
10	chr18:11519034-11519084	Jurkat	blood:	n/a
11	chr18:11519034-11519084	AoSMC	blood vessel:	n/a
12	chr18:11519034-11519084	CMK	blood:	n/a
13	chr18:11519034-11519084	GM19239	blood:	n/a
14	chr18:11519034-11519084	SKMC	muscle:	n/a
15	chr18:11519034-11519084	HCM	heart:	n/a
16	chr18:11519034-11519084	HRE	kidney:	n/a
17	chr18:11519034-11519084	HL-60	blood:	n/a
18	chr18:11519034-11519084	BE2_C	brain:	n/a
19	chr18:11519034-11519084	T-47D	breast:	n/a
20	chr18:11519034-11519084	ovcar-3	ovarian:	n/a
21	chr18:11519034-11519084	HCF	heart:	n/a
22	chr18:11519034-11519084	GM12892	blood:	n/a
23	chr18:11519034-11519084	GM12891	blood:	n/a
24	chr18:11519034-11519084	SK-N-MC	brain:	n/a
25	chr18:11519034-11519084	AG04450	lung:	fetal
26	chr18:11519034-11519084	HNPCEpiC	eye:	n/a
27	chr18:11519034-11519084	AG09309	skin:	n/a
28	chr18:11519034-11519084	MCF10A-Er-Src	breast:	n/a
29	chr18:11519034-11519084	HIPEpiC	eye:	n/a
30	chr18:11519034-11519084	HAEpiC	amniotic membrane:	n/a
31	chr18:11519034-11519084	PrEC	prostate:	n/a
32	chr18:11519034-11519084	HPAEpiC	pulmonary alveolar:	n/a
33	chr18:11519034-11519084	SK-N-SH_RA	brain:	n/a
34	chr18:11519034-11519084	HCPEpiC	choroid plexus:	n/a
35	chr18:11519034-11519084	BJ	skin:	n/a
36	chr18:11519034-11519084	NH-A	brain:	n/a
37	chr18:11519034-11519084	RPTEC	kidney:	n/a
38	chr18:11519034-11519084	AG09319	gingival:	n/a
39	chr18:11519034-11519084	HCT-116	colon:	n/a
40	chr18:11519034-11519084	PANC-1	pancreas:	n/a
41	chr18:11519034-11519084	PFSK-1	brain:	n/a
42	chr18:11519034-11519084	HMEC	breast:	n/a
43	chr18:11519034-11519084	HRCEpiC	kidney:	n/a
44	chr18:11519034-11519084	Hepatocyte	liver:	n/a
45	chr18:11519034-11519084	K562	blood:	n/a
46	chr18:11519034-11519084	H1-hESC	embryonic stem cell:	embryo
47	chr18:11519034-11519084	AG10803	skin:	n/a
48	chr18:11519034-11519084	SAEC	small airway:	n/a
49	chr18:11519034-11519084	HRPEpiC	eye:	n/a
50	chr18:11519034-11519084	SK-N-SH	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:11513286..11515221-chr18:11517194..11519674,2	K562	blood:
2	chr18:11487890..11489675-chr18:11493773..11495986,2	K562	blood:
3	chr18:11387860..11389856-chr18:11391492..11394424,2	MCF-7	breast:
4	chr18:11440473..11443094-chr18:11444494..11446221,2	K562	blood:
5	chr1:151965186..151965687-chr18:11365448..11365948,2	Hela-S3	cervix:
6	chr18:11464572..11467266-chr18:11469004..11470524,2	K562	blood:
7	chr18:11494387..11496981-chr18:11498491..11500808,2	MCF-7	breast:
8	chr18:11518713..11519703-chr18:11552996..11553743,6	MCF-7	breast:
9	chr18:11518713..11519703-chr18:11552996..11553743,6	MCF-7	breast:
10	chr18:11440473..11443094-chr18:11444494..11446221,2	K562	blood:
11	chr18:11324796..11327150-chr18:11338669..11340267,2	MCF-7	breast:
12	chr18:11268822..11269508-chr18:11500370..11501110,2	MCF-7	breast:
13	chr18:11518909..11519601-chr18:11549107..11549874,2	MCF-7	breast:
14	chr18:11454276..11456483-chr18:11456790..11459275,2	MCF-7	breast:
15	chr18:11484260..11486472-chr18:11488941..11490761,2	MCF-7	breast:
16	chr18:11494387..11496981-chr18:11498491..11500808,2	MCF-7	breast:
17	chr18:11365422..11368107-chr18:11369028..11370592,2	K562	blood:
18	chr18:11310565..11311185-chr18:11413212..11414156,2	K562	blood:
19	chr18:11310235..11310873-chr18:11387558..11388316,3	MCF-7	breast:
20	chr18:11487890..11489890-chr18:11494486..11496353,2	K562	blood:
21	chr18:11310495..11311249-chr18:11553049..11553579,2	MCF-7	breast:
22	chr18:11518909..11519601-chr18:11549107..11549874,2	MCF-7	breast:
23	chr18:11309816..11310769-chr18:11512438..11513268,3	MCF-7	breast:
24	chr18:11387860..11389856-chr18:11391492..11394424,2	MCF-7	breast:
25	chr18:11464572..11467266-chr18:11469004..11470524,2	K562	blood:
26	chr18:11365422..11368107-chr18:11369028..11370592,2	K562	blood:
27	chr18:11513286..11515221-chr18:11517194..11519674,2	K562	blood:

(count:90 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC35G4-1	chr18:11503733-11503883	ENSG00000267252.1
2	lnc-RP11-677O4.1.1-2	chr18:11471228-11471279	XLOC_012769
3	lnc-PIEZO2-11	chr18:11358532-11358651	l_1525_chr18:11356975-11368345_testes
4	lnc-SLC35G4-6	chr18:11465276-11465509	ENSG00000267425.1
5	lnc-PIEZO2-3	chr18:11376001-11376371	XLOC_012768
6	lnc-RP11-677O4.1.1-2	chr18:11489325-11489912	XLOC_012769
7	lnc-RP11-677O4.1.1-4	chr18:11390032-11390728	ENSG00000273119.1
8	lnc-SLC35G4-1	chr18:11506531-11506635	NONHSAT057308
9	lnc-SLC35G4-1	chr18:11490109-11490240	ENSG00000267252.1
10	lnc-RP11-677O4.1.1-2	chr18:11447755-11447989	ENSG00000267564.1
11	lnc-SLC35G4-1	chr18:11490769-11490964	ENSG00000267252.1
12	lnc-RP11-677O4.1.1-2	chr18:11447748-11447989	XLOC_012769
13	lnc-SLC35G4-1	chr18:11490029-11490240	XLOC_012626
14	lnc-SLC35G4-1	chr18:11506756-11506982	XLOC_012626
15	lnc-RP11-677O4.1.1-2	chr18:11489325-11489368	ENSG00000267564.1
16	lnc-RP11-677O4.1.1-2	chr18:11447608-11447989	XLOC_012769
17	lnc-SLC35G4-1	chr18:11506756-11506979	XLOC_012626
18	lnc-SLC35G4-4	chr18:11480379-11480950	l_1528_chr18:11480028-11481803_testes
19	lnc-SLC35G4-5	chr18:11477426-11478594	l_1527_chr18:11477425-11478921_testes
20	lnc-SLC35G4-1	chr18:11504827-11505056	XLOC_012626
21	lnc-SLC35G4-6	chr18:11454055-11454532	NONHSAT057303
22	lnc-PIEZO2-3	chr18:11378261-11378345	XLOC_012768
23	lnc-SLC35G4-1	chr18:11506756-11506967	ENSG00000267252.1
24	lnc-SLC35G4-1	chr18:11488569-11488594	ENSG00000267252.1
25	lnc-SLC35G4-1	chr18:11505778-11505923	ENSG00000267252.1
26	lnc-SLC35G4-1	chr18:11491562-11491788	ENSG00000267252.1
27	lnc-RP11-677O4.1.1-2	chr18:11490466-11490670	XLOC_012769
28	lnc-PIEZO2-3	chr18:11378254-11378408	ENSG00000267051.1
29	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
30	lnc-RP11-677O4.1.1-3	chr18:11479325-11480012	l_1526_chr18:11437747-11480012_testes
31	lnc-SLC35G4-1	chr18:11490047-11490240	ENSG00000267252.1
32	lnc-SLC35G4-6	chr18:11454751-11454837	NONHSAT057303
33	lnc-SLC35G4-1	chr18:11506756-11506982	XLOC_012626
34	lnc-RP11-677O4.1.1-3	chr18:11480466-11480670	l_1526_chr18:11437747-11480012_testes
35	lnc-PIEZO2-11	chr18:11356976-11357446	l_1525_chr18:11356975-11368345_testes
36	lnc-SLC35G4-6	chr18:11465869-11466469	NONHSAT057303
37	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
38	lnc-SLC35G4-1	chr18:11490029-11490240	XLOC_012626
39	lnc-SLC35G4-1	chr18:11506755-11506982	NONHSAT057314
40	lnc-SLC35G4-2	chr18:11491562-11491767	XLOC_012627
41	lnc-PIEZO2-11	chr18:11368259-11368392	l_1525_chr18:11356975-11368345_testes
42	lnc-SLC35G4-1	chr18:11506756-11506975	ENSG00000267252.1
43	lnc-SLC35G4-6	chr18:11454751-11454837	ENSG00000267425.1
44	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
45	lnc-SLC35G4-1	chr18:11506756-11506982	ENSG00000267252.1
46	lnc-SLC35G4-1	chr18:11489032-11490240	XLOC_012626
47	lnc-SLC35G4-1	chr18:11490223-11490240	ENSG00000267252.1
48	lnc-PIEZO2-3	chr18:11368532-11368651	ENSG00000267051.1
49	lnc-SLC35G4-1	chr18:11487834-11488594	XLOC_012626
50	lnc-SLC35G4-4	chr18:11493733-11494026	l_1528_chr18:11480028-11481803_testes

No data

Variant related genes	Relation type
ENSG00000267252	TF binding region
ENSG00000267425	TF binding region
ENSG00000267051	TF binding region
ENSG00000267371	TF binding region
ENSG00000273119	TF binding region
ENSG00000267564	TF binding region
ENSG00000267252	CpG island
ENSG00000267425	CpG island
ENSG00000267051	CpG island
ENSG00000267371	CpG island
ENSG00000273119	CpG island
ENSG00000267564	CpG island
ENSG00000267425	chromatin interactions
ENSG00000267252	chromatin interactions
ENSG00000263682	chromatin interactions
ENSG00000267564	chromatin interactions
SLC30A6	miRNA target sites
SLC30A7	miRNA target sites
BICD2	miRNA target sites
TGFBR2	miRNA target sites
EPB41	miRNA target sites
CLCN3	miRNA target sites
TMEM9B	miRNA target sites
TMF1	miRNA target sites
NUP153	miRNA target sites

Extended variants
information (count: 7174 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7174 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs66871790	chr18:11336730-11336731	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372195925	chr18:11336739-11336740	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs192615823	chr18:11336804-11336805	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547733375	chr18:11336813-11336814	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs566367078	chr18:11336823-11336824	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs183658202	chr18:11336889-11336890	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs550054264	chr18:11336893-11336894	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs565368765	chr18:11336948-11336949	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs532534480	chr18:11336956-11336957	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs375215722	chr18:11337075-11337076	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs541207577	chr18:11337086-11337087	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs186871151	chr18:11337088-11337089	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530249352	chr18:11337103-11337104	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs548433759	chr18:11337106-11337107	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs191619736	chr18:11337117-11337118	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs184920776	chr18:11337123-11337124	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs189751403	chr18:11337124-11337125	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs551928014	chr18:11337151-11337152	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs570505163	chr18:11337152-11337153	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs374312653	chr18:11337153-11337154	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs181738875	chr18:11337166-11337167	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs369714029	chr18:11337192-11337193	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs75793855	chr18:11337237-11337238	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs568220693	chr18:11337290-11337291	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs535646934	chr18:11337294-11337295	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs374134579	chr18:11337299-11337300	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs185305627	chr18:11337308-11337309	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs189197923	chr18:11337322-11337323	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs145555021	chr18:11337415-11337416	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs576851251	chr18:11337434-11337435	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs541095589	chr18:11337440-11337441	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181953595	chr18:11337463-11337464	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs369417738	chr18:11337477-11337478	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs574645916	chr18:11337478-11337479	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs184901426	chr18:11337485-11337486	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs114724444	chr18:11337549-11337550	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs150736865	chr18:11337556-11337557	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs552855343	chr18:11337565-11337566	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs369773670	chr18:11337569-11337570	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs528101756	chr18:11337598-11337599	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs546670970	chr18:11337643-11337644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs8093332	chr18:11337673-11337674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs8092521	chr18:11337689-11337690	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550534838	chr18:11337690-11337691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs8092523	chr18:11337692-11337693	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs539328206	chr18:11337698-11337699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566154594	chr18:11337713-11337714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189756638	chr18:11337771-11337772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576789457	chr18:11337812-11337813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539983381	chr18:11337841-11337842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
Melanoma	18172304	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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11335800-11337400	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr18:11336000-11337400	Enhancers	Psoas Muscle	Psoas
3	chr18:11336600-11336800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr18:11336600-11336800	Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr18:11336800-11337000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr18:11336800-11338800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr18:11337000-11337600	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr18:11337400-11339000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr18:11338800-11339200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr18:11338800-11339400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr18:11338800-11339400	Enhancers	NHDF-Ad	bronchial
12	chr18:11339000-11339200	Enhancers	Psoas Muscle	Psoas
13	chr18:11339000-11339200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr18:11339000-11339400	Enhancers	Osteobl	bone
15	chr18:11339400-11349000	Weak transcription	NHDF-Ad	bronchial
16	chr18:11342000-11344000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr18:11344000-11344800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr18:11349000-11349200	Enhancers	NHDF-Ad	bronchial
19	chr18:11357600-11358200	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr18:11358000-11358200	Enhancers	Fetal Heart	heart
21	chr18:11358000-11358400	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr18:11361000-11361200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr18:11361200-11364400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr18:11364400-11369400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr18:11364800-11365000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr18:11365000-11366000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr18:11365200-11366400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr18:11366000-11366200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr18:11366000-11366200	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr18:11366000-11366400	Enhancers	HSMMtube	muscle
31	chr18:11366000-11367400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr18:11366000-11367800	Enhancers	Fetal Heart	heart
33	chr18:11366000-11367800	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr18:11366200-11366400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr18:11366200-11366400	Enhancers	Osteobl	bone
36	chr18:11366200-11366600	Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr18:11366200-11367000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr18:11366200-11367200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr18:11366200-11368200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr18:11366200-11368600	Enhancers	HSMM	muscle
41	chr18:11366400-11366800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr18:11366400-11366800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr18:11366400-11366800	Enhancers	NH-A	brain
44	chr18:11366400-11366800	Enhancers	NHLF	lung
45	chr18:11366400-11366800	Flanking Active TSS	Osteobl	bone
46	chr18:11366400-11367000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr18:11366400-11367000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr18:11366400-11367000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr18:11366400-11367000	Flanking Active TSS	HSMMtube	muscle
50	chr18:11366400-11367400	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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