Variant report

Variant	nsv524125
Chromosome Location	chr1:224902054-225021860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1052)
CpG islands
(count:488)
Chromatin interactive
region (count:71)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1052 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:224969526-224969892	HepG2	liver:	n/a	n/a
2	ATF1	chr1:224921105-224921307	K562	blood:	n/a	n/a
3	ATF1	chr1:224914645-224914695	K562	blood:	n/a	n/a
4	ATF2	chr1:224924308-224925050	GM12878	blood:	n/a	n/a
5	ATF2	chr1:224933517-224933985	GM12878	blood:	n/a	n/a
6	ATF2	chr1:224920738-224921262	GM12878	blood:	n/a	n/a
7	ATF2	chr1:224920594-224921147	GM12878	blood:	n/a	n/a
8	ATF2	chr1:224924365-224924910	GM12878	blood:	n/a	n/a
9	ATF2	chr1:224927537-224928226	GM12878	blood:	n/a	n/a
10	ATF3	chr1:224958034-224958332	K562	blood:	n/a	n/a
11	ATF3	chr1:224914487-224914809	K562	blood:	n/a	n/a
12	BACH1	chr1:224925313-224925511	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr1:224920622-224921010	GM12878	blood:	n/a	chr1:224920831-224920841 chr1:224920830-224920841
14	BATF	chr1:224993642-224993901	GM12878	blood:	n/a	n/a
15	BATF	chr1:224927595-224927945	GM12878	blood:	n/a	n/a
16	BATF	chr1:224974488-224974724	GM12878	blood:	n/a	chr1:224974613-224974624
17	BATF	chr1:224924444-224924882	GM12878	blood:	n/a	n/a
18	BATF	chr1:224920647-224920985	GM12878	blood:	n/a	chr1:224920831-224920841 chr1:224920830-224920841
19	BATF	chr1:224974496-224974792	GM12878	blood:	n/a	chr1:224974613-224974624
20	BATF	chr1:224927577-224928001	GM12878	blood:	n/a	n/a
21	BATF	chr1:225003449-225003652	GM12878	blood:	n/a	n/a
22	BATF	chr1:224933576-224933898	GM12878	blood:	n/a	n/a
23	BATF	chr1:224921246-224921615	GM12878	blood:	n/a	chr1:224921428-224921439
24	BATF	chr1:224933657-224933895	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:224924434-224924909	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:224927679-224927989	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:224927625-224928311	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:224920813-224921176	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:224924456-224924884	GM12878	blood:	n/a	n/a
30	BCL3	chr1:224924409-224924919	GM12878	blood:	n/a	n/a
31	BCLAF1	chr1:224927608-224928089	GM12878	blood:	n/a	n/a
32	BCLAF1	chr1:224927575-224928222	GM12878	blood:	n/a	n/a
33	BHLHE40	chr1:224938834-224938979	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:224927557-224928398	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:224972452-224972570	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:224970905-224971377	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:224924355-224925254	GM12878	blood:	n/a	n/a
38	BHLHE40	chr1:224922917-224923255	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:224920673-224921861	GM12878	blood:	n/a	n/a
40	BRCA1	chr1:224988404-224988428	HepG2	liver:	n/a	n/a
41	CBX3	chr1:225009556-225009762	K562	blood:	n/a	n/a
42	CBX3	chr1:224946893-224947109	K562	blood:	n/a	n/a
43	CBX3	chr1:225009498-225009783	K562	blood:	n/a	n/a
44	CBX3	chr1:224946769-224947267	HCT-116	colon:	n/a	n/a
45	CBX3	chr1:224924665-224924977	K562	blood:	n/a	n/a
46	CBX3	chr1:224946885-224947180	K562	blood:	n/a	n/a
47	CEBPB	chr1:224918801-224918940	A549	lung:	n/a	n/a
48	CEBPB	chr1:224979306-224979568	IMR90	lung:	n/a	chr1:224979424-224979435
49	CEBPB	chr1:225013286-225013568	MCF-7	breast:	n/a	n/a
50	CEBPB	chr1:224981078-224981312	IMR90	lung:	n/a	chr1:224981198-224981209 chr1:224981200-224981209 chr1:224981199-224981210

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224958213-224958263	SAEC	small airway:	n/a
2	chr1:224989041-224989091	CMK	blood:	n/a
3	chr1:224989041-224989091	HRCEpiC	kidney:	n/a
4	chr1:224927238-224927288	Caco-2	colon:	n/a
5	chr1:224972796-224972846	BE2_C	brain:	n/a
6	chr1:224927238-224927288	MCF-7	breast:	n/a
7	chr1:224927238-224927288	LNCaP	prostate:	n/a
8	chr1:224925516-224925566	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:224989041-224989091	NHBE	bronchial:	n/a
10	chr1:224954584-224954634	HL-60	blood:	n/a
11	chr1:224914799-224914849	NHBE	bronchial:	n/a
12	chr1:224927238-224927288	ovcar-3	ovarian:	n/a
13	chr1:224958213-224958263	GM06990	blood:	n/a
14	chr1:224927238-224927288	AoSMC	blood vessel:	n/a
15	chr1:224989041-224989091	HEK293	kidney:	embryo
16	chr1:224989041-224989091	MCF-7	breast:	n/a
17	chr1:224927238-224927288	GM12891	blood:	n/a
18	chr1:224927238-224927288	NHDF-neo	bronchial:	n/a
19	chr1:224958213-224958263	HAEpiC	amniotic membrane:	n/a
20	chr1:224925516-224925566	HEK293	kidney:	embryo
21	chr1:224972796-224972846	SAEC	small airway:	n/a
22	chr1:224914799-224914849	HCPEpiC	choroid plexus:	n/a
23	chr1:224968206-224968256	H1-hESC	embryonic stem cell:	embryo
24	chr1:224958213-224958263	MCF-7	breast:	n/a
25	chr1:224968206-224968256	NHBE	bronchial:	n/a
26	chr1:224958213-224958263	PANC-1	pancreas:	n/a
27	chr1:224972796-224972846	HCM	heart:	n/a
28	chr1:224914799-224914849	HRE	kidney:	n/a
29	chr1:224989041-224989091	HCM	heart:	n/a
30	chr1:224954584-224954634	HCF	heart:	n/a
31	chr1:224968206-224968256	IMR90	lung:	fetal
32	chr1:224954584-224954634	H1-hESC	embryonic stem cell:	embryo
33	chr1:224927238-224927288	GM12878	blood:	n/a
34	chr1:224927238-224927288	Hepatocyte	liver:	n/a
35	chr1:224914799-224914849	HEK293	kidney:	embryo
36	chr1:224989041-224989091	HCT-116	colon:	n/a
37	chr1:224972796-224972846	Hepatocyte	liver:	n/a
38	chr1:224914799-224914849	CMK	blood:	n/a
39	chr1:224954584-224954634	SKMC	muscle:	n/a
40	chr1:224989041-224989091	Jurkat	blood:	n/a
41	chr1:224927238-224927288	AG04450	lung:	fetal
42	chr1:224958213-224958263	AG04449	skin:	fetal
43	chr1:224954584-224954634	NH-A	brain:	n/a
44	chr1:224958213-224958263	ovcar-3	ovarian:	n/a
45	chr1:224989041-224989091	HAEpiC	amniotic membrane:	n/a
46	chr1:224958213-224958263	AoSMC	blood vessel:	n/a
47	chr1:224914799-224914849	AG09309	skin:	n/a
48	chr1:224972796-224972846	HAEpiC	amniotic membrane:	n/a
49	chr1:224972796-224972846	MCF10A-Er-Src	breast:	n/a
50	chr1:224914799-224914849	Hela-S3	cervix:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:224912065..224916127-chr1:224919460..224922896,4	MCF-7	breast:
2	chr1:225018962..225021561-chr1:225021627..225023637,2	MCF-7	breast:
3	chr1:224903179..224905151-chr1:224906238..224908958,2	K562	blood:
4	chr1:224922062..224922859-chr1:225040254..225041009,2	MCF-7	breast:
5	chr1:224903173..224906981-chr1:224925522..224929021,3	K562	blood:
6	chr1:224958593..224960248-chr1:224966899..224969772,2	MCF-7	breast:
7	chr1:224969277..224969796-chr1:225038870..225039554,2	MCF-7	breast:
8	chr1:224917954..224920800-chr1:224921444..224923051,2	MCF-7	breast:
9	chr1:225002421..225004034-chr1:225006348..225008275,2	K562	blood:
10	chr1:225018962..225021561-chr1:225021627..225023637,2	MCF-7	breast:
11	chr1:224944665..224946199-chr1:224947747..224949532,2	K562	blood:
12	chr1:224962064..224964754-chr1:224973948..224976755,2	MCF-7	breast:
13	chr1:224926041..224927693-chr1:224941147..224943121,2	MCF-7	breast:
14	chr1:224923808..224926549-chr1:224941724..224943859,2	MCF-7	breast:
15	chr1:225012142..225014836-chr1:225016307..225017906,2	K562	blood:
16	chr1:224910297..224912551-chr1:224913621..224915881,2	K562	blood:
17	chr1:224921057..224922857-chr1:225011412..225013045,2	MCF-7	breast:
18	chr1:224910297..224912551-chr1:224913621..224915881,2	K562	blood:
19	chr1:224958593..224960248-chr1:224966899..224969772,2	MCF-7	breast:
20	chr1:224891874..224893385-chr1:224991193..224992708,2	K562	blood:
21	chr1:225019310..225022612-chr1:225026038..225029818,3	K562	blood:
22	chr1:224832157..224833040-chr1:224961843..224962368,3	MCF-7	breast:
23	chr1:224920081..224922903-chr1:224922930..224927181,4	MCF-7	breast:
24	chr1:224949023..224950840-chr1:224954199..224956791,2	MCF-7	breast:
25	chr1:224924141..224925837-chr1:224931757..224934189,2	K562	blood:
26	chr1:224923508..224926598-chr1:224928145..224929773,3	K562	blood:
27	chr1:225016483..225019106-chr1:225019764..225021563,2	K562	blood:
28	chr1:224944665..224946199-chr1:224947747..224949532,2	K562	blood:
29	chr1:224896062..224897742-chr1:224902518..224904337,2	K562	blood:
30	chr1:224992713..224995103-chr1:224995787..224998414,2	K562	blood:
31	chr1:224974307..224977047-chr1:224979429..224981257,2	K562	blood:
32	chr1:224992713..224995103-chr1:224995787..224998414,2	K562	blood:
33	chr1:224932630..224934863-chr1:224937638..224939409,2	K562	blood:
34	chr1:224899513..224902997-chr1:224905625..224908310,3	MCF-7	breast:
35	chr1:225004248..225005816-chr1:225039220..225040837,2	MCF-7	breast:
36	chr1:224974307..224977047-chr1:224979429..224981257,2	K562	blood:
37	chr1:224903173..224906981-chr1:224925522..224929021,3	K562	blood:
38	chr1:224914462..224916100-chr1:224917587..224919956,2	K562	blood:
39	chr1:224968181..224972472-chr1:224972623..224976659,4	MCF-7	breast:
40	chr1:224832200..224833011-chr1:224921824..224922821,2	MCF-7	breast:
41	chr1:225012142..225014836-chr1:225016307..225017906,2	K562	blood:
42	chr1:224932630..224934863-chr1:224937638..224939409,2	K562	blood:
43	chr1:224980293..224982435-chr15:65595974..65597659,2	MCF-7	breast:
44	chr1:224923808..224926549-chr1:224941724..224943859,2	MCF-7	breast:
45	chr1:225016483..225019106-chr1:225019764..225021563,2	K562	blood:
46	chr1:224923508..224926598-chr1:224928145..224929773,3	K562	blood:
47	chr1:224920081..224922903-chr1:224922930..224927181,4	MCF-7	breast:
48	chr1:224976705..224978932-chr1:224981542..224984436,2	MCF-7	breast:
49	chr1:225018653..225020810-chr1:225024865..225027538,2	K562	blood:
50	chr1:224898628..224901270-chr1:224902141..224904049,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNIH3-1	chr1:224966875-224967057	XLOC_000584
2	lnc-CNIH3-1	chr1:224960875-224960974	NONHSAT009826
3	lnc-CNIH3-1	chr1:224954602-224954855	XLOC_000584
4	lnc-CNIH3-1	chr1:224960875-224961043	XLOC_000584
5	lnc-CNIH3-1	chr1:224954074-224954855	NONHSAT009826
6	lnc-CNIH3-1	chr1:224954058-224954855	XLOC_000584

No data

Variant related genes	Relation type
ENSG00000251933	TF binding region
ENSG00000225334	TF binding region
ENSG00000229400	TF binding region
ENSG00000251933	CpG island
ENSG00000225334	CpG island
ENSG00000229400	CpG island
ENSG00000225334	chromatin interactions
ENSG00000185842	chromatin interactions
ENSG00000251933	chromatin interactions
ENSG00000229400	chromatin interactions
ENSG00000200156	chromatin interactions
EIF2C1	miRNA target sites

Extended variants
information (count: 3563 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3563 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10915704	chr1:224902054-224902055	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575379971	chr1:224902111-224902112	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs116468983	chr1:224902114-224902115	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs544349773	chr1:224902131-224902132	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs557571194	chr1:224902162-224902163	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs557175805	chr1:224902172-224902173	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs546712856	chr1:224902173-224902174	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs568156519	chr1:224902175-224902176	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs535293320	chr1:224902218-224902219	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs550444021	chr1:224902286-224902287	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs141386585	chr1:224902289-224902290	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs184951345	chr1:224902299-224902300	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs558683105	chr1:224902325-224902326	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs577209208	chr1:224902384-224902385	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs146240116	chr1:224902388-224902389	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs6669564	chr1:224902412-224902413	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs553461930	chr1:224902441-224902442	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs574920950	chr1:224902452-224902453	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs542460513	chr1:224902477-224902478	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs139340098	chr1:224902478-224902479	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs115869662	chr1:224902533-224902534	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs187374598	chr1:224902544-224902545	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs373587670	chr1:224902624-224902625	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs192153222	chr1:224902627-224902628	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs528132494	chr1:224902649-224902650	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs115370023	chr1:224902651-224902652	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs554198525	chr1:224902763-224902764	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs550382623	chr1:224902766-224902767	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs568764052	chr1:224902774-224902775	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs375239165	chr1:224902813-224902814	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs539339785	chr1:224902848-224902849	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs551700762	chr1:224902868-224902869	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs570735576	chr1:224902934-224902935	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs73132709	chr1:224902950-224902951	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs144109274	chr1:224902957-224902958	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs2117941	chr1:224902962-224902963	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs185458062	chr1:224902963-224902964	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs557601439	chr1:224902972-224902973	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs528791413	chr1:224903035-224903036	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs569320061	chr1:224903052-224903053	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs546174953	chr1:224903161-224903162	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs564826892	chr1:224903162-224903163	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs572732926	chr1:224903170-224903171	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs540238169	chr1:224903190-224903191	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs561599974	chr1:224903199-224903200	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs528958564	chr1:224903202-224903203	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189514899	chr1:224903219-224903220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562340984	chr1:224903222-224903223	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146081520	chr1:224903231-224903232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570246238	chr1:224903322-224903323	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224885000-224920200	Weak transcription	Right Atrium	heart
2	chr1:224896200-224914000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:224896400-224910600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:224896400-224913800	Weak transcription	NHLF	lung
5	chr1:224896400-224914000	Weak transcription	NH-A	brain
6	chr1:224896600-224902600	Weak transcription	NHDF-Ad	bronchial
7	chr1:224898400-224904400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:224900600-224904200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:224901000-224904200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr1:224901200-224907000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:224901600-224906800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:224902000-224902400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:224902000-224903000	Enhancers	Pancreas	Pancrea
14	chr1:224902000-224903200	ZNF genes & repeats	Dnd41	blood
15	chr1:224902400-224906200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:224902600-224902800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:224902600-224905000	Strong transcription	NHDF-Ad	bronchial
18	chr1:224902800-224903000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:224902800-224903000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:224903000-224906600	Weak transcription	Pancreas	Pancrea
21	chr1:224903000-224907600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:224903000-224914000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:224903200-224904800	Enhancers	Dnd41	blood
24	chr1:224904200-224906600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:224904400-224906800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:224904600-224908600	Enhancers	Fetal Thymus	thymus
27	chr1:224904800-224905600	Genic enhancers	Dnd41	blood
28	chr1:224905000-224909400	Weak transcription	NHDF-Ad	bronchial
29	chr1:224905600-224905800	Enhancers	Dnd41	blood
30	chr1:224905800-224906800	Flanking Active TSS	Dnd41	blood
31	chr1:224906200-224906800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:224906200-224907000	Enhancers	Thymus	Thymus
33	chr1:224906400-224906600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
34	chr1:224906400-224906600	Weak transcription	Gastric	stomach
35	chr1:224906400-224911000	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr1:224906600-224906800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr1:224906600-224907000	Enhancers	Gastric	stomach
38	chr1:224906600-224907000	Enhancers	Pancreas	Pancrea
39	chr1:224906600-224907400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:224906600-224908200	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr1:224906800-224908000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:224906800-224908400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr1:224906800-224910400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:224906800-224910800	Enhancers	Dnd41	blood
45	chr1:224906800-224911000	Enhancers	Psoas Muscle	Psoas
46	chr1:224907000-224912400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:224907000-224920200	Weak transcription	Gastric	stomach
48	chr1:224907400-224908000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:224907400-224908000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:224907400-224911400	Enhancers	Cortex derived primary cultured neurospheres	brain

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