Variant report

Variant	nsv832537
Chromosome Location	chr1:215509026-215705105
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1198)
CpG islands
(count:305)
Chromatin interactive
region (count:97)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1198 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:215698179-215698390	K562	blood:	n/a	n/a
2	BHLHE40	chr1:215573275-215573299	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:215673057-215673225	HepG2	liver:	n/a	n/a
4	BRCA1	chr1:215674811-215674940	GM12878	blood:	n/a	n/a
5	BRCA1	chr1:215699930-215700075	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr1:215528370-215528613	K562	blood:	n/a	n/a
7	CEBPB	chr1:215699886-215700169	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:215663351-215663712	MCF-7	breast:	n/a	n/a
9	CEBPB	chr1:215649354-215650108	MCF-7	breast:	n/a	n/a
10	CEBPB	chr1:215704070-215704283	IMR90	lung:	n/a	chr1:215704197-215704208
11	CEBPB	chr1:215691867-215692216	MCF-7	breast:	n/a	n/a
12	CEBPB	chr1:215654413-215654558	HepG2	liver:	n/a	chr1:215654491-215654502 chr1:215654491-215654504
13	CEBPB	chr1:215621425-215621637	HepG2	liver:	n/a	chr1:215621562-215621573 chr1:215621563-215621572 chr1:215621561-215621574 chr1:215621561-215621572
14	CEBPB	chr1:215662114-215662718	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:215704027-215704257	A549	lung:	n/a	chr1:215704197-215704208
16	CEBPB	chr1:215681715-215681969	HepG2	liver:	n/a	chr1:215681834-215681845
17	CEBPB	chr1:215688543-215688802	A549	lung:	n/a	chr1:215688676-215688687
18	CEBPB	chr1:215690682-215691237	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:215654410-215654637	A549	lung:	n/a	chr1:215654491-215654502 chr1:215654491-215654504
20	CEBPB	chr1:215704036-215704339	HepG2	liver:	n/a	chr1:215704197-215704208
21	CEBPB	chr1:215621405-215621639	IMR90	lung:	n/a	chr1:215621562-215621573 chr1:215621563-215621572 chr1:215621561-215621574 chr1:215621561-215621572
22	CEBPB	chr1:215688593-215688835	HepG2	liver:	n/a	chr1:215688676-215688687
23	CEBPB	chr1:215688659-215688714	K562	blood:	n/a	chr1:215688676-215688687
24	CEBPB	chr1:215699990-215700183	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr1:215649544-215650006	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:215649472-215650093	MCF-7	breast:	n/a	n/a
27	CEBPB	chr1:215598454-215598830	MCF-7	breast:	n/a	chr1:215598580-215598591
28	CEBPB	chr1:215614672-215614771	HepG2	liver:	n/a	chr1:215614715-215614726
29	CHD2	chr1:215696281-215696381	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:215699980-215700130	GM12865	blood:	n/a	chr1:215700080-215700098 chr1:215700075-215700096 chr1:215700085-215700093
31	CTCF	chr1:215691060-215691210	AG10803	skin:	n/a	n/a
32	CTCF	chr1:215696940-215697090	AG09309	skin:	n/a	n/a
33	CTCF	chr1:215700400-215700550	K562	blood:	n/a	n/a
34	CTCF	chr1:215696920-215697070	AG09319	gingival:	n/a	n/a
35	CTCF	chr1:215696940-215697106	LNCaP	prostate:	n/a	n/a
36	CTCF	chr1:215696969-215697098	K562	blood:	n/a	n/a
37	CTCF	chr1:215576670-215576746	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:215696980-215697096	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr1:215696960-215697110	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:215699882-215700220	SK-N-SH_RA	brain:	n/a	chr1:215700080-215700098 chr1:215700075-215700096 chr1:215700085-215700093
41	CTCF	chr1:215696949-215697125	LNCaP	prostate:	n/a	n/a
42	CTCF	chr1:215513520-215513670	AG09319	gingival:	n/a	n/a
43	CTCF	chr1:215691020-215691170	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr1:215700040-215700190	HPAF	blood vessel:	n/a	chr1:215700080-215700098 chr1:215700075-215700096 chr1:215700085-215700093
45	CTCF	chr1:215700000-215700150	GM12864	blood:	n/a	chr1:215700080-215700098 chr1:215700075-215700096 chr1:215700085-215700093
46	CTCF	chr1:215700020-215700170	AoAF	blood vessel:	n/a	chr1:215700080-215700098 chr1:215700075-215700096 chr1:215700085-215700093
47	CTCF	chr1:215513520-215513670	BJ	skin:	n/a	n/a
48	CTCF	chr1:215700000-215700150	BJ	skin:	n/a	chr1:215700080-215700098 chr1:215700075-215700096 chr1:215700085-215700093
49	CTCF	chr1:215699988-215700185	GM10248	blood:	n/a	chr1:215700080-215700098 chr1:215700075-215700096 chr1:215700085-215700093
50	CTCF	chr1:215700200-215700350	GM06990	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:215567839-215567889	ProgFib	skin:	n/a
2	chr1:215567477-215567527	MCF10A-Er-Src	breast:	n/a
3	chr1:215586699-215586749	HCPEpiC	choroid plexus:	n/a
4	chr1:215586699-215586749	HCT-116	colon:	n/a
5	chr1:215586523-215586573	SAEC	small airway:	n/a
6	chr1:215567839-215567889	HCM	heart:	n/a
7	chr1:215586523-215586573	AG04450	lung:	fetal
8	chr1:215648453-215648503	HEK293	kidney:	embryo
9	chr1:215586699-215586749	MCF10A-Er-Src	breast:	n/a
10	chr1:215586523-215586573	HRE	kidney:	n/a
11	chr1:215648453-215648503	K562	blood:	n/a
12	chr1:215567477-215567527	CMK	blood:	n/a
13	chr1:215567477-215567527	HIPEpiC	eye:	n/a
14	chr1:215586699-215586749	LNCaP	prostate:	n/a
15	chr1:215567839-215567889	HMEC	breast:	n/a
16	chr1:215586523-215586573	ovcar-3	ovarian:	n/a
17	chr1:215648453-215648503	HRPEpiC	eye:	n/a
18	chr1:215586699-215586749	PFSK-1	brain:	n/a
19	chr1:215567839-215567889	Caco-2	colon:	n/a
20	chr1:215586523-215586573	PFSK-1	brain:	n/a
21	chr1:215567477-215567527	Jurkat	blood:	n/a
22	chr1:215586699-215586749	BJ	skin:	n/a
23	chr1:215586699-215586749	AG04449	skin:	fetal
24	chr1:215567477-215567527	PFSK-1	brain:	n/a
25	chr1:215567477-215567527	AoSMC	blood vessel:	n/a
26	chr1:215648453-215648503	SK-N-MC	brain:	n/a
27	chr1:215586699-215586749	HRE	kidney:	n/a
28	chr1:215648453-215648503	AG04449	skin:	fetal
29	chr1:215567839-215567889	HRE	kidney:	n/a
30	chr1:215648453-215648503	HEEpiC	esophagus:	n/a
31	chr1:215586699-215586749	AG09319	gingival:	n/a
32	chr1:215567477-215567527	Hepatocyte	liver:	n/a
33	chr1:215567477-215567527	HNPCEpiC	eye:	n/a
34	chr1:215648453-215648503	HRE	kidney:	n/a
35	chr1:215567477-215567527	RPTEC	kidney:	n/a
36	chr1:215648453-215648503	NH-A	brain:	n/a
37	chr1:215586523-215586573	IMR90	lung:	fetal
38	chr1:215586523-215586573	HCT-116	colon:	n/a
39	chr1:215567839-215567889	HIPEpiC	eye:	n/a
40	chr1:215586523-215586573	CMK	blood:	n/a
41	chr1:215586699-215586749	HIPEpiC	eye:	n/a
42	chr1:215567477-215567527	HEEpiC	esophagus:	n/a
43	chr1:215567839-215567889	HCF	heart:	n/a
44	chr1:215586523-215586573	SK-N-SH_RA	brain:	n/a
45	chr1:215567839-215567889	GM12878	blood:	n/a
46	chr1:215567839-215567889	HAEpiC	amniotic membrane:	n/a
47	chr1:215586699-215586749	GM12892	blood:	n/a
48	chr1:215567477-215567527	HUVEC	blood vessel:	n/a
49	chr1:215586523-215586573	HRPEpiC	eye:	n/a
50	chr1:215586523-215586573	PrEC	prostate:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:215652527..215655000-chr1:215655463..215657420,3	MCF-7	breast:
2	chr1:214832291..214832816-chr1:215696580..215697541,3	MCF-7	breast:
3	chr1:215572966..215575563-chr1:215579724..215582468,2	K562	blood:
4	chr1:214831934..214833558-chr1:215696482..215697599,5	MCF-7	breast:
5	chr1:215646701..215647850-chr1:215655247..215656051,5	MCF-7	breast:
6	chr1:215699599..215700316-chr1:215779687..215780673,3	MCF-7	breast:
7	chr1:215542629..215544748-chr1:215545652..215547267,2	K562	blood:
8	chr1:214506031..214506834-chr1:215699653..215700161,2	K562	blood:
9	chr1:215624948..215626572-chr1:215631438..215633502,2	MCF-7	breast:
10	chr1:215530323..215533254-chr1:215538502..215541402,2	K562	blood:
11	chr1:215690701..215691338-chrX:53321371..53322017,2	MCF-7	breast:
12	chr1:215598452..215599119-chr1:215662801..215663769,2	MCF-7	breast:
13	chr1:215598275..215599042-chr1:215647338..215647850,2	MCF-7	breast:
14	chr1:215624948..215626572-chr1:215631438..215633502,2	MCF-7	breast:
15	chr1:215354644..215355511-chr1:215690679..215691509,5	MCF-7	breast:
16	chr1:215646701..215647818-chr1:215655247..215656051,4	MCF-7	breast:
17	chr1:215531029..215532667-chr1:215653579..215655433,2	K562	blood:
18	chr1:215641789..215644876-chr1:215645316..215648235,3	K562	blood:
19	chr1:215622337..215625097-chr1:215626697..215628486,2	K562	blood:
20	chr1:215628691..215630584-chr1:215630925..215633155,2	MCF-7	breast:
21	chr1:215598617..215599182-chr1:215655318..215656103,2	MCF-7	breast:
22	chr1:215572784..215574532-chr1:215574857..215577668,2	K562	blood:
23	chr1:215646701..215647818-chr1:215655247..215656051,4	MCF-7	breast:
24	chr1:215641789..215644876-chr1:215645316..215648235,3	K562	blood:
25	chr1:215530323..215533254-chr1:215538502..215541402,2	K562	blood:
26	chr1:215531102..215532894-chr1:215533168..215535488,2	MCF-7	breast:
27	chr1:215667479..215669365-chr1:215673688..215676316,2	MCF-7	breast:
28	chr1:215598355..215599119-chr1:215661939..215663301,3	MCF-7	breast:
29	chr1:215676034..215678522-chr1:215684144..215685735,2	K562	blood:
30	chr1:215660646..215662869-chr1:215670952..215673694,2	MCF-7	breast:
31	chr1:214981919..214982804-chr1:215690586..215691218,5	MCF-7	breast:
32	chr1:215670287..215672769-chr1:215675480..215677186,2	MCF-7	breast:
33	chr1:215655508..215656065-chr1:215718108..215718963,2	MCF-7	breast:
34	chr1:215696600..215699320-chr1:215739621..215741254,2	K562	blood:
35	chr1:215652527..215655000-chr1:215655463..215657420,3	MCF-7	breast:
36	chr1:215667479..215669365-chr1:215673688..215676316,2	MCF-7	breast:
37	chr1:215507541..215509380-chr1:215510952..215512628,2	K562	blood:
38	chr1:215676034..215678522-chr1:215684144..215685735,2	K562	blood:
39	chr1:215653919..215659650-chr1:215659919..215663792,9	MCF-7	breast:
40	chr1:215550395..215553289-chr1:215632429..215635331,2	MCF-7	breast:
41	chr1:215693481..215695189-chr1:215695315..215696992,2	MCF-7	breast:
42	chr1:215693481..215695189-chr1:215695315..215696992,2	MCF-7	breast:
43	chr1:215576335..215577189-chr1:215690702..215691423,2	MCF-7	breast:
44	chr1:215598325..215599086-chr1:215646834..215647759,3	MCF-7	breast:
45	chr1:215656949..215659189-chr1:215661543..215664424,2	K562	blood:
46	chr1:215598275..215599042-chr1:215647338..215647850,2	MCF-7	breast:
47	chr1:215531029..215532667-chr1:215653579..215655433,2	K562	blood:
48	chr1:215649830..215650771-chr1:215662339..215662875,2	MCF-7	breast:
49	chr1:215645440..215647544-chr1:215658602..215661519,2	MCF-7	breast:
50	chr1:215550395..215553289-chr1:215632429..215635331,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCTD3-6	chr1:215588007-215588179	NONHSAT009470
2	lnc-USH2A-2	chr1:215627371-215627472	NONHSAT009472
3	lnc-KCTD3-5	chr1:215588920-215588980	NONHSAT009471
4	lnc-USH2A-2	chr1:215627031-215627183	NONHSAT009472
5	lnc-USH2A-2	chr1:215627065-215627166	FPKM1_group_2309_transcript_1
6	lnc-KCTD3-6	chr1:215584407-215584506	NONHSAT009470
7	lnc-USH2A-2	chr1:215627031-215627183	FPKM1_group_2309_transcript_1
8	lnc-KCTD3-5	chr1:215586199-215586279	NONHSAT009471
9	lnc-KCTD3-5	chr1:215584887-215585105	NONHSAT009471
10	lnc-KCTD3-6	chr1:215584407-215584506	FPKM1_group_2308_transcript_1
11	lnc-KCTD3-6	chr1:215584443-215584615	FPKM1_group_2308_transcript_1

No data

Variant related genes	Relation type
VDAC1P10	TF binding region
VDAC1P10	CpG island
ENSG00000232809	chromatin interactions
ENSG00000196562	chromatin interactions
ENSG00000136636	chromatin interactions
ENSG00000087086	chromatin interactions
ENSG00000143756	chromatin interactions

Extended variants
information (count: 5004 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5004 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12077731	chr1:215517219-215517220	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12077775	chr1:215517319-215517320	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532554894	chr1:215517363-215517364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546016954	chr1:215517448-215517449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564967227	chr1:215517466-215517467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184871682	chr1:215517499-215517500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11120567	chr1:215517500-215517501	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs148078104	chr1:215517524-215517525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529760137	chr1:215517533-215517534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539108705	chr1:215517539-215517540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs60454150	chr1:215517550-215517551	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs61057668	chr1:215517556-215517557	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182043847	chr1:215517577-215517578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142673424	chr1:215517604-215517605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369885318	chr1:215517654-215517655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187659750	chr1:215517672-215517673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537956730	chr1:215517750-215517751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146016291	chr1:215517771-215517772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556659144	chr1:215517775-215517776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543125510	chr1:215517786-215517787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533967410	chr1:215517818-215517819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554024812	chr1:215517821-215517822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189798218	chr1:215517844-215517845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77384957	chr1:215517887-215517888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555565596	chr1:215517989-215517990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12074526	chr1:215518000-215518001	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs544693486	chr1:215518032-215518033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116307414	chr1:215518040-215518041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181966641	chr1:215518051-215518052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561077991	chr1:215518055-215518056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529696942	chr1:215518059-215518060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546646380	chr1:215518119-215518120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560458557	chr1:215518125-215518126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141781754	chr1:215518140-215518141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540661666	chr1:215518155-215518156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560484871	chr1:215518191-215518192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552303386	chr1:215518221-215518222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185321020	chr1:215518261-215518262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368047332	chr1:215518272-215518273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538085497	chr1:215518278-215518279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548380011	chr1:215518321-215518322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375502031	chr1:215518334-215518335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533907977	chr1:215518341-215518342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150765682	chr1:215518359-215518360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139103584	chr1:215518362-215518363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6686570	chr1:215518364-215518365	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556860737	chr1:215518376-215518377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548469029	chr1:215518386-215518387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376996786	chr1:215518419-215518420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561927472	chr1:215518433-215518434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
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
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215517200-215519200	Enhancers	Adipose Nuclei	Adipose
2	chr1:215517200-215519400	Enhancers	Fetal Lung	lung
3	chr1:215517400-215519600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:215518000-215518200	Enhancers	Right Atrium	heart
5	chr1:215518000-215518400	Enhancers	Fetal Stomach	stomach
6	chr1:215518400-215520200	Weak transcription	Right Atrium	heart
7	chr1:215519000-215519400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:215519400-215530600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:215530600-215534200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:215531400-215532400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:215532400-215533000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:215533000-215534000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr1:215533200-215533800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr1:215533200-215534400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:215533400-215534000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:215533400-215534000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:215533400-215534000	Enhancers	Psoas Muscle	Psoas
18	chr1:215533400-215534400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:215548400-215548600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:215548600-215549600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:215548800-215549800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:215549000-215551600	Enhancers	Osteobl	bone
23	chr1:215549600-215549800	Enhancers	NHDF-Ad	bronchial
24	chr1:215549600-215551600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:215549800-215550000	Bivalent Enhancer	NHDF-Ad	bronchial
26	chr1:215549800-215550200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:215549800-215550800	Enhancers	Adipose Nuclei	Adipose
28	chr1:215549800-215551200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:215549800-215551800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:215550000-215550200	Flanking Active TSS	NHDF-Ad	bronchial
31	chr1:215550000-215550800	Enhancers	HSMM	muscle
32	chr1:215550000-215550800	Enhancers	HSMMtube	muscle
33	chr1:215550200-215550600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:215550200-215550600	Enhancers	HepG2	liver
35	chr1:215550200-215551200	Enhancers	NHDF-Ad	bronchial
36	chr1:215550600-215550800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:215550800-215551400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:215562200-215563200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr1:215563200-215563400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr1:215563400-215564000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr1:215563400-215568000	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr1:215565400-215567400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:215567000-215567400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr1:215567400-215567800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr1:215567400-215568400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:215568000-215568200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
47	chr1:215568400-215572600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:215570400-215571000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:215570400-215571000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:215570600-215571000	Active TSS	NHDF-Ad	bronchial

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