Variant report

Variant	nsv531880
Chromosome Location	chr1:71724941-71964501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:654)
CpG islands
(count:183)
Chromatin interactive
region (count:28)
LncRNA
region (count:55)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:71778691-71778792	K562	blood:	n/a	n/a
2	ATF1	chr1:71839584-71839653	K562	blood:	n/a	n/a
3	ATF1	chr1:71758441-71758554	K562	blood:	n/a	n/a
4	BACH1	chr1:71773289-71773496	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:71950573-71950579	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:71773244-71773527	GM12878	blood:	n/a	chr1:71773395-71773406
7	BCL11A	chr1:71927983-71928296	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr1:71928031-71928271	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr1:71953142-71953384	GM12878	blood:	n/a	n/a
10	BCL3	chr1:71953062-71953428	GM12878	blood:	n/a	n/a
11	BCL3	chr1:71956137-71956395	GM12878	blood:	n/a	n/a
12	BCL3	chr1:71956157-71956480	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:71727383-71727432	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:71823557-71823623	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:71961511-71961727	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:71857351-71857492	K562	blood:	n/a	chr1:71857386-71857397
17	CEBPB	chr1:71902907-71903169	IMR90	lung:	n/a	chr1:71903029-71903040
18	CEBPB	chr1:71831103-71831451	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:71857313-71857530	H1-hESC	embryonic stem cell:	n/a	chr1:71857386-71857397
20	CEBPB	chr1:71959918-71960236	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:71928888-71929212	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:71859079-71859300	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr1:71930968-71931163	A549	lung:	n/a	chr1:71931145-71931162 chr1:71931065-71931076
24	CEBPB	chr1:71956153-71956490	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:71964324-71964524	H1-hESC	embryonic stem cell:	n/a	chr1:71964419-71964432 chr1:71964419-71964430 chr1:71964419-71964432 chr1:71964419-71964432 chr1:71964420-71964431
26	CEBPB	chr1:71914156-71914512	IMR90	lung:	n/a	chr1:71914318-71914331 chr1:71914318-71914331 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914319-71914330
27	CEBPB	chr1:71857247-71857472	HepG2	liver:	n/a	chr1:71857386-71857397
28	CEBPB	chr1:71914196-71914408	Hela-S3	cervix:	n/a	chr1:71914318-71914331 chr1:71914318-71914331 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914319-71914330
29	CEBPB	chr1:71888601-71888799	HepG2	liver:	n/a	chr1:71888661-71888674 chr1:71888663-71888672 chr1:71888661-71888672
30	CEBPB	chr1:71956151-71956460	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:71817163-71817558	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:71959895-71960217	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:71769898-71770122	Hela-S3	cervix:	n/a	chr1:71769975-71769986 chr1:71769975-71769988
34	CEBPB	chr1:71914147-71914509	HepG2	liver:	n/a	chr1:71914318-71914331 chr1:71914318-71914331 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914319-71914330
35	CEBPB	chr1:71923017-71923331	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:71914163-71914470	H1-hESC	embryonic stem cell:	n/a	chr1:71914318-71914331 chr1:71914318-71914331 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914319-71914330
37	CEBPB	chr1:71857220-71857566	IMR90	lung:	n/a	chr1:71857386-71857397
38	CEBPB	chr1:71930934-71931218	HepG2	liver:	n/a	chr1:71931145-71931162 chr1:71931065-71931076
39	CEBPB	chr1:71964266-71964603	IMR90	lung:	n/a	chr1:71964419-71964432 chr1:71964419-71964430 chr1:71964419-71964432 chr1:71964419-71964432 chr1:71964420-71964431
40	CEBPB	chr1:71857297-71857513	A549	lung:	n/a	chr1:71857386-71857397
41	CEBPB	chr1:71914161-71914482	A549	lung:	n/a	chr1:71914318-71914331 chr1:71914318-71914331 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914319-71914330
42	CEBPB	chr1:71964273-71964584	HepG2	liver:	n/a	chr1:71964419-71964432 chr1:71964419-71964430 chr1:71964419-71964432 chr1:71964419-71964432 chr1:71964420-71964431
43	CEBPB	chr1:71927446-71927664	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:71902874-71903109	HepG2	liver:	n/a	chr1:71903029-71903040
45	CEBPB	chr1:71914227-71914476	K562	blood:	n/a	chr1:71914318-71914331 chr1:71914318-71914331 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914319-71914330
46	CEBPB	chr1:71914214-71914552	MCF-7	breast:	n/a	chr1:71914318-71914331 chr1:71914318-71914331 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914320-71914329 chr1:71914319-71914330
47	CEBPB	chr1:71956190-71956394	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr1:71928390-71928678	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr1:71823524-71823637	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:71737420-71737570	HFF-Myc	foreskin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71830814-71830864	AG09319	gingival:	n/a
2	chr1:71929976-71930026	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:71929976-71930026	K562	blood:	n/a
4	chr1:71929976-71930026	HCF	heart:	n/a
5	chr1:71830814-71830864	HEEpiC	esophagus:	n/a
6	chr1:71830814-71830864	GM12878	blood:	n/a
7	chr1:71929976-71930026	GM06990	blood:	n/a
8	chr1:71929976-71930026	A549	lung:	n/a
9	chr1:71904426-71904476	T-47D	breast:	n/a
10	chr1:71830814-71830864	AG09309	skin:	n/a
11	chr1:71929976-71930026	GM12878	blood:	n/a
12	chr1:71929976-71930026	HIPEpiC	eye:	n/a
13	chr1:71830814-71830864	ECC-1	luminal epithelium:	n/a
14	chr1:71904426-71904476	HIPEpiC	eye:	n/a
15	chr1:71929976-71930026	AoSMC	blood vessel:	n/a
16	chr1:71830814-71830864	MCF10A-Er-Src	breast:	n/a
17	chr1:71830814-71830864	ProgFib	skin:	n/a
18	chr1:71904426-71904476	SK-N-MC	brain:	n/a
19	chr1:71904426-71904476	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:71904426-71904476	SK-N-SH	brain:	n/a
21	chr1:71904426-71904476	LNCaP	prostate:	n/a
22	chr1:71929976-71930026	HEEpiC	esophagus:	n/a
23	chr1:71830814-71830864	AG04450	lung:	fetal
24	chr1:71830814-71830864	HL-60	blood:	n/a
25	chr1:71904426-71904476	A549	lung:	n/a
26	chr1:71904426-71904476	HRPEpiC	eye:	n/a
27	chr1:71929976-71930026	HepG2	liver:	n/a
28	chr1:71904426-71904476	BE2_C	brain:	n/a
29	chr1:71929976-71930026	HCM	heart:	n/a
30	chr1:71904426-71904476	GM06990	blood:	n/a
31	chr1:71929976-71930026	BE2_C	brain:	n/a
32	chr1:71830814-71830864	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:71830814-71830864	AG04449	skin:	fetal
34	chr1:71830814-71830864	HUVEC	blood vessel:	n/a
35	chr1:71904426-71904476	BJ	skin:	n/a
36	chr1:71904426-71904476	HepG2	liver:	n/a
37	chr1:71904426-71904476	H1-hESC	embryonic stem cell:	embryo
38	chr1:71929976-71930026	AG04449	skin:	fetal
39	chr1:71830814-71830864	NHDF-neo	bronchial:	n/a
40	chr1:71929976-71930026	NHBE	bronchial:	n/a
41	chr1:71929976-71930026	HUVEC	blood vessel:	n/a
42	chr1:71929976-71930026	ProgFib	skin:	n/a
43	chr1:71904426-71904476	Jurkat	blood:	n/a
44	chr1:71929976-71930026	SAEC	small airway:	n/a
45	chr1:71929976-71930026	MCF10A-Er-Src	breast:	n/a
46	chr1:71929976-71930026	ovcar-3	ovarian:	n/a
47	chr1:71830814-71830864	GM06990	blood:	n/a
48	chr1:71830814-71830864	A549	lung:	n/a
49	chr1:71929976-71930026	Hela-S3	cervix:	n/a
50	chr1:71929976-71930026	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:71914328..71914976-chr1:71927298..71927813,2	MCF-7	breast:
2	chr1:71926381..71928732-chr1:71944427..71946345,2	K562	blood:
3	chr1:71914037..71914921-chr1:71926795..71927704,3	MCF-7	breast:
4	chr1:71942559..71944248-chr1:71944744..71947074,2	MCF-7	breast:
5	chr1:71915989..71918426-chr1:72103464..72106010,2	K562	blood:
6	chr1:71813943..71816406-chr1:71819082..71821648,2	K562	blood:
7	chr1:71920535..71922572-chr1:71923828..71926094,2	MCF-7	breast:
8	chr1:71924869..71926479-chr1:71926979..71928831,2	MCF-7	breast:
9	chr1:71924869..71926479-chr1:71926979..71928831,2	MCF-7	breast:
10	chr1:71913901..71916757-chr1:71917212..71919277,2	K562	blood:
11	chr1:71941950..71944127-chr1:71948756..71950368,2	K562	blood:
12	chr1:71914108..71914677-chr16:85554351..85554911,2	MCF-7	breast:
13	chr1:71926381..71928732-chr1:71944427..71946345,2	K562	blood:
14	chr1:71941950..71944127-chr1:71948756..71950368,2	K562	blood:
15	chr1:71941193..71943663-chr1:71947061..71948900,2	K562	blood:
16	chr1:71914037..71914921-chr1:71926795..71927704,3	MCF-7	breast:
17	chr1:71942559..71944248-chr1:71944744..71947074,2	MCF-7	breast:
18	chr1:71941193..71943663-chr1:71947061..71948900,2	K562	blood:
19	chr1:71914328..71914851-chr1:71927223..71927813,2	MCF-7	breast:
20	chr1:71513260..71514174-chr1:71822945..71823752,2	K562	blood:
21	chr1:71885933..71887641-chr1:71889181..71890999,2	K562	blood:
22	chr1:71813943..71816406-chr1:71819082..71821648,2	K562	blood:
23	chr1:71914328..71914851-chr1:71927223..71927813,2	MCF-7	breast:
24	chr1:71914328..71914976-chr1:71927298..71927813,2	MCF-7	breast:
25	chr1:71914181..71914987-chr1:71994857..71995392,2	MCF-7	breast:
26	chr1:71920535..71922572-chr1:71923828..71926094,2	MCF-7	breast:
27	chr1:71885933..71887641-chr1:71889181..71890999,2	K562	blood:
28	chr1:71913901..71916757-chr1:71917212..71919277,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-6	chr1:71933967-71934193	ENSG00000229956.5
2	lnc-CTH-6	chr1:71952081-71952130	ENSG00000229956.5
3	lnc-CTH-6	chr1:71950469-71950519	ENSG00000229956.5
4	lnc-CTH-6	chr1:71929014-71929208	ENSG00000229956.5
5	lnc-CTH-6	chr1:71927244-71927500	ENSG00000229956.5
6	lnc-CTH-6	chr1:71953674-71953831	ENSG00000229956.5
7	lnc-CTH-6	chr1:71873316-71873554	ENSG00000229956.5
8	lnc-CTH-6	chr1:71929092-71929208	ENSG00000229956.5
9	lnc-CTH-6	chr1:71927244-71927500	ENSG00000229956.5
10	lnc-CTH-6	chr1:71887053-71887155	ENSG00000229956.5
11	lnc-CTH-6	chr1:71833738-71833771	ENSG00000229956.5
12	lnc-CTH-6	chr1:71938265-71938324	ENSG00000229956.5
13	lnc-CTH-6	chr1:71873304-71873367	ENSG00000229956.5
14	lnc-CTH-6	chr1:71867782-71868254	ENSG00000229956.5
15	lnc-CTH-6	chr1:71874621-71874694	ENSG00000229956.5
16	lnc-CTH-6	chr1:71938265-71938324	ENSG00000229956.5
17	lnc-CTH-6	chr1:71874622-71874694	ENSG00000229956.5
18	lnc-CTH-6	chr1:71873304-71873362	ENSG00000229956.5
19	lnc-CTH-6	chr1:71867406-71867562	ENSG00000229956.5
20	lnc-CTH-6	chr1:71955391-71955586	ENSG00000229956.5
21	lnc-CTH-6	chr1:71873316-71873554	ENSG00000229956.5
22	lnc-CTH-6	chr1:71867405-71867562	ENSG00000229956.5
23	lnc-CTH-6	chr1:71952081-71952196	ENSG00000229956.5
24	lnc-CTH-6	chr1:71952081-71952217	ENSG00000229956.5
25	lnc-CTH-6	chr1:71873327-71873498	ENSG00000229956.5
26	lnc-CTH-6	chr1:71929014-71929063	ENSG00000229956.5
27	lnc-CTH-6	chr1:71868179-71868254	ENSG00000227126.1
28	lnc-CTH-6	chr1:71770042-71770098	ENSG00000229956.5
29	lnc-CTH-6	chr1:71952081-71952751	ENSG00000229956.5
30	lnc-CTH-6	chr1:71867530-71867562	ENSG00000227126.1
31	lnc-CTH-6	chr1:71953674-71953831	ENSG00000229956.5
32	lnc-CTH-6	chr1:71873327-71873498	ENSG00000229956.5
33	lnc-CTH-6	chr1:71833738-71833771	ENSG00000229956.2
34	lnc-CTH-6	chr1:71887053-71887155	ENSG00000229956.5
35	lnc-CTH-6	chr1:71929014-71929208	ENSG00000229956.5
36	lnc-CTH-6	chr1:71873304-71873367	ENSG00000229956.5
37	lnc-CTH-6	chr1:71950469-71950519	ENSG00000229956.5
38	lnc-CTH-6	chr1:71867406-71867562	ENSG00000229956.5
39	lnc-CTH-6	chr1:71874621-71874694	ENSG00000229956.5
40	lnc-CTH-6	chr1:71867406-71867562	ENSG00000229956.2
41	lnc-CTH-6	chr1:71955391-71955652	ENSG00000229956.5
42	lnc-CTH-6	chr1:71733588-71733913	ENSG00000229956
43	lnc-CTH-6	chr1:71888187-71888658	ENSG00000229956.5
44	lnc-CTH-6	chr1:71874621-71874694	ENSG00000229956.5
45	lnc-CTH-6	chr1:71929014-71929184	ENSG00000229956.2
46	lnc-CTH-6	chr1:71867406-71867562	ENSG00000229956.5
47	lnc-CTH-6	chr1:71873304-71873341	ENSG00000229956.5
48	lnc-NEGR1-2	chr1:71832737-71832986	NONHSAT003896
49	lnc-CTH-6	chr1:71873304-71873407	ENSG00000227126.1
50	lnc-CTH-6	chr1:71873323-71873554	ENSG00000229956.5

No data

Variant related genes	Relation type
ENSG00000226324	TF binding region
ZRANB2-AS2	TF binding region
NEGR1	TF binding region
ENSG00000226324	CpG island
ZRANB2-AS2	CpG island
NEGR1	CpG island
ENSG00000050628	chromatin interactions
CDK19	miRNA target sites

Extended variants
information (count: 4282 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:4282 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571213981	chr1:71725826-71725827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534100181	chr1:71725882-71725883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375642625	chr1:71725892-71725893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147276193	chr1:71725918-71725919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117781165	chr1:71725996-71725997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542488552	chr1:71725998-71725999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538853777	chr1:71727266-71727267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558326226	chr1:71727269-71727270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577756029	chr1:71727305-71727306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533987934	chr1:71727308-71727309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553751127	chr1:71727353-71727354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145206753	chr1:71727472-71727473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542965584	chr1:71727486-71727487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549526096	chr1:71727492-71727493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563228819	chr1:71727522-71727523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113564298	chr1:71727643-71727644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576641730	chr1:71727698-71727699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545666575	chr1:71727714-71727715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565471959	chr1:71727753-71727754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112800770	chr1:71727775-71727776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17091044	chr1:71727795-71727796	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs560891227	chr1:71727879-71727880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529659599	chr1:71727907-71727908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111329732	chr1:71727908-71727909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61777294	chr1:71727911-71727912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569979641	chr1:71727945-71727946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532295060	chr1:71727980-71727981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557157282	chr1:71728000-71728001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569835055	chr1:71728014-71728015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535382077	chr1:71728066-71728067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551961943	chr1:71728085-71728086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565487987	chr1:71728151-71728152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534046660	chr1:71728264-71728265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140898941	chr1:71728292-71728293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143152479	chr1:71728294-71728295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531679998	chr1:71728322-71728323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192680787	chr1:71728327-71728328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555673258	chr1:71728331-71728332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574331572	chr1:71728367-71728368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556282705	chr1:71728543-71728544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576715828	chr1:71728565-71728566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543627401	chr1:71728636-71728637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565107528	chr1:71728657-71728658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185477761	chr1:71728697-71728698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368524862	chr1:71728751-71728752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559198580	chr1:71728801-71728802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375625854	chr1:71728813-71728814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188991170	chr1:71728824-71728825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532083633	chr1:71728866-71728867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2694947	chr1:71728893-71728894	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71725800-71726000	Enhancers	Fetal Brain Female	brain
2	chr1:71727200-71733000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:71728400-71729000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:71728400-71729000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:71729200-71729600	Enhancers	Fetal Brain Male	brain
6	chr1:71729800-71733600	Weak transcription	Fetal Brain Male	brain
7	chr1:71732600-71733800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:71733000-71734400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:71733000-71736400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:71733400-71736400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:71733600-71733800	Enhancers	Fetal Brain Male	brain
12	chr1:71733600-71736600	Enhancers	NHDF-Ad	bronchial
13	chr1:71733800-71734400	Weak transcription	Fetal Brain Male	brain
14	chr1:71734400-71736000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:71734600-71734800	Enhancers	Fetal Brain Male	brain
16	chr1:71734800-71735600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr1:71735800-71736200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:71736200-71736800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:71736400-71737800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:71736400-71739200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:71736600-71738800	Weak transcription	NHDF-Ad	bronchial
22	chr1:71737000-71737800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr1:71737800-71738000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr1:71737800-71739400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:71738800-71739600	Enhancers	NHDF-Ad	bronchial
26	chr1:71739200-71740400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:71740200-71740800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:71742200-71742400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:71742400-71751000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:71751000-71751200	ZNF genes & repeats	Pancreas	Pancrea
31	chr1:71751000-71751400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:71751000-71751400	Enhancers	HMEC	breast
33	chr1:71751200-71754000	Weak transcription	Pancreas	Pancrea
34	chr1:71759600-71762400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:71759600-71762800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:71760000-71760200	Enhancers	HMEC	breast
37	chr1:71760200-71760400	Enhancers	NHDF-Ad	bronchial
38	chr1:71760200-71761000	Weak transcription	HMEC	breast
39	chr1:71760400-71761200	Weak transcription	NHDF-Ad	bronchial
40	chr1:71761000-71761400	Enhancers	Adipose Nuclei	Adipose
41	chr1:71761000-71763200	Enhancers	HMEC	breast
42	chr1:71761000-71763400	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr1:71761000-71763400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:71761200-71762600	Enhancers	NHDF-Ad	bronchial
45	chr1:71762200-71763200	Enhancers	Fetal Muscle Leg	muscle
46	chr1:71762400-71764400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:71762800-71764200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:71763200-71764200	Weak transcription	HMEC	breast
49	chr1:71763400-71763800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:71763800-71764800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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