Variant report

Variant	nsv873200
Chromosome Location	chr1:221644180-221843191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1613)
CpG islands
(count:489)
Chromatin interactive
region (count:63)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:221840917-221841233	K562	blood:	n/a	n/a
2	ARID3A	chr1:221829368-221829547	K562	blood:	n/a	n/a
3	ATF1	chr1:221785596-221786177	K562	blood:	n/a	n/a
4	ATF1	chr1:221805498-221805778	K562	blood:	n/a	n/a
5	ATF1	chr1:221685219-221685419	K562	blood:	n/a	n/a
6	ATF1	chr1:221651441-221651841	K562	blood:	n/a	n/a
7	ATF1	chr1:221757163-221757521	K562	blood:	n/a	n/a
8	ATF1	chr1:221701385-221701508	K562	blood:	n/a	n/a
9	ATF1	chr1:221768533-221768534	K562	blood:	n/a	n/a
10	ATF1	chr1:221836820-221837456	K562	blood:	n/a	n/a
11	ATF1	chr1:221840853-221841254	K562	blood:	n/a	n/a
12	ATF1	chr1:221728375-221728513	K562	blood:	n/a	n/a
13	ATF1	chr1:221738143-221738299	K562	blood:	n/a	n/a
14	ATF1	chr1:221741072-221741272	K562	blood:	n/a	n/a
15	ATF2	chr1:221842665-221843223	GM12878	blood:	n/a	n/a
16	ATF2	chr1:221816985-221817657	GM12878	blood:	n/a	n/a
17	ATF2	chr1:221840686-221841296	GM12878	blood:	n/a	n/a
18	ATF2	chr1:221840763-221841267	GM12878	blood:	n/a	n/a
19	ATF2	chr1:221651312-221651802	GM12878	blood:	n/a	n/a
20	ATF3	chr1:221840846-221841242	K562	blood:	n/a	n/a
21	ATF3	chr1:221785855-221786116	K562	blood:	n/a	chr1:221786032-221786045
22	BATF	chr1:221842743-221843102	GM12878	blood:	n/a	chr1:221842898-221842909
23	BATF	chr1:221840760-221841219	GM12878	blood:	n/a	n/a
24	BATF	chr1:221817211-221817535	GM12878	blood:	n/a	n/a
25	BATF	chr1:221840765-221841177	GM12878	blood:	n/a	n/a
26	BATF	chr1:221842646-221843102	GM12878	blood:	n/a	chr1:221842898-221842909
27	BATF	chr1:221817194-221817496	GM12878	blood:	n/a	n/a
28	BATF	chr1:221683067-221683246	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:221840737-221841219	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:221840803-221841107	GM12878	blood:	n/a	n/a
31	BCL3	chr1:221785727-221786201	A549	lung:	n/a	chr1:221785986-221785995 chr1:221785987-221785996
32	BCL3	chr1:221840836-221841264	GM12878	blood:	n/a	n/a
33	BCLAF1	chr1:221840722-221841210	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:221829299-221829805	K562	blood:	n/a	n/a
35	BHLHE40	chr1:221840822-221841182	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:221651431-221651726	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:221803644-221803794	K562	blood:	n/a	n/a
38	BHLHE40	chr1:221840886-221841466	K562	blood:	n/a	n/a
39	BHLHE40	chr1:221817096-221817550	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:221788141-221788416	K562	blood:	n/a	n/a
41	BHLHE40	chr1:221842867-221843061	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:221810373-221810574	K562	blood:	n/a	n/a
43	BRCA1	chr1:221785455-221786284	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr1:221811059-221811110	GM12878	blood:	n/a	n/a
45	BRCA1	chr1:221840950-221841133	GM12878	blood:	n/a	n/a
46	BRCA1	chr1:221728602-221728604	GM12878	blood:	n/a	n/a
47	BRCA1	chr1:221651377-221651748	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr1:221667961-221668430	HCT-116	colon:	n/a	n/a
49	CCNT2	chr1:221785610-221786019	K562	blood:	n/a	n/a
50	CCNT2	chr1:221829286-221829519	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:221737032-221737082	PFSK-1	brain:	n/a
2	chr1:221737032-221737082	PFSK-1	brain:	n/a
3	chr1:221818304-221818354	NB4	blood:	n/a
4	chr1:221818304-221818354	PrEC	prostate:	n/a
5	chr1:221785710-221785760	AG09319	gingival:	n/a
6	chr1:221737032-221737082	NT2-D1	testis:	n/a
7	chr1:221747446-221747496	BE2_C	brain:	n/a
8	chr1:221737032-221737082	AG09319	gingival:	n/a
9	chr1:221818304-221818354	NHDF-neo	bronchial:	n/a
10	chr1:221838383-221838433	Caco-2	colon:	n/a
11	chr1:221838383-221838433	HepG2	liver:	n/a
12	chr1:221747446-221747496	HRCEpiC	kidney:	n/a
13	chr1:221737032-221737082	LNCaP	prostate:	n/a
14	chr1:221737032-221737082	PANC-1	pancreas:	n/a
15	chr1:221785710-221785760	U87	brain:	n/a
16	chr1:221785710-221785760	RPTEC	kidney:	n/a
17	chr1:221737206-221737256	HRCEpiC	kidney:	n/a
18	chr1:221651747-221651797	GM12878	blood:	n/a
19	chr1:221747446-221747496	HepG2	liver:	n/a
20	chr1:221747446-221747496	HRE	kidney:	n/a
21	chr1:221737032-221737082	Jurkat	blood:	n/a
22	chr1:221785710-221785760	HCT-116	colon:	n/a
23	chr1:221651747-221651797	PrEC	prostate:	n/a
24	chr1:221737206-221737256	AoSMC	blood vessel:	n/a
25	chr1:221741553-221741603	PrEC	prostate:	n/a
26	chr1:221818304-221818354	ProgFib	skin:	n/a
27	chr1:221747446-221747496	Hela-S3	cervix:	n/a
28	chr1:221737032-221737082	SK-N-SH	brain:	n/a
29	chr1:221785710-221785760	AG04449	skin:	fetal
30	chr1:221785710-221785760	SK-N-SH_RA	brain:	n/a
31	chr1:221838383-221838433	H1-hESC	embryonic stem cell:	embryo
32	chr1:221747446-221747496	NHBE	bronchial:	n/a
33	chr1:221838383-221838433	NHDF-neo	bronchial:	n/a
34	chr1:221737206-221737256	PrEC	prostate:	n/a
35	chr1:221651747-221651797	A549	lung:	n/a
36	chr1:221737032-221737082	Caco-2	colon:	n/a
37	chr1:221737032-221737082	ECC-1	luminal epithelium:	n/a
38	chr1:221785710-221785760	HAEpiC	amniotic membrane:	n/a
39	chr1:221747446-221747496	AG10803	skin:	n/a
40	chr1:221785710-221785760	HRPEpiC	eye:	n/a
41	chr1:221651747-221651797	H1-hESC	embryonic stem cell:	embryo
42	chr1:221785710-221785760	LNCaP	prostate:	n/a
43	chr1:221838383-221838433	HCF	heart:	n/a
44	chr1:221785710-221785760	NHBE	bronchial:	n/a
45	chr1:221737032-221737082	GM12878	blood:	n/a
46	chr1:221651747-221651797	HRPEpiC	eye:	n/a
47	chr1:221737032-221737082	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:221741553-221741603	NB4	blood:	n/a
49	chr1:221737032-221737082	HEK293	kidney:	embryo
50	chr1:221651747-221651797	HMEC	breast:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:221804015..221806371-chr1:221811621..221813998,2	K562	blood:
2	chr1:221696861..221698748-chr1:221709544..221711266,2	K562	blood:
3	chr1:221746909..221748850-chr1:221913979..221916326,2	MCF-7	breast:
4	chr1:221644700..221647006-chr1:221650503..221652903,2	MCF-7	breast:
5	chr1:221651383..221651959-chr1:221811085..221811756,3	MCF-7	breast:
6	chr1:221716979..221717540-chr1:221914806..221915585,2	MCF-7	breast:
7	chr1:221812228..221814162-chr1:221815406..221817221,2	K562	blood:
8	chr1:221826366..221828507-chr1:221841172..221843520,2	MCF-7	breast:
9	chr1:221840278..221843127-chr1:221844989..221847688,2	MCF-7	breast:
10	chr1:221644525..221647511-chr1:221668649..221670160,2	K562	blood:
11	chr1:221830865..221833221-chr1:221836408..221838119,2	MCF-7	breast:
12	chr1:221796853..221799053-chr1:221805880..221808710,2	K562	blood:
13	chr1:221804697..221805537-chr1:222182197..222182723,2	MCF-7	breast:
14	chr1:221774036..221776758-chr1:221913845..221916015,2	MCF-7	breast:
15	chr1:221766487..221768171-chr1:221768648..221770195,2	MCF-7	breast:
16	chr1:221766078..221767726-chr1:221770721..221773346,2	MCF-7	breast:
17	chr1:221766487..221768171-chr1:221768648..221770195,2	MCF-7	breast:
18	chr1:221732770..221734353-chr1:221737338..221739600,2	MCF-7	breast:
19	chr1:221651308..221651811-chr1:221837665..221838257,2	MCF-7	breast:
20	chr1:221651383..221651959-chr1:221811085..221811756,3	MCF-7	breast:
21	chr1:221684140..221685754-chr1:221914882..221917290,2	MCF-7	breast:
22	chr1:221644525..221647511-chr1:221668649..221670160,2	K562	blood:
23	chr1:221828900..221831688-chr1:221913117..221915245,2	K562	blood:
24	chr1:221826366..221828507-chr1:221841172..221843520,2	MCF-7	breast:
25	chr1:221809737..221812639-chr1:221914030..221916413,2	MCF-7	breast:
26	chr1:221716861..221717502-chr1:222278572..222279282,2	MCF-7	breast:
27	chr1:221766078..221767726-chr1:221770721..221773346,2	MCF-7	breast:
28	chr1:221751248..221753271-chr1:221864470..221866458,2	MCF-7	breast:
29	chr1:221812817..221813738-chr8:53687326..53688171,2	MCF-7	breast:
30	chr1:221651337..221652127-chr1:222628247..222629064,2	MCF-7	breast:
31	chr1:221746221..221748385-chr1:221914504..221916703,2	MCF-7	breast:
32	chr1:221644700..221647006-chr1:221650503..221652903,2	MCF-7	breast:
33	chr1:221725072..221727435-chr1:221733629..221736016,2	K562	blood:
34	chr1:221768064..221770595-chr1:221774994..221777506,2	MCF-7	breast:
35	chr1:221804015..221806371-chr1:221811621..221813998,2	K562	blood:
36	chr1:221651204..221652055-chr1:222065020..222066030,3	MCF-7	breast:
37	chr1:221651308..221651811-chr1:221837665..221838257,2	MCF-7	breast:
38	chr1:221696861..221698748-chr1:221709544..221711266,2	K562	blood:
39	chr1:221651246..221652054-chr1:222340121..222340653,3	MCF-7	breast:
40	chr1:221842453..221844829-chr1:221845406..221848131,2	MCF-7	breast:
41	chr1:221768064..221770595-chr1:221774994..221777506,2	MCF-7	breast:
42	chr1:221651148..221651987-chr1:222182537..222183210,2	MCF-7	breast:
43	chr1:221716805..221717802-chr1:221811163..221812344,4	MCF-7	breast:
44	chr1:221816826..221819415-chr1:221839496..221842221,2	MCF-7	breast:
45	chr1:221782617..221784755-chr1:221788045..221789610,2	MCF-7	breast:
46	chr1:221793515..221795187-chr1:221798481..221800380,2	K562	blood:
47	chr1:221746709..221748888-chr1:221752322..221754674,2	K562	blood:
48	chr1:221716805..221717802-chr1:221811163..221812344,4	MCF-7	breast:
49	chr1:221816826..221819415-chr1:221839496..221842221,2	MCF-7	breast:
50	chr1:221830865..221833221-chr1:221836408..221838119,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DUSP10-2	chr1:221734408-221734479	NONHSAT009644
2	lnc-DUSP10-2	chr1:221736650-221736978	XLOC_001212
3	lnc-DUSP10-2	chr1:221736650-221736994	NONHSAT009644
4	lnc-DUSP10-2	chr1:221734408-221734479	XLOC_001212
5	lnc-HLX-1	chr1:221681901-221682512	ENSG00000232436
6	lnc-HLX-5	chr1:221727429-221727771	NONHSAT009642
7	lnc-HLX-1	chr1:221684127-221684321	ENSG00000232436
8	lnc-DUSP10-2	chr1:221728928-221729770	NONHSAT009644
9	lnc-HLX-5	chr1:221722606-221722817	NONHSAT009642
10	lnc-DUSP10-6	chr1:221723128-221723985	NONHSAT009643
11	lnc-DUSP10-2	chr1:221728934-221729770	XLOC_001212

No data

Variant related genes	Relation type
ENSG00000227585	TF binding region
ENSG00000232436	TF binding region
ENSG00000227585	CpG island
ENSG00000232436	CpG island
ENSG00000227585	chromatin interactions
ENSG00000143507	chromatin interactions
CORO2B	miRNA target sites
ARID4A	miRNA target sites
RGPD4	miRNA target sites

Extended variants
information (count: 6019 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:6019 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17010076	chr1:221644180-221644181	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549669979	chr1:221644186-221644187	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs57553315	chr1:221644211-221644212	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs569339211	chr1:221644304-221644305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577940682	chr1:221644339-221644340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189461997	chr1:221644379-221644380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113062313	chr1:221644410-221644411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551452743	chr1:221644479-221644480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373092423	chr1:221644482-221644483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527813496	chr1:221644493-221644494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549594612	chr1:221644495-221644496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561503708	chr1:221644519-221644520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140663071	chr1:221644527-221644528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550446771	chr1:221644539-221644540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181117563	chr1:221644572-221644573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539387847	chr1:221644622-221644623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551126668	chr1:221644641-221644642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566541647	chr1:221644672-221644673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76326982	chr1:221644748-221644749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12085691	chr1:221644762-221644763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555134865	chr1:221644812-221644813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573461928	chr1:221644828-221644829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537654023	chr1:221644850-221644851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554462536	chr1:221644872-221644873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186611565	chr1:221644873-221644874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11118721	chr1:221644874-221644875	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545363241	chr1:221644901-221644902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560329933	chr1:221644928-221644929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536855350	chr1:221644930-221644931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145917820	chr1:221644946-221644947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555782991	chr1:221644949-221644950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147814782	chr1:221645013-221645014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61710732	chr1:221645014-221645015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397975567	chr1:221645016-221645017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561368609	chr1:221645069-221645070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531917012	chr1:221645133-221645134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550124910	chr1:221645139-221645140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112417972	chr1:221645170-221645171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376566790	chr1:221645191-221645192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190560809	chr1:221645192-221645193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555136901	chr1:221645212-221645213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181719218	chr1:221645215-221645216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556523091	chr1:221645247-221645248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566386695	chr1:221645270-221645271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186415649	chr1:221645279-221645280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548622177	chr1:221645282-221645283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191224076	chr1:221645297-221645298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368018663	chr1:221645321-221645322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138457388	chr1:221645365-221645366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571513287	chr1:221645380-221645381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221636400-221651200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:221642200-221651200	Weak transcription	HSMM	muscle
3	chr1:221642800-221645000	Enhancers	Hela-S3	cervix
4	chr1:221643000-221644200	Enhancers	NHEK	skin
5	chr1:221643200-221644200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:221643400-221644200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:221643800-221644200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:221644000-221644600	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr1:221644200-221644600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:221645000-221651000	Weak transcription	Hela-S3	cervix
11	chr1:221646600-221646800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr1:221646800-221647000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr1:221646800-221647200	Enhancers	Fetal Kidney	kidney
14	chr1:221649400-221650200	Enhancers	Fetal Lung	lung
15	chr1:221650200-221651200	Weak transcription	Fetal Lung	lung
16	chr1:221650200-221651800	Enhancers	Fetal Muscle Leg	muscle
17	chr1:221650600-221652600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:221651000-221651800	Enhancers	Colon Smooth Muscle	Colon
19	chr1:221651000-221652200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:221651000-221652600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:221651000-221652800	Enhancers	Hela-S3	cervix
22	chr1:221651200-221651400	Enhancers	Osteobl	bone
23	chr1:221651200-221651800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr1:221651200-221651800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr1:221651200-221651800	Enhancers	Fetal Lung	lung
26	chr1:221651200-221652000	Enhancers	NHEK	skin
27	chr1:221651200-221652000	Enhancers	NHLF	lung
28	chr1:221651200-221652200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:221651200-221652200	Enhancers	HMEC	breast
30	chr1:221651200-221652200	Enhancers	HSMM	muscle
31	chr1:221651200-221652200	Enhancers	NHDF-Ad	bronchial
32	chr1:221651200-221652400	Enhancers	A549	lung
33	chr1:221651200-221652800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:221651400-221651800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr1:221651400-221651800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr1:221651400-221651800	Enhancers	Brain Substantia Nigra	brain
37	chr1:221651400-221651800	Enhancers	Dnd41	blood
38	chr1:221651400-221651800	Flanking Active TSS	Osteobl	bone
39	chr1:221651400-221652000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:221651400-221652000	Enhancers	Brain Hippocampus Middle	brain
41	chr1:221651400-221652000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr1:221651400-221652000	Enhancers	NH-A	brain
43	chr1:221651400-221652200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:221651400-221652200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:221651400-221652200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr1:221651400-221652200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr1:221651400-221652200	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr1:221651400-221652600	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr1:221651600-221651800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr1:221651600-221651800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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