Variant report

Variant	esv3512582
Chromosome Location	chr1:145080158-145189464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2694)
CpG islands
(count:1773)
Chromatin interactive
region (count:94)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2694 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145091964-145092746	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:145096149-145096769	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:145083440-145084471	K562	blood:	n/a	n/a
4	ARID3A	chr1:145098092-145098776	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:145089768-145090509	K562	blood:	n/a	n/a
6	ATF1	chr1:145117631-145118374	K562	blood:	n/a	n/a
7	ATF1	chr1:145090189-145090575	K562	blood:	n/a	n/a
8	ATF1	chr1:145107917-145107980	K562	blood:	n/a	n/a
9	ATF1	chr1:145109420-145111084	K562	blood:	n/a	n/a
10	ATF1	chr1:145112421-145113298	K562	blood:	n/a	n/a
11	ATF1	chr1:145096190-145096629	K562	blood:	n/a	n/a
12	ATF1	chr1:145113871-145114613	K562	blood:	n/a	n/a
13	ATF1	chr1:145083579-145084451	K562	blood:	n/a	n/a
14	ATF1	chr1:145080812-145081067	K562	blood:	n/a	n/a
15	ATF1	chr1:145086819-145087312	K562	blood:	n/a	n/a
16	ATF1	chr1:145098857-145100009	K562	blood:	n/a	n/a
17	ATF1	chr1:145082093-145082887	K562	blood:	n/a	n/a
18	ATF1	chr1:145108235-145108438	K562	blood:	n/a	n/a
19	ATF1	chr1:145111322-145111864	K562	blood:	n/a	n/a
20	ATF2	chr1:145096082-145096678	GM12878	blood:	n/a	n/a
21	ATF2	chr1:145092143-145092822	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr1:145096141-145096582	GM12878	blood:	n/a	n/a
23	ATF2	chr1:145159486-145159715	GM12878	blood:	n/a	n/a
24	ATF2	chr1:145129724-145130023	GM12878	blood:	n/a	n/a
25	ATF2	chr1:145092073-145092999	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr1:145129655-145130099	GM12878	blood:	n/a	n/a
27	ATF2	chr1:145096133-145096595	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr1:145096106-145096616	K562	blood:	n/a	n/a
29	BACH1	chr1:145080726-145081101	K562	blood:	n/a	n/a
30	BACH1	chr1:145091823-145092943	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr1:145105218-145105521	K562	blood:	n/a	n/a
32	BACH1	chr1:145083544-145084558	K562	blood:	n/a	n/a
33	BATF	chr1:145171479-145171789	GM12878	blood:	n/a	n/a
34	BATF	chr1:145159043-145159865	GM12878	blood:	n/a	n/a
35	BATF	chr1:145159059-145159858	GM12878	blood:	n/a	n/a
36	BATF	chr1:145189103-145189407	GM12878	blood:	n/a	n/a
37	BATF	chr1:145138847-145139124	GM12878	blood:	n/a	n/a
38	BATF	chr1:145138847-145139218	GM12878	blood:	n/a	n/a
39	BATF	chr1:145139292-145139563	GM12878	blood:	n/a	n/a
40	BATF	chr1:145129645-145130292	GM12878	blood:	n/a	n/a
41	BATF	chr1:145152894-145153398	GM12878	blood:	n/a	n/a
42	BATF	chr1:145122920-145123245	GM12878	blood:	n/a	n/a
43	BATF	chr1:145128460-145128759	GM12878	blood:	n/a	n/a
44	BATF	chr1:145122815-145123217	GM12878	blood:	n/a	n/a
45	BATF	chr1:145153039-145153342	GM12878	blood:	n/a	n/a
46	BATF	chr1:145129688-145130263	GM12878	blood:	n/a	n/a
47	BATF	chr1:145096205-145096592	GM12878	blood:	n/a	n/a
48	BATF	chr1:145154286-145155318	GM12878	blood:	n/a	n/a
49	BATF	chr1:145154309-145155270	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:145139734-145139968	GM12878	blood:	n/a	chr1:145139838-145139847

(count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145139063-145139113	GM06990	blood:	n/a
2	chr1:145092576-145092626	CMK	blood:	n/a
3	chr1:145100564-145100614	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:145096125-145096175	RPTEC	kidney:	n/a
5	chr1:145139063-145139113	GM06990	blood:	n/a
6	chr1:145092576-145092626	CMK	blood:	n/a
7	chr1:145100564-145100614	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:145096125-145096175	RPTEC	kidney:	n/a
9	chr1:145096567-145096617	AoSMC	blood vessel:	n/a
10	chr1:145139896-145139946	HUVEC	blood vessel:	n/a
11	chr1:145139908-145139958	NT2-D1	testis:	n/a
12	chr1:145116797-145116847	HCM	heart:	n/a
13	chr1:145139908-145139958	PFSK-1	brain:	n/a
14	chr1:145110972-145111022	HCM	heart:	n/a
15	chr1:145097220-145097270	SK-N-SH_RA	brain:	n/a
16	chr1:145096375-145096425	BJ	skin:	n/a
17	chr1:145096479-145096529	GM06990	blood:	n/a
18	chr1:145100564-145100614	HRPEpiC	eye:	n/a
19	chr1:145112981-145113031	MCF-7	breast:	n/a
20	chr1:145096403-145096453	HIPEpiC	eye:	n/a
21	chr1:145092485-145092535	AG09309	skin:	n/a
22	chr1:145096723-145096773	LNCaP	prostate:	n/a
23	chr1:145092576-145092626	HCT-116	colon:	n/a
24	chr1:145096567-145096617	A549	lung:	n/a
25	chr1:145096403-145096453	HepG2	liver:	n/a
26	chr1:145096479-145096529	NH-A	brain:	n/a
27	chr1:145115872-145115922	SAEC	small airway:	n/a
28	chr1:145096479-145096529	CMK	blood:	n/a
29	chr1:145096403-145096453	HNPCEpiC	eye:	n/a
30	chr1:145096602-145096652	ECC-1	luminal epithelium:	n/a
31	chr1:145096567-145096617	BJ	skin:	n/a
32	chr1:145092485-145092535	Hela-S3	cervix:	n/a
33	chr1:145112981-145113031	Hepatocyte	liver:	n/a
34	chr1:145096375-145096425	NT2-D1	testis:	n/a
35	chr1:145092330-145092380	HAEpiC	amniotic membrane:	n/a
36	chr1:145096375-145096425	ECC-1	luminal epithelium:	n/a
37	chr1:145096403-145096453	LNCaP	prostate:	n/a
38	chr1:145097220-145097270	PrEC	prostate:	n/a
39	chr1:145096849-145096899	CMK	blood:	n/a
40	chr1:145139679-145139729	T-47D	breast:	n/a
41	chr1:145089017-145089067	NB4	blood:	n/a
42	chr1:145096567-145096617	RPTEC	kidney:	n/a
43	chr1:145104707-145104757	Jurkat	blood:	n/a
44	chr1:145096321-145096371	GM06990	blood:	n/a
45	chr1:145139063-145139113	NHDF-neo	bronchial:	n/a
46	chr1:145100564-145100614	HL-60	blood:	n/a
47	chr1:145116797-145116847	ECC-1	luminal epithelium:	n/a
48	chr1:145092485-145092535	NB4	blood:	n/a
49	chr1:145092485-145092535	IMR90	lung:	fetal
50	chr1:145096319-145096369	IMR90	lung:	fetal

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:145096186..145098889-chr12:66522673..66525529,2	MCF-7	breast:
2	chr1:145028195..145030084-chr1:145108356..145110933,3	K562	blood:
3	chr1:145096397..145097357-chr5:168006463..168007379,2	Hela-S3	cervix:
4	chr1:144929981..144935077-chr1:145095230..145100493,10	MCF-7	breast:
5	chr1:145138455..145140955-chr1:145381729..145384293,2	MCF-7	breast:
6	chr1:145015783..145017477-chr1:145099868..145103885,3	K562	blood:
7	chr1:144532668..144535961-chr1:145101125..145103299,5	K562	blood:
8	chr1:144932003..144934560-chr1:145095329..145097401,2	MCF-7	breast:
9	chr1:145115000..145117272-chr1:145119775..145122289,2	MCF-7	breast:
10	chr1:144987485..144989370-chr1:145102673..145104230,2	K562	blood:
11	chr1:145112612..145114533-chr20:60808919..60810723,2	MCF-7	breast:
12	chr1:144931106..144933247-chr1:145112848..145115806,3	MCF-7	breast:
13	chr1:145116481..145119033-chr1:145122356..145124040,2	K562	blood:
14	chr1:144930691..144932405-chr1:145101538..145103976,2	MCF-7	breast:
15	chr1:145069959..145072647-chr1:145097335..145099798,3	K562	blood:
16	chr1:145115000..145117272-chr1:145119775..145122289,2	MCF-7	breast:
17	chr1:145108662..145110529-chr1:145382748..145385386,2	K562	blood:
18	chr1:144531776..144534178-chr1:145095593..145097406,2	K562	blood:
19	chr1:145096224..145096777-chr2:143635158..143635659,2	Hela-S3	cervix:
20	chr1:144532674..144534262-chr1:145089036..145091259,2	K562	blood:
21	chr1:145041147..145043858-chr1:145090158..145092282,3	K562	blood:
22	chr1:145069991..145072792-chr1:145078438..145080718,2	K562	blood:
23	chr1:145044375..145046639-chr1:145102991..145105034,2	K562	blood:
24	chr1:145074665..145076679-chr1:145080108..145082967,2	MCF-7	breast:
25	chr1:145110007..145112621-chr1:149221905..149225544,4	MCF-7	breast:
26	chr1:145057641..145059158-chr1:145100599..145102878,2	MCF-7	breast:
27	chr1:145079205..145081578-chr1:145083280..145086175,3	K562	blood:
28	chr1:144928278..144930809-chr1:145113028..145115664,2	MCF-7	breast:
29	chr1:145043102..145046639-chr1:145102991..145106582,3	K562	blood:
30	chr1:145082670..145085511-chr1:145092846..145095216,2	MCF-7	breast:
31	chr1:145065982..145068200-chr1:145088629..145091493,2	K562	blood:
32	chr1:145112491..145115929-chr1:145116059..145118132,3	MCF-7	breast:
33	chr1:120480674..120483081-chr1:145098868..145100829,2	MCF-7	breast:
34	chr1:120691948..120694351-chr1:145121998..145123840,2	K562	blood:
35	chr1:145097859..145099647-chr1:147805751..147808247,2	K562	blood:
36	chr1:144930939..144933225-chr1:145098255..145100189,2	MCF-7	breast:
37	chr1:145137959..145140660-chr1:145381811..145384748,2	K562	blood:
38	chr1:145116552..145118106-chr1:145382522..145384612,2	MCF-7	breast:
39	chr1:145116481..145119033-chr1:145122356..145124040,2	K562	blood:
40	chr1:145124431..145127072-chr1:145381606..145383214,2	K562	blood:
41	chr1:145054217..145054913-chr1:145103284..145104051,2	K562	blood:
42	chr1:145006961..145008693-chr1:145104666..145107384,2	K562	blood:
43	chr1:145095997..145096821-chr11:66384044..66384600,2	NB4	blood:
44	chr1:144533808..144536803-chr1:145107932..145113896,6	K562	blood:
45	chr1:145083894..145086416-chr1:145095361..145097533,3	MCF-7	breast:
46	chr1:145082537..145085433-chr1:145102296..145104665,3	MCF-7	breast:
47	chr1:145082860..145085361-chr1:145086854..145088510,5	K562	blood:
48	chr1:120688084..120688694-chr1:145126764..145127269,2	MCF-7	breast:
49	chr1:145077663..145080122-chr1:145080911..145082669,2	MCF-7	breast:
50	chr1:145076679..145079296-chr1:145102825..145104399,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2NL-3	chr1:145112627-145113408	ucscGeneNc_uc001epf_1
2	lnc-NOTCH2NL-3	chr1:145110974-145111762	ucscGeneNc_uc001epf_1
3	lnc-PDE4DIP-5	chr1:145088039-145088567	NONHSAT005874

No data

Variant related genes	Relation type
PDE4DIP	TF binding region
ENSG00000271546	TF binding region
NUDT4P1	TF binding region
SEC22B	TF binding region
RNU6-1071P	TF binding region
PDE4DIP	CpG island
ENSG00000271546	CpG island
NUDT4P1	CpG island
SEC22B	CpG island
RNU6-1071P	CpG island
ENSG00000273131	chromatin interactions
ENSG00000171735	chromatin interactions
ENSG00000115919	chromatin interactions
ENSG00000237436	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000248643	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000167904	chromatin interactions
ENSG00000239335	chromatin interactions
ENSG00000271546	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000137574	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000139233	chromatin interactions
ENSG00000120137	chromatin interactions
ENSG00000239306	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000201558	chromatin interactions
SMAD7	miRNA target sites
NSMAF	miRNA target sites

Extended variants
information (count: 3719 )
Associated
traits (count: 181 )

Variant overlapped rSNPs/rCNVs (count:3719 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2762703	chr1:145080207-145080208	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs587625304	chr1:145080226-145080227	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587657397	chr1:145080227-145080228	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs10910739	chr1:145080229-145080230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587741534	chr1:145080231-145080232	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs587613067	chr1:145080249-145080250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11578742	chr1:145080252-145080253	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs111347044	chr1:145080294-145080295	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs587696696	chr1:145080329-145080330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587729934	chr1:145080351-145080352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2762704	chr1:145080355-145080356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587632380	chr1:145080357-145080358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs12068696	chr1:145080393-145080394	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs3979406	chr1:145080403-145080404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587691654	chr1:145080425-145080426	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs376291083	chr1:145080456-145080457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2590070	chr1:145080457-145080458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587646942	chr1:145080497-145080498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587697371	chr1:145080503-145080504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587761219	chr1:145080605-145080606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112169101	chr1:145080627-145080628	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs66826129	chr1:145080634-145080635	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs138706774	chr1:145080640-145080641	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs587628965	chr1:145080683-145080684	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs2762705	chr1:145080722-145080723	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112367746	chr1:145080732-145080733	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs587716951	chr1:145080770-145080771	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs587594960	chr1:145080788-145080789	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs587671084	chr1:145080815-145080816	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs111553715	chr1:145080834-145080835	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs202100360	chr1:145080872-145080873	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs587625602	chr1:145080913-145080914	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs587664893	chr1:145080951-145080952	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs587738450	chr1:145081055-145081056	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs2596332	chr1:145081066-145081067	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs587602194	chr1:145081107-145081108	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs587670056	chr1:145081157-145081158	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs587736913	chr1:145081160-145081161	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs587632798	chr1:145081177-145081178	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs587669453	chr1:145081178-145081179	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs111818122	chr1:145081190-145081191	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs3845335	chr1:145081232-145081233	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs3933672	chr1:145081262-145081263	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2762706	chr1:145081302-145081303	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373922748	chr1:145081309-145081310	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs587680179	chr1:145081327-145081328	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs587756980	chr1:145081341-145081342	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs587613891	chr1:145081366-145081367	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs609586	chr1:145081390-145081391	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs587691100	chr1:145081405-145081406	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:181)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Autism	22543975	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:3388 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145076800-145080600	Weak transcription	NHDF-Ad	bronchial
2	chr1:145079600-145080600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr1:145079800-145080600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:145079800-145081600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:145079800-145085400	Weak transcription	Aorta	Aorta
6	chr1:145079800-145088400	Weak transcription	Pancreas	Pancrea
7	chr1:145080000-145089800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:145080600-145080800	Enhancers	Osteobl	bone
9	chr1:145080600-145081000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr1:145080600-145081000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:145080600-145081000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:145080600-145081000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:145080600-145081200	Enhancers	NHDF-Ad	bronchial
14	chr1:145081000-145082000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:145081000-145082200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:145081000-145082800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr1:145081000-145087600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:145081200-145082800	Weak transcription	Osteobl	bone
19	chr1:145081200-145083000	Weak transcription	NHDF-Ad	bronchial
20	chr1:145081600-145081800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr1:145081600-145082000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:145081600-145082000	Bivalent Enhancer	Fetal Heart	heart
23	chr1:145081800-145082400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr1:145082000-145085200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:145082200-145083400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:145082400-145083800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr1:145082800-145083000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr1:145082800-145083800	Enhancers	Osteobl	bone
29	chr1:145082800-145084400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:145083000-145083600	Enhancers	NHDF-Ad	bronchial
31	chr1:145083000-145084600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr1:145083000-145084600	Enhancers	Hela-S3	cervix
33	chr1:145083200-145083600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:145083200-145083800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:145083200-145084600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr1:145083200-145084600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:145083400-145084400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:145083400-145084400	Enhancers	K562	blood
39	chr1:145083600-145084400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:145083600-145084400	Enhancers	NH-A	brain
41	chr1:145083600-145084400	Flanking Active TSS	NHDF-Ad	bronchial
42	chr1:145083600-145084600	Enhancers	HSMM	muscle
43	chr1:145083600-145089800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:145083800-145084200	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr1:145083800-145084200	Flanking Active TSS	Osteobl	bone
46	chr1:145083800-145084400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:145083800-145084600	Enhancers	NHLF	lung
48	chr1:145084000-145084400	Enhancers	HSMMtube	muscle
49	chr1:145084200-145085000	Enhancers	Osteobl	bone
50	chr1:145084400-145084600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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