Variant report

Variant	esv3415227
Chromosome Location	chr12:63228121-63591615
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3319)
CpG islands
(count:2872)
Chromatin interactive
region (count:248)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3319 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63476870-63477179	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:63371319-63371987	K562	blood:	n/a	n/a
3	ARID3A	chr12:63438998-63439080	K562	blood:	n/a	n/a
4	ARID3A	chr12:63254350-63254843	K562	blood:	n/a	n/a
5	ARID3A	chr12:63285344-63286798	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:63294910-63295100	K562	blood:	n/a	n/a
7	ARID3A	chr12:63286334-63286586	K562	blood:	n/a	n/a
8	ARID3A	chr12:63289230-63289440	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:63497272-63497631	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:63360264-63361606	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:63297280-63297288	K562	blood:	n/a	n/a
12	ARID3A	chr12:63249160-63249320	K562	blood:	n/a	n/a
13	ARID3A	chr12:63294385-63295188	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:63260351-63260761	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:63462602-63463008	K562	blood:	n/a	chr12:63462745-63462761
16	ARID3A	chr12:63304189-63304733	K562	blood:	n/a	n/a
17	ARID3A	chr12:63260910-63261150	K562	blood:	n/a	n/a
18	ARID3A	chr12:63308839-63308845	K562	blood:	n/a	n/a
19	ARID3A	chr12:63307845-63308119	K562	blood:	n/a	n/a
20	ARID3A	chr12:63237306-63237814	HepG2	liver:	n/a	n/a
21	ARID3A	chr12:63328780-63329249	HepG2	liver:	n/a	n/a
22	ARID3A	chr12:63293456-63294017	HepG2	liver:	n/a	n/a
23	ATF1	chr12:63254297-63254889	K562	blood:	n/a	n/a
24	ATF1	chr12:63294403-63294745	K562	blood:	n/a	n/a
25	ATF1	chr12:63523763-63524061	K562	blood:	n/a	n/a
26	ATF1	chr12:63253175-63253362	K562	blood:	n/a	n/a
27	ATF1	chr12:63363163-63363212	K562	blood:	n/a	n/a
28	ATF1	chr12:63304289-63304687	K562	blood:	n/a	n/a
29	ATF1	chr12:63307746-63308778	K562	blood:	n/a	n/a
30	ATF1	chr12:63341081-63341281	K562	blood:	n/a	n/a
31	ATF1	chr12:63325385-63325532	K562	blood:	n/a	n/a
32	ATF1	chr12:63247467-63247625	K562	blood:	n/a	n/a
33	ATF2	chr12:63328915-63329240	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF3	chr12:63304301-63304734	K562	blood:	n/a	n/a
35	ATF3	chr12:63328829-63329287	H1-hESC	embryonic stem cell:	n/a	chr12:63328924-63328933
36	ATF3	chr12:63328821-63329274	H1-hESC	embryonic stem cell:	n/a	chr12:63328924-63328933 chr12:63328827-63328836
37	ATF3	chr12:63328522-63329137	A549	lung:	n/a	chr12:63328924-63328933 chr12:63328827-63328836
38	ATF3	chr12:63328780-63329266	K562	blood:	n/a	chr12:63328924-63328933 chr12:63328827-63328836
39	BACH1	chr12:63297268-63297271	K562	blood:	n/a	n/a
40	BACH1	chr12:63371676-63371853	K562	blood:	n/a	n/a
41	BACH1	chr12:63545234-63545470	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr12:63460694-63460961	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr12:63327254-63327630	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr12:63328322-63329341	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr12:63544074-63544342	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr12:63422249-63422298	K562	blood:	n/a	n/a
47	BACH1	chr12:63412000-63412583	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr12:63229132-63229371	GM12878	blood:	n/a	chr12:63229265-63229275
49	BATF	chr12:63229061-63229386	GM12878	blood:	n/a	chr12:63229265-63229275
50	BATF	chr12:63360209-63360413	GM12878	blood:	n/a	chr12:63360339-63360350 chr12:63360311-63360322

(count:2872 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63396701-63396751	T-47D	breast:	n/a
2	chr12:63545523-63545573	SK-N-SH_RA	brain:	n/a
3	chr12:63544175-63544225	PANC-1	pancreas:	n/a
4	chr12:63397289-63397339	HCPEpiC	choroid plexus:	n/a
5	chr12:63327172-63327222	SK-N-SH_RA	brain:	n/a
6	chr12:63396701-63396751	T-47D	breast:	n/a
7	chr12:63545523-63545573	SK-N-SH_RA	brain:	n/a
8	chr12:63544175-63544225	PANC-1	pancreas:	n/a
9	chr12:63397289-63397339	HCPEpiC	choroid plexus:	n/a
10	chr12:63327172-63327222	SK-N-SH_RA	brain:	n/a
11	chr12:63324472-63324522	PANC-1	pancreas:	n/a
12	chr12:63544175-63544225	HNPCEpiC	eye:	n/a
13	chr12:63327172-63327222	NH-A	brain:	n/a
14	chr12:63358135-63358185	HPAEpiC	pulmonary alveolar:	n/a
15	chr12:63396701-63396751	AG10803	skin:	n/a
16	chr12:63544319-63544369	BE2_C	brain:	n/a
17	chr12:63359135-63359185	SK-N-SH	brain:	n/a
18	chr12:63544430-63544480	PrEC	prostate:	n/a
19	chr12:63294404-63294454	T-47D	breast:	n/a
20	chr12:63260327-63260377	NB4	blood:	n/a
21	chr12:63544175-63544225	MCF10A-Er-Src	breast:	n/a
22	chr12:63328717-63328767	GM12892	blood:	n/a
23	chr12:63329258-63329308	HEEpiC	esophagus:	n/a
24	chr12:63545783-63545833	HEEpiC	esophagus:	n/a
25	chr12:63329258-63329308	PFSK-1	brain:	n/a
26	chr12:63545523-63545573	BJ	skin:	n/a
27	chr12:63328556-63328606	HRCEpiC	kidney:	n/a
28	chr12:63547716-63547766	HEEpiC	esophagus:	n/a
29	chr12:63544430-63544480	GM12878	blood:	n/a
30	chr12:63327172-63327222	PrEC	prostate:	n/a
31	chr12:63544319-63544369	HCPEpiC	choroid plexus:	n/a
32	chr12:63544319-63544369	HEK293	kidney:	embryo
33	chr12:63327235-63327285	A549	lung:	n/a
34	chr12:63359135-63359185	PrEC	prostate:	n/a
35	chr12:63328158-63328208	HL-60	blood:	n/a
36	chr12:63328524-63328574	ECC-1	luminal epithelium:	n/a
37	chr12:63352052-63352102	RPTEC	kidney:	n/a
38	chr12:63545288-63545338	HCF	heart:	n/a
39	chr12:63544857-63544907	HEK293	kidney:	embryo
40	chr12:63359181-63359231	PANC-1	pancreas:	n/a
41	chr12:63324472-63324522	Jurkat	blood:	n/a
42	chr12:63479872-63479922	NH-A	brain:	n/a
43	chr12:63324472-63324522	HCT-116	colon:	n/a
44	chr12:63396701-63396751	HepG2	liver:	n/a
45	chr12:63544857-63544907	GM12891	blood:	n/a
46	chr12:63328158-63328208	HRCEpiC	kidney:	n/a
47	chr12:63328158-63328208	NB4	blood:	n/a
48	chr12:63545956-63546006	HIPEpiC	eye:	n/a
49	chr12:63545783-63545833	HAEpiC	amniotic membrane:	n/a
50	chr12:63544857-63544907	HUVEC	blood vessel:	n/a

(count:248 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:63239285..63241895-chr12:63253265..63255649,2	MCF-7	breast:
2	chr12:63522003..63524350-chr12:63527022..63529275,2	K562	blood:
3	chr12:63327252..63328936-chr12:63486552..63489469,2	MCF-7	breast:
4	chr12:63314546..63316947-chr12:63317010..63319516,2	K562	blood:
5	chr12:63453202..63455984-chr12:63460677..63462283,2	MCF-7	breast:
6	chr12:63326696..63327449-chr3:117961931..117962815,2	MCF-7	breast:
7	chr12:63321809..63323411-chr12:63325612..63327297,2	K562	blood:
8	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
9	chr12:63297848..63300168-chr12:63310835..63312662,2	MCF-7	breast:
10	chr12:63429516..63431734-chr8:91673428..91674948,2	MCF-7	breast:
11	chr12:63545428..63546206-chr12:63674883..63675724,2	MCF-7	breast:
12	chr12:63312289..63315021-chr12:63318945..63321153,2	MCF-7	breast:
13	chr12:63461645..63464045-chr12:63491435..63493739,2	MCF-7	breast:
14	chr12:63278653..63281020-chr12:63327180..63328937,2	MCF-7	breast:
15	chr12:63407510..63410577-chr12:63417588..63419660,3	MCF-7	breast:
16	chr12:63230714..63233409-chr12:63236744..63239259,2	MCF-7	breast:
17	chr12:63351575..63353883-chr12:63354242..63355934,2	MCF-7	breast:
18	chr12:63298722..63300428-chr12:63300794..63302294,2	MCF-7	breast:
19	chr12:63278268..63280209-chr12:63326131..63327723,2	MCF-7	breast:
20	chr12:63244647..63247922-chr12:63326690..63328475,3	MCF-7	breast:
21	chr12:63219854..63222833-chr12:63226244..63229699,3	MCF-7	breast:
22	chr12:63237375..63239412-chr12:63328282..63330219,2	MCF-7	breast:
23	chr12:63329161..63330688-chr12:63333077..63335873,2	K562	blood:
24	chr12:62997417..63000223-chr12:63319548..63321193,2	MCF-7	breast:
25	chr12:63227346..63229238-chr12:63238157..63241100,2	K562	blood:
26	chr12:63432302..63435436-chr12:63436957..63439553,3	MCF-7	breast:
27	chr12:63503782..63505766-chr12:63506813..63509120,2	K562	blood:
28	chr12:63497332..63498958-chr12:63670308..63671121,8	MCF-7	breast:
29	chr12:63535701..63537481-chr12:63551924..63553918,2	MCF-7	breast:
30	chr12:63460043..63460554-chr12:63480000..63480756,2	MCF-7	breast:
31	chr12:63298722..63300428-chr12:63300794..63302294,2	MCF-7	breast:
32	chr12:63302887..63305750-chr12:63328233..63330331,2	K562	blood:
33	chr12:63326223..63329085-chr20:52208224..52210688,2	MCF-7	breast:
34	chr12:63514993..63517783-chr12:63522556..63524545,2	MCF-7	breast:
35	chr12:63227346..63229238-chr12:63238157..63241100,2	K562	blood:
36	chr12:63370726..63372632-chr12:63374198..63375972,2	K562	blood:
37	chr12:63311089..63313901-chr12:63317542..63319982,2	K562	blood:
38	chr12:63298026..63301472-chr12:63301744..63306217,4	K562	blood:
39	chr12:63255973..63257618-chr12:63326751..63328622,2	MCF-7	breast:
40	chr12:63327385..63330661-chr12:63331841..63334943,4	K562	blood:
41	chr12:63246101..63246646-chr12:63377150..63378063,4	MCF-7	breast:
42	chr12:63376679..63380388-chr12:63381374..63383929,4	K562	blood:
43	chr12:63303196..63305906-chr12:63305926..63307721,2	K562	blood:
44	chr12:63522003..63524350-chr12:63527022..63529275,2	K562	blood:
45	chr12:63311089..63313901-chr12:63317542..63319982,2	K562	blood:
46	chr12:63275413..63276960-chr12:63307773..63310580,2	K562	blood:
47	chr12:63257305..63259336-chr12:63259485..63261884,2	K562	blood:
48	chr12:63239407..63241171-chr12:63244280..63246692,2	MCF-7	breast:
49	chr12:63257305..63259336-chr12:63259485..63261884,2	K562	blood:
50	chr12:63244647..63247922-chr12:63326690..63328475,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AVPR1A-2	chr12:63519180-63519254	NONHSAT029106
2	lnc-TMEM5-5	chr12:63563605-63563746	l_664_chr12:63563604-63657550_brain
3	lnc-MON2-3	chr12:63544845-63544872	ENSG00000257973.1
4	lnc-PPM1H-1	chr12:63398590-63400681	ENSG00000250314
5	lnc-PPM1H-1	chr12:63397459-63398430	ENSG00000250314
6	lnc-MON2-3	chr12:63547640-63547786	ENSG00000257973.1
7	lnc-AVPR1A-2	chr12:63504632-63504765	NONHSAT029106
8	lnc-MON2-3	chr12:63546261-63546418	ENSG00000257973.1
9	lnc-MON2-9	chr12:63396249-63396575	NONHSAT029103
10	lnc-AVPR1A-3	chr12:63449055-63449545	NONHSAT029105
11	lnc-TMEM5-5	chr12:63563762-63563912	l_664_chr12:63563604-63657550_brain
12	lnc-MON2-8	chr12:63376818-63377527	expReg_chr12_6799_+
13	lnc-TMEM5-5	chr12:63580624-63580735	l_664_chr12:63563604-63657550_brain

No data

Variant related genes	Relation type
ENSG00000257235	TF binding region
RPL14P1	TF binding region
RNU1-83P	TF binding region
AVPR1A	TF binding region
PPM1H	TF binding region
ENSG00000252660	TF binding region
LDHAL6CP	TF binding region
ENSG00000257779	TF binding region
RSL24D1P5	TF binding region
ENSG00000257235	CpG island
RPL14P1	CpG island
RNU1-83P	CpG island
AVPR1A	CpG island
PPM1H	CpG island
ENSG00000252660	CpG island
LDHAL6CP	CpG island
ENSG00000257779	CpG island
RSL24D1P5	CpG island
ENSG00000250517	chromatin interactions
ENSG00000139239	chromatin interactions
ENSG00000257235	chromatin interactions
ENSG00000174206	chromatin interactions
ENSG00000257354	chromatin interactions
ENSG00000111110	chromatin interactions
ENSG00000196227	chromatin interactions
ENSG00000199179	chromatin interactions
ENSG00000257779	chromatin interactions
ENSG00000118600	chromatin interactions
ENSG00000252660	chromatin interactions
ENSG00000200296	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000243024	chromatin interactions
ENSG00000257664	chromatin interactions
PTEN	miRNA target sites

Extended variants
information (count: 9887 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:9887 , 50 per page) page: 1 2 3 4 5 6 7 ... 198

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556392641	chr12:63228137-63228138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11610395	chr12:63228171-63228172	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs538616722	chr12:63228174-63228175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530964145	chr12:63228188-63228189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558160558	chr12:63228211-63228212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550720207	chr12:63228259-63228260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560008234	chr12:63228271-63228272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529135424	chr12:63228273-63228274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548910316	chr12:63228289-63228290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568992912	chr12:63228290-63228291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182691553	chr12:63228320-63228321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571807045	chr12:63228331-63228332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147111793	chr12:63228366-63228367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571290922	chr12:63228461-63228462	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs533753572	chr12:63228489-63228490	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs554544876	chr12:63228495-63228496	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs567857583	chr12:63228513-63228514	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs534453300	chr12:63228523-63228524	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs144100813	chr12:63228541-63228542	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs556486243	chr12:63228544-63228545	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs147130240	chr12:63228617-63228618	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs545202633	chr12:63228659-63228660	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs74369999	chr12:63228710-63228711	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs572150606	chr12:63228713-63228714	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs541026250	chr12:63228723-63228724	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs560902192	chr12:63228728-63228729	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs554255485	chr12:63228799-63228800	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs377140412	chr12:63228812-63228813	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs574929704	chr12:63228879-63228880	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs562563635	chr12:63228901-63228902	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs531510572	chr12:63228949-63228950	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs73135681	chr12:63228962-63228963	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs148616257	chr12:63229017-63229018	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs141189605	chr12:63229055-63229056	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs150753803	chr12:63229079-63229080	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs369338048	chr12:63229113-63229114	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs11174685	chr12:63229170-63229171	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs547267223	chr12:63229214-63229215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs536558086	chr12:63229239-63229240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs546215046	chr12:63229294-63229295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs371833361	chr12:63229306-63229307	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs376378529	chr12:63229333-63229334	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs556785279	chr12:63229354-63229355	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs369475956	chr12:63229454-63229455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35695836	chr12:63229511-63229512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs398019877	chr12:63229520-63229521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570191396	chr12:63229537-63229538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376086747	chr12:63229543-63229544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373774844	chr12:63229672-63229673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77661238	chr12:63229717-63229718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3326 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63195800-63228600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:63207200-63228600	Weak transcription	A549	lung
3	chr12:63207200-63231200	Weak transcription	Pancreas	Pancrea
4	chr12:63211800-63228200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:63211800-63228200	Weak transcription	Aorta	Aorta
6	chr12:63212000-63228200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr12:63212400-63228200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr12:63212400-63228200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr12:63212400-63228400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:63212400-63228600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:63212400-63228800	Weak transcription	Brain Anterior Caudate	brain
12	chr12:63212400-63229000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:63212600-63234600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr12:63214000-63228400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr12:63218400-63234800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:63221200-63228200	Weak transcription	Ovary	ovary
17	chr12:63221400-63228800	Weak transcription	Fetal Kidney	kidney
18	chr12:63221600-63234200	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr12:63222200-63228200	Weak transcription	Left Ventricle	heart
20	chr12:63222200-63235200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr12:63223800-63229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr12:63225400-63237600	Weak transcription	Liver	Liver
23	chr12:63225600-63231800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:63225800-63230200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:63226000-63228200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:63226000-63234200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr12:63226000-63234600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:63226200-63228400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:63226200-63228800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:63226200-63240600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:63226400-63234000	Weak transcription	HepG2	liver
32	chr12:63226600-63229200	Enhancers	K562	blood
33	chr12:63226800-63228400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr12:63227600-63231000	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr12:63227600-63237200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr12:63227800-63228600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr12:63227800-63228600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr12:63227800-63229200	Enhancers	Brain Substantia Nigra	brain
39	chr12:63228000-63228200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr12:63228000-63228400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:63228000-63228400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:63228000-63228600	Enhancers	Brain Angular Gyrus	brain
43	chr12:63228000-63228600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr12:63228000-63228800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr12:63228000-63229000	Enhancers	Adipose Nuclei	Adipose
46	chr12:63228000-63229200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr12:63228000-63229200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr12:63228000-63229400	Enhancers	Brain Hippocampus Middle	brain
49	chr12:63228200-63228400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr12:63228200-63228600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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