Variant report

Variant	esv3324282
Chromosome Location	chr12:120971394-120973942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:547)
CpG islands
(count:427)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:120972763-120973402	K562	blood:	n/a	n/a
2	ATF1	chr12:120972905-120973218	K562	blood:	n/a	n/a
3	ATF3	chr12:120972673-120973325	K562	blood:	n/a	n/a
4	ATF3	chr12:120971874-120972328	A549	lung:	n/a	n/a
5	BACH1	chr12:120972782-120973170	K562	blood:	n/a	n/a
6	BCL3	chr12:120971875-120972430	A549	lung:	n/a	chr12:120971995-120972004 chr12:120972414-120972427 chr12:120972355-120972364 chr12:120972408-120972421
7	BCLAF1	chr12:120972525-120972846	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:120972831-120973244	K562	blood:	n/a	n/a
9	BHLHE40	chr12:120971962-120972385	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:120971927-120972268	K562	blood:	n/a	n/a
11	BHLHE40	chr12:120972537-120972608	K562	blood:	n/a	n/a
12	BRCA1	chr12:120972513-120972691	HepG2	liver:	n/a	n/a
13	BRCA1	chr12:120972119-120972248	GM12878	blood:	n/a	n/a
14	CBX3	chr12:120972711-120973335	K562	blood:	n/a	n/a
15	CCNT2	chr12:120972003-120973156	K562	blood:	n/a	n/a
16	CEBPD	chr12:120972053-120972301	HepG2	liver:	n/a	n/a
17	CHD1	chr12:120971909-120972331	GM12878	blood:	n/a	n/a
18	CHD1	chr12:120971902-120972423	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr12:120972648-120972788	HepG2	liver:	n/a	n/a
20	CHD2	chr12:120972807-120973222	K562	blood:	n/a	n/a
21	CHD2	chr12:120971946-120972328	GM12878	blood:	n/a	n/a
22	CHD2	chr12:120972165-120972368	HepG2	liver:	n/a	n/a
23	CHD2	chr12:120972110-120972391	K562	blood:	n/a	n/a
24	CHD2	chr12:120972016-120973096	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr12:120972036-120972287	A549	lung:	n/a	n/a
26	CREB1	chr12:120972013-120972874	A549	lung:	n/a	n/a
27	CREB1	chr12:120971893-120972471	GM12878	blood:	n/a	n/a
28	CTCF	chr12:120972740-120972890	AG09309	skin:	n/a	chr12:120972808-120972821
29	CTCF	chr12:120972780-120972930	GM12864	blood:	n/a	chr12:120972808-120972821
30	CTCF	chr12:120972720-120972870	HUVEC	blood vessel:	n/a	chr12:120972808-120972821
31	CTCF	chr12:120972740-120972890	GM12866	blood:	n/a	chr12:120972808-120972821
32	CTCF	chr12:120972820-120972970	GM06990	blood:	n/a	n/a
33	CTCF	chr12:120972769-120972830	GM13977	blood:	n/a	chr12:120972808-120972821
34	CTCF	chr12:120972700-120972850	AG04449	skin:	n/a	chr12:120972808-120972821
35	CTCF	chr12:120972700-120972850	GM12869	blood:	n/a	chr12:120972808-120972821
36	CTCF	chr12:120972700-120972850	HVMF	connective:	n/a	chr12:120972808-120972821
37	CTCF	chr12:120972700-120972850	HRPEpiC	eye:	n/a	chr12:120972808-120972821
38	CTCF	chr12:120972760-120972910	HCPEpiC	choroid plexus:	n/a	chr12:120972808-120972821
39	CTCF	chr12:120972780-120972930	HPAF	blood vessel:	n/a	chr12:120972808-120972821
40	CTCF	chr12:120972680-120972830	GM12878	blood:	n/a	chr12:120972808-120972821
41	CTCF	chr12:120972660-120972810	GM12875	blood:	n/a	n/a
42	CTCF	chr12:120972720-120972870	HMF	breast:	n/a	chr12:120972808-120972821
43	CTCF	chr12:120972700-120972850	HAc	cerebellar:	n/a	chr12:120972808-120972821
44	CTCF	chr12:120972799-120972835	GM12891	blood:	n/a	chr12:120972808-120972821
45	CTCF	chr12:120972720-120972870	AoAF	blood vessel:	n/a	chr12:120972808-120972821
46	CTCF	chr12:120972720-120972870	GM12873	blood:	n/a	chr12:120972808-120972821
47	CTCF	chr12:120972788-120972837	GM19239	blood:	n/a	chr12:120972808-120972821
48	CTCF	chr12:120972660-120972810	GM12868	blood:	n/a	n/a
49	CTCF	chr12:120972700-120972850	HBMEC	blood vessel:	n/a	chr12:120972808-120972821
50	CTCF	chr12:120972660-120972810	SAEC	small airway:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120972797-120972847	HCM	heart:	n/a
2	chr12:120972601-120972651	SK-N-SH	brain:	n/a
3	chr12:120971999-120972049	PFSK-1	brain:	n/a
4	chr12:120971538-120971588	MCF10A-Er-Src	breast:	n/a
5	chr12:120971999-120972049	SAEC	small airway:	n/a
6	chr12:120972173-120972223	AG10803	skin:	n/a
7	chr12:120971999-120972049	U87	brain:	n/a
8	chr12:120972070-120972120	NB4	blood:	n/a
9	chr12:120972173-120972223	RPTEC	kidney:	n/a
10	chr12:120972070-120972120	RPTEC	kidney:	n/a
11	chr12:120972070-120972120	BE2_C	brain:	n/a
12	chr12:120971358-120971408	LNCaP	prostate:	n/a
13	chr12:120971538-120971588	PrEC	prostate:	n/a
14	chr12:120971999-120972049	MCF10A-Er-Src	breast:	n/a
15	chr12:120971999-120972049	ProgFib	skin:	n/a
16	chr12:120972173-120972223	Jurkat	blood:	n/a
17	chr12:120971538-120971588	HCF	heart:	n/a
18	chr12:120972601-120972651	PFSK-1	brain:	n/a
19	chr12:120972173-120972223	PANC-1	pancreas:	n/a
20	chr12:120971999-120972049	AG04450	lung:	fetal
21	chr12:120972173-120972223	HCPEpiC	choroid plexus:	n/a
22	chr12:120971538-120971588	NHBE	bronchial:	n/a
23	chr12:120972173-120972223	Hela-S3	cervix:	n/a
24	chr12:120971358-120971408	HIPEpiC	eye:	n/a
25	chr12:120972173-120972223	SK-N-MC	brain:	n/a
26	chr12:120971538-120971588	IMR90	lung:	fetal
27	chr12:120971358-120971408	CMK	blood:	n/a
28	chr12:120972601-120972651	AG09319	gingival:	n/a
29	chr12:120972173-120972223	LNCaP	prostate:	n/a
30	chr12:120972797-120972847	HL-60	blood:	n/a
31	chr12:120972797-120972847	SK-N-SH_RA	brain:	n/a
32	chr12:120971358-120971408	SK-N-SH_RA	brain:	n/a
33	chr12:120971999-120972049	T-47D	breast:	n/a
34	chr12:120972173-120972223	MCF-7	breast:	n/a
35	chr12:120971538-120971588	BE2_C	brain:	n/a
36	chr12:120971358-120971408	HL-60	blood:	n/a
37	chr12:120972797-120972847	AG09319	gingival:	n/a
38	chr12:120971358-120971408	HMEC	breast:	n/a
39	chr12:120972601-120972651	AoSMC	blood vessel:	n/a
40	chr12:120971538-120971588	LNCaP	prostate:	n/a
41	chr12:120972173-120972223	NB4	blood:	n/a
42	chr12:120971358-120971408	HCF	heart:	n/a
43	chr12:120972070-120972120	Caco-2	colon:	n/a
44	chr12:120972601-120972651	GM06990	blood:	n/a
45	chr12:120972070-120972120	AoSMC	blood vessel:	n/a
46	chr12:120971538-120971588	Hepatocyte	liver:	n/a
47	chr12:120972601-120972651	IMR90	lung:	fetal
48	chr12:120972797-120972847	HEK293	kidney:	embryo
49	chr12:120972173-120972223	U87	brain:	n/a
50	chr12:120971358-120971408	GM12891	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120931985..120935585-chr12:120970035..120974742,8	MCF-7	breast:
2	chr12:120972120..120972749-chr18:29671926..29672687,2	Hela-S3	cervix:
3	chr12:120906126..120908752-chr12:120971938..120973464,2	MCF-7	breast:
4	chr12:120905043..120908623-chr12:120970585..120973644,4	K562	blood:
5	chr12:120906583..120908236-chr12:120972144..120973710,2	K562	blood:
6	chr12:120882042..120885526-chr12:120971268..120975128,6	K562	blood:
7	chr1:212458466..212459172-chr12:120972086..120972631,2	Hela-S3	cervix:
8	chr12:120973210..120975541-chr12:121135063..121137387,2	K562	blood:
9	chr12:120727107..120731318-chr12:120971335..120975286,11	K562	blood:
10	chr12:120728453..120733011-chr12:120965347..120973411,16	MCF-7	breast:
11	chr12:120971743..120974059-chr12:121017467..121020168,3	MCF-7	breast:
12	chr12:120933021..120935221-chr12:120970996..120973452,2	MCF-7	breast:
13	chr12:120972451..120974167-chr19:10764022..10766297,2	K562	blood:
14	chr12:120905762..120908724-chr12:120970875..120974820,5	MCF-7	breast:
15	chr12:120932493..120935871-chr12:120970423..120972998,4	K562	blood:
16	chr12:120932857..120935871-chr12:120969535..120974885,9	K562	blood:
17	chr12:120883164..120885526-chr12:120971268..120972852,2	K562	blood:
18	chr12:120925184..120926895-chr12:120973583..120975847,2	K562	blood:
19	chr12:120729269..120732334-chr12:120971435..120974602,3	K562	blood:
20	chr12:120970635..120973356-chr12:121018386..121020894,3	K562	blood:
21	chr12:120874999..120877444-chr12:120972685..120975166,2	K562	blood:
22	chr12:120964646..120969249-chr12:120969286..120973951,11	MCF-7	breast:
23	chr12:120972103..120972651-chr17:80250321..80251237,2	Hela-S3	cervix:
24	chr12:120728052..120732322-chr12:120971723..120974902,6	MCF-7	breast:

No data

Variant related genes	Relation type
RNF10	TF binding region
COQ5	TF binding region
RNF10	CpG island
COQ5	CpG island
ENSG00000088986	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000129351	chromatin interactions
ENSG00000248008	chromatin interactions
ENSG00000257218	chromatin interactions
ENSG00000111775	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000267100	chromatin interactions
ENSG00000134758	chromatin interactions
ENSG00000066027	chromatin interactions
ENSG00000111786	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000170855	chromatin interactions
ENSG00000111780	chromatin interactions
ENSG00000265692	chromatin interactions
ENSG00000256364	chromatin interactions
ENSG00000265008	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11065154	chr12:120971417-120971418	Weak transcription Enhancers Active TSS	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375363253	chr12:120971421-120971422	Weak transcription Enhancers Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs187300824	chr12:120971435-120971436	Weak transcription Enhancers Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs567649720	chr12:120971484-120971485	Weak transcription Enhancers Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs73225248	chr12:120971517-120971518	Weak transcription Enhancers Active TSS	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs191983114	chr12:120971522-120971523	Weak transcription Enhancers Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs117311262	chr12:120971532-120971533	Weak transcription Enhancers Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs545295371	chr12:120971678-120971679	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs140980445	chr12:120971735-120971736	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs373837828	chr12:120971768-120971769	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs544081011	chr12:120971778-120971779	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs560683610	chr12:120971780-120971781	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs78198329	chr12:120971807-120971808	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs78225964	chr12:120971808-120971809	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs79287466	chr12:120971809-120971810	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs10709360	chr12:120971817-120971818	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs199816721	chr12:120971823-120971824	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs541536016	chr12:120971881-120971882	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs561500717	chr12:120971895-120971896	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs10774555	chr12:120971978-120971979	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs540891308	chr12:120972063-120972064	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs182574759	chr12:120972085-120972086	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs79736037	chr12:120972110-120972111	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs552148097	chr12:120972112-120972113	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs571845293	chr12:120972135-120972136	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs527920471	chr12:120972181-120972182	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs533283511	chr12:120972186-120972187	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs548026363	chr12:120972199-120972200	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs567734248	chr12:120972240-120972241	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs536753633	chr12:120972266-120972267	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs549864764	chr12:120972270-120972271	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs11542860	chr12:120972333-120972334	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs562942343	chr12:120972351-120972352	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs140042315	chr12:120972396-120972397	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs547079038	chr12:120972424-120972425	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs558453334	chr12:120972509-120972510	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
37	rs571894300	chr12:120972514-120972515	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
38	rs1043097	chr12:120972584-120972585	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
39	rs113139244	chr12:120972586-120972587	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
40	rs184077395	chr12:120972707-120972708	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
41	rs374593114	chr12:120972755-120972756	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs377054423	chr12:120972756-120972757	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs574404871	chr12:120972777-120972778	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs543516224	chr12:120972829-120972830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs73225249	chr12:120972839-120972840	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576797532	chr12:120972868-120972869	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs545697530	chr12:120972884-120972885	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs565541805	chr12:120972885-120972886	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs117319218	chr12:120972994-120972995	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs547964044	chr12:120973061-120973062	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120967200-120972200	Weak transcription	Spleen	Spleen
2	chr12:120967400-120972000	Weak transcription	Esophagus	oesophagus
3	chr12:120967400-120972200	Weak transcription	Lung	lung
4	chr12:120967400-120972200	Weak transcription	Small Intestine	intestine
5	chr12:120967600-120972200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr12:120967800-120971600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr12:120967800-120971800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr12:120967800-120971800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:120967800-120971800	Weak transcription	Left Ventricle	heart
10	chr12:120967800-120971800	Weak transcription	HSMMtube	muscle
11	chr12:120967800-120972000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr12:120967800-120972000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:120968000-120971600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr12:120968000-120971800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:120968000-120971800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr12:120968000-120971800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:120968000-120971800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:120968000-120971800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr12:120968000-120971800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr12:120968000-120971800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr12:120968000-120971800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:120968000-120971800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr12:120968000-120971800	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr12:120968000-120971800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:120968000-120971800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:120968000-120971800	Weak transcription	Colon Smooth Muscle	Colon
27	chr12:120968000-120971800	Weak transcription	Fetal Lung	lung
28	chr12:120968000-120971800	Weak transcription	Ovary	ovary
29	chr12:120968000-120971800	Weak transcription	Stomach Mucosa	stomach
30	chr12:120968000-120971800	Weak transcription	Thymus	Thymus
31	chr12:120968000-120972000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:120968000-120972000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr12:120968000-120972000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr12:120968000-120972000	Weak transcription	NH-A	brain
35	chr12:120968200-120971600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:120968200-120971600	Weak transcription	Fetal Muscle Trunk	muscle
37	chr12:120968200-120971800	Weak transcription	Primary B cells from peripheral blood	blood
38	chr12:120968200-120971800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:120968200-120971800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr12:120968200-120971800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr12:120968200-120971800	Weak transcription	Fetal Intestine Large	intestine
42	chr12:120968200-120971800	Weak transcription	Fetal Kidney	kidney
43	chr12:120968200-120971800	Weak transcription	A549	lung
44	chr12:120968200-120971800	Weak transcription	HMEC	breast
45	chr12:120968200-120971800	Weak transcription	HUVEC	blood vessel
46	chr12:120968200-120971800	Weak transcription	Osteobl	bone
47	chr12:120968400-120971400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr12:120968400-120971800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:120968400-120971800	Weak transcription	Fetal Brain Male	brain
50	chr12:120968400-120971800	Weak transcription	Fetal Intestine Small	intestine

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