Variant report

Variant	nsv1042181
Chromosome Location	chr12:124037400-124152950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3939)
CpG islands
(count:3057)
Chromatin interactive
region (count:217)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3939 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124055016-124055130	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:124086179-124086778	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:124066719-124067024	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:124086169-124086751	K562	blood:	n/a	n/a
5	ARID3A	chr12:124055889-124056158	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:124080339-124081019	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:124068840-124069198	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:124118202-124118430	K562	blood:	n/a	n/a
9	ARID3A	chr12:124066707-124067005	K562	blood:	n/a	n/a
10	ARID3A	chr12:124118134-124118531	HepG2	liver:	n/a	n/a
11	ATF1	chr12:124086461-124086850	K562	blood:	n/a	n/a
12	ATF1	chr12:124068826-124069223	K562	blood:	n/a	n/a
13	ATF1	chr12:124118054-124118572	K562	blood:	n/a	n/a
14	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
15	ATF2	chr12:124118102-124118636	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr12:124085993-124086936	GM12878	blood:	n/a	n/a
17	ATF2	chr12:124118133-124118718	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr12:124086364-124086783	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr12:124068644-124069075	GM12878	blood:	n/a	n/a
20	ATF2	chr12:124086303-124086746	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr12:124068668-124069206	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr12:124086369-124086785	GM12878	blood:	n/a	n/a
23	ATF2	chr12:124117993-124118726	GM12878	blood:	n/a	n/a
24	ATF2	chr12:124068622-124069127	GM12878	blood:	n/a	n/a
25	ATF2	chr12:124118041-124118671	GM12878	blood:	n/a	n/a
26	ATF2	chr12:124068634-124069051	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr12:124066738-124067088	K562	blood:	n/a	n/a
28	ATF3	chr12:124085987-124086914	A549	lung:	n/a	n/a
29	ATF3	chr12:124086537-124086818	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr12:124068610-124069255	A549	lung:	n/a	n/a
31	ATF3	chr12:124118087-124118409	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
32	ATF3	chr12:124118019-124118526	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
33	ATF3	chr12:124055844-124056095	HepG2	liver:	n/a	n/a
34	ATF3	chr12:124117981-124118734	A549	lung:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
35	ATF3	chr12:124086400-124086896	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF3	chr12:124055844-124056086	K562	blood:	n/a	n/a
37	ATF3	chr12:124118039-124118550	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
38	ATF3	chr12:124118056-124118549	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
39	ATF3	chr12:124118070-124118525	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
40	ATF3	chr12:124086465-124086828	K562	blood:	n/a	n/a
41	ATF3	chr12:124055837-124056188	HepG2	liver:	n/a	n/a
42	ATF3	chr12:124068575-124069116	A549	lung:	n/a	n/a
43	ATF3	chr12:124117986-124118648	A549	lung:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
44	ATF3	chr12:124055748-124056205	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF3	chr12:124118016-124118688	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
46	ATF3	chr12:124086213-124086916	A549	lung:	n/a	n/a
47	ATF3	chr12:124086541-124086734	GM12878	blood:	n/a	n/a
48	ATF3	chr12:124118086-124118563	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
49	ATF3	chr12:124118019-124118591	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
50	ATF3	chr12:124117982-124118633	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332

(count:3057 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124068984-124069034	AG04449	skin:	fetal
2	chr12:124087057-124087107	HCM	heart:	n/a
3	chr12:124118326-124118376	PrEC	prostate:	n/a
4	chr12:124069324-124069374	HUVEC	blood vessel:	n/a
5	chr12:124116920-124116970	MCF10A-Er-Src	breast:	n/a
6	chr12:124086667-124086717	HEK293	kidney:	embryo
7	chr12:124069324-124069374	CMK	blood:	n/a
8	chr12:124068984-124069034	AG04449	skin:	fetal
9	chr12:124087057-124087107	HCM	heart:	n/a
10	chr12:124118326-124118376	PrEC	prostate:	n/a
11	chr12:124069324-124069374	HUVEC	blood vessel:	n/a
12	chr12:124116920-124116970	MCF10A-Er-Src	breast:	n/a
13	chr12:124086667-124086717	HEK293	kidney:	embryo
14	chr12:124069324-124069374	CMK	blood:	n/a
15	chr12:124118360-124118410	T-47D	breast:	n/a
16	chr12:124105880-124105930	GM12892	blood:	n/a
17	chr12:124119657-124119707	ECC-1	luminal epithelium:	n/a
18	chr12:124086301-124086351	K562	blood:	n/a
19	chr12:124066860-124066910	AG04449	skin:	fetal
20	chr12:124145110-124145160	T-47D	breast:	n/a
21	chr12:124068984-124069034	Hepatocyte	liver:	n/a
22	chr12:124082333-124082383	H1-hESC	embryonic stem cell:	embryo
23	chr12:124086403-124086453	ECC-1	luminal epithelium:	n/a
24	chr12:124069168-124069218	GM19239	blood:	n/a
25	chr12:124086301-124086351	SK-N-SH	brain:	n/a
26	chr12:124087057-124087107	HUVEC	blood vessel:	n/a
27	chr12:124145110-124145160	IMR90	lung:	fetal
28	chr12:124090996-124091046	HEK293	kidney:	embryo
29	chr12:124086218-124086268	GM12878	blood:	n/a
30	chr12:124145110-124145160	HRE	kidney:	n/a
31	chr12:124068903-124068953	SKMC	muscle:	n/a
32	chr12:124116920-124116970	HUVEC	blood vessel:	n/a
33	chr12:124069168-124069218	H1-hESC	embryonic stem cell:	embryo
34	chr12:124086301-124086351	HEEpiC	esophagus:	n/a
35	chr12:124066860-124066910	HL-60	blood:	n/a
36	chr12:124043090-124043140	SK-N-SH_RA	brain:	n/a
37	chr12:124066860-124066910	HRE	kidney:	n/a
38	chr12:124086301-124086351	ovcar-3	ovarian:	n/a
39	chr12:124086727-124086777	AG09319	gingival:	n/a
40	chr12:124069475-124069525	GM19239	blood:	n/a
41	chr12:124118329-124118379	BJ	skin:	n/a
42	chr12:124068984-124069034	U87	brain:	n/a
43	chr12:124086903-124086953	LNCaP	prostate:	n/a
44	chr12:124118360-124118410	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:124069649-124069699	SK-N-SH	brain:	n/a
46	chr12:124118184-124118234	Hela-S3	cervix:	n/a
47	chr12:124069168-124069218	BJ	skin:	n/a
48	chr12:124086403-124086453	AG04450	lung:	fetal
49	chr12:124090996-124091046	HIPEpiC	eye:	n/a
50	chr12:124043090-124043140	ProgFib	skin:	n/a

(count:217 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:124084988..124092992-chr12:124114351..124121638,14	K562	blood:
2	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
3	chr12:124097957..124100584-chr12:124101045..124103171,2	MCF-7	breast:
4	chr12:124068784..124069610-chr17:35766980..35767756,2	NB4	blood:
5	chr12:124119318..124121767-chr12:124194183..124197056,2	MCF-7	breast:
6	chr12:123867412..123869840-chr12:124105069..124107721,2	K562	blood:
7	chr12:124090616..124092389-chr12:124114546..124116542,2	MCF-7	breast:
8	chr12:124067363..124072745-chr12:124084857..124088217,7	K562	blood:
9	chr12:124015697..124018727-chr12:124070609..124072770,3	K562	blood:
10	chr12:123868517..123870959-chr12:124065640..124068402,2	MCF-7	breast:
11	chr12:123755830..123757417-chr12:124116609..124118455,2	MCF-7	breast:
12	chr12:124065661..124069328-chr12:124081746..124084446,4	K562	blood:
13	chr12:124085496..124088026-chr12:124116630..124119648,4	MCF-7	breast:
14	chr12:123753500..123755086-chr12:124068992..124070507,2	MCF-7	breast:
15	chr12:124084893..124086565-chr12:124117453..124119818,2	K562	blood:
16	chr12:124105734..124108451-chr12:124133249..124135719,2	K562	blood:
17	chr12:124117920..124120001-chr12:124129132..124130798,2	MCF-7	breast:
18	chr12:124017387..124020298-chr12:124054468..124057519,3	MCF-7	breast:
19	chr12:123794013..123795517-chr12:124095818..124097432,2	K562	blood:
20	chr12:123867386..123869300-chr12:124085669..124087822,2	K562	blood:
21	chr12:124066647..124068350-chr12:124118155..124119898,2	K562	blood:
22	chr12:123846861..123850261-chr12:124066655..124071408,9	MCF-7	breast:
23	chr12:124116692..124118630-chr12:124144717..124146823,2	MCF-7	breast:
24	chr12:124068907..124069507-chr19:10763953..10764535,2	NB4	blood:
25	chr12:123866683..123868660-chr12:124118535..124120956,2	K562	blood:
26	chr12:124104075..124107132-chr12:124195548..124198352,3	MCF-7	breast:
27	chr12:124067363..124072745-chr12:124084857..124088217,7	K562	blood:
28	chr12:124109158..124110697-chr12:124113991..124116759,2	K562	blood:
29	chr12:124117633..124120865-chr12:124133499..124139438,5	K562	blood:
30	chr12:124117495..124119400-chr12:124126684..124128895,2	MCF-7	breast:
31	chr12:124138422..124140008-chr12:124142075..124144430,2	MCF-7	breast:
32	chr12:124098297..124101264-chr12:124101448..124103367,2	MCF-7	breast:
33	chr12:123755058..123757440-chr12:124084744..124087456,3	K562	blood:
34	chr12:124067567..124070616-chr12:124116717..124118360,3	K562	blood:
35	chr12:124112554..124115997-chr12:124116047..124118023,3	MCF-7	breast:
36	chr12:124067553..124070106-chr12:124116767..124119854,4	MCF-7	breast:
37	chr12:124130618..124132144-chr12:124154341..124156246,2	MCF-7	breast:
38	chr12:124084509..124086598-chr12:124112180..124115159,2	K562	blood:
39	chr12:123847713..123850022-chr12:124067528..124071055,3	MCF-7	breast:
40	chr12:124063601..124065298-chr12:124067381..124068906,2	MCF-7	breast:
41	chr12:124087290..124089167-chr12:124099421..124102129,2	MCF-7	breast:
42	chr12:124120951..124123869-chr12:124130412..124132116,2	K562	blood:
43	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
44	chr12:124068085..124074131-chr12:124076456..124078821,7	K562	blood:
45	chr12:124084509..124086598-chr12:124112180..124115159,2	K562	blood:
46	chr12:124137852..124140530-chr12:124458317..124460698,2	K562	blood:
47	chr12:124018224..124020563-chr12:124065688..124070487,5	K562	blood:
48	chr12:124085449..124088387-chr12:124115552..124120028,6	MCF-7	breast:
49	chr12:123752175..123754799-chr12:124094511..124096299,2	K562	blood:
50	chr1:149223310..149224289-chr12:124068656..124069362,2	HCT-116	colon:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2B1-1	chr12:124066709-124068936	NONHSAT031599
2	lnc-EIF2B1-1	chr12:124068759-124068874	XLOC_010229
3	lnc-EIF2B1-1	chr12:124068148-124068245	XLOC_010229
4	lnc-EIF2B1-2	chr12:124062808-124062838	XLOC_010228
5	lnc-EIF2B1-1	chr12:124065632-124067714	NR_110049
6	lnc-EIF2B1-2	chr12:124060445-124060779	XLOC_010228
7	lnc-EIF2B1-1	chr12:124068148-124068245	NR_110049
8	lnc-EIF2B1-1	chr12:124065613-124067714	XLOC_010229
9	lnc-EIF2B1-1	chr12:124068759-124068874	NR_110049
10	lnc-DDX55-1	chr12:124080952-124081554	expReg_chr12_11962_+

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	EIF2B1	hsa-miR-30a-5p	chr12:124105656-124105677
2	TMED2	hsa-miR-30a-5p	chr12:124081299-124081320
3	EIF2B1	hsa-miR-26b-5p	chr12:124105615-124105637
4	TMED2	hsa-miR-7-5p	chr12:124081277-124081289
5	EIF2B1	hsa-miR-30b-5p	chr12:124105656-124105681

Variant related genes	Relation type
ENSG00000206897	TF binding region
GTF2H3	TF binding region
ENSG00000247373	TF binding region
DDX55	TF binding region
TCTN2	TF binding region
TMED2	TF binding region
EIF2B1	TF binding region
ENSG00000206897	CpG island
GTF2H3	CpG island
ENSG00000247373	CpG island
DDX55	CpG island
TCTN2	CpG island
TMED2	CpG island
EIF2B1	CpG island
ENSG00000146834	chromatin interactions
ENSG00000179912	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000185344	chromatin interactions
ENSG00000184575	chromatin interactions
ENSG00000270095	chromatin interactions
ENSG00000184209	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000150977	chromatin interactions
ENSG00000179195	chromatin interactions
ENSG00000141543	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000267100	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000108264	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000108813	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000206897	chromatin interactions
ENSG00000270113	chromatin interactions
ENSG00000163125	chromatin interactions
CD2AP	miRNA target sites
CD44	miRNA target sites

Extended variants
information (count: 4313 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:4313 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150270741	chr12:124037417-124037418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559557551	chr12:124037424-124037425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192771012	chr12:124037435-124037436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184254953	chr12:124037586-124037587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138947470	chr12:124037615-124037616	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375961488	chr12:124037659-124037660	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143380468	chr12:124037664-124037665	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373605959	chr12:124037748-124037749	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187275416	chr12:124037778-124037779	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528153999	chr12:124037841-124037842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145787760	chr12:124037844-124037845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551508009	chr12:124037860-124037861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373372887	chr12:124037862-124037863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551150494	chr12:124037889-124037890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564864694	chr12:124037912-124037913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138682765	chr12:124037940-124037941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536914168	chr12:124037952-124037953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192155025	chr12:124037977-124037978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372947491	chr12:124038055-124038056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550807037	chr12:124038060-124038061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534071950	chr12:124038082-124038083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184553668	chr12:124038188-124038189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142734976	chr12:124038201-124038202	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576879951	chr12:124038217-124038218	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538455522	chr12:124038344-124038345	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556702809	chr12:124038351-124038352	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575186015	chr12:124038399-124038400	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189336035	chr12:124038407-124038408	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560757554	chr12:124038408-124038409	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144841076	chr12:124038456-124038457	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142001949	chr12:124038457-124038458	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370719036	chr12:124038459-124038460	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192711496	chr12:124038485-124038486	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147460725	chr12:124038535-124038536	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs35881147	chr12:124038548-124038549	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184517618	chr12:124038572-124038573	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564978136	chr12:124038597-124038598	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532207537	chr12:124038641-124038642	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148443617	chr12:124038684-124038685	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189793543	chr12:124038696-124038697	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530358791	chr12:124038804-124038805	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181394615	chr12:124038838-124038839	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28880346	chr12:124038995-124038996	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs150586790	chr12:124039011-124039012	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs139990165	chr12:124039030-124039031	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs570627323	chr12:124039041-124039042	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs185798219	chr12:124039044-124039045	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143564973	chr12:124039102-124039103	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs575081324	chr12:124039165-124039166	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs536194701	chr12:124039166-124039167	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4262 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124034400-124039000	Weak transcription	Primary B cells from cord blood	blood
2	chr12:124035600-124038000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr12:124036000-124037600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr12:124036000-124037600	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr12:124036600-124037400	Enhancers	Placenta	Placenta
6	chr12:124037200-124038600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:124037600-124037800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr12:124037600-124040400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr12:124037800-124038200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr12:124038000-124040400	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr12:124038200-124038600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:124038200-124040200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr12:124038400-124038800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr12:124039000-124040200	Enhancers	Primary B cells from cord blood	blood
15	chr12:124040200-124041800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr12:124040400-124043600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr12:124040400-124043800	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr12:124041800-124042800	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr12:124042600-124045000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr12:124042800-124043000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr12:124043000-124044400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr12:124043600-124044600	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr12:124043800-124044400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr12:124044000-124044400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr12:124044000-124044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:124044000-124044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:124044200-124044400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr12:124044200-124044600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr12:124044400-124045200	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr12:124044600-124044800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr12:124044800-124045200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr12:124045000-124045200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:124045200-124046000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr12:124046000-124046200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:124050400-124050600	Enhancers	HepG2	liver
36	chr12:124051800-124053000	Weak transcription	HepG2	liver
37	chr12:124054200-124055400	Enhancers	Dnd41	blood
38	chr12:124054600-124054800	Enhancers	HepG2	liver
39	chr12:124054600-124056000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr12:124054600-124056200	Enhancers	Fetal Thymus	thymus
41	chr12:124054600-124056400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:124054800-124055000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr12:124054800-124055000	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr12:124054800-124055000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr12:124054800-124055000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:124054800-124055000	Enhancers	NHDF-Ad	bronchial
47	chr12:124054800-124055200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:124054800-124055400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:124054800-124055400	Flanking Active TSS	HepG2	liver
50	chr12:124054800-124055800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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