Variant report

Variant	nsv832408
Chromosome Location	chr12:51696605-51871339
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3742)
CpG islands
(count:3791)
Chromatin interactive
region (count:213)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3742 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:51745791-51746000	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:51762519-51762654	K562	blood:	n/a	n/a
3	ARID3A	chr12:51783150-51783551	K562	blood:	n/a	n/a
4	ARID3A	chr12:51765410-51765783	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:51714725-51715166	K562	blood:	n/a	n/a
6	ARID3A	chr12:51863978-51864156	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:51729914-51729925	K562	blood:	n/a	n/a
8	ARID3A	chr12:51781855-51782190	K562	blood:	n/a	n/a
9	ARID3A	chr12:51755369-51755375	K562	blood:	n/a	n/a
10	ARID3A	chr12:51712319-51712572	K562	blood:	n/a	n/a
11	ARID3A	chr12:51720510-51720934	K562	blood:	n/a	n/a
12	ATF1	chr12:51789381-51789904	K562	blood:	n/a	n/a
13	ATF1	chr12:51734969-51735478	K562	blood:	n/a	n/a
14	ATF1	chr12:51762553-51763105	K562	blood:	n/a	n/a
15	ATF1	chr12:51756790-51757117	K562	blood:	n/a	n/a
16	ATF1	chr12:51783127-51783470	K562	blood:	n/a	n/a
17	ATF1	chr12:51720465-51720878	K562	blood:	n/a	n/a
18	ATF2	chr12:51762620-51763238	GM12878	blood:	n/a	n/a
19	ATF2	chr12:51735008-51735562	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr12:51867732-51868163	GM12878	blood:	n/a	n/a
21	ATF2	chr12:51762571-51763305	GM12878	blood:	n/a	n/a
22	ATF2	chr12:51720370-51720948	GM12878	blood:	n/a	n/a
23	ATF2	chr12:51788954-51789423	GM12878	blood:	n/a	n/a
24	ATF2	chr12:51788674-51789620	GM12878	blood:	n/a	n/a
25	ATF2	chr12:51714629-51715214	GM12878	blood:	n/a	n/a
26	ATF2	chr12:51750988-51751699	GM12878	blood:	n/a	n/a
27	ATF2	chr12:51783469-51783869	GM12878	blood:	n/a	n/a
28	ATF2	chr12:51734906-51735460	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr12:51783020-51783903	GM12878	blood:	n/a	n/a
30	ATF3	chr12:51783106-51783532	K562	blood:	n/a	n/a
31	ATF3	chr12:51756687-51756855	K562	blood:	n/a	n/a
32	BACH1	chr12:51745733-51745990	K562	blood:	n/a	n/a
33	BACH1	chr12:51781801-51782031	K562	blood:	n/a	n/a
34	BACH1	chr12:51720521-51720953	K562	blood:	n/a	n/a
35	BACH1	chr12:51762793-51763053	K562	blood:	n/a	n/a
36	BACH1	chr12:51739520-51739720	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr12:51720624-51720970	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr12:51751170-51751576	GM12878	blood:	n/a	n/a
39	BATF	chr12:51796912-51797305	GM12878	blood:	n/a	chr12:51797118-51797129
40	BATF	chr12:51796987-51797213	GM12878	blood:	n/a	chr12:51797118-51797129
41	BATF	chr12:51867768-51868062	GM12878	blood:	n/a	chr12:51867942-51867953 chr12:51867924-51867935
42	BATF	chr12:51736703-51736982	GM12878	blood:	n/a	n/a
43	BATF	chr12:51788975-51789458	GM12878	blood:	n/a	n/a
44	BATF	chr12:51762571-51763073	GM12878	blood:	n/a	n/a
45	BATF	chr12:51762580-51763214	GM12878	blood:	n/a	n/a
46	BATF	chr12:51788979-51789405	GM12878	blood:	n/a	n/a
47	BATF	chr12:51867715-51868032	GM12878	blood:	n/a	chr12:51867942-51867953 chr12:51867924-51867935
48	BCL11A	chr12:51762649-51763206	GM12878	blood:	n/a	n/a
49	BCL11A	chr12:51867765-51868055	GM12878	blood:	n/a	n/a
50	BCL11A	chr12:51762672-51763124	GM12878	blood:	n/a	n/a

(count:3791 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:51773409-51773459	AG04450	lung:	fetal
2	chr12:51785378-51785428	MCF-7	breast:	n/a
3	chr12:51818681-51818731	AoSMC	blood vessel:	n/a
4	chr12:51849767-51849817	AG09319	gingival:	n/a
5	chr12:51718088-51718138	PrEC	prostate:	n/a
6	chr12:51740751-51740801	HAEpiC	amniotic membrane:	n/a
7	chr12:51717978-51718028	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:51773594-51773644	HUVEC	blood vessel:	n/a
9	chr12:51783393-51783443	NH-A	brain:	n/a
10	chr12:51773409-51773459	AG04450	lung:	fetal
11	chr12:51785378-51785428	MCF-7	breast:	n/a
12	chr12:51818681-51818731	AoSMC	blood vessel:	n/a
13	chr12:51849767-51849817	AG09319	gingival:	n/a
14	chr12:51718088-51718138	PrEC	prostate:	n/a
15	chr12:51740751-51740801	HAEpiC	amniotic membrane:	n/a
16	chr12:51717978-51718028	HPAEpiC	pulmonary alveolar:	n/a
17	chr12:51773594-51773644	HUVEC	blood vessel:	n/a
18	chr12:51783393-51783443	NH-A	brain:	n/a
19	chr12:51740751-51740801	GM19239	blood:	n/a
20	chr12:51819019-51819069	NHBE	bronchial:	n/a
21	chr12:51828070-51828120	ProgFib	skin:	n/a
22	chr12:51783393-51783443	AoSMC	blood vessel:	n/a
23	chr12:51815083-51815133	U87	brain:	n/a
24	chr12:51819149-51819199	NB4	blood:	n/a
25	chr12:51715252-51715302	ECC-1	luminal epithelium:	n/a
26	chr12:51782159-51782209	ProgFib	skin:	n/a
27	chr12:51718112-51718162	HRCEpiC	kidney:	n/a
28	chr12:51715252-51715302	GM06990	blood:	n/a
29	chr12:51722300-51722350	HAEpiC	amniotic membrane:	n/a
30	chr12:51720755-51720805	AoSMC	blood vessel:	n/a
31	chr12:51794933-51794983	AG09309	skin:	n/a
32	chr12:51818350-51818400	AG04449	skin:	fetal
33	chr12:51783393-51783443	PFSK-1	brain:	n/a
34	chr12:51701979-51702029	GM12892	blood:	n/a
35	chr12:51717674-51717724	PANC-1	pancreas:	n/a
36	chr12:51849767-51849817	LNCaP	prostate:	n/a
37	chr12:51713220-51713270	MCF-7	breast:	n/a
38	chr12:51828070-51828120	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:51776460-51776510	HIPEpiC	eye:	n/a
40	chr12:51788285-51788335	SKMC	muscle:	n/a
41	chr12:51819149-51819199	HCT-116	colon:	n/a
42	chr12:51740751-51740801	MCF10A-Er-Src	breast:	n/a
43	chr12:51740751-51740801	GM12878	blood:	n/a
44	chr12:51722300-51722350	PFSK-1	brain:	n/a
45	chr12:51718108-51718158	ProgFib	skin:	n/a
46	chr12:51701979-51702029	GM12891	blood:	n/a
47	chr12:51773594-51773644	HAEpiC	amniotic membrane:	n/a
48	chr12:51784644-51784694	SAEC	small airway:	n/a
49	chr12:51828070-51828120	GM06990	blood:	n/a
50	chr12:51835919-51835969	SK-N-MC	brain:	n/a

(count:213 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:51766723..51770541-chr12:51770868..51773253,4	K562	blood:
2	chr12:51735794..51738588-chr12:51760014..51762063,2	K562	blood:
3	chr12:51461072..51462629-chr12:51782020..51784509,2	MCF-7	breast:
4	chr12:51851591..51853710-chr12:51854624..51856829,2	MCF-7	breast:
5	chr12:51441397..51442221-chr12:51735006..51735798,3	MCF-7	breast:
6	chr12:51663027..51663961-chr12:51734595..51735757,6	MCF-7	breast:
7	chr12:51661930..51666177-chr12:51732145..51735624,5	MCF-7	breast:
8	chr12:51780059..51782698-chr12:51806494..51808055,2	MCF-7	breast:
9	chr12:51771653..51774170-chr12:51775864..51778994,3	MCF-7	breast:
10	chr12:51662651..51666835-chr12:51728817..51731606,3	MCF-7	breast:
11	chr12:51717645..51719204-chr12:51757324..51760023,2	MCF-7	breast:
12	chr12:51823526..51825878-chr12:51828204..51829965,2	MCF-7	breast:
13	chr12:51475962..51477532-chr12:51714487..51716389,2	K562	blood:
14	chr12:51720048..51722146-chr12:51747016..51749714,2	K562	blood:
15	chr12:51475890..51478856-chr12:51719210..51722345,3	K562	blood:
16	chr12:51747253..51748969-chr12:51752047..51753827,2	K562	blood:
17	chr12:51772633..51775258-chr12:51778475..51780611,2	K562	blood:
18	chr12:51751580..51754546-chr12:51755369..51757595,3	MCF-7	breast:
19	chr12:51786487..51790707-chr12:51791778..51797846,7	MCF-7	breast:
20	chr12:51720048..51722146-chr12:51747016..51749714,2	K562	blood:
21	chr12:51735794..51738588-chr12:51760014..51762063,2	K562	blood:
22	chr12:51816067..51817942-chr12:51924198..51925817,2	MCF-7	breast:
23	chr12:51818349..51820345-chr12:51823032..51825189,2	MCF-7	breast:
24	chr12:51712710..51716828-chr12:51719754..51724043,5	K562	blood:
25	chr12:51770709..51771496-chr12:51813074..51813863,2	MCF-7	breast:
26	chr12:51816861..51818635-chr12:51821373..51823097,2	K562	blood:
27	chr12:51438469..51440828-chr12:51713413..51715859,2	K562	blood:
28	chr12:51800589..51802507-chr12:51810515..51813200,2	K562	blood:
29	chr12:51784285..51786349-chr12:51786444..51790807,4	MCF-7	breast:
30	chr12:51765744..51766522-chr12:51925449..51926130,2	MCF-7	breast:
31	chr12:51726670..51729630-chr12:51730629..51732198,2	K562	blood:
32	chr12:51754890..51757082-chr12:51783252..51784847,2	K562	blood:
33	chr12:51656622..51657136-chr12:51734891..51735412,2	MCF-7	breast:
34	chr12:51734941..51739498-chr12:51744423..51748065,5	K562	blood:
35	chr12:51710356..51713645-chr12:51720668..51723733,3	MCF-7	breast:
36	chr12:51762201..51772634-chr12:51780037..51787148,16	MCF-7	breast:
37	chr12:51814446..51815641-chr12:52071629..52072553,3	K562	blood:
38	chr12:51719185..51720763-chr12:51721819..51723856,2	MCF-7	breast:
39	chr12:51712004..51713863-chr12:51716596..51718189,2	K562	blood:
40	chr12:51633168..51635077-chr12:51718759..51720463,2	MCF-7	breast:
41	chr12:51841850..51843356-chr12:51869641..51871923,2	MCF-7	breast:
42	chr12:51566806..51568529-chr12:51720798..51723312,2	K562	blood:
43	chr12:51475846..51477585-chr12:51782020..51786385,4	MCF-7	breast:
44	chr12:51783714..51787101-chr12:51795661..51799785,4	MCF-7	breast:
45	chr12:51814764..51815691-chr12:51922340..51923305,6	MCF-7	breast:
46	chr12:51796589..51798593-chr12:51799869..51802526,2	K562	blood:
47	chr12:51815017..51815657-chr12:52071869..52072477,2	MCF-7	breast:
48	chr12:51632808..51635025-chr12:51730960..51733837,2	MCF-7	breast:
49	chr12:51734275..51737716-chr12:51737747..51740483,3	K562	blood:
50	chr12:51761603..51763662-chr12:51775969..51778368,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CELA1-2	chr12:51784634-51784721	NONHSAT028257
2	lnc-CELA1-2	chr12:51776097-51776293	NONHSAT028259
3	lnc-CELA1-2	chr12:51773625-51773668	NONHSAT028259
4	lnc-CELA1-2	chr12:51785385-51785435	NONHSAT028257
5	lnc-CELA1-1	chr12:51716369-51717042	NONHSAT028255
6	lnc-GALNT6-2	chr12:51860570-51860955	NONHSAT028269
7	lnc-CELA1-2	chr12:51776119-51776293	NONHSAT028260
8	lnc-CELA1-2	chr12:51777245-51777366	NONHSAT028260
9	lnc-CELA1-2	chr12:51777245-51777366	NONHSAT028257
10	lnc-CELA1-2	chr12:51785071-51785174	NONHSAT028259
11	lnc-CELA1-2	chr12:51785385-51785459	NONHSAT028260
12	lnc-CELA1-2	chr12:51776097-51776293	NONHSAT028257
13	lnc-CELA1-2	chr12:51777245-51777366	NONHSAT028261
14	lnc-CELA1-2	chr12:51773597-51773668	NONHSAT028258
15	lnc-CELA1-2	chr12:51784866-51785188	NONHSAT028261
16	lnc-GALNT6-1	chr12:51815740-51815961	ENSG00000271065.1
17	lnc-CELA1-2	chr12:51776245-51776293	NONHSAT028261
18	lnc-CELA1-2	chr12:51777245-51777366	NONHSAT028258
19	lnc-CELA1-1	chr12:51717806-51717869	NONHSAT028255
20	lnc-DAZAP2-6	chr12:51705285-51705526	expReg_chr12_4589_+
21	lnc-CELA1-2	chr12:51777245-51777366	NONHSAT028259
22	lnc-CELA1-2	chr12:51773570-51773668	NONHSAT028257
23	lnc-CELA1-2	chr12:51785385-51785739	NONHSAT028258
24	lnc-GALNT6-1	chr12:51818271-51818395	ENSG00000271065.1
25	lnc-CELA1-2	chr12:51785071-51785375	NONHSAT028262
26	lnc-CELA1-2	chr12:51777245-51777366	NONHSAT028262
27	lnc-GALNT6-2	chr12:51861202-51861334	NONHSAT028269
28	lnc-CELA1-2	chr12:51776245-51776293	NONHSAT028262
29	lnc-CELA1-2	chr12:51784634-51784721	NONHSAT028259

No data

Variant related genes	Relation type
GALNT6	TF binding region
CELA1	TF binding region
SLC4A8	TF binding region
ENSG00000271065	TF binding region
BIN2	TF binding region
GALNT6	CpG island
CELA1	CpG island
SLC4A8	CpG island
ENSG00000271065	CpG island
BIN2	CpG island
ENSG00000196562	chromatin interactions
ENSG00000183971	chromatin interactions
ENSG00000050426	chromatin interactions
ENSG00000135457	chromatin interactions
ENSG00000110911	chromatin interactions
ENSG00000167962	chromatin interactions
ENSG00000139629	chromatin interactions
ENSG00000271065	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000170545	chromatin interactions
ENSG00000183283	chromatin interactions
ENSG00000110934	chromatin interactions
ENSG00000184271	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000139610	chromatin interactions
ENSG00000050438	chromatin interactions

Extended variants
information (count: 6445 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:6445 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370511380	chr12:51696612-51696613	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550030235	chr12:51696716-51696717	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563835313	chr12:51696723-51696724	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576677906	chr12:51696818-51696819	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200797995	chr12:51696841-51696842	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372942644	chr12:51696847-51696848	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201010283	chr12:51696852-51696853	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377310382	chr12:51696868-51696869	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201895934	chr12:51696875-51696876	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147235873	chr12:51696879-51696880	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34119627	chr12:51696886-51696887	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370919677	chr12:51696937-51696938	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375508894	chr12:51696945-51696946	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528398940	chr12:51696950-51696951	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12580979	chr12:51697029-51697030	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185553450	chr12:51697037-51697038	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571280539	chr12:51697039-51697040	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148722720	chr12:51697086-51697087	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556763765	chr12:51697118-51697119	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567395307	chr12:51697152-51697153	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190268026	chr12:51697153-51697154	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7308177	chr12:51697162-51697163	Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141429486	chr12:51697199-51697200	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150846919	chr12:51697212-51697213	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557704325	chr12:51697231-51697232	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577938106	chr12:51697235-51697236	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559595718	chr12:51697300-51697301	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182848030	chr12:51697339-51697340	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563624618	chr12:51697361-51697362	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529436648	chr12:51697515-51697516	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186765177	chr12:51697567-51697568	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559598641	chr12:51697574-51697575	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534076369	chr12:51697613-51697614	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551677300	chr12:51697617-51697618	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571551278	chr12:51697624-51697625	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530414431	chr12:51697690-51697691	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550597369	chr12:51697691-51697692	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143327024	chr12:51697738-51697739	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535949158	chr12:51697755-51697756	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555504002	chr12:51697787-51697788	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs796504	chr12:51697809-51697810	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565953041	chr12:51697890-51697891	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs68042460	chr12:51697891-51697892	Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs558015686	chr12:51697895-51697896	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190882938	chr12:51697897-51697898	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578227026	chr12:51697898-51697899	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567650281	chr12:51697904-51697905	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543452160	chr12:51697919-51697920	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146728974	chr12:51697943-51697944	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114147157	chr12:51697956-51697957	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Seminomas	18059402	CNVD
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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	20409316	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Adenoid cystic carcinoma	18332873	CNVD

Chromatin state (count:4905 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51673800-51697600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:51674000-51698400	Strong transcription	Fetal Thymus	thymus
3	chr12:51674000-51701400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr12:51674200-51704000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:51674400-51698400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr12:51674400-51698600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:51674400-51698800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:51674400-51700600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:51678000-51697600	Weak transcription	Adipose Nuclei	Adipose
10	chr12:51680600-51701600	Weak transcription	Small Intestine	intestine
11	chr12:51681800-51714200	Weak transcription	Gastric	stomach
12	chr12:51685800-51697600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:51686200-51702800	Weak transcription	Colonic Mucosa	Colon
14	chr12:51686600-51698800	Strong transcription	Primary B cells from peripheral blood	blood
15	chr12:51686800-51698600	Strong transcription	Primary T cells from cord blood	blood
16	chr12:51686800-51701200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr12:51687000-51703800	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr12:51687000-51707400	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr12:51687200-51696800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr12:51687200-51697200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
21	chr12:51687800-51697200	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr12:51687800-51700000	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr12:51687800-51708000	Strong transcription	Thymus	Thymus
24	chr12:51688000-51698400	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr12:51688800-51696800	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr12:51691000-51696800	Strong transcription	Placenta	Placenta
27	chr12:51691800-51702200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr12:51692600-51698200	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr12:51692800-51698400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
30	chr12:51692800-51698600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr12:51693000-51697200	Strong transcription	Primary hematopoietic stem cells	blood
32	chr12:51693000-51698000	Strong transcription	GM12878-XiMat	blood
33	chr12:51693000-51698400	Strong transcription	Primary B cells from cord blood	blood
34	chr12:51693800-51701600	Weak transcription	Duodenum Mucosa	Duodenum
35	chr12:51694800-51701400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr12:51696000-51698400	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr12:51696200-51698400	Strong transcription	Spleen	Spleen
38	chr12:51696400-51696800	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr12:51696600-51700400	Weak transcription	A549	lung
40	chr12:51696600-51712400	Genic enhancers	Primary T cells fromperipheralblood	blood
41	chr12:51696800-51698000	Weak transcription	Placenta	Placenta
42	chr12:51696800-51698400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr12:51696800-51701600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr12:51697200-51698400	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr12:51697200-51699000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
46	chr12:51697200-51699800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr12:51697600-51697800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr12:51697600-51698400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr12:51697800-51698200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr12:51697800-51701600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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