Variant report

Variant	nsv973944
Chromosome Location	chr12:121017088-121027122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1025)
CpG islands
(count:1161)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1025 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121018694-121018835	K562	blood:	n/a	n/a
2	ARID3A	chr12:121019212-121019513	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121019281-121019700	K562	blood:	n/a	n/a
4	ARID3A	chr12:121022326-121022526	K562	blood:	n/a	n/a
5	ATF1	chr12:121019725-121020200	K562	blood:	n/a	n/a
6	ATF2	chr12:121018992-121019649	GM12878	blood:	n/a	n/a
7	ATF2	chr12:121021125-121021525	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:121021128-121021571	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:121019386-121019765	K562	blood:	n/a	n/a
10	BACH1	chr12:121017152-121017257	K562	blood:	n/a	n/a
11	BACH1	chr12:121018908-121019072	K562	blood:	n/a	n/a
12	BACH1	chr12:121021129-121021504	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr12:121018746-121018999	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr12:121022329-121022614	GM12878	blood:	n/a	chr12:121022499-121022512 chr12:121022503-121022516 chr12:121022515-121022528 chr12:121022434-121022447
15	BCL3	chr12:121018607-121019840	A549	lung:	n/a	n/a
16	BCL3	chr12:121018210-121019709	A549	lung:	n/a	chr12:121018532-121018541
17	BCL3	chr12:121018715-121019503	GM12878	blood:	n/a	n/a
18	BCLAF1	chr12:121018810-121019652	GM12878	blood:	n/a	n/a
19	BHLHE40	chr12:121022392-121022604	K562	blood:	n/a	n/a
20	BHLHE40	chr12:121018957-121019377	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:121017063-121017302	K562	blood:	n/a	n/a
22	BHLHE40	chr12:121021294-121021626	K562	blood:	n/a	n/a
23	BHLHE40	chr12:121018856-121019501	K562	blood:	n/a	n/a
24	BRCA1	chr12:121018990-121019187	GM12878	blood:	n/a	n/a
25	BRCA1	chr12:121018839-121019110	HepG2	liver:	n/a	n/a
26	BRCA1	chr12:121022704-121022788	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr12:121019926-121020141	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr12:121022241-121022441	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr12:121021323-121021478	HepG2	liver:	n/a	n/a
30	CBX3	chr12:121021128-121021937	K562	blood:	n/a	chr12:121021332-121021343
31	CBX3	chr12:121018813-121019606	K562	blood:	n/a	n/a
32	CBX3	chr12:121021360-121021845	K562	blood:	n/a	n/a
33	CCNT2	chr12:121022296-121022781	K562	blood:	n/a	chr12:121022668-121022677
34	CCNT2	chr12:121018784-121019422	K562	blood:	n/a	n/a
35	CCNT2	chr12:121016994-121017387	K562	blood:	n/a	chr12:121017216-121017236
36	CEBPB	chr12:121022349-121022631	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:121020029-121020147	K562	blood:	n/a	n/a
38	CEBPB	chr12:121022409-121022421	K562	blood:	n/a	n/a
39	CEBPD	chr12:121018908-121019523	HepG2	liver:	n/a	n/a
40	CHD1	chr12:121019396-121019592	GM12878	blood:	n/a	n/a
41	CHD2	chr12:121018944-121019517	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr12:121021223-121021618	HepG2	liver:	n/a	n/a
43	CHD2	chr12:121018918-121019639	K562	blood:	n/a	n/a
44	CHD2	chr12:121018920-121019543	GM12878	blood:	n/a	n/a
45	CHD2	chr12:121018823-121019504	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr12:121022315-121022681	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr12:121022712-121022779	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr12:121018947-121019449	HepG2	liver:	n/a	n/a
49	CREB1	chr12:121022537-121022925	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr12:121018898-121019525	A549	lung:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121019343-121019393	BE2_C	brain:	n/a
2	chr12:121021560-121021610	HAEpiC	amniotic membrane:	n/a
3	chr12:121019343-121019393	BE2_C	brain:	n/a
4	chr12:121021560-121021610	HAEpiC	amniotic membrane:	n/a
5	chr12:121021560-121021610	A549	lung:	n/a
6	chr12:121019729-121019779	MCF10A-Er-Src	breast:	n/a
7	chr12:121021560-121021610	HCM	heart:	n/a
8	chr12:121022843-121022893	RPTEC	kidney:	n/a
9	chr12:121021560-121021610	ECC-1	luminal epithelium:	n/a
10	chr12:121021560-121021610	HCT-116	colon:	n/a
11	chr12:121019603-121019653	AoSMC	blood vessel:	n/a
12	chr12:121019603-121019653	HepG2	liver:	n/a
13	chr12:121021673-121021723	PrEC	prostate:	n/a
14	chr12:121021490-121021540	AoSMC	blood vessel:	n/a
15	chr12:121017209-121017259	AG04450	lung:	fetal
16	chr12:121021673-121021723	Jurkat	blood:	n/a
17	chr12:121022424-121022474	HMEC	breast:	n/a
18	chr12:121022439-121022489	HepG2	liver:	n/a
19	chr12:121022424-121022474	HRE	kidney:	n/a
20	chr12:121019201-121019251	Hepatocyte	liver:	n/a
21	chr12:121022843-121022893	PrEC	prostate:	n/a
22	chr12:121022843-121022893	U87	brain:	n/a
23	chr12:121019412-121019462	NB4	blood:	n/a
24	chr12:121022424-121022474	HCPEpiC	choroid plexus:	n/a
25	chr12:121019019-121019069	HUVEC	blood vessel:	n/a
26	chr12:121019192-121019242	HCM	heart:	n/a
27	chr12:121022439-121022489	SK-N-SH_RA	brain:	n/a
28	chr12:121022703-121022753	AG04450	lung:	fetal
29	chr12:121019523-121019573	MCF-7	breast:	n/a
30	chr12:121021673-121021723	BE2_C	brain:	n/a
31	chr12:121019242-121019292	SKMC	muscle:	n/a
32	chr12:121019242-121019292	K562	blood:	n/a
33	chr12:121022703-121022753	BE2_C	brain:	n/a
34	chr12:121019412-121019462	AG10803	skin:	n/a
35	chr12:121022703-121022753	AG10803	skin:	n/a
36	chr12:121019242-121019292	HEEpiC	esophagus:	n/a
37	chr12:121019343-121019393	HIPEpiC	eye:	n/a
38	chr12:121019019-121019069	Hela-S3	cervix:	n/a
39	chr12:121024974-121025024	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:121018746-121018796	NHDF-neo	bronchial:	n/a
41	chr12:121021673-121021723	HCT-116	colon:	n/a
42	chr12:121019242-121019292	ProgFib	skin:	n/a
43	chr12:121022703-121022753	HCF	heart:	n/a
44	chr12:121019729-121019779	HCF	heart:	n/a
45	chr12:121019523-121019573	Hela-S3	cervix:	n/a
46	chr12:121022843-121022893	HCT-116	colon:	n/a
47	chr12:121021490-121021540	HMEC	breast:	n/a
48	chr12:121019192-121019242	HIPEpiC	eye:	n/a
49	chr12:121019343-121019393	SK-N-SH_RA	brain:	n/a
50	chr12:121021673-121021723	ovcar-3	ovarian:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120728472..120731126-chr12:121019042..121021642,2	K562	blood:
2	chr12:120905819..120908222-chr12:121018300..121020103,2	MCF-7	breast:
3	chr12:121007178..121009795-chr12:121014880..121017443,2	MCF-7	breast:
4	chr12:120994023..120996050-chr12:121018061..121019874,2	K562	blood:
5	chr12:121020917..121021868-chr12:121533219..121533885,3	K562	blood:
6	chr12:121021974..121024111-chr12:121148529..121150037,2	MCF-7	breast:
7	chr12:121021138..121021783-chr12:121084881..121085562,2	K562	blood:
8	chr12:121021265..121021846-chr12:121151493..121152375,2	MCF-7	breast:
9	chr12:121020090..121020910-chr12:121086635..121087738,3	MCF-7	breast:
10	chr12:121020899..121021841-chr12:121409286..121409915,3	K562	blood:
11	chr12:121021209..121021867-chr12:121087027..121087660,3	MCF-7	breast:
12	chr1:19923267..19923950-chr12:121018737..121019591,2	Hela-S3	cervix:
13	chr12:120970635..120973356-chr12:121018386..121020894,3	K562	blood:
14	chr12:121015961..121017626-chr12:121019497..121021092,2	K562	blood:
15	chr12:121018818..121020507-chr12:121022267..121023983,3	K562	blood:
16	chr12:121018252..121018999-chr3:48228737..48229264,2	Hela-S3	cervix:
17	chr12:121018584..121021388-chr12:121022313..121024823,2	MCF-7	breast:
18	chr12:121020907..121021484-chr12:121077869..121078415,2	MCF-7	breast:
19	chr12:121019025..121020943-chr12:121076838..121078875,3	K562	blood:
20	chr12:121017632..121023235-chr12:121123750..121127979,5	K562	blood:
21	chr12:121021041..121021897-chr12:121661173..121662030,2	MCF-7	breast:
22	chr12:121020875..121021804-chr12:121150905..121152345,4	K562	blood:
23	chr12:121019438..121021278-chr12:121153857..121156212,2	K562	blood:
24	chr12:121020078..121022631-chr12:121125640..121127142,2	K562	blood:
25	chr12:121020419..121023213-chr12:121085697..121088719,3	MCF-7	breast:
26	chr12:121021971..121022484-chr12:121124436..121124969,2	K562	blood:
27	chr12:121021368..121022342-chr12:121149363..121149884,2	K562	blood:
28	chr12:121021284..121022852-chr12:121123778..121125938,2	MCF-7	breast:
29	chr12:120965360..120967085-chr12:121018477..121020344,2	MCF-7	breast:
30	chr12:120999355..121001147-chr12:121014486..121017310,2	K562	blood:
31	chr12:121021176..121021954-chr12:121086681..121088032,8	MCF-7	breast:
32	chr12:120971743..120974059-chr12:121017467..121020168,3	MCF-7	breast:
33	chr12:121018631..121021385-chr12:121124185..121125689,2	MCF-7	breast:
34	chr12:121018631..121020878-chr12:121162530..121164769,2	MCF-7	breast:
35	chr12:121020996..121021955-chr12:121087894..121088614,2	K562	blood:
36	chr12:121002647..121005056-chr12:121017144..121019429,2	MCF-7	breast:

No data

Variant related genes	Relation type
POP5	TF binding region
POP5	CpG island
ENSG00000256008	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000111786	chromatin interactions
ENSG00000157782	chromatin interactions
ENSG00000110917	chromatin interactions
ENSG00000173436	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000270136	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000122971	chromatin interactions
ENSG00000235185	chromatin interactions
ENSG00000022840	chromatin interactions
ENSG00000088986	chromatin interactions

Extended variants
information (count: 411 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375439034	chr12:121017108-121017109	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559948050	chr12:121017136-121017137	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143447072	chr12:121017144-121017145	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369463367	chr12:121017154-121017155	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs188092231	chr12:121017156-121017157	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372790098	chr12:121017170-121017171	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7174	chr12:121017171-121017172	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs549041831	chr12:121017202-121017203	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs377021428	chr12:121017213-121017214	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541098610	chr12:121017239-121017240	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs509445	chr12:121017243-121017244	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs201521846	chr12:121017245-121017246	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2301456	chr12:121017264-121017265	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs376416552	chr12:121017271-121017272	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190786826	chr12:121017276-121017277	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554222502	chr12:121017277-121017278	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563191858	chr12:121017283-121017284	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370911432	chr12:121017288-121017289	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552061593	chr12:121017299-121017300	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201098854	chr12:121017320-121017321	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140784734	chr12:121017333-121017334	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376390708	chr12:121017334-121017335	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374290893	chr12:121017396-121017397	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368277242	chr12:121017427-121017428	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563920	chr12:121017439-121017440	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs373663945	chr12:121017443-121017444	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs114788845	chr12:121017444-121017445	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567455742	chr12:121017473-121017474	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs3833953	chr12:121017475-121017476	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs536225136	chr12:121017487-121017488	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs549954697	chr12:121017494-121017495	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs570041222	chr12:121017507-121017508	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs371641220	chr12:121017527-121017528	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs182834091	chr12:121017534-121017535	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs377306788	chr12:121017539-121017540	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs538509460	chr12:121017553-121017554	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs34425419	chr12:121017561-121017562	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs368559910	chr12:121017562-121017563	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs372578822	chr12:121017565-121017566	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs142190925	chr12:121017612-121017613	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs150135150	chr12:121017628-121017629	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs151192790	chr12:121017688-121017689	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs188049856	chr12:121017723-121017724	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs138708878	chr12:121017727-121017728	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs554680248	chr12:121017735-121017736	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs574630193	chr12:121017763-121017764	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs543394371	chr12:121017779-121017780	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs576558998	chr12:121017780-121017781	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs563100289	chr12:121017815-121017816	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs576778701	chr12:121017895-121017896	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	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
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
Breast cancer	22522925	CNVD

Chromatin state (count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120976000-121018000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:120976400-121018200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:120977400-121017600	Strong transcription	Fetal Thymus	thymus
4	chr12:120977400-121018200	Strong transcription	Fetal Stomach	stomach
5	chr12:120982200-121017600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:120983600-121017600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:120983600-121017600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr12:120983600-121017800	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:120983600-121017800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:120983600-121017800	Strong transcription	Fetal Muscle Trunk	muscle
11	chr12:120983800-121017800	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr12:120983800-121017800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:120984000-121017800	Strong transcription	H1 Cell Line	embryonic stem cell
14	chr12:120984000-121017800	Strong transcription	Fetal Intestine Large	intestine
15	chr12:120984000-121017800	Strong transcription	Thymus	Thymus
16	chr12:120984000-121018200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:120984200-121017400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:120984400-121018000	Strong transcription	Brain Germinal Matrix	brain
19	chr12:120985600-121018200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:120988200-121017800	Strong transcription	Stomach Smooth Muscle	stomach
21	chr12:120988200-121018200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr12:120988400-121017800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:120989200-121017600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr12:120989400-121017800	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr12:120989600-121017600	Strong transcription	Placenta	Placenta
26	chr12:120990000-121018000	Strong transcription	Spleen	Spleen
27	chr12:120990200-121017800	Strong transcription	HUVEC	blood vessel
28	chr12:120990600-121017600	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr12:120990800-121017200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr12:120990800-121017200	Strong transcription	Duodenum Mucosa	Duodenum
31	chr12:120990800-121017400	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr12:120990800-121017400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr12:120990800-121017400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr12:120990800-121017600	Strong transcription	Primary B cells from peripheral blood	blood
35	chr12:120990800-121017600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr12:120990800-121017600	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr12:120990800-121017800	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr12:120990800-121017800	Strong transcription	Liver	Liver
39	chr12:120990800-121018200	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr12:120991000-121017600	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr12:120991400-121018200	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr12:120992000-121017400	Strong transcription	Ovary	ovary
43	chr12:120992000-121017800	Strong transcription	Fetal Lung	lung
44	chr12:120992800-121017800	Strong transcription	Brain Anterior Caudate	brain
45	chr12:120993000-121018000	Strong transcription	Fetal Muscle Leg	muscle
46	chr12:120994600-121017800	Strong transcription	HSMMtube	muscle
47	chr12:120995800-121017800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:120996800-121017600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:120997000-121017600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr12:120997000-121018000	Strong transcription	Lung	lung

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