Variant report

Variant	nsv1034358
Chromosome Location	chr7:26142380-26219559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1372)
CpG islands
(count:1344)
Chromatin interactive
region (count:122)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:26170965-26171130	K562	blood:	n/a	n/a
2	ATF1	chr7:26196017-26196304	K562	blood:	n/a	n/a
3	ATF2	chr7:26195846-26196477	GM12878	blood:	n/a	n/a
4	ATF2	chr7:26192743-26193985	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:26192958-26193943	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:26195933-26196525	GM12878	blood:	n/a	n/a
7	BACH1	chr7:26191502-26191790	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:26195194-26195761	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:26193593-26194113	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:26195971-26196302	GM12878	blood:	n/a	n/a
11	BATF	chr7:26196002-26196468	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:26195985-26196383	GM12878	blood:	n/a	chr7:26196143-26196152 chr7:26196099-26196108
13	BCL3	chr7:26195916-26196360	GM12878	blood:	n/a	chr7:26196143-26196152 chr7:26196099-26196108
14	BCL3	chr7:26218186-26218815	A549	lung:	n/a	n/a
15	BCL3	chr7:26166958-26167372	GM12878	blood:	n/a	n/a
16	BCL3	chr7:26219133-26220180	A549	lung:	n/a	n/a
17	BCL3	chr7:26217644-26229718	A549	lung:	n/a	chr7:26226946-26226953 chr7:26220505-26220512 chr7:26220601-26220614
18	BCLAF1	chr7:26191348-26192153	GM12878	blood:	n/a	chr7:26191796-26191809 chr7:26191834-26191847 chr7:26191813-26191822 chr7:26191798-26191811 chr7:26191802-26191815 chr7:26191919-26191932
19	BCLAF1	chr7:26195986-26196488	GM12878	blood:	n/a	chr7:26196143-26196152 chr7:26196099-26196108
20	BCLAF1	chr7:26195878-26196566	GM12878	blood:	n/a	chr7:26196143-26196152 chr7:26196099-26196108
21	BHLHE40	chr7:26192626-26193938	K562	blood:	n/a	n/a
22	BHLHE40	chr7:26191507-26192202	GM12878	blood:	n/a	chr7:26191795-26191811 chr7:26192019-26192035 chr7:26191803-26191819 chr7:26191830-26191846 chr7:26191917-26191933 chr7:26191796-26191812
23	BHLHE40	chr7:26191604-26192176	HepG2	liver:	n/a	chr7:26191795-26191811 chr7:26192019-26192035 chr7:26191803-26191819 chr7:26191830-26191846 chr7:26191917-26191933 chr7:26191796-26191812
24	BHLHE40	chr7:26206582-26207381	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:26195711-26197084	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:26155922-26156187	K562	blood:	n/a	chr7:26156013-26156026 chr7:26156016-26156025 chr7:26156015-26156024 chr7:26156009-26156030
27	BHLHE40	chr7:26191546-26192306	K562	blood:	n/a	chr7:26191795-26191811 chr7:26192019-26192035 chr7:26191803-26191819 chr7:26191830-26191846 chr7:26191917-26191933 chr7:26191796-26191812
28	BHLHE40	chr7:26196013-26196515	K562	blood:	n/a	n/a
29	BHLHE40	chr7:26157126-26157288	K562	blood:	n/a	n/a
30	BHLHE40	chr7:26195215-26195616	K562	blood:	n/a	n/a
31	BRCA1	chr7:26193206-26193808	H1-hESC	embryonic stem cell:	n/a	n/a
32	CCNT2	chr7:26196063-26196263	K562	blood:	n/a	n/a
33	CCNT2	chr7:26191569-26192234	K562	blood:	n/a	n/a
34	CCNT2	chr7:26192589-26192874	K562	blood:	n/a	n/a
35	CEBPB	chr7:26184085-26184572	A549	lung:	n/a	n/a
36	CEBPB	chr7:26183197-26183638	A549	lung:	n/a	n/a
37	CEBPB	chr7:26161113-26161137	HepG2	liver:	n/a	chr7:26161121-26161134
38	CEBPB	chr7:26170757-26170931	A549	lung:	n/a	chr7:26170861-26170872
39	CEBPB	chr7:26206607-26206918	K562	blood:	n/a	n/a
40	CEBPB	chr7:26193180-26193762	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr7:26183275-26183615	A549	lung:	n/a	n/a
42	CEBPB	chr7:26184190-26184500	A549	lung:	n/a	n/a
43	CEBPB	chr7:26183152-26183778	A549	lung:	n/a	n/a
44	CEBPB	chr7:26206611-26206913	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:26175377-26175473	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:26170700-26171016	HepG2	liver:	n/a	chr7:26170861-26170872
47	CEBPB	chr7:26195195-26195433	A549	lung:	n/a	n/a
48	CEBPB	chr7:26206664-26206845	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr7:26177193-26177381	HepG2	liver:	n/a	chr7:26177263-26177274
50	CEBPB	chr7:26170731-26171020	K562	blood:	n/a	chr7:26170861-26170872

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:26191633-26191683	Hela-S3	cervix:	n/a
2	chr7:26193805-26193855	SAEC	small airway:	n/a
3	chr7:26191633-26191683	Hela-S3	cervix:	n/a
4	chr7:26193805-26193855	SAEC	small airway:	n/a
5	chr7:26183581-26183631	GM06990	blood:	n/a
6	chr7:26193109-26193159	AG09319	gingival:	n/a
7	chr7:26196274-26196324	AoSMC	blood vessel:	n/a
8	chr7:26193805-26193855	NHBE	bronchial:	n/a
9	chr7:26191489-26191539	HepG2	liver:	n/a
10	chr7:26191696-26191746	AG04450	lung:	fetal
11	chr7:26192034-26192084	MCF10A-Er-Src	breast:	n/a
12	chr7:26192032-26192082	Caco-2	colon:	n/a
13	chr7:26183581-26183631	AoSMC	blood vessel:	n/a
14	chr7:26193607-26193657	NH-A	brain:	n/a
15	chr7:26187634-26187684	BE2_C	brain:	n/a
16	chr7:26192966-26193016	K562	blood:	n/a
17	chr7:26191633-26191683	CMK	blood:	n/a
18	chr7:26192966-26193016	U87	brain:	n/a
19	chr7:26193032-26193082	HepG2	liver:	n/a
20	chr7:26191633-26191683	AG09309	skin:	n/a
21	chr7:26192966-26193016	CMK	blood:	n/a
22	chr7:26191633-26191683	GM12891	blood:	n/a
23	chr7:26199872-26199922	MCF10A-Er-Src	breast:	n/a
24	chr7:26196274-26196324	NHDF-neo	bronchial:	n/a
25	chr7:26191726-26191776	BE2_C	brain:	n/a
26	chr7:26196274-26196324	NH-A	brain:	n/a
27	chr7:26192199-26192249	HCM	heart:	n/a
28	chr7:26196274-26196324	HAEpiC	amniotic membrane:	n/a
29	chr7:26192034-26192084	NHDF-neo	bronchial:	n/a
30	chr7:26199872-26199922	GM19239	blood:	n/a
31	chr7:26191458-26191508	HEEpiC	esophagus:	n/a
32	chr7:26191696-26191746	HCF	heart:	n/a
33	chr7:26191696-26191746	K562	blood:	n/a
34	chr7:26183581-26183631	AG09309	skin:	n/a
35	chr7:26192756-26192806	GM12891	blood:	n/a
36	chr7:26192756-26192806	SAEC	small airway:	n/a
37	chr7:26192034-26192084	H1-hESC	embryonic stem cell:	embryo
38	chr7:26192756-26192806	AG04449	skin:	fetal
39	chr7:26192032-26192082	SK-N-MC	brain:	n/a
40	chr7:26191489-26191539	HRPEpiC	eye:	n/a
41	chr7:26191726-26191776	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:26183581-26183631	Hepatocyte	liver:	n/a
43	chr7:26193805-26193855	HRPEpiC	eye:	n/a
44	chr7:26191726-26191776	MCF10A-Er-Src	breast:	n/a
45	chr7:26196274-26196324	CMK	blood:	n/a
46	chr7:26192199-26192249	GM12891	blood:	n/a
47	chr7:26188268-26188318	HCM	heart:	n/a
48	chr7:26156403-26156453	HCT-116	colon:	n/a
49	chr7:26192756-26192806	AG09309	skin:	n/a
50	chr7:26191696-26191746	GM12878	blood:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:26166131..26167830-chr7:26224029..26225600,2	K562	blood:
2	chr7:26218241..26220346-chr7:26316988..26319565,2	K562	blood:
3	chr7:26189963..26195377-chr7:26195444..26205125,17	K562	blood:
4	chr7:26187762..26202698-chr7:26218693..26233402,42	K562	blood:
5	chr7:26195498..26197303-chr7:26213085..26215858,2	MCF-7	breast:
6	chr7:26171147..26177551-chr7:26225022..26228862,6	K562	blood:
7	chr7:26186252..26188116-chr7:26188165..26190170,2	K562	blood:
8	chr7:26179857..26181935-chr7:26183757..26186621,2	MCF-7	breast:
9	chr7:26205548..26209207-chr7:26238110..26241194,3	MCF-7	breast:
10	chr7:26154961..26157764-chr7:26173715..26175460,2	MCF-7	breast:
11	chr7:26152221..26157308-chr7:26225005..26229751,7	K562	blood:
12	chr7:26180704..26182826-chr7:26222240..26224296,2	K562	blood:
13	chr7:26204181..26207055-chr7:26208718..26211585,2	K562	blood:
14	chr7:26149919..26152511-chr7:26155274..26157717,3	K562	blood:
15	chr7:26204554..26206378-chr7:26234760..26236409,2	MCF-7	breast:
16	chr7:25931446..25933941-chr7:26194696..26196288,2	K562	blood:
17	chr7:26195366..26198244-chr7:26238444..26241052,4	MCF-7	breast:
18	chr7:26205194..26207129-chr7:26211869..26214201,2	K562	blood:
19	chr7:26135924..26137855-chr7:26144469..26146230,4	MCF-7	breast:
20	chr7:26212218..26214993-chr7:26226282..26231933,7	K562	blood:
21	chr7:26208099..26210370-chr7:26211210..26213726,2	K562	blood:
22	chr7:26149910..26152831-chr7:26237358..26241131,4	MCF-7	breast:
23	chr7:26138953..26140614-chr7:26142057..26143746,2	K562	blood:
24	chr7:26212776..26215168-chr7:26216411..26218758,2	MCF-7	breast:
25	chr19:16186941..16187691-chr7:26191732..26192335,2	NB4	blood:
26	chr7:26176340..26179625-chr7:26179869..26182859,3	K562	blood:
27	chr7:26190306..26191845-chr7:26238643..26241387,3	K562	blood:
28	chr7:26181706..26184362-chr7:26226921..26229070,2	K562	blood:
29	chr7:26174239..26175923-chr7:26189473..26191347,2	K562	blood:
30	chr7:26196217..26197790-chr7:26198735..26200576,2	K562	blood:
31	chr7:26152455..26156873-chr7:26226826..26229761,5	K562	blood:
32	chr7:26174282..26175870-chr7:26191828..26193448,2	K562	blood:
33	chr7:26191421..26193047-chr7:26221749..26224345,2	MCF-7	breast:
34	chr7:26156563..26159032-chr7:26159643..26162118,2	K562	blood:
35	chr7:26164394..26166417-chr7:26171304..26173771,2	K562	blood:
36	chr7:26217885..26219634-chr7:26219672..26221889,2	MCF-7	breast:
37	chr7:26161276..26164225-chr7:26165809..26167407,2	K562	blood:
38	chr7:26163228..26165901-chr7:26223007..26225996,2	K562	blood:
39	chr7:26148861..26152196-chr7:26192517..26195999,3	K562	blood:
40	chr7:26212301..26214165-chr7:26238438..26240076,2	MCF-7	breast:
41	chr7:26182928..26187601-chr7:26190385..26193241,6	MCF-7	breast:
42	chr7:26202823..26205559-chr7:26239912..26241448,2	K562	blood:
43	chr7:26212943..26215260-chr7:26216372..26218499,2	MCF-7	breast:
44	chr7:26204327..26208311-chr7:26225894..26230203,6	K562	blood:
45	chr7:26188352..26191164-chr7:26239205..26240759,2	MCF-7	breast:
46	chr7:26196259..26200156-chr7:26237694..26241726,5	MCF-7	breast:
47	chr7:26146073..26148941-chr7:26224609..26227830,4	K562	blood:
48	chr7:26184369..26187148-chr7:26227369..26229065,2	K562	blood:
49	chr7:26214375..26216195-chr7:26219360..26221662,2	MCF-7	breast:
50	chr7:26205835..26207422-chr7:26220316..26222090,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPA2B1-7	chr7:26213604-26214402	NONHSAT119618
2	lnc-HNRNPA2B1-3	chr7:26168027-26168087	NONHSAT119617
3	lnc-HNRNPA2B1-2	chr7:26170211-26170398	XLOC_006385
4	lnc-HNRNPA2B1-3	chr7:26170211-26170479	NONHSAT119611
5	lnc-HNRNPA2B1-2	chr7:26167953-26168087	XLOC_006385
6	lnc-HNRNPA2B1-3	chr7:26170211-26170479	NONHSAT119617
7	lnc-HNRNPA2B1-2	chr7:26170211-26170398	XLOC_006385
8	lnc-HNRNPA2B1-3	chr7:26170211-26170479	NONHSAT119612
9	lnc-HNRNPA2B1-2	chr7:26167953-26168090	XLOC_006385
10	lnc-HNRNPA2B1-8	chr7:26190725-26191065	expRegAs_chr7_2078_-
11	lnc-HNRNPA2B1-2	chr7:26170211-26170398	XLOC_006385
12	lnc-CBX3-1	chr7:26208574-26209088	expReg_chr7_1618_+
13	lnc-HNRNPA2B1-7	chr7:26213153-26214565	ENSG00000273237.1

No data

Variant related genes	Relation type
ENSG00000273237	TF binding region
NFE2L3	TF binding region
ENSG00000273237	CpG island
NFE2L3	CpG island
ENSG00000167460	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000050344	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000273237	chromatin interactions
ANKRD52	miRNA target sites

Extended variants
information (count: 2793 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2793 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555675571	chr7:26142395-26142396	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs376160302	chr7:26142401-26142402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369204029	chr7:26142422-26142423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569929444	chr7:26142441-26142442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs55989554	chr7:26142442-26142443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397788016	chr7:26142456-26142457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181433386	chr7:26142499-26142500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6461915	chr7:26142507-26142508	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs373231498	chr7:26142532-26142533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533672635	chr7:26142542-26142543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532928752	chr7:26142563-26142564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4722568	chr7:26142608-26142609	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs4722569	chr7:26142624-26142625	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528651690	chr7:26142629-26142630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539310214	chr7:26142632-26142633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568442308	chr7:26142640-26142641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531092578	chr7:26142690-26142691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550609919	chr7:26142728-26142729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202033769	chr7:26142748-26142749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4722570	chr7:26142755-26142756	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs539560533	chr7:26142756-26142757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553398425	chr7:26142765-26142766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371733339	chr7:26142784-26142785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141607625	chr7:26142908-26142909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535671340	chr7:26142937-26142938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575548398	chr7:26142939-26142940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4722571	chr7:26142963-26142964	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs111599292	chr7:26143035-26143036	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs4722572	chr7:26143066-26143067	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185526747	chr7:26143093-26143094	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs6959296	chr7:26143106-26143107	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs369524746	chr7:26143113-26143114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs143243045	chr7:26143155-26143156	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs4722573	chr7:26143174-26143175	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560388405	chr7:26143198-26143199	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs147506599	chr7:26143238-26143239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371042355	chr7:26143245-26143246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542051570	chr7:26143277-26143278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561935787	chr7:26143318-26143319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375853845	chr7:26143344-26143345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531115008	chr7:26143373-26143374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183541466	chr7:26143463-26143464	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs187304828	chr7:26143570-26143571	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs533331597	chr7:26143758-26143759	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs13247421	chr7:26143888-26143889	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs546040724	chr7:26144010-26144011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78267778	chr7:26144025-26144026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549248192	chr7:26144026-26144027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562660338	chr7:26144051-26144052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376653650	chr7:26144066-26144067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Breast cancer	18852474	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26136400-26142400	Enhancers	Primary T cells fromperipheralblood	blood
2	chr7:26138800-26143600	Enhancers	Placenta	Placenta
3	chr7:26139600-26142400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr7:26140000-26142400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr7:26140400-26142400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
6	chr7:26140600-26142400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:26140600-26142400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
8	chr7:26140600-26142400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:26140600-26142400	Active TSS	Adipose Nuclei	Adipose
10	chr7:26140600-26142400	Flanking Active TSS	GM12878-XiMat	blood
11	chr7:26140800-26142400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:26141000-26142400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:26141000-26142400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:26141000-26142400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr7:26141000-26142400	Active TSS	Right Atrium	heart
16	chr7:26141400-26142400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:26141400-26144800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:26141400-26145000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr7:26141600-26142400	Enhancers	Fetal Kidney	kidney
20	chr7:26141800-26142400	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr7:26141800-26142400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr7:26141800-26143000	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr7:26141800-26143600	Enhancers	Primary B cells from peripheral blood	blood
24	chr7:26142000-26142400	Enhancers	Primary T cells from cord blood	blood
25	chr7:26142000-26142400	Enhancers	Primary hematopoietic stem cells	blood
26	chr7:26142000-26142400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr7:26142000-26142400	Enhancers	Fetal Intestine Large	intestine
28	chr7:26142000-26142600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:26142000-26143200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr7:26142000-26143600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:26142200-26142600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:26142200-26142600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:26142200-26143000	Weak transcription	Primary B cells from cord blood	blood
34	chr7:26142200-26143000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:26142200-26143400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr7:26142200-26144000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:26142200-26145400	Weak transcription	Thymus	Thymus
38	chr7:26142200-26145600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr7:26142200-26145600	Weak transcription	Fetal Thymus	thymus
40	chr7:26142200-26145800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr7:26142200-26156600	Weak transcription	Fetal Intestine Small	intestine
42	chr7:26142400-26142800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr7:26142400-26142800	Weak transcription	Fetal Kidney	kidney
44	chr7:26142400-26143000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr7:26142400-26143400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr7:26142400-26144600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:26142400-26144600	Weak transcription	Adipose Nuclei	Adipose
48	chr7:26142400-26145800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr7:26142400-26145800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr7:26142400-26146000	Enhancers	Primary monocytes fromperipheralblood	blood

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