Variant report

Variant	nsv1032005
Chromosome Location	chr7:26096504-26127670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:26124155-26124371	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:26124122-26124308	K562	blood:	n/a	n/a
3	BACH1	chr7:26118646-26118885	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr7:26101253-26101643	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:26114648-26114915	HepG2	liver:	n/a	chr7:26114765-26114778 chr7:26114767-26114776 chr7:26114761-26114782 chr7:26114766-26114775 chr7:26114767-26114776 chr7:26114768-26114777
6	BHLHE40	chr7:26118652-26118870	K562	blood:	n/a	n/a
7	BHLHE40	chr7:26114691-26114850	GM12878	blood:	n/a	chr7:26114765-26114778 chr7:26114767-26114776 chr7:26114761-26114782 chr7:26114766-26114775 chr7:26114767-26114776 chr7:26114768-26114777
8	BHLHE40	chr7:26114567-26114951	K562	blood:	n/a	chr7:26114765-26114778 chr7:26114767-26114776 chr7:26114761-26114782 chr7:26114766-26114775 chr7:26114767-26114776 chr7:26114768-26114777
9	BHLHE40	chr7:26101343-26101531	K562	blood:	n/a	n/a
10	BHLHE40	chr7:26101304-26101622	GM12878	blood:	n/a	n/a
11	CCNT2	chr7:26114596-26114921	K562	blood:	n/a	n/a
12	CCNT2	chr7:26118676-26118851	K562	blood:	n/a	n/a
13	CEBPB	chr7:26113403-26113603	HepG2	liver:	n/a	chr7:26113507-26113518
14	CEBPB	chr7:26118723-26118989	K562	blood:	n/a	n/a
15	CEBPB	chr7:26121149-26121727	MCF-7	breast:	n/a	n/a
16	CEBPB	chr7:26122768-26123153	MCF-7	breast:	n/a	n/a
17	CEBPB	chr7:26118459-26118991	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:26113425-26113625	H1-hESC	embryonic stem cell:	n/a	chr7:26113507-26113518
19	CHD1	chr7:26101346-26101348	GM12878	blood:	n/a	n/a
20	CREB1	chr7:26118585-26118928	A549	lung:	n/a	n/a
21	CTCF	chr7:26118600-26118750	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr7:26118535-26118832	HepG2	liver:	n/a	n/a
23	CTCF	chr7:26121400-26121550	HepG2	liver:	n/a	n/a
24	CTCF	chr7:26101296-26101616	A549	lung:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
25	CTCF	chr7:26101354-26101661	Spleen_OC	spleen:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
26	CTCF	chr7:26101400-26101550	GM12869	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
27	CTCF	chr7:26118600-26118750	GM12865	blood:	n/a	n/a
28	CTCF	chr7:26101400-26101550	NHDF-neo	bronchial:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
29	CTCF	chr7:26101420-26101570	BJ	skin:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
30	CTCF	chr7:26118620-26118770	AG04449	skin:	n/a	n/a
31	CTCF	chr7:26118640-26118790	AG09309	skin:	n/a	n/a
32	CTCF	chr7:26118600-26118750	GM12864	blood:	n/a	n/a
33	CTCF	chr7:26101368-26101632	Fibrobl	skin:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
34	CTCF	chr7:26118700-26118850	HVMF	connective:	n/a	n/a
35	CTCF	chr7:26101380-26101530	HFF-Myc	foreskin:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
36	CTCF	chr7:26101377-26101624	GM19239	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
37	CTCF	chr7:26101440-26101590	NHEK	skin:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
38	CTCF	chr7:26101420-26101570	K562	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
39	CTCF	chr7:26101420-26101570	HBMEC	blood vessel:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
40	CTCF	chr7:26118560-26118710	HPF	lung:	n/a	n/a
41	CTCF	chr7:26101440-26101590	WERI-Rb-1	eye:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
42	CTCF	chr7:26118583-26118815	GM10266	blood:	n/a	n/a
43	CTCF	chr7:26118620-26118770	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr7:26101378-26101610	MCF-7	breast:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
45	CTCF	chr7:26121440-26121590	HepG2	liver:	n/a	n/a
46	CTCF	chr7:26101367-26101641	LNCaP	prostate:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
47	CTCF	chr7:26105405-26105459	GM12878	blood:	n/a	n/a
48	CTCF	chr7:26101862-26101873	GM12891	blood:	n/a	n/a
49	CTCF	chr7:26104520-26104670	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:26121292-26121592	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:26112215-26112265	MCF-7	breast:	n/a
2	chr7:26112215-26112265	GM06990	blood:	n/a
3	chr7:26119300-26119350	SK-N-MC	brain:	n/a
4	chr7:26112215-26112265	GM12891	blood:	n/a
5	chr7:26112215-26112265	SK-N-SH_RA	brain:	n/a
6	chr7:26112215-26112265	ProgFib	skin:	n/a
7	chr7:26119300-26119350	U87	brain:	n/a
8	chr7:26112215-26112265	HL-60	blood:	n/a
9	chr7:26119300-26119350	ovcar-3	ovarian:	n/a
10	chr7:26112215-26112265	HCF	heart:	n/a
11	chr7:26119300-26119350	GM12878	blood:	n/a
12	chr7:26119300-26119350	HEEpiC	esophagus:	n/a
13	chr7:26112215-26112265	LNCaP	prostate:	n/a
14	chr7:26112215-26112265	H1-hESC	embryonic stem cell:	embryo
15	chr7:26112215-26112265	AG09309	skin:	n/a
16	chr7:26112215-26112265	HIPEpiC	eye:	n/a
17	chr7:26119300-26119350	HepG2	liver:	n/a
18	chr7:26119300-26119350	SAEC	small airway:	n/a
19	chr7:26112215-26112265	HEEpiC	esophagus:	n/a
20	chr7:26119300-26119350	H1-hESC	embryonic stem cell:	embryo
21	chr7:26119300-26119350	SK-N-SH	brain:	n/a
22	chr7:26119300-26119350	PANC-1	pancreas:	n/a
23	chr7:26112215-26112265	PFSK-1	brain:	n/a
24	chr7:26119300-26119350	NHBE	bronchial:	n/a
25	chr7:26112215-26112265	NT2-D1	testis:	n/a
26	chr7:26112215-26112265	HRE	kidney:	n/a
27	chr7:26112215-26112265	Hepatocyte	liver:	n/a
28	chr7:26119300-26119350	AG09319	gingival:	n/a
29	chr7:26119300-26119350	HCM	heart:	n/a
30	chr7:26112215-26112265	BJ	skin:	n/a
31	chr7:26119300-26119350	BJ	skin:	n/a
32	chr7:26119300-26119350	Caco-2	colon:	n/a
33	chr7:26119300-26119350	GM12891	blood:	n/a
34	chr7:26119300-26119350	PrEC	prostate:	n/a
35	chr7:26112215-26112265	HUVEC	blood vessel:	n/a
36	chr7:26119300-26119350	HRE	kidney:	n/a
37	chr7:26119300-26119350	K562	blood:	n/a
38	chr7:26119300-26119350	Jurkat	blood:	n/a
39	chr7:26119300-26119350	Hela-S3	cervix:	n/a
40	chr7:26112215-26112265	MCF10A-Er-Src	breast:	n/a
41	chr7:26119300-26119350	HAEpiC	amniotic membrane:	n/a
42	chr7:26112215-26112265	T-47D	breast:	n/a
43	chr7:26112215-26112265	GM19239	blood:	n/a
44	chr7:26112215-26112265	BE2_C	brain:	n/a
45	chr7:26119300-26119350	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:26119300-26119350	RPTEC	kidney:	n/a
47	chr7:26112215-26112265	AG10803	skin:	n/a
48	chr7:26112215-26112265	IMR90	lung:	fetal
49	chr7:26119300-26119350	AG09309	skin:	n/a
50	chr7:26112215-26112265	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:26109451..26111180-chr7:26113272..26116179,2	MCF-7	breast:
2	chr7:26112064..26114800-chr7:26118641..26120981,2	K562	blood:
3	chr7:26121331..26123679-chr7:26220972..26223224,2	MCF-7	breast:
4	chr7:26100956..26102621-chr7:26104473..26107390,2	K562	blood:
5	chr7:26122863..26125751-chr7:26125996..26128926,3	K562	blood:
6	chr7:26120022..26122895-chr7:26235605..26238728,3	MCF-7	breast:
7	chr7:26110644..26115952-chr7:26225900..26230055,7	K562	blood:
8	chr7:26126882..26129598-chr7:26130419..26133130,2	K562	blood:
9	chr7:26112064..26114800-chr7:26118641..26120981,2	K562	blood:
10	chr7:26126305..26129045-chr7:26235519..26238243,2	MCF-7	breast:
11	chr7:25990207..25991830-chr7:26094178..26097069,2	MCF-7	breast:
12	chr7:26119926..26122266-chr7:26227984..26229588,2	MCF-7	breast:
13	chr7:26111175..26113730-chr7:26115998..26118801,2	MCF-7	breast:
14	chr7:26124079..26126684-chr7:26237086..26240273,4	MCF-7	breast:
15	chr7:25935063..25935626-chr7:26100854..26101524,2	K562	blood:
16	chr7:25989381..25991698-chr7:26116313..26118529,2	K562	blood:
17	chr6:8102268..8102945-chr7:26101163..26101679,2	HCT-116	colon:
18	chr7:26108059..26110541-chr7:26114751..26116494,2	K562	blood:
19	chr7:26107192..26109459-chr7:26238936..26241371,3	MCF-7	breast:
20	chr7:25989811..25992726-chr7:26096097..26097704,2	MCF-7	breast:
21	chr7:26111985..26114950-chr7:26225900..26229450,4	K562	blood:
22	chr7:26116496..26120025-chr7:26124167..26127570,3	MCF-7	breast:
23	chr7:26118254..26119023-chr7:26227436..26228387,2	MCF-7	breast:
24	chr7:26117230..26119075-chr7:26243956..26245762,2	K562	blood:
25	chr7:26044346..26047065-chr7:26096452..26098804,2	MCF-7	breast:
26	chr7:26126033..26128739-chr7:26129365..26131958,3	MCF-7	breast:
27	chr7:26127005..26130353-chr7:26231092..26235350,4	MCF-7	breast:
28	chr7:26122079..26124239-chr7:26127253..26128768,2	MCF-7	breast:
29	chr7:26112324..26114738-chr7:26221263..26223725,2	MCF-7	breast:
30	chr7:26100956..26102621-chr7:26104473..26107390,2	K562	blood:
31	chr7:26117300..26119853-chr7:26222397..26224212,2	MCF-7	breast:
32	chr7:26122079..26124239-chr7:26127253..26128768,2	MCF-7	breast:
33	chr7:26125161..26128089-chr7:26129488..26132458,4	MCF-7	breast:
34	chr7:26126753..26129598-chr7:26130419..26132828,3	K562	blood:
35	chr7:26126507..26129554-chr7:26238695..26242281,4	K562	blood:
36	chr7:26122995..26125751-chr7:26126126..26128926,3	K562	blood:
37	chr7:26108042..26110669-chr7:26111318..26113129,2	K562	blood:
38	chr7:26126519..26129493-chr7:26238695..26242874,4	K562	blood:
39	chr7:26127176..26132084-chr7:26132908..26137367,5	K562	blood:
40	chr7:26120211..26123074-chr7:26126513..26128042,2	MCF-7	breast:
41	chr7:26035423..26036364-chr7:26100860..26101483,2	MCF-7	breast:
42	chr7:26096714..26102069-chr7:26240159..26243560,6	MCF-7	breast:
43	chr7:26123460..26125747-chr7:26131738..26134099,3	K562	blood:
44	chr7:26102797..26105180-chr7:26108229..26111038,2	K562	blood:
45	chr7:26102797..26105180-chr7:26108229..26111038,2	K562	blood:
46	chr7:26121372..26122991-chr7:26241151..26242996,2	MCF-7	breast:
47	chr7:26120079..26121816-chr7:26128176..26130468,2	K562	blood:
48	chr7:26125058..26127925-chr7:26238815..26242707,3	MCF-7	breast:
49	chr7:26121029..26121778-chr7:26237338..26237969,2	MCF-7	breast:
50	chr7:25934813..25935616-chr7:26101041..26101955,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPA2B1-3	chr7:26101163-26101262	XLOC_006384
2	lnc-HNRNPA2B1-3	chr7:26097439-26098434	XLOC_006384
3	lnc-HNRNPA2B1-2	chr7:26109126-26109421	XLOC_006385
4	lnc-HNRNPA2B1-2	chr7:26112307-26112316	XLOC_006385
5	lnc-HNRNPA2B1-2	chr7:26109126-26109421	XLOC_006385
6	lnc-HNRNPA2B1-3	chr7:26097832-26098434	NONHSAT119611

Variant related genes	Relation type
ENSG00000266430	TF binding region
ENSG00000266430	CpG island
ENSG00000199085	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000124802	chromatin interactions
ENSG00000050344	chromatin interactions
ENSG00000265818	chromatin interactions
ENSG00000122566	chromatin interactions
ZEB1	miRNA target sites
LRRFIP1	miRNA target sites
ZNF700	miRNA target sites
EP300	miRNA target sites

Extended variants
information (count: 913 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144043322	chr7:26096510-26096511	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557466822	chr7:26096536-26096537	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs57174018	chr7:26096544-26096545	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs539627013	chr7:26096546-26096547	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187078875	chr7:26096617-26096618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572818383	chr7:26096645-26096646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74508143	chr7:26096658-26096659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147293499	chr7:26096741-26096742	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs538021219	chr7:26096745-26096746	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs141057934	chr7:26096753-26096754	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs543855544	chr7:26096758-26096759	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs529969576	chr7:26096801-26096802	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs564217662	chr7:26096824-26096825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs191833594	chr7:26096903-26096904	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs112350691	chr7:26097023-26097024	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs113910475	chr7:26097058-26097059	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144946636	chr7:26097149-26097150	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548943979	chr7:26097150-26097151	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184813489	chr7:26097235-26097236	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs111818872	chr7:26097338-26097339	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73683211	chr7:26097354-26097355	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs570948564	chr7:26097355-26097356	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371177832	chr7:26097358-26097359	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574968207	chr7:26097370-26097371	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs539517158	chr7:26097401-26097402	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145841123	chr7:26097452-26097453	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs376518900	chr7:26097491-26097492	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs543205209	chr7:26097527-26097528	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs535268372	chr7:26097538-26097539	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs555283988	chr7:26097557-26097558	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs554207872	chr7:26097599-26097600	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs148510369	chr7:26097733-26097734	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs557433670	chr7:26097749-26097750	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs372840188	chr7:26097763-26097764	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs577267663	chr7:26097778-26097779	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs546221318	chr7:26097829-26097830	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs577549646	chr7:26097840-26097841	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs376225505	chr7:26097842-26097843	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs561660683	chr7:26097859-26097860	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs190185259	chr7:26097882-26097883	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs370851717	chr7:26097905-26097906	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs560284454	chr7:26097909-26097910	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs562941316	chr7:26097933-26097934	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs193025350	chr7:26097940-26097941	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs542399351	chr7:26097961-26097962	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs142786811	chr7:26098015-26098016	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs531085907	chr7:26098050-26098051	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs151074911	chr7:26098079-26098080	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs564359657	chr7:26098087-26098088	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs185556541	chr7:26098127-26098128	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Breast cancer	18852474	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26091600-26099800	Weak transcription	Gastric	stomach
2	chr7:26093800-26098000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:26096400-26096600	ZNF genes & repeats	Aorta	Aorta
4	chr7:26096400-26097000	Enhancers	Pancreas	Pancrea
5	chr7:26096600-26096800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr7:26096800-26097000	Enhancers	Lung	lung
7	chr7:26096800-26097800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr7:26097000-26100200	Weak transcription	Pancreas	Pancrea
9	chr7:26097800-26098200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr7:26097800-26098200	Enhancers	Spleen	Spleen
11	chr7:26098000-26098200	Bivalent Enhancer	Left Ventricle	heart
12	chr7:26098000-26098200	Bivalent Enhancer	K562	blood
13	chr7:26098000-26098800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:26098200-26098600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:26098200-26101200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr7:26098600-26100200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:26098800-26100000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:26100000-26101000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr7:26100000-26101800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:26100200-26100600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:26100200-26100600	Enhancers	Pancreas	Pancrea
22	chr7:26100200-26100600	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr7:26100200-26100800	Enhancers	Fetal Muscle Leg	muscle
24	chr7:26100200-26101000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:26100200-26101000	Enhancers	Dnd41	blood
26	chr7:26100200-26101400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:26100200-26101400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:26100200-26101400	Enhancers	Colon Smooth Muscle	Colon
29	chr7:26100200-26101400	Enhancers	Fetal Stomach	stomach
30	chr7:26100200-26101800	Enhancers	Brain Germinal Matrix	brain
31	chr7:26100400-26100800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:26100400-26101000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:26100400-26101400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr7:26100400-26101400	Enhancers	Primary hematopoietic stem cells	blood
35	chr7:26100400-26101400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:26100400-26101400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:26100400-26101400	Enhancers	Duodenum Mucosa	Duodenum
38	chr7:26100600-26101400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr7:26100600-26101400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr7:26100600-26101400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:26100600-26101400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr7:26100600-26101400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr7:26100800-26101200	Weak transcription	Fetal Muscle Leg	muscle
44	chr7:26100800-26101400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:26101000-26101200	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr7:26101000-26101400	Enhancers	HMEC	breast
47	chr7:26101000-26101600	Enhancers	Liver	Liver
48	chr7:26101200-26101400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:26101200-26101400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:26101200-26101400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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