Variant report

Variant	esv3406348
Chromosome Location	chr7:150779369-150781767
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	ARID3A	chr7:150779712-150779985	K562	blood:	n/a	n/a
2	ATF3	chr7:150780402-150780813	K562	blood:	n/a	chr7:150780505-150780514
3	BACH1	chr7:150780634-150781000	K562	blood:	n/a	n/a
4	BACH1	chr7:150780581-150781114	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:150780093-150781029	GM12878	blood:	n/a	chr7:150780784-150780800 chr7:150780733-150780749
6	BHLHE40	chr7:150779972-150780891	K562	blood:	n/a	chr7:150780784-150780800 chr7:150780733-150780749
7	BRCA1	chr7:150780728-150780791	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr7:150780244-150780257	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr7:150780391-150780985	K562	blood:	n/a	n/a
10	CBX3	chr7:150778354-150780326	K562	blood:	n/a	n/a
11	CCNT2	chr7:150779406-150780927	K562	blood:	n/a	chr7:150780134-150780143 chr7:150780800-150780809 chr7:150780128-150780137 chr7:150780394-150780403
12	CEBPB	chr7:150780443-150780709	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:150780452-150780784	K562	blood:	n/a	n/a
14	CEBPB	chr7:150780503-150780826	K562	blood:	n/a	n/a
15	CEBPD	chr7:150779966-150780747	HepG2	liver:	n/a	n/a
16	CHD2	chr7:150780191-150780770	HepG2	liver:	n/a	chr7:150780565-150780575
17	CHD2	chr7:150780237-150780774	H1-hESC	embryonic stem cell:	n/a	chr7:150780565-150780575
18	CHD2	chr7:150780171-150780918	K562	blood:	n/a	chr7:150780565-150780575
19	CHD2	chr7:150779519-150779955	K562	blood:	n/a	n/a
20	CHD2	chr7:150780153-150781086	Hela-S3	cervix:	n/a	chr7:150780565-150780575
21	CHD2	chr7:150779919-150781101	GM12878	blood:	n/a	chr7:150780565-150780575
22	CREB1	chr7:150779897-150781161	K562	blood:	n/a	n/a
23	CREB1	chr7:150776969-150779696	HepG2	liver:	n/a	n/a
24	CREB1	chr7:150779980-150781144	GM12878	blood:	n/a	n/a
25	CREB1	chr7:150780608-150781104	ECC-1	luminal epithelium:	n/a	n/a
26	CREB1	chr7:150779957-150781113	HepG2	liver:	n/a	n/a
27	CREB1	chr7:150780120-150781102	A549	lung:	n/a	n/a
28	CREB1	chr7:150780416-150781067	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:150780683-150780841	GM12878	blood:	n/a	chr7:150780757-150780778 chr7:150780762-150780780
30	CTCF	chr7:150780680-150780830	K562	blood:	n/a	chr7:150780757-150780778 chr7:150780762-150780780
31	CTCF	chr7:150780660-150780810	GM12871	blood:	n/a	chr7:150780757-150780778 chr7:150780762-150780780 chr7:150780669-150780682
32	CTCF	chr7:150780680-150780830	HUVEC	blood vessel:	n/a	chr7:150780757-150780778 chr7:150780762-150780780
33	CTCF	chr7:150780587-150780956	K562	blood:	n/a	chr7:150780757-150780778 chr7:150780762-150780780 chr7:150780669-150780682 chr7:150780937-150780953
34	CTCF	chr7:150779337-150779667	K562	blood:	n/a	n/a
35	CTCF	chr7:150780740-150780893	IMR90	lung:	n/a	chr7:150780757-150780778 chr7:150780762-150780780
36	CTCF	chr7:150780700-150780850	HEK293	kidney:	n/a	chr7:150780757-150780778 chr7:150780762-150780780
37	CTCF	chr7:150780640-150780790	GM12878	blood:	n/a	chr7:150780757-150780778 chr7:150780762-150780780 chr7:150780669-150780682
38	CTCF	chr7:150780676-150780881	K562	blood:	n/a	chr7:150780757-150780778 chr7:150780762-150780780
39	CTCF	chr7:150779264-150779539	T-47D	breast:	n/a	n/a
40	E2F4	chr7:150779996-150780081	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr7:150780554-150780770	MCF10A-Er-Src	breast:	n/a	chr7:150780563-150780574 chr7:150780569-150780578
42	E2F4	chr7:150780031-150781070	K562	blood:	n/a	chr7:150780134-150780143 chr7:150780424-150780436 chr7:150780483-150780492 chr7:150780314-150780323 chr7:150780563-150780574 chr7:150780569-150780578
43	E2F6	chr7:150780382-150780948	K562	blood:	n/a	chr7:150780424-150780436 chr7:150780483-150780492 chr7:150780569-150780578
44	E2F6	chr7:150780392-150780810	K562	blood:	n/a	chr7:150780424-150780436 chr7:150780483-150780492 chr7:150780569-150780578
45	E2F6	chr7:150777236-150780026	K562	blood:	n/a	chr7:150777982-150777991 chr7:150778035-150778042 chr7:150778130-150778139
46	E2F6	chr7:150779593-150779823	K562	blood:	n/a	n/a
47	E2F6	chr7:150779193-150779433	K562	blood:	n/a	n/a
48	E2F6	chr7:150778197-150779589	K562	blood:	n/a	n/a
49	E2F6	chr7:150780120-150780838	K562	blood:	n/a	chr7:150780134-150780143 chr7:150780424-150780436 chr7:150780483-150780492 chr7:150780314-150780323 chr7:150780569-150780578
50	EBF1	chr7:150780626-150780822	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150779710-150779760	Caco-2	colon:	n/a
2	chr7:150779710-150779760	Caco-2	colon:	n/a
3	chr7:150779390-150779440	NHDF-neo	bronchial:	n/a
4	chr7:150780797-150780847	T-47D	breast:	n/a
5	chr7:150780657-150780707	ProgFib	skin:	n/a
6	chr7:150779334-150779384	AG09309	skin:	n/a
7	chr7:150780784-150780834	HCF	heart:	n/a
8	chr7:150780878-150780928	ProgFib	skin:	n/a
9	chr7:150780510-150780560	SK-N-SH	brain:	n/a
10	chr7:150781341-150781391	BE2_C	brain:	n/a
11	chr7:150780797-150780847	GM12892	blood:	n/a
12	chr7:150780510-150780560	AG04449	skin:	fetal
13	chr7:150781341-150781391	HEK293	kidney:	embryo
14	chr7:150780086-150780136	Hepatocyte	liver:	n/a
15	chr7:150779334-150779384	Hepatocyte	liver:	n/a
16	chr7:150779390-150779440	A549	lung:	n/a
17	chr7:150779710-150779760	HRE	kidney:	n/a
18	chr7:150780657-150780707	BE2_C	brain:	n/a
19	chr7:150780797-150780847	GM12878	blood:	n/a
20	chr7:150780878-150780928	AG10803	skin:	n/a
21	chr7:150780878-150780928	HepG2	liver:	n/a
22	chr7:150780872-150780922	SAEC	small airway:	n/a
23	chr7:150780657-150780707	AG04449	skin:	fetal
24	chr7:150780797-150780847	BJ	skin:	n/a
25	chr7:150779710-150779760	AG09319	gingival:	n/a
26	chr7:150780872-150780922	GM12892	blood:	n/a
27	chr7:150779710-150779760	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:150780878-150780928	Jurkat	blood:	n/a
29	chr7:150779334-150779384	BE2_C	brain:	n/a
30	chr7:150781341-150781391	Jurkat	blood:	n/a
31	chr7:150780086-150780136	HRPEpiC	eye:	n/a
32	chr7:150780872-150780922	HCF	heart:	n/a
33	chr7:150780657-150780707	MCF-7	breast:	n/a
34	chr7:150780872-150780922	AoSMC	blood vessel:	n/a
35	chr7:150781341-150781391	H1-hESC	embryonic stem cell:	embryo
36	chr7:150779334-150779384	AoSMC	blood vessel:	n/a
37	chr7:150780797-150780847	RPTEC	kidney:	n/a
38	chr7:150779710-150779760	NB4	blood:	n/a
39	chr7:150781341-150781391	HCT-116	colon:	n/a
40	chr7:150780878-150780928	H1-hESC	embryonic stem cell:	embryo
41	chr7:150780317-150780367	MCF10A-Er-Src	breast:	n/a
42	chr7:150779390-150779440	HL-60	blood:	n/a
43	chr7:150779334-150779384	HRCEpiC	kidney:	n/a
44	chr7:150780086-150780136	RPTEC	kidney:	n/a
45	chr7:150779710-150779760	BJ	skin:	n/a
46	chr7:150780510-150780560	HIPEpiC	eye:	n/a
47	chr7:150779334-150779384	IMR90	lung:	fetal
48	chr7:150780086-150780136	PANC-1	pancreas:	n/a
49	chr7:150780086-150780136	Jurkat	blood:	n/a
50	chr7:150780086-150780136	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150776319..150779502-chr7:150929825..150933736,3	K562	blood:
2	chr7:150695075..150697082-chr7:150780811..150782403,2	MCF-7	breast:
3	chr7:5568664..5571530-chr7:150777332..150779644,2	MCF-7	breast:
4	chr7:150754830..150755615-chr7:150780087..150780650,2	MCF-7	breast:
5	chr7:150781128..150782793-chr7:150928748..150931080,2	MCF-7	breast:
6	chr1:155049689..155051785-chr7:150780053..150782856,2	MCF-7	breast:

Variant related genes	Relation type
AGAP3	TF binding region
TMUB1	TF binding region
FASTK	TF binding region
AGAP3	CpG island
TMUB1	CpG island
FASTK	CpG island
ENSG00000075624	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000164889	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000033100	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372875041	chr7:150779373-150779374	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs377291570	chr7:150779382-150779383	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs140276178	chr7:150779388-150779389	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs145390788	chr7:150779443-150779444	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs137941603	chr7:150779447-150779448	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs145461493	chr7:150779463-150779464	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs150093605	chr7:150779508-150779509	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs561501779	chr7:150779509-150779510	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs370840691	chr7:150779514-150779515	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs200729897	chr7:150779529-150779530	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs199755955	chr7:150779542-150779543	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs566745055	chr7:150779544-150779545	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs550079227	chr7:150779552-150779553	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs552342919	chr7:150779567-150779568	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs368738720	chr7:150779571-150779572	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs370142456	chr7:150779572-150779573	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs138927705	chr7:150779577-150779578	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs149440789	chr7:150779594-150779595	Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs373854929	chr7:150779612-150779613	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs367740872	chr7:150779615-150779616	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs373776715	chr7:150779668-150779669	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs377010543	chr7:150779683-150779684	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs201041502	chr7:150779695-150779696	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs186527326	chr7:150779710-150779711	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
25	rs148391516	chr7:150779715-150779716	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
26	rs533825008	chr7:150779779-150779780	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs554041646	chr7:150779851-150779852	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs114649980	chr7:150779867-150779868	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs545802307	chr7:150779921-150779922	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs555949492	chr7:150779927-150779928	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs73474675	chr7:150779962-150779963	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs541976955	chr7:150779971-150779972	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs189795429	chr7:150779989-150779990	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs371573527	chr7:150780019-150780020	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs376609921	chr7:150780032-150780033	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs560844770	chr7:150780042-150780043	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
37	rs532374706	chr7:150780068-150780069	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs376478894	chr7:150780132-150780133	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs552557527	chr7:150780133-150780134	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs562769991	chr7:150780137-150780138	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs182439780	chr7:150780169-150780170	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs553061910	chr7:150780178-150780179	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs567872423	chr7:150780225-150780226	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs187963073	chr7:150780245-150780246	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs574484778	chr7:150780343-150780344	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs570737755	chr7:150780403-150780404	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs539384222	chr7:150780432-150780433	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs191009319	chr7:150780436-150780437	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs576156508	chr7:150780526-150780527	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs143982550	chr7:150780530-150780531	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150776200-150779400	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr7:150776400-150780000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
3	chr7:150776800-150781000	Active TSS	H9 Cell Line	embryonic stem cell
4	chr7:150776800-150781200	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr7:150777000-150781000	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr7:150777200-150780600	Active TSS	Small Intestine	intestine
7	chr7:150777200-150780800	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr7:150777600-150780600	Enhancers	Fetal Brain Male	brain
9	chr7:150778000-150779800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:150778000-150779800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr7:150778000-150780000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:150778000-150780000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:150778000-150780000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr7:150778000-150780000	Flanking Active TSS	Liver	Liver
15	chr7:150778000-150780000	Flanking Active TSS	Colonic Mucosa	Colon
16	chr7:150778000-150780000	Flanking Active TSS	Pancreas	Pancrea
17	chr7:150778000-150780000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr7:150778000-150780000	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr7:150778000-150780000	Flanking Active TSS	HUVEC	blood vessel
20	chr7:150778000-150780000	Flanking Active TSS	Osteobl	bone
21	chr7:150778000-150780200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:150778000-150780200	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr7:150778000-150780200	Flanking Active TSS	Fetal Muscle Leg	muscle
24	chr7:150778200-150779400	Enhancers	Fetal Lung	lung
25	chr7:150778200-150779600	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr7:150778200-150779600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr7:150778200-150779600	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
28	chr7:150778200-150779800	Enhancers	Primary B cells from cord blood	blood
29	chr7:150778200-150780000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr7:150778200-150780000	Flanking Active TSS	Hela-S3	cervix
31	chr7:150778200-150780200	Flanking Active TSS	Brain Germinal Matrix	brain
32	chr7:150778400-150779400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:150778400-150779400	Enhancers	Primary T cells from cord blood	blood
34	chr7:150778400-150779400	Enhancers	Primary T cells fromperipheralblood	blood
35	chr7:150778400-150779400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr7:150778400-150779400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:150778400-150779400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:150778400-150779400	Enhancers	Fetal Thymus	thymus
39	chr7:150778400-150779400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr7:150778400-150779600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:150778400-150779600	Enhancers	Primary B cells from peripheral blood	blood
42	chr7:150778400-150779600	Enhancers	Primary hematopoietic stem cells	blood
43	chr7:150778400-150779600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:150778400-150779600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:150778400-150779600	Weak transcription	Aorta	Aorta
46	chr7:150778400-150779600	Enhancers	Brain Substantia Nigra	brain
47	chr7:150778400-150779600	Weak transcription	Fetal Kidney	kidney
48	chr7:150778400-150779800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:150778400-150779800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr7:150778400-150779800	Enhancers	Primary neutrophils fromperipheralblood	blood

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