Variant report

Variant	nsv831160
Chromosome Location	chr7:141009011-141188046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:800)
CpG islands
(count:733)
Chromatin interactive
region (count:76)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:800 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:141042310-141042316	K562	blood:	n/a	n/a
2	ATF1	chr7:141178689-141178794	K562	blood:	n/a	n/a
3	ATF2	chr7:141109711-141110235	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr7:141077247-141077464	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr7:141160547-141160868	K562	blood:	n/a	n/a
6	ATF3	chr7:141077251-141077511	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:141182940-141183177	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:141062874-141063098	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr7:141152913-141153158	GM12878	blood:	n/a	chr7:141153015-141153026
10	BATF	chr7:141152826-141153207	GM12878	blood:	n/a	chr7:141153015-141153026
11	BATF	chr7:141016927-141017222	GM12878	blood:	n/a	n/a
12	BATF	chr7:141182884-141183131	GM12878	blood:	n/a	chr7:141183056-141183066 chr7:141183020-141183031
13	BATF	chr7:141016902-141017172	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:141152910-141153123	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:141141847-141141973	K562	blood:	n/a	chr7:141141899-141141908 chr7:141141900-141141909 chr7:141141899-141141908 chr7:141141893-141141914
16	BRCA1	chr7:141118065-141118155	GM12878	blood:	n/a	n/a
17	BRCA1	chr7:141152165-141152307	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:141059089-141059233	H1-hESC	embryonic stem cell:	n/a	chr7:141059113-141059126 chr7:141059113-141059126 chr7:141059115-141059126
19	CEBPB	chr7:141160566-141160946	K562	blood:	n/a	chr7:141160751-141160762
20	CEBPB	chr7:141160542-141160846	MCF-7	breast:	n/a	chr7:141160751-141160762
21	CEBPB	chr7:141064620-141064820	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:141106291-141106500	HepG2	liver:	n/a	chr7:141106352-141106363
23	CEBPB	chr7:141110967-141111338	A549	lung:	n/a	chr7:141111151-141111162
24	CEBPB	chr7:141077351-141077519	HepG2	liver:	n/a	chr7:141077421-141077432
25	CEBPB	chr7:141077331-141077493	A549	lung:	n/a	chr7:141077421-141077432
26	CEBPB	chr7:141110964-141111339	IMR90	lung:	n/a	chr7:141111151-141111162
27	CEBPB	chr7:141077338-141077530	K562	blood:	n/a	chr7:141077421-141077432
28	CEBPB	chr7:141033180-141033543	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:141111712-141111800	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:141111028-141111311	ECC-1	luminal epithelium:	n/a	chr7:141111151-141111162
31	CEBPB	chr7:141110958-141111360	H1-hESC	embryonic stem cell:	n/a	chr7:141111151-141111162
32	CEBPB	chr7:141098538-141098634	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr7:141111032-141111424	A549	lung:	n/a	chr7:141111151-141111162
34	CEBPB	chr7:141024456-141024802	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:141160574-141160910	A549	lung:	n/a	chr7:141160751-141160762
36	CEBPB	chr7:141077291-141077563	H1-hESC	embryonic stem cell:	n/a	chr7:141077421-141077432
37	CEBPB	chr7:141110977-141111342	Hela-S3	cervix:	n/a	chr7:141111151-141111162
38	CEBPB	chr7:141111027-141111299	MCF-7	breast:	n/a	chr7:141111151-141111162
39	CEBPB	chr7:141110959-141111387	K562	blood:	n/a	chr7:141111151-141111162
40	CEBPB	chr7:141110920-141111305	A549	lung:	n/a	chr7:141111151-141111162
41	CEBPB	chr7:141103292-141103572	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:141160590-141160928	HepG2	liver:	n/a	chr7:141160751-141160762
43	CEBPB	chr7:141139630-141139899	HepG2	liver:	n/a	chr7:141139750-141139759 chr7:141139748-141139759
44	CEBPB	chr7:141160579-141160913	H1-hESC	embryonic stem cell:	n/a	chr7:141160751-141160762
45	CEBPB	chr7:141160556-141160913	K562	blood:	n/a	chr7:141160751-141160762
46	CEBPB	chr7:141111024-141111354	ECC-1	luminal epithelium:	n/a	chr7:141111151-141111162
47	CEBPB	chr7:141139621-141139910	K562	blood:	n/a	chr7:141139750-141139759 chr7:141139748-141139759
48	CEBPB	chr7:141103260-141103563	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:141110974-141111351	K562	blood:	n/a	chr7:141111151-141111162
50	CEBPB	chr7:141160573-141160844	K562	blood:	n/a	chr7:141160751-141160762

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:141130687-141130737	HNPCEpiC	eye:	n/a
2	chr7:141130687-141130737	HNPCEpiC	eye:	n/a
3	chr7:141136170-141136220	HMEC	breast:	n/a
4	chr7:141115018-141115068	NH-A	brain:	n/a
5	chr7:141176413-141176463	CMK	blood:	n/a
6	chr7:141130199-141130249	CMK	blood:	n/a
7	chr7:141175075-141175125	SK-N-SH	brain:	n/a
8	chr7:141130687-141130737	GM06990	blood:	n/a
9	chr7:141176264-141176314	GM19239	blood:	n/a
10	chr7:141108956-141109006	BE2_C	brain:	n/a
11	chr7:141175902-141175952	IMR90	lung:	fetal
12	chr7:141175075-141175125	HCM	heart:	n/a
13	chr7:141175075-141175125	GM12891	blood:	n/a
14	chr7:141130199-141130249	K562	blood:	n/a
15	chr7:141165430-141165480	PrEC	prostate:	n/a
16	chr7:141108956-141109006	ECC-1	luminal epithelium:	n/a
17	chr7:141115018-141115068	PANC-1	pancreas:	n/a
18	chr7:141165430-141165480	A549	lung:	n/a
19	chr7:141175902-141175952	HRPEpiC	eye:	n/a
20	chr7:141175075-141175125	Hepatocyte	liver:	n/a
21	chr7:141130199-141130249	HRCEpiC	kidney:	n/a
22	chr7:141130199-141130249	HNPCEpiC	eye:	n/a
23	chr7:141130687-141130737	ECC-1	luminal epithelium:	n/a
24	chr7:141175075-141175125	AG09319	gingival:	n/a
25	chr7:141130687-141130737	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:141130199-141130249	GM12891	blood:	n/a
27	chr7:141130199-141130249	HMEC	breast:	n/a
28	chr7:141175075-141175125	Caco-2	colon:	n/a
29	chr7:141175902-141175952	HUVEC	blood vessel:	n/a
30	chr7:141175902-141175952	Hepatocyte	liver:	n/a
31	chr7:141130687-141130737	GM12878	blood:	n/a
32	chr7:141108956-141109006	GM12878	blood:	n/a
33	chr7:141130687-141130737	HMEC	breast:	n/a
34	chr7:141024673-141024723	PANC-1	pancreas:	n/a
35	chr7:141115018-141115068	HL-60	blood:	n/a
36	chr7:141176413-141176463	HUVEC	blood vessel:	n/a
37	chr7:141176264-141176314	AG04449	skin:	fetal
38	chr7:141175075-141175125	PrEC	prostate:	n/a
39	chr7:141024673-141024723	ProgFib	skin:	n/a
40	chr7:141175902-141175952	HCF	heart:	n/a
41	chr7:141115018-141115068	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:141115018-141115068	HEK293	kidney:	embryo
43	chr7:141024673-141024723	SK-N-MC	brain:	n/a
44	chr7:141165430-141165480	HRPEpiC	eye:	n/a
45	chr7:141115018-141115068	AG09309	skin:	n/a
46	chr7:141115018-141115068	NHDF-neo	bronchial:	n/a
47	chr7:141136170-141136220	BE2_C	brain:	n/a
48	chr7:141136170-141136220	BJ	skin:	n/a
49	chr7:141130199-141130249	PANC-1	pancreas:	n/a
50	chr7:141024673-141024723	SK-N-SH_RA	brain:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:141139379..141141342-chr7:141160311..141162457,2	MCF-7	breast:
2	chr7:141034745..141035250-chr7:141232846..141233551,2	MCF-7	breast:
3	chr7:141092974..141095041-chr7:141096828..141098850,2	K562	blood:
4	chr7:141181798..141183802-chr7:141196664..141199285,2	K562	blood:
5	chr7:141167941..141170244-chr7:141172525..141175115,2	MCF-7	breast:
6	chr7:141156797..141159784-chr7:141174259..141175958,2	MCF-7	breast:
7	chr7:141144316..141147029-chr7:141147161..141149930,2	K562	blood:
8	chr7:141075863..141077708-chr7:141079059..141080787,2	K562	blood:
9	chr7:141185695..141187643-chr7:141191163..141193243,2	MCF-7	breast:
10	chr7:141186693..141187320-chr7:141233115..141233805,2	MCF-7	breast:
11	chr7:141167941..141170244-chr7:141172525..141175115,2	MCF-7	breast:
12	chr7:141139134..141142034-chr7:141165484..141168427,2	K562	blood:
13	chr7:141169797..141173422-chr7:141175617..141177527,3	K562	blood:
14	chr13:42845563..42848555-chr7:141137680..141139878,2	MCF-7	breast:
15	chr7:140976512..140978529-chr7:141117067..141120019,2	MCF-7	breast:
16	chr7:141104268..141105938-chr7:141109130..141111493,2	K562	blood:
17	chr7:141113173..141114678-chr7:141115849..141118099,2	MCF-7	breast:
18	chr7:141151518..141153052-chr7:141163328..141166045,2	K562	blood:
19	chr7:141180840..141183339-chr7:141185725..141188556,2	MCF-7	breast:
20	chr7:141111204..141113482-chr7:141117735..141120654,3	K562	blood:
21	chr7:141082802..141085142-chr7:141086740..141088714,2	K562	blood:
22	chr7:141087677..141089408-chr7:141091994..141093848,2	K562	blood:
23	chr7:141141171..141143340-chr7:141149747..141151734,2	K562	blood:
24	chr7:141125361..141126933-chr7:141182956..141185699,2	K562	blood:
25	chr7:141029015..141031882-chr7:141078726..141080854,2	K562	blood:
26	chr7:141029015..141031882-chr7:141078726..141080854,2	K562	blood:
27	chr7:141026635..141028691-chr7:141030665..141032279,2	K562	blood:
28	chr7:141183273..141185827-chr7:141188275..141189870,2	K562	blood:
29	chr7:141141171..141143340-chr7:141149747..141151734,2	K562	blood:
30	chr7:141139134..141142034-chr7:141165484..141168427,2	K562	blood:
31	chr7:141161346..141164355-chr7:141165026..141168332,3	K562	blood:
32	chr7:141151518..141153052-chr7:141163328..141166045,2	K562	blood:
33	chr7:141104268..141105938-chr7:141109130..141111493,2	K562	blood:
34	chr7:141087677..141089408-chr7:141091994..141093848,2	K562	blood:
35	chr7:141139379..141141342-chr7:141160311..141162457,2	MCF-7	breast:
36	chr7:141161346..141164355-chr7:141165026..141168332,3	K562	blood:
37	chr7:141149416..141151049-chr7:141154833..141157038,2	MCF-7	breast:
38	chr6:5445214..5446148-chr7:141145714..141146573,2	MCF-7	breast:
39	chr7:141075863..141077708-chr7:141079059..141080787,2	K562	blood:
40	chr7:141156797..141159784-chr7:141174259..141175958,2	MCF-7	breast:
41	chr7:141050550..141052321-chr7:141091904..141093431,2	MCF-7	breast:
42	chr7:141111204..141113482-chr7:141117735..141120654,3	K562	blood:
43	chr7:141125361..141126933-chr7:141182956..141185699,2	K562	blood:
44	chr7:141169797..141173422-chr7:141175617..141177527,3	K562	blood:
45	chr7:141180840..141183339-chr7:141185725..141188556,2	MCF-7	breast:
46	chr7:141090003..141092037-chr7:141092400..141096560,4	K562	blood:
47	chr7:141056651..141059376-chr7:141061286..141063035,2	K562	blood:
48	chr7:141138600..141140845-chr7:141142664..141144473,2	MCF-7	breast:
49	chr7:141079961..141081760-chr7:141089399..141092125,3	K562	blood:
50	chr7:141010882..141013752-chr7:141015205..141017324,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1147-5	chr7:141112379-141113876	XLOC_006624
2	lnc-KIAA1147-6	chr7:141074261-141074414	refGeneNc_2015_NR_015392
3	lnc-KIAA1147-6	chr7:141083652-141083836	refGeneNc_2015_NR_015392
4	lnc-KIAA1147-5	chr7:141115805-141116190	XLOC_006624
5	lnc-KIAA1147-6	chr7:141050607-141052026	refGeneNc_2015_NR_015392
6	lnc-KIAA1147-4	chr7:141129511-141129994	ENSG00000261629.1
7	lnc-AGK-2	chr7:141176431-141180177	NONHSAT123713
8	lnc-AGK-4	chr7:141051777-141052163	NONHSAT123709
9	lnc-KIAA1147-6	chr7:141060458-141060643	refGeneNc_2015_NR_015392
10	lnc-AGK-4	chr7:141052478-141052568	NONHSAT123709
11	lnc-KIAA1147-6	chr7:141070185-141070293	refGeneNc_2015_NR_015392
12	lnc-KIAA1147-5	chr7:141114183-141115235	XLOC_006624
13	lnc-AGK-3	chr7:141110031-141110321	expReg_chr7_11441_+
14	lnc-KIAA1147-5	chr7:141115805-141116190	XLOC_006624
15	lnc-KIAA1147-6	chr7:141084467-141084499	refGeneNc_2015_NR_015392
16	lnc-KIAA1147-4	chr7:141130957-141131068	ENSG00000261629.1
17	lnc-KIAA1147-6	chr7:141073473-141073647	refGeneNc_2015_NR_015392
18	lnc-KIAA1147-5	chr7:141114196-141115235	XLOC_006624

No data

Variant related genes	Relation type
ENSG00000204990	TF binding region
ENSG00000261624	TF binding region
ENSG00000261629	TF binding region
ENSG00000204990	CpG island
ENSG00000261624	CpG island
ENSG00000261629	CpG island
ENSG00000163382	chromatin interactions
ENSG00000023516	chromatin interactions
ENSG00000204990	chromatin interactions
ENSG00000261624	chromatin interactions
TRPS1	miRNA target sites

Extended variants
information (count: 6571 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:6571 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552117016	chr7:141009079-141009080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557964892	chr7:141009100-141009101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570148731	chr7:141009107-141009108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117484847	chr7:141009187-141009188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572942130	chr7:141009189-141009190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145256189	chr7:141009198-141009199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151003975	chr7:141009207-141009208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191179562	chr7:141009209-141009210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139652282	chr7:141009228-141009229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182978895	chr7:141009238-141009239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537500839	chr7:141009247-141009248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572664158	chr7:141009259-141009260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539777815	chr7:141009284-141009285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558108576	chr7:141009303-141009304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576553795	chr7:141009313-141009314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188065822	chr7:141009357-141009358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191708624	chr7:141009375-141009376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs60881706	chr7:141009394-141009395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541980303	chr7:141009395-141009396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577757601	chr7:141009402-141009403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13221383	chr7:141009503-141009504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527568198	chr7:141009583-141009584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs559538045	chr7:141009594-141009595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530128874	chr7:141009623-141009624	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552234655	chr7:141009698-141009699	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554014670	chr7:141009720-141009721	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563728067	chr7:141009743-141009744	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145732146	chr7:141009798-141009799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs57011411	chr7:141009931-141009932	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112542708	chr7:141009962-141009963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567785011	chr7:141009964-141009965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535210563	chr7:141010068-141010069	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547953498	chr7:141010071-141010072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566168069	chr7:141010077-141010078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540124549	chr7:141010098-141010099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs78811808	chr7:141010106-141010107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6944144	chr7:141010114-141010115	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs74193510	chr7:141010116-141010117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78285329	chr7:141010119-141010120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145308370	chr7:141010123-141010124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs79590057	chr7:141010135-141010136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561238554	chr7:141010153-141010154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576616173	chr7:141010155-141010156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6962669	chr7:141010169-141010170	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs531262166	chr7:141010238-141010239	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555820335	chr7:141010247-141010248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574148227	chr7:141010257-141010258	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565382019	chr7:141010341-141010342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187480789	chr7:141010347-141010348	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572186934	chr7:141010371-141010372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Low-grade astrocytoma	19016743	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Melanoma	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1431 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140994400-141018000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:141004600-141014200	Weak transcription	Right Atrium	heart
3	chr7:141005000-141013000	Weak transcription	Right Ventricle	heart
4	chr7:141006200-141012600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:141008800-141011600	Weak transcription	Left Ventricle	heart
6	chr7:141011600-141012000	Enhancers	Left Ventricle	heart
7	chr7:141012000-141013000	Weak transcription	Left Ventricle	heart
8	chr7:141012000-141013400	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr7:141012400-141012800	Enhancers	Brain Germinal Matrix	brain
10	chr7:141012400-141012800	Enhancers	Psoas Muscle	Psoas
11	chr7:141012400-141013400	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr7:141012400-141013800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:141012600-141012800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:141012800-141013200	Weak transcription	Psoas Muscle	Psoas
15	chr7:141013000-141013800	Enhancers	Right Ventricle	heart
16	chr7:141013000-141016000	Enhancers	Left Ventricle	heart
17	chr7:141013200-141013400	Enhancers	Psoas Muscle	Psoas
18	chr7:141013200-141013600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr7:141013400-141017000	Weak transcription	Psoas Muscle	Psoas
20	chr7:141013400-141019800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr7:141013800-141014200	Weak transcription	Right Ventricle	heart
22	chr7:141013800-141016800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr7:141014000-141014200	Enhancers	Fetal Brain Male	brain
24	chr7:141014200-141014400	Enhancers	Right Ventricle	heart
25	chr7:141014200-141014600	Enhancers	Right Atrium	heart
26	chr7:141014200-141018000	Weak transcription	Fetal Brain Male	brain
27	chr7:141014400-141029000	Weak transcription	Right Ventricle	heart
28	chr7:141014600-141025200	Weak transcription	Right Atrium	heart
29	chr7:141015600-141015800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:141015800-141016000	Enhancers	Fetal Brain Female	brain
31	chr7:141015800-141016800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:141016000-141018400	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr7:141016000-141024800	Weak transcription	Fetal Brain Female	brain
34	chr7:141016600-141016800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:141016800-141017400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr7:141016800-141017600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:141016800-141025200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr7:141017000-141017400	Enhancers	Psoas Muscle	Psoas
39	chr7:141017600-141024800	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr7:141018000-141018200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr7:141018000-141019200	Enhancers	Fetal Brain Male	brain
42	chr7:141018200-141019000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr7:141019000-141019200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr7:141019200-141024400	Weak transcription	Fetal Brain Male	brain
45	chr7:141019800-141020400	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr7:141020000-141020400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:141020200-141020400	Enhancers	Left Ventricle	heart
48	chr7:141020400-141025000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr7:141020400-141028200	Weak transcription	Left Ventricle	heart
50	chr7:141020600-141023800	Weak transcription	H1 Cell Line	embryonic stem cell

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