Variant report

Variant	nsv1029128
Chromosome Location	chr7:140293389-140335570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:338)
CpG islands
(count:427)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:140304553-140304843	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:140328155-140328321	HepG2	liver:	n/a	n/a
3	ATF1	chr7:140294131-140294412	K562	blood:	n/a	n/a
4	BACH1	chr7:140305279-140305375	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:140305226-140305238	K562	blood:	n/a	n/a
6	BHLHE40	chr7:140294307-140294423	K562	blood:	n/a	n/a
7	BHLHE40	chr7:140326263-140326484	A549	lung:	n/a	n/a
8	BHLHE40	chr7:140326270-140326432	K562	blood:	n/a	n/a
9	BHLHE40	chr7:140326163-140326532	HepG2	liver:	n/a	n/a
10	BHLHE40	chr7:140302625-140302825	K562	blood:	n/a	n/a
11	CEBPB	chr7:140319843-140320131	K562	blood:	n/a	n/a
12	CEBPB	chr7:140304517-140305378	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:140326163-140326711	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:140304759-140305061	A549	lung:	n/a	n/a
15	CEBPB	chr7:140328069-140328399	K562	blood:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
16	CEBPB	chr7:140303968-140304287	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:140320552-140320725	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:140304723-140305065	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:140321523-140321878	IMR90	lung:	n/a	chr7:140321686-140321697
20	CEBPB	chr7:140319839-140320079	K562	blood:	n/a	n/a
21	CEBPB	chr7:140319888-140320027	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:140326019-140326784	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr7:140319097-140319403	IMR90	lung:	n/a	chr7:140319262-140319273
24	CEBPB	chr7:140295444-140295641	K562	blood:	n/a	n/a
25	CEBPB	chr7:140319831-140320070	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:140311198-140311885	IMR90	lung:	n/a	chr7:140311288-140311299 chr7:140311694-140311705
27	CEBPB	chr7:140311278-140311328	HepG2	liver:	n/a	chr7:140311288-140311299
28	CEBPB	chr7:140311680-140311737	HepG2	liver:	n/a	chr7:140311694-140311705
29	CEBPB	chr7:140319091-140319411	K562	blood:	n/a	chr7:140319262-140319273
30	CEBPB	chr7:140328062-140328390	A549	lung:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
31	CEBPB	chr7:140311598-140311835	A549	lung:	n/a	chr7:140311694-140311705
32	CEBPB	chr7:140316313-140316446	K562	blood:	n/a	n/a
33	CEBPB	chr7:140328089-140328416	K562	blood:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
34	CEBPB	chr7:140311251-140312070	K562	blood:	n/a	chr7:140311288-140311299 chr7:140311694-140311705
35	CEBPB	chr7:140328069-140328312	HepG2	liver:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
36	CEBPB	chr7:140327268-140327562	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:140328005-140328367	A549	lung:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
38	CEBPB	chr7:140328062-140328444	HepG2	liver:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
39	CEBPB	chr7:140328036-140328357	MCF-7	breast:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
40	CEBPB	chr7:140328095-140328315	HepG2	liver:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
41	CEBPB	chr7:140328038-140328446	IMR90	lung:	n/a	chr7:140328252-140328261 chr7:140328251-140328262 chr7:140328250-140328263 chr7:140328250-140328261
42	CEBPB	chr7:140319087-140319402	HepG2	liver:	n/a	chr7:140319262-140319273
43	CEBPB	chr7:140331427-140331570	IMR90	lung:	n/a	n/a
44	CEBPD	chr7:140328117-140328313	HepG2	liver:	n/a	chr7:140328251-140328262
45	CHD2	chr7:140335442-140335735	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr7:140325984-140326503	A549	lung:	n/a	n/a
47	CTCF	chr7:140312880-140313030	GM12868	blood:	n/a	n/a
48	CTCF	chr7:140305200-140305350	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:140305320-140305470	HFF	foreskin:	n/a	n/a
50	CTCF	chr7:140295599-140295604	MCF-7	breast:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140303471-140303521	K562	blood:	n/a
2	chr7:140302680-140302730	U87	brain:	n/a
3	chr7:140306908-140306958	AG04449	skin:	fetal
4	chr7:140305368-140305418	HRCEpiC	kidney:	n/a
5	chr7:140296664-140296714	SAEC	small airway:	n/a
6	chr7:140306908-140306958	HRPEpiC	eye:	n/a
7	chr7:140305368-140305418	T-47D	breast:	n/a
8	chr7:140296664-140296714	SK-N-SH	brain:	n/a
9	chr7:140301450-140301500	U87	brain:	n/a
10	chr7:140301450-140301500	Hela-S3	cervix:	n/a
11	chr7:140306908-140306958	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:140302727-140302777	GM12878	blood:	n/a
13	chr7:140296664-140296714	NB4	blood:	n/a
14	chr7:140301450-140301500	SAEC	small airway:	n/a
15	chr7:140301450-140301500	K562	blood:	n/a
16	chr7:140306908-140306958	SK-N-SH_RA	brain:	n/a
17	chr7:140302680-140302730	Jurkat	blood:	n/a
18	chr7:140302727-140302777	MCF-7	breast:	n/a
19	chr7:140296664-140296714	RPTEC	kidney:	n/a
20	chr7:140303471-140303521	MCF10A-Er-Src	breast:	n/a
21	chr7:140302727-140302777	NT2-D1	testis:	n/a
22	chr7:140302727-140302777	HEK293	kidney:	embryo
23	chr7:140302680-140302730	NT2-D1	testis:	n/a
24	chr7:140296664-140296714	Jurkat	blood:	n/a
25	chr7:140305368-140305418	AG04450	lung:	fetal
26	chr7:140306908-140306958	HRCEpiC	kidney:	n/a
27	chr7:140306908-140306958	K562	blood:	n/a
28	chr7:140302727-140302777	NH-A	brain:	n/a
29	chr7:140302680-140302730	BJ	skin:	n/a
30	chr7:140305368-140305418	AG09309	skin:	n/a
31	chr7:140301450-140301500	HCT-116	colon:	n/a
32	chr7:140301450-140301500	MCF10A-Er-Src	breast:	n/a
33	chr7:140296664-140296714	AoSMC	blood vessel:	n/a
34	chr7:140302680-140302730	Caco-2	colon:	n/a
35	chr7:140302727-140302777	BE2_C	brain:	n/a
36	chr7:140302727-140302777	Jurkat	blood:	n/a
37	chr7:140302680-140302730	ProgFib	skin:	n/a
38	chr7:140306908-140306958	BJ	skin:	n/a
39	chr7:140302680-140302730	H1-hESC	embryonic stem cell:	embryo
40	chr7:140301450-140301500	RPTEC	kidney:	n/a
41	chr7:140306908-140306958	HIPEpiC	eye:	n/a
42	chr7:140303471-140303521	U87	brain:	n/a
43	chr7:140303471-140303521	SK-N-SH	brain:	n/a
44	chr7:140303471-140303521	T-47D	breast:	n/a
45	chr7:140306908-140306958	U87	brain:	n/a
46	chr7:140296664-140296714	HRCEpiC	kidney:	n/a
47	chr7:140301450-140301500	SK-N-MC	brain:	n/a
48	chr7:140305368-140305418	U87	brain:	n/a
49	chr7:140302727-140302777	BJ	skin:	n/a
50	chr7:140306908-140306958	PFSK-1	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:140293470..140295582-chr7:140296257..140297930,2	MCF-7	breast:
2	chr7:140316179..140319018-chr7:140328202..140329746,2	MCF-7	breast:
3	chr7:140287756..140290360-chr7:140292366..140296132,3	K562	blood:
4	chr7:140320485..140322777-chr7:140324198..140327820,3	K562	blood:
5	chr7:140283049..140285377-chr7:140334649..140337248,2	K562	blood:
6	chr7:140326135..140327836-chr7:140331660..140333245,2	K562	blood:
7	chr7:140288394..140290360-chr7:140293265..140296132,2	K562	blood:
8	chr7:140326135..140328395-chr7:140330259..140333160,2	K562	blood:
9	chr7:140319770..140321765-chr7:140333430..140335076,2	K562	blood:
10	chr7:140326135..140327836-chr7:140331660..140333245,2	K562	blood:
11	chr7:140306776..140309175-chr7:140310789..140312888,2	K562	blood:
12	chr7:140304917..140305573-chr7:140352877..140353424,2	MCF-7	breast:
13	chr7:140316179..140319018-chr7:140328202..140329746,2	MCF-7	breast:
14	chr7:140295798..140297761-chr7:140298299..140300028,2	K562	blood:
15	chr7:140299787..140302664-chr7:140303935..140306575,2	K562	blood:
16	chr7:140296522..140298552-chr7:140299428..140301578,2	MCF-7	breast:
17	chr7:140296522..140298552-chr7:140299428..140301578,2	MCF-7	breast:
18	chr7:140293470..140295582-chr7:140296257..140297930,2	MCF-7	breast:
19	chr7:140319770..140321765-chr7:140333430..140335076,2	K562	blood:
20	chr7:140323962..140324769-chr7:140346590..140347490,2	MCF-7	breast:
21	chr7:140320485..140322777-chr7:140324198..140327820,3	K562	blood:
22	chr7:140330889..140333777-chr7:140334738..140338747,3	K562	blood:
23	chr7:140330889..140333777-chr7:140334738..140338747,3	K562	blood:
24	chr7:140177738..140180621-chr7:140323233..140327044,4	MCF-7	breast:
25	chr7:140295798..140297761-chr7:140298299..140300028,2	K562	blood:
26	chr7:140285688..140288608-chr7:140322285..140325056,3	MCF-7	breast:
27	chr7:140323886..140324547-chr7:140338246..140338841,2	MCF-7	breast:
28	chr7:140314792..140316521-chr7:140318510..140320433,2	K562	blood:
29	chr7:140299787..140302664-chr7:140303935..140306575,2	K562	blood:
30	chr7:140301959..140304839-chr7:140305867..140308448,2	MCF-7	breast:
31	chr7:140314792..140316521-chr7:140318510..140320433,2	K562	blood:
32	chr7:140326135..140328395-chr7:140330259..140333160,2	K562	blood:
33	chr7:140306776..140309175-chr7:140310789..140312888,2	K562	blood:
34	chr7:140296966..140299312-chr7:140301445..140303256,2	K562	blood:
35	chr7:140224000..140226834-chr7:140322770..140324470,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000201354	TF binding region
DENND2A	TF binding region
ENSG00000201354	CpG island
DENND2A	CpG island
ENSG00000146966	chromatin interactions
ENSG00000133606	chromatin interactions

Extended variants
information (count: 1656 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544012560	chr7:140293390-140293391	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562610039	chr7:140293448-140293449	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77022550	chr7:140293458-140293459	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141184622	chr7:140293476-140293477	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560051847	chr7:140293484-140293485	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188228716	chr7:140293572-140293573	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552098240	chr7:140293576-140293577	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564016709	chr7:140293635-140293636	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561529208	chr7:140293683-140293684	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113149894	chr7:140293698-140293699	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549530429	chr7:140293711-140293712	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370516056	chr7:140293713-140293714	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78824837	chr7:140293714-140293715	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568483766	chr7:140293781-140293782	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535896556	chr7:140293808-140293809	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4448176	chr7:140293809-140293810	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28678005	chr7:140293831-140293832	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs539840358	chr7:140293857-140293858	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558518092	chr7:140293891-140293892	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138760151	chr7:140293892-140293893	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537659944	chr7:140293899-140293900	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377181547	chr7:140293902-140293903	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148958098	chr7:140293910-140293911	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574455387	chr7:140293927-140293928	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369857081	chr7:140293987-140293988	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373372376	chr7:140293997-140293998	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200878125	chr7:140294001-140294002	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533037959	chr7:140294017-140294018	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370493808	chr7:140294043-140294044	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184016443	chr7:140294051-140294052	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374200553	chr7:140294096-140294097	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76733497	chr7:140294122-140294123	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74759847	chr7:140294123-140294124	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571735385	chr7:140294199-140294200	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545377854	chr7:140294206-140294207	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs564055347	chr7:140294209-140294210	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs550651038	chr7:140294258-140294259	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs551335418	chr7:140294269-140294270	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs562690997	chr7:140294293-140294294	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs531473370	chr7:140294366-140294367	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs549569186	chr7:140294370-140294371	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs74566475	chr7:140294404-140294405	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562676200	chr7:140294421-140294422	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190053649	chr7:140294430-140294431	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370913806	chr7:140294437-140294438	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143759742	chr7:140294440-140294441	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539878968	chr7:140294446-140294447	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551769333	chr7:140294448-140294449	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138496109	chr7:140294466-140294467	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74558397	chr7:140294487-140294488	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	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

Chromatin state (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140247000-140297400	Weak transcription	Spleen	Spleen
2	chr7:140263800-140303600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:140263800-140303600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr7:140263800-140305200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:140263800-140305600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:140265200-140304400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr7:140267800-140300800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr7:140267800-140326000	Weak transcription	Gastric	stomach
9	chr7:140269400-140306600	Weak transcription	Right Atrium	heart
10	chr7:140274000-140301400	Weak transcription	Right Ventricle	heart
11	chr7:140276600-140296200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:140279800-140302000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:140281400-140294600	Weak transcription	Fetal Intestine Small	intestine
14	chr7:140281600-140306400	Weak transcription	Brain Angular Gyrus	brain
15	chr7:140281800-140304200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr7:140285800-140297400	Weak transcription	NHDF-Ad	bronchial
17	chr7:140285800-140301400	Weak transcription	Left Ventricle	heart
18	chr7:140285800-140306400	Weak transcription	Colon Smooth Muscle	Colon
19	chr7:140286000-140304000	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr7:140286600-140299800	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr7:140286600-140300000	Weak transcription	Fetal Intestine Large	intestine
22	chr7:140287000-140299600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:140287200-140295800	Weak transcription	Brain Anterior Caudate	brain
24	chr7:140287200-140296200	Weak transcription	NH-A	brain
25	chr7:140287400-140295600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:140287400-140300000	Weak transcription	Brain Hippocampus Middle	brain
27	chr7:140287400-140301400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr7:140287400-140301400	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr7:140287600-140293800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:140287600-140294200	Weak transcription	Ovary	ovary
31	chr7:140287600-140295200	Weak transcription	NHLF	lung
32	chr7:140287600-140295400	Weak transcription	Placenta	Placenta
33	chr7:140287600-140299800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:140287600-140299800	Weak transcription	Fetal Brain Female	brain
35	chr7:140287600-140300800	Weak transcription	Brain Substantia Nigra	brain
36	chr7:140287600-140301400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr7:140287600-140301400	Weak transcription	Adipose Nuclei	Adipose
38	chr7:140287600-140301400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr7:140287600-140304800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr7:140287600-140305600	Weak transcription	Stomach Smooth Muscle	stomach
41	chr7:140287600-140326000	Weak transcription	Fetal Brain Male	brain
42	chr7:140287800-140295800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr7:140288000-140295400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:140288200-140299800	Weak transcription	Brain Germinal Matrix	brain
45	chr7:140288400-140294600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:140290400-140294400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:140291000-140299600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr7:140291200-140294200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:140291400-140295600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:140291600-140297000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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