Variant report

Variant	nsv888826
Chromosome Location	chr7:101230768-101277334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:736)
CpG islands
(count:611)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101245724-101245971	HepG2	liver:	n/a	n/a
2	ATF1	chr7:101238094-101238243	K562	blood:	n/a	n/a
3	ATF3	chr7:101230683-101230956	K562	blood:	n/a	n/a
4	BHLHE40	chr7:101245709-101246072	K562	blood:	n/a	n/a
5	BHLHE40	chr7:101245701-101246022	GM12878	blood:	n/a	n/a
6	BRCA1	chr7:101245819-101246007	HepG2	liver:	n/a	n/a
7	CBX3	chr7:101275855-101276304	K562	blood:	n/a	n/a
8	CBX3	chr7:101230583-101231078	K562	blood:	n/a	n/a
9	CBX3	chr7:101263705-101263991	K562	blood:	n/a	n/a
10	CCNT2	chr7:101245808-101246087	K562	blood:	n/a	n/a
11	CEBPB	chr7:101238692-101239000	HepG2	liver:	n/a	chr7:101238847-101238858
12	CEBPB	chr7:101240325-101240479	H1-hESC	embryonic stem cell:	n/a	chr7:101240359-101240370
13	CEBPB	chr7:101238716-101238945	A549	lung:	n/a	chr7:101238847-101238858
14	CEBPB	chr7:101240268-101240492	Hela-S3	cervix:	n/a	chr7:101240359-101240370
15	CEBPB	chr7:101240222-101240513	A549	lung:	n/a	chr7:101240359-101240370
16	CEBPB	chr7:101240174-101240501	K562	blood:	n/a	chr7:101240359-101240370
17	CEBPB	chr7:101240178-101240495	A549	lung:	n/a	chr7:101240359-101240370
18	CEBPB	chr7:101238750-101238959	IMR90	lung:	n/a	chr7:101238847-101238858
19	CEBPB	chr7:101240139-101240501	MCF-7	breast:	n/a	chr7:101240359-101240370
20	CEBPB	chr7:101268069-101268201	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:101240214-101240518	IMR90	lung:	n/a	chr7:101240359-101240370
22	CEBPB	chr7:101248559-101248594	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:101240171-101240524	K562	blood:	n/a	chr7:101240359-101240370
24	CEBPB	chr7:101238763-101238974	K562	blood:	n/a	chr7:101238847-101238858
25	CEBPB	chr7:101240201-101240536	HepG2	liver:	n/a	chr7:101240359-101240370
26	CHD2	chr7:101245769-101246045	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr7:101245821-101246010	GM12878	blood:	n/a	n/a
28	CHD2	chr7:101258453-101258643	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr7:101242163-101242305	HepG2	liver:	n/a	n/a
30	CHD2	chr7:101245738-101246094	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:101267977-101268203	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr7:101245866-101245976	K562	blood:	n/a	n/a
33	CHD2	chr7:101268599-101268747	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr7:101245762-101246027	A549	lung:	n/a	n/a
35	CREB1	chr7:101241533-101242488	HepG2	liver:	n/a	chr7:101242169-101242182
36	CTBP2	chr7:101252049-101252633	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr7:101267763-101268319	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr7:101245716-101246055	A549	lung:	n/a	chr7:101245860-101245881 chr7:101245859-101245875 chr7:101245858-101245876
39	CTCF	chr7:101245780-101245930	WERI-Rb-1	eye:	n/a	chr7:101245860-101245881 chr7:101245859-101245875 chr7:101245858-101245876
40	CTCF	chr7:101251980-101252130	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr7:101245780-101245930	NHEK	skin:	n/a	chr7:101245860-101245881 chr7:101245859-101245875 chr7:101245858-101245876
42	CTCF	chr7:101245340-101245490	HVMF	connective:	n/a	n/a
43	CTCF	chr7:101268514-101268694	H1-hESC	embryonic stem cell:	n/a	chr7:101268601-101268610
44	CTCF	chr7:101245700-101245850	HMEC	breast:	n/a	n/a
45	CTCF	chr7:101245780-101245930	BE2_C	brain:	n/a	chr7:101245860-101245881 chr7:101245859-101245875 chr7:101245858-101245876
46	CTCF	chr7:101245800-101245950	GM12872	blood:	n/a	chr7:101245860-101245881 chr7:101245859-101245875 chr7:101245858-101245876
47	CTCF	chr7:101245723-101246014	GM19239	blood:	n/a	chr7:101245860-101245881 chr7:101245859-101245875 chr7:101245858-101245876
48	CTCF	chr7:101268400-101268550	HCM	heart:	n/a	n/a
49	CTCF	chr7:101252152-101252207	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr7:101245420-101245570	GM12874	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101273741-101273791	NH-A	brain:	n/a
2	chr7:101273741-101273791	NH-A	brain:	n/a
3	chr7:101268430-101268480	SK-N-SH	brain:	n/a
4	chr7:101274027-101274077	T-47D	breast:	n/a
5	chr7:101273741-101273791	SK-N-MC	brain:	n/a
6	chr7:101256647-101256697	U87	brain:	n/a
7	chr7:101256647-101256697	HEEpiC	esophagus:	n/a
8	chr7:101272582-101272632	SAEC	small airway:	n/a
9	chr7:101268430-101268480	H1-hESC	embryonic stem cell:	embryo
10	chr7:101272582-101272632	U87	brain:	n/a
11	chr7:101257675-101257725	U87	brain:	n/a
12	chr7:101272515-101272565	AG09309	skin:	n/a
13	chr7:101273741-101273791	AG04449	skin:	fetal
14	chr7:101272515-101272565	HCM	heart:	n/a
15	chr7:101274027-101274077	SAEC	small airway:	n/a
16	chr7:101274027-101274077	SKMC	muscle:	n/a
17	chr7:101272484-101272534	LNCaP	prostate:	n/a
18	chr7:101272484-101272534	PrEC	prostate:	n/a
19	chr7:101268430-101268480	HCPEpiC	choroid plexus:	n/a
20	chr7:101272484-101272534	SAEC	small airway:	n/a
21	chr7:101268430-101268480	HepG2	liver:	n/a
22	chr7:101273741-101273791	HRPEpiC	eye:	n/a
23	chr7:101272484-101272534	SK-N-MC	brain:	n/a
24	chr7:101274037-101274087	HAEpiC	amniotic membrane:	n/a
25	chr7:101274037-101274087	AG09319	gingival:	n/a
26	chr7:101268430-101268480	BE2_C	brain:	n/a
27	chr7:101268430-101268480	SK-N-MC	brain:	n/a
28	chr7:101274037-101274087	SKMC	muscle:	n/a
29	chr7:101274037-101274087	PrEC	prostate:	n/a
30	chr7:101272096-101272146	HIPEpiC	eye:	n/a
31	chr7:101272484-101272534	HCM	heart:	n/a
32	chr7:101272515-101272565	Caco-2	colon:	n/a
33	chr7:101273741-101273791	K562	blood:	n/a
34	chr7:101272582-101272632	GM12878	blood:	n/a
35	chr7:101257675-101257725	NHBE	bronchial:	n/a
36	chr7:101257675-101257725	AoSMC	blood vessel:	n/a
37	chr7:101272484-101272534	HAEpiC	amniotic membrane:	n/a
38	chr7:101257675-101257725	NT2-D1	testis:	n/a
39	chr7:101257675-101257725	Hepatocyte	liver:	n/a
40	chr7:101273741-101273791	CMK	blood:	n/a
41	chr7:101274037-101274087	HL-60	blood:	n/a
42	chr7:101272096-101272146	NB4	blood:	n/a
43	chr7:101272484-101272534	HRCEpiC	kidney:	n/a
44	chr7:101272515-101272565	MCF10A-Er-Src	breast:	n/a
45	chr7:101272484-101272534	AoSMC	blood vessel:	n/a
46	chr7:101272582-101272632	NHBE	bronchial:	n/a
47	chr7:101273741-101273791	LNCaP	prostate:	n/a
48	chr7:101268430-101268480	T-47D	breast:	n/a
49	chr7:101274037-101274087	SAEC	small airway:	n/a
50	chr7:101272484-101272534	NT2-D1	testis:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:101264267..101265986-chr7:101459473..101461138,2	MCF-7	breast:
2	chr7:101245631..101247804-chr7:101249820..101253085,4	MCF-7	breast:
3	chr7:101241906..101244609-chr7:101517882..101520597,2	MCF-7	breast:
4	chr7:101242393..101247738-chr7:101456834..101460384,5	MCF-7	breast:
5	chr7:101237649..101239948-chr7:101241103..101242929,2	MCF-7	breast:
6	chr7:101230299..101232623-chr7:101237127..101239473,3	K562	blood:
7	chr7:101239160..101242958-chr7:101243756..101248056,5	MCF-7	breast:
8	chr7:101265195..101267380-chr7:101272779..101275035,3	MCF-7	breast:
9	chr7:101230210..101233751-chr7:101237509..101240350,3	K562	blood:
10	chr7:101207965..101209956-chr7:101246300..101248561,2	MCF-7	breast:
11	chr7:101272795..101275451-chr7:101277536..101279709,2	MCF-7	breast:
12	chr7:101239160..101242958-chr7:101243756..101248056,5	MCF-7	breast:
13	chr7:101232884..101235194-chr7:101237010..101238742,3	K562	blood:
14	chr7:101219940..101222421-chr7:101228950..101232494,3	K562	blood:
15	chr7:101232884..101235194-chr7:101237010..101238742,3	K562	blood:
16	chr7:101255927..101262461-chr7:101262750..101268268,7	MCF-7	breast:
17	chr7:101230659..101232950-chr7:101241327..101243345,2	K562	blood:
18	chr7:101230659..101232950-chr7:101241327..101243345,2	K562	blood:
19	chr7:101230210..101233751-chr7:101237509..101240350,3	K562	blood:
20	chr7:101249674..101252052-chr7:101267585..101269354,2	K562	blood:
21	chr7:101240345..101242548-chr7:101441803..101443372,2	MCF-7	breast:
22	chr7:101255927..101262461-chr7:101262750..101268268,7	MCF-7	breast:
23	chr7:101248988..101252731-chr7:101456839..101459495,3	MCF-7	breast:
24	chr7:101245631..101247804-chr7:101249820..101253085,4	MCF-7	breast:
25	chr7:101252945..101257038-chr7:101259636..101262173,3	MCF-7	breast:
26	chr7:101271948..101273835-chr7:101457651..101460196,2	MCF-7	breast:
27	chr7:101263736..101266044-chr7:101274498..101276590,2	MCF-7	breast:
28	chr7:101230299..101232623-chr7:101237127..101239473,3	K562	blood:
29	chr7:101245522..101246394-chr7:101457419..101458061,2	K562	blood:
30	chr7:101264280..101265109-chr7:101915196..101916107,2	K562	blood:
31	chr1:145400746..145403511-chr7:101258057..101260091,2	MCF-7	breast:
32	chr7:101245559..101246104-chr7:101916727..101917460,2	K562	blood:
33	chr7:101240848..101242506-chr7:101458651..101461014,2	MCF-7	breast:
34	chr7:101245451..101246297-chr7:101914933..101915725,2	MCF-7	breast:
35	chr7:101237649..101239948-chr7:101241103..101242929,2	MCF-7	breast:
36	chr7:101252945..101257038-chr7:101259636..101262173,3	MCF-7	breast:
37	chr7:101245401..101246357-chr7:101879322..101880688,4	K562	blood:
38	chr7:101223546..101226775-chr7:101229478..101232006,3	K562	blood:
39	chr7:101263737..101265953-chr7:101458871..101461158,2	K562	blood:
40	chr7:101245091..101246357-chr7:101457101..101458459,9	MCF-7	breast:
41	chr7:101185812..101186322-chr7:101245513..101246339,2	K562	blood:
42	chr7:101245468..101246352-chr7:101915597..101916163,4	K562	blood:
43	chr7:101244039..101255564-chr7:101454524..101463981,21	MCF-7	breast:
44	chr7:101263736..101266044-chr7:101274498..101276590,2	MCF-7	breast:
45	chr7:101260930..101263826-chr7:101271438..101273640,2	MCF-7	breast:
46	chr7:101265195..101267380-chr7:101272779..101275035,3	MCF-7	breast:
47	chr7:101245574..101246182-chr7:101331380..101332228,3	MCF-7	breast:
48	chr7:101249674..101252052-chr7:101267585..101269354,2	K562	blood:

No data

Variant related genes	Relation type
MYL10	TF binding region
MYL10	CpG island
ENSG00000106436	chromatin interactions
ENSG00000257923	chromatin interactions

Extended variants
information (count: 1943 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1943 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10242865	chr7:101230768-101230769	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141656168	chr7:101230780-101230781	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs367979422	chr7:101230892-101230893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150538050	chr7:101230923-101230924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139443573	chr7:101230945-101230946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185783657	chr7:101230946-101230947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190106185	chr7:101230979-101230980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565931848	chr7:101230980-101230981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537122785	chr7:101230996-101230997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548919831	chr7:101231018-101231019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567318210	chr7:101231059-101231060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs56240036	chr7:101231082-101231083	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182618243	chr7:101231189-101231190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571775295	chr7:101231201-101231202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143191175	chr7:101231249-101231250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554181528	chr7:101231269-101231270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146674282	chr7:101231286-101231287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186202153	chr7:101231295-101231296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376854763	chr7:101231305-101231306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554647617	chr7:101231311-101231312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191568548	chr7:101231323-101231324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543572855	chr7:101231340-101231341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564967276	chr7:101231366-101231367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139396557	chr7:101231390-101231391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541180807	chr7:101231397-101231398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6972183	chr7:101231407-101231408	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184212637	chr7:101231462-101231463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74902037	chr7:101231467-101231468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115173022	chr7:101231549-101231550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13226495	chr7:101231555-101231556	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs550026053	chr7:101231631-101231632	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs55995100	chr7:101231632-101231633	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs549513884	chr7:101231734-101231735	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs188620273	chr7:101231812-101231813	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs10276555	chr7:101231849-101231850	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192721395	chr7:101231903-101231904	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs77580251	chr7:101231923-101231924	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs551852098	chr7:101231931-101231932	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs569074684	chr7:101231944-101231945	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182115563	chr7:101231974-101231975	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs543409886	chr7:101231999-101232000	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs558379249	chr7:101232011-101232012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576826154	chr7:101232026-101232027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372691855	chr7:101232067-101232068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7790294	chr7:101232159-101232160	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs145795102	chr7:101232219-101232220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537656689	chr7:101232253-101232254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10247942	chr7:101232299-101232300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187078969	chr7:101232319-101232320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563213037	chr7:101232351-101232352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101227400-101235200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:101227600-101233400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:101227800-101231600	Enhancers	Fetal Intestine Small	intestine
4	chr7:101228000-101230800	Enhancers	Fetal Intestine Large	intestine
5	chr7:101230000-101232400	Weak transcription	Placenta	Placenta
6	chr7:101230200-101231400	Weak transcription	HepG2	liver
7	chr7:101230200-101231600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:101230400-101232600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:101230600-101230800	Flanking Active TSS	K562	blood
10	chr7:101231400-101232200	Enhancers	HepG2	liver
11	chr7:101231600-101231800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:101231600-101232200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:101231600-101232200	Enhancers	NHDF-Ad	bronchial
14	chr7:101231600-101232600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:101231800-101232000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr7:101232400-101232600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:101232400-101232600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:101232400-101234400	Enhancers	Placenta	Placenta
19	chr7:101232600-101232800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr7:101232600-101234000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:101233400-101233800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:101233400-101234200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:101233400-101234400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:101233600-101234200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:101233600-101234200	Enhancers	HMEC	breast
26	chr7:101233600-101234400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:101233600-101234800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:101234000-101234200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:101234000-101234400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:101234000-101234600	Enhancers	Esophagus	oesophagus
31	chr7:101234200-101238000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:101234400-101235800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:101234400-101237000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr7:101235800-101236000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:101236000-101241600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:101238000-101238400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:101238200-101238400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr7:101239600-101241600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr7:101240400-101241200	Enhancers	HepG2	liver
40	chr7:101241200-101241400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:101241200-101242200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
42	chr7:101241200-101242200	Flanking Active TSS	HepG2	liver
43	chr7:101241200-101242400	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr7:101241200-101242400	Enhancers	HMEC	breast
45	chr7:101241200-101242600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:101241200-101242600	Enhancers	Fetal Intestine Small	intestine
47	chr7:101241200-101242600	Enhancers	Fetal Lung	lung
48	chr7:101241200-101242600	Enhancers	Pancreas	Pancrea
49	chr7:101241200-101242800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:101241200-101242800	Enhancers	Placenta Amnion	Placenta Amnion

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