Variant report

Variant	nsv888757
Chromosome Location	chr7:97003503-97461115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1504)
CpG islands
(count:1284)
Chromatin interactive
region (count:65)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97079843-97080204	K562	blood:	n/a	n/a
2	ARID3A	chr7:97142218-97142424	K562	blood:	n/a	n/a
3	ATF1	chr7:97079821-97080180	K562	blood:	n/a	n/a
4	ATF1	chr7:97266556-97266599	K562	blood:	n/a	n/a
5	ATF1	chr7:97400219-97400518	K562	blood:	n/a	n/a
6	ATF2	chr7:97361030-97361449	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:97252581-97253055	GM12878	blood:	n/a	n/a
8	ATF2	chr7:97252591-97253138	GM12878	blood:	n/a	n/a
9	ATF3	chr7:97387199-97387488	K562	blood:	n/a	n/a
10	ATF3	chr7:97360990-97361408	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:97361066-97361396	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:97142143-97142390	K562	blood:	n/a	n/a
13	BACH1	chr7:97360792-97361684	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:97141760-97142405	K562	blood:	n/a	chr7:97141939-97141953
15	BACH1	chr7:97362622-97363312	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:97399997-97400286	K562	blood:	n/a	n/a
17	BACH1	chr7:97362075-97362381	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:97268425-97268731	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr7:97142136-97142450	GM12878	blood:	n/a	n/a
20	BATF	chr7:97252659-97252955	GM12878	blood:	n/a	chr7:97252763-97252774
21	BCL11A	chr7:97252748-97252957	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:97252567-97253084	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:97252623-97253022	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:97387337-97387422	K562	blood:	n/a	n/a
25	BHLHE40	chr7:97109242-97109273	K562	blood:	n/a	n/a
26	BHLHE40	chr7:97136039-97136375	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:97029233-97029287	K562	blood:	n/a	n/a
28	BHLHE40	chr7:97142169-97142494	K562	blood:	n/a	n/a
29	BHLHE40	chr7:97182605-97182802	K562	blood:	n/a	chr7:97182653-97182662 chr7:97182654-97182663 chr7:97182648-97182669 chr7:97182652-97182665 chr7:97182655-97182664 chr7:97182654-97182663
30	BHLHE40	chr7:97361206-97361218	K562	blood:	n/a	n/a
31	BHLHE40	chr7:97076314-97076607	K562	blood:	n/a	n/a
32	BHLHE40	chr7:97252705-97253062	GM12878	blood:	n/a	n/a
33	CBX3	chr7:97068966-97069246	K562	blood:	n/a	n/a
34	CBX3	chr7:97090943-97091222	K562	blood:	n/a	n/a
35	CBX3	chr7:97079806-97080241	K562	blood:	n/a	n/a
36	CBX3	chr7:97068902-97069413	HCT-116	colon:	n/a	n/a
37	CBX3	chr7:97068948-97069360	K562	blood:	n/a	n/a
38	CBX3	chr7:97068871-97069405	HCT-116	colon:	n/a	n/a
39	CCNT2	chr7:97371177-97371373	K562	blood:	n/a	n/a
40	CCNT2	chr7:97079799-97080109	K562	blood:	n/a	n/a
41	CCNT2	chr7:97157423-97157513	K562	blood:	n/a	n/a
42	CEBPB	chr7:97337604-97337779	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:97037123-97037414	HepG2	liver:	n/a	chr7:97037166-97037179 chr7:97037255-97037266
44	CEBPB	chr7:97177725-97177912	K562	blood:	n/a	n/a
45	CEBPB	chr7:97040197-97040361	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:97359557-97359757	K562	blood:	n/a	n/a
47	CEBPB	chr7:97256176-97256418	HepG2	liver:	n/a	chr7:97256312-97256323
48	CEBPB	chr7:97361154-97361225	HepG2	liver:	n/a	chr7:97361195-97361206 chr7:97361195-97361208
49	CEBPB	chr7:97205467-97205743	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:97201687-97201920	K562	blood:	n/a	chr7:97201772-97201783

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97361408-97361458	NT2-D1	testis:	n/a
2	chr7:97363080-97363130	SAEC	small airway:	n/a
3	chr7:97361148-97361198	SKMC	muscle:	n/a
4	chr7:97361408-97361458	NT2-D1	testis:	n/a
5	chr7:97363080-97363130	SAEC	small airway:	n/a
6	chr7:97361148-97361198	SKMC	muscle:	n/a
7	chr7:97366840-97366890	Hepatocyte	liver:	n/a
8	chr7:97360615-97360665	AoSMC	blood vessel:	n/a
9	chr7:97361026-97361076	Caco-2	colon:	n/a
10	chr7:97158782-97158832	AG04449	skin:	fetal
11	chr7:97401062-97401112	CMK	blood:	n/a
12	chr7:97401062-97401112	HL-60	blood:	n/a
13	chr7:97361759-97361809	U87	brain:	n/a
14	chr7:97401062-97401112	HUVEC	blood vessel:	n/a
15	chr7:97361244-97361294	T-47D	breast:	n/a
16	chr7:97361241-97361291	Jurkat	blood:	n/a
17	chr7:97362308-97362358	HCT-116	colon:	n/a
18	chr7:97158782-97158832	AoSMC	blood vessel:	n/a
19	chr7:97361244-97361294	PrEC	prostate:	n/a
20	chr7:97361252-97361302	HEK293	kidney:	embryo
21	chr7:97361241-97361291	AG04449	skin:	fetal
22	chr7:97361114-97361164	A549	lung:	n/a
23	chr7:97157869-97157919	AG09309	skin:	n/a
24	chr7:97361026-97361076	BJ	skin:	n/a
25	chr7:97366840-97366890	SK-N-SH_RA	brain:	n/a
26	chr7:97363080-97363130	HEK293	kidney:	embryo
27	chr7:97361759-97361809	HEK293	kidney:	embryo
28	chr7:97361114-97361164	AG04450	lung:	fetal
29	chr7:97162175-97162225	HRPEpiC	eye:	n/a
30	chr7:97361759-97361809	RPTEC	kidney:	n/a
31	chr7:97361114-97361164	HEK293	kidney:	embryo
32	chr7:97359829-97359879	RPTEC	kidney:	n/a
33	chr7:97362523-97362573	HCM	heart:	n/a
34	chr7:97360615-97360665	A549	lung:	n/a
35	chr7:97361148-97361198	HIPEpiC	eye:	n/a
36	chr7:97361148-97361198	HCM	heart:	n/a
37	chr7:97158782-97158832	A549	lung:	n/a
38	chr7:97361759-97361809	MCF10A-Er-Src	breast:	n/a
39	chr7:97366840-97366890	ProgFib	skin:	n/a
40	chr7:97359829-97359879	HCPEpiC	choroid plexus:	n/a
41	chr7:97362308-97362358	HCF	heart:	n/a
42	chr7:97362523-97362573	ECC-1	luminal epithelium:	n/a
43	chr7:97401062-97401112	HAEpiC	amniotic membrane:	n/a
44	chr7:97361114-97361164	NHDF-neo	bronchial:	n/a
45	chr7:97357470-97357520	SKMC	muscle:	n/a
46	chr7:97361201-97361251	U87	brain:	n/a
47	chr7:97361244-97361294	BJ	skin:	n/a
48	chr7:97157869-97157919	ProgFib	skin:	n/a
49	chr7:97401062-97401112	HCF	heart:	n/a
50	chr7:97359829-97359879	HCM	heart:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:97372375..97375018-chr7:97378274..97380975,3	K562	blood:
2	chr13:39258683..39259458-chr7:97325089..97325609,2	MCF-7	breast:
3	chr7:97460832..97463550-chr7:97466876..97469674,2	K562	blood:
4	chr7:97150187..97152185-chr7:97153537..97156038,2	K562	blood:
5	chr7:97235082..97237692-chr7:97239276..97241532,2	K562	blood:
6	chr7:97424753..97427686-chr7:97428619..97431033,2	K562	blood:
7	chr7:97076230..97078215-chr7:97082351..97084350,2	K562	blood:
8	chr7:97038233..97040741-chr7:97056603..97058477,2	K562	blood:
9	chr7:97144562..97147344-chr7:97147622..97149562,2	K562	blood:
10	chr7:97049254..97050948-chr7:97055423..97058355,2	K562	blood:
11	chr7:97024861..97027776-chr7:97033571..97035191,2	MCF-7	breast:
12	chr7:97105914..97108921-chr7:97111052..97113024,3	K562	blood:
13	chr7:97315518..97317984-chr7:97320788..97322969,2	K562	blood:
14	chr7:97399083..97401485-chr7:97404504..97407058,2	K562	blood:
15	chr7:97038071..97039952-chr7:97040393..97042517,2	K562	blood:
16	chr7:97128692..97129417-chr7:97464626..97465345,2	MCF-7	breast:
17	chr7:97144562..97147344-chr7:97147622..97149562,2	K562	blood:
18	chr7:96946869..96947558-chr7:97448317..97449019,2	MCF-7	breast:
19	chr7:97103018..97105848-chr7:97107556..97110700,3	K562	blood:
20	chr7:97355540..97357624-chr7:97360814..97362547,2	K562	blood:
21	chr17:78169900..78170447-chr7:97276087..97276587,2	K562	blood:
22	chr7:97317770..97320003-chr7:97320998..97323004,2	K562	blood:
23	chr7:97197850..97199672-chr7:97203982..97205606,2	K562	blood:
24	chr7:97150187..97153466-chr7:97153537..97156915,4	K562	blood:
25	chr6:15954730..15955700-chr7:97086457..97086982,2	MCF-7	breast:
26	chr7:97128256..97128858-chr7:97465708..97466442,2	K562	blood:
27	chr7:97367330..97369358-chr7:97372378..97374711,2	K562	blood:
28	chr7:97015958..97018724-chr7:97019357..97022553,3	K562	blood:
29	chr7:97024861..97027776-chr7:97033571..97035191,2	MCF-7	breast:
30	chr7:97195807..97198146-chr7:97228960..97231165,2	MCF-7	breast:
31	chr7:97015958..97018724-chr7:97019357..97022553,3	K562	blood:
32	chr7:97317770..97320003-chr7:97320998..97323004,2	K562	blood:
33	chr7:97150187..97152185-chr7:97153537..97156038,2	K562	blood:
34	chr7:97103018..97105848-chr7:97107556..97110700,3	K562	blood:
35	chr5:57754807..57755506-chr7:97052674..97053220,2	Hela-S3	cervix:
36	chr7:97128674..97129320-chr7:97474641..97475573,2	K562	blood:
37	chr7:97367998..97369892-chr7:97372461..97374150,2	MCF-7	breast:
38	chr7:97038233..97040741-chr7:97056603..97058477,2	K562	blood:
39	chr7:97049254..97050948-chr7:97055423..97058355,2	K562	blood:
40	chr7:97115929..97118142-chr7:97120900..97123183,2	K562	blood:
41	chr7:96774346..96775064-chr7:97011084..97011839,3	MCF-7	breast:
42	chr7:97182433..97184162-chr7:97187152..97189011,2	K562	blood:
43	chr7:97367998..97369892-chr7:97372461..97374150,2	MCF-7	breast:
44	chr7:97367330..97369358-chr7:97372378..97374711,2	K562	blood:
45	chr7:97115929..97118142-chr7:97120900..97123183,2	K562	blood:
46	chr7:97195807..97198146-chr7:97228960..97231165,2	MCF-7	breast:
47	chr7:97150187..97153466-chr7:97153537..97156915,4	K562	blood:
48	chr7:97007234..97008904-chr7:97014307..97016794,2	K562	blood:
49	chr7:97032690..97034318-chr7:97039801..97041810,2	K562	blood:
50	chr7:97105914..97108921-chr7:97111052..97113024,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASNS-2	chr7:97228245-97228572	NONHSAT122144

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TAC1	hsa-miR-130a-3p	chr7:97369284-97369306
2	TAC1	hsa-miR-320a	chr7:97369242-97369263

Variant related genes	Relation type
ENSG00000226046	TF binding region
RN7SKP104	TF binding region
TAC1	TF binding region
ENSG00000226046	CpG island
RN7SKP104	CpG island
TAC1	CpG island
ENSG00000145632	chromatin interactions
ENSG00000006128	chromatin interactions
ENSG00000070669	chromatin interactions

Extended variants
information (count: 4901 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:4901 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10435325	chr7:97003503-97003504	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577212683	chr7:97003542-97003543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189404202	chr7:97003573-97003574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573353550	chr7:97003577-97003578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182252699	chr7:97003653-97003654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530888200	chr7:97003688-97003689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544285382	chr7:97003743-97003744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573859044	chr7:97003755-97003756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561207118	chr7:97003826-97003827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529958915	chr7:97003855-97003856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74919071	chr7:97003859-97003860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150386461	chr7:97003883-97003884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116185195	chr7:97003884-97003885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs367709411	chr7:97003896-97003897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs80110397	chr7:97004010-97004011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549006359	chr7:97004094-97004095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537401658	chr7:97004098-97004099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554285547	chr7:97004124-97004125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567934072	chr7:97004128-97004129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536572367	chr7:97004185-97004186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138091920	chr7:97004238-97004239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573521601	chr7:97004294-97004295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531775321	chr7:97004296-97004297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186856496	chr7:97004314-97004315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191644240	chr7:97004343-97004344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10260716	chr7:97004409-97004410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs149550107	chr7:97004419-97004420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112825529	chr7:97004423-97004424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112223099	chr7:97004475-97004476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34160499	chr7:97004477-97004478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77220341	chr7:97004483-97004484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111946831	chr7:97004484-97004485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529976438	chr7:97004491-97004492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540203074	chr7:97004522-97004523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116955017	chr7:97004537-97004538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532134042	chr7:97004539-97004540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570349625	chr7:97004542-97004543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181316284	chr7:97004615-97004616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551955428	chr7:97004646-97004647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533250518	chr7:97004647-97004648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76775085	chr7:97004668-97004669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531341807	chr7:97004741-97004742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548148244	chr7:97004767-97004768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185441016	chr7:97004787-97004788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146066269	chr7:97004788-97004789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71108209	chr7:97004843-97004844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10435326	chr7:97004859-97004860	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs567175909	chr7:97004874-97004875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10261241	chr7:97004878-97004879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs10245862	chr7:97004908-97004909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
abnormal development	18461090	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Chronic myeloid leukemia	21384125	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell lymphomas	22341440	CNVD
Bladder cancer	21909424	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96998400-97003600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:96999000-97004000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:97003000-97003600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:97003000-97003800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr7:97003000-97003800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:97003000-97003800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr7:97003000-97003800	Enhancers	Brain Anterior Caudate	brain
8	chr7:97003200-97003800	Enhancers	Brain Angular Gyrus	brain
9	chr7:97003600-97003800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr7:97003600-97003800	Enhancers	Brain Cingulate Gyrus	brain
11	chr7:97004000-97011600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:97011600-97012400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:97011600-97012600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:97011600-97012600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr7:97012200-97012600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr7:97012400-97013000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:97019400-97019800	Enhancers	K562	blood
18	chr7:97019400-97020000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr7:97019600-97019800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr7:97019800-97020800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr7:97020400-97021000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:97020400-97021200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:97020400-97021200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:97020800-97021000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr7:97020800-97021200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:97026800-97027200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr7:97026800-97027200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr7:97034800-97035800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:97034800-97035800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:97035200-97035400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:97035600-97036000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:97050000-97051600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:97050000-97052000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:97050200-97052000	Enhancers	Fetal Muscle Leg	muscle
35	chr7:97052000-97055600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:97055600-97056600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:97055600-97056600	Enhancers	Brain Anterior Caudate	brain
38	chr7:97055800-97056600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:97056000-97056400	Enhancers	Brain Germinal Matrix	brain
40	chr7:97056200-97056600	Enhancers	Brain Cingulate Gyrus	brain
41	chr7:97056200-97056600	Enhancers	Brain Hippocampus Middle	brain
42	chr7:97056600-97059400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:97056600-97060400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:97059200-97059600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:97059200-97059600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr7:97059200-97059600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr7:97059400-97059600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:97059400-97059600	Enhancers	Gastric	stomach
49	chr7:97059600-97060000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:97060000-97060800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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