Variant report

Variant	nsv834645
Chromosome Location	chr3:25363723-25555107
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1500)
CpG islands
(count:1894)
Chromatin interactive
region (count:44)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1500 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:25463305-25463603	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:25468675-25468953	HepG2	liver:	n/a	n/a
3	ATF1	chr3:25475397-25475755	K562	blood:	n/a	n/a
4	ATF1	chr3:25469470-25469846	K562	blood:	n/a	n/a
5	ATF1	chr3:25472057-25472314	K562	blood:	n/a	n/a
6	ATF2	chr3:25469410-25469875	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:25469485-25469792	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:25502250-25502645	GM12878	blood:	n/a	n/a
9	ATF3	chr3:25465749-25466612	A549	lung:	n/a	n/a
10	ATF3	chr3:25469270-25469956	A549	lung:	n/a	n/a
11	ATF3	chr3:25513766-25513910	K562	blood:	n/a	n/a
12	ATF3	chr3:25468515-25469173	A549	lung:	n/a	n/a
13	BACH1	chr3:25508831-25509204	K562	blood:	n/a	n/a
14	BACH1	chr3:25535439-25535468	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr3:25461767-25462099	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr3:25465703-25466576	A549	lung:	n/a	n/a
17	BCL3	chr3:25468534-25470580	A549	lung:	n/a	chr3:25469982-25469991
18	BCL3	chr3:25463184-25463739	A549	lung:	n/a	n/a
19	BCL3	chr3:25469327-25470636	A549	lung:	n/a	chr3:25469982-25469991
20	BCL3	chr3:25465823-25466657	A549	lung:	n/a	n/a
21	BCL3	chr3:25468552-25469285	A549	lung:	n/a	n/a
22	BHLHE40	chr3:25508831-25509205	K562	blood:	n/a	n/a
23	BHLHE40	chr3:25469813-25470072	A549	lung:	n/a	n/a
24	BHLHE40	chr3:25469726-25469982	K562	blood:	n/a	n/a
25	BHLHE40	chr3:25508832-25509205	GM12878	blood:	n/a	n/a
26	BRCA1	chr3:25508833-25509033	GM12878	blood:	n/a	n/a
27	BRCA1	chr3:25508830-25509206	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:25499647-25500595	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr3:25475400-25475737	K562	blood:	n/a	n/a
30	CCNT2	chr3:25472070-25472270	K562	blood:	n/a	n/a
31	CEBPB	chr3:25462671-25462962	K562	blood:	n/a	chr3:25462825-25462838 chr3:25462825-25462838 chr3:25462826-25462837 chr3:25462825-25462838
32	CEBPB	chr3:25469537-25469867	K562	blood:	n/a	chr3:25469726-25469737 chr3:25469725-25469736
33	CEBPB	chr3:25463251-25463632	HepG2	liver:	n/a	n/a
34	CEBPB	chr3:25462649-25462986	A549	lung:	n/a	chr3:25462825-25462838 chr3:25462825-25462838 chr3:25462826-25462837 chr3:25462825-25462838
35	CEBPB	chr3:25469422-25469996	A549	lung:	n/a	chr3:25469726-25469737 chr3:25469725-25469736
36	CEBPB	chr3:25490259-25490734	A549	lung:	n/a	chr3:25490470-25490481 chr3:25490468-25490479 chr3:25490468-25490481 chr3:25490470-25490479
37	CEBPB	chr3:25465773-25466865	A549	lung:	n/a	n/a
38	CEBPB	chr3:25474661-25474940	A549	lung:	n/a	n/a
39	CEBPB	chr3:25550467-25550818	A549	lung:	n/a	chr3:25550585-25550594
40	CEBPB	chr3:25463086-25463768	A549	lung:	n/a	n/a
41	CEBPB	chr3:25531725-25532073	K562	blood:	n/a	chr3:25531863-25531874 chr3:25531863-25531876 chr3:25531863-25531876 chr3:25532000-25532012 chr3:25531864-25531875 chr3:25531863-25531876 chr3:25531863-25531874 chr3:25531862-25531879
42	CEBPB	chr3:25469536-25469910	IMR90	lung:	n/a	chr3:25469726-25469737 chr3:25469725-25469736
43	CEBPB	chr3:25463203-25463629	A549	lung:	n/a	n/a
44	CEBPB	chr3:25468474-25469009	A549	lung:	n/a	n/a
45	CEBPB	chr3:25490284-25490853	Hela-S3	cervix:	n/a	chr3:25490470-25490481 chr3:25490468-25490479 chr3:25490468-25490481 chr3:25490470-25490479
46	CEBPB	chr3:25421949-25422376	MCF-7	breast:	n/a	chr3:25422162-25422171 chr3:25422162-25422171 chr3:25422161-25422172 chr3:25422162-25422171 chr3:25422160-25422173
47	CEBPB	chr3:25537234-25537533	A549	lung:	n/a	n/a
48	CEBPB	chr3:25421861-25422434	A549	lung:	n/a	chr3:25422162-25422171 chr3:25422162-25422171 chr3:25422161-25422172 chr3:25422162-25422171 chr3:25422160-25422173
49	CEBPB	chr3:25465707-25466482	A549	lung:	n/a	n/a
50	CEBPB	chr3:25469020-25470405	A549	lung:	n/a	chr3:25469726-25469737 chr3:25469725-25469736

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:25493807-25493857	ECC-1	luminal epithelium:	n/a
2	chr3:25469872-25469922	RPTEC	kidney:	n/a
3	chr3:25469430-25469480	AG04449	skin:	fetal
4	chr3:25493807-25493857	ECC-1	luminal epithelium:	n/a
5	chr3:25469872-25469922	RPTEC	kidney:	n/a
6	chr3:25469430-25469480	AG04449	skin:	fetal
7	chr3:25469148-25469198	HCF	heart:	n/a
8	chr3:25468324-25468374	CMK	blood:	n/a
9	chr3:25469720-25469770	NT2-D1	testis:	n/a
10	chr3:25426534-25426584	HCF	heart:	n/a
11	chr3:25469430-25469480	T-47D	breast:	n/a
12	chr3:25468324-25468374	PANC-1	pancreas:	n/a
13	chr3:25493807-25493857	GM12892	blood:	n/a
14	chr3:25469402-25469452	HAEpiC	amniotic membrane:	n/a
15	chr3:25469125-25469175	NB4	blood:	n/a
16	chr3:25426563-25426613	GM12892	blood:	n/a
17	chr3:25482937-25482987	Hela-S3	cervix:	n/a
18	chr3:25461111-25461161	SK-N-SH	brain:	n/a
19	chr3:25472652-25472702	NHBE	bronchial:	n/a
20	chr3:25426534-25426584	BE2_C	brain:	n/a
21	chr3:25469860-25469910	NT2-D1	testis:	n/a
22	chr3:25365560-25365610	GM06990	blood:	n/a
23	chr3:25467237-25467287	HEEpiC	esophagus:	n/a
24	chr3:25469708-25469758	SKMC	muscle:	n/a
25	chr3:25472652-25472702	NB4	blood:	n/a
26	chr3:25469872-25469922	SK-N-SH	brain:	n/a
27	chr3:25461111-25461161	GM19239	blood:	n/a
28	chr3:25467534-25467584	HRPEpiC	eye:	n/a
29	chr3:25469694-25469744	GM12892	blood:	n/a
30	chr3:25469991-25470041	HEK293	kidney:	embryo
31	chr3:25426563-25426613	RPTEC	kidney:	n/a
32	chr3:25469872-25469922	HepG2	liver:	n/a
33	chr3:25469991-25470041	NHDF-neo	bronchial:	n/a
34	chr3:25469914-25469964	HNPCEpiC	eye:	n/a
35	chr3:25469577-25469627	AG09309	skin:	n/a
36	chr3:25391527-25391577	CMK	blood:	n/a
37	chr3:25482937-25482987	AG09319	gingival:	n/a
38	chr3:25426534-25426584	HCT-116	colon:	n/a
39	chr3:25493807-25493857	ProgFib	skin:	n/a
40	chr3:25472652-25472702	HEK293	kidney:	embryo
41	chr3:25469148-25469198	BJ	skin:	n/a
42	chr3:25469860-25469910	NHBE	bronchial:	n/a
43	chr3:25427224-25427274	SK-N-SH_RA	brain:	n/a
44	chr3:25426563-25426613	BJ	skin:	n/a
45	chr3:25365560-25365610	ovcar-3	ovarian:	n/a
46	chr3:25426563-25426613	NHBE	bronchial:	n/a
47	chr3:25472652-25472702	AG09319	gingival:	n/a
48	chr3:25426534-25426584	ProgFib	skin:	n/a
49	chr3:25469919-25469969	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:25469573-25469623	HNPCEpiC	eye:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:25537595..25539847-chr3:25543355..25545556,2	K562	blood:
2	chr3:25487672..25489209-chr3:25493785..25496614,2	K562	blood:
3	chr3:25510947..25513375-chr3:25521256..25523814,2	K562	blood:
4	chr3:23957476..23960072-chr3:25467685..25470119,2	K562	blood:
5	chr3:25485607..25487240-chr3:25500715..25502781,2	K562	blood:
6	chr3:25402908..25405265-chr3:25407637..25410309,2	K562	blood:
7	chr3:25534068..25536188-chr3:25718697..25720754,2	K562	blood:
8	chr3:25457826..25461683-chr3:25463810..25466915,4	K562	blood:
9	chr3:25458396..25460211-chr3:25468832..25470804,2	K562	blood:
10	chr3:25468622..25472449-chr3:25473366..25475962,3	K562	blood:
11	chr3:25497283..25499638-chr3:25505573..25507305,2	MCF-7	breast:
12	chr3:25468072..25472151-chr3:25476799..25480393,4	K562	blood:
13	chr3:25523167..25526128-chr3:25537959..25540465,2	K562	blood:
14	chr3:25501340..25503913-chr3:25512511..25514935,2	K562	blood:
15	chr3:25515577..25518929-chr3:25519264..25523048,3	K562	blood:
16	chr3:25385596..25387245-chr3:25390667..25392200,2	K562	blood:
17	chr3:25499125..25502104-chr3:25520661..25522813,2	MCF-7	breast:
18	chr3:25485607..25487240-chr3:25500715..25502781,2	K562	blood:
19	chr3:25487622..25488496-chr6:25269914..25270525,2	MCF-7	breast:
20	chr3:25501912..25504372-chr3:25504768..25507425,2	K562	blood:
21	chr3:25385596..25387245-chr3:25390667..25392200,2	K562	blood:
22	chr3:25510947..25513375-chr3:25521256..25523814,2	K562	blood:
23	chr3:25537595..25539847-chr3:25543355..25545556,2	K562	blood:
24	chr3:25523167..25526128-chr3:25537959..25540465,2	K562	blood:
25	chr3:25544422..25547348-chr3:25549041..25550865,2	K562	blood:
26	chr3:25501340..25503913-chr3:25512511..25514935,2	K562	blood:
27	chr3:25515260..25517004-chr3:25622098..25624114,2	MCF-7	breast:
28	chr3:25510012..25511690-chr3:25569831..25571365,2	K562	blood:
29	chr3:25497131..25499173-chr3:25538554..25540372,2	K562	blood:
30	chr3:25553583..25555488-chr3:25562706..25565371,2	K562	blood:
31	chr3:25515577..25518929-chr3:25519264..25523048,3	K562	blood:
32	chr3:25544422..25547348-chr3:25549041..25550865,2	K562	blood:
33	chr3:25497283..25499638-chr3:25505573..25507305,2	MCF-7	breast:
34	chr3:25513903..25516202-chr3:25541774..25543673,2	K562	blood:
35	chr3:25511658..25514317-chr3:25515224..25516952,2	K562	blood:
36	chr3:25511658..25514317-chr3:25515224..25516952,2	K562	blood:
37	chr3:25457826..25461683-chr3:25463810..25466915,4	K562	blood:
38	chr3:25487672..25489209-chr3:25493785..25496614,2	K562	blood:
39	chr3:25402908..25405265-chr3:25407637..25410309,2	K562	blood:
40	chr3:25497131..25499173-chr3:25538554..25540372,2	K562	blood:
41	chr3:25469479..25471668-chr3:25472348..25474075,2	K562	blood:
42	chr3:25513903..25516202-chr3:25541774..25543673,2	K562	blood:
43	chr3:25468072..25470085-chr3:25478893..25481695,2	K562	blood:
44	chr3:25501912..25504372-chr3:25504768..25507425,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOP2B-4	chr3:25424599-25424870	NONHSAT088710
2	lnc-TOP2B-4	chr3:25426137-25426409	NONHSAT088710
3	lnc-TOP2B-5	chr3:25401141-25401413	ucscGeneNc_uc003cdf_1
4	lnc-TOP2B-3	chr3:25482655-25482993	NONHSAT088711
5	lnc-TOP2B-5	chr3:25399603-25399874	ucscGeneNc_uc003cdf_1

No data

Variant related genes	Relation type
ENSG00000229421	TF binding region
RARB	TF binding region
RNA5SP126	TF binding region
CFL1P7	TF binding region
ENSG00000229421	CpG island
RARB	CpG island
RNA5SP126	CpG island
CFL1P7	CpG island
ENSG00000197885	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000077092	chromatin interactions

Extended variants
information (count: 7564 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:7564 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369642486	chr3:25364437-25364438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552204150	chr3:25364468-25364469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565937041	chr3:25364474-25364475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534583586	chr3:25364508-25364509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372295252	chr3:25364529-25364530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150312355	chr3:25364563-25364564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568104146	chr3:25364572-25364573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537194284	chr3:25364604-25364605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79312569	chr3:25364617-25364618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375235570	chr3:25364620-25364621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200578510	chr3:25364640-25364641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187879625	chr3:25364643-25364644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs137937224	chr3:25364662-25364663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553410208	chr3:25364722-25364723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573604993	chr3:25364758-25364759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145943703	chr3:25364760-25364761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138542787	chr3:25364772-25364773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574440786	chr3:25364780-25364781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543163911	chr3:25364786-25364787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs578246411	chr3:25364791-25364792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563363603	chr3:25364822-25364823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75812834	chr3:25364838-25364839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552377312	chr3:25364875-25364876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559107515	chr3:25364899-25364900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528410266	chr3:25364905-25364906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548075217	chr3:25364908-25364909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73051671	chr3:25364947-25364948	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs560734920	chr3:25364952-25364953	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs1564744	chr3:25364972-25364973	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs74982394	chr3:25364978-25364979	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs185821802	chr3:25364982-25364983	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs2164476	chr3:25365011-25365012	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs553562285	chr3:25365056-25365057	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs573474788	chr3:25365058-25365059	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs536160283	chr3:25365066-25365067	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs556057334	chr3:25365102-25365103	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs574501574	chr3:25365126-25365127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373404346	chr3:25365178-25365179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144647964	chr3:25365246-25365247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563116731	chr3:25365252-25365253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76243897	chr3:25365275-25365276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545571469	chr3:25365280-25365281	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs77309070	chr3:25365286-25365287	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs189896050	chr3:25365290-25365291	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs181689369	chr3:25365316-25365317	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs75648383	chr3:25365365-25365366	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs77291579	chr3:25365383-25365384	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs533053535	chr3:25365426-25365427	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs148445241	chr3:25365431-25365432	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs142618933	chr3:25365497-25365498	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Tracheal agenesis	20877625	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Glioblastoma multiforme	21510904	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:2630 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25364400-25366000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:25364600-25365000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr3:25364600-25366000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:25365000-25365400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr3:25365000-25365800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr3:25365000-25365800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:25365000-25366000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:25365000-25366000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr3:25365000-25366000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr3:25365200-25365600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr3:25365400-25365600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr3:25365400-25366000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:25365600-25366000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:25366400-25366800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:25366400-25366800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:25366400-25367200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:25366800-25367200	Enhancers	Left Ventricle	heart
18	chr3:25376400-25377200	Enhancers	Fetal Lung	lung
19	chr3:25376600-25377400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr3:25377200-25384000	Weak transcription	Fetal Lung	lung
21	chr3:25377400-25379800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr3:25378200-25378400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:25378200-25378600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr3:25378200-25380800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:25378400-25379600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:25378600-25380200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr3:25379000-25382600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:25379200-25380800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:25379400-25380400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:25379600-25380000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:25379600-25380200	Enhancers	Brain Germinal Matrix	brain
32	chr3:25379800-25380400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr3:25380200-25381000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:25380400-25382000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:25380800-25382200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:25380800-25384200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr3:25381000-25389200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr3:25381800-25382200	Enhancers	Fetal Heart	heart
39	chr3:25382000-25382800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr3:25382200-25383000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:25382400-25382600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr3:25382600-25384000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr3:25382600-25384000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr3:25383000-25388000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:25384000-25384400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:25384000-25384600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr3:25384000-25384800	Enhancers	Fetal Lung	lung
48	chr3:25384200-25384400	Enhancers	Fetal Stomach	stomach
49	chr3:25384400-25386400	Weak transcription	Fetal Stomach	stomach
50	chr3:25384400-25388200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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