Variant report

Variant	nsv887976
Chromosome Location	chr7:39874986-40018693
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2315)
CpG islands
(count:1099)
Chromatin interactive
region (count:111)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2315 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39935977-39936271	K562	blood:	n/a	n/a
2	ARID3A	chr7:39959353-39959612	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:39988795-39989318	K562	blood:	n/a	n/a
4	ARID3A	chr7:39935950-39936284	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:39988952-39989394	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:39991137-39991565	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:39970740-39971068	HepG2	liver:	n/a	n/a
8	ATF1	chr7:39988895-39989464	K562	blood:	n/a	n/a
9	ATF2	chr7:39989525-39990022	GM12878	blood:	n/a	n/a
10	ATF2	chr7:39988069-39989384	GM12878	blood:	n/a	n/a
11	ATF2	chr7:39988795-39989521	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:39988181-39990121	GM12878	blood:	n/a	n/a
13	ATF3	chr7:39988701-39989220	A549	lung:	n/a	n/a
14	ATF3	chr7:39955520-39955767	K562	blood:	n/a	n/a
15	ATF3	chr7:39960570-39960810	K562	blood:	n/a	n/a
16	BACH1	chr7:40018632-40018639	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:39938784-39938796	K562	blood:	n/a	n/a
18	BACH1	chr7:39989782-39989879	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:39988728-39989113	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr7:39988644-39989114	GM12878	blood:	n/a	n/a
21	BATF	chr7:39989596-39989936	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:39989569-39989907	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:39989551-39990003	GM12878	blood:	n/a	chr7:39989938-39989951
24	BCL3	chr7:39988598-39989279	A549	lung:	n/a	chr7:39989107-39989116
25	BCL3	chr7:39988778-39990038	GM12878	blood:	n/a	chr7:39990008-39990017 chr7:39989461-39989470 chr7:39989107-39989116 chr7:39989462-39989475 chr7:39989460-39989473 chr7:39989457-39989470 chr7:39989938-39989951 chr7:39989421-39989430 chr7:39989458-39989467 chr7:39989459-39989472 chr7:39989464-39989473
26	BCL3	chr7:39989559-39990015	A549	lung:	n/a	chr7:39989938-39989951
27	BCL3	chr7:39931941-39932267	A549	lung:	n/a	chr7:39932072-39932081
28	BCL3	chr7:39988684-39989394	A549	lung:	n/a	chr7:39989107-39989116
29	BCLAF1	chr7:39991025-39991531	GM12878	blood:	n/a	n/a
30	BCLAF1	chr7:39988575-39990198	GM12878	blood:	n/a	chr7:39990008-39990017 chr7:39990144-39990153 chr7:39989461-39989470 chr7:39989107-39989116 chr7:39989462-39989475 chr7:39989460-39989473 chr7:39989457-39989470 chr7:39989938-39989951 chr7:39989421-39989430 chr7:39989458-39989467 chr7:39989459-39989472 chr7:39989464-39989473 chr7:39990147-39990156
31	BCLAF1	chr7:39988557-39990046	GM12878	blood:	n/a	chr7:39990008-39990017 chr7:39989461-39989470 chr7:39989107-39989116 chr7:39989462-39989475 chr7:39989460-39989473 chr7:39989457-39989470 chr7:39989938-39989951 chr7:39989421-39989430 chr7:39989458-39989467 chr7:39989459-39989472 chr7:39989464-39989473
32	BCLAF1	chr7:39987990-39988386	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:39990833-39991549	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:39990238-39990381	K562	blood:	n/a	n/a
35	BHLHE40	chr7:39987958-39988524	K562	blood:	n/a	n/a
36	BHLHE40	chr7:39988791-39990038	K562	blood:	n/a	chr7:39989452-39989468 chr7:39989459-39989475 chr7:39989457-39989473
37	BHLHE40	chr7:39987846-39988555	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:39991058-39991549	K562	blood:	n/a	n/a
39	BHLHE40	chr7:39991187-39991428	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:39988761-39990023	GM12878	blood:	n/a	chr7:39989452-39989468 chr7:39989459-39989475 chr7:39989457-39989473
41	BHLHE40	chr7:39878152-39878266	K562	blood:	n/a	n/a
42	BHLHE40	chr7:39997596-39997914	GM12878	blood:	n/a	n/a
43	BRCA1	chr7:39989104-39989335	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr7:39989041-39989388	HepG2	liver:	n/a	n/a
45	BRCA1	chr7:39989734-39989832	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr7:39991212-39992274	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr7:39991726-39991826	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr7:39989508-39989907	GM12878	blood:	n/a	n/a
49	BRCA1	chr7:39988609-39990172	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr7:39989680-39989844	HepG2	liver:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39989474-39989524	T-47D	breast:	n/a
2	chr7:39989474-39989524	T-47D	breast:	n/a
3	chr7:39985400-39985450	Caco-2	colon:	n/a
4	chr7:39989860-39989910	T-47D	breast:	n/a
5	chr7:39988923-39988973	GM12878	blood:	n/a
6	chr7:39993440-39993490	BJ	skin:	n/a
7	chr7:39991217-39991267	HIPEpiC	eye:	n/a
8	chr7:39989860-39989910	PANC-1	pancreas:	n/a
9	chr7:39989090-39989140	RPTEC	kidney:	n/a
10	chr7:39991217-39991267	AG10803	skin:	n/a
11	chr7:39985400-39985450	SK-N-MC	brain:	n/a
12	chr7:39989544-39989594	PANC-1	pancreas:	n/a
13	chr7:39988923-39988973	HUVEC	blood vessel:	n/a
14	chr7:39990532-39990582	Jurkat	blood:	n/a
15	chr7:39994617-39994667	HCPEpiC	choroid plexus:	n/a
16	chr7:39990042-39990092	U87	brain:	n/a
17	chr7:39989723-39989773	AG09319	gingival:	n/a
18	chr7:39989474-39989524	AoSMC	blood vessel:	n/a
19	chr7:39993440-39993490	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:39990532-39990582	GM12891	blood:	n/a
21	chr7:39989544-39989594	IMR90	lung:	fetal
22	chr7:39989860-39989910	NHDF-neo	bronchial:	n/a
23	chr7:39985400-39985450	HCF	heart:	n/a
24	chr7:39990729-39990779	SK-N-SH_RA	brain:	n/a
25	chr7:39994617-39994667	ProgFib	skin:	n/a
26	chr7:39991463-39991513	H1-hESC	embryonic stem cell:	embryo
27	chr7:39989867-39989917	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:39990532-39990582	PFSK-1	brain:	n/a
29	chr7:39994617-39994667	AoSMC	blood vessel:	n/a
30	chr7:39985400-39985450	HCM	heart:	n/a
31	chr7:39988923-39988973	SAEC	small airway:	n/a
32	chr7:39989867-39989917	GM12878	blood:	n/a
33	chr7:39985400-39985450	NT2-D1	testis:	n/a
34	chr7:39989544-39989594	HMEC	breast:	n/a
35	chr7:39991463-39991513	BJ	skin:	n/a
36	chr7:39990544-39990594	ECC-1	luminal epithelium:	n/a
37	chr7:39991217-39991267	ovcar-3	ovarian:	n/a
38	chr7:39990729-39990779	PrEC	prostate:	n/a
39	chr7:39990544-39990594	NT2-D1	testis:	n/a
40	chr7:39989860-39989910	PFSK-1	brain:	n/a
41	chr7:39985400-39985450	PrEC	prostate:	n/a
42	chr7:39989544-39989594	HEK293	kidney:	embryo
43	chr7:39989867-39989917	H1-hESC	embryonic stem cell:	embryo
44	chr7:39990532-39990582	PANC-1	pancreas:	n/a
45	chr7:39989860-39989910	HCT-116	colon:	n/a
46	chr7:39988923-39988973	AG09319	gingival:	n/a
47	chr7:39985400-39985450	IMR90	lung:	fetal
48	chr7:39989090-39989140	Jurkat	blood:	n/a
49	chr7:39991217-39991267	AG09319	gingival:	n/a
50	chr7:39985400-39985450	HIPEpiC	eye:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:39991743..39994324-chr7:40009939..40012634,2	K562	blood:
2	chr11:96122465..96123203-chr7:39988642..39989631,2	Hela-S3	cervix:
3	chr7:39989834..39993162-chr7:40018221..40020870,3	K562	blood:
4	chr7:39992179..39995720-chr7:40011134..40014847,3	K562	blood:
5	chr7:40006687..40008469-chr7:40010129..40011913,2	K562	blood:
6	chr7:39987318..39990027-chr8:101962750..101965742,2	MCF-7	breast:
7	chr7:39988014..39992779-chr7:40016991..40021232,5	K562	blood:
8	chr7:40005726..40008469-chr7:40010129..40013269,3	K562	blood:
9	chr7:39989281..39990257-chr9:4679240..4680185,2	Hela-S3	cervix:
10	chr7:39925804..39928770-chr7:39934507..39936424,2	K562	blood:
11	chr7:39987924..39989879-chr7:39999761..40002554,2	K562	blood:
12	chr7:39988793..39991340-chr7:40008054..40010425,3	MCF-7	breast:
13	chr7:39963368..39965638-chr7:39986641..39989237,2	K562	blood:
14	chr12:56551913..56552508-chr7:39988805..39989416,2	Hela-S3	cervix:
15	chr7:39920454..39923588-chr7:39927259..39930788,3	MCF-7	breast:
16	chr1:94311521..94312144-chr7:39988387..39989256,2	HCT-116	colon:
17	chr7:39925804..39927840-chr7:39933103..39935350,2	MCF-7	breast:
18	chr10:75011864..75012841-chr7:39989467..39990350,2	NB4	blood:
19	chr16:85060770..85061475-chr7:39989435..39989944,2	Hela-S3	cervix:
20	chr7:39955812..39957588-chr7:39989391..39990971,2	K562	blood:
21	chr7:39993833..39995767-chr7:39996251..39998539,2	MCF-7	breast:
22	chr7:39933111..39934686-chr7:39937937..39939707,2	K562	blood:
23	chr7:39988178..39991178-chr7:40012997..40016738,6	MCF-7	breast:
24	chr7:39989010..39992398-chr7:40024722..40029040,5	MCF-7	breast:
25	chr7:39922523..39924083-chr7:40170762..40172465,2	K562	blood:
26	chr7:39961241..39963014-chr7:39971580..39973102,2	MCF-7	breast:
27	chr7:39987907..39993068-chr7:39995715..40000293,13	MCF-7	breast:
28	chr19:48824897..48825730-chr7:39988705..39989640,2	NB4	blood:
29	chr14:96968408..96969093-chr7:39989276..39989838,2	Hela-S3	cervix:
30	chr7:40005726..40008469-chr7:40010129..40013269,3	K562	blood:
31	chr7:39987721..39990242-chr7:40174056..40176267,2	MCF-7	breast:
32	chr2:64067918..64068649-chr7:39987965..39988470,2	Hela-S3	cervix:
33	chr7:39934240..39937212-chr7:39987156..39990695,5	MCF-7	breast:
34	chr20:48598768..48599760-chr7:39989242..39989944,2	Hela-S3	cervix:
35	chr7:39662538..39665289-chr7:39934013..39936040,2	K562	blood:
36	chr7:39992179..39995720-chr7:40011134..40014847,3	K562	blood:
37	chr19:39897400..39897939-chr7:39988698..39989697,2	Hela-S3	cervix:
38	chr7:39663090..39665724-chr7:39988469..39990285,2	MCF-7	breast:
39	chr17:33914316..33914947-chr7:39988751..39989359,2	NB4	blood:
40	chr7:39975051..39978175-chr7:39986837..39989689,3	MCF-7	breast:
41	chr1:150550230..150550897-chr7:39988646..39989310,2	Hela-S3	cervix:
42	chr2:63815667..63816442-chr7:39988724..39989292,2	NB4	blood:
43	chr1:41156987..41157841-chr7:39988968..39989713,2	NB4	blood:
44	chr14:92587219..92588097-chr7:39989268..39989812,2	Hela-S3	cervix:
45	chr6:26157666..26158376-chr7:39988958..39989905,3	Hela-S3	cervix:
46	chr5:36876363..36877049-chr7:39989868..39990637,2	Hela-S3	cervix:
47	chr7:39932888..39935926-chr7:39987671..39991292,5	MCF-7	breast:
48	chr7:39991743..39994324-chr7:40009939..40012634,2	K562	blood:
49	chr7:39930986..39932784-chr7:39989575..39991330,2	MCF-7	breast:
50	chr7:39988142..39991064-chr7:40007061..40008566,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDK13-6	chr7:39905911-39906030	NONHSAT120234
2	lnc-C7orf11-1	chr7:39987121-39989354	ENSG00000259826.1
3	lnc-CDK13-1	chr7:39894632-39894854	ENSG00000249078
4	lnc-CDK13-1	chr7:39893117-39894444	ENSG00000249078
5	lnc-CDK13-6	chr7:39907545-39907739	NONHSAT120234
6	lnc-CDK13-6	chr7:39876357-39876510	NONHSAT120234
7	lnc-CDK13-5	chr7:39927972-39928261	NONHSAT120238

No data

Variant related genes	Relation type
CDK13	TF binding region
RN7SL496P	TF binding region
RWDD4P2	TF binding region
ENSG00000259826	TF binding region
ENSG00000231198	TF binding region
CDK13	CpG island
RN7SL496P	CpG island
RWDD4P2	CpG island
ENSG00000259826	CpG island
ENSG00000231198	CpG island
ENSG00000168303	chromatin interactions
ENSG00000182180	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000169764	chromatin interactions
ENSG00000014641	chromatin interactions
ENSG00000242855	chromatin interactions
ENSG00000198824	chromatin interactions
ENSG00000107020	chromatin interactions
ENSG00000183340	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000198162	chromatin interactions
ENSG00000143951	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000128016	chromatin interactions
ENSG00000241127	chromatin interactions
ENSG00000273061	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000263764	chromatin interactions
ENSG00000006451	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000227540	chromatin interactions
ENSG00000183648	chromatin interactions
ENSG00000100316	chromatin interactions
ENSG00000179950	chromatin interactions
ENSG00000257809	chromatin interactions
ENSG00000227172	chromatin interactions
ENSG00000149231	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000106993	chromatin interactions
ENSG00000272145	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000135709	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000175600	chromatin interactions
ENSG00000092841	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000066136	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000166266	chromatin interactions
ENSG00000260806	chromatin interactions
ENSG00000124216	chromatin interactions

Extended variants
information (count: 3980 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3980 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10272635	chr7:39874986-39874987	Bivalent/Poised TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35286787	chr7:39875013-39875014	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs73132706	chr7:39875014-39875015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561812441	chr7:39875022-39875023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192750433	chr7:39875043-39875044	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs6969532	chr7:39875108-39875109	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs75924032	chr7:39875118-39875119	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs536046981	chr7:39875122-39875123	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs555708926	chr7:39875131-39875132	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572554273	chr7:39875139-39875140	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs35251766	chr7:39875140-39875141	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs138703427	chr7:39875164-39875165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558155956	chr7:39875168-39875169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs578072452	chr7:39875273-39875274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6970005	chr7:39875277-39875278	Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs563589801	chr7:39875320-39875321	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs184270618	chr7:39875343-39875344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189215471	chr7:39875376-39875377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559138232	chr7:39875391-39875392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6952352	chr7:39875408-39875409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551067752	chr7:39875438-39875439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564503469	chr7:39875524-39875525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530519191	chr7:39875541-39875542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142762363	chr7:39875570-39875571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111977199	chr7:39875623-39875624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146924838	chr7:39875656-39875657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531727426	chr7:39875773-39875774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375372702	chr7:39875799-39875800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs137939145	chr7:39875809-39875810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566295485	chr7:39875893-39875894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541267271	chr7:39875910-39875911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558292842	chr7:39875966-39875967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199520798	chr7:39875988-39875989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112594430	chr7:39875989-39875990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371767435	chr7:39875994-39875995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578171854	chr7:39875995-39875996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4442036	chr7:39876015-39876016	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs79260433	chr7:39876041-39876042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112258512	chr7:39876042-39876043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570047639	chr7:39876043-39876044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542578789	chr7:39876071-39876072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141781044	chr7:39876086-39876087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75279094	chr7:39876111-39876112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544847474	chr7:39876121-39876122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564637023	chr7:39876136-39876137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4576335	chr7:39876138-39876139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550532162	chr7:39876159-39876160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs59418652	chr7:39876162-39876163	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529559653	chr7:39876188-39876189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150601932	chr7:39876222-39876223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1757 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39872600-39875000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr7:39873400-39877800	Weak transcription	Ovary	ovary
3	chr7:39873400-39878000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr7:39873400-39878000	Weak transcription	Pancreas	Pancrea
5	chr7:39873800-39877800	Weak transcription	Adipose Nuclei	Adipose
6	chr7:39873800-39878000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:39873800-39878000	Weak transcription	HMEC	breast
8	chr7:39874400-39875400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:39875200-39875600	Enhancers	HepG2	liver
10	chr7:39877600-39878000	Bivalent Enhancer	Fetal Lung	lung
11	chr7:39877800-39878200	Enhancers	Adipose Nuclei	Adipose
12	chr7:39877800-39879600	Enhancers	Ovary	ovary
13	chr7:39878000-39878200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:39878000-39878200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
15	chr7:39878000-39878200	Flanking Active TSS	Duodenum Mucosa	Duodenum
16	chr7:39878000-39878200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
17	chr7:39878000-39878200	Bivalent Enhancer	Fetal Muscle Leg	muscle
18	chr7:39878000-39878200	Enhancers	Pancreas	Pancrea
19	chr7:39878000-39878200	Bivalent Enhancer	NHEK	skin
20	chr7:39878000-39878400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr7:39878000-39878400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:39878000-39878400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:39878000-39878400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:39878000-39878400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:39878000-39878400	Enhancers	HMEC	breast
26	chr7:39884600-39884800	Bivalent Enhancer	Fetal Lung	lung
27	chr7:39884600-39885600	Enhancers	Hela-S3	cervix
28	chr7:39894000-39894200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:39894200-39894400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:39894200-39894400	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:39894200-39894400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:39894200-39894400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:39894200-39894400	Bivalent Enhancer	NH-A	brain
34	chr7:39894200-39894600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:39894200-39894800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:39894200-39894800	Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr7:39894200-39895000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
38	chr7:39894200-39895000	Active TSS	Primary hematopoietic stem cells	blood
39	chr7:39894200-39895000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:39894200-39895000	Active TSS	Brain Angular Gyrus	brain
41	chr7:39894200-39895000	Active TSS	Brain Substantia Nigra	brain
42	chr7:39894200-39895000	Bivalent/Poised TSS	Fetal Lung	lung
43	chr7:39894200-39895000	Active TSS	Fetal Muscle Trunk	muscle
44	chr7:39894200-39895000	Active TSS	Right Atrium	heart
45	chr7:39894200-39895000	Active TSS	Right Ventricle	heart
46	chr7:39894200-39895000	Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr7:39894200-39895200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:39894200-39895200	Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr7:39894200-39895200	Active TSS	Psoas Muscle	Psoas
50	chr7:39894200-39895200	Bivalent/Poised TSS	NHDF-Ad	bronchial

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