Variant report

Variant	nsv464437
Chromosome Location	chr7:40094641-40197168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1351)
CpG islands
(count:1100)
Chromatin interactive
region (count:52)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:40139011-40139191	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:40163349-40163518	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:40174061-40174516	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:40138413-40138773	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:40098322-40098610	K562	blood:	n/a	n/a
6	ARID3A	chr7:40174131-40174567	K562	blood:	n/a	n/a
7	ARID3A	chr7:40110475-40110675	K562	blood:	n/a	n/a
8	ARID3A	chr7:40135727-40135825	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:40134894-40135287	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:40162343-40162462	HepG2	liver:	n/a	n/a
11	ATF1	chr7:40117561-40117768	K562	blood:	n/a	n/a
12	ATF2	chr7:40174002-40174636	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:40173849-40174728	GM12878	blood:	n/a	n/a
14	ATF2	chr7:40173956-40174637	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr7:40174016-40174606	GM12878	blood:	n/a	n/a
16	ATF3	chr7:40173976-40174641	A549	lung:	n/a	n/a
17	ATF3	chr7:40173901-40174629	A549	lung:	n/a	n/a
18	ATF3	chr7:40096977-40097167	K562	blood:	n/a	n/a
19	BACH1	chr7:40174222-40174905	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:40098245-40098605	K562	blood:	n/a	n/a
21	BACH1	chr7:40134033-40134217	K562	blood:	n/a	n/a
22	BACH1	chr7:40098271-40098628	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr7:40174134-40174601	GM12878	blood:	n/a	chr7:40174245-40174254
24	BATF	chr7:40181515-40181798	GM12878	blood:	n/a	chr7:40181662-40181673
25	BCL11A	chr7:40174137-40174355	GM12878	blood:	n/a	chr7:40174323-40174332
26	BCL3	chr7:40173835-40174647	A549	lung:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
27	BCL3	chr7:40173988-40174683	A549	lung:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
28	BCLAF1	chr7:40173790-40174695	GM12878	blood:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
29	BCLAF1	chr7:40174018-40174592	K562	blood:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
30	BCLAF1	chr7:40173997-40174755	K562	blood:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
31	BCLAF1	chr7:40173871-40174728	GM12878	blood:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
32	BHLHE40	chr7:40174103-40175029	HepG2	liver:	n/a	chr7:40174959-40174975
33	BHLHE40	chr7:40174090-40174761	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:40098417-40098988	K562	blood:	n/a	n/a
35	BHLHE40	chr7:40174170-40174571	A549	lung:	n/a	n/a
36	BHLHE40	chr7:40173931-40174967	K562	blood:	n/a	n/a
37	BHLHE40	chr7:40133785-40133889	K562	blood:	n/a	n/a
38	BHLHE40	chr7:40096875-40097314	K562	blood:	n/a	n/a
39	BRCA1	chr7:40174088-40174514	GM12878	blood:	n/a	n/a
40	BRCA1	chr7:40174122-40174683	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr7:40174112-40174925	HepG2	liver:	n/a	n/a
42	BRCA1	chr7:40173982-40174672	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr7:40173829-40174749	K562	blood:	n/a	n/a
44	CBX3	chr7:40174090-40174469	K562	blood:	n/a	n/a
45	CBX3	chr7:40173906-40174948	HCT-116	colon:	n/a	n/a
46	CBX3	chr7:40096872-40097273	K562	blood:	n/a	n/a
47	CBX3	chr7:40181450-40182008	HCT-116	colon:	n/a	n/a
48	CCNT2	chr7:40173858-40175059	K562	blood:	n/a	n/a
49	CCNT2	chr7:40143597-40143730	K562	blood:	n/a	n/a
50	CEBPB	chr7:40124115-40124426	HepG2	liver:	n/a	chr7:40124257-40124268

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40098119-40098169	H1-hESC	embryonic stem cell:	embryo
2	chr7:40177071-40177121	NT2-D1	testis:	n/a
3	chr7:40098119-40098169	H1-hESC	embryonic stem cell:	embryo
4	chr7:40177071-40177121	NT2-D1	testis:	n/a
5	chr7:40174463-40174513	CMK	blood:	n/a
6	chr7:40172521-40172571	NH-A	brain:	n/a
7	chr7:40174463-40174513	AoSMC	blood vessel:	n/a
8	chr7:40174463-40174513	A549	lung:	n/a
9	chr7:40174274-40174324	HRPEpiC	eye:	n/a
10	chr7:40173613-40173663	HCPEpiC	choroid plexus:	n/a
11	chr7:40171342-40171392	ovcar-3	ovarian:	n/a
12	chr7:40174330-40174380	HIPEpiC	eye:	n/a
13	chr7:40174191-40174241	RPTEC	kidney:	n/a
14	chr7:40174463-40174513	HEK293	kidney:	embryo
15	chr7:40172521-40172571	NHBE	bronchial:	n/a
16	chr7:40173613-40173663	GM06990	blood:	n/a
17	chr7:40098119-40098169	PFSK-1	brain:	n/a
18	chr7:40174410-40174460	HCPEpiC	choroid plexus:	n/a
19	chr7:40177071-40177121	HEEpiC	esophagus:	n/a
20	chr7:40175036-40175086	HEEpiC	esophagus:	n/a
21	chr7:40174490-40174540	ovcar-3	ovarian:	n/a
22	chr7:40174843-40174893	BE2_C	brain:	n/a
23	chr7:40174274-40174324	ECC-1	luminal epithelium:	n/a
24	chr7:40172521-40172571	NHDF-neo	bronchial:	n/a
25	chr7:40174191-40174241	NB4	blood:	n/a
26	chr7:40177071-40177121	HL-60	blood:	n/a
27	chr7:40098119-40098169	GM12878	blood:	n/a
28	chr7:40174490-40174540	H1-hESC	embryonic stem cell:	embryo
29	chr7:40174274-40174324	GM12878	blood:	n/a
30	chr7:40098119-40098169	Caco-2	colon:	n/a
31	chr7:40172521-40172571	BE2_C	brain:	n/a
32	chr7:40174463-40174513	HL-60	blood:	n/a
33	chr7:40171342-40171392	GM06990	blood:	n/a
34	chr7:40172521-40172571	Hela-S3	cervix:	n/a
35	chr7:40174330-40174380	HCT-116	colon:	n/a
36	chr7:40174463-40174513	GM12878	blood:	n/a
37	chr7:40174274-40174324	HCT-116	colon:	n/a
38	chr7:40174270-40174320	ProgFib	skin:	n/a
39	chr7:40174330-40174380	Jurkat	blood:	n/a
40	chr7:40174274-40174324	HMEC	breast:	n/a
41	chr7:40177071-40177121	ECC-1	luminal epithelium:	n/a
42	chr7:40173613-40173663	NH-A	brain:	n/a
43	chr7:40174270-40174320	SK-N-SH_RA	brain:	n/a
44	chr7:40172521-40172571	H1-hESC	embryonic stem cell:	embryo
45	chr7:40174327-40174377	HEEpiC	esophagus:	n/a
46	chr7:40175036-40175086	LNCaP	prostate:	n/a
47	chr7:40174490-40174540	BE2_C	brain:	n/a
48	chr7:40174191-40174241	NT2-D1	testis:	n/a
49	chr7:40098119-40098169	HRE	kidney:	n/a
50	chr7:40174843-40174893	SK-N-MC	brain:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:
2	chr7:39874655..39876948-chr7:40167976..40170537,2	MCF-7	breast:
3	chr7:39987649..39989294-chr7:40160123..40163099,2	K562	blood:
4	chr7:40157076..40159444-chr7:40173522..40176316,2	K562	blood:
5	chr7:40105682..40108224-chr7:40109570..40112415,2	K562	blood:
6	chr7:40165267..40167211-chr7:40171970..40173571,2	K562	blood:
7	chr7:40148186..40149710-chr7:40154500..40156968,2	K562	blood:
8	chr7:39985235..39991458-chr7:40172332..40176244,8	K562	blood:
9	chr7:40183573..40185979-chr7:40191227..40192891,2	K562	blood:
10	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
11	chr7:40109257..40111529-chr7:40116739..40118703,2	K562	blood:
12	chr7:40165267..40167211-chr7:40171970..40173571,2	K562	blood:
13	chr7:39987485..39989678-chr7:40173138..40176244,4	K562	blood:
14	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
15	chr5:72111975..72112885-chr7:40174048..40174680,2	Hela-S3	cervix:
16	chr7:39987353..39988943-chr7:40114287..40116137,2	K562	blood:
17	chr7:39989838..39991458-chr7:40172726..40174247,2	K562	blood:
18	chr7:40093916..40096892-chr7:40098882..40101191,2	K562	blood:
19	chr7:39957754..39959391-chr7:40170682..40173574,2	MCF-7	breast:
20	chr20:45945819..45948556-chr7:40171300..40173134,2	MCF-7	breast:
21	chr7:40167264..40171884-chr7:40172209..40175327,5	K562	blood:
22	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
23	chr7:40098014..40099578-chr7:40101201..40104032,2	K562	blood:
24	chr7:40162725..40164570-chr7:40170579..40173215,2	MCF-7	breast:
25	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:
26	chr7:40139705..40142810-chr7:40143193..40146222,3	K562	blood:
27	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
28	chr20:30326378..30327220-chr7:40174029..40174591,2	Hela-S3	cervix:
29	chr7:39987767..39989590-chr7:40096379..40098788,2	K562	blood:
30	chr7:40105682..40108224-chr7:40109570..40112415,2	K562	blood:
31	chr7:40167562..40171134-chr7:40171634..40175290,4	MCF-7	breast:
32	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
33	chr7:40161714..40163470-chr7:40165770..40168688,2	MCF-7	breast:
34	chr7:40098014..40099578-chr7:40101201..40104032,2	K562	blood:
35	chr7:40090602..40093136-chr7:40095056..40097125,2	K562	blood:
36	chr7:40130215..40132846-chr7:40133657..40135422,2	K562	blood:
37	chr7:39922523..39924083-chr7:40170762..40172465,2	K562	blood:
38	chr7:10979872..10980668-chr7:40173740..40174309,2	Hela-S3	cervix:
39	chr15:93351708..93352444-chr7:40174029..40174595,2	Hela-S3	cervix:
40	chr7:40162391..40165100-chr7:40174021..40176292,2	K562	blood:
41	chr7:40162725..40164570-chr7:40170579..40173215,2	MCF-7	breast:
42	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
43	chr7:40139705..40142810-chr7:40143193..40146222,3	K562	blood:
44	chr7:40093916..40096892-chr7:40098882..40101191,2	K562	blood:
45	chr7:40167562..40171134-chr7:40171634..40175290,4	MCF-7	breast:
46	chr7:40117676..40119529-chr7:40167964..40170464,2	K562	blood:
47	chr17:59501958..59502789-chr7:40112228..40112887,2	MCF-7	breast:
48	chr7:40167264..40171884-chr7:40172209..40175327,5	K562	blood:
49	chr7:40157051..40160727-chr7:40165883..40170112,5	K562	blood:
50	chr7:40183573..40185979-chr7:40191227..40192891,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDK13-4	chr7:40192631-40193750	NONHSAT120248
2	lnc-CDK13-4	chr7:40192040-40192296	NONHSAT120248
3	lnc-CDK13-3	chr7:40155284-40155542	NONHSAT120244
4	lnc-C7orf10-3	chr7:40174482-40174719	NONHSAT120247
5	lnc-C7orf10-4	chr7:40172588-40174207	NONHSAT120246
6	lnc-CDK13-4	chr7:40191212-40191314	NONHSAT120248
7	lnc-C7orf10-5	chr7:40135564-40136731	NONHSAT120243

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDK13	hsa-miR-133b	chr7:40134910-40134934
2	CDK13	hsa-miR-133b	chr7:40134927-40134933

Variant related genes	Relation type
CDK13	TF binding region
ENSG00000199273	TF binding region
SUGCT	TF binding region
ENSG00000270577	TF binding region
ENSG00000248711	TF binding region
ENSG00000273444	TF binding region
MPLKIP	TF binding region
CDK13	CpG island
ENSG00000199273	CpG island
SUGCT	CpG island
ENSG00000270577	CpG island
ENSG00000248711	CpG island
ENSG00000273444	CpG island
MPLKIP	CpG island
ENSG00000271185	chromatin interactions
ENSG00000175600	chromatin interactions
ENSG00000267882	chromatin interactions
ENSG00000088325	chromatin interactions
ENSG00000199273	chromatin interactions
ENSG00000083312	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000270577	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000258922	chromatin interactions
ENSG00000249085	chromatin interactions
ENSG00000189043	chromatin interactions
ENSG00000168303	chromatin interactions

Extended variants
information (count: 3823 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3823 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9639820	chr7:40094641-40094642	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554895758	chr7:40094650-40094651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76784924	chr7:40094662-40094663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555923580	chr7:40094679-40094680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569845621	chr7:40094712-40094713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368906424	chr7:40094756-40094757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56001601	chr7:40094795-40094796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs59114022	chr7:40094796-40094797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192258350	chr7:40094809-40094810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558165307	chr7:40094862-40094863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578216857	chr7:40094871-40094872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10234693	chr7:40094917-40094918	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183251267	chr7:40094919-40094920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574303264	chr7:40094920-40094921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543094648	chr7:40094926-40094927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559893556	chr7:40094961-40094962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373369752	chr7:40094995-40094996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528483213	chr7:40095003-40095004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545448184	chr7:40095008-40095009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565019392	chr7:40095072-40095073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530801780	chr7:40095107-40095108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550625013	chr7:40095218-40095219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567407865	chr7:40095273-40095274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369067411	chr7:40095307-40095308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558567748	chr7:40095313-40095314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113710505	chr7:40095407-40095408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535310846	chr7:40095420-40095421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143986269	chr7:40095473-40095474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538224454	chr7:40095521-40095522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558557069	chr7:40095561-40095562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568775562	chr7:40095586-40095587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537721225	chr7:40095614-40095615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557370672	chr7:40095622-40095623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574242329	chr7:40095647-40095648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543281981	chr7:40095700-40095701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553499653	chr7:40095761-40095762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573411238	chr7:40095825-40095826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545188577	chr7:40095869-40095870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553730030	chr7:40095889-40095890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565257066	chr7:40095907-40095908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187977115	chr7:40095972-40095973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28706701	chr7:40096060-40096061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148663018	chr7:40096077-40096078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529836976	chr7:40096096-40096097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546418891	chr7:40096197-40096198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566212622	chr7:40096249-40096250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142890164	chr7:40096256-40096257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12533272	chr7:40096299-40096300	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs575021055	chr7:40096301-40096302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568787606	chr7:40096327-40096328	Weak transcription Strong 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
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2002 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40026600-40096800	Weak transcription	Right Ventricle	heart
2	chr7:40028000-40127800	Weak transcription	Colonic Mucosa	Colon
3	chr7:40043600-40095200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:40043600-40127800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr7:40044400-40096000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:40047600-40102600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:40048000-40102400	Weak transcription	HMEC	breast
8	chr7:40048000-40102400	Weak transcription	NHEK	skin
9	chr7:40049000-40096200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr7:40055600-40126400	Weak transcription	Aorta	Aorta
11	chr7:40055800-40097000	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr7:40055800-40102400	Weak transcription	NHLF	lung
13	chr7:40055800-40110000	Weak transcription	Gastric	stomach
14	chr7:40055800-40127600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr7:40055800-40127600	Weak transcription	Rectal Smooth Muscle	rectum
16	chr7:40056000-40097000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:40056000-40097800	Weak transcription	Brain Hippocampus Middle	brain
18	chr7:40056000-40097800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr7:40056000-40105400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr7:40056000-40112200	Weak transcription	HepG2	liver
21	chr7:40056200-40128600	Weak transcription	A549	lung
22	chr7:40058400-40101800	Weak transcription	Fetal Brain Male	brain
23	chr7:40058600-40126800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:40059000-40125200	Weak transcription	Fetal Kidney	kidney
25	chr7:40060200-40102400	Weak transcription	NHDF-Ad	bronchial
26	chr7:40060400-40098800	Weak transcription	Brain Anterior Caudate	brain
27	chr7:40067400-40096000	Weak transcription	NH-A	brain
28	chr7:40067600-40096800	Weak transcription	Left Ventricle	heart
29	chr7:40067800-40095600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:40070600-40104000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:40072000-40096000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr7:40072000-40098800	Weak transcription	Ovary	ovary
33	chr7:40072000-40104000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr7:40072000-40130400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr7:40072600-40101000	Weak transcription	Primary hematopoietic stem cells	blood
36	chr7:40074000-40097000	Weak transcription	Right Atrium	heart
37	chr7:40074000-40102600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr7:40074600-40097000	Weak transcription	Adipose Nuclei	Adipose
39	chr7:40075200-40096000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr7:40075800-40096600	Weak transcription	Lung	lung
41	chr7:40075800-40102400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:40076200-40102400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr7:40076200-40106800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:40076400-40096000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:40077200-40098800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:40077200-40102400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr7:40077200-40102600	Weak transcription	GM12878-XiMat	blood
48	chr7:40077200-40127800	Weak transcription	Esophagus	oesophagus
49	chr7:40077400-40096200	Weak transcription	HSMM	muscle
50	chr7:40080200-40132400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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