Variant report

Variant	esv2756801
Chromosome Location	chr7:40060180-40269583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2212)
CpG islands
(count:1221)
Chromatin interactive
region (count:84)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2212 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:40163349-40163518	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:40162343-40162462	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:40110475-40110675	K562	blood:	n/a	n/a
4	ARID3A	chr7:40174061-40174516	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:40139011-40139191	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:40092188-40092405	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:40138413-40138773	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:40098322-40098610	K562	blood:	n/a	n/a
9	ARID3A	chr7:40174131-40174567	K562	blood:	n/a	n/a
10	ARID3A	chr7:40135727-40135825	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:40134894-40135287	HepG2	liver:	n/a	n/a
12	ATF1	chr7:40117561-40117768	K562	blood:	n/a	n/a
13	ATF2	chr7:40174016-40174606	GM12878	blood:	n/a	n/a
14	ATF2	chr7:40173956-40174637	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr7:40174002-40174636	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr7:40173849-40174728	GM12878	blood:	n/a	n/a
17	ATF3	chr7:40173976-40174641	A549	lung:	n/a	n/a
18	ATF3	chr7:40096977-40097167	K562	blood:	n/a	n/a
19	ATF3	chr7:40173901-40174629	A549	lung:	n/a	n/a
20	BACH1	chr7:40078099-40078178	K562	blood:	n/a	n/a
21	BACH1	chr7:40174222-40174905	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:40098245-40098605	K562	blood:	n/a	n/a
23	BACH1	chr7:40098271-40098628	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:40134033-40134217	K562	blood:	n/a	n/a
25	BATF	chr7:40174134-40174601	GM12878	blood:	n/a	chr7:40174245-40174254
26	BATF	chr7:40181515-40181798	GM12878	blood:	n/a	chr7:40181662-40181673
27	BCL11A	chr7:40174137-40174355	GM12878	blood:	n/a	chr7:40174323-40174332
28	BCL3	chr7:40173835-40174647	A549	lung:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
29	BCL3	chr7:40173988-40174683	A549	lung:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
30	BCLAF1	chr7:40174018-40174592	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	BCLAF1	chr7:40173790-40174695	GM12878	blood:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
33	BCLAF1	chr7:40173997-40174755	K562	blood:	n/a	chr7:40174553-40174566 chr7:40174323-40174332
34	BHLHE40	chr7:40174170-40174571	A549	lung:	n/a	n/a
35	BHLHE40	chr7:40174090-40174761	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:40092120-40092431	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:40098417-40098988	K562	blood:	n/a	n/a
38	BHLHE40	chr7:40174103-40175029	HepG2	liver:	n/a	chr7:40174959-40174975
39	BHLHE40	chr7:40133785-40133889	K562	blood:	n/a	n/a
40	BHLHE40	chr7:40096875-40097314	K562	blood:	n/a	n/a
41	BHLHE40	chr7:40173931-40174967	K562	blood:	n/a	n/a
42	BRCA1	chr7:40173982-40174672	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr7:40174088-40174514	GM12878	blood:	n/a	n/a
44	BRCA1	chr7:40174112-40174925	HepG2	liver:	n/a	n/a
45	BRCA1	chr7:40174122-40174683	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr7:40174090-40174469	K562	blood:	n/a	n/a
47	CBX3	chr7:40173906-40174948	HCT-116	colon:	n/a	n/a
48	CBX3	chr7:40173829-40174749	K562	blood:	n/a	n/a
49	CBX3	chr7:40181450-40182008	HCT-116	colon:	n/a	n/a
50	CBX3	chr7:40096872-40097273	K562	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40175036-40175086	HepG2	liver:	n/a
2	chr7:40175036-40175086	HepG2	liver:	n/a
3	chr7:40174653-40174703	SKMC	muscle:	n/a
4	chr7:40098119-40098169	GM12892	blood:	n/a
5	chr7:40174274-40174324	SKMC	muscle:	n/a
6	chr7:40174653-40174703	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:40174490-40174540	HL-60	blood:	n/a
8	chr7:40173613-40173663	Jurkat	blood:	n/a
9	chr7:40174330-40174380	GM06990	blood:	n/a
10	chr7:40174653-40174703	NB4	blood:	n/a
11	chr7:40171342-40171392	NHBE	bronchial:	n/a
12	chr7:40174653-40174703	HMEC	breast:	n/a
13	chr7:40174490-40174540	U87	brain:	n/a
14	chr7:40177071-40177121	HepG2	liver:	n/a
15	chr7:40240143-40240193	HAEpiC	amniotic membrane:	n/a
16	chr7:40173882-40173932	BE2_C	brain:	n/a
17	chr7:40098119-40098169	HUVEC	blood vessel:	n/a
18	chr7:40174327-40174377	SK-N-SH	brain:	n/a
19	chr7:40174463-40174513	CMK	blood:	n/a
20	chr7:40172521-40172571	GM12891	blood:	n/a
21	chr7:40098119-40098169	K562	blood:	n/a
22	chr7:40174653-40174703	RPTEC	kidney:	n/a
23	chr7:40098119-40098169	LNCaP	prostate:	n/a
24	chr7:40240143-40240193	HRE	kidney:	n/a
25	chr7:40174843-40174893	U87	brain:	n/a
26	chr7:40174463-40174513	GM06990	blood:	n/a
27	chr7:40174490-40174540	SK-N-SH_RA	brain:	n/a
28	chr7:40174653-40174703	Hepatocyte	liver:	n/a
29	chr7:40171342-40171392	AG04449	skin:	fetal
30	chr7:40177071-40177121	SK-N-MC	brain:	n/a
31	chr7:40174274-40174324	SAEC	small airway:	n/a
32	chr7:40174270-40174320	PFSK-1	brain:	n/a
33	chr7:40172521-40172571	K562	blood:	n/a
34	chr7:40174653-40174703	ProgFib	skin:	n/a
35	chr7:40174463-40174513	AG09319	gingival:	n/a
36	chr7:40172521-40172571	GM06990	blood:	n/a
37	chr7:40174327-40174377	IMR90	lung:	fetal
38	chr7:40171342-40171392	HEK293	kidney:	embryo
39	chr7:40174410-40174460	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:40174327-40174377	SAEC	small airway:	n/a
41	chr7:40173613-40173663	NHDF-neo	bronchial:	n/a
42	chr7:40173613-40173663	HRE	kidney:	n/a
43	chr7:40174463-40174513	Hela-S3	cervix:	n/a
44	chr7:40174270-40174320	HMEC	breast:	n/a
45	chr7:40174274-40174324	NH-A	brain:	n/a
46	chr7:40174330-40174380	NHBE	bronchial:	n/a
47	chr7:40174225-40174275	RPTEC	kidney:	n/a
48	chr7:40175036-40175086	NB4	blood:	n/a
49	chr7:40174327-40174377	MCF10A-Er-Src	breast:	n/a
50	chr7:40172521-40172571	SKMC	muscle:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:72111975..72112885-chr7:40174048..40174680,2	Hela-S3	cervix:
2	chr7:40048549..40051232-chr7:40060255..40062264,2	K562	blood:
3	chr7:40259840..40262064-chr7:40262266..40264754,2	K562	blood:
4	chr7:40157076..40159444-chr7:40173522..40176316,2	K562	blood:
5	chr7:39985235..39991458-chr7:40172332..40176244,8	K562	blood:
6	chr7:40165267..40167211-chr7:40171970..40173571,2	K562	blood:
7	chr7:40241300..40243620-chr7:40251162..40253022,2	K562	blood:
8	chr7:39988782..39993568-chr7:40089798..40094373,7	MCF-7	breast:
9	chr7:39935762..39936421-chr7:40091763..40092363,2	K562	blood:
10	chr7:40130215..40132846-chr7:40133657..40135422,2	K562	blood:
11	chr7:40259840..40262064-chr7:40262266..40264754,2	K562	blood:
12	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
13	chr7:40167264..40171884-chr7:40172209..40175327,5	K562	blood:
14	chr11:126173275..126173777-chr7:40061848..40062348,2	NB4	blood:
15	chr7:40162725..40164570-chr7:40170579..40173215,2	MCF-7	breast:
16	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
17	chr7:40157051..40160727-chr7:40165883..40170112,5	K562	blood:
18	chr7:40080571..40083008-chr7:40084879..40087447,2	MCF-7	breast:
19	chr7:40109257..40111529-chr7:40116739..40118703,2	K562	blood:
20	chr7:39989467..39991419-chr7:40087056..40089179,2	K562	blood:
21	chr7:40139705..40142810-chr7:40143193..40146222,3	K562	blood:
22	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
23	chr7:40055192..40057711-chr7:40058795..40061552,3	K562	blood:
24	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
25	chr15:93351708..93352444-chr7:40174029..40174595,2	Hela-S3	cervix:
26	chr7:40162391..40165100-chr7:40174021..40176292,2	K562	blood:
27	chr7:39619647..39620204-chr7:40092201..40092766,2	K562	blood:
28	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:
29	chr7:40084993..40087566-chr7:40090698..40092927,2	K562	blood:
30	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
31	chr7:40167264..40171884-chr7:40172209..40175327,5	K562	blood:
32	chr7:40162725..40164570-chr7:40170579..40173215,2	MCF-7	breast:
33	chr7:40090602..40093136-chr7:40095056..40097125,2	K562	blood:
34	chr7:40131598..40134106-chr7:40137449..40139937,2	MCF-7	breast:
35	chr7:39987485..39989678-chr7:40173138..40176244,4	K562	blood:
36	chr7:40167562..40171134-chr7:40171634..40175290,4	MCF-7	breast:
37	chr7:39874655..39876948-chr7:40167976..40170537,2	MCF-7	breast:
38	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
39	chr7:39922523..39924083-chr7:40170762..40172465,2	K562	blood:
40	chr7:40167562..40171134-chr7:40171634..40175290,4	MCF-7	breast:
41	chr7:40093916..40096892-chr7:40098882..40101191,2	K562	blood:
42	chr20:45945819..45948556-chr7:40171300..40173134,2	MCF-7	breast:
43	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
44	chr7:40148186..40149710-chr7:40154500..40156968,2	K562	blood:
45	chr7:39784501..39786932-chr7:40060004..40061750,2	MCF-7	breast:
46	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
47	chr7:39987767..39989590-chr7:40096379..40098788,2	K562	blood:
48	chr7:40183573..40185979-chr7:40191227..40192891,2	K562	blood:
49	chr7:39987353..39988943-chr7:40114287..40116137,2	K562	blood:
50	chr7:39988058..39990368-chr7:40072620..40075295,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDK13-4	chr7:40191212-40191314	NONHSAT120248
2	lnc-C7orf10-4	chr7:40172588-40174207	NONHSAT120246
3	lnc-CDK13-4	chr7:40192631-40193750	NONHSAT120248
4	lnc-C7orf10-3	chr7:40174482-40174719	NONHSAT120247
5	lnc-C7orf10-3	chr7:40220547-40220597	NONHSAT120247
6	lnc-C7orf10-3	chr7:40221555-40221615	NONHSAT120247
7	lnc-CDK13-3	chr7:40155284-40155542	NONHSAT120244
8	lnc-C7orf11-8	chr7:40264706-40264758	NONHSAT120249
9	lnc-C7orf10-5	chr7:40135564-40136731	NONHSAT120243
10	lnc-CDK13-4	chr7:40192040-40192296	NONHSAT120248

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
ENSG00000270577	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000088325	chromatin interactions
ENSG00000267882	chromatin interactions
ENSG00000199273	chromatin interactions
ENSG00000168303	chromatin interactions
ENSG00000110063	chromatin interactions
ENSG00000249085	chromatin interactions
ENSG00000258922	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000175600	chromatin interactions
ENSG00000189043	chromatin interactions
ENSG00000271185	chromatin interactions
ENSG00000083312	chromatin interactions

Extended variants
information (count: 7739 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:7739 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17526699	chr7:40060180-40060181	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575952365	chr7:40060189-40060190	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs190992683	chr7:40060220-40060221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543406301	chr7:40060245-40060246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569308999	chr7:40060270-40060271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73392711	chr7:40060325-40060326	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114091036	chr7:40060351-40060352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574653177	chr7:40060388-40060389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533940192	chr7:40060397-40060398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17496436	chr7:40060400-40060401	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371702407	chr7:40060410-40060411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545526975	chr7:40060419-40060420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562118986	chr7:40060429-40060430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575961072	chr7:40060450-40060451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541479047	chr7:40060534-40060535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561589108	chr7:40060550-40060551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377174346	chr7:40060554-40060555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183243531	chr7:40060559-40060560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187898684	chr7:40060563-40060564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568920054	chr7:40060646-40060647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532230011	chr7:40060660-40060661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12701790	chr7:40060690-40060691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13239627	chr7:40060696-40060697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201663660	chr7:40060698-40060699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111490308	chr7:40060699-40060700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201387544	chr7:40060702-40060703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202141003	chr7:40060703-40060704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532636967	chr7:40060707-40060708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552733621	chr7:40060709-40060710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200884223	chr7:40060721-40060722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs118159040	chr7:40060751-40060752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538198465	chr7:40060767-40060768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548294618	chr7:40060777-40060778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190516012	chr7:40060790-40060791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533880971	chr7:40060858-40060859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12673210	chr7:40060866-40060867	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs576653202	chr7:40060898-40060899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530284556	chr7:40060930-40060931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150288765	chr7:40060993-40060994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138212815	chr7:40061002-40061003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576069427	chr7:40061020-40061021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs17496457	chr7:40061035-40061036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561578066	chr7:40061078-40061079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76028602	chr7:40061088-40061089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201434638	chr7:40061089-40061090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs398085741	chr7:40061096-40061097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs397807844	chr7:40061097-40061098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376453377	chr7:40061178-40061179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570324945	chr7:40061237-40061238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369705206	chr7:40061269-40061270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2921 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40020400-40077600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:40025800-40062800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:40025800-40082200	Weak transcription	Spleen	Spleen
4	chr7:40026000-40071200	Weak transcription	Brain Germinal Matrix	brain
5	chr7:40026600-40096800	Weak transcription	Right Ventricle	heart
6	chr7:40028000-40077800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr7:40028000-40127800	Weak transcription	Colonic Mucosa	Colon
8	chr7:40028200-40073000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr7:40034400-40072200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr7:40042800-40070400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr7:40043000-40061600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:40043600-40067000	Weak transcription	K562	blood
13	chr7:40043600-40071600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr7:40043600-40076000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:40043600-40079800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:40043600-40095200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr7:40043600-40127800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr7:40044400-40096000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:40047600-40102600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr7:40048000-40102400	Weak transcription	HMEC	breast
21	chr7:40048000-40102400	Weak transcription	NHEK	skin
22	chr7:40048400-40066600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:40048600-40074800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr7:40049000-40085600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr7:40049000-40085800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:40049000-40096200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr7:40049200-40074800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:40050000-40075400	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr7:40050400-40075000	Weak transcription	Esophagus	oesophagus
30	chr7:40051000-40071200	Weak transcription	Lung	lung
31	chr7:40052000-40066400	Weak transcription	NH-A	brain
32	chr7:40052400-40062600	Weak transcription	Fetal Intestine Small	intestine
33	chr7:40053200-40065400	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr7:40054400-40070800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:40055600-40064400	Weak transcription	Small Intestine	intestine
36	chr7:40055600-40126400	Weak transcription	Aorta	Aorta
37	chr7:40055800-40062800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:40055800-40070800	Weak transcription	Fetal Brain Female	brain
39	chr7:40055800-40070800	Weak transcription	Pancreas	Pancrea
40	chr7:40055800-40072000	Weak transcription	Stomach Mucosa	stomach
41	chr7:40055800-40074200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr7:40055800-40077000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:40055800-40077000	Weak transcription	Psoas Muscle	Psoas
44	chr7:40055800-40082600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr7:40055800-40092200	Weak transcription	Colon Smooth Muscle	Colon
46	chr7:40055800-40097000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr7:40055800-40102400	Weak transcription	NHLF	lung
48	chr7:40055800-40110000	Weak transcription	Gastric	stomach
49	chr7:40055800-40127600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr7:40055800-40127600	Weak transcription	Rectal Smooth Muscle	rectum

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