Variant report

Variant	nsv892052
Chromosome Location	chr9:1980819-2072470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2072)
CpG islands
(count:1468)
Chromatin interactive
region (count:59)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2072 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2015069-2015470	K562	blood:	n/a	n/a
2	ARID3A	chr9:2017419-2017721	K562	blood:	n/a	n/a
3	ARID3A	chr9:2014707-2015574	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:2022275-2022865	K562	blood:	n/a	n/a
5	ARID3A	chr9:1994315-1994445	HepG2	liver:	n/a	n/a
6	ATF1	chr9:2014946-2015514	K562	blood:	n/a	n/a
7	ATF1	chr9:2023624-2023993	K562	blood:	n/a	n/a
8	ATF2	chr9:2054946-2055805	GM12878	blood:	n/a	n/a
9	ATF2	chr9:2014754-2015575	GM12878	blood:	n/a	n/a
10	ATF2	chr9:2012168-2013278	GM12878	blood:	n/a	n/a
11	ATF2	chr9:2043068-2043725	GM12878	blood:	n/a	n/a
12	ATF2	chr9:2053700-2054321	GM12878	blood:	n/a	n/a
13	ATF2	chr9:2014857-2015545	GM12878	blood:	n/a	n/a
14	ATF2	chr9:2012174-2012977	GM12878	blood:	n/a	n/a
15	ATF2	chr9:2043092-2043667	GM12878	blood:	n/a	n/a
16	ATF2	chr9:2017261-2017815	GM12878	blood:	n/a	n/a
17	ATF2	chr9:2053653-2054478	GM12878	blood:	n/a	n/a
18	ATF2	chr9:2055011-2055808	GM12878	blood:	n/a	n/a
19	ATF3	chr9:1995224-1995511	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr9:2015135-2015500	K562	blood:	n/a	chr9:2015196-2015205
21	ATF3	chr9:2012355-2012584	K562	blood:	n/a	n/a
22	BACH1	chr9:2016045-2016494	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr9:2015202-2015228	K562	blood:	n/a	n/a
24	BACH1	chr9:2014722-2015365	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr9:2016857-2018078	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr9:2043195-2043566	GM12878	blood:	n/a	n/a
27	BATF	chr9:2012130-2012836	GM12878	blood:	n/a	chr9:2012489-2012500 chr9:2012494-2012504
28	BATF	chr9:2066304-2066596	GM12878	blood:	n/a	n/a
29	BATF	chr9:2055036-2055733	GM12878	blood:	n/a	chr9:2055534-2055544
30	BATF	chr9:2053830-2054274	GM12878	blood:	n/a	n/a
31	BATF	chr9:2015231-2015430	GM12878	blood:	n/a	n/a
32	BATF	chr9:2043270-2043543	GM12878	blood:	n/a	n/a
33	BATF	chr9:2012231-2012720	GM12878	blood:	n/a	chr9:2012489-2012500 chr9:2012494-2012504
34	BATF	chr9:2017409-2017661	GM12878	blood:	n/a	n/a
35	BATF	chr9:2015151-2015474	GM12878	blood:	n/a	n/a
36	BATF	chr9:2055078-2055684	GM12878	blood:	n/a	chr9:2055534-2055544
37	BATF	chr9:1982196-1982410	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:1982176-1982424	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:2053866-2054307	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:2018869-2019105	H1-hESC	embryonic stem cell:	n/a	n/a
41	BCL11A	chr9:2055123-2055702	GM12878	blood:	n/a	n/a
42	BCL11A	chr9:2053878-2054277	GM12878	blood:	n/a	n/a
43	BCL11A	chr9:2059398-2059873	GM12878	blood:	n/a	n/a
44	BCL11A	chr9:1982181-1982398	GM12878	blood:	n/a	n/a
45	BCL11A	chr9:2012367-2012638	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
46	BCL11A	chr9:2012252-2012716	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
47	BCL11A	chr9:2017312-2017744	GM12878	blood:	n/a	chr9:2017349-2017358
48	BCL11A	chr9:2055057-2055743	GM12878	blood:	n/a	n/a
49	BCL3	chr9:2012231-2012873	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
50	BCL3	chr9:2055084-2055684	GM12878	blood:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2047800-2047850	MCF-7	breast:	n/a
2	chr9:2050899-2050949	SK-N-MC	brain:	n/a
3	chr9:2016262-2016312	AoSMC	blood vessel:	n/a
4	chr9:2013970-2014020	AG09309	skin:	n/a
5	chr9:2047800-2047850	MCF-7	breast:	n/a
6	chr9:2050899-2050949	SK-N-MC	brain:	n/a
7	chr9:2016262-2016312	AoSMC	blood vessel:	n/a
8	chr9:2013970-2014020	AG09309	skin:	n/a
9	chr9:2047373-2047423	AG09309	skin:	n/a
10	chr9:2016340-2016390	SKMC	muscle:	n/a
11	chr9:2015788-2015838	BJ	skin:	n/a
12	chr9:2016253-2016303	NH-A	brain:	n/a
13	chr9:2017199-2017249	BJ	skin:	n/a
14	chr9:2011564-2011614	GM12892	blood:	n/a
15	chr9:2015039-2015089	HepG2	liver:	n/a
16	chr9:2016340-2016390	HL-60	blood:	n/a
17	chr9:2022036-2022086	GM12891	blood:	n/a
18	chr9:2016253-2016303	RPTEC	kidney:	n/a
19	chr9:2018164-2018214	NHBE	bronchial:	n/a
20	chr9:2016262-2016312	Jurkat	blood:	n/a
21	chr9:2024387-2024437	ovcar-3	ovarian:	n/a
22	chr9:2016608-2016658	HCT-116	colon:	n/a
23	chr9:2047595-2047645	K562	blood:	n/a
24	chr9:2018164-2018214	NH-A	brain:	n/a
25	chr9:2005484-2005534	HIPEpiC	eye:	n/a
26	chr9:2047160-2047210	HEK293	kidney:	embryo
27	chr9:2015788-2015838	SK-N-MC	brain:	n/a
28	chr9:2015635-2015685	U87	brain:	n/a
29	chr9:2005484-2005534	HAEpiC	amniotic membrane:	n/a
30	chr9:1995528-1995578	HRCEpiC	kidney:	n/a
31	chr9:2015039-2015089	MCF10A-Er-Src	breast:	n/a
32	chr9:2016608-2016658	H1-hESC	embryonic stem cell:	embryo
33	chr9:2017884-2017934	HIPEpiC	eye:	n/a
34	chr9:2011564-2011614	MCF10A-Er-Src	breast:	n/a
35	chr9:2018164-2018214	HRE	kidney:	n/a
36	chr9:2013970-2014020	K562	blood:	n/a
37	chr9:2005484-2005534	K562	blood:	n/a
38	chr9:2017884-2017934	IMR90	lung:	fetal
39	chr9:2017884-2017934	HNPCEpiC	eye:	n/a
40	chr9:2022036-2022086	HPAEpiC	pulmonary alveolar:	n/a
41	chr9:2024387-2024437	HEEpiC	esophagus:	n/a
42	chr9:2016608-2016658	PFSK-1	brain:	n/a
43	chr9:2017199-2017249	HUVEC	blood vessel:	n/a
44	chr9:2016253-2016303	SAEC	small airway:	n/a
45	chr9:2047373-2047423	A549	lung:	n/a
46	chr9:2044055-2044105	AG04449	skin:	fetal
47	chr9:2015788-2015838	RPTEC	kidney:	n/a
48	chr9:2015635-2015685	SAEC	small airway:	n/a
49	chr9:2015039-2015089	AoSMC	blood vessel:	n/a
50	chr9:2013970-2014020	GM19239	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:2014683..2019202-chr9:2026620..2030174,6	MCF-7	breast:
2	chr9:2009959..2012169-chr9:2015635..2018101,3	MCF-7	breast:
3	chr9:2015057..2017007-chr9:2029405..2032085,2	K562	blood:
4	chr9:2000498..2002228-chr9:2014699..2016855,2	K562	blood:
5	chr9:2061237..2063006-chr9:2063719..2066539,2	K562	blood:
6	chr9:2009046..2010738-chr9:2013715..2015276,2	K562	blood:
7	chr9:2061237..2063006-chr9:2063719..2066539,2	K562	blood:
8	chr9:2015290..2017230-chr9:2035454..2037354,2	MCF-7	breast:
9	chr9:2015281..2016857-chr9:6006319..6008670,2	K562	blood:
10	chr14:51410677..51411191-chr9:2017301..2017897,2	Hela-S3	cervix:
11	chr9:2009046..2010738-chr9:2013715..2015276,2	K562	blood:
12	chr9:2027542..2030484-chr9:2031269..2033941,3	K562	blood:
13	chr17:41465202..41465809-chr9:2016258..2017217,2	NB4	blood:
14	chr9:2019942..2022254-chr9:2022481..2024574,2	MCF-7	breast:
15	chr9:2038457..2040329-chr9:2040850..2042831,2	K562	blood:
16	chr9:2025406..2027101-chr9:2041465..2044182,2	K562	blood:
17	chr9:2014489..2016511-chr9:2066212..2068333,2	MCF-7	breast:
18	chr8:56986335..56987104-chr9:2016512..2017193,2	Hela-S3	cervix:
19	chr9:2016568..2019114-chr9:2030660..2033552,2	MCF-7	breast:
20	chr9:2012580..2014743-chr9:2038420..2041072,2	K562	blood:
21	chr9:1989591..1991606-chr9:2004303..2006836,2	MCF-7	breast:
22	chr9:2016568..2019114-chr9:2030660..2033552,2	MCF-7	breast:
23	chr9:2014683..2019202-chr9:2026620..2030174,6	MCF-7	breast:
24	chr9:2031596..2033809-chr9:2036447..2038109,2	MCF-7	breast:
25	chr9:2005250..2009172-chr9:2015225..2018704,4	K562	blood:
26	chr9:2038457..2040329-chr9:2040850..2042831,2	K562	blood:
27	chr9:2035810..2037705-chr9:2044015..2046964,2	K562	blood:
28	chr9:2006922..2009253-chr9:2013169..2015088,2	MCF-7	breast:
29	chr9:2006922..2009253-chr9:2013169..2015088,2	MCF-7	breast:
30	chr6:56407223..56407766-chr9:2014757..2015410,2	NB4	blood:
31	chr9:2016948..2019401-chr9:2068781..2070385,2	MCF-7	breast:
32	chr9:2025406..2027101-chr9:2041465..2044182,2	K562	blood:
33	chr9:2025445..2029095-chr9:2029321..2031633,5	K562	blood:
34	chr9:2013479..2017608-chr9:2017826..2022083,7	MCF-7	breast:
35	chr9:2004426..2007121-chr9:2015163..2018162,2	MCF-7	breast:
36	chr9:2016219..2019918-chr9:2022215..2026324,5	MCF-7	breast:
37	chr9:2027773..2030143-chr9:2034628..2037514,2	K562	blood:
38	chr9:2016166..2018399-chr9:2051368..2053339,2	MCF-7	breast:
39	chr9:2027542..2030484-chr9:2031269..2033941,3	K562	blood:
40	chr9:2012580..2014743-chr9:2038420..2041072,2	K562	blood:
41	chr9:2018308..2020609-chr9:2085608..2087272,2	K562	blood:
42	chr9:2015330..2018297-chr9:2035684..2039047,3	MCF-7	breast:
43	chr9:2017363..2019516-chr9:2029024..2032521,3	K562	blood:
44	chr9:2013479..2017608-chr9:2017826..2022083,7	MCF-7	breast:
45	chr9:2006630..2009336-chr9:2010265..2012993,2	K562	blood:
46	chr9:2014709..2017122-chr9:2062966..2067398,3	MCF-7	breast:
47	chr9:2014062..2016473-chr9:2041837..2045472,3	MCF-7	breast:
48	chr9:2009885..2011957-chr9:2013522..2016362,3	K562	blood:
49	chr9:1981753..1984012-chr9:2012148..2014267,2	K562	blood:
50	chr9:2019923..2022306-chr9:2028801..2031582,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCA2-4	chr9:2001764-2001896	NONHSAT129982
2	lnc-KIAA0020-2	chr9:2041900-2042130	ENSG00000236199.1
3	lnc-SMARCA2-3	chr9:2007539-2007793	expReg_chr9_128_+
4	lnc-KIAA0020-2	chr9:2045835-2046023	ENSG00000236199.1
5	lnc-VLDLR-4	chr9:2042994-2046019	NONHSAT129986
6	lnc-SMARCA2-4	chr9:2001907-2002409	NONHSAT129982

No data

Variant related genes	Relation type
ENSG00000236199	TF binding region
SMARCA2	TF binding region
ENSG00000224092	TF binding region
ENSG00000236199	CpG island
SMARCA2	CpG island
ENSG00000224092	CpG island
ENSG00000183354	chromatin interactions
ENSG00000151914	chromatin interactions
ENSG00000238650	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000236199	chromatin interactions
ENSG00000263575	chromatin interactions
ENSG00000080503	chromatin interactions
ENSG00000100504	chromatin interactions
ENSG00000008988	chromatin interactions

Extended variants
information (count: 4162 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:4162 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7858803	chr9:1980819-1980820	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536268659	chr9:1980883-1980884	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77879815	chr9:1980892-1980893	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs7847882	chr9:1980918-1980919	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs536352552	chr9:1980940-1980941	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs386731619	chr9:1980947-1980948	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs199667384	chr9:1980948-1980949	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs7858947	chr9:1980949-1980950	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs577779308	chr9:1980968-1980969	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs540297225	chr9:1980989-1980990	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553932335	chr9:1980990-1980991	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7858062	chr9:1980996-1980997	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs542632733	chr9:1981047-1981048	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs562547928	chr9:1981054-1981055	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs140454314	chr9:1981065-1981066	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs376427879	chr9:1981069-1981070	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545683655	chr9:1981116-1981117	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs565294195	chr9:1981126-1981127	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs527892814	chr9:1981135-1981136	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs144092161	chr9:1981164-1981165	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs117629573	chr9:1981201-1981202	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs146497664	chr9:1981209-1981210	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs530167199	chr9:1981262-1981263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549897318	chr9:1981277-1981278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192288006	chr9:1981282-1981283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544981472	chr9:1981287-1981288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537708566	chr9:1981315-1981316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551671787	chr9:1981342-1981343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61230160	chr9:1981353-1981354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554044797	chr9:1981396-1981397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112851031	chr9:1981397-1981398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140884720	chr9:1981414-1981415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555837077	chr9:1981445-1981446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150120474	chr9:1981450-1981451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532917040	chr9:1981464-1981465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78953625	chr9:1981472-1981473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182303026	chr9:1981487-1981488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185922598	chr9:1981512-1981513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190800160	chr9:1981532-1981533	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561186266	chr9:1981546-1981547	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530131152	chr9:1981574-1981575	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550258406	chr9:1981598-1981599	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs563501622	chr9:1981622-1981623	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs10120400	chr9:1981634-1981635	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs552318606	chr9:1981638-1981639	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs376599873	chr9:1981659-1981660	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571552921	chr9:1981698-1981699	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs182436141	chr9:1981733-1981734	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs376856492	chr9:1981737-1981738	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs374317271	chr9:1981743-1981744	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2911 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1976800-1981400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr9:1978200-1981600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:1979000-1981000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:1979000-1981000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:1979000-1981000	Enhancers	Left Ventricle	heart
6	chr9:1979000-1981000	Enhancers	HSMM	muscle
7	chr9:1979000-1982000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr9:1980200-1981000	Flanking Active TSS	NHDF-Ad	bronchial
9	chr9:1980200-1981200	Flanking Active TSS	Liver	Liver
10	chr9:1980400-1981000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr9:1980400-1981600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:1980400-1981800	Weak transcription	GM12878-XiMat	blood
13	chr9:1980600-1981000	Active TSS	Brain Germinal Matrix	brain
14	chr9:1980600-1981000	Enhancers	Fetal Lung	lung
15	chr9:1980600-1981000	Enhancers	Fetal Muscle Leg	muscle
16	chr9:1980600-1981000	Weak transcription	Fetal Stomach	stomach
17	chr9:1980600-1982000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr9:1980800-1981000	Enhancers	Ovary	ovary
19	chr9:1980800-1981400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:1981000-1981400	Enhancers	Fetal Stomach	stomach
21	chr9:1981000-1982200	Enhancers	NHDF-Ad	bronchial
22	chr9:1981200-1982200	Enhancers	Liver	Liver
23	chr9:1981800-1982400	Enhancers	GM12878-XiMat	blood
24	chr9:1982200-1982400	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr9:1982200-1989400	Weak transcription	Liver	Liver
26	chr9:1983200-1984000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr9:1983200-1984000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr9:1990600-1991000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:1990600-1991200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr9:1990600-1991200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr9:1990600-1991400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr9:1990600-1994200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:1990800-1991000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:1990800-1991000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr9:1990800-1991200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:1990800-1991400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr9:1991000-1993800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr9:1991200-1993800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr9:1991200-1994000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr9:1991200-1994200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:1991400-1993800	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr9:1993000-1993200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr9:1993200-1994200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr9:1993800-1995200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr9:1993800-1995800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr9:1993800-1995800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr9:1993800-1996800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr9:1994000-1995000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr9:1994000-1996200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr9:1994000-1996200	Enhancers	H1 Cell Line	embryonic stem cell

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