Variant report

Variant	nsv1007522
Chromosome Location	chr3:121200563-121374051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1735)
CpG islands
(count:1891)
Chromatin interactive
region (count:64)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:121264632-121265235	K562	blood:	n/a	n/a
2	ARID3A	chr3:121316377-121316483	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:121265480-121265882	K562	blood:	n/a	n/a
4	ARID3A	chr3:121265453-121265941	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:121361606-121361746	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:121293291-121293628	K562	blood:	n/a	n/a
7	ARID3A	chr3:121316361-121316430	K562	blood:	n/a	n/a
8	ARID3A	chr3:121264757-121265250	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:121293415-121293609	HepG2	liver:	n/a	n/a
10	ATF1	chr3:121293341-121293636	K562	blood:	n/a	n/a
11	ATF2	chr3:121267479-121267985	GM12878	blood:	n/a	n/a
12	ATF2	chr3:121311674-121312713	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr3:121311633-121312689	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr3:121264597-121265169	GM12878	blood:	n/a	n/a
15	ATF2	chr3:121267420-121267944	GM12878	blood:	n/a	n/a
16	ATF2	chr3:121264561-121265245	GM12878	blood:	n/a	n/a
17	ATF2	chr3:121373211-121373782	GM12878	blood:	n/a	n/a
18	ATF2	chr3:121265572-121266011	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr3:121264594-121265142	A549	lung:	n/a	chr3:121264846-121264855
20	ATF3	chr3:121312116-121312453	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr3:121293358-121293722	K562	blood:	n/a	n/a
22	BACH1	chr3:121370532-121370903	K562	blood:	n/a	n/a
23	BACH1	chr3:121293357-121293710	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr3:121311672-121312712	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr3:121370567-121370886	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr3:121373309-121373740	GM12878	blood:	n/a	n/a
27	BATF	chr3:121267535-121267976	GM12878	blood:	n/a	n/a
28	BATF	chr3:121267576-121267909	GM12878	blood:	n/a	n/a
29	BATF	chr3:121373310-121373733	GM12878	blood:	n/a	n/a
30	BCL3	chr3:121271688-121271931	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:121267517-121268093	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:121264518-121265140	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:121264580-121265251	GM12878	blood:	n/a	n/a
34	BCLAF1	chr3:121373280-121373842	GM12878	blood:	n/a	n/a
35	BCLAF1	chr3:121373301-121373736	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:121264738-121264916	K562	blood:	n/a	n/a
37	BHLHE40	chr3:121264707-121265217	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:121356973-121357138	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:121267547-121267919	GM12878	blood:	n/a	n/a
40	BRCA1	chr3:121264554-121265265	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr3:121293244-121293683	K562	blood:	n/a	n/a
42	CBX3	chr3:121234709-121235051	K562	blood:	n/a	n/a
43	CBX3	chr3:121234787-121234973	K562	blood:	n/a	n/a
44	CBX3	chr3:121264666-121265161	K562	blood:	n/a	chr3:121265149-121265160
45	CCNT2	chr3:121264449-121264875	K562	blood:	n/a	n/a
46	CCNT2	chr3:121373404-121373517	K562	blood:	n/a	n/a
47	CEBPB	chr3:121264671-121265977	MCF-7	breast:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
48	CEBPB	chr3:121265317-121265984	HCT-116	colon:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
49	CEBPB	chr3:121261808-121262108	A549	lung:	n/a	chr3:121261903-121261914
50	CEBPB	chr3:121264730-121265961	K562	blood:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506

(count:1891 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121264693-121264743	AG04449	skin:	fetal
2	chr3:121285779-121285829	AoSMC	blood vessel:	n/a
3	chr3:121265395-121265445	U87	brain:	n/a
4	chr3:121265726-121265776	NHBE	bronchial:	n/a
5	chr3:121348609-121348659	GM12878	blood:	n/a
6	chr3:121262503-121262553	SK-N-MC	brain:	n/a
7	chr3:121312127-121312177	HepG2	liver:	n/a
8	chr3:121264923-121264973	NHBE	bronchial:	n/a
9	chr3:121286563-121286613	HRCEpiC	kidney:	n/a
10	chr3:121285779-121285829	SK-N-SH	brain:	n/a
11	chr3:121286563-121286613	RPTEC	kidney:	n/a
12	chr3:121286354-121286404	AG09319	gingival:	n/a
13	chr3:121264278-121264328	HCM	heart:	n/a
14	chr3:121264929-121264979	AG09319	gingival:	n/a
15	chr3:121265395-121265445	GM12892	blood:	n/a
16	chr3:121264929-121264979	IMR90	lung:	fetal
17	chr3:121264278-121264328	PANC-1	pancreas:	n/a
18	chr3:121286563-121286613	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:121264942-121264992	AG04450	lung:	fetal
20	chr3:121363104-121363154	SAEC	small airway:	n/a
21	chr3:121310923-121310973	GM12878	blood:	n/a
22	chr3:121264849-121264899	Caco-2	colon:	n/a
23	chr3:121264819-121264869	AG10803	skin:	n/a
24	chr3:121285779-121285829	K562	blood:	n/a
25	chr3:121262503-121262553	HIPEpiC	eye:	n/a
26	chr3:121264942-121264992	PrEC	prostate:	n/a
27	chr3:121280760-121280810	HUVEC	blood vessel:	n/a
28	chr3:121286563-121286613	BE2_C	brain:	n/a
29	chr3:121285779-121285829	GM06990	blood:	n/a
30	chr3:121312164-121312214	AG09319	gingival:	n/a
31	chr3:121312127-121312177	SK-N-SH_RA	brain:	n/a
32	chr3:121264844-121264894	SK-N-SH_RA	brain:	n/a
33	chr3:121285779-121285829	Hela-S3	cervix:	n/a
34	chr3:121264819-121264869	HRCEpiC	kidney:	n/a
35	chr3:121264538-121264588	HNPCEpiC	eye:	n/a
36	chr3:121262503-121262553	AG04450	lung:	fetal
37	chr3:121312241-121312291	HAEpiC	amniotic membrane:	n/a
38	chr3:121348609-121348659	HNPCEpiC	eye:	n/a
39	chr3:121312127-121312177	Hela-S3	cervix:	n/a
40	chr3:121267733-121267783	ProgFib	skin:	n/a
41	chr3:121310923-121310973	Jurkat	blood:	n/a
42	chr3:121264923-121264973	AG04450	lung:	fetal
43	chr3:121310923-121310973	RPTEC	kidney:	n/a
44	chr3:121264903-121264953	LNCaP	prostate:	n/a
45	chr3:121311075-121311125	HEK293	kidney:	embryo
46	chr3:121264693-121264743	ProgFib	skin:	n/a
47	chr3:121264942-121264992	NH-A	brain:	n/a
48	chr3:121286563-121286613	AG09319	gingival:	n/a
49	chr3:121363104-121363154	HIPEpiC	eye:	n/a
50	chr3:121286820-121286870	BE2_C	brain:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:121257674..121260535-chr3:121261894..121265462,3	MCF-7	breast:
2	chr3:121339257..121341104-chr3:121379300..121381638,2	K562	blood:
3	chr3:121216865..121219603-chr3:121221676..121223246,2	MCF-7	breast:
4	chr3:121259538..121263018-chr3:121263022..121266683,5	K562	blood:
5	chr3:121264864..121267091-chr3:122101354..122103102,2	MCF-7	breast:
6	chr3:121216865..121219603-chr3:121221676..121223246,2	MCF-7	breast:
7	chr3:121256811..121260221-chr3:121262363..121264764,4	MCF-7	breast:
8	chr3:121242146..121244903-chr3:121250057..121252456,2	K562	blood:
9	chr3:121262393..121265271-chr3:121277271..121279560,2	MCF-7	breast:
10	chr3:121205722..121207237-chr3:121210537..121212477,2	K562	blood:
11	chr3:121288728..121291116-chr3:121291333..121293786,2	MCF-7	breast:
12	chr3:121257218..121258726-chr3:121258912..121261843,2	K562	blood:
13	chr3:121344119..121346108-chr3:121348732..121350963,2	K562	blood:
14	chr3:121291865..121293689-chr3:121466098..121468278,2	K562	blood:
15	chr3:121256811..121260221-chr3:121262363..121264764,4	MCF-7	breast:
16	chr3:121264298..121266034-chr3:122100794..122102974,2	MCF-7	breast:
17	chr3:121344119..121346108-chr3:121348732..121350963,2	K562	blood:
18	chr3:121249276..121252211-chr3:121260575..121262874,2	MCF-7	breast:
19	chr3:121298924..121301111-chr3:121307868..121309748,2	MCF-7	breast:
20	chr3:121265697..121266207-chr3:122977401..122978341,2	K562	blood:
21	chr3:121210505..121212714-chr3:121217216..121218928,2	K562	blood:
22	chr3:121228286..121231093-chr3:121234825..121237774,2	K562	blood:
23	chr3:121271397..121273219-chr3:122101468..122103033,2	K562	blood:
24	chr3:121265150..121267222-chr3:121267374..121269393,2	K562	blood:
25	chr3:121256672..121259266-chr3:121264172..121266746,4	K562	blood:
26	chr3:121361933..121363730-chr3:121367165..121368759,2	K562	blood:
27	chr3:121206534..121207799-chr3:121247617..121248857,4	MCF-7	breast:
28	chr3:121197599..121199340-chr3:121205840..121207439,2	K562	blood:
29	chr3:121263260..121265570-chr3:121468289..121470216,2	K562	blood:
30	chr17:60095074..60095939-chr3:121314935..121315693,2	MCF-7	breast:
31	chr3:121242146..121244586-chr3:121250057..121252591,2	K562	blood:
32	chr3:121206957..121207672-chr3:121248079..121248871,2	MCF-7	breast:
33	chr3:121150437..121151324-chr3:121212003..121212905,2	MCF-7	breast:
34	chr3:121047561..121048621-chr3:121247919..121248785,3	MCF-7	breast:
35	chr3:121325183..121326691-chr3:121327746..121330379,2	K562	blood:
36	chr3:121261975..121264944-chr3:121467360..121470216,3	K562	blood:
37	chr3:121325183..121326691-chr3:121327746..121330379,2	K562	blood:
38	chr3:121251819..121253772-chr3:121257661..121259674,3	K562	blood:
39	chr1:145382746..145383629-chr3:121264432..121265003,2	Hela-S3	cervix:
40	chr3:121206957..121207672-chr3:121248079..121248871,2	MCF-7	breast:
41	chr3:121206534..121207799-chr3:121247617..121248857,4	MCF-7	breast:
42	chr3:121216264..121219327-chr3:121238004..121241014,4	K562	blood:
43	chr3:121265303..121265930-chr3:121811130..121811872,2	MCF-7	breast:
44	chr3:121264895..121265445-chr3:121468081..121468931,2	HCT-116	colon:
45	chr3:121262548..121264431-chr3:121401420..121403788,2	K562	blood:
46	chr3:121248468..121250741-chr3:121250884..121254091,3	K562	blood:
47	chr3:121210505..121212714-chr3:121217216..121218928,2	K562	blood:
48	chr3:121205722..121207237-chr3:121210537..121212477,2	K562	blood:
49	chr3:121221546..121223153-chr3:121223525..121225297,2	K562	blood:
50	chr3:121264432..121265085-chr8:141467270..141468232,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLQ-1	chr3:121295924-121296127	expReg_chr3_8545_-
2	lnc-GOLGB1-2	chr3:121372843-121373143	NONHSAT091474

No data

Variant related genes	Relation type
HCLS1	TF binding region
ENSG00000238670	TF binding region
ARGFX	TF binding region
RN7SL172P	TF binding region
POLQ	TF binding region
RPL7AP11	TF binding region
FBXO40	TF binding region
HCLS1	CpG island
ENSG00000238670	CpG island
ARGFX	CpG island
RN7SL172P	CpG island
POLQ	CpG island
RPL7AP11	CpG island
FBXO40	CpG island
ENSG00000138496	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000167632	chromatin interactions
ENSG00000173230	chromatin interactions
ENSG00000180353	chromatin interactions
ENSG00000114023	chromatin interactions
ENSG00000051341	chromatin interactions
ENSG00000173193	chromatin interactions
ENSG00000186103	chromatin interactions
ENSG00000160124	chromatin interactions
ENSG00000163840	chromatin interactions

Extended variants
information (count: 6756 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:6756 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71329221	chr3:121200589-121200590	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370501550	chr3:121200601-121200602	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372762164	chr3:121200621-121200622	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371363050	chr3:121200674-121200675	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs202000977	chr3:121200682-121200683	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566370751	chr3:121200731-121200732	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563386750	chr3:121200851-121200852	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs116345605	chr3:121200906-121200907	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs16832333	chr3:121200908-121200909	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs371101456	chr3:121200940-121200941	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs548757997	chr3:121200948-121200949	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs188252880	chr3:121200980-121200981	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182031802	chr3:121201041-121201042	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536866312	chr3:121201137-121201138	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557082506	chr3:121201142-121201143	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574082468	chr3:121201185-121201186	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs812102	chr3:121201207-121201208	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs794322	chr3:121201228-121201229	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543085486	chr3:121201230-121201231	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553138011	chr3:121201241-121201242	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs811117	chr3:121201310-121201311	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185747967	chr3:121201316-121201317	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34216699	chr3:121201367-121201368	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs199996842	chr3:121201373-121201374	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs397731470	chr3:121201381-121201382	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs545380504	chr3:121201424-121201425	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs565580948	chr3:121201443-121201444	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs202053110	chr3:121201457-121201458	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs397875020	chr3:121201464-121201465	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs531203632	chr3:121201500-121201501	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs373985113	chr3:121201534-121201535	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs561517544	chr3:121201550-121201551	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs569668041	chr3:121201657-121201658	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529009245	chr3:121201736-121201737	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs149462244	chr3:121201739-121201740	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs73193625	chr3:121201756-121201757	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs528087732	chr3:121201778-121201779	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550931099	chr3:121201786-121201787	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs571220353	chr3:121201841-121201842	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs537334827	chr3:121201852-121201853	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs373281801	chr3:121201974-121201975	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs143921963	chr3:121202021-121202022	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567450631	chr3:121202047-121202048	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs536387278	chr3:121202083-121202084	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370387790	chr3:121202131-121202132	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200015135	chr3:121202132-121202133	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201147155	chr3:121202133-121202134	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs397755922	chr3:121202134-121202135	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs189873617	chr3:121202165-121202166	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs374439731	chr3:121202183-121202184	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	17953491	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2067 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121151200-121263800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr3:121176400-121214800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr3:121176400-121224200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:121177200-121237000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr3:121177400-121204000	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr3:121177400-121205200	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr3:121177800-121214800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:121178000-121208600	Weak transcription	Fetal Heart	heart
9	chr3:121178200-121263800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr3:121178400-121204800	Strong transcription	Dnd41	blood
11	chr3:121181000-121219600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:121181600-121204000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:121183800-121234400	Weak transcription	Primary B cells from cord blood	blood
14	chr3:121186400-121255600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr3:121186600-121211600	Weak transcription	Primary T cells from cord blood	blood
16	chr3:121186800-121213000	Weak transcription	Fetal Intestine Small	intestine
17	chr3:121187000-121209600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr3:121187200-121223400	Weak transcription	Fetal Intestine Large	intestine
19	chr3:121192200-121233600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr3:121193000-121212400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr3:121193200-121237000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr3:121195200-121208200	Weak transcription	Thymus	Thymus
23	chr3:121195600-121233800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr3:121195800-121207400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:121196000-121207000	Weak transcription	Primary hematopoietic stem cells	blood
26	chr3:121196000-121208800	Weak transcription	Fetal Muscle Leg	muscle
27	chr3:121196800-121208600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr3:121197000-121202000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr3:121197000-121207600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr3:121197200-121201400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:121197200-121201400	Weak transcription	HSMM	muscle
32	chr3:121197200-121201800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:121197200-121206800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:121197200-121207600	Weak transcription	HepG2	liver
35	chr3:121197200-121217400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:121197200-121233400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:121197400-121200800	Weak transcription	NH-A	brain
38	chr3:121197600-121201800	Weak transcription	Osteobl	bone
39	chr3:121198200-121204000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr3:121198800-121210000	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr3:121199000-121205000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:121199200-121202600	Strong transcription	Fetal Thymus	thymus
43	chr3:121199200-121203600	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr3:121199200-121203600	Strong transcription	GM12878-XiMat	blood
45	chr3:121199200-121204000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:121199200-121205000	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr3:121199200-121216200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr3:121199400-121200600	Strong transcription	HMEC	breast
49	chr3:121199400-121201000	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr3:121199400-121201000	Strong transcription	Hela-S3	cervix

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