Variant report

Variant	nsv539099
Chromosome Location	chr7:120667937-120887301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2809)
CpG islands
(count:671)
Chromatin interactive
region (count:310)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2809 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:120683006-120683949	K562	blood:	n/a	n/a
2	ARID3A	chr7:120719020-120719586	K562	blood:	n/a	n/a
3	ARID3A	chr7:120684739-120686576	K562	blood:	n/a	n/a
4	ARID3A	chr7:120686842-120687556	K562	blood:	n/a	n/a
5	ARID3A	chr7:120735693-120736439	K562	blood:	n/a	chr7:120736063-120736079
6	ARID3A	chr7:120678225-120679868	K562	blood:	n/a	n/a
7	ARID3A	chr7:120695431-120695493	K562	blood:	n/a	n/a
8	ARID3A	chr7:120747983-120748273	K562	blood:	n/a	n/a
9	ARID3A	chr7:120714923-120715159	K562	blood:	n/a	n/a
10	ARID3A	chr7:120720624-120722162	K562	blood:	n/a	n/a
11	ARID3A	chr7:120689326-120689898	K562	blood:	n/a	n/a
12	ARID3A	chr7:120723039-120723664	K562	blood:	n/a	n/a
13	ARID3A	chr7:120709444-120709898	K562	blood:	n/a	n/a
14	ARID3A	chr7:120709160-120709188	K562	blood:	n/a	n/a
15	ARID3A	chr7:120778432-120778625	K562	blood:	n/a	n/a
16	ARID3A	chr7:120724896-120725031	K562	blood:	n/a	n/a
17	ARID3A	chr7:120800023-120800487	K562	blood:	n/a	n/a
18	ARID3A	chr7:120724859-120725121	HepG2	liver:	n/a	n/a
19	ARID3A	chr7:120672785-120673244	K562	blood:	n/a	n/a
20	ARID3A	chr7:120721437-120721773	HepG2	liver:	n/a	n/a
21	ARID3A	chr7:120670423-120670663	K562	blood:	n/a	n/a
22	ARID3A	chr7:120680858-120682413	K562	blood:	n/a	chr7:120681232-120681248
23	ARID3A	chr7:120675441-120675454	K562	blood:	n/a	n/a
24	ARID3A	chr7:120715862-120717615	K562	blood:	n/a	n/a
25	ARID3A	chr7:120711748-120712087	K562	blood:	n/a	n/a
26	ARID3A	chr7:120719901-120720326	K562	blood:	n/a	n/a
27	ATF1	chr7:120689365-120689889	K562	blood:	n/a	n/a
28	ATF1	chr7:120741816-120741840	K562	blood:	n/a	n/a
29	ATF1	chr7:120721397-120721954	K562	blood:	n/a	n/a
30	ATF1	chr7:120799677-120800576	K562	blood:	n/a	n/a
31	ATF1	chr7:120681589-120682195	K562	blood:	n/a	n/a
32	ATF1	chr7:120716345-120716834	K562	blood:	n/a	n/a
33	ATF1	chr7:120778322-120778731	K562	blood:	n/a	n/a
34	ATF1	chr7:120678690-120679689	K562	blood:	n/a	n/a
35	ATF1	chr7:120672914-120673500	K562	blood:	n/a	n/a
36	ATF1	chr7:120687065-120687405	K562	blood:	n/a	n/a
37	ATF2	chr7:120778277-120778721	GM12878	blood:	n/a	n/a
38	ATF2	chr7:120820349-120820987	GM12878	blood:	n/a	n/a
39	ATF2	chr7:120778230-120778840	GM12878	blood:	n/a	n/a
40	ATF2	chr7:120820324-120820939	GM12878	blood:	n/a	n/a
41	ATF3	chr7:120800134-120800510	K562	blood:	n/a	n/a
42	ATF3	chr7:120678622-120679093	K562	blood:	n/a	n/a
43	ATF3	chr7:120723078-120723515	K562	blood:	n/a	n/a
44	ATF3	chr7:120778265-120778713	K562	blood:	n/a	n/a
45	ATF3	chr7:120687007-120687368	K562	blood:	n/a	n/a
46	ATF3	chr7:120715926-120716892	K562	blood:	n/a	n/a
47	ATF3	chr7:120716978-120717420	K562	blood:	n/a	n/a
48	BACH1	chr7:120678768-120679173	K562	blood:	n/a	n/a
49	BACH1	chr7:120736364-120736379	K562	blood:	n/a	n/a
50	BACH1	chr7:120716017-120716863	K562	blood:	n/a	chr7:120716591-120716605

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:120852287-120852337	AG09319	gingival:	n/a
2	chr7:120689323-120689373	NB4	blood:	n/a
3	chr7:120704511-120704561	HAEpiC	amniotic membrane:	n/a
4	chr7:120702049-120702099	RPTEC	kidney:	n/a
5	chr7:120852287-120852337	HL-60	blood:	n/a
6	chr7:120704511-120704561	PANC-1	pancreas:	n/a
7	chr7:120704511-120704561	H1-hESC	embryonic stem cell:	embryo
8	chr7:120725046-120725096	GM12891	blood:	n/a
9	chr7:120701829-120701879	HCT-116	colon:	n/a
10	chr7:120704511-120704561	SK-N-SH_RA	brain:	n/a
11	chr7:120725046-120725096	Caco-2	colon:	n/a
12	chr7:120702049-120702099	HCF	heart:	n/a
13	chr7:120716340-120716390	MCF10A-Er-Src	breast:	n/a
14	chr7:120725046-120725096	BJ	skin:	n/a
15	chr7:120701829-120701879	NT2-D1	testis:	n/a
16	chr7:120725046-120725096	HCM	heart:	n/a
17	chr7:120701829-120701879	HL-60	blood:	n/a
18	chr7:120702049-120702099	CMK	blood:	n/a
19	chr7:120716340-120716390	NT2-D1	testis:	n/a
20	chr7:120689323-120689373	RPTEC	kidney:	n/a
21	chr7:120852287-120852337	H1-hESC	embryonic stem cell:	embryo
22	chr7:120689323-120689373	HNPCEpiC	eye:	n/a
23	chr7:120725046-120725096	ECC-1	luminal epithelium:	n/a
24	chr7:120721606-120721656	GM19239	blood:	n/a
25	chr7:120702049-120702099	K562	blood:	n/a
26	chr7:120701829-120701879	RPTEC	kidney:	n/a
27	chr7:120721606-120721656	HL-60	blood:	n/a
28	chr7:120725046-120725096	Jurkat	blood:	n/a
29	chr7:120716340-120716390	U87	brain:	n/a
30	chr7:120721606-120721656	HCT-116	colon:	n/a
31	chr7:120725046-120725096	HCT-116	colon:	n/a
32	chr7:120701117-120701167	NT2-D1	testis:	n/a
33	chr7:120701829-120701879	HRPEpiC	eye:	n/a
34	chr7:120721606-120721656	AG10803	skin:	n/a
35	chr7:120852287-120852337	A549	lung:	n/a
36	chr7:120716340-120716390	HEEpiC	esophagus:	n/a
37	chr7:120721606-120721656	HEK293	kidney:	embryo
38	chr7:120701829-120701879	AG10803	skin:	n/a
39	chr7:120725046-120725096	T-47D	breast:	n/a
40	chr7:120725046-120725096	HCF	heart:	n/a
41	chr7:120721606-120721656	HCF	heart:	n/a
42	chr7:120704511-120704561	GM12892	blood:	n/a
43	chr7:120725046-120725096	HL-60	blood:	n/a
44	chr7:120742600-120742650	Hepatocyte	liver:	n/a
45	chr7:120742600-120742650	NH-A	brain:	n/a
46	chr7:120852287-120852337	Hepatocyte	liver:	n/a
47	chr7:120742600-120742650	HNPCEpiC	eye:	n/a
48	chr7:120689323-120689373	HRCEpiC	kidney:	n/a
49	chr7:120721606-120721656	Hepatocyte	liver:	n/a
50	chr7:120704511-120704561	HPAEpiC	pulmonary alveolar:	n/a

(count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr7:120826513..120828364-chr7:120831445..120833082,2	K562	blood:
2	chr7:120651629..120654433-chr7:120773346..120775726,2	K562	blood:
3	chr7:120624020..120645873-chr7:120713358..120727138,77	K562	blood:
4	chr7:120682875..120684877-chr7:120691015..120693627,2	K562	blood:
5	chr7:120870734..120873223-chr7:120882275..120885118,2	K562	blood:
6	chr7:120589698..120592018-chr7:120727687..120730624,2	K562	blood:
7	chr7:120692006..120694534-chr7:120721905..120723814,2	K562	blood:
8	chr7:120627515..120628244-chr7:120719065..120719854,2	MCF-7	breast:
9	chr7:120665801..120667354-chr7:120675569..120677821,2	K562	blood:
10	chr7:120684359..120686005-chr7:120688473..120690743,2	MCF-7	breast:
11	chr7:120589479..120591049-chr7:120760761..120762508,2	MCF-7	breast:
12	chr7:120814118..120818051-chr7:120821660..120824436,5	K562	blood:
13	chr7:120655270..120658134-chr7:120709646..120711499,2	K562	blood:
14	chr7:120868481..120870338-chr7:120872297..120875239,2	K562	blood:
15	chr7:120701678..120704158-chr7:120722578..120725881,3	K562	blood:
16	chr7:120680122..120681952-chr7:120727272..120728827,2	K562	blood:
17	chr7:120775298..120777729-chr7:120784980..120787236,2	K562	blood:
18	chr7:120800390..120802719-chr7:120816367..120819301,2	K562	blood:
19	chr7:120658657..120661112-chr7:120743405..120745049,2	K562	blood:
20	chr7:120762968..120765297-chr7:120774508..120778182,3	K562	blood:
21	chr7:120774713..120776221-chr7:120777852..120779454,2	K562	blood:
22	chr7:120854329..120856810-chr7:120876127..120877752,2	K562	blood:
23	chr7:120703590..120707044-chr7:120707756..120711872,8	K562	blood:
24	chr7:120590916..120593428-chr7:120771496..120774928,3	K562	blood:
25	chr7:120631497..120633631-chr7:120731853..120734107,2	K562	blood:
26	chr7:120729541..120731923-chr7:120745410..120747271,2	K562	blood:
27	chr7:120695659..120698795-chr7:120708123..120711912,4	K562	blood:
28	chr7:120685095..120691151-chr7:120712234..120720635,10	K562	blood:
29	chr7:120873011..120874844-chr7:120878339..120881386,3	K562	blood:
30	chr7:120445860..120446622-chr7:120721053..120722016,4	MCF-7	breast:
31	chr7:120773227..120776221-chr7:120776532..120780949,5	K562	blood:
32	chr7:120747233..120749938-chr7:120774365..120776379,3	K562	blood:
33	chr7:120774713..120776221-chr7:120777852..120779454,2	K562	blood:
34	chr7:120756984..120759314-chr7:120759581..120762409,4	K562	blood:
35	chr7:120711582..120714500-chr7:120752923..120755177,2	K562	blood:
36	chr7:120836283..120838682-chr7:120872699..120875576,2	K562	blood:
37	chr7:120674115..120676104-chr7:120725405..120727477,2	K562	blood:
38	chr7:120848908..120852746-chr7:120854048..120856854,5	K562	blood:
39	chr7:120778481..120780848-chr7:120786003..120787680,2	K562	blood:
40	chr7:120724755..120727043-chr8:49082625..49084125,2	K562	blood:
41	chr7:120723287..120725669-chr7:120740976..120742923,2	K562	blood:
42	chr7:120696002..120698090-chr7:120700790..120703179,3	K562	blood:
43	chr7:120701560..120707048-chr7:120714809..120721907,9	K562	blood:
44	chr7:120778509..120781370-chr7:120785067..120788347,3	K562	blood:
45	chr7:120748117..120751439-chr7:120760191..120762453,3	K562	blood:
46	chr7:120805499..120808232-chr7:120819576..120821319,3	K562	blood:
47	chr7:120719872..120722285-chr8:115706379..115707879,2	K562	blood:
48	chr7:120778481..120780848-chr7:120786003..120787680,2	K562	blood:
49	chr7:120431798..120432733-chr7:120748046..120748607,2	K562	blood:
50	chr7:120629478..120632230-chr7:120728269..120729776,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ING3-5	chr7:120690445-120690496	NONHSAT122999
2	lnc-ING3-6	chr7:120702382-120702597	expReg_chr7_8599_+
3	lnc-ING3-5	chr7:120686941-120687047	NONHSAT122999
4	lnc-ING3-3	chr7:120671720-120671974	expReg_chr7_8572_+
5	lnc-ING3-4	chr7:120671993-120672337	expReg_chr7_8573_+

No data

Variant related genes	Relation type
RNU6-517P	TF binding region
CPED1	TF binding region
HMGN1P18	TF binding region
RNA5SP241	TF binding region
RNU6-517P	CpG island
CPED1	CpG island
HMGN1P18	CpG island
RNA5SP241	CpG island
ENSG00000202225	chromatin interactions
ENSG00000071243	chromatin interactions
ENSG00000212628	chromatin interactions
ENSG00000207090	chromatin interactions
ENSG00000196937	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000106034	chromatin interactions
ENSG00000234927	chromatin interactions

Extended variants
information (count: 7785 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:7785 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145511592	chr7:120667953-120667954	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367954175	chr7:120667955-120667956	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73221244	chr7:120667976-120667977	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs367601657	chr7:120667980-120667981	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115317741	chr7:120667998-120667999	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370774250	chr7:120667999-120668000	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117051948	chr7:120668004-120668005	Enhancers Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148878834	chr7:120668050-120668051	Enhancers Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543720113	chr7:120668112-120668113	Enhancers Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571495790	chr7:120668119-120668120	Enhancers Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146974363	chr7:120668134-120668135	Enhancers Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550718857	chr7:120668159-120668160	Enhancers Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567473145	chr7:120668202-120668203	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188112384	chr7:120668217-120668218	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34280118	chr7:120668282-120668283	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563610026	chr7:120668294-120668295	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552706671	chr7:120668423-120668424	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572492704	chr7:120668465-120668466	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538390190	chr7:120668477-120668478	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147646903	chr7:120668498-120668499	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192865051	chr7:120668502-120668503	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528887641	chr7:120668507-120668508	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111387912	chr7:120668516-120668517	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111671097	chr7:120668597-120668598	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183522505	chr7:120668612-120668613	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540880301	chr7:120668623-120668624	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560331854	chr7:120668638-120668639	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77422769	chr7:120668641-120668642	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552740081	chr7:120668652-120668653	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549048017	chr7:120668655-120668656	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562988117	chr7:120668708-120668709	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10258610	chr7:120668737-120668738	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550508221	chr7:120668745-120668746	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565544733	chr7:120668750-120668751	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528151486	chr7:120668764-120668765	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566096681	chr7:120668784-120668785	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536190812	chr7:120668934-120668935	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10229719	chr7:120669027-120669028	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs10259031	chr7:120669054-120669055	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375490578	chr7:120669111-120669112	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187392405	chr7:120669242-120669243	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538230533	chr7:120669262-120669263	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6954847	chr7:120669299-120669300	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575017298	chr7:120669318-120669319	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537899057	chr7:120669335-120669336	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554873815	chr7:120669339-120669340	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs80122144	chr7:120669391-120669392	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146116381	chr7:120669513-120669514	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs192540895	chr7:120669562-120669563	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs577579912	chr7:120669578-120669579	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120656000-120668000	Weak transcription	Right Atrium	heart
2	chr7:120661000-120668000	Weak transcription	HSMMtube	muscle
3	chr7:120661600-120669400	Genic enhancers	K562	blood
4	chr7:120662000-120668000	Weak transcription	Fetal Stomach	stomach
5	chr7:120664000-120668400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:120664400-120668200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:120664400-120668400	Weak transcription	Aorta	Aorta
8	chr7:120664600-120668000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:120664600-120668000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr7:120664600-120668000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:120664600-120672800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr7:120665000-120668000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:120665000-120668000	Weak transcription	Adipose Nuclei	Adipose
14	chr7:120665000-120668000	Weak transcription	Osteobl	bone
15	chr7:120665200-120668000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:120665200-120668400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:120665200-120672800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr7:120666200-120668000	Weak transcription	Colon Smooth Muscle	Colon
19	chr7:120666200-120668000	Weak transcription	Fetal Kidney	kidney
20	chr7:120666400-120668200	Weak transcription	Right Ventricle	heart
21	chr7:120666400-120668600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:120666600-120668000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr7:120666600-120668000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr7:120666600-120668000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:120666600-120668000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr7:120666600-120668600	Weak transcription	NHDF-Ad	bronchial
27	chr7:120666600-120672800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:120666600-120673000	Weak transcription	Small Intestine	intestine
29	chr7:120666600-120683600	Weak transcription	Liver	Liver
30	chr7:120666800-120668800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr7:120667000-120668000	Weak transcription	Ovary	ovary
32	chr7:120667200-120668000	Weak transcription	HepG2	liver
33	chr7:120667200-120668200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:120667200-120668400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:120667200-120668400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:120667200-120670400	Enhancers	Fetal Heart	heart
37	chr7:120667200-120672600	Weak transcription	Left Ventricle	heart
38	chr7:120667400-120668200	Enhancers	Fetal Lung	lung
39	chr7:120667600-120668600	Enhancers	Psoas Muscle	Psoas
40	chr7:120667600-120668800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr7:120667600-120669000	Enhancers	NHLF	lung
42	chr7:120667800-120668400	Genic enhancers	HSMM	muscle
43	chr7:120668000-120668200	Enhancers	Colon Smooth Muscle	Colon
44	chr7:120668000-120668200	Active TSS	Stomach Smooth Muscle	stomach
45	chr7:120668000-120668600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:120668000-120668600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr7:120668000-120668600	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:120668000-120668600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:120668000-120668600	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:120668000-120668600	Enhancers	Fetal Kidney	kidney

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