Variant report

Variant	nsv608070
Chromosome Location	chr7:105504201-105533735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:759)
CpG islands
(count:672)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105516671-105517184	HepG2	liver:	n/a	chr7:105516839-105516847
2	ARID3A	chr7:105517709-105517938	HepG2	liver:	n/a	n/a
3	ATF1	chr7:105516707-105517162	K562	blood:	n/a	n/a
4	ATF1	chr7:105509515-105509522	K562	blood:	n/a	n/a
5	ATF2	chr7:105516752-105517105	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr7:105517069-105517275	K562	blood:	n/a	n/a
7	BCL3	chr7:105516608-105517180	A549	lung:	n/a	chr7:105517163-105517176
8	BCL3	chr7:105518226-105518460	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:105516830-105517987	HepG2	liver:	n/a	chr7:105517155-105517171 chr7:105517157-105517173
10	BHLHE40	chr7:105516839-105517370	GM12878	blood:	n/a	chr7:105517155-105517171 chr7:105517157-105517173
11	BHLHE40	chr7:105530867-105531067	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:105516783-105517426	K562	blood:	n/a	chr7:105517155-105517171 chr7:105517157-105517173
13	BRCA1	chr7:105523466-105523512	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr7:105517869-105518143	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr7:105516722-105517178	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr7:105516661-105517532	K562	blood:	n/a	n/a
17	CCNT2	chr7:105516482-105517477	K562	blood:	n/a	n/a
18	CEBPB	chr7:105516835-105517009	K562	blood:	n/a	n/a
19	CEBPB	chr7:105512983-105513303	A549	lung:	n/a	chr7:105513126-105513137
20	CEBPB	chr7:105516858-105517006	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:105516724-105517174	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:105513109-105513231	Hela-S3	cervix:	n/a	chr7:105513126-105513137
23	CEBPB	chr7:105513024-105513278	K562	blood:	n/a	chr7:105513126-105513137
24	CEBPB	chr7:105526712-105526972	HepG2	liver:	n/a	chr7:105526830-105526841 chr7:105526758-105526769
25	CEBPB	chr7:105513001-105513296	IMR90	lung:	n/a	chr7:105513126-105513137
26	CEBPB	chr7:105516788-105517059	A549	lung:	n/a	n/a
27	CEBPB	chr7:105518753-105518827	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:105512987-105513239	HepG2	liver:	n/a	chr7:105513126-105513137
29	CEBPD	chr7:105516786-105517500	HepG2	liver:	n/a	n/a
30	CHD1	chr7:105516642-105516949	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:105516882-105517893	HepG2	liver:	n/a	n/a
32	CHD2	chr7:105516516-105517363	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr7:105517778-105518009	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr7:105522732-105522914	K562	blood:	n/a	n/a
35	CHD2	chr7:105516763-105517490	GM12878	blood:	n/a	n/a
36	CHD2	chr7:105516479-105517211	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr7:105516543-105517408	K562	blood:	n/a	n/a
38	CREB1	chr7:105516695-105517658	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr7:105516724-105517368	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr7:105516877-105517182	A549	lung:	n/a	n/a
41	CREB1	chr7:105517620-105518043	A549	lung:	n/a	n/a
42	CREB1	chr7:105516762-105517534	A549	lung:	n/a	n/a
43	CREB1	chr7:105516545-105518159	HepG2	liver:	n/a	n/a
44	CREB1	chr7:105516679-105517827	K562	blood:	n/a	n/a
45	CTCF	chr7:105526968-105527050	Hela-S3	cervix:	n/a	chr7:105526989-105527010
46	CTCF	chr7:105517059-105517307	LNCaP	prostate:	n/a	chr7:105517183-105517191 chr7:105517161-105517170 chr7:105517161-105517174
47	CTCF	chr7:105527105-105527123	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr7:105517445-105517496	GM10248	blood:	n/a	n/a
49	CTCF	chr7:105517080-105517230	HCPEpiC	choroid plexus:	n/a	chr7:105517183-105517191 chr7:105517161-105517170 chr7:105517161-105517174
50	CTCF	chr7:105517914-105517958	MCF-7	breast:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105515896-105515946	Caco-2	colon:	n/a
2	chr7:105515896-105515946	Caco-2	colon:	n/a
3	chr7:105514694-105514744	ovcar-3	ovarian:	n/a
4	chr7:105515896-105515946	IMR90	lung:	fetal
5	chr7:105515896-105515946	T-47D	breast:	n/a
6	chr7:105517962-105518012	T-47D	breast:	n/a
7	chr7:105515896-105515946	K562	blood:	n/a
8	chr7:105515896-105515946	AG10803	skin:	n/a
9	chr7:105515896-105515946	GM12878	blood:	n/a
10	chr7:105519144-105519194	PrEC	prostate:	n/a
11	chr7:105519144-105519194	GM12878	blood:	n/a
12	chr7:105518489-105518539	GM12891	blood:	n/a
13	chr7:105521116-105521166	AG04449	skin:	fetal
14	chr7:105516956-105517006	HUVEC	blood vessel:	n/a
15	chr7:105518489-105518539	AG10803	skin:	n/a
16	chr7:105514694-105514744	AoSMC	blood vessel:	n/a
17	chr7:105516956-105517006	HepG2	liver:	n/a
18	chr7:105517962-105518012	GM06990	blood:	n/a
19	chr7:105518489-105518539	AG04450	lung:	fetal
20	chr7:105518489-105518539	ovcar-3	ovarian:	n/a
21	chr7:105521116-105521166	NH-A	brain:	n/a
22	chr7:105515896-105515946	MCF10A-Er-Src	breast:	n/a
23	chr7:105517962-105518012	A549	lung:	n/a
24	chr7:105521116-105521166	HRCEpiC	kidney:	n/a
25	chr7:105515219-105515269	HMEC	breast:	n/a
26	chr7:105515219-105515269	HCT-116	colon:	n/a
27	chr7:105517962-105518012	AG04449	skin:	fetal
28	chr7:105516956-105517006	SKMC	muscle:	n/a
29	chr7:105517689-105517739	BE2_C	brain:	n/a
30	chr7:105521116-105521166	HL-60	blood:	n/a
31	chr7:105517962-105518012	HCM	heart:	n/a
32	chr7:105515896-105515946	HRE	kidney:	n/a
33	chr7:105517689-105517739	HCT-116	colon:	n/a
34	chr7:105516956-105517006	HL-60	blood:	n/a
35	chr7:105515896-105515946	NT2-D1	testis:	n/a
36	chr7:105521116-105521166	A549	lung:	n/a
37	chr7:105514694-105514744	HepG2	liver:	n/a
38	chr7:105516956-105517006	ProgFib	skin:	n/a
39	chr7:105519144-105519194	NH-A	brain:	n/a
40	chr7:105518489-105518539	PFSK-1	brain:	n/a
41	chr7:105514694-105514744	HRCEpiC	kidney:	n/a
42	chr7:105517689-105517739	AG04450	lung:	fetal
43	chr7:105516985-105517035	HMEC	breast:	n/a
44	chr7:105521116-105521166	Jurkat	blood:	n/a
45	chr7:105519144-105519194	U87	brain:	n/a
46	chr7:105516985-105517035	MCF10A-Er-Src	breast:	n/a
47	chr7:105515896-105515946	AG09319	gingival:	n/a
48	chr7:105516956-105517006	AoSMC	blood vessel:	n/a
49	chr7:105516956-105517006	HRE	kidney:	n/a
50	chr7:105514694-105514744	HAEpiC	amniotic membrane:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:105481154..105482832-chr7:105524732..105527543,2	MCF-7	breast:
2	chr7:105524776..105526800-chr7:105527754..105529376,2	MCF-7	breast:
3	chr7:105417593..105419833-chr7:105514684..105516854,2	MCF-7	breast:
4	chr7:105529246..105532232-chr7:105533599..105537801,4	K562	blood:
5	chr7:105516911..105517651-chr7:105526775..105527447,2	K562	blood:
6	chr7:105528969..105534140-chr7:105534279..105538473,8	MCF-7	breast:
7	chr7:105529246..105532232-chr7:105533599..105537801,4	K562	blood:
8	chr7:105529710..105531248-chr7:105533599..105536485,2	K562	blood:
9	chr7:105516995..105519157-chr7:105532768..105536422,4	MCF-7	breast:
10	chr7:105504589..105506448-chr7:105515307..105516867,2	MCF-7	breast:
11	chr7:105502403..105505060-chr7:105511687..105514344,2	MCF-7	breast:
12	chr7:105171193..105173393-chr7:105516904..105519168,2	K562	blood:
13	chr7:105515766..105519471-chr7:105525958..105528344,4	K562	blood:
14	chr7:105513448..105515426-chr7:105522353..105525334,2	MCF-7	breast:
15	chr7:105506919..105509240-chr7:105515267..105517245,3	MCF-7	breast:
16	chr7:105516810..105518543-chr7:105750750..105753587,2	K562	blood:
17	chr7:105513806..105516596-chr7:105523378..105525448,2	K562	blood:
18	chr7:105508618..105511146-chr7:105522403..105524816,2	K562	blood:
19	chr7:105493324..105495060-chr7:105505004..105507170,2	K562	blood:
20	chr7:105508618..105511146-chr7:105522403..105524816,2	K562	blood:
21	chr7:102715242..102717974-chr7:105515259..105517980,2	MCF-7	breast:
22	chr7:105501942..105503890-chr7:105514726..105516451,2	MCF-7	breast:
23	chr7:105506358..105508649-chr7:105509377..105511928,3	MCF-7	breast:
24	chr7:105514771..105518088-chr7:105519640..105522126,3	K562	blood:
25	chr7:105400423..105401271-chr7:105526515..105527388,4	MCF-7	breast:
26	chr7:105513448..105515426-chr7:105522353..105525334,2	MCF-7	breast:
27	chr7:105500508..105505322-chr7:105509824..105513208,4	K562	blood:
28	chr7:105500053..105503749-chr7:105509417..105511445,3	MCF-7	breast:
29	chr7:105499355..105501635-chr7:105503534..105506439,2	K562	blood:
30	chr7:105513806..105516596-chr7:105523378..105525448,2	K562	blood:
31	chr7:105496031..105498783-chr7:105510711..105513346,2	MCF-7	breast:
32	chr7:105526646..105528203-chr7:105571811..105574702,2	MCF-7	breast:
33	chr7:105500508..105505322-chr7:105509824..105513208,4	K562	blood:
34	chr7:105502403..105505060-chr7:105511687..105514344,2	MCF-7	breast:
35	chr7:105504589..105506448-chr7:105515307..105516867,2	MCF-7	breast:
36	chr7:105514782..105516451-chr7:105517322..105519469,2	MCF-7	breast:
37	chr7:105506358..105508649-chr7:105509377..105511928,3	MCF-7	breast:
38	chr7:105515024..105519848-chr7:105525937..105530815,8	MCF-7	breast:
39	chr7:105533117..105535181-chr7:105536193..105537994,2	K562	blood:
40	chr7:105529710..105531248-chr7:105533599..105536485,2	K562	blood:
41	chr7:105298862..105301241-chr7:105519713..105521805,2	K562	blood:
42	chr7:105501689..105503971-chr7:105506813..105509071,2	K562	blood:
43	chr7:105497685..105504581-chr7:105514330..105518670,5	K562	blood:
44	chr7:105524776..105526800-chr7:105527754..105529376,2	MCF-7	breast:
45	chr7:105509564..105513213-chr7:105514359..105518751,5	MCF-7	breast:
46	chr7:105171304..105173778-chr7:105510120..105512763,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATXN7L1-1	chr7:105529972-105530577	NONHSAT122632

No data

Variant related genes	Relation type
CDHR3	TF binding region
ATXN7L1	TF binding region
CDHR3	CpG island
ATXN7L1	CpG island
ENSG00000161040	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000008282	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000170632	chromatin interactions

Extended variants
information (count: 1109 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1109 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs212423	chr7:105504201-105504202	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565595198	chr7:105504253-105504254	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs183395280	chr7:105504343-105504344	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200151276	chr7:105504360-105504361	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35632276	chr7:105504361-105504362	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs547758535	chr7:105504379-105504380	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs567737070	chr7:105504407-105504408	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs536934537	chr7:105504470-105504471	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557004709	chr7:105504479-105504480	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186913576	chr7:105504490-105504491	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs539297444	chr7:105504563-105504564	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530139605	chr7:105504585-105504586	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553141291	chr7:105504595-105504596	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573328677	chr7:105504609-105504610	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142767623	chr7:105504614-105504615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555783288	chr7:105504630-105504631	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374365587	chr7:105504739-105504740	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77624654	chr7:105504746-105504747	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377538741	chr7:105504754-105504755	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6972533	chr7:105504788-105504789	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs527515571	chr7:105504818-105504819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559360993	chr7:105504819-105504820	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533686588	chr7:105504837-105504838	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540422719	chr7:105504840-105504841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191351491	chr7:105504869-105504870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147506659	chr7:105504872-105504873	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528142664	chr7:105504888-105504889	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113264683	chr7:105504890-105504891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34739253	chr7:105504903-105504904	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs71155487	chr7:105504928-105504929	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62482806	chr7:105504930-105504931	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182078936	chr7:105504949-105504950	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187775135	chr7:105504968-105504969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368065257	chr7:105504980-105504981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530471852	chr7:105504992-105504993	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138487982	chr7:105504993-105504994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193300999	chr7:105505048-105505049	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75443697	chr7:105505088-105505089	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs367844591	chr7:105505089-105505090	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539722939	chr7:105505102-105505103	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546442504	chr7:105505122-105505123	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35900202	chr7:105505124-105505125	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149633348	chr7:105505128-105505129	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144393213	chr7:105505149-105505150	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555942940	chr7:105505155-105505156	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575698075	chr7:105505166-105505167	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185522219	chr7:105505213-105505214	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148706436	chr7:105505217-105505218	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553012885	chr7:105505229-105505230	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs578165056	chr7:105505280-105505281	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1311 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105465400-105506600	Weak transcription	Fetal Intestine Large	intestine
2	chr7:105479600-105506200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:105480000-105515600	Weak transcription	Ovary	ovary
4	chr7:105482200-105506400	Weak transcription	Psoas Muscle	Psoas
5	chr7:105483000-105506400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr7:105488000-105515600	Weak transcription	Aorta	Aorta
7	chr7:105489800-105506600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr7:105490200-105515600	Weak transcription	Gastric	stomach
9	chr7:105490200-105516200	Weak transcription	Thymus	Thymus
10	chr7:105490800-105509200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:105491000-105511600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:105491600-105511600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr7:105491600-105515200	Weak transcription	Spleen	Spleen
14	chr7:105491800-105515400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:105492800-105515800	Weak transcription	A549	lung
16	chr7:105493000-105506400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr7:105493200-105516400	Weak transcription	Lung	lung
18	chr7:105494600-105514000	Weak transcription	Placenta	Placenta
19	chr7:105494800-105506400	Weak transcription	Adipose Nuclei	Adipose
20	chr7:105494800-105508600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:105494800-105510000	Weak transcription	Small Intestine	intestine
22	chr7:105494800-105515600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:105495000-105514800	Weak transcription	Brain Germinal Matrix	brain
24	chr7:105495000-105515200	Weak transcription	Right Atrium	heart
25	chr7:105495000-105515600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:105495200-105506200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:105495200-105506200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:105495200-105507000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr7:105495200-105508600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:105495200-105508800	Weak transcription	Fetal Brain Female	brain
31	chr7:105495200-105511400	Weak transcription	HUVEC	blood vessel
32	chr7:105495200-105512800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:105495200-105513000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:105495200-105515000	Weak transcription	Fetal Brain Male	brain
35	chr7:105495200-105515200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:105495200-105515400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:105495200-105515400	Weak transcription	Brain Angular Gyrus	brain
38	chr7:105495200-105515400	Weak transcription	Brain Anterior Caudate	brain
39	chr7:105495200-105515400	Weak transcription	Fetal Kidney	kidney
40	chr7:105495200-105515400	Weak transcription	Fetal Lung	lung
41	chr7:105495200-105515600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:105495200-105515600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr7:105495400-105508600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:105495400-105515200	Weak transcription	Brain Hippocampus Middle	brain
45	chr7:105495600-105513000	Weak transcription	NHLF	lung
46	chr7:105495800-105506400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr7:105495800-105506600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr7:105495800-105506600	Weak transcription	Fetal Muscle Leg	muscle
49	chr7:105496000-105515000	Weak transcription	NHDF-Ad	bronchial
50	chr7:105498000-105515600	Weak transcription	Colonic Mucosa	Colon

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