Variant report

Variant	nsv482365
Chromosome Location	chr7:107122401-107271861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2303)
CpG islands
(count:2260)
Chromatin interactive
region (count:196)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2303 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:107220275-107220630	K562	blood:	n/a	n/a
2	ARID3A	chr7:107200966-107201010	K562	blood:	n/a	n/a
3	ARID3A	chr7:107135270-107135661	K562	blood:	n/a	n/a
4	ARID3A	chr7:107214069-107214179	K562	blood:	n/a	n/a
5	ARID3A	chr7:107220484-107220694	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:107204257-107204702	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:107136091-107136277	K562	blood:	n/a	n/a
8	ARID3A	chr7:107123148-107123204	K562	blood:	n/a	n/a
9	ARID3A	chr7:107203702-107203898	K562	blood:	n/a	n/a
10	ARID3A	chr7:107142042-107142424	K562	blood:	n/a	n/a
11	ARID3A	chr7:107220972-107222372	K562	blood:	n/a	n/a
12	ARID3A	chr7:107134973-107135199	HepG2	liver:	n/a	n/a
13	ATF1	chr7:107134729-107135061	K562	blood:	n/a	n/a
14	ATF1	chr7:107220165-107221087	K562	blood:	n/a	n/a
15	ATF1	chr7:107204090-107205131	K562	blood:	n/a	n/a
16	ATF1	chr7:107142051-107142370	K562	blood:	n/a	n/a
17	ATF2	chr7:107220309-107220851	GM12878	blood:	n/a	n/a
18	ATF2	chr7:107204129-107204700	GM12878	blood:	n/a	n/a
19	ATF2	chr7:107204096-107204691	GM12878	blood:	n/a	n/a
20	ATF2	chr7:107204103-107204585	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr7:107204184-107204582	HepG2	liver:	n/a	n/a
22	ATF3	chr7:107220283-107221108	K562	blood:	n/a	n/a
23	ATF3	chr7:107204044-107204900	K562	blood:	n/a	n/a
24	ATF3	chr7:107204086-107204630	K562	blood:	n/a	n/a
25	ATF3	chr7:107204154-107204596	GM12878	blood:	n/a	n/a
26	ATF3	chr7:107204174-107204498	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr7:107204196-107204997	K562	blood:	n/a	n/a
28	ATF3	chr7:107204091-107204614	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF3	chr7:107204082-107204682	HepG2	liver:	n/a	n/a
30	ATF3	chr7:107204280-107204562	GM12878	blood:	n/a	n/a
31	BACH1	chr7:107220155-107220366	K562	blood:	n/a	n/a
32	BACH1	chr7:107220484-107221181	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr7:107196405-107196688	GM12878	blood:	n/a	n/a
34	BCL3	chr7:107220018-107220803	A549	lung:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
35	BCL3	chr7:107219957-107220571	A549	lung:	n/a	chr7:107220398-107220411
36	BCL3	chr7:107204082-107204609	A549	lung:	n/a	n/a
37	BCL3	chr7:107220236-107220948	GM12878	blood:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
38	BCLAF1	chr7:107220355-107220916	GM12878	blood:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
39	BCLAF1	chr7:107204103-107204471	GM12878	blood:	n/a	n/a
40	BCLAF1	chr7:107219873-107221326	K562	blood:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
41	BHLHE40	chr7:107204773-107205162	A549	lung:	n/a	n/a
42	BHLHE40	chr7:107135448-107135629	K562	blood:	n/a	n/a
43	BHLHE40	chr7:107203783-107205250	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:107204064-107205290	HepG2	liver:	n/a	n/a
45	BHLHE40	chr7:107204216-107204452	A549	lung:	n/a	n/a
46	BHLHE40	chr7:107221584-107221652	K562	blood:	n/a	n/a
47	BHLHE40	chr7:107203611-107205486	K562	blood:	n/a	n/a
48	BHLHE40	chr7:107220120-107221211	K562	blood:	n/a	chr7:107220399-107220415 chr7:107220666-107220682
49	BHLHE40	chr7:107142213-107142276	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:107220430-107221177	GM12878	blood:	n/a	chr7:107220666-107220682

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:107223076-107223126	BE2_C	brain:	n/a
2	chr7:107221327-107221377	Jurkat	blood:	n/a
3	chr7:107219178-107219228	ECC-1	luminal epithelium:	n/a
4	chr7:107223076-107223126	BE2_C	brain:	n/a
5	chr7:107221327-107221377	Jurkat	blood:	n/a
6	chr7:107219178-107219228	ECC-1	luminal epithelium:	n/a
7	chr7:107235907-107235957	ovcar-3	ovarian:	n/a
8	chr7:107220080-107220130	AoSMC	blood vessel:	n/a
9	chr7:107220345-107220395	HMEC	breast:	n/a
10	chr7:107221074-107221124	Caco-2	colon:	n/a
11	chr7:107205253-107205303	Jurkat	blood:	n/a
12	chr7:107220968-107221018	LNCaP	prostate:	n/a
13	chr7:107205105-107205155	HEEpiC	esophagus:	n/a
14	chr7:107220040-107220090	GM19239	blood:	n/a
15	chr7:107219178-107219228	BJ	skin:	n/a
16	chr7:107204399-107204449	HepG2	liver:	n/a
17	chr7:107205105-107205155	GM12892	blood:	n/a
18	chr7:107220357-107220407	GM12878	blood:	n/a
19	chr7:107219178-107219228	AG10803	skin:	n/a
20	chr7:107220345-107220395	HRPEpiC	eye:	n/a
21	chr7:107220372-107220422	HMEC	breast:	n/a
22	chr7:107205105-107205155	HCPEpiC	choroid plexus:	n/a
23	chr7:107219178-107219228	PANC-1	pancreas:	n/a
24	chr7:107204135-107204185	ovcar-3	ovarian:	n/a
25	chr7:107235907-107235957	IMR90	lung:	fetal
26	chr7:107204195-107204245	HNPCEpiC	eye:	n/a
27	chr7:107204399-107204449	HUVEC	blood vessel:	n/a
28	chr7:107205253-107205303	HAEpiC	amniotic membrane:	n/a
29	chr7:107204385-107204435	RPTEC	kidney:	n/a
30	chr7:107220040-107220090	HNPCEpiC	eye:	n/a
31	chr7:107204399-107204449	ProgFib	skin:	n/a
32	chr7:107220345-107220395	HUVEC	blood vessel:	n/a
33	chr7:107205105-107205155	AG04450	lung:	fetal
34	chr7:107221141-107221191	ECC-1	luminal epithelium:	n/a
35	chr7:107204581-107204631	HCT-116	colon:	n/a
36	chr7:107219178-107219228	MCF-7	breast:	n/a
37	chr7:107235907-107235957	HEEpiC	esophagus:	n/a
38	chr7:107219178-107219228	HCF	heart:	n/a
39	chr7:107205105-107205155	NHBE	bronchial:	n/a
40	chr7:107205157-107205207	AoSMC	blood vessel:	n/a
41	chr7:107204195-107204245	SK-N-SH_RA	brain:	n/a
42	chr7:107148409-107148459	AoSMC	blood vessel:	n/a
43	chr7:107220080-107220130	Hepatocyte	liver:	n/a
44	chr7:107204581-107204631	H1-hESC	embryonic stem cell:	embryo
45	chr7:107204581-107204631	HNPCEpiC	eye:	n/a
46	chr7:107148409-107148459	HUVEC	blood vessel:	n/a
47	chr7:107204135-107204185	BE2_C	brain:	n/a
48	chr7:107221141-107221191	HIPEpiC	eye:	n/a
49	chr7:107220262-107220312	PrEC	prostate:	n/a
50	chr7:107220345-107220395	HCM	heart:	n/a

(count:196 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:107133036..107135324-chr7:107145398..107148368,3	MCF-7	breast:
2	chr7:106808633..106810263-chr7:107202578..107204471,2	K562	blood:
3	chr7:107264623..107267190-chr7:107267957..107271121,3	K562	blood:
4	chr7:107132036..107135481-chr7:107143415..107147537,5	K562	blood:
5	chr7:107258308..107259893-chr7:107260426..107263262,2	K562	blood:
6	chr7:107195231..107197923-chr7:107218574..107220615,2	K562	blood:
7	chr7:107262077..107263608-chr7:107265529..107267087,2	K562	blood:
8	chr7:107166936..107168955-chr7:107170505..107173136,2	MCF-7	breast:
9	chr7:107116237..107119401-chr7:107133412..107136186,3	MCF-7	breast:
10	chr7:107129731..107132088-chr7:107135002..107137252,2	MCF-7	breast:
11	chr7:107164671..107167823-chr7:107168530..107171856,3	K562	blood:
12	chr7:106808633..106810586-chr7:107202578..107204934,3	K562	blood:
13	chr7:107249634..107253526-chr7:107253696..107258280,6	K562	blood:
14	chr7:107190837..107193195-chr7:107215687..107218303,2	K562	blood:
15	chr7:107220649..107224781-chr7:107243854..107248319,6	K562	blood:
16	chr7:107188089..107190681-chr7:107220054..107222160,2	MCF-7	breast:
17	chr7:107189106..107191821-chr7:107204481..107207285,3	K562	blood:
18	chr7:107120115..107121857-chr7:107137628..107139612,2	K562	blood:
19	chr7:107134045..107136740-chr7:107137894..107140171,2	MCF-7	breast:
20	chr7:107261454..107263851-chr7:107267426..107269612,2	K562	blood:
21	chr7:107115877..107118056-chr7:107127031..107129912,2	K562	blood:
22	chr7:107188089..107190681-chr7:107220054..107222160,2	MCF-7	breast:
23	chr1:145507347..145508204-chr7:107203872..107204602,2	Hela-S3	cervix:
24	chr7:107199299..107201422-chr7:107219574..107221620,2	MCF-7	breast:
25	chr7:107259288..107259940-chr7:107270769..107271431,2	K562	blood:
26	chr7:107201923..107207041-chr7:107381527..107386474,7	K562	blood:
27	chr7:107259288..107259940-chr7:107270769..107271431,2	K562	blood:
28	chr7:107261469..107264518-chr7:107270573..107273343,3	K562	blood:
29	chr7:107126321..107129066-chr7:107219098..107220671,2	K562	blood:
30	chr7:107232356..107233858-chr7:107262506..107264853,2	K562	blood:
31	chr2:95830717..95831431-chr7:107220273..107221008,2	HCT-116	colon:
32	chr7:107134560..107137629-chr7:107140496..107142146,3	K562	blood:
33	chr7:107190433..107193195-chr7:107214406..107217187,2	K562	blood:
34	chr7:107129283..107132125-chr7:107690846..107692465,2	K562	blood:
35	chr1:92763878..92764562-chr7:107220034..107220754,2	Hela-S3	cervix:
36	chr7:107262077..107263608-chr7:107265529..107267087,2	K562	blood:
37	chr7:107187820..107189357-chr7:107192646..107194427,2	K562	blood:
38	chr7:107243569..107245525-chr7:107254509..107256969,2	K562	blood:
39	chr7:107249922..107251734-chr7:107254251..107256132,2	K562	blood:
40	chr7:107219418..107222356-chr7:107237027..107239369,2	MCF-7	breast:
41	chr7:107241065..107243964-chr7:107244649..107247131,2	K562	blood:
42	chr7:106420213..106422890-chr7:107201706..107205184,3	K562	blood:
43	chr7:107143924..107148910-chr7:107218443..107222194,8	MCF-7	breast:
44	chr7:107178929..107181687-chr7:107183616..107186437,2	K562	blood:
45	chr7:107144788..107149242-chr7:107202871..107206314,6	MCF-7	breast:
46	chr7:107219336..107222149-chr7:107234347..107238081,3	MCF-7	breast:
47	chr7:107213784..107216037-chr7:107241685..107244437,2	K562	blood:
48	chr7:107165422..107167408-chr7:107219933..107221750,2	K562	blood:
49	chr7:107134186..107135883-chr7:107215334..107217413,2	K562	blood:
50	chr7:107265867..107267996-chr7:107270274..107272239,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COG5-4	chr7:107220002-107220502	ENSG00000272854.1
2	lnc-DUS4L-2	chr7:107236278-107236447	NONHSAT122691
3	lnc-DUS4L-2	chr7:107240842-107240880	NONHSAT122691
4	lnc-SLC26A3-3	chr7:107188723-107188777	NONHSAT122681
5	lnc-DUS4L-1	chr7:107207495-107207592	NONHSAT122684
6	lnc-DUS4L-1	chr7:107204476-107205121	NONHSAT122684
7	lnc-BCAP29-2	chr7:107270458-107271165	NONHSAT122694
8	lnc-SLC26A3-3	chr7:107188443-107188625	NONHSAT122681

No data

Variant related genes	Relation type
BCAP29	TF binding region
ENSG00000272854	TF binding region
WBP1LP2	TF binding region
COG5	TF binding region
DUS4L	TF binding region
ENSG00000238832	TF binding region
BCAP29	CpG island
ENSG00000272854	CpG island
WBP1LP2	CpG island
COG5	CpG island
DUS4L	CpG island
ENSG00000238832	CpG island
ENSG00000197734	chromatin interactions
ENSG00000251978	chromatin interactions
ENSG00000131795	chromatin interactions
ENSG00000100603	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000105879	chromatin interactions
ENSG00000144026	chromatin interactions
ENSG00000238832	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000164597	chromatin interactions
ENSG00000234222	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000103591	chromatin interactions
ENSG00000075790	chromatin interactions
ENSG00000241764	chromatin interactions
ENSG00000272854	chromatin interactions
ENSG00000091137	chromatin interactions
ENSG00000185344	chromatin interactions
ENSG00000250474	chromatin interactions
ENSG00000272072	chromatin interactions
ENSG00000163067	chromatin interactions
ENSG00000105865	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000105856	chromatin interactions
ENSG00000091140	chromatin interactions
ENSG00000197191	chromatin interactions

Extended variants
information (count: 5806 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5806 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187221224	chr7:107122408-107122409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532100697	chr7:107122409-107122410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574996834	chr7:107122576-107122577	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200866030	chr7:107122585-107122586	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs575925648	chr7:107122586-107122587	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs200184170	chr7:107122587-107122588	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs370609728	chr7:107122597-107122598	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs539742215	chr7:107122618-107122619	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs191222684	chr7:107122651-107122652	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs562559818	chr7:107122653-107122654	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183237632	chr7:107122672-107122673	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs541629993	chr7:107122746-107122747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555540204	chr7:107122749-107122750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112413859	chr7:107122756-107122757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574950776	chr7:107122767-107122768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116982440	chr7:107122771-107122772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563732260	chr7:107122818-107122819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529746958	chr7:107122838-107122839	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs6466172	chr7:107122901-107122902	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs540908648	chr7:107122904-107122905	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560592773	chr7:107122934-107122935	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs145434344	chr7:107122959-107122960	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs549265835	chr7:107122999-107123000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs11365572	chr7:107123050-107123051	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs187776461	chr7:107123099-107123100	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs531834747	chr7:107123106-107123107	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs140884363	chr7:107123149-107123150	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs192648211	chr7:107123155-107123156	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs79037687	chr7:107123214-107123215	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147684762	chr7:107123256-107123257	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs554158207	chr7:107123353-107123354	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs566602179	chr7:107123374-107123375	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs535750024	chr7:107123383-107123384	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs142458081	chr7:107123440-107123441	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs145186622	chr7:107123485-107123486	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs112041565	chr7:107123489-107123490	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs185044391	chr7:107123497-107123498	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs557461816	chr7:107123547-107123548	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs577336529	chr7:107123548-107123549	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs527646645	chr7:107123645-107123646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78393140	chr7:107123652-107123653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574211268	chr7:107123679-107123680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187949662	chr7:107123710-107123711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563069850	chr7:107123807-107123808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192429034	chr7:107123812-107123813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538983086	chr7:107123845-107123846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557177964	chr7:107123854-107123855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552019271	chr7:107123878-107123879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565350755	chr7:107123905-107123906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527788126	chr7:107123928-107123929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Biliary cancer	19435499	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4143 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107035800-107133000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr7:107052600-107126400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr7:107088600-107126000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr7:107090800-107146000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:107091000-107145800	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr7:107098800-107132600	Weak transcription	Primary B cells from cord blood	blood
7	chr7:107112800-107145800	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr7:107113000-107124800	Weak transcription	HUVEC	blood vessel
9	chr7:107113400-107126200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr7:107115400-107132800	Weak transcription	Primary T cells from cord blood	blood
11	chr7:107115600-107135200	Weak transcription	Left Ventricle	heart
12	chr7:107120000-107145600	Weak transcription	Right Ventricle	heart
13	chr7:107120200-107135200	Weak transcription	Fetal Intestine Small	intestine
14	chr7:107122000-107126800	Enhancers	Fetal Heart	heart
15	chr7:107122000-107147000	Weak transcription	HSMM	muscle
16	chr7:107123200-107155800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr7:107123600-107166200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr7:107126000-107126800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:107126000-107127400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr7:107126200-107127400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:107126400-107126600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:107126400-107126600	Enhancers	Adipose Nuclei	Adipose
23	chr7:107126600-107135600	Weak transcription	Pancreas	Pancrea
24	chr7:107126600-107145600	Weak transcription	Adipose Nuclei	Adipose
25	chr7:107126800-107131000	Weak transcription	Fetal Heart	heart
26	chr7:107126800-107184800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr7:107127400-107175400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr7:107129800-107130800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:107130800-107145400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr7:107130800-107163400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:107131000-107131200	Enhancers	Fetal Heart	heart
32	chr7:107131200-107131600	Weak transcription	Fetal Heart	heart
33	chr7:107131400-107135400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:107131400-107179800	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr7:107131600-107131800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr7:107131600-107131800	Enhancers	Fetal Heart	heart
37	chr7:107131600-107132400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:107131800-107133000	Weak transcription	Fetal Heart	heart
39	chr7:107131800-107146000	Weak transcription	Dnd41	blood
40	chr7:107131800-107175000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr7:107132000-107146200	Weak transcription	Colonic Mucosa	Colon
42	chr7:107132000-107146800	Weak transcription	Fetal Thymus	thymus
43	chr7:107132200-107146400	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:107132200-107146800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr7:107132400-107133000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:107132400-107133000	Weak transcription	Aorta	Aorta
47	chr7:107132600-107132800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:107132600-107133000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:107132600-107133600	Strong transcription	Primary B cells from cord blood	blood
50	chr7:107132800-107133200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived

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