Variant report

Variant	nsv608069
Chromosome Location	chr7:105088693-105208492
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2171)
CpG islands
(count:2079)
Chromatin interactive
region (count:179)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2171 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105172276-105172771	K562	blood:	n/a	n/a
2	ARID3A	chr7:105162532-105162842	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
4	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
5	ARID3A	chr7:105162675-105163137	K562	blood:	n/a	n/a
6	ARID3A	chr7:105172230-105172894	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:105173865-105174045	HepG2	liver:	n/a	n/a
8	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
9	ATF2	chr7:105172257-105172894	GM12878	blood:	n/a	n/a
10	ATF2	chr7:105162441-105162701	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:105172329-105172807	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:105171988-105172822	GM12878	blood:	n/a	n/a
13	ATF3	chr7:105162419-105162922	K562	blood:	n/a	chr7:105162516-105162525
14	ATF3	chr7:105162479-105162756	A549	lung:	n/a	chr7:105162516-105162525
15	ATF3	chr7:105172202-105172799	K562	blood:	n/a	n/a
16	BACH1	chr7:105113662-105113870	K562	blood:	n/a	n/a
17	BACH1	chr7:105113653-105113991	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:105172328-105172846	K562	blood:	n/a	n/a
19	BACH1	chr7:105161884-105162223	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:105172426-105172817	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:105162629-105162935	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:105103081-105103084	K562	blood:	n/a	n/a
23	BATF	chr7:105172440-105172791	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:105172537-105172868	GM12878	blood:	n/a	n/a
25	BCL3	chr7:105172316-105172982	A549	lung:	n/a	n/a
26	BCL3	chr7:105172270-105172911	A549	lung:	n/a	n/a
27	BCL3	chr7:105162453-105163079	A549	lung:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
28	BCLAF1	chr7:105172346-105172920	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:105162157-105163019	K562	blood:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
30	BCLAF1	chr7:105172218-105172996	K562	blood:	n/a	n/a
31	BCLAF1	chr7:105172328-105172981	K562	blood:	n/a	n/a
32	BCLAF1	chr7:105172265-105172905	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:105161948-105162953	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:105174117-105174180	K562	blood:	n/a	n/a
35	BHLHE40	chr7:105172056-105172791	HepG2	liver:	n/a	n/a
36	BHLHE40	chr7:105172018-105173029	K562	blood:	n/a	n/a
37	BHLHE40	chr7:105128299-105128701	K562	blood:	n/a	n/a
38	BHLHE40	chr7:105171963-105172867	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:105088647-105088769	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:105161582-105163259	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:105162517-105162823	A549	lung:	n/a	n/a
42	BHLHE40	chr7:105161610-105163105	K562	blood:	n/a	n/a
43	BHLHE40	chr7:105162519-105162872	HepG2	liver:	n/a	n/a
44	BRCA1	chr7:105162680-105163061	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:105172446-105172663	GM12878	blood:	n/a	n/a
46	BRCA1	chr7:105172361-105172945	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr7:105161980-105162068	HepG2	liver:	n/a	n/a
48	CBX3	chr7:105161068-105162276	K562	blood:	n/a	n/a
49	CBX3	chr7:105172354-105173016	K562	blood:	n/a	n/a
50	CBX3	chr7:105162379-105163324	K562	blood:	n/a	n/a

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105162577-105162627	GM19239	blood:	n/a
2	chr7:105128488-105128538	Hepatocyte	liver:	n/a
3	chr7:105112740-105112790	SK-N-MC	brain:	n/a
4	chr7:105172403-105172453	HCM	heart:	n/a
5	chr7:105162855-105162905	AG09319	gingival:	n/a
6	chr7:105162577-105162627	GM19239	blood:	n/a
7	chr7:105128488-105128538	Hepatocyte	liver:	n/a
8	chr7:105112740-105112790	SK-N-MC	brain:	n/a
9	chr7:105172403-105172453	HCM	heart:	n/a
10	chr7:105162855-105162905	AG09319	gingival:	n/a
11	chr7:105162735-105162785	Jurkat	blood:	n/a
12	chr7:105094993-105095043	H1-hESC	embryonic stem cell:	embryo
13	chr7:105171843-105171893	GM06990	blood:	n/a
14	chr7:105162878-105162928	AG09319	gingival:	n/a
15	chr7:105172403-105172453	AG10803	skin:	n/a
16	chr7:105161983-105162033	MCF-7	breast:	n/a
17	chr7:105173132-105173182	AoSMC	blood vessel:	n/a
18	chr7:105172722-105172772	HMEC	breast:	n/a
19	chr7:105162855-105162905	T-47D	breast:	n/a
20	chr7:105172403-105172453	T-47D	breast:	n/a
21	chr7:105172722-105172772	GM12892	blood:	n/a
22	chr7:105158109-105158159	LNCaP	prostate:	n/a
23	chr7:105162888-105162938	PFSK-1	brain:	n/a
24	chr7:105162577-105162627	HCM	heart:	n/a
25	chr7:105137683-105137733	AG04450	lung:	fetal
26	chr7:105162470-105162520	ECC-1	luminal epithelium:	n/a
27	chr7:105172520-105172570	NB4	blood:	n/a
28	chr7:105172168-105172218	Hepatocyte	liver:	n/a
29	chr7:105097168-105097218	NB4	blood:	n/a
30	chr7:105170241-105170291	AG09309	skin:	n/a
31	chr7:105172664-105172714	AG10803	skin:	n/a
32	chr7:105170241-105170291	GM06990	blood:	n/a
33	chr7:105172664-105172714	K562	blood:	n/a
34	chr7:105134734-105134784	HCPEpiC	choroid plexus:	n/a
35	chr7:105172820-105172870	AoSMC	blood vessel:	n/a
36	chr7:105162814-105162864	K562	blood:	n/a
37	chr7:105172520-105172570	SK-N-MC	brain:	n/a
38	chr7:105163736-105163786	Hepatocyte	liver:	n/a
39	chr7:105128488-105128538	HCF	heart:	n/a
40	chr7:105162888-105162938	AG09319	gingival:	n/a
41	chr7:105128488-105128538	ProgFib	skin:	n/a
42	chr7:105162941-105162991	HRE	kidney:	n/a
43	chr7:105161983-105162033	AG09319	gingival:	n/a
44	chr7:105134734-105134784	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:105176805-105176855	HCT-116	colon:	n/a
46	chr7:105172403-105172453	A549	lung:	n/a
47	chr7:105162859-105162909	MCF10A-Er-Src	breast:	n/a
48	chr7:105173132-105173182	RPTEC	kidney:	n/a
49	chr7:105172664-105172714	RPTEC	kidney:	n/a
50	chr7:105172820-105172870	SAEC	small airway:	n/a

(count:179 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:105127051..105129077-chr7:105161518..105164006,2	K562	blood:
2	chr7:105123891..105126807-chr7:105127065..105130619,3	K562	blood:
3	chr7:105126837..105131294-chr7:105131811..105135446,3	K562	blood:
4	chr7:105126837..105131294-chr7:105131811..105135446,3	K562	blood:
5	chr14:20937110..20938110-chr7:105172278..105173069,2	Hela-S3	cervix:
6	chr7:105171231..105172860-chr7:105185302..105187081,2	MCF-7	breast:
7	chr7:105160687..105164718-chr7:105170642..105174239,14	MCF-7	breast:
8	chr7:105115487..105117775-chr7:105123011..105125006,2	K562	blood:
9	chr7:104653054..104655993-chr7:105161169..105164095,3	MCF-7	breast:
10	chr7:104772977..104775390-chr7:105160456..105162601,2	K562	blood:
11	chr7:105123891..105126807-chr7:105127065..105130619,3	K562	blood:
12	chr7:105110346..105111937-chr7:105127717..105129867,2	K562	blood:
13	chr7:104652163..104655972-chr7:105160292..105163807,4	MCF-7	breast:
14	chr7:105160261..105165362-chr7:105168599..105174293,22	MCF-7	breast:
15	chr17:41465807..41466363-chr7:105162224..105162878,2	NB4	blood:
16	chr7:105125271..105127106-chr7:105136833..105138910,2	K562	blood:
17	chr7:105135383..105138778-chr7:105145127..105148143,3	MCF-7	breast:
18	chr7:65958424..65959012-chr7:105162357..105162865,2	NB4	blood:
19	chr7:105171303..105174411-chr7:105176077..105181251,7	MCF-7	breast:
20	chr7:105171405..105173628-chr7:105221272..105223628,2	MCF-7	breast:
21	chr17:33914164..33914765-chr7:105161584..105162384,2	Hela-S3	cervix:
22	chr7:105116272..105117859-chr7:105118414..105120932,2	K562	blood:
23	chr6:96969151..96969942-chr7:105161938..105162970,3	Hela-S3	cervix:
24	chr7:105143860..105146568-chr7:105160476..105162753,4	K562	blood:
25	chr7:105152955..105155476-chr7:105155749..105158829,5	K562	blood:
26	chr7:105027071..105029412-chr7:105096317..105098709,3	K562	blood:
27	chr7:105158727..105165017-chr7:105166972..105176993,56	K562	blood:
28	chr7:105178950..105184769-chr7:105189536..105192769,5	K562	blood:
29	chr7:105135206..105139003-chr7:105202925..105206444,3	K562	blood:
30	chr11:66056148..66056859-chr7:105172413..105173177,2	Hela-S3	cervix:
31	chr7:105143706..105147161-chr7:105171378..105174621,4	K562	blood:
32	chr7:104651944..104654760-chr7:105154090..105156667,3	K562	blood:
33	chr7:105088778..105090320-chr7:105090980..105093442,3	MCF-7	breast:
34	chr7:105171071..105173381-chr7:105188092..105190983,2	MCF-7	breast:
35	chr7:105192153..105195079-chr7:105203440..105205877,2	K562	blood:
36	chr7:105171396..105173975-chr7:105194252..105196859,3	K562	blood:
37	chr7:105078529..105081334-chr7:105089630..105092260,2	MCF-7	breast:
38	chr7:105136272..105139151-chr7:105160934..105162836,3	MCF-7	breast:
39	chr7:105148472..105150405-chr7:105160556..105162918,2	MCF-7	breast:
40	chr7:105125271..105127106-chr7:105136833..105138910,2	K562	blood:
41	chr7:105189456..105192064-chr7:105194767..105196325,2	K562	blood:
42	chr7:105171185..105172981-chr7:105198987..105201219,2	MCF-7	breast:
43	chr7:105171919..105174630-chr7:105210042..105212382,2	K562	blood:
44	chr7:105162077..105162858-chr7:105172193..105173344,3	MCF-7	breast:
45	chr7:105115487..105117775-chr7:105123011..105125006,2	K562	blood:
46	chr7:104652625..104654760-chr7:105154090..105155879,2	K562	blood:
47	chr7:105121563..105123153-chr7:105161155..105163117,2	MCF-7	breast:
48	chr7:105147334..105150075-chr7:105152769..105155658,2	K562	blood:
49	chr7:105161102..105162655-chr7:105181498..105183213,2	K562	blood:
50	chr7:105162459..105163197-chr7:105172183..105173025,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDHR3-5	chr7:105182855-105183003	NONHSAT122624
2	lnc-RINT1-2	chr7:105170656-105171118	NONHSAT122622
3	lnc-PUS7-1	chr7:105171944-105171973	NONHSAT122623
4	lnc-CDHR3-5	chr7:105182048-105182302	NONHSAT122624
5	lnc-RINT1-1	chr7:105208142-105208836	NONHSAT122625
6	lnc-PUS7-1	chr7:105170677-105170904	NONHSAT122623

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PUS7	hsa-miR-155-5p	chr7:105097684-105097705
2	PUS7	hsa-miR-32-5p	chr7:105098074-105098095

Variant related genes	Relation type
ENSG00000272604	TF binding region
RINT1	TF binding region
ENSG00000223886	TF binding region
PUS7	TF binding region
ENSG00000272604	CpG island
RINT1	CpG island
ENSG00000223886	CpG island
PUS7	CpG island
ENSG00000223473	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000223886	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000230508	chromatin interactions
ENSG00000233797	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000231167	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000272604	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000185055	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000014123	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000146776	chromatin interactions

Extended variants
information (count: 4831 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4831 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6977560	chr7:105088693-105088694	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537887044	chr7:105088721-105088722	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs13244551	chr7:105088758-105088759	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs6466066	chr7:105088813-105088814	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs577764375	chr7:105088833-105088834	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540336953	chr7:105088834-105088835	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553928551	chr7:105088851-105088852	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs58094192	chr7:105088872-105088873	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs59819945	chr7:105088908-105088909	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs563230685	chr7:105088928-105088929	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370501443	chr7:105088930-105088931	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532021404	chr7:105088933-105088934	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79921000	chr7:105088936-105088937	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375096264	chr7:105088939-105088940	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532916444	chr7:105088942-105088943	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113390131	chr7:105088952-105088953	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541936682	chr7:105088987-105088988	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566417357	chr7:105089020-105089021	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145431862	chr7:105089024-105089025	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548892130	chr7:105089054-105089055	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193189920	chr7:105089094-105089095	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537747243	chr7:105089100-105089101	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184086351	chr7:105089105-105089106	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571309086	chr7:105089110-105089111	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533903771	chr7:105089149-105089150	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554253875	chr7:105089150-105089151	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2091160	chr7:105089161-105089162	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs377217996	chr7:105089174-105089175	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536878324	chr7:105089192-105089193	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs143373939	chr7:105089239-105089240	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563264008	chr7:105089253-105089254	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576847151	chr7:105089295-105089296	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116052537	chr7:105089296-105089297	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139261971	chr7:105089321-105089322	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577737395	chr7:105089363-105089364	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539813639	chr7:105089411-105089412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188830716	chr7:105089435-105089436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528961266	chr7:105089446-105089447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549208926	chr7:105089475-105089476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191811200	chr7:105089498-105089499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7778869	chr7:105089506-105089507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7778494	chr7:105089508-105089509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531354843	chr7:105089525-105089526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369988845	chr7:105089567-105089568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183607781	chr7:105089590-105089591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188359372	chr7:105089592-105089593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564479321	chr7:105089602-105089603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181959078	chr7:105089623-105089624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567793689	chr7:105089624-105089625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536337483	chr7:105089656-105089657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:3626 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105080000-105093000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:105080000-105094400	Weak transcription	NHLF	lung
3	chr7:105080000-105108400	Weak transcription	Spleen	Spleen
4	chr7:105080000-105161200	Weak transcription	Pancreas	Pancrea
5	chr7:105080200-105104600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:105080200-105126800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr7:105084800-105090000	Enhancers	Primary B cells from cord blood	blood
8	chr7:105084800-105091200	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:105086800-105098200	Weak transcription	Ovary	ovary
10	chr7:105087000-105091600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr7:105087200-105098200	Weak transcription	Fetal Stomach	stomach
12	chr7:105087200-105101400	Weak transcription	Left Ventricle	heart
13	chr7:105087200-105102000	Weak transcription	Aorta	Aorta
14	chr7:105087800-105090000	Enhancers	Primary T cells fromperipheralblood	blood
15	chr7:105087800-105090800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr7:105088000-105089400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
17	chr7:105088000-105089600	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr7:105088000-105089600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:105088000-105090000	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr7:105088000-105090200	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr7:105088000-105090400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr7:105088000-105090800	Enhancers	GM12878-XiMat	blood
23	chr7:105088000-105091600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:105088200-105089200	Enhancers	Primary hematopoietic stem cells	blood
25	chr7:105088200-105089400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:105088200-105090000	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr7:105088200-105099000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr7:105088200-105142600	Weak transcription	Esophagus	oesophagus
29	chr7:105088200-105152800	Weak transcription	Gastric	stomach
30	chr7:105088400-105089000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr7:105088400-105089000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr7:105088400-105089000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr7:105088400-105089600	Enhancers	Primary T cells from cord blood	blood
34	chr7:105088400-105097200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:105088400-105140400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr7:105088600-105088800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:105088600-105088800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:105088600-105088800	Enhancers	Dnd41	blood
39	chr7:105088800-105089000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:105088800-105089200	Enhancers	Fetal Thymus	thymus
41	chr7:105088800-105092600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:105088800-105096200	Weak transcription	Dnd41	blood
43	chr7:105088800-105096600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:105089000-105096200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr7:105089000-105096600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:105089200-105127000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr7:105089200-105142600	Weak transcription	Fetal Thymus	thymus
48	chr7:105089400-105091800	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr7:105089400-105094200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr7:105089600-105090000	Weak transcription	Primary T cells from cord blood	blood

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