Variant report

Variant	nsv932138
Chromosome Location	chr7:104826194-105152816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4385)
CpG islands
(count:3059)
Chromatin interactive
region (count:347)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:4385 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
2	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
3	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
4	ARID3A	chr7:104972080-104972123	K562	blood:	n/a	n/a
5	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
6	ARID3A	chr7:104999428-104999583	K562	blood:	n/a	n/a
7	ARID3A	chr7:105080108-105080325	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
9	ARID3A	chr7:104924529-104924792	K562	blood:	n/a	n/a
10	ARID3A	chr7:104994259-104994459	K562	blood:	n/a	n/a
11	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
13	ARID3A	chr7:105015076-105015149	K562	blood:	n/a	n/a
14	ARID3A	chr7:104999465-104999651	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:105070152-105070549	K562	blood:	n/a	n/a
16	ARID3A	chr7:105008783-105009038	K562	blood:	n/a	n/a
17	ARID3A	chr7:104909404-104910342	K562	blood:	n/a	chr7:104910069-104910085 chr7:104909863-104909879 chr7:104909862-104909878
18	ARID3A	chr7:104873284-104873810	K562	blood:	n/a	n/a
19	ARID3A	chr7:104976432-104976788	K562	blood:	n/a	n/a
20	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
21	ARID3A	chr7:104897645-104898076	K562	blood:	n/a	n/a
22	ARID3A	chr7:104909503-104909771	HepG2	liver:	n/a	n/a
23	ARID3A	chr7:104944460-104945017	HepG2	liver:	n/a	n/a
24	ARID3A	chr7:104999888-105000102	K562	blood:	n/a	n/a
25	ARID3A	chr7:104976462-104976771	HepG2	liver:	n/a	n/a
26	ARID3A	chr7:105006603-105006770	K562	blood:	n/a	n/a
27	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
28	ARID3A	chr7:104970982-104971041	K562	blood:	n/a	n/a
29	ARID3A	chr7:105070221-105070610	HepG2	liver:	n/a	n/a
30	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
31	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
32	ARID3A	chr7:105007981-105008379	HepG2	liver:	n/a	n/a
33	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
34	ATF1	chr7:104897712-104898056	K562	blood:	n/a	n/a
35	ATF1	chr7:104865550-104866001	K562	blood:	n/a	n/a
36	ATF1	chr7:104902188-104902552	K562	blood:	n/a	n/a
37	ATF1	chr7:105007289-105007410	K562	blood:	n/a	n/a
38	ATF1	chr7:105070205-105070516	K562	blood:	n/a	n/a
39	ATF1	chr7:104908668-104908848	K562	blood:	n/a	n/a
40	ATF1	chr7:104897219-104897309	K562	blood:	n/a	n/a
41	ATF2	chr7:104944617-104945385	GM12878	blood:	n/a	n/a
42	ATF2	chr7:104992448-104993159	GM12878	blood:	n/a	n/a
43	ATF3	chr7:104944489-104944823	HCT-116	colon:	n/a	n/a
44	BACH1	chr7:105042903-105043365	K562	blood:	n/a	n/a
45	BACH1	chr7:105103081-105103084	K562	blood:	n/a	n/a
46	BACH1	chr7:104871499-104871667	K562	blood:	n/a	n/a
47	BACH1	chr7:105029014-105029308	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr7:105027844-105028042	K562	blood:	n/a	n/a
49	BACH1	chr7:105113662-105113870	K562	blood:	n/a	n/a
50	BACH1	chr7:105028171-105028753	H1-hESC	embryonic stem cell:	n/a	n/a

(count:3059 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:104945248-104945298	ovcar-3	ovarian:	n/a
2	chr7:104943515-104943565	Jurkat	blood:	n/a
3	chr7:105094993-105095043	IMR90	lung:	fetal
4	chr7:105110948-105110998	H1-hESC	embryonic stem cell:	embryo
5	chr7:104994322-104994372	RPTEC	kidney:	n/a
6	chr7:104941977-104942027	NB4	blood:	n/a
7	chr7:104909815-104909865	HEK293	kidney:	embryo
8	chr7:104885248-104885298	HCPEpiC	choroid plexus:	n/a
9	chr7:104869189-104869239	U87	brain:	n/a
10	chr7:104945248-104945298	ovcar-3	ovarian:	n/a
11	chr7:104943515-104943565	Jurkat	blood:	n/a
12	chr7:105094993-105095043	IMR90	lung:	fetal
13	chr7:105110948-105110998	H1-hESC	embryonic stem cell:	embryo
14	chr7:104994322-104994372	RPTEC	kidney:	n/a
15	chr7:104941977-104942027	NB4	blood:	n/a
16	chr7:104909815-104909865	HEK293	kidney:	embryo
17	chr7:104885248-104885298	HCPEpiC	choroid plexus:	n/a
18	chr7:104869189-104869239	U87	brain:	n/a
19	chr7:104909430-104909480	K562	blood:	n/a
20	chr7:104892331-104892381	HMEC	breast:	n/a
21	chr7:104869288-104869338	HAEpiC	amniotic membrane:	n/a
22	chr7:105028539-105028589	HRE	kidney:	n/a
23	chr7:104869132-104869182	SK-N-SH	brain:	n/a
24	chr7:105026171-105026221	SK-N-MC	brain:	n/a
25	chr7:104888858-104888908	HMEC	breast:	n/a
26	chr7:105029385-105029435	U87	brain:	n/a
27	chr7:104879299-104879349	HNPCEpiC	eye:	n/a
28	chr7:104939331-104939381	GM19239	blood:	n/a
29	chr7:104859800-104859850	Jurkat	blood:	n/a
30	chr7:104941898-104941948	AG04449	skin:	fetal
31	chr7:104829801-104829851	PFSK-1	brain:	n/a
32	chr7:104939331-104939381	NT2-D1	testis:	n/a
33	chr7:104883450-104883500	Hela-S3	cervix:	n/a
34	chr7:105079663-105079713	GM12878	blood:	n/a
35	chr7:104837830-104837880	CMK	blood:	n/a
36	chr7:104887042-104887092	GM12891	blood:	n/a
37	chr7:105029497-105029547	SAEC	small airway:	n/a
38	chr7:104909815-104909865	AG04449	skin:	fetal
39	chr7:104941977-104942027	RPTEC	kidney:	n/a
40	chr7:105110948-105110998	PFSK-1	brain:	n/a
41	chr7:105134734-105134784	HCT-116	colon:	n/a
42	chr7:104892331-104892381	HepG2	liver:	n/a
43	chr7:104892331-104892381	SK-N-MC	brain:	n/a
44	chr7:105112740-105112790	ProgFib	skin:	n/a
45	chr7:105030168-105030218	U87	brain:	n/a
46	chr7:104869189-104869239	GM19239	blood:	n/a
47	chr7:105018109-105018159	T-47D	breast:	n/a
48	chr7:104885375-104885425	SKMC	muscle:	n/a
49	chr7:104909815-104909865	GM19239	blood:	n/a
50	chr7:105030752-105030802	CMK	blood:	n/a

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr7:104851087..104853973-chr7:104856176..104858967,3	K562	blood:
2	chr7:105039517..105040114-chr7:105128184..105128801,2	MCF-7	breast:
3	chr7:105078529..105081334-chr7:105089630..105092260,2	MCF-7	breast:
4	chr7:104835386..104838119-chr7:104841515..104843730,2	K562	blood:
5	chr7:104861681..104863242-chr7:104872431..104874616,2	K562	blood:
6	chr7:104974522..104976847-chr7:104979071..104980731,2	K562	blood:
7	chr7:105103366..105105752-chr7:105109309..105111791,2	K562	blood:
8	chr7:104922381..104923956-chr7:104935072..104936834,2	MCF-7	breast:
9	chr7:104902229..104905190-chr7:104911272..104913681,2	MCF-7	breast:
10	chr7:104893338..104895687-chr7:104903857..104906194,3	K562	blood:
11	chr7:104909811..104911853-chr7:104934398..104937099,2	K562	blood:
12	chr7:105026529..105029377-chr7:105162488..105165118,2	MCF-7	breast:
13	chr7:104873668..104875334-chr7:104875685..104877257,2	MCF-7	breast:
14	chr7:104801800..104804505-chr7:104876427..104879424,2	K562	blood:
15	chr7:105041648..105042543-chr7:105069609..105070839,7	MCF-7	breast:
16	chr7:104621634..104622334-chr7:105128158..105128926,3	K562	blood:
17	chr7:105065275..105067790-chr7:105068952..105071449,2	K562	blood:
18	chr7:104998328..105001969-chr7:105010062..105013711,3	K562	blood:
19	chr7:105134519..105138273-chr7:105140684..105142940,4	K562	blood:
20	chr7:104974522..104976847-chr7:104979071..104980731,2	K562	blood:
21	chr7:105129766..105132024-chr7:105147808..105150041,2	MCF-7	breast:
22	chr7:104924217..104925131-chr7:104956599..104958078,10	MCF-7	breast:
23	chr7:104651787..104654517-chr7:104949816..104951712,2	MCF-7	breast:
24	chr7:104895826..104898177-chr7:105161985..105164646,2	K562	blood:
25	chr7:104893974..104896006-chr7:104900694..104903454,2	K562	blood:
26	chr7:104914487..104916145-chr7:104922195..104924067,2	K562	blood:
27	chr7:104994593..104996936-chr7:105006253..105008097,2	K562	blood:
28	chr7:104943318..104946165-chr7:104949324..104952244,3	K562	blood:
29	chr7:105065275..105067790-chr7:105068952..105071449,2	K562	blood:
30	chr7:104956419..104959017-chr7:104967499..104969539,3	MCF-7	breast:
31	chr7:104906168..104907747-chr7:104911064..104912802,2	K562	blood:
32	chr7:104855097..104857884-chr7:104863691..104866292,2	K562	blood:
33	chr7:104652744..104654842-chr7:105028526..105031470,2	MCF-7	breast:
34	chr7:105139514..105141337-chr7:105172365..105174838,2	K562	blood:
35	chr7:105108727..105111208-chr7:105115281..105117815,3	K562	blood:
36	chr7:104857529..104859234-chr7:104868508..104871222,2	MCF-7	breast:
37	chr7:105088778..105090320-chr7:105090980..105093442,3	MCF-7	breast:
38	chr7:104965775..104968018-chr7:104970482..104972338,2	MCF-7	breast:
39	chr7:104985604..104988009-chr7:104988661..104992551,3	MCF-7	breast:
40	chr7:105028909..105031014-chr7:105085186..105086946,2	K562	blood:
41	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
42	chr7:105012234..105014245-chr7:105022510..105026066,3	K562	blood:
43	chr7:104649613..104651128-chr7:104876520..104878391,2	K562	blood:
44	chr7:105039634..105040417-chr7:105069590..105070567,3	MCF-7	breast:
45	chr7:104621410..104622279-chr7:105069837..105070818,3	K562	blood:
46	chr7:104853847..104856619-chr7:104856817..104860250,3	MCF-7	breast:
47	chr7:105135383..105138778-chr7:105145127..105148143,3	MCF-7	breast:
48	chr7:104829354..104831168-chr7:104834858..104836763,2	K562	blood:
49	chr7:105039296..105040112-chr7:105127763..105129034,3	MCF-7	breast:
50	chr7:105128652..105130431-chr7:105155897..105157484,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MLL5-5	chr7:104845047-104845306	NONHSAT122615
2	lnc-SRPK2-5	chr7:104909253-104909316	NONHSAT122614
3	lnc-MLL5-1	chr7:104946699-104947089	ENSG00000242154.1
4	lnc-SRPK2-5	chr7:104844170-104844232	NONHSAT122614
5	lnc-MLL5-4	chr7:104829637-104829934	NONHSAT122612
6	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614
7	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
8	lnc-MLL5-6	chr7:104941969-104942533	NONHSAT122616
9	lnc-MLL5-4	chr7:104830195-104830261	NONHSAT122612
10	lnc-MLL5-1	chr7:104944724-104944878	ENSG00000242154.1

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
ENSG00000271482	TF binding region
ENSG00000213361	TF binding region
ENSG00000270764	TF binding region
RWDD4P1	TF binding region
RNU6-1322P	TF binding region
PUS7	TF binding region
ENSG00000242154	TF binding region
SRPK2	TF binding region
ENSG00000271482	CpG island
ENSG00000213361	CpG island
ENSG00000270764	CpG island
RWDD4P1	CpG island
RNU6-1322P	CpG island
PUS7	CpG island
ENSG00000242154	CpG island
SRPK2	CpG island
ENSG00000135249	chromatin interactions
ENSG00000213361	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000271482	chromatin interactions
ENSG00000242154	chromatin interactions
ENSG00000270764	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000244490	chromatin interactions

Extended variants
information (count: 12805 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:12805 , 50 per page) page: 1 2 3 4 5 6 7 ... 257

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547912585	chr7:104826215-104826216	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs183853408	chr7:104826245-104826246	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs73186008	chr7:104826263-104826264	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs188628140	chr7:104826376-104826377	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs376616244	chr7:104826380-104826381	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs553108339	chr7:104826381-104826382	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577600517	chr7:104826427-104826428	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs573086086	chr7:104826436-104826437	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs542072129	chr7:104826440-104826441	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555496995	chr7:104826472-104826473	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs73186009	chr7:104826484-104826485	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs113118407	chr7:104826569-104826570	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374263435	chr7:104826609-104826610	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180686114	chr7:104826618-104826619	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563267733	chr7:104826630-104826631	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs150019771	chr7:104826669-104826670	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs540500242	chr7:104826716-104826717	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs560720997	chr7:104826768-104826769	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs575626595	chr7:104826769-104826770	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs185120901	chr7:104826826-104826827	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs55638165	chr7:104826910-104826911	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs561355426	chr7:104826925-104826926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530463512	chr7:104826950-104826951	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373286951	chr7:104826975-104826976	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570237807	chr7:104826996-104826997	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539501919	chr7:104826999-104827000	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73186011	chr7:104827010-104827011	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190349500	chr7:104827013-104827014	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117974725	chr7:104827141-104827142	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555597643	chr7:104827288-104827289	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs79435087	chr7:104827294-104827295	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs561069288	chr7:104827416-104827417	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs538291658	chr7:104827445-104827446	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs528294750	chr7:104827457-104827458	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs578168759	chr7:104827485-104827486	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs376329100	chr7:104827525-104827526	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs55671517	chr7:104827528-104827529	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs560543898	chr7:104827533-104827534	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs574135210	chr7:104827535-104827536	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs144290272	chr7:104827539-104827540	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs148730561	chr7:104827565-104827566	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs71562646	chr7:104827587-104827588	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs533435511	chr7:104827597-104827598	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs143610928	chr7:104827603-104827604	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs563701530	chr7:104827626-104827627	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs80268591	chr7:104827658-104827659	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs182592758	chr7:104827741-104827742	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs528988384	chr7:104827789-104827790	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs376760772	chr7:104827790-104827791	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs146776043	chr7:104827833-104827834	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Bladder cancer	21909424	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
Cancer	20164919	CNVD
Myxofibrosarcoma	20639860	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:7427 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104754400-104850400	Weak transcription	Fetal Kidney	kidney
2	chr7:104782800-104845600	Weak transcription	Spleen	Spleen
3	chr7:104806400-104838200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:104806600-104836800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:104806600-104842000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:104807600-104829800	Weak transcription	Thymus	Thymus
7	chr7:104809000-104836600	Weak transcription	HSMM	muscle
8	chr7:104809000-104838800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:104809600-104838000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr7:104809800-104826600	Weak transcription	Primary B cells from cord blood	blood
11	chr7:104809800-104838000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:104810200-104840600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr7:104814000-104839800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr7:104814200-104827000	Weak transcription	Pancreas	Pancrea
15	chr7:104815600-104836600	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr7:104819800-104829400	Weak transcription	Brain Angular Gyrus	brain
17	chr7:104820000-104827800	Weak transcription	Stomach Mucosa	stomach
18	chr7:104820800-104833800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:104821000-104828400	Weak transcription	Brain Substantia Nigra	brain
20	chr7:104821000-104829200	Weak transcription	Brain Hippocampus Middle	brain
21	chr7:104821000-104829800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr7:104821000-104838400	Weak transcription	Fetal Lung	lung
23	chr7:104821200-104830000	Weak transcription	Fetal Thymus	thymus
24	chr7:104821200-104830400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr7:104821600-104838400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:104822000-104836400	Weak transcription	A549	lung
27	chr7:104822000-104858800	Weak transcription	Gastric	stomach
28	chr7:104822200-104826200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:104822800-104838200	Weak transcription	Primary T cells from cord blood	blood
30	chr7:104823600-104829400	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:104823600-104848600	Strong transcription	Dnd41	blood
32	chr7:104824800-104828800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:104825000-104837800	Weak transcription	NH-A	brain
34	chr7:104825200-104826400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:104825200-104829800	Enhancers	HMEC	breast
36	chr7:104825800-104826200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:104825800-104826200	Weak transcription	Brain Anterior Caudate	brain
38	chr7:104825800-104826400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:104825800-104826400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:104825800-104826400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:104825800-104826400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:104826000-104826400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr7:104826000-104826400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:104826000-104826400	Active TSS	NHEK	skin
45	chr7:104826000-104826800	Enhancers	Osteobl	bone
46	chr7:104826200-104826400	Enhancers	Brain Anterior Caudate	brain
47	chr7:104826200-104827400	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr7:104826200-104829800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr7:104826200-104831600	Weak transcription	Primary B cells from peripheral blood	blood
50	chr7:104826400-104826600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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