Variant report

Variant	nsv1028228
Chromosome Location	chr7:104807207-105182998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5848)
CpG islands
(count:4705)
Chromatin interactive
region (count:439)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:5848 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
2	ARID3A	chr7:104999465-104999651	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:104944460-104945017	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:104994259-104994459	K562	blood:	n/a	n/a
5	ARID3A	chr7:104924529-104924792	K562	blood:	n/a	n/a
6	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
7	ARID3A	chr7:104999888-105000102	K562	blood:	n/a	n/a
8	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
9	ARID3A	chr7:104976432-104976788	K562	blood:	n/a	n/a
10	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:105070152-105070549	K562	blood:	n/a	n/a
12	ARID3A	chr7:104970982-104971041	K562	blood:	n/a	n/a
13	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:104909503-104909771	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:105007981-105008379	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:104999428-104999583	K562	blood:	n/a	n/a
17	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
18	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
19	ARID3A	chr7:105173865-105174045	HepG2	liver:	n/a	n/a
20	ARID3A	chr7:104909404-104910342	K562	blood:	n/a	chr7:104910069-104910085 chr7:104909863-104909879 chr7:104909862-104909878
21	ARID3A	chr7:105172276-105172771	K562	blood:	n/a	n/a
22	ARID3A	chr7:105172230-105172894	HepG2	liver:	n/a	n/a
23	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
24	ARID3A	chr7:105008783-105009038	K562	blood:	n/a	n/a
25	ARID3A	chr7:105162675-105163137	K562	blood:	n/a	n/a
26	ARID3A	chr7:104819345-104819786	HepG2	liver:	n/a	n/a
27	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
28	ARID3A	chr7:104873284-104873810	K562	blood:	n/a	n/a
29	ARID3A	chr7:104976462-104976771	HepG2	liver:	n/a	n/a
30	ARID3A	chr7:105006603-105006770	K562	blood:	n/a	n/a
31	ARID3A	chr7:104897645-104898076	K562	blood:	n/a	n/a
32	ARID3A	chr7:105015076-105015149	K562	blood:	n/a	n/a
33	ARID3A	chr7:105070221-105070610	HepG2	liver:	n/a	n/a
34	ARID3A	chr7:104972080-104972123	K562	blood:	n/a	n/a
35	ARID3A	chr7:105162532-105162842	HepG2	liver:	n/a	n/a
36	ARID3A	chr7:105080108-105080325	HepG2	liver:	n/a	n/a
37	ARID3A	chr7:104819987-104820013	HepG2	liver:	n/a	n/a
38	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
39	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
40	ATF1	chr7:104902188-104902552	K562	blood:	n/a	n/a
41	ATF1	chr7:105070205-105070516	K562	blood:	n/a	n/a
42	ATF1	chr7:104897712-104898056	K562	blood:	n/a	n/a
43	ATF1	chr7:104865550-104866001	K562	blood:	n/a	n/a
44	ATF1	chr7:104897219-104897309	K562	blood:	n/a	n/a
45	ATF1	chr7:104908668-104908848	K562	blood:	n/a	n/a
46	ATF1	chr7:105007289-105007410	K562	blood:	n/a	n/a
47	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
48	ATF2	chr7:105172329-105172807	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF2	chr7:105162441-105162701	H1-hESC	embryonic stem cell:	n/a	n/a
50	ATF2	chr7:104944617-104945385	GM12878	blood:	n/a	n/a

(count:4705 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:104879299-104879349	HAEpiC	amniotic membrane:	n/a
2	chr7:105158109-105158159	ovcar-3	ovarian:	n/a
3	chr7:104909430-104909480	GM12878	blood:	n/a
4	chr7:105162855-105162905	Jurkat	blood:	n/a
5	chr7:105110948-105110998	SAEC	small airway:	n/a
6	chr7:105030752-105030802	HMEC	breast:	n/a
7	chr7:105018109-105018159	ProgFib	skin:	n/a
8	chr7:104939819-104939869	MCF-7	breast:	n/a
9	chr7:104879299-104879349	HAEpiC	amniotic membrane:	n/a
10	chr7:105158109-105158159	ovcar-3	ovarian:	n/a
11	chr7:104909430-104909480	GM12878	blood:	n/a
12	chr7:105162855-105162905	Jurkat	blood:	n/a
13	chr7:105110948-105110998	SAEC	small airway:	n/a
14	chr7:105030752-105030802	HMEC	breast:	n/a
15	chr7:105018109-105018159	ProgFib	skin:	n/a
16	chr7:104939819-104939869	MCF-7	breast:	n/a
17	chr7:105029385-105029435	SAEC	small airway:	n/a
18	chr7:104885375-104885425	LNCaP	prostate:	n/a
19	chr7:104939819-104939869	SKMC	muscle:	n/a
20	chr7:104888858-104888908	K562	blood:	n/a
21	chr7:105172664-105172714	SK-N-SH_RA	brain:	n/a
22	chr7:105134734-105134784	HRPEpiC	eye:	n/a
23	chr7:104829801-104829851	ovcar-3	ovarian:	n/a
24	chr7:105162577-105162627	NHDF-neo	bronchial:	n/a
25	chr7:104865796-104865846	K562	blood:	n/a
26	chr7:105172820-105172870	GM06990	blood:	n/a
27	chr7:105018109-105018159	H1-hESC	embryonic stem cell:	embryo
28	chr7:105162814-105162864	BJ	skin:	n/a
29	chr7:105029125-105029175	LNCaP	prostate:	n/a
30	chr7:105029499-105029549	H1-hESC	embryonic stem cell:	embryo
31	chr7:105028539-105028589	SK-N-MC	brain:	n/a
32	chr7:104837830-104837880	PANC-1	pancreas:	n/a
33	chr7:105094993-105095043	HRCEpiC	kidney:	n/a
34	chr7:105027541-105027591	GM12891	blood:	n/a
35	chr7:105172664-105172714	BJ	skin:	n/a
36	chr7:105172168-105172218	HNPCEpiC	eye:	n/a
37	chr7:105161983-105162033	MCF10A-Er-Src	breast:	n/a
38	chr7:105128488-105128538	HEEpiC	esophagus:	n/a
39	chr7:104941898-104941948	PFSK-1	brain:	n/a
40	chr7:105171843-105171893	NB4	blood:	n/a
41	chr7:105030168-105030218	GM12892	blood:	n/a
42	chr7:105029895-105029945	PFSK-1	brain:	n/a
43	chr7:105162878-105162928	HMEC	breast:	n/a
44	chr7:105030752-105030802	SK-N-SH_RA	brain:	n/a
45	chr7:104879299-104879349	IMR90	lung:	fetal
46	chr7:104881282-104881332	NH-A	brain:	n/a
47	chr7:105173132-105173182	NH-A	brain:	n/a
48	chr7:105173132-105173182	NHDF-neo	bronchial:	n/a
49	chr7:105162814-105162864	HAEpiC	amniotic membrane:	n/a
50	chr7:104892331-104892381	PANC-1	pancreas:	n/a

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Distal block	Cell Line	Cell type
1	chr7:104836648..104838790-chr7:104846781..104848427,3	K562	blood:
2	chr7:105095176..105096749-chr7:105098441..105100955,2	MCF-7	breast:
3	chr7:104905394..104907568-chr7:104922706..104925372,2	MCF-7	breast:
4	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:
5	chr7:105077610..105079593-chr7:105277215..105278771,2	MCF-7	breast:
6	chr7:105143860..105146568-chr7:105160476..105162753,4	K562	blood:
7	chr7:105160687..105164718-chr7:105170642..105174239,14	MCF-7	breast:
8	chr7:104907817..104909444-chr7:104949572..104952100,2	MCF-7	breast:
9	chr7:104805654..104807783-chr7:104838268..104840997,2	K562	blood:
10	chr7:104955875..104958627-chr7:104961394..104962913,2	MCF-7	breast:
11	chr7:105078097..105081437-chr7:105081895..105086252,7	MCF-7	breast:
12	chr1:156698268..156698938-chr7:105162358..105162859,2	Hela-S3	cervix:
13	chr7:105069108..105071061-chr7:105077063..105078737,2	MCF-7	breast:
14	chr7:104945506..104947169-chr7:104948934..104951564,2	MCF-7	breast:
15	chr7:104862522..104864551-chr7:104866607..104868300,2	K562	blood:
16	chr7:105134519..105138273-chr7:105140684..105142940,4	K562	blood:
17	chr7:104563090..104564028-chr7:105069801..105070415,2	K562	blood:
18	chr7:105126748..105128626-chr7:105155718..105158086,2	K562	blood:
19	chr7:104877972..104880415-chr7:104883761..104886456,5	K562	blood:
20	chr7:105065275..105067790-chr7:105068952..105071449,2	K562	blood:
21	chr7:105139662..105141341-chr7:105152826..105155555,3	K562	blood:
22	chr7:104902229..104905190-chr7:104911272..104913681,2	MCF-7	breast:
23	chr7:105093737..105097449-chr7:105099816..105103606,4	K562	blood:
24	chr7:104960628..104963813-chr7:104964024..104966847,3	MCF-7	breast:
25	chr7:104649613..104651128-chr7:104876520..104878391,2	K562	blood:
26	chr7:104906464..104909306-chr7:104939170..104942038,3	MCF-7	breast:
27	chr7:104652744..104654842-chr7:105028526..105031470,2	MCF-7	breast:
28	chr7:105029824..105032086-chr7:105067490..105069979,2	K562	blood:
29	chr7:105171895..105174076-chr7:105174094..105176454,2	MCF-7	breast:
30	chr7:104652163..104655972-chr7:105160292..105163807,4	MCF-7	breast:
31	chr7:104955875..104958627-chr7:104961394..104962913,2	MCF-7	breast:
32	chr7:105019571..105021474-chr7:105027326..105029018,2	MCF-7	breast:
33	chr7:105148185..105149870-chr7:105160014..105161672,2	K562	blood:
34	chr7:104584351..104587135-chr7:105088477..105090953,2	K562	blood:
35	chr7:104956419..104959017-chr7:104967499..104969539,3	MCF-7	breast:
36	chr7:105019911..105021910-chr7:105024677..105026313,2	K562	blood:
37	chr7:105155451..105157293-chr7:105221576..105223932,2	K562	blood:
38	chr7:104944940..104946853-chr7:104951503..104953129,2	MCF-7	breast:
39	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
40	chr7:104944150..104946367-chr7:104948630..104950865,4	MCF-7	breast:
41	chr7:104842758..104847197-chr7:104847496..104851366,4	MCF-7	breast:
42	chr7:104914487..104916145-chr7:104922195..104924067,2	K562	blood:
43	chr7:65958424..65959012-chr7:105162357..105162865,2	NB4	blood:
44	chr17:41465807..41466363-chr7:105162224..105162878,2	NB4	blood:
45	chr7:104850289..104852047-chr7:104854189..104856772,3	MCF-7	breast:
46	chr7:105172788..105175282-chr7:105215933..105219450,4	K562	blood:
47	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
48	chr7:105009330..105013041-chr7:105014599..105017566,3	K562	blood:
49	chr7:104857529..104859234-chr7:104868508..104871222,2	MCF-7	breast:
50	chr7:104651829..104654559-chr7:104857384..104858979,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPK2-5	chr7:104844170-104844232	NONHSAT122614
2	lnc-CDHR3-5	chr7:105182855-105183003	NONHSAT122624
3	lnc-SRPK2-5	chr7:104909253-104909316	NONHSAT122614
4	lnc-MLL5-1	chr7:104944724-104944878	ENSG00000242154.1
5	lnc-MLL5-1	chr7:104946699-104947089	ENSG00000242154.1
6	lnc-MLL5-6	chr7:104941969-104942533	NONHSAT122616
7	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
8	lnc-RINT1-2	chr7:105170656-105171118	NONHSAT122622
9	lnc-MLL5-5	chr7:104845047-104845306	NONHSAT122615
10	lnc-CDHR3-5	chr7:105182048-105182302	NONHSAT122624
11	lnc-MLL5-4	chr7:104830195-104830261	NONHSAT122612
12	lnc-PUS7-1	chr7:105170677-105170904	NONHSAT122623
13	lnc-MLL5-4	chr7:104829637-104829934	NONHSAT122612
14	lnc-PUS7-1	chr7:105171944-105171973	NONHSAT122623
15	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614

No data

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

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

Variant related genes	Relation type
ENSG00000271482	TF binding region
ENSG00000213361	TF binding region
ENSG00000223886	TF binding region
PUS7	TF binding region
ENSG00000270764	TF binding region
RINT1	TF binding region
RWDD4P1	TF binding region
RNU6-1322P	TF binding region
ENSG00000242154	TF binding region
SRPK2	TF binding region
ENSG00000271482	CpG island
ENSG00000213361	CpG island
ENSG00000223886	CpG island
PUS7	CpG island
ENSG00000270764	CpG island
RINT1	CpG island
RWDD4P1	CpG island
RNU6-1322P	CpG island
ENSG00000242154	CpG island
SRPK2	CpG island
ENSG00000172244	chromatin interactions
ENSG00000242154	chromatin interactions
ENSG00000231167	chromatin interactions
ENSG00000244490	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000223886	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000270764	chromatin interactions
ENSG00000233797	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000185055	chromatin interactions
ENSG00000230508	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000014123	chromatin interactions
ENSG00000271482	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000213361	chromatin interactions
ENSG00000272604	chromatin interactions

Extended variants
information (count: 14851 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:14851 , 50 per page) page: 1 2 3 4 5 6 7 ... 298

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10238507	chr7:104807207-104807208	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2214928	chr7:104807248-104807249	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs77352257	chr7:104807259-104807260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377180513	chr7:104807268-104807269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538395708	chr7:104807295-104807296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558498209	chr7:104807364-104807365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191965695	chr7:104807365-104807366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370553176	chr7:104807389-104807390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556421327	chr7:104807414-104807415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78681769	chr7:104807415-104807416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574334390	chr7:104807443-104807444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376597101	chr7:104807447-104807448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552963350	chr7:104807469-104807470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs55715849	chr7:104807494-104807495	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs532416551	chr7:104807505-104807506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541537955	chr7:104807524-104807525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142346494	chr7:104807540-104807541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183495374	chr7:104807613-104807614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575096280	chr7:104807691-104807692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554674551	chr7:104807704-104807705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs61159115	chr7:104807712-104807713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564116369	chr7:104807717-104807718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144805594	chr7:104807719-104807720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540133299	chr7:104807738-104807739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73715406	chr7:104807757-104807758	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529279200	chr7:104807778-104807779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201263517	chr7:104807855-104807856	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs562930765	chr7:104807860-104807861	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs375950727	chr7:104807861-104807862	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs201440842	chr7:104807875-104807876	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs143338018	chr7:104807882-104807883	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs531835080	chr7:104807970-104807971	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs148554622	chr7:104807984-104807985	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs571728301	chr7:104807987-104807988	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs534544954	chr7:104807988-104807989	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs547737325	chr7:104808069-104808070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112074718	chr7:104808096-104808097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188536120	chr7:104808126-104808127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542931773	chr7:104808136-104808137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555050985	chr7:104808154-104808155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369277901	chr7:104808205-104808206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs60714423	chr7:104808230-104808231	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545729167	chr7:104808243-104808244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537544509	chr7:104808258-104808259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557958932	chr7:104808300-104808301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577746655	chr7:104808333-104808334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540543082	chr7:104808336-104808337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573023425	chr7:104808377-104808378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143276009	chr7:104808386-104808387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs60505353	chr7:104808391-104808392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	22522925	CNVD
Myxofibrosarcoma	20639860	CNVD
Chordoma	21215367	CNVD
Pancreatic cancer	17952125	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:9286 , 50 per page) page: 1 2 3 4 5 6 7 ... 186

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104678000-104812200	Strong transcription	Dnd41	blood
2	chr7:104752800-104807400	Weak transcription	Fetal Brain Male	brain
3	chr7:104753800-104822000	Weak transcription	Small Intestine	intestine
4	chr7:104754400-104850400	Weak transcription	Fetal Kidney	kidney
5	chr7:104777200-104809800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:104778000-104807800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:104780000-104807400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:104780000-104818800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:104780200-104818800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:104782600-104814000	Weak transcription	Colonic Mucosa	Colon
11	chr7:104782800-104845600	Weak transcription	Spleen	Spleen
12	chr7:104784200-104810400	Weak transcription	NHLF	lung
13	chr7:104784400-104818800	Weak transcription	Colon Smooth Muscle	Colon
14	chr7:104786400-104812200	Weak transcription	Fetal Intestine Small	intestine
15	chr7:104787000-104808400	Weak transcription	HepG2	liver
16	chr7:104787000-104813800	Weak transcription	Right Atrium	heart
17	chr7:104787600-104813400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr7:104791000-104813800	Weak transcription	Pancreas	Pancrea
19	chr7:104793200-104809600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:104796000-104809200	Strong transcription	Primary T cells from cord blood	blood
21	chr7:104796000-104810200	Strong transcription	Fetal Thymus	thymus
22	chr7:104799800-104810000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr7:104799800-104810000	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr7:104799800-104811000	Weak transcription	Esophagus	oesophagus
25	chr7:104799800-104813800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr7:104800000-104809800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:104802000-104810800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr7:104802400-104810200	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr7:104802800-104809200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:104803200-104808400	Strong transcription	Primary hematopoietic stem cells	blood
31	chr7:104803200-104809000	Strong transcription	HSMM	muscle
32	chr7:104803200-104809600	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr7:104803200-104809600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr7:104803200-104809600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:104803200-104809800	Strong transcription	Primary B cells from peripheral blood	blood
36	chr7:104803200-104809800	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr7:104803400-104809600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:104803600-104808000	Strong transcription	Stomach Smooth Muscle	stomach
39	chr7:104803600-104809200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr7:104803600-104809600	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr7:104803800-104809000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr7:104803800-104809600	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr7:104803800-104809600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:104803800-104809800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:104803800-104810000	Strong transcription	Fetal Muscle Leg	muscle
46	chr7:104803800-104810200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr7:104804000-104808000	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr7:104804000-104808200	Strong transcription	Fetal Intestine Large	intestine
49	chr7:104804200-104807600	Strong transcription	Thymus	Thymus
50	chr7:104804200-104808000	Strong transcription	Rectal Mucosa Donor 29	rectum

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