Variant report

Variant	esv2758156
Chromosome Location	chr8:48788293-49008014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4399)
CpG islands
(count:2013)
Chromatin interactive
region (count:189)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:4399 , 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	chr8:48909052-48909241	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48954659-48955530	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48905475-48905861	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:48909809-48910128	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:48915966-48916230	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:48909808-48910086	K562	blood:	n/a	n/a
7	ARID3A	chr8:48895484-48895695	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:48986390-48986586	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:48920792-48921191	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:48872863-48873605	K562	blood:	n/a	chr8:48873270-48873278
11	ARID3A	chr8:48872565-48873634	HepG2	liver:	n/a	chr8:48873270-48873278
12	ARID3A	chr8:48987503-48987712	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:48989035-48989075	K562	blood:	n/a	n/a
14	ARID3A	chr8:48879708-48880140	HepG2	liver:	n/a	n/a
15	ATF1	chr8:48920761-48921122	K562	blood:	n/a	n/a
16	ATF1	chr8:48975614-48975808	K562	blood:	n/a	n/a
17	ATF1	chr8:48873182-48873558	K562	blood:	n/a	n/a
18	ATF1	chr8:48911599-48911799	K562	blood:	n/a	n/a
19	ATF2	chr8:48872630-48873618	GM12878	blood:	n/a	n/a
20	ATF2	chr8:48873078-48873648	GM12878	blood:	n/a	n/a
21	ATF2	chr8:48872229-48873077	GM12878	blood:	n/a	n/a
22	ATF2	chr8:48814692-48815306	GM12878	blood:	n/a	n/a
23	ATF2	chr8:48814851-48815342	GM12878	blood:	n/a	n/a
24	ATF2	chr8:48790878-48791451	GM12878	blood:	n/a	n/a
25	ATF2	chr8:48812278-48812924	GM12878	blood:	n/a	n/a
26	ATF2	chr8:48790887-48791278	GM12878	blood:	n/a	n/a
27	ATF2	chr8:48920689-48921069	GM12878	blood:	n/a	n/a
28	ATF2	chr8:48812173-48812889	GM12878	blood:	n/a	n/a
29	ATF2	chr8:48872671-48873661	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr8:48872659-48873677	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr8:48873139-48873694	A549	lung:	n/a	chr8:48873579-48873588
32	ATF3	chr8:48920846-48921194	A549	lung:	n/a	n/a
33	ATF3	chr8:48988882-48989250	K562	blood:	n/a	n/a
34	ATF3	chr8:48987856-48987995	K562	blood:	n/a	chr8:48987957-48987966
35	ATF3	chr8:48920715-48921150	K562	blood:	n/a	n/a
36	ATF3	chr8:48872471-48872782	K562	blood:	n/a	chr8:48872766-48872775
37	ATF3	chr8:48920796-48921148	A549	lung:	n/a	n/a
38	ATF3	chr8:48872460-48872962	A549	lung:	n/a	chr8:48872766-48872775
39	ATF3	chr8:48873076-48873396	A549	lung:	n/a	n/a
40	BACH1	chr8:48872877-48873374	K562	blood:	n/a	n/a
41	BACH1	chr8:48988916-48989245	K562	blood:	n/a	n/a
42	BACH1	chr8:48873138-48874173	H1-hESC	embryonic stem cell:	n/a	chr8:48873984-48873998
43	BACH1	chr8:48892735-48892903	K562	blood:	n/a	n/a
44	BACH1	chr8:48920856-48921088	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr8:48874797-48874813	K562	blood:	n/a	n/a
46	BACH1	chr8:48872546-48872866	H1-hESC	embryonic stem cell:	n/a	n/a
47	BATF	chr8:48793513-48793779	GM12878	blood:	n/a	n/a
48	BATF	chr8:48886372-48886721	GM12878	blood:	n/a	n/a
49	BATF	chr8:48790867-48791261	GM12878	blood:	n/a	n/a
50	BATF	chr8:48793523-48793761	GM12878	blood:	n/a	n/a

(count:2013 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48889520-48889570	T-47D	breast:	n/a
2	chr8:48826017-48826067	HMEC	breast:	n/a
3	chr8:48871883-48871933	NH-A	brain:	n/a
4	chr8:48921337-48921387	HCPEpiC	choroid plexus:	n/a
5	chr8:48872865-48872915	ProgFib	skin:	n/a
6	chr8:48921062-48921112	SAEC	small airway:	n/a
7	chr8:48873906-48873956	Jurkat	blood:	n/a
8	chr8:48889520-48889570	GM12892	blood:	n/a
9	chr8:48872822-48872872	PFSK-1	brain:	n/a
10	chr8:48920858-48920908	GM19239	blood:	n/a
11	chr8:48920838-48920888	HRE	kidney:	n/a
12	chr8:48871883-48871933	MCF-7	breast:	n/a
13	chr8:48877513-48877563	NB4	blood:	n/a
14	chr8:48920838-48920888	SK-N-SH_RA	brain:	n/a
15	chr8:48872822-48872872	HIPEpiC	eye:	n/a
16	chr8:48921554-48921604	BE2_C	brain:	n/a
17	chr8:48872865-48872915	GM12892	blood:	n/a
18	chr8:48986813-48986863	ovcar-3	ovarian:	n/a
19	chr8:48872865-48872915	ovcar-3	ovarian:	n/a
20	chr8:48869819-48869869	HMEC	breast:	n/a
21	chr8:48826017-48826067	MCF-7	breast:	n/a
22	chr8:48921062-48921112	Hepatocyte	liver:	n/a
23	chr8:48921062-48921112	CMK	blood:	n/a
24	chr8:48872865-48872915	GM19239	blood:	n/a
25	chr8:48973636-48973686	ProgFib	skin:	n/a
26	chr8:48889520-48889570	SAEC	small airway:	n/a
27	chr8:48877513-48877563	HepG2	liver:	n/a
28	chr8:48872822-48872872	HepG2	liver:	n/a
29	chr8:48920818-48920868	HepG2	liver:	n/a
30	chr8:48920838-48920888	Hepatocyte	liver:	n/a
31	chr8:48910778-48910828	GM12891	blood:	n/a
32	chr8:48920460-48920510	PFSK-1	brain:	n/a
33	chr8:48920858-48920908	LNCaP	prostate:	n/a
34	chr8:48986813-48986863	NB4	blood:	n/a
35	chr8:48872801-48872851	AG09309	skin:	n/a
36	chr8:48869819-48869869	NHDF-neo	bronchial:	n/a
37	chr8:48873951-48874001	ProgFib	skin:	n/a
38	chr8:48910636-48910686	BJ	skin:	n/a
39	chr8:48920818-48920868	NB4	blood:	n/a
40	chr8:48873190-48873240	SAEC	small airway:	n/a
41	chr8:48973636-48973686	K562	blood:	n/a
42	chr8:48873533-48873583	BE2_C	brain:	n/a
43	chr8:48921062-48921112	NHBE	bronchial:	n/a
44	chr8:48872865-48872915	MCF10A-Er-Src	breast:	n/a
45	chr8:48921337-48921387	AG10803	skin:	n/a
46	chr8:48920460-48920510	HRPEpiC	eye:	n/a
47	chr8:48872822-48872872	GM19239	blood:	n/a
48	chr8:48920838-48920888	HAEpiC	amniotic membrane:	n/a
49	chr8:48854968-48855018	SK-N-MC	brain:	n/a
50	chr8:48920761-48920811	T-47D	breast:	n/a

(count:189 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:48870843..48877121-chr8:48919292..48922738,10	K562	blood:
2	chr8:48787397..48789499-chr8:48791391..48793520,2	K562	blood:
3	chr8:48872949..48874764-chr8:48927442..48928965,2	K562	blood:
4	chr8:48870802..48875414-chr8:48919446..48923770,8	MCF-7	breast:
5	chr8:48898201..48900058-chr8:48903051..48905001,2	K562	blood:
6	chr8:48795937..48796818-chr8:49837936..49838689,2	MCF-7	breast:
7	chr8:48800554..48803077-chr8:48803975..48806027,3	K562	blood:
8	chr8:48871246..48875685-chr8:48919504..48923066,10	K562	blood:
9	chr8:48938195..48942344-chr8:48943305..48947689,4	K562	blood:
10	chr8:48787397..48789499-chr8:48791391..48793520,2	K562	blood:
11	chr8:48898201..48900058-chr8:48903051..48905001,2	K562	blood:
12	chr8:48871178..48874087-chr8:48899526..48903049,3	MCF-7	breast:
13	chr8:48915545..48918522-chr8:48918892..48921377,2	MCF-7	breast:
14	chr8:48872462..48875163-chr8:48911695..48914343,2	K562	blood:
15	chr8:48853605..48856725-chr8:48865845..48868250,3	MCF-7	breast:
16	chr8:48871644..48875335-chr8:48903503..48906313,3	MCF-7	breast:
17	chr8:48843317..48847035-chr8:48871031..48874795,6	K562	blood:
18	chr8:48909845..48912339-chr8:48920798..48922536,2	MCF-7	breast:
19	chr8:48848253..48849969-chr8:48851774..48853317,2	MCF-7	breast:
20	chr8:48870534..48872766-chr8:48885611..48888462,2	MCF-7	breast:
21	chr8:48851587..48857130-chr8:48871349..48874968,8	MCF-7	breast:
22	chr8:48869692..48871263-chr8:48950585..48953419,2	MCF-7	breast:
23	chr8:48878378..48881135-chr8:48887828..48890847,3	MCF-7	breast:
24	chr8:48849661..48851317-chr8:48858106..48860426,2	K562	blood:
25	chr21:40176802..40177797-chr8:48872778..48873309,2	Hela-S3	cervix:
26	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
27	chr8:48871629..48874079-chr8:48980802..48983659,2	MCF-7	breast:
28	chr8:48846197..48849935-chr8:48851023..48856886,6	K562	blood:
29	chr8:48803324..48804836-chr8:48807142..48809364,2	K562	blood:
30	chr8:48949897..48951407-chr8:48952676..48954247,2	MCF-7	breast:
31	chr8:48818457..48820091-chr8:48825193..48827901,2	MCF-7	breast:
32	chr15:66797411..66797929-chr8:48872333..48873322,2	Hela-S3	cervix:
33	chr8:48852381..48854358-chr8:48859418..48862066,2	MCF-7	breast:
34	chr8:48924342..48926810-chr8:48928221..48931397,3	K562	blood:
35	chr8:48869236..48871124-chr8:48909959..48911972,2	K562	blood:
36	chr8:48830577..48833973-chr8:48871114..48874120,3	MCF-7	breast:
37	chr1:28974788..28975451-chr8:48920936..48921691,2	Hela-S3	cervix:
38	chr8:48871080..48872628-chr8:48898193..48900084,2	K562	blood:
39	chr8:48919638..48923031-chr8:48924229..48928095,7	MCF-7	breast:
40	chr8:48824273..48826627-chr8:48840417..48843621,4	K562	blood:
41	chr8:48799441..48801272-chr8:48808121..48809759,2	K562	blood:
42	chr8:48836211..48838209-chr8:48842073..48843953,2	MCF-7	breast:
43	chr8:48886822..48888941-chr8:48919839..48922442,3	MCF-7	breast:
44	chr8:48907169..48911737-chr8:48918914..48922421,4	K562	blood:
45	chr8:48881714..48884143-chr8:48924954..48927887,2	MCF-7	breast:
46	chr8:48858446..48860800-chr8:48864491..48866014,2	K562	blood:
47	chr8:48924792..48926393-chr8:48927338..48929721,2	K562	blood:
48	chr8:48839901..48842172-chr8:48844421..48847174,2	K562	blood:
49	chr11:75273252..75273856-chr8:48873481..48874356,2	NB4	blood:
50	chr8:48869692..48871263-chr8:48950585..48953419,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCM4-1	chr8:48855141-48855324	NONHSAT126462
2	lnc-MCM4-1	chr8:48857309-48857338	NONHSAT126462
3	lnc-MCM4-2	chr8:48854790-48855069	NONHSAT126461
4	lnc-MCM4-2	chr8:48854048-48854246	NONHSAT126461

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MCM4	hsa-miR-183-5p	chr8:48889872-48889892
2	MCM4	hsa-miR-24-3p	chr8:48875505-48875525
3	MCM4	hsa-miR-24-3p	chr8:48875419-48875419

Variant related genes	Relation type
PRKDC	TF binding region
MCM4	TF binding region
ENSG00000211562	TF binding region
UBE2V2	TF binding region
RNU6-519P	TF binding region
PRKDC	CpG island
MCM4	CpG island
ENSG00000211562	CpG island
UBE2V2	CpG island
RNU6-519P	CpG island
ENSG00000270103	chromatin interactions
ENSG00000101213	chromatin interactions
ENSG00000075303	chromatin interactions
ENSG00000222522	chromatin interactions
ENSG00000143633	chromatin interactions
ENSG00000174442	chromatin interactions
ENSG00000253729	chromatin interactions
ENSG00000245534	chromatin interactions
ENSG00000006634	chromatin interactions
ENSG00000169139	chromatin interactions
ENSG00000211562	chromatin interactions
ENSG00000128915	chromatin interactions
ENSG00000104738	chromatin interactions
ENSG00000157557	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000131408	chromatin interactions

Extended variants
information (count: 8162 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:8162 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558603842	chr8:48788319-48788320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577179176	chr8:48788330-48788331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570639596	chr8:48788367-48788368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186290767	chr8:48788394-48788395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565363213	chr8:48788400-48788401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151306159	chr8:48788447-48788448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369064107	chr8:48788465-48788466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529886492	chr8:48788490-48788491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560776056	chr8:48788493-48788494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539975052	chr8:48788502-48788503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560336180	chr8:48788549-48788550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527789194	chr8:48788582-48788583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552118511	chr8:48788653-48788654	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570541034	chr8:48788714-48788715	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531868892	chr8:48788725-48788726	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550249402	chr8:48788788-48788789	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568637346	chr8:48788815-48788816	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535630439	chr8:48788829-48788830	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531457570	chr8:48788854-48788855	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566413447	chr8:48788891-48788892	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533893330	chr8:48788892-48788893	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558563624	chr8:48788893-48788894	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576946912	chr8:48788910-48788911	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544507614	chr8:48788935-48788936	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556229713	chr8:48788948-48788949	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190785741	chr8:48788963-48788964	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139375596	chr8:48788979-48788980	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541619850	chr8:48788981-48788982	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183974709	chr8:48788991-48788992	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572185660	chr8:48789005-48789006	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545928270	chr8:48789020-48789021	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150058905	chr8:48789048-48789049	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186917630	chr8:48789078-48789079	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191801558	chr8:48789091-48789092	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536628847	chr8:48789104-48789105	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs367731273	chr8:48789126-48789127	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562206189	chr8:48789163-48789164	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77871023	chr8:48789178-48789179	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373481753	chr8:48789184-48789185	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529609501	chr8:48789198-48789199	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183224487	chr8:48789209-48789210	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570005149	chr8:48789248-48789249	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533853975	chr8:48789258-48789259	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114476398	chr8:48789266-48789267	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556844432	chr8:48789268-48789269	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147757499	chr8:48789312-48789313	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372719713	chr8:48789357-48789358	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556132501	chr8:48789382-48789383	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574610599	chr8:48789412-48789413	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535851677	chr8:48789452-48789453	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
22q11 deletion syndrome	20357662	CNVD
Autism	20531469	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Ovarian cancer	21781307	CNVD
Renal cell carcinoma	21215367	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5353 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48684400-48861600	Strong transcription	Dnd41	blood
2	chr8:48685000-48818800	Strong transcription	Fetal Thymus	thymus
3	chr8:48722600-48798800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr8:48723000-48793400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:48726200-48793400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr8:48726400-48870400	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr8:48730000-48871600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:48738400-48818800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr8:48739600-48793400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr8:48739600-48799400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:48739600-48822200	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr8:48739600-48870600	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr8:48739800-48793400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
14	chr8:48739800-48870400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr8:48751400-48805800	Strong transcription	Fetal Lung	lung
16	chr8:48756600-48793400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:48758200-48799600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:48759800-48808400	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr8:48761000-48793400	Strong transcription	Primary B cells from cord blood	blood
20	chr8:48775200-48796000	Weak transcription	Small Intestine	intestine
21	chr8:48775400-48788600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:48775400-48800200	Weak transcription	Stomach Mucosa	stomach
23	chr8:48775600-48791400	Weak transcription	Fetal Heart	heart
24	chr8:48776800-48797200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr8:48777200-48788400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr8:48777200-48788600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr8:48777200-48789400	Weak transcription	Brain Substantia Nigra	brain
28	chr8:48777200-48790800	Weak transcription	Psoas Muscle	Psoas
29	chr8:48777200-48791000	Weak transcription	HSMMtube	muscle
30	chr8:48777400-48788600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr8:48778600-48793400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr8:48778600-48838200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr8:48778800-48795800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:48778800-48808200	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr8:48778800-48818200	Strong transcription	H1 Cell Line	embryonic stem cell
36	chr8:48778800-48818800	Strong transcription	Duodenum Mucosa	Duodenum
37	chr8:48779400-48808200	Strong transcription	Primary B cells from peripheral blood	blood
38	chr8:48779400-48815800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:48779600-48793400	Strong transcription	Fetal Intestine Large	intestine
40	chr8:48779800-48822200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:48780000-48822800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:48781600-48788400	Weak transcription	NHDF-Ad	bronchial
43	chr8:48782800-48790800	Weak transcription	Spleen	Spleen
44	chr8:48782800-48793400	Weak transcription	Gastric	stomach
45	chr8:48782800-48794800	Weak transcription	Right Ventricle	heart
46	chr8:48782800-48832200	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr8:48783000-48789400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr8:48783000-48789400	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr8:48783000-48794800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:48783000-48794800	Weak transcription	Esophagus	oesophagus

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