Variant report

Variant	esv1794084
Chromosome Location	chr16:47478207-47676184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2361)
CpG islands
(count:1100)
Chromatin interactive
region (count:157)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2361 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47615141-47615378	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:47526816-47527197	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:47524403-47524722	K562	blood:	n/a	n/a
4	ARID3A	chr16:47556945-47557537	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47519386-47519410	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:47554148-47554743	K562	blood:	n/a	n/a
7	ARID3A	chr16:47498536-47498645	K562	blood:	n/a	n/a
8	ARID3A	chr16:47482890-47483076	K562	blood:	n/a	n/a
9	ARID3A	chr16:47500293-47502483	K562	blood:	n/a	n/a
10	ARID3A	chr16:47538556-47538932	K562	blood:	n/a	n/a
11	ARID3A	chr16:47533067-47533932	HepG2	liver:	n/a	n/a
12	ARID3A	chr16:47507738-47508382	HepG2	liver:	n/a	n/a
13	ARID3A	chr16:47499795-47500033	K562	blood:	n/a	n/a
14	ARID3A	chr16:47658634-47659953	K562	blood:	n/a	n/a
15	ARID3A	chr16:47526802-47527555	K562	blood:	n/a	n/a
16	ARID3A	chr16:47495283-47496261	K562	blood:	n/a	n/a
17	ARID3A	chr16:47612461-47612663	K562	blood:	n/a	n/a
18	ARID3A	chr16:47494825-47496228	HepG2	liver:	n/a	n/a
19	ARID3A	chr16:47507313-47507485	HepG2	liver:	n/a	n/a
20	ARID3A	chr16:47509336-47510111	HepG2	liver:	n/a	n/a
21	ARID3A	chr16:47572269-47572803	HepG2	liver:	n/a	n/a
22	ARID3A	chr16:47484519-47484647	HepG2	liver:	n/a	n/a
23	ARID3A	chr16:47667679-47668530	HepG2	liver:	n/a	n/a
24	ATF1	chr16:47501985-47502361	K562	blood:	n/a	n/a
25	ATF1	chr16:47599472-47599607	K562	blood:	n/a	n/a
26	ATF1	chr16:47554214-47554593	K562	blood:	n/a	n/a
27	ATF1	chr16:47495611-47496214	K562	blood:	n/a	n/a
28	ATF1	chr16:47658917-47659475	K562	blood:	n/a	n/a
29	ATF1	chr16:47526819-47527180	K562	blood:	n/a	n/a
30	ATF1	chr16:47626832-47626837	K562	blood:	n/a	n/a
31	ATF2	chr16:47608501-47609078	GM12878	blood:	n/a	n/a
32	ATF2	chr16:47526273-47527368	GM12878	blood:	n/a	n/a
33	ATF2	chr16:47557169-47557724	GM12878	blood:	n/a	n/a
34	ATF3	chr16:47494617-47495423	HepG2	liver:	n/a	n/a
35	ATF3	chr16:47494783-47495259	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF3	chr16:47494797-47495311	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF3	chr16:47494755-47495369	HepG2	liver:	n/a	n/a
38	ATF3	chr16:47501997-47502334	K562	blood:	n/a	n/a
39	ATF3	chr16:47494801-47495349	K562	blood:	n/a	n/a
40	ATF3	chr16:47494735-47495286	K562	blood:	n/a	n/a
41	ATF3	chr16:47494883-47495224	GM12878	blood:	n/a	n/a
42	ATF3	chr16:47494770-47495381	GM12878	blood:	n/a	n/a
43	BACH1	chr16:47495724-47496205	K562	blood:	n/a	n/a
44	BACH1	chr16:47538552-47539389	K562	blood:	n/a	n/a
45	BACH1	chr16:47495280-47495285	K562	blood:	n/a	n/a
46	BACH1	chr16:47502025-47502424	K562	blood:	n/a	n/a
47	BACH1	chr16:47651620-47652054	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr16:47502056-47502356	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr16:47495881-47496208	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr16:47578156-47578439	GM12878	blood:	n/a	chr16:47578328-47578339

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47539203-47539253	HRE	kidney:	n/a
2	chr16:47494824-47494874	A549	lung:	n/a
3	chr16:47539203-47539253	HRE	kidney:	n/a
4	chr16:47494824-47494874	A549	lung:	n/a
5	chr16:47495445-47495495	AG04449	skin:	fetal
6	chr16:47495541-47495591	ovcar-3	ovarian:	n/a
7	chr16:47495110-47495160	HCPEpiC	choroid plexus:	n/a
8	chr16:47527034-47527084	PANC-1	pancreas:	n/a
9	chr16:47494711-47494761	GM19239	blood:	n/a
10	chr16:47588660-47588710	AG10803	skin:	n/a
11	chr16:47492286-47492336	SAEC	small airway:	n/a
12	chr16:47494258-47494308	LNCaP	prostate:	n/a
13	chr16:47495541-47495591	AG04449	skin:	fetal
14	chr16:47539137-47539187	HAEpiC	amniotic membrane:	n/a
15	chr16:47539137-47539187	SK-N-SH	brain:	n/a
16	chr16:47495113-47495163	ovcar-3	ovarian:	n/a
17	chr16:47495746-47495796	HEEpiC	esophagus:	n/a
18	chr16:47527034-47527084	SK-N-MC	brain:	n/a
19	chr16:47495110-47495160	AG10803	skin:	n/a
20	chr16:47495113-47495163	HCPEpiC	choroid plexus:	n/a
21	chr16:47539166-47539216	HRE	kidney:	n/a
22	chr16:47539137-47539187	HepG2	liver:	n/a
23	chr16:47495541-47495591	HNPCEpiC	eye:	n/a
24	chr16:47497822-47497872	SKMC	muscle:	n/a
25	chr16:47497822-47497872	K562	blood:	n/a
26	chr16:47539137-47539187	HL-60	blood:	n/a
27	chr16:47494258-47494308	Jurkat	blood:	n/a
28	chr16:47492286-47492336	CMK	blood:	n/a
29	chr16:47588660-47588710	ProgFib	skin:	n/a
30	chr16:47494258-47494308	NHDF-neo	bronchial:	n/a
31	chr16:47539166-47539216	NH-A	brain:	n/a
32	chr16:47495541-47495591	SK-N-SH	brain:	n/a
33	chr16:47588660-47588710	MCF10A-Er-Src	breast:	n/a
34	chr16:47494711-47494761	GM12878	blood:	n/a
35	chr16:47495113-47495163	HPAEpiC	pulmonary alveolar:	n/a
36	chr16:47527034-47527084	HIPEpiC	eye:	n/a
37	chr16:47494711-47494761	NT2-D1	testis:	n/a
38	chr16:47588660-47588710	HMEC	breast:	n/a
39	chr16:47492286-47492336	HRCEpiC	kidney:	n/a
40	chr16:47495746-47495796	HRPEpiC	eye:	n/a
41	chr16:47539137-47539187	GM12878	blood:	n/a
42	chr16:47495746-47495796	AG04450	lung:	fetal
43	chr16:47495541-47495591	NHDF-neo	bronchial:	n/a
44	chr16:47539137-47539187	NT2-D1	testis:	n/a
45	chr16:47494711-47494761	GM12891	blood:	n/a
46	chr16:47495541-47495591	SK-N-SH_RA	brain:	n/a
47	chr16:47494824-47494874	SK-N-MC	brain:	n/a
48	chr16:47494258-47494308	Hela-S3	cervix:	n/a
49	chr16:47495541-47495591	H1-hESC	embryonic stem cell:	embryo
50	chr16:47495746-47495796	IMR90	lung:	fetal

(count:157 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
2	chr16:47490166..47492489-chr16:47495627..47497742,2	MCF-7	breast:
3	chr16:47500719..47503610-chr16:47510639..47513571,4	K562	blood:
4	chr16:47542191..47545156-chr16:47546024..47549181,3	K562	blood:
5	chr16:47646276..47649578-chr16:47653598..47656458,3	K562	blood:
6	chr16:47506877..47508389-chr16:47511649..47513909,2	K562	blood:
7	chr16:47668276..47670957-chr16:47675128..47677879,2	K562	blood:
8	chr16:47638901..47640593-chr16:47647628..47649175,2	K562	blood:
9	chr16:47484770..47486422-chr16:47488487..47490664,2	K562	blood:
10	chr16:47165353..47167030-chr16:47501273..47503652,2	K562	blood:
11	chr16:47517170..47520211-chr16:47526974..47528925,3	K562	blood:
12	chr16:47416227..47418087-chr16:47500282..47502102,2	K562	blood:
13	chr16:47489451..47492163-chr16:47492304..47496167,3	K562	blood:
14	chr16:47495762..47498105-chr16:47514546..47516108,2	K562	blood:
15	chr16:47673393..47675073-chr16:47721240..47723950,2	K562	blood:
16	chr16:47512020..47514843-chr16:47517675..47520024,2	K562	blood:
17	chr16:47315203..47316940-chr16:47529898..47531487,2	K562	blood:
18	chr16:47594118..47597140-chr16:47598345..47602068,5	K562	blood:
19	chr16:47560964..47562749-chr16:47565268..47567477,2	K562	blood:
20	chr16:47487581..47489813-chr16:47498979..47501357,2	K562	blood:
21	chr16:47538624..47539255-chr19:24184251..24185320,3	MCF-7	breast:
22	chr16:47500040..47503767-chr16:47514818..47518136,4	K562	blood:
23	chr16:47500719..47503610-chr16:47510639..47513571,4	K562	blood:
24	chr16:47493569..47497883-chr16:47557067..47559084,4	K562	blood:
25	chr16:47657682..47661918-chr16:47662510..47665105,4	K562	blood:
26	chr16:47538686..47539206-chr5:50081215..50081735,2	MCF-7	breast:
27	chr16:47514982..47517180-chr16:47517561..47520425,2	MCF-7	breast:
28	chr16:47541164..47545156-chr16:47546024..47549793,5	K562	blood:
29	chr16:47491892..47494084-chr16:47494205..47496711,2	MCF-7	breast:
30	chr16:47657682..47661918-chr16:47662510..47665105,4	K562	blood:
31	chr16:47521997..47524877-chr16:47525537..47527944,2	K562	blood:
32	chr16:47525470..47528929-chr16:47529310..47531688,3	K562	blood:
33	chr16:47480331..47482328-chr16:47492246..47495576,3	MCF-7	breast:
34	chr16:47560964..47562749-chr16:47565268..47567477,2	K562	blood:
35	chr16:47671896..47674537-chr16:47675667..47678409,3	K562	blood:
36	chr16:47652198..47653880-chr16:47657938..47660462,2	K562	blood:
37	chr16:47505221..47508195-chr16:47519032..47520673,2	K562	blood:
38	chr16:47527728..47529779-chr16:47631706..47633843,2	K562	blood:
39	chr16:47535504..47537200-chr16:47537688..47539463,2	K562	blood:
40	chr16:47177492..47179325-chr16:47500185..47502883,2	K562	blood:
41	chr16:47502629..47504464-chr16:47550187..47553009,2	K562	blood:
42	chr16:47607769..47610118-chr16:47633916..47636393,2	K562	blood:
43	chr16:47541164..47545156-chr16:47546024..47549793,5	K562	blood:
44	chr16:47504741..47507121-chr16:47699160..47701122,2	K562	blood:
45	chr16:47497589..47499344-chr8:19675035..19676685,2	K562	blood:
46	chr16:47652198..47653880-chr16:47657938..47660462,2	K562	blood:
47	chr16:47648657..47650524-chr16:47658477..47661384,2	K562	blood:
48	chr16:47542191..47545156-chr16:47546024..47549181,3	K562	blood:
49	chr16:47502808..47504633-chr16:47527127..47529319,2	K562	blood:
50	chr16:47502099..47504584-chr16:47526951..47528627,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPT2-4	chr16:47563101-47563152	NONHSAT142298
2	lnc-GPT2-12	chr16:47495240-47495337	NONHSAT142295
3	lnc-GPT2-4	chr16:47563101-47563152	ENSG00000262038.1
4	lnc-ITFG1-3	chr16:47652232-47652439	uc_396_-
5	lnc-LONP2-12	chr16:47652232-47652439	uc_396_+
6	lnc-GPT2-4	chr16:47563386-47563827	NONHSAT142298
7	lnc-ITFG1-2	chr16:47632565-47632907	NONHSAT142302
8	lnc-GPT2-4	chr16:47563387-47563827	ENSG00000262038.1
9	lnc-ITFG1-1	chr16:47595218-47596391	NONHSAT142300
10	lnc-GPT2-12	chr16:47497009-47497433	NONHSAT142295

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ITFG1	hsa-miR-23b-3p	chr16:47484216-47484236

Variant related genes	Relation type
ENSG00000262038	TF binding region
NDUFA5P11	TF binding region
ENSG00000259866	TF binding region
EIF4BP5	TF binding region
RNA5SP424	TF binding region
PHKB	TF binding region
ITFG1	TF binding region
RNA5SP425	TF binding region
ENSG00000262038	CpG island
NDUFA5P11	CpG island
ENSG00000259866	CpG island
EIF4BP5	CpG island
RNA5SP424	CpG island
PHKB	CpG island
ITFG1	CpG island
RNA5SP425	CpG island
ENSG00000222268	chromatin interactions
ENSG00000212290	chromatin interactions
ENSG00000259866	chromatin interactions
ENSG00000104613	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000102893	chromatin interactions
ENSG00000260281	chromatin interactions
ENSG00000171208	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000133703	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000261336	chromatin interactions
ENSG00000259918	chromatin interactions
ENSG00000162664	chromatin interactions
ENSG00000152147	chromatin interactions

Extended variants
information (count: 6295 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6295 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28404995	chr16:47478207-47478208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540200082	chr16:47478218-47478219	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs151069532	chr16:47478220-47478221	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs538532917	chr16:47478235-47478236	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142385653	chr16:47478241-47478242	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs575089252	chr16:47478258-47478259	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561915730	chr16:47478275-47478276	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs536030013	chr16:47478295-47478296	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs34545360	chr16:47478305-47478306	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540736310	chr16:47478320-47478321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572487669	chr16:47478333-47478334	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs545904732	chr16:47478357-47478358	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs564502040	chr16:47478381-47478382	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs9932230	chr16:47478473-47478474	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs146372731	chr16:47478476-47478477	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs561599210	chr16:47478482-47478483	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548182796	chr16:47478500-47478501	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs547153239	chr16:47478514-47478515	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559215766	chr16:47478525-47478526	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs533045531	chr16:47478612-47478613	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs139077811	chr16:47478644-47478645	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551132872	chr16:47478695-47478696	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142992491	chr16:47478713-47478714	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537001662	chr16:47478738-47478739	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563537035	chr16:47478751-47478752	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs113582839	chr16:47478760-47478761	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs552985866	chr16:47478772-47478773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs150173591	chr16:47478791-47478792	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536092418	chr16:47478800-47478801	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74016208	chr16:47478859-47478860	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149301630	chr16:47478863-47478864	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs57884999	chr16:47478931-47478932	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs371450669	chr16:47478935-47478936	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs186290836	chr16:47478946-47478947	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144532505	chr16:47478963-47478964	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs71380992	chr16:47478981-47478982	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs137937493	chr16:47478994-47478995	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540396640	chr16:47479023-47479024	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201350519	chr16:47479029-47479030	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs573581684	chr16:47479031-47479032	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs61015312	chr16:47479037-47479038	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12918561	chr16:47479039-47479040	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs540876870	chr16:47479093-47479094	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs191046166	chr16:47479100-47479101	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs183661049	chr16:47479143-47479144	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545094284	chr16:47479197-47479198	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs563209805	chr16:47479202-47479203	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376147469	chr16:47479235-47479236	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562889599	chr16:47479286-47479287	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs368461755	chr16:47479294-47479295	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	22341455	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5456 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47426400-47482800	Weak transcription	NH-A	brain
2	chr16:47430400-47485600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr16:47442600-47483800	Weak transcription	Hela-S3	cervix
4	chr16:47445400-47482600	Weak transcription	NHEK	skin
5	chr16:47445800-47483800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr16:47451600-47484000	Weak transcription	Small Intestine	intestine
7	chr16:47459200-47493400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr16:47459400-47484000	Weak transcription	Pancreas	Pancrea
9	chr16:47459400-47487200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr16:47459400-47493800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr16:47459600-47487200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr16:47459600-47493400	Weak transcription	Esophagus	oesophagus
13	chr16:47459800-47484600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr16:47459800-47484800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr16:47459800-47493400	Weak transcription	Right Ventricle	heart
16	chr16:47459800-47494400	Weak transcription	Aorta	Aorta
17	chr16:47460000-47485400	Weak transcription	HSMMtube	muscle
18	chr16:47460200-47479600	Weak transcription	Ovary	ovary
19	chr16:47460200-47482600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr16:47460200-47482800	Weak transcription	Brain Germinal Matrix	brain
21	chr16:47460200-47483800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr16:47460200-47485600	Weak transcription	Colonic Mucosa	Colon
23	chr16:47460200-47485600	Weak transcription	NHLF	lung
24	chr16:47460200-47486800	Weak transcription	Fetal Kidney	kidney
25	chr16:47460400-47479400	Weak transcription	HepG2	liver
26	chr16:47460400-47483400	Weak transcription	Fetal Brain Male	brain
27	chr16:47461400-47482800	Weak transcription	A549	lung
28	chr16:47461600-47485600	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr16:47461800-47485400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr16:47462000-47479400	Weak transcription	Fetal Intestine Large	intestine
31	chr16:47462000-47479600	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr16:47462000-47479600	Weak transcription	Adipose Nuclei	Adipose
33	chr16:47462000-47479600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr16:47462000-47479800	Weak transcription	Brain Hippocampus Middle	brain
35	chr16:47462000-47480400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr16:47462000-47482600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr16:47462000-47482600	Weak transcription	Fetal Lung	lung
38	chr16:47462000-47482800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr16:47462000-47482800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr16:47462000-47482800	Weak transcription	Osteobl	bone
41	chr16:47462000-47483000	Weak transcription	Fetal Muscle Leg	muscle
42	chr16:47462000-47483800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr16:47462000-47484000	Weak transcription	Thymus	Thymus
44	chr16:47462000-47484200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr16:47462000-47485600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr16:47462000-47486800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr16:47462000-47493400	Weak transcription	Gastric	stomach
48	chr16:47462000-47493400	Weak transcription	Spleen	Spleen
49	chr16:47462200-47479400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr16:47462200-47479600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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