Variant report

Variant	esv20058
Chromosome Location	chr16:70145134-70285081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2867)
CpG islands
(count:1405)
Chromatin interactive
region (count:39)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2867 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70186462-70187162	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:70191181-70192253	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:70199076-70199303	K562	blood:	n/a	n/a
4	ARID3A	chr16:70195992-70196417	HepG2	liver:	n/a	n/a
5	ATF1	chr16:70147951-70148282	K562	blood:	n/a	chr16:70148098-70148112
6	ATF1	chr16:70195925-70196369	K562	blood:	n/a	n/a
7	ATF1	chr16:70199108-70199250	K562	blood:	n/a	n/a
8	ATF3	chr16:70285052-70285235	K562	blood:	n/a	n/a
9	ATF3	chr16:70148048-70148187	GM12878	blood:	n/a	chr16:70148090-70148110 chr16:70148074-70148094
10	ATF3	chr16:70147960-70148270	K562	blood:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
11	ATF3	chr16:70147959-70148367	HepG2	liver:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
12	ATF3	chr16:70147973-70148328	H1-hESC	embryonic stem cell:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
13	ATF3	chr16:70147962-70148260	HepG2	liver:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
14	ATF3	chr16:70147950-70148330	GM12878	blood:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
15	BACH1	chr16:70147926-70148170	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr16:70190168-70190514	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr16:70269196-70269455	GM12878	blood:	n/a	n/a
18	BATF	chr16:70266179-70266523	GM12878	blood:	n/a	n/a
19	BATF	chr16:70272645-70272986	GM12878	blood:	n/a	n/a
20	BATF	chr16:70274531-70275234	GM12878	blood:	n/a	n/a
21	BATF	chr16:70148023-70148328	GM12878	blood:	n/a	n/a
22	BATF	chr16:70249268-70249471	GM12878	blood:	n/a	n/a
23	BATF	chr16:70199070-70199298	GM12878	blood:	n/a	n/a
24	BATF	chr16:70251010-70251261	GM12878	blood:	n/a	n/a
25	BATF	chr16:70277954-70278184	GM12878	blood:	n/a	n/a
26	BATF	chr16:70269207-70269408	GM12878	blood:	n/a	n/a
27	BATF	chr16:70275330-70275612	GM12878	blood:	n/a	n/a
28	BATF	chr16:70265769-70265977	GM12878	blood:	n/a	n/a
29	BATF	chr16:70266143-70266490	GM12878	blood:	n/a	n/a
30	BATF	chr16:70259711-70260057	GM12878	blood:	n/a	n/a
31	BATF	chr16:70275352-70275629	GM12878	blood:	n/a	n/a
32	BATF	chr16:70274761-70275229	GM12878	blood:	n/a	n/a
33	BATF	chr16:70270340-70270551	GM12878	blood:	n/a	n/a
34	BATF	chr16:70272693-70272978	GM12878	blood:	n/a	n/a
35	BATF	chr16:70242991-70243230	GM12878	blood:	n/a	n/a
36	BATF	chr16:70252521-70252845	GM12878	blood:	n/a	chr16:70252736-70252746
37	BATF	chr16:70243288-70243494	GM12878	blood:	n/a	n/a
38	BATF	chr16:70251089-70251362	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:70247717-70247954	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:70274796-70275305	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:70267253-70267439	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:70274544-70275641	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:70274569-70274791	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:70256901-70257158	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:70260079-70260328	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:70266040-70266508	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:70252607-70252876	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:70252674-70252910	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:70272603-70273149	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:70265235-70265407	GM12878	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70190513-70190563	MCF-7	breast:	n/a
2	chr16:70190398-70190448	ECC-1	luminal epithelium:	n/a
3	chr16:70190513-70190563	MCF-7	breast:	n/a
4	chr16:70190398-70190448	ECC-1	luminal epithelium:	n/a
5	chr16:70190513-70190563	CMK	blood:	n/a
6	chr16:70193705-70193755	AG04449	skin:	fetal
7	chr16:70284893-70284943	MCF10A-Er-Src	breast:	n/a
8	chr16:70145696-70145746	GM19239	blood:	n/a
9	chr16:70284928-70284978	HRCEpiC	kidney:	n/a
10	chr16:70148758-70148808	HIPEpiC	eye:	n/a
11	chr16:70259186-70259236	AG09309	skin:	n/a
12	chr16:70148511-70148561	Jurkat	blood:	n/a
13	chr16:70283421-70283471	NH-A	brain:	n/a
14	chr16:70259186-70259236	SKMC	muscle:	n/a
15	chr16:70207304-70207354	HCPEpiC	choroid plexus:	n/a
16	chr16:70207297-70207347	NT2-D1	testis:	n/a
17	chr16:70283421-70283471	SK-N-SH_RA	brain:	n/a
18	chr16:70207801-70207851	PANC-1	pancreas:	n/a
19	chr16:70226235-70226285	GM12891	blood:	n/a
20	chr16:70284893-70284943	GM12892	blood:	n/a
21	chr16:70220191-70220241	Hela-S3	cervix:	n/a
22	chr16:70207304-70207354	LNCaP	prostate:	n/a
23	chr16:70207297-70207347	H1-hESC	embryonic stem cell:	embryo
24	chr16:70196247-70196297	GM12891	blood:	n/a
25	chr16:70220191-70220241	HUVEC	blood vessel:	n/a
26	chr16:70283421-70283471	GM12891	blood:	n/a
27	chr16:70196247-70196297	HCF	heart:	n/a
28	chr16:70147964-70148014	HRCEpiC	kidney:	n/a
29	chr16:70147964-70148014	MCF-7	breast:	n/a
30	chr16:70148795-70148845	HNPCEpiC	eye:	n/a
31	chr16:70284928-70284978	HCT-116	colon:	n/a
32	chr16:70190329-70190379	AoSMC	blood vessel:	n/a
33	chr16:70207722-70207772	SAEC	small airway:	n/a
34	chr16:70259186-70259236	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:70145696-70145746	SKMC	muscle:	n/a
36	chr16:70284928-70284978	ProgFib	skin:	n/a
37	chr16:70226235-70226285	HRE	kidney:	n/a
38	chr16:70207304-70207354	Hela-S3	cervix:	n/a
39	chr16:70220191-70220241	NB4	blood:	n/a
40	chr16:70207304-70207354	HUVEC	blood vessel:	n/a
41	chr16:70148511-70148561	HCPEpiC	choroid plexus:	n/a
42	chr16:70146610-70146660	HPAEpiC	pulmonary alveolar:	n/a
43	chr16:70148511-70148561	HCM	heart:	n/a
44	chr16:70283421-70283471	ECC-1	luminal epithelium:	n/a
45	chr16:70207722-70207772	PANC-1	pancreas:	n/a
46	chr16:70284928-70284978	HAEpiC	amniotic membrane:	n/a
47	chr16:70151549-70151599	AoSMC	blood vessel:	n/a
48	chr16:70207722-70207772	A549	lung:	n/a
49	chr16:70283421-70283471	HRCEpiC	kidney:	n/a
50	chr16:70220191-70220241	HRCEpiC	kidney:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70191657..70193675-chr16:70283732..70285560,2	K562	blood:
2	chr16:70283799..70285737-chr6:44213868..44216847,2	K562	blood:
3	chr16:70197328..70198092-chr16:70301268..70302134,2	MCF-7	breast:
4	chr16:70284511..70286776-chr16:70330314..70334173,3	MCF-7	breast:
5	chr16:70192894..70195380-chr16:70284264..70288568,4	MCF-7	breast:
6	chr16:70283970..70285913-chr16:70380669..70382950,2	K562	blood:
7	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
8	chr16:70170309..70171136-chr16:72947288..72947878,2	MCF-7	breast:
9	chr16:70170285..70171145-chr16:72963448..72963968,2	MCF-7	breast:
10	chr16:70185026..70185664-chr16:74657267..74657783,2	MCF-7	breast:
11	chr16:70191657..70193675-chr16:70283732..70285560,2	K562	blood:
12	chr16:70195628..70198229-chr16:70323197..70325854,2	MCF-7	breast:
13	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
14	chr16:70189713..70191262-chr16:70193819..70195441,2	MCF-7	breast:
15	chr16:70194900..70197913-chr16:70284304..70286530,3	MCF-7	breast:
16	chr16:70284251..70286200-chr16:70298122..70301114,5	MCF-7	breast:
17	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
18	chr16:70190180..70193178-chr16:70320490..70323768,3	K562	blood:
19	chr16:70185546..70188215-chr16:74330413..74333077,2	K562	blood:
20	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
21	chr16:70098076..70099819-chr16:70146086..70148783,2	MCF-7	breast:
22	chr16:70190124..70192979-chr16:70192985..70196334,3	MCF-7	breast:
23	chr16:70284207..70286196-chr16:70321648..70323975,3	MCF-7	breast:
24	chr16:70194744..70197032-chr16:70317749..70321532,3	K562	blood:
25	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
26	chr16:70190124..70192979-chr16:70192985..70196334,3	MCF-7	breast:
27	chr16:70283625..70285831-chr16:70321379..70323186,2	K562	blood:
28	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
29	chr16:70185001..70186006-chr16:74463672..74464734,4	MCF-7	breast:
30	chr16:70183960..70187287-chr16:70187613..70192158,4	MCF-7	breast:
31	chr16:70198641..70199632-chr16:74343397..74344233,2	K562	blood:
32	chr16:70284271..70287113-chr16:70301564..70303205,2	MCF-7	breast:
33	chr16:70284505..70286615-chr16:70556732..70559559,2	MCF-7	breast:
34	chr16:70183960..70187287-chr16:70187613..70192158,4	MCF-7	breast:
35	chr16:70285081..70287489-chr16:70291525..70295571,5	K562	blood:
36	chr16:70284942..70287057-chr16:70291525..70294943,4	K562	blood:
37	chr16:70190723..70192786-chr16:74330377..74332345,2	K562	blood:
38	chr16:70189713..70191262-chr16:70193819..70195441,2	MCF-7	breast:
39	chr16:70245449..70247912-chr16:70284379..70285973,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOSC6-2	chr16:70192708-70192792	ENSG00000247228.2
2	lnc-EXOSC6-2	chr16:70190243-70190407	ENSG00000247228.2
3	lnc-EXOSC6-2	chr16:70195347-70195796	ENSG00000247228
4	lnc-EXOSC6-2	chr16:70192860-70193983	ENSG00000247228
5	lnc-DDX19B-2	chr16:70273803-70273904	NONHSAT143414
6	lnc-EXOSC6-2	chr16:70207031-70207351	ENSG00000247228
7	lnc-DDX19B-2	chr16:70280560-70282018	NONHSAT143414
8	lnc-EXOSC6-2	chr16:70194638-70194844	ENSG00000247228
9	lnc-EXOSC6-2	chr16:70194075-70194214	ENSG00000247228
10	lnc-EXOSC6-2	chr16:70207031-70207322	ENSG00000247228.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PDPR	hsa-let-7b-5p	chr16:70191322-70191343
2	PDPR	hsa-miR-16-5p	chr16:70191655-70191661
3	PDPR	hsa-let-7b-5p	chr16:70191336-70191343
4	PDPR	hsa-miR-155-5p	chr16:70192265-70192271

Variant related genes	Relation type
PDPR	TF binding region
ENSG00000247228	TF binding region
ENSG00000238734	TF binding region
ENSG00000269866	TF binding region
ENSG00000269746	TF binding region
CLEC18C	TF binding region
ENSG00000261145	TF binding region
ENSG00000261556	TF binding region
PDPR	CpG island
ENSG00000247228	CpG island
ENSG00000238734	CpG island
ENSG00000269866	CpG island
ENSG00000269746	CpG island
CLEC18C	CpG island
ENSG00000261145	CpG island
ENSG00000261556	CpG island
ENSG00000103051	chromatin interactions
ENSG00000260537	chromatin interactions
ENSG00000265230	chromatin interactions
ENSG00000196696	chromatin interactions
ENSG00000223496	chromatin interactions
ENSG00000261556	chromatin interactions
ENSG00000157349	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000090861	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000259972	chromatin interactions
ENSG00000168872	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000255185	chromatin interactions
ACOT8	miRNA target sites
ATAD5	miRNA target sites
ZNRF3	miRNA target sites
FAM122B	miRNA target sites
ARHGDIA	miRNA target sites

Extended variants
information (count: 5310 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:5310 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547337605	chr16:70145139-70145140	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs571832949	chr16:70145145-70145146	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs539751453	chr16:70145177-70145178	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs557560158	chr16:70145240-70145241	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs569248655	chr16:70145254-70145255	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs149685195	chr16:70145261-70145262	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs3972162	chr16:70145272-70145273	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368328967	chr16:70145309-70145310	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs553291729	chr16:70145310-70145311	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs3972163	chr16:70145327-70145328	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
11	rs572906171	chr16:70145344-70145345	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs189859436	chr16:70145347-70145348	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192189955	chr16:70145358-70145359	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs141289361	chr16:70145397-70145398	Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs544857321	chr16:70145403-70145404	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563547218	chr16:70145414-70145415	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs575242368	chr16:70145432-70145433	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs555508647	chr16:70145446-70145447	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs3972164	chr16:70145448-70145449	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs3972165	chr16:70145475-70145476	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560691383	chr16:70145500-70145501	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs11489915	chr16:70145525-70145526	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs11489916	chr16:70145529-70145530	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs565556210	chr16:70145559-70145560	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs375797267	chr16:70145660-70145661	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532903360	chr16:70145666-70145667	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs550883654	chr16:70145667-70145668	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs8060042	chr16:70145675-70145676	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
29	rs536302881	chr16:70145697-70145698	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs548686264	chr16:70145758-70145759	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566495396	chr16:70145764-70145765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141427785	chr16:70145788-70145789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533918260	chr16:70145793-70145794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558558903	chr16:70145805-70145806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577515450	chr16:70145816-70145817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183692602	chr16:70145819-70145820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556839429	chr16:70145826-70145827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575416059	chr16:70145828-70145829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542321395	chr16:70145896-70145897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560946689	chr16:70145915-70145916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573002527	chr16:70145919-70145920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540229731	chr16:70145923-70145924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564913358	chr16:70145981-70145982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113356395	chr16:70146057-70146058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578097793	chr16:70146089-70146090	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs532653723	chr16:70146124-70146125	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2911017	chr16:70146129-70146130	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs9928167	chr16:70146188-70146189	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs201032305	chr16:70146220-70146221	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs554463355	chr16:70146223-70146224	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:2672 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70135000-70148200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr16:70142400-70147000	Weak transcription	Adipose Nuclei	Adipose
3	chr16:70144000-70145200	Weak transcription	HepG2	liver
4	chr16:70145200-70145400	Flanking Bivalent TSS/Enh	HepG2	liver
5	chr16:70145600-70146800	Weak transcription	HepG2	liver
6	chr16:70145800-70147600	Enhancers	Primary B cells from peripheral blood	blood
7	chr16:70146200-70146400	Enhancers	Primary B cells from cord blood	blood
8	chr16:70146400-70147800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr16:70146400-70147800	Weak transcription	Primary B cells from cord blood	blood
10	chr16:70147000-70147200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr16:70147000-70147200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr16:70147000-70147200	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr16:70147000-70147200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr16:70147000-70147200	Enhancers	Liver	Liver
15	chr16:70147000-70147200	Enhancers	Fetal Stomach	stomach
16	chr16:70147000-70147200	Enhancers	Left Ventricle	heart
17	chr16:70147000-70147200	Enhancers	Ovary	ovary
18	chr16:70147000-70147200	Enhancers	Pancreas	Pancrea
19	chr16:70147000-70147200	Flanking Active TSS	HepG2	liver
20	chr16:70147000-70147200	Enhancers	NH-A	brain
21	chr16:70147000-70147400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr16:70147000-70147400	Enhancers	Primary T cells fromperipheralblood	blood
23	chr16:70147000-70147400	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr16:70147000-70147400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr16:70147000-70147400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr16:70147000-70147400	Enhancers	Brain Anterior Caudate	brain
27	chr16:70147000-70147400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr16:70147000-70147400	Enhancers	Colon Smooth Muscle	Colon
29	chr16:70147000-70147400	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr16:70147000-70147400	Enhancers	Fetal Intestine Small	intestine
31	chr16:70147000-70147400	Enhancers	Fetal Muscle Trunk	muscle
32	chr16:70147000-70147400	Enhancers	Fetal Thymus	thymus
33	chr16:70147000-70147400	Enhancers	Psoas Muscle	Psoas
34	chr16:70147000-70147400	Enhancers	Right Ventricle	heart
35	chr16:70147000-70147400	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr16:70147000-70147400	Enhancers	Stomach Smooth Muscle	stomach
37	chr16:70147000-70147600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr16:70147000-70147600	Enhancers	Adipose Nuclei	Adipose
39	chr16:70147000-70147600	Enhancers	Fetal Muscle Leg	muscle
40	chr16:70147000-70147600	Enhancers	Dnd41	blood
41	chr16:70147000-70147800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr16:70147000-70147800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr16:70147000-70149600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr16:70147200-70148600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr16:70147200-70149000	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr16:70147200-70149000	Active TSS	HepG2	liver
47	chr16:70147200-70149200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr16:70147200-70149400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr16:70147200-70149600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr16:70147400-70147800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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