Variant report

Variant	nsv528263
Chromosome Location	chr17:16097430-16196996
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2950)
CpG islands
(count:1527)
Chromatin interactive
region (count:106)
LncRNA
region (count:4)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2950 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:16147276-16147449	K562	blood:	n/a	n/a
2	ARID3A	chr17:16110586-16110700	K562	blood:	n/a	n/a
3	ARID3A	chr17:16192208-16192853	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:16102393-16102644	K562	blood:	n/a	n/a
5	ARID3A	chr17:16188276-16188280	K562	blood:	n/a	n/a
6	ARID3A	chr17:16189226-16190064	K562	blood:	n/a	n/a
7	ARID3A	chr17:16118713-16119045	HepG2	liver:	n/a	n/a
8	ARID3A	chr17:16189122-16190127	HepG2	liver:	n/a	n/a
9	ARID3A	chr17:16117740-16117755	K562	blood:	n/a	n/a
10	ARID3A	chr17:16118775-16118975	K562	blood:	n/a	n/a
11	ARID3A	chr17:16150559-16150882	HepG2	liver:	n/a	n/a
12	ARID3A	chr17:16154007-16154298	HepG2	liver:	n/a	n/a
13	ATF1	chr17:16176843-16177155	K562	blood:	n/a	n/a
14	ATF1	chr17:16120297-16120606	K562	blood:	n/a	n/a
15	ATF1	chr17:16187993-16188034	K562	blood:	n/a	n/a
16	ATF1	chr17:16130064-16130290	K562	blood:	n/a	n/a
17	ATF1	chr17:16189151-16190166	K562	blood:	n/a	n/a
18	ATF1	chr17:16190955-16191384	K562	blood:	n/a	n/a
19	ATF1	chr17:16178409-16178659	K562	blood:	n/a	n/a
20	ATF1	chr17:16132896-16133096	K562	blood:	n/a	n/a
21	ATF2	chr17:16190626-16191343	GM12878	blood:	n/a	n/a
22	ATF2	chr17:16120111-16120859	GM12878	blood:	n/a	n/a
23	ATF2	chr17:16132738-16133261	GM12878	blood:	n/a	n/a
24	ATF2	chr17:16189972-16191467	GM12878	blood:	n/a	n/a
25	ATF2	chr17:16189038-16189830	GM12878	blood:	n/a	n/a
26	ATF2	chr17:16189108-16189571	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr17:16190158-16190569	GM12878	blood:	n/a	n/a
28	ATF2	chr17:16120266-16120766	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr17:16132790-16133207	GM12878	blood:	n/a	n/a
30	ATF2	chr17:16189102-16189601	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr17:16189161-16190136	GM12878	blood:	n/a	n/a
32	ATF2	chr17:16120146-16120936	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr17:16120326-16120617	K562	blood:	n/a	n/a
34	ATF3	chr17:16118535-16119370	A549	lung:	n/a	chr17:16119135-16119144
35	ATF3	chr17:16132862-16133158	HCT-116	colon:	n/a	n/a
36	ATF3	chr17:16189018-16190294	A549	lung:	n/a	n/a
37	ATF3	chr17:16189051-16190255	A549	lung:	n/a	n/a
38	ATF3	chr17:16132878-16133166	K562	blood:	n/a	n/a
39	ATF3	chr17:16118571-16119176	A549	lung:	n/a	chr17:16119135-16119144
40	ATF3	chr17:16120079-16120890	A549	lung:	n/a	n/a
41	ATF3	chr17:16120109-16120859	A549	lung:	n/a	n/a
42	BACH1	chr17:16118591-16119509	H1-hESC	embryonic stem cell:	n/a	n/a
43	BATF	chr17:16120282-16120647	GM12878	blood:	n/a	n/a
44	BATF	chr17:16118764-16119022	GM12878	blood:	n/a	chr17:16118842-16118853
45	BATF	chr17:16106444-16106772	GM12878	blood:	n/a	n/a
46	BATF	chr17:16132823-16133129	GM12878	blood:	n/a	n/a
47	BATF	chr17:16106468-16106751	GM12878	blood:	n/a	n/a
48	BCL11A	chr17:16190202-16190580	GM12878	blood:	n/a	n/a
49	BCL11A	chr17:16132846-16133134	GM12878	blood:	n/a	n/a
50	BCL11A	chr17:16191086-16191313	GM12878	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16120890-16120940	LNCaP	prostate:	n/a
2	chr17:16176891-16176941	NT2-D1	testis:	n/a
3	chr17:16120890-16120940	LNCaP	prostate:	n/a
4	chr17:16176891-16176941	NT2-D1	testis:	n/a
5	chr17:16185300-16185350	Hela-S3	cervix:	n/a
6	chr17:16118138-16118188	T-47D	breast:	n/a
7	chr17:16120428-16120478	SK-N-SH	brain:	n/a
8	chr17:16119456-16119506	MCF10A-Er-Src	breast:	n/a
9	chr17:16120399-16120449	HIPEpiC	eye:	n/a
10	chr17:16118806-16118856	U87	brain:	n/a
11	chr17:16120890-16120940	HRE	kidney:	n/a
12	chr17:16120890-16120940	MCF-7	breast:	n/a
13	chr17:16120399-16120449	NH-A	brain:	n/a
14	chr17:16120431-16120481	HRCEpiC	kidney:	n/a
15	chr17:16120465-16120515	PrEC	prostate:	n/a
16	chr17:16185300-16185350	GM12891	blood:	n/a
17	chr17:16120465-16120515	SK-N-SH_RA	brain:	n/a
18	chr17:16120569-16120619	NT2-D1	testis:	n/a
19	chr17:16119439-16119489	HMEC	breast:	n/a
20	chr17:16120428-16120478	NB4	blood:	n/a
21	chr17:16184961-16185011	HEEpiC	esophagus:	n/a
22	chr17:16119344-16119394	IMR90	lung:	fetal
23	chr17:16119344-16119394	SK-N-SH_RA	brain:	n/a
24	chr17:16120448-16120498	AoSMC	blood vessel:	n/a
25	chr17:16120693-16120743	T-47D	breast:	n/a
26	chr17:16120569-16120619	PFSK-1	brain:	n/a
27	chr17:16185300-16185350	AG10803	skin:	n/a
28	chr17:16120431-16120481	HMEC	breast:	n/a
29	chr17:16118700-16118750	HCT-116	colon:	n/a
30	chr17:16184961-16185011	HepG2	liver:	n/a
31	chr17:16119441-16119491	Hepatocyte	liver:	n/a
32	chr17:16158686-16158736	HEK293	kidney:	embryo
33	chr17:16120515-16120565	HIPEpiC	eye:	n/a
34	chr17:16118251-16118301	AG04449	skin:	fetal
35	chr17:16158686-16158736	SAEC	small airway:	n/a
36	chr17:16119441-16119491	T-47D	breast:	n/a
37	chr17:16120448-16120498	K562	blood:	n/a
38	chr17:16118138-16118188	AoSMC	blood vessel:	n/a
39	chr17:16119441-16119491	H1-hESC	embryonic stem cell:	embryo
40	chr17:16118919-16118969	NT2-D1	testis:	n/a
41	chr17:16119441-16119491	HepG2	liver:	n/a
42	chr17:16120890-16120940	AG10803	skin:	n/a
43	chr17:16184961-16185011	GM06990	blood:	n/a
44	chr17:16120465-16120515	ovcar-3	ovarian:	n/a
45	chr17:16176891-16176941	HRCEpiC	kidney:	n/a
46	chr17:16120448-16120498	T-47D	breast:	n/a
47	chr17:16120515-16120565	A549	lung:	n/a
48	chr17:16120569-16120619	LNCaP	prostate:	n/a
49	chr17:16114743-16114793	Jurkat	blood:	n/a
50	chr17:16118806-16118856	H1-hESC	embryonic stem cell:	embryo

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:16188072..16192244-chr17:16282440..16289447,10	K562	blood:
2	chr17:16189235..16191423-chr8:145514360..145516525,2	MCF-7	breast:
3	chr17:16117873..16120120-chr17:16255453..16257553,2	MCF-7	breast:
4	chr17:16145216..16149469-chr17:16187670..16191741,4	K562	blood:
5	chr17:16117370..16118876-chr17:16121320..16122865,2	K562	blood:
6	chr1:113497995..113498938-chr17:16118772..16119540,2	Hela-S3	cervix:
7	chr17:16118960..16120810-chr17:16254534..16257203,3	K562	blood:
8	chr1:145382530..145383456-chr17:16118328..16119083,2	Hela-S3	cervix:
9	chr17:16189274..16189815-chr17:16492735..16493319,2	K562	blood:
10	chr17:16189886..16192515-chr17:16344238..16345817,2	K562	blood:
11	chr17:16131263..16133081-chr17:16135992..16138257,2	K562	blood:
12	chr17:16188539..16190770-chr17:16316162..16319521,3	K562	blood:
13	chr17:16112257..16115014-chr17:16118157..16121007,4	MCF-7	breast:
14	chr17:16117875..16121026-chr17:16318413..16323261,4	K562	blood:
15	chr17:16145216..16149469-chr17:16187670..16191741,4	K562	blood:
16	chr17:16133803..16136363-chr17:16137901..16140091,2	MCF-7	breast:
17	chr17:16117370..16118876-chr17:16121320..16122865,2	K562	blood:
18	chr17:16188324..16192785-chr17:16195612..16200767,7	K562	blood:
19	chr17:16105475..16107770-chr17:16118140..16120504,3	MCF-7	breast:
20	chr17:16115662..16122557-chr17:16186487..16191394,14	K562	blood:
21	chr17:16117769..16122024-chr17:16284027..16287393,3	K562	blood:
22	chr17:15987048..15989365-chr17:16117375..16120147,2	MCF-7	breast:
23	chr17:16116365..16119285-chr17:16395133..16397532,2	K562	blood:
24	chr17:16187978..16191408-chr17:16282408..16285625,11	K562	blood:
25	chr17:16182895..16184855-chr17:16188164..16190735,2	K562	blood:
26	chr17:16102233..16105436-chr17:16117478..16120410,3	MCF-7	breast:
27	chr17:16196597..16198455-chr17:16199967..16201476,2	K562	blood:
28	chr17:16102885..16105162-chr17:16114131..16115658,2	K562	blood:
29	chr17:16171393..16174312-chr17:16182076..16184658,2	K562	blood:
30	chr17:16174439..16177068-chr17:16182949..16184575,2	MCF-7	breast:
31	chr17:16188817..16191161-chr17:16192710..16195262,3	K562	blood:
32	chr17:16189482..16191401-chr17:16347392..16349028,2	K562	blood:
33	chr17:16188324..16192785-chr17:16195612..16200767,7	K562	blood:
34	chr17:16116452..16122627-chr17:16187627..16192896,12	K562	blood:
35	chr17:16174439..16177068-chr17:16182949..16184575,2	MCF-7	breast:
36	chr17:16158983..16161004-chr17:16162947..16164808,2	K562	blood:
37	chr17:16115684..16120775-chr17:16282002..16285784,4	MCF-7	breast:
38	chr17:16189283..16191732-chr17:16340312..16342740,3	K562	blood:
39	chr17:16187896..16189680-chr17:16346072..16348174,2	MCF-7	breast:
40	chr17:16195813..16198372-chr17:16206381..16207960,2	K562	blood:
41	chr17:16133803..16136363-chr17:16137901..16140091,2	MCF-7	breast:
42	chr17:16165701..16168526-chr17:16175025..16177234,2	K562	blood:
43	chr17:16175415..16178833-chr17:16340980..16343676,3	K562	blood:
44	chr17:16118549..16119334-chr22:19419377..19419924,2	Hela-S3	cervix:
45	chr17:16118010..16120268-chr17:16181462..16183688,2	MCF-7	breast:
46	chr17:16121383..16123280-chr17:16341991..16343713,2	K562	blood:
47	chr17:16115419..16117298-chr17:56706385..56708749,2	MCF-7	breast:
48	chr17:16187182..16191519-chr17:16253380..16257839,12	K562	blood:
49	chr17:16118309..16118871-chr7:128116620..128117465,2	Hela-S3	cervix:
50	chr17:16188284..16190570-chr17:16196788..16199758,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBB-5	chr17:16120862-16121473	NONHSAT145898
2	lnc-CENPV-4	chr17:16118676-16118715	NONHSAT145897
3	lnc-UBB-5	chr17:16120560-16120775	NONHSAT145898
4	lnc-CENPV-4	chr17:16101485-16102033	NONHSAT145897

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1288-5p	chr17:16185342-16185364	MIMAT0026743
hsa-miR-1288-3p	chr17:16185372-16185392	MIMAT0005942

No data

Variant related genes	Relation type
PIGL	TF binding region
MIR1288	TF binding region
NCOR1	TF binding region
PIGL	CpG island
MIR1288	CpG island
NCOR1	CpG island
ENSG00000087263	chromatin interactions
ENSG00000165055	chromatin interactions
ENSG00000173156	chromatin interactions
ENSG00000128699	chromatin interactions
ENSG00000064933	chromatin interactions
ENSG00000265401	chromatin interactions
ENSG00000198363	chromatin interactions
ENSG00000264408	chromatin interactions
ENSG00000181350	chromatin interactions
ENSG00000221355	chromatin interactions
ENSG00000147799	chromatin interactions
ENSG00000185122	chromatin interactions
ENSG00000166582	chromatin interactions
ENSG00000170315	chromatin interactions
ENSG00000185608	chromatin interactions
ENSG00000168556	chromatin interactions
ENSG00000264739	chromatin interactions
ENSG00000167005	chromatin interactions
ENSG00000108474	chromatin interactions
ENSG00000100387	chromatin interactions
ENSG00000246705	chromatin interactions
ENSG00000232648	chromatin interactions
ENSG00000197483	chromatin interactions
ENSG00000266651	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000175061	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000011295	chromatin interactions
ENSG00000269859	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000126267	chromatin interactions
ENSG00000239203	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000233979	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000170727	chromatin interactions
ENSG00000187688	chromatin interactions
ENSG00000214941	chromatin interactions
ENSG00000111912	chromatin interactions

Extended variants
information (count: 3779 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:3779 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs178810	chr17:16097430-16097431	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371033725	chr17:16097451-16097452	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373808575	chr17:16097468-16097469	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558844200	chr17:16097539-16097540	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183697174	chr17:16097562-16097563	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189636761	chr17:16097601-16097602	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35644251	chr17:16097602-16097603	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372427987	chr17:16097603-16097604	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113022990	chr17:16097604-16097605	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71150276	chr17:16097606-16097607	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561194363	chr17:16097609-16097610	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542563440	chr17:16097623-16097624	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574968303	chr17:16097692-16097693	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374840459	chr17:16097697-16097698	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543590490	chr17:16097720-16097721	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371039277	chr17:16097737-16097738	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376259190	chr17:16097742-16097743	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563783794	chr17:16097748-16097749	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201037902	chr17:16097786-16097787	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75360338	chr17:16097788-16097789	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs202117316	chr17:16097792-16097793	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199610082	chr17:16097808-16097809	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200699286	chr17:16097809-16097810	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs202168825	chr17:16097810-16097811	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368974418	chr17:16097820-16097821	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73281920	chr17:16097825-16097826	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76145228	chr17:16097870-16097871	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149293452	chr17:16097899-16097900	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552573190	chr17:16097907-16097908	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142702166	chr17:16097910-16097911	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201806069	chr17:16097912-16097913	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79572007	chr17:16097921-16097922	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79346200	chr17:16097953-16097954	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs565185491	chr17:16098024-16098025	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs80257917	chr17:16098030-16098031	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs527533104	chr17:16098048-16098049	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs199955216	chr17:16098057-16098058	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs547708980	chr17:16098072-16098073	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200958402	chr17:16098073-16098074	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs182072577	chr17:16098133-16098134	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs202243015	chr17:16098134-16098135	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201451317	chr17:16098148-16098149	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529883288	chr17:16098193-16098194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185731466	chr17:16098205-16098206	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189816600	chr17:16098237-16098238	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374343452	chr17:16098260-16098261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182075049	chr17:16098305-16098306	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372048890	chr17:16098314-16098315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558085003	chr17:16098358-16098359	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77274360	chr17:16098385-16098386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	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
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	17550852	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:3303 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16035800-16103400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr17:16049200-16103400	Weak transcription	Spleen	Spleen
3	chr17:16049200-16108600	Weak transcription	Esophagus	oesophagus
4	chr17:16052200-16100400	Weak transcription	Ovary	ovary
5	chr17:16055200-16102600	Weak transcription	Brain Angular Gyrus	brain
6	chr17:16055400-16104000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr17:16055800-16102000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr17:16059400-16102400	Weak transcription	Small Intestine	intestine
9	chr17:16059400-16102400	Weak transcription	NHLF	lung
10	chr17:16059400-16102800	Weak transcription	Pancreas	Pancrea
11	chr17:16064000-16101000	Weak transcription	Lung	lung
12	chr17:16064600-16106000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr17:16084800-16098000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr17:16086000-16098000	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr17:16086600-16101600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr17:16086600-16102400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr17:16086800-16102200	Weak transcription	Stomach Mucosa	stomach
18	chr17:16087200-16097600	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr17:16087200-16098000	Strong transcription	Fetal Intestine Large	intestine
20	chr17:16087200-16108200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr17:16088000-16117000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr17:16088200-16101800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr17:16088200-16102200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr17:16088200-16116200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr17:16088600-16101200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr17:16089400-16103400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr17:16089400-16104000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr17:16089600-16104400	Weak transcription	HSMMtube	muscle
29	chr17:16089600-16114600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr17:16090000-16100200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr17:16090000-16116800	Weak transcription	NH-A	brain
32	chr17:16090400-16102600	Weak transcription	Stomach Smooth Muscle	stomach
33	chr17:16090400-16105200	Weak transcription	Colonic Mucosa	Colon
34	chr17:16091200-16098600	Strong transcription	HepG2	liver
35	chr17:16091800-16099200	Strong transcription	Placenta	Placenta
36	chr17:16092000-16097800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:16092000-16098000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr17:16092000-16103400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr17:16092200-16097600	Strong transcription	Duodenum Mucosa	Duodenum
40	chr17:16092400-16098000	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr17:16092400-16098000	Strong transcription	Fetal Muscle Trunk	muscle
42	chr17:16092400-16102400	Weak transcription	Right Atrium	heart
43	chr17:16092600-16098000	Strong transcription	Fetal Thymus	thymus
44	chr17:16092800-16098000	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr17:16092800-16098000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr17:16092800-16098000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr17:16092800-16098000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr17:16092800-16098000	Strong transcription	Liver	Liver
49	chr17:16092800-16098200	Strong transcription	Osteobl	bone
50	chr17:16092800-16099200	Strong transcription	Dnd41	blood

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