Variant report

Variant	nsv907718
Chromosome Location	chr17:16080849-16143709
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1645)
CpG islands
(count:1160)
Chromatin interactive
region (count:53)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1645 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:16117740-16117755	K562	blood:	n/a	n/a
2	ARID3A	chr17:16110586-16110700	K562	blood:	n/a	n/a
3	ARID3A	chr17:16102393-16102644	K562	blood:	n/a	n/a
4	ARID3A	chr17:16118775-16118975	K562	blood:	n/a	n/a
5	ARID3A	chr17:16118713-16119045	HepG2	liver:	n/a	n/a
6	ATF1	chr17:16130064-16130290	K562	blood:	n/a	n/a
7	ATF1	chr17:16132896-16133096	K562	blood:	n/a	n/a
8	ATF1	chr17:16120297-16120606	K562	blood:	n/a	n/a
9	ATF2	chr17:16120111-16120859	GM12878	blood:	n/a	n/a
10	ATF2	chr17:16120146-16120936	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr17:16132738-16133261	GM12878	blood:	n/a	n/a
12	ATF2	chr17:16132790-16133207	GM12878	blood:	n/a	n/a
13	ATF2	chr17:16120266-16120766	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr17:16120109-16120859	A549	lung:	n/a	n/a
15	ATF3	chr17:16120326-16120617	K562	blood:	n/a	n/a
16	ATF3	chr17:16118535-16119370	A549	lung:	n/a	chr17:16119135-16119144
17	ATF3	chr17:16132878-16133166	K562	blood:	n/a	n/a
18	ATF3	chr17:16132862-16133158	HCT-116	colon:	n/a	n/a
19	ATF3	chr17:16118571-16119176	A549	lung:	n/a	chr17:16119135-16119144
20	ATF3	chr17:16120079-16120890	A549	lung:	n/a	n/a
21	BACH1	chr17:16118591-16119509	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr17:16106444-16106772	GM12878	blood:	n/a	n/a
23	BATF	chr17:16118764-16119022	GM12878	blood:	n/a	chr17:16118842-16118853
24	BATF	chr17:16106468-16106751	GM12878	blood:	n/a	n/a
25	BATF	chr17:16120282-16120647	GM12878	blood:	n/a	n/a
26	BATF	chr17:16132823-16133129	GM12878	blood:	n/a	n/a
27	BCL11A	chr17:16132846-16133134	GM12878	blood:	n/a	n/a
28	BCL3	chr17:16132835-16133147	GM12878	blood:	n/a	n/a
29	BCL3	chr17:16120084-16120936	A549	lung:	n/a	n/a
30	BCL3	chr17:16118598-16119548	A549	lung:	n/a	chr17:16119207-16119216 chr17:16119223-16119236 chr17:16119222-16119231 chr17:16119225-16119234 chr17:16119022-16119035
31	BCL3	chr17:16118680-16119082	GM12878	blood:	n/a	chr17:16119022-16119035
32	BCL3	chr17:16120109-16120940	A549	lung:	n/a	n/a
33	BCLAF1	chr17:16120113-16120759	K562	blood:	n/a	n/a
34	BCLAF1	chr17:16120031-16120757	GM12878	blood:	n/a	n/a
35	BCLAF1	chr17:16118352-16119737	GM12878	blood:	n/a	chr17:16118478-16118487 chr17:16118587-16118600 chr17:16119207-16119216 chr17:16119223-16119236 chr17:16119222-16119231 chr17:16119225-16119234 chr17:16119022-16119035
36	BCLAF1	chr17:16120081-16120911	GM12878	blood:	n/a	n/a
37	BCLAF1	chr17:16120110-16120702	K562	blood:	n/a	n/a
38	BCLAF1	chr17:16118638-16119121	GM12878	blood:	n/a	chr17:16119022-16119035
39	BHLHE40	chr17:16118810-16119071	K562	blood:	n/a	n/a
40	BHLHE40	chr17:16120199-16120722	GM12878	blood:	n/a	n/a
41	BHLHE40	chr17:16119288-16119601	K562	blood:	n/a	n/a
42	BHLHE40	chr17:16118646-16119081	GM12878	blood:	n/a	n/a
43	BHLHE40	chr17:16118381-16118391	K562	blood:	n/a	n/a
44	BHLHE40	chr17:16120212-16120640	K562	blood:	n/a	n/a
45	BHLHE40	chr17:16120326-16120997	HepG2	liver:	n/a	n/a
46	BRCA1	chr17:16117588-16118208	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr17:16120357-16120650	HepG2	liver:	n/a	n/a
48	BRCA1	chr17:16118710-16118739	HepG2	liver:	n/a	n/a
49	BRCA1	chr17:16118686-16118946	GM12878	blood:	n/a	n/a
50	BRCA1	chr17:16120323-16120665	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16119344-16119394	CMK	blood:	n/a
2	chr17:16119344-16119394	CMK	blood:	n/a
3	chr17:16120428-16120478	IMR90	lung:	fetal
4	chr17:16119439-16119489	AG04449	skin:	fetal
5	chr17:16120431-16120481	HEK293	kidney:	embryo
6	chr17:16118251-16118301	Hepatocyte	liver:	n/a
7	chr17:16118700-16118750	NT2-D1	testis:	n/a
8	chr17:16120515-16120565	H1-hESC	embryonic stem cell:	embryo
9	chr17:16118138-16118188	HCPEpiC	choroid plexus:	n/a
10	chr17:16120890-16120940	HAEpiC	amniotic membrane:	n/a
11	chr17:16120515-16120565	IMR90	lung:	fetal
12	chr17:16120515-16120565	Caco-2	colon:	n/a
13	chr17:16118806-16118856	Hela-S3	cervix:	n/a
14	chr17:16120431-16120481	Caco-2	colon:	n/a
15	chr17:16120448-16120498	GM12891	blood:	n/a
16	chr17:16114743-16114793	HCM	heart:	n/a
17	chr17:16120399-16120449	MCF10A-Er-Src	breast:	n/a
18	chr17:16120515-16120565	Jurkat	blood:	n/a
19	chr17:16118700-16118750	NB4	blood:	n/a
20	chr17:16120448-16120498	NHBE	bronchial:	n/a
21	chr17:16119441-16119491	HIPEpiC	eye:	n/a
22	chr17:16118251-16118301	GM12878	blood:	n/a
23	chr17:16120515-16120565	SK-N-SH	brain:	n/a
24	chr17:16118700-16118750	HCPEpiC	choroid plexus:	n/a
25	chr17:16120515-16120565	HCT-116	colon:	n/a
26	chr17:16119441-16119491	NB4	blood:	n/a
27	chr17:16118251-16118301	HMEC	breast:	n/a
28	chr17:16118138-16118188	HIPEpiC	eye:	n/a
29	chr17:16120569-16120619	Caco-2	colon:	n/a
30	chr17:16119441-16119491	HAEpiC	amniotic membrane:	n/a
31	chr17:16120890-16120940	HL-60	blood:	n/a
32	chr17:16118700-16118750	HIPEpiC	eye:	n/a
33	chr17:16120448-16120498	AG09319	gingival:	n/a
34	chr17:16119439-16119489	PrEC	prostate:	n/a
35	chr17:16118251-16118301	AG04450	lung:	fetal
36	chr17:16120428-16120478	AG10803	skin:	n/a
37	chr17:16120569-16120619	SAEC	small airway:	n/a
38	chr17:16120693-16120743	ProgFib	skin:	n/a
39	chr17:16118138-16118188	HRCEpiC	kidney:	n/a
40	chr17:16118919-16118969	ECC-1	luminal epithelium:	n/a
41	chr17:16120465-16120515	GM06990	blood:	n/a
42	chr17:16119456-16119506	HL-60	blood:	n/a
43	chr17:16118806-16118856	HL-60	blood:	n/a
44	chr17:16120569-16120619	GM19239	blood:	n/a
45	chr17:16119439-16119489	ECC-1	luminal epithelium:	n/a
46	chr17:16120399-16120449	AG04450	lung:	fetal
47	chr17:16118251-16118301	HRE	kidney:	n/a
48	chr17:16120515-16120565	NT2-D1	testis:	n/a
49	chr17:16118806-16118856	HRE	kidney:	n/a
50	chr17:16119344-16119394	AoSMC	blood vessel:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:16118623..16119597-chr3:100120034..100120875,2	Hela-S3	cervix:
2	chr17:16117769..16122024-chr17:16284027..16287393,3	K562	blood:
3	chr17:16108186..16110773-chr17:16115629..16120771,4	MCF-7	breast:
4	chr17:15901763..15905062-chr17:16117309..16121912,5	MCF-7	breast:
5	chr1:113497995..113498938-chr17:16118772..16119540,2	Hela-S3	cervix:
6	chr15:60689206..60690030-chr17:16118605..16119334,2	Hela-S3	cervix:
7	chr17:16092087..16094482-chr17:16096479..16099127,2	MCF-7	breast:
8	chr17:16128076..16130079-chr17:16132114..16135046,2	K562	blood:
9	chr17:16099413..16101155-chr17:16118369..16120104,2	K562	blood:
10	chr17:16092491..16094768-chr17:16118634..16120351,2	K562	blood:
11	chr17:16118917..16121426-chr17:16341120..16343503,3	MCF-7	breast:
12	chr17:16117370..16118876-chr17:16121320..16122865,2	K562	blood:
13	chr17:16118960..16120810-chr17:16254534..16257203,3	K562	blood:
14	chr17:16118752..16119403-chr22:41347099..41347775,2	NB4	blood:
15	chr17:16102233..16105436-chr17:16117478..16120410,3	MCF-7	breast:
16	chr17:16117555..16120555-chr17:16284027..16286497,3	K562	blood:
17	chr17:15902955..15905510-chr17:16117213..16119076,2	K562	blood:
18	chr17:16117873..16120120-chr17:16255453..16257553,2	MCF-7	breast:
19	chr17:16118765..16119327-chr2:190649095..190649706,2	NB4	blood:
20	chr17:16118309..16118871-chr7:128116620..128117465,2	Hela-S3	cervix:
21	chr12:14926760..14928352-chr17:16118616..16120352,2	MCF-7	breast:
22	chr17:16120523..16122902-chr17:16284277..16285939,2	MCF-7	breast:
23	chr17:16102885..16105162-chr17:16114131..16115658,2	K562	blood:
24	chr17:16118549..16119334-chr22:19419377..19419924,2	Hela-S3	cervix:
25	chr17:16089561..16091475-chr17:16117842..16119372,2	MCF-7	breast:
26	chr17:16118736..16121992-chr17:16123895..16128426,5	MCF-7	breast:
27	chr17:16118435..16121280-chr8:145831040..145833997,2	MCF-7	breast:
28	chr17:16118268..16119159-chr8:62627070..62627630,2	Hela-S3	cervix:
29	chr17:15987048..15989365-chr17:16117375..16120147,2	MCF-7	breast:
30	chr17:16133803..16136363-chr17:16137901..16140091,2	MCF-7	breast:
31	chr17:16117370..16118876-chr17:16121320..16122865,2	K562	blood:
32	chr17:16115419..16117298-chr17:56706385..56708749,2	MCF-7	breast:
33	chr17:16116365..16119285-chr17:16395133..16397532,2	K562	blood:
34	chr17:16118306..16119162-chr19:36139052..36139638,2	Hela-S3	cervix:
35	chr17:16117875..16121026-chr17:16318413..16323261,4	K562	blood:
36	chr17:16105475..16107770-chr17:16118140..16120504,3	MCF-7	breast:
37	chr17:16133803..16136363-chr17:16137901..16140091,2	MCF-7	breast:
38	chr17:16128076..16130079-chr17:16132114..16135046,2	K562	blood:
39	chr17:16118406..16118944-chr6:126101530..126102507,2	Hela-S3	cervix:
40	chr17:16118757..16122338-chr17:16126613..16132237,5	MCF-7	breast:
41	chr17:16085958..16087608-chr17:16095092..16097243,2	MCF-7	breast:
42	chr17:16115684..16120775-chr17:16282002..16285784,4	MCF-7	breast:
43	chr17:16121383..16123280-chr17:16341991..16343713,2	K562	blood:
44	chr17:16118192..16118876-chr19:55987576..55988208,2	Hela-S3	cervix:
45	chr1:145382530..145383456-chr17:16118328..16119083,2	Hela-S3	cervix:
46	chr17:16102885..16105162-chr17:16114131..16115658,2	K562	blood:
47	chr17:16118974..16121859-chr17:16134370..16136827,2	K562	blood:
48	chr17:16108588..16110753-chr17:16116954..16119421,3	K562	blood:
49	chr17:16112257..16115014-chr17:16118157..16121007,4	MCF-7	breast:
50	chr17:16131263..16133081-chr17:16135992..16138257,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGL-2	chr17:16095146-16095466	NONHSAT145896
2	lnc-CENPV-4	chr17:16118676-16118715	NONHSAT145897
3	lnc-UBB-5	chr17:16120560-16120775	NONHSAT145898
4	lnc-CENPV-4	chr17:16101485-16102033	NONHSAT145897
5	lnc-UBB-5	chr17:16120862-16121473	NONHSAT145898

No data

Variant related genes	Relation type
PIGL	TF binding region
NCOR1	TF binding region
RN7SL442P	TF binding region
PIGL	CpG island
NCOR1	CpG island
RN7SL442P	CpG island
ENSG00000264408	chromatin interactions
ENSG00000147799	chromatin interactions
ENSG00000266651	chromatin interactions
ENSG00000214941	chromatin interactions
ENSG00000197483	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000170315	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000011295	chromatin interactions
ENSG00000111912	chromatin interactions
ENSG00000187688	chromatin interactions
ENSG00000126267	chromatin interactions
ENSG00000246705	chromatin interactions
ENSG00000064933	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000181350	chromatin interactions
ENSG00000269859	chromatin interactions
ENSG00000233979	chromatin interactions
ENSG00000264739	chromatin interactions
ENSG00000100387	chromatin interactions
ENSG00000166582	chromatin interactions
ENSG00000165055	chromatin interactions
ENSG00000198363	chromatin interactions
ENSG00000265401	chromatin interactions
ENSG00000108474	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000175061	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000239221	chromatin interactions
ENSG00000128699	chromatin interactions
ENSG00000185608	chromatin interactions
ENSG00000155380	chromatin interactions

Extended variants
information (count: 2520 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:2520 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs178831	chr17:16080849-16080850	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540417793	chr17:16080893-16080894	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560639136	chr17:16080913-16080914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375146513	chr17:16080919-16080920	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573912343	chr17:16080993-16080994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543024525	chr17:16081042-16081043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141545394	chr17:16081080-16081081	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530743692	chr17:16081091-16081092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540938985	chr17:16081127-16081128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543990483	chr17:16081154-16081155	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183701097	chr17:16081199-16081200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189360333	chr17:16081242-16081243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375405579	chr17:16081243-16081244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182352015	chr17:16081263-16081264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185585883	chr17:16081278-16081279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146764392	chr17:16081294-16081295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566576241	chr17:16081298-16081299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190045878	chr17:16081322-16081323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577538545	chr17:16081329-16081330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181602538	chr17:16081355-16081356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569555067	chr17:16081360-16081361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545070176	chr17:16081375-16081376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558380479	chr17:16081401-16081402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564867625	chr17:16081441-16081442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530521381	chr17:16081451-16081452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147755390	chr17:16081470-16081471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551176944	chr17:16081478-16081479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199645449	chr17:16081504-16081505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs202235556	chr17:16081507-16081508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534415484	chr17:16081614-16081615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149213634	chr17:16081625-16081626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143356378	chr17:16081670-16081671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542636527	chr17:16081705-16081706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556175125	chr17:16081706-16081707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185319153	chr17:16081808-16081809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148517119	chr17:16081810-16081811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564320622	chr17:16081812-16081813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79297565	chr17:16081816-16081817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12948503	chr17:16081835-16081836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79672548	chr17:16081839-16081840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575179329	chr17:16081903-16081904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs178830	chr17:16081958-16081959	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs564047188	chr17:16081961-16081962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190034946	chr17:16081965-16081966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111761031	chr17:16081969-16081970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181297149	chr17:16081990-16081991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546511118	chr17:16082025-16082026	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372228185	chr17:16082045-16082046	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529017812	chr17:16082093-16082094	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548692667	chr17:16082104-16082105	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:160)

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

Chromatin state (count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16021800-16087600	Weak transcription	Fetal Brain Male	brain
2	chr17:16035800-16103400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr17:16039200-16096800	Weak transcription	K562	blood
4	chr17:16042000-16094200	Weak transcription	Psoas Muscle	Psoas
5	chr17:16048400-16088000	Weak transcription	Fetal Brain Female	brain
6	chr17:16049200-16088600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr17:16049200-16093200	Weak transcription	Aorta	Aorta
8	chr17:16049200-16103400	Weak transcription	Spleen	Spleen
9	chr17:16049200-16108600	Weak transcription	Esophagus	oesophagus
10	chr17:16051800-16089400	Weak transcription	Brain Germinal Matrix	brain
11	chr17:16052000-16089000	Weak transcription	HSMMtube	muscle
12	chr17:16052200-16100400	Weak transcription	Ovary	ovary
13	chr17:16055000-16088600	Weak transcription	Colonic Mucosa	Colon
14	chr17:16055200-16089400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr17:16055200-16102600	Weak transcription	Brain Angular Gyrus	brain
16	chr17:16055400-16094000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr17:16055400-16104000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr17:16055800-16102000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr17:16056200-16083800	Weak transcription	Gastric	stomach
20	chr17:16059400-16083400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr17:16059400-16094200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr17:16059400-16102400	Weak transcription	Small Intestine	intestine
23	chr17:16059400-16102400	Weak transcription	NHLF	lung
24	chr17:16059400-16102800	Weak transcription	Pancreas	Pancrea
25	chr17:16059800-16093200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr17:16060000-16083600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr17:16060600-16087800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr17:16061200-16089200	Weak transcription	Colon Smooth Muscle	Colon
29	chr17:16061400-16087200	Weak transcription	Fetal Kidney	kidney
30	chr17:16062200-16093200	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr17:16063200-16088600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr17:16063600-16082000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr17:16064000-16101000	Weak transcription	Lung	lung
34	chr17:16064200-16088200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr17:16064600-16083400	Weak transcription	Brain Hippocampus Middle	brain
36	chr17:16064600-16106000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr17:16067400-16094000	Weak transcription	Brain Anterior Caudate	brain
38	chr17:16069000-16093800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr17:16072200-16083600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr17:16072400-16088800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr17:16074400-16081000	Strong transcription	Duodenum Mucosa	Duodenum
42	chr17:16074800-16088200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr17:16075200-16087000	Weak transcription	NH-A	brain
44	chr17:16075400-16083400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr17:16075400-16083400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr17:16075400-16083400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr17:16075400-16084800	Weak transcription	Adipose Nuclei	Adipose
48	chr17:16075400-16085000	Weak transcription	Liver	Liver
49	chr17:16075400-16086600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr17:16075400-16086800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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