Variant report

Variant	nsv830853
Chromosome Location	chr6:161180005-161376481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1820)
CpG islands
(count:1893)
Chromatin interactive
region (count:72)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1820 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:161222959-161223156	K562	blood:	n/a	n/a
2	ARID3A	chr6:161231207-161231570	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:161214851-161215153	K562	blood:	n/a	n/a
4	ARID3A	chr6:161253322-161253858	K562	blood:	n/a	n/a
5	ARID3A	chr6:161339622-161339783	HepG2	liver:	n/a	chr6:161339720-161339736
6	ARID3A	chr6:161213056-161213435	K562	blood:	n/a	n/a
7	ARID3A	chr6:161195588-161195744	K562	blood:	n/a	n/a
8	ATF1	chr6:161195553-161195712	K562	blood:	n/a	n/a
9	ATF1	chr6:161214879-161214958	K562	blood:	n/a	n/a
10	ATF1	chr6:161354421-161354518	K562	blood:	n/a	n/a
11	ATF2	chr6:161210268-161211235	GM12878	blood:	n/a	n/a
12	ATF2	chr6:161292270-161292825	GM12878	blood:	n/a	n/a
13	ATF2	chr6:161212461-161213256	GM12878	blood:	n/a	n/a
14	ATF2	chr6:161188260-161188782	GM12878	blood:	n/a	n/a
15	ATF2	chr6:161210135-161211249	GM12878	blood:	n/a	n/a
16	ATF2	chr6:161298726-161299101	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr6:161253561-161253714	K562	blood:	n/a	n/a
18	ATF3	chr6:161212860-161213233	K562	blood:	n/a	n/a
19	BACH1	chr6:161351808-161352158	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:161195553-161195793	K562	blood:	n/a	n/a
21	BACH1	chr6:161188007-161188814	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:161195550-161195750	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr6:161292319-161292640	GM12878	blood:	n/a	n/a
24	BATF	chr6:161292357-161292666	GM12878	blood:	n/a	n/a
25	BATF	chr6:161210642-161211215	GM12878	blood:	n/a	n/a
26	BATF	chr6:161212542-161212977	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:161298746-161299079	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr6:161210478-161210819	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:161210821-161211126	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:161210278-161211237	GM12878	blood:	n/a	n/a
31	BCL3	chr6:161210293-161210999	GM12878	blood:	n/a	n/a
32	BCL3	chr6:161231111-161231617	A549	lung:	n/a	chr6:161231445-161231454
33	BCL3	chr6:161210287-161211171	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:161212630-161213026	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:161210293-161210934	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:161188232-161188830	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:161352988-161353350	K562	blood:	n/a	n/a
38	BHLHE40	chr6:161353075-161353311	GM12878	blood:	n/a	n/a
39	BHLHE40	chr6:161292517-161292673	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:161188391-161188713	GM12878	blood:	n/a	n/a
41	BHLHE40	chr6:161210246-161211108	GM12878	blood:	n/a	n/a
42	BHLHE40	chr6:161372287-161372674	K562	blood:	n/a	n/a
43	BRCA1	chr6:161187996-161188190	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr6:161351821-161352054	HepG2	liver:	n/a	n/a
45	BRCA1	chr6:161351585-161351882	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr6:161188458-161188461	HepG2	liver:	n/a	n/a
47	BRCA1	chr6:161189398-161189449	GM12878	blood:	n/a	n/a
48	CBX3	chr6:161219674-161220076	K562	blood:	n/a	n/a
49	CBX3	chr6:161260019-161260358	K562	blood:	n/a	n/a
50	CBX3	chr6:161210757-161211651	K562	blood:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:161352297-161352347	AG09309	skin:	n/a
2	chr6:161188022-161188072	HEK293	kidney:	embryo
3	chr6:161352297-161352347	AG09309	skin:	n/a
4	chr6:161188022-161188072	HEK293	kidney:	embryo
5	chr6:161188183-161188233	HCT-116	colon:	n/a
6	chr6:161347129-161347179	CMK	blood:	n/a
7	chr6:161188529-161188579	Jurkat	blood:	n/a
8	chr6:161348903-161348953	ECC-1	luminal epithelium:	n/a
9	chr6:161188322-161188372	GM06990	blood:	n/a
10	chr6:161347129-161347179	PFSK-1	brain:	n/a
11	chr6:161351879-161351929	NHBE	bronchial:	n/a
12	chr6:161285451-161285501	HAEpiC	amniotic membrane:	n/a
13	chr6:161188574-161188624	A549	lung:	n/a
14	chr6:161348903-161348953	BJ	skin:	n/a
15	chr6:161285451-161285501	SK-N-SH	brain:	n/a
16	chr6:161185585-161185635	SK-N-SH_RA	brain:	n/a
17	chr6:161188022-161188072	AG09309	skin:	n/a
18	chr6:161353323-161353373	HRE	kidney:	n/a
19	chr6:161188822-161188872	SKMC	muscle:	n/a
20	chr6:161354531-161354581	A549	lung:	n/a
21	chr6:161258479-161258529	SAEC	small airway:	n/a
22	chr6:161188337-161188387	PrEC	prostate:	n/a
23	chr6:161188529-161188579	GM19239	blood:	n/a
24	chr6:161347487-161347537	NHDF-neo	bronchial:	n/a
25	chr6:161258479-161258529	ECC-1	luminal epithelium:	n/a
26	chr6:161258456-161258506	K562	blood:	n/a
27	chr6:161258421-161258471	H1-hESC	embryonic stem cell:	embryo
28	chr6:161347348-161347398	T-47D	breast:	n/a
29	chr6:161185585-161185635	Hela-S3	cervix:	n/a
30	chr6:161258456-161258506	SKMC	muscle:	n/a
31	chr6:161347129-161347179	U87	brain:	n/a
32	chr6:161188322-161188372	T-47D	breast:	n/a
33	chr6:161188529-161188579	HEK293	kidney:	embryo
34	chr6:161258922-161258972	U87	brain:	n/a
35	chr6:161186852-161186902	ProgFib	skin:	n/a
36	chr6:161258752-161258802	HMEC	breast:	n/a
37	chr6:161188183-161188233	HCPEpiC	choroid plexus:	n/a
38	chr6:161347348-161347398	HCF	heart:	n/a
39	chr6:161258456-161258506	CMK	blood:	n/a
40	chr6:161188638-161188688	NH-A	brain:	n/a
41	chr6:161185585-161185635	HEK293	kidney:	embryo
42	chr6:161258752-161258802	HIPEpiC	eye:	n/a
43	chr6:161354531-161354581	K562	blood:	n/a
44	chr6:161347487-161347537	SK-N-MC	brain:	n/a
45	chr6:161186852-161186902	HL-60	blood:	n/a
46	chr6:161188337-161188387	GM19239	blood:	n/a
47	chr6:161188574-161188624	Jurkat	blood:	n/a
48	chr6:161185585-161185635	BJ	skin:	n/a
49	chr6:161352113-161352163	ovcar-3	ovarian:	n/a
50	chr6:161188638-161188688	BE2_C	brain:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:161346875..161349133-chr6:161350824..161353127,2	MCF-7	breast:
2	chr6:161196367..161198386-chr6:161199110..161200907,2	K562	blood:
3	chr6:161346875..161349133-chr6:161350824..161353127,2	MCF-7	breast:
4	chr6:161196367..161198386-chr6:161199110..161200907,2	K562	blood:
5	chr6:161375159..161377891-chr6:161412077..161413734,2	MCF-7	breast:
6	chr6:161366897..161368711-chr6:161371406..161373943,2	MCF-7	breast:
7	chr6:161323886..161325793-chr6:161330752..161333163,2	K562	blood:
8	chr6:161373053..161374579-chr6:161376569..161379258,2	K562	blood:
9	chr6:161271079..161273454-chr6:161275442..161277966,2	K562	blood:
10	chr6:161295209..161297877-chr6:161302548..161304249,2	K562	blood:
11	chr6:161235361..161237238-chr6:161238681..161240959,2	K562	blood:
12	chr6:161178222..161180525-chr6:161182750..161185405,2	K562	blood:
13	chr6:161366897..161368711-chr6:161371406..161373943,2	MCF-7	breast:
14	chr6:161213757..161216214-chr6:161411268..161413950,3	MCF-7	breast:
15	chr6:161342992..161345118-chr6:161348741..161350289,2	K562	blood:
16	chr6:161183337..161185501-chr6:161187046..161189123,2	K562	blood:
17	chr6:161295209..161297877-chr6:161302548..161304249,2	K562	blood:
18	chr6:161271079..161273700-chr6:161275442..161277966,3	K562	blood:
19	chr6:161362872..161367165-chr6:161367890..161370793,5	K562	blood:
20	chr6:161355190..161357461-chr6:161362771..161365212,2	K562	blood:
21	chr6:161328809..161330497-chr6:161338500..161340123,2	K562	blood:
22	chr6:161282793..161285621-chr6:161332343..161335165,2	K562	blood:
23	chr6:161183337..161185501-chr6:161187046..161189123,2	K562	blood:
24	chr6:161347613..161349495-chr6:161362654..161364258,2	K562	blood:
25	chr6:161231600..161233858-chr6:161239225..161241427,2	K562	blood:
26	chr6:161342992..161345118-chr6:161348741..161350289,2	K562	blood:
27	chr6:161178222..161180525-chr6:161182750..161185405,2	K562	blood:
28	chr6:161322905..161327205-chr6:161327539..161331040,3	K562	blood:
29	chr6:161231600..161233858-chr6:161239225..161241427,2	K562	blood:
30	chr6:161271079..161273454-chr6:161275442..161277966,2	K562	blood:
31	chr6:161235361..161237238-chr6:161238681..161240959,2	K562	blood:
32	chr6:161369702..161372936-chr6:161374234..161376186,3	K562	blood:
33	chr6:161260541..161262340-chr6:161262561..161265121,3	K562	blood:
34	chr6:161248150..161249930-chr6:161255516..161257589,2	K562	blood:
35	chr6:161315007..161317430-chr6:161326001..161327653,2	K562	blood:
36	chr6:161362872..161367165-chr6:161367890..161370793,5	K562	blood:
37	chr6:161347613..161349495-chr6:161362654..161364258,2	K562	blood:
38	chr6:161227565..161229491-chr6:161229972..161232150,2	MCF-7	breast:
39	chr6:161303689..161305703-chr6:161311421..161313341,2	K562	blood:
40	chr6:161255639..161258104-chr6:161293113..161295110,2	K562	blood:
41	chr6:161358647..161361913-chr6:161364919..161367564,3	K562	blood:
42	chr6:161339436..161341259-chr6:161343117..161345271,2	K562	blood:
43	chr6:161303689..161305703-chr6:161311421..161313341,2	K562	blood:
44	chr6:161323886..161325793-chr6:161330752..161333163,2	K562	blood:
45	chr6:161369702..161372936-chr6:161374234..161376186,3	K562	blood:
46	chr6:161369420..161372191-chr6:161411916..161414445,2	MCF-7	breast:
47	chr6:161266955..161270556-chr6:161271678..161274838,4	K562	blood:
48	chr6:161282793..161285621-chr6:161332343..161335165,2	K562	blood:
49	chr6:161185948..161188243-chr6:161411812..161413951,2	K562	blood:
50	chr6:161250769..161254707-chr6:161411304..161414099,3	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPA-3	chr6:161339469-161339681	ENSG00000224371
2	lnc-PLG-3	chr6:161268885-161269038	l_3310_chr6:161267548-161283742_testes
3	lnc-MAP3K4-4	chr6:161311768-161312561	NONHSAT115922
4	lnc-MAP3K4-2	chr6:161347401-161347610	ENSG00000233342
5	lnc-LPA-3	chr6:161293926-161294157	ENSG00000224371
6	lnc-PLG-3	chr6:161268128-161268254	l_3310_chr6:161267548-161283742_testes
7	lnc-MAP3K4-4	chr6:161307675-161307898	NONHSAT115922
8	lnc-PLG-4	chr6:161299991-161300086	NONHSAT115917
9	lnc-PLG-4	chr6:161310740-161310793	NONHSAT115917
10	lnc-PLG-4	chr6:161297593-161297722	NONHSAT115917
11	lnc-MAP3K4-1	chr6:161352112-161352404	XLOC_005529
12	lnc-MAP3K4-2	chr6:161348595-161348656	NONHSAT115924
13	lnc-PLG-3	chr6:161283570-161283773	l_3310_chr6:161267548-161283742_testes
14	lnc-LPA-1	chr6:161227975-161228213	XLOC_005905
15	lnc-LPA-1	chr6:161216349-161216488	XLOC_005905
16	lnc-LPA-2	chr6:161237596-161237875	XLOC_005906
17	lnc-LPA-2	chr6:161236582-161237293	XLOC_005906
18	lnc-LPA-3	chr6:161336811-161336889	ENSG00000224371
19	lnc-LPA-3	chr6:161294048-161294157	ENSG00000224371
20	lnc-MAP3K4-2	chr6:161348026-161348194	ENSG00000233342
21	lnc-LPA-3	chr6:161294118-161294157	ENSG00000224371
22	lnc-PLG-3	chr6:161267549-161267600	l_3310_chr6:161267548-161283742_testes
23	lnc-LPA-2	chr6:161238186-161238383	XLOC_005906
24	lnc-LPA-3	chr6:161339434-161339561	ENSG00000224371
25	lnc-MAP3K4-2	chr6:161348895-161349017	NONHSAT115924
26	lnc-MAP3K4-2	chr6:161347014-161347163	NONHSAT115924
27	lnc-LPA-3	chr6:161336811-161336889	ENSG00000224371
28	lnc-MAP3K4-2	chr6:161348138-161348264	NONHSAT115924
29	lnc-PLG-4	chr6:161272102-161272394	NONHSAT115917
30	lnc-LPA-3	chr6:161293920-161294157	ENSG00000224371
31	lnc-LPA-3	chr6:161321256-161321431	ENSG00000224371
32	lnc-LPA-3	chr6:161339434-161339481	ENSG00000224371
33	lnc-LPA-3	chr6:161336811-161336889	ENSG00000224371
34	lnc-PLG-3	chr6:161268016-161268184	NONHSAT115916
35	lnc-PLG-3	chr6:161267391-161267600	NONHSAT115916
36	lnc-LPA-3	chr6:161301355-161301426	ENSG00000224371

No data

Variant related genes	Relation type
ENSG00000224371	TF binding region
ENSG00000231863	TF binding region
ENSG00000233342	TF binding region
ENSG00000220913	TF binding region
ENSG00000224371	CpG island
ENSG00000231863	CpG island
ENSG00000233342	CpG island
ENSG00000220913	CpG island
ENSG00000085511	chromatin interactions
ENSG00000231863	chromatin interactions
ENSG00000220913	chromatin interactions
ENSG00000233342	chromatin interactions
ENSG00000224371	chromatin interactions
ENSG00000272841	chromatin interactions

Extended variants
information (count: 5573 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:5573 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78410778	chr6:161180045-161180046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149094524	chr6:161180110-161180111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527652171	chr6:161180193-161180194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373846448	chr6:161180198-161180199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576442575	chr6:161180209-161180210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143139560	chr6:161180228-161180229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553326613	chr6:161180241-161180242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201098688	chr6:161180362-161180363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147463306	chr6:161180363-161180364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs58582567	chr6:161180365-161180366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs202163440	chr6:161180366-161180367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1084658	chr6:161180477-161180478	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs11969328	chr6:161180493-161180494	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541129298	chr6:161180507-161180508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183141073	chr6:161180508-161180509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116716500	chr6:161180533-161180534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117052245	chr6:161180575-161180576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537581279	chr6:161180609-161180610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529571041	chr6:161180617-161180618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113680885	chr6:161180619-161180620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151213837	chr6:161180657-161180658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559360117	chr6:161180661-161180662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528429389	chr6:161180665-161180666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368689401	chr6:161180691-161180692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544698350	chr6:161180731-161180732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185993938	chr6:161180754-161180755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140393431	chr6:161180755-161180756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146919714	chr6:161180781-161180782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192024696	chr6:161180787-161180788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569864816	chr6:161180820-161180821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs137946234	chr6:161180829-161180830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183883545	chr6:161180964-161180965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572009627	chr6:161180991-161180992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546876986	chr6:161180993-161180994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143502340	chr6:161181033-161181034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145901294	chr6:161181084-161181085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115426297	chr6:161181108-161181109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79983377	chr6:161181115-161181116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116480834	chr6:161181133-161181134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573885515	chr6:161181161-161181162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542921765	chr6:161181174-161181175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559590156	chr6:161181206-161181207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377509888	chr6:161181214-161181215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551519131	chr6:161181259-161181260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1084657	chr6:161181271-161181272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs74570655	chr6:161181290-161181291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1084656	chr6:161181292-161181293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs74341379	chr6:161181339-161181340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548981298	chr6:161181348-161181349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549317922	chr6:161181475-161181476	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1111 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161169600-161181400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:161171400-161187800	Weak transcription	Pancreas	Pancrea
3	chr6:161179000-161186000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:161181400-161181600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:161181400-161187800	Weak transcription	Gastric	stomach
6	chr6:161181600-161187800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:161185200-161187600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr6:161185600-161186000	Weak transcription	Fetal Kidney	kidney
9	chr6:161185600-161187800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:161186000-161186200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:161186000-161186200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:161186000-161186200	ZNF genes & repeats	Fetal Kidney	kidney
13	chr6:161186000-161186400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:161186200-161187600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:161186400-161187600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr6:161186800-161187000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:161187000-161188800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:161187400-161187600	Active TSS	GM12878-XiMat	blood
19	chr6:161187400-161188800	Active TSS	Fetal Brain Female	brain
20	chr6:161187600-161187800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr6:161187600-161187800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr6:161187600-161187800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:161187600-161187800	Enhancers	Brain Angular Gyrus	brain
24	chr6:161187600-161187800	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr6:161187600-161187800	Enhancers	Colon Smooth Muscle	Colon
26	chr6:161187600-161187800	Bivalent Enhancer	HepG2	liver
27	chr6:161187600-161187800	Enhancers	HMEC	breast
28	chr6:161187600-161188000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr6:161187600-161188000	Active TSS	Fetal Brain Male	brain
30	chr6:161187600-161188000	Flanking Active TSS	GM12878-XiMat	blood
31	chr6:161187600-161188400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
32	chr6:161187600-161188400	Enhancers	Primary B cells from peripheral blood	blood
33	chr6:161187600-161188600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
34	chr6:161187600-161188600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:161187600-161188600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr6:161187600-161188600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr6:161187600-161188600	Active TSS	Brain Cingulate Gyrus	brain
38	chr6:161187600-161188600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr6:161187600-161188800	Active TSS	Brain Anterior Caudate	brain
40	chr6:161187600-161188800	Enhancers	Fetal Lung	lung
41	chr6:161187600-161188800	Active TSS	NHEK	skin
42	chr6:161187800-161188000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
43	chr6:161187800-161188000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr6:161187800-161188000	Enhancers	Adipose Nuclei	Adipose
45	chr6:161187800-161188000	Enhancers	Aorta	Aorta
46	chr6:161187800-161188000	Active TSS	Liver	Liver
47	chr6:161187800-161188000	Enhancers	Esophagus	oesophagus
48	chr6:161187800-161188000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr6:161187800-161188000	Enhancers	Fetal Intestine Large	intestine
50	chr6:161187800-161188000	Enhancers	Gastric	stomach

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