Variant report

Variant	esv3427182
Chromosome Location	chr6:161411987-161414535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:755)
CpG islands
(count:550)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:161413850-161414311	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:161412215-161412877	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:161413548-161414155	K562	blood:	n/a	n/a
4	ATF2	chr6:161412619-161412999	GM12878	blood:	n/a	n/a
5	ATF3	chr6:161412279-161413050	K562	blood:	n/a	chr6:161412490-161412499 chr6:161412408-161412419
6	BACH1	chr6:161414044-161414221	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr6:161412224-161413018	GM12878	blood:	n/a	chr6:161412563-161412576 chr6:161412933-161412942 chr6:161412794-161412807 chr6:161412934-161412947
8	BHLHE40	chr6:161412465-161413077	HepG2	liver:	n/a	chr6:161412693-161412709
9	BHLHE40	chr6:161413323-161414140	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:161411973-161414136	K562	blood:	n/a	chr6:161412693-161412709
11	BHLHE40	chr6:161412462-161414137	GM12878	blood:	n/a	chr6:161412693-161412709
12	BRCA1	chr6:161412573-161412847	HepG2	liver:	n/a	n/a
13	CBX3	chr6:161412044-161414226	K562	blood:	n/a	n/a
14	CCNT2	chr6:161412039-161413458	K562	blood:	n/a	chr6:161412681-161412690
15	CEBPD	chr6:161412401-161413021	HepG2	liver:	n/a	n/a
16	CEBPD	chr6:161412039-161413107	K562	blood:	n/a	n/a
17	CHD1	chr6:161413158-161413422	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr6:161412618-161413551	GM12878	blood:	n/a	chr6:161412623-161412633 chr6:161412679-161412689
19	CHD1	chr6:161411694-161414825	IMR90	lung:	n/a	chr6:161412623-161412633 chr6:161412679-161412689
20	CHD1	chr6:161412414-161412416	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr6:161412606-161412947	HepG2	liver:	n/a	chr6:161412623-161412633 chr6:161412679-161412689
22	CHD2	chr6:161413245-161413463	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr6:161412476-161413384	K562	blood:	n/a	chr6:161412623-161412633 chr6:161412679-161412689
24	CHD2	chr6:161412225-161412915	Hela-S3	cervix:	n/a	chr6:161412623-161412633 chr6:161412679-161412689
25	CHD2	chr6:161413754-161414037	GM12878	blood:	n/a	n/a
26	CHD2	chr6:161412157-161412973	GM12878	blood:	n/a	chr6:161412623-161412633 chr6:161412679-161412689
27	CHD2	chr6:161412803-161412976	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:161412310-161412578	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr6:161412255-161413641	GM12878	blood:	n/a	n/a
30	CREB1	chr6:161412231-161412996	A549	lung:	n/a	n/a
31	CREB1	chr6:161412283-161412778	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr6:161412151-161413649	HepG2	liver:	n/a	n/a
33	CREB1	chr6:161412187-161414204	K562	blood:	n/a	n/a
34	CTBP2	chr6:161412277-161412912	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:161413900-161414050	K562	blood:	n/a	n/a
36	CTCF	chr6:161413920-161414070	BJ	skin:	n/a	n/a
37	CTCF	chr6:161413480-161413630	GM12870	blood:	n/a	n/a
38	CTCF	chr6:161413877-161414097	GM10266	blood:	n/a	n/a
39	CTCF	chr6:161413200-161413350	AG04449	skin:	n/a	chr6:161413232-161413245
40	CTCF	chr6:161413920-161414070	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr6:161413900-161414050	HMF	breast:	n/a	n/a
42	CTCF	chr6:161413869-161414115	LNCaP	prostate:	n/a	n/a
43	CTCF	chr6:161413940-161414090	HepG2	liver:	n/a	n/a
44	CTCF	chr6:161413880-161414030	HCT-116	colon:	n/a	n/a
45	CTCF	chr6:161413920-161414070	AG10803	skin:	n/a	n/a
46	CTCF	chr6:161412640-161412790	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr6:161413900-161414050	Caco-2	colon:	n/a	n/a
48	CTCF	chr6:161412520-161412670	GM12872	blood:	n/a	chr6:161412601-161412614 chr6:161412604-161412617
49	CTCF	chr6:161413786-161414137	A549	lung:	n/a	n/a
50	CTCF	chr6:161413920-161414070	NHDF-neo	bronchial:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:161413652-161413702	AoSMC	blood vessel:	n/a
2	chr6:161413652-161413702	AoSMC	blood vessel:	n/a
3	chr6:161413055-161413105	K562	blood:	n/a
4	chr6:161413055-161413105	AG04450	lung:	fetal
5	chr6:161413433-161413483	HAEpiC	amniotic membrane:	n/a
6	chr6:161412518-161412568	NB4	blood:	n/a
7	chr6:161413652-161413702	HRE	kidney:	n/a
8	chr6:161413055-161413105	HAEpiC	amniotic membrane:	n/a
9	chr6:161413484-161413534	GM06990	blood:	n/a
10	chr6:161413484-161413534	PANC-1	pancreas:	n/a
11	chr6:161413442-161413492	ovcar-3	ovarian:	n/a
12	chr6:161413442-161413492	AoSMC	blood vessel:	n/a
13	chr6:161412392-161412442	T-47D	breast:	n/a
14	chr6:161412518-161412568	HepG2	liver:	n/a
15	chr6:161413652-161413702	GM12891	blood:	n/a
16	chr6:161413652-161413702	A549	lung:	n/a
17	chr6:161413433-161413483	ProgFib	skin:	n/a
18	chr6:161412392-161412442	K562	blood:	n/a
19	chr6:161412505-161412555	AG09319	gingival:	n/a
20	chr6:161413484-161413534	HRCEpiC	kidney:	n/a
21	chr6:161413442-161413492	HL-60	blood:	n/a
22	chr6:161412518-161412568	PFSK-1	brain:	n/a
23	chr6:161413442-161413492	MCF-7	breast:	n/a
24	chr6:161412505-161412555	MCF-7	breast:	n/a
25	chr6:161413126-161413176	GM12878	blood:	n/a
26	chr6:161412518-161412568	NT2-D1	testis:	n/a
27	chr6:161413126-161413176	HL-60	blood:	n/a
28	chr6:161413484-161413534	PrEC	prostate:	n/a
29	chr6:161412392-161412442	NH-A	brain:	n/a
30	chr6:161413442-161413492	HRCEpiC	kidney:	n/a
31	chr6:161413442-161413492	HRE	kidney:	n/a
32	chr6:161413652-161413702	NT2-D1	testis:	n/a
33	chr6:161412392-161412442	HUVEC	blood vessel:	n/a
34	chr6:161413652-161413702	H1-hESC	embryonic stem cell:	embryo
35	chr6:161412392-161412442	HCF	heart:	n/a
36	chr6:161412505-161412555	GM12891	blood:	n/a
37	chr6:161412392-161412442	HCT-116	colon:	n/a
38	chr6:161412505-161412555	AG10803	skin:	n/a
39	chr6:161413484-161413534	ECC-1	luminal epithelium:	n/a
40	chr6:161413126-161413176	GM06990	blood:	n/a
41	chr6:161413652-161413702	GM06990	blood:	n/a
42	chr6:161413652-161413702	AG09319	gingival:	n/a
43	chr6:161413055-161413105	IMR90	lung:	fetal
44	chr6:161413652-161413702	AG04450	lung:	fetal
45	chr6:161413442-161413492	SK-N-SH	brain:	n/a
46	chr6:161412505-161412555	NHDF-neo	bronchial:	n/a
47	chr6:161413055-161413105	RPTEC	kidney:	n/a
48	chr6:161413433-161413483	HEEpiC	esophagus:	n/a
49	chr6:161413652-161413702	Hela-S3	cervix:	n/a
50	chr6:161413055-161413105	PANC-1	pancreas:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:161411809..161413437-chr6:161693885..161696604,2	K562	blood:
2	chr6:161411531..161413327-chr6:161653025..161655728,2	K562	blood:
3	chr6:161411372..161413087-chr6:161442452..161444110,2	K562	blood:
4	chr6:161414058..161416452-chr6:161484999..161486533,2	K562	blood:
5	chr6:161413545..161416445-chr6:161589800..161592180,2	K562	blood:
6	chr6:160940621..160941316-chr6:161413631..161414342,2	MCF-7	breast:
7	chr6:161413290..161415523-chr6:161493926..161495745,2	K562	blood:
8	chr6:161153719..161154752-chr6:161413517..161414074,3	K562	blood:
9	chr6:161171347..161171874-chr6:161413503..161414501,3	K562	blood:
10	chr6:161412566..161414577-chr6:161651798..161653599,2	K562	blood:
11	chr6:161349966..161354183-chr6:161410810..161413824,4	MCF-7	breast:
12	chr6:158243442..158245618-chr6:161412032..161413556,2	K562	blood:
13	chr6:161300742..161302528-chr6:161411919..161413550,2	K562	blood:
14	chr6:161351755..161352361-chr6:161413554..161414480,3	MCF-7	breast:
15	chr6:161409929..161412719-chr6:161465318..161467396,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGPAT4-1	chr6:161411382-161412758	NONHSAT115928
2	lnc-AGPAT4-1	chr6:161411350-161413374	ENSG00000272841.1

No data

Variant related genes	Relation type
ENSG00000272841	TF binding region
MAP3K4	TF binding region
ENSG00000272841	CpG island
MAP3K4	CpG island
ENSG00000026652	chromatin interactions
ENSG00000231863	chromatin interactions
ENSG00000130340	chromatin interactions
ENSG00000085511	chromatin interactions
ENSG00000224371	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570380693	chr6:161412062-161412063	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
2	rs532925730	chr6:161412119-161412120	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
3	rs528224844	chr6:161412131-161412132	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
4	rs142364326	chr6:161412161-161412162	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
5	rs568027251	chr6:161412224-161412225	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
6	rs142843134	chr6:161412280-161412281	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
7	rs9456608	chr6:161412320-161412321	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs147436460	chr6:161412400-161412401	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
9	rs183410009	chr6:161412411-161412412	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
10	rs71565784	chr6:161412419-161412420	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs565909602	chr6:161412494-161412495	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
12	rs188640681	chr6:161412519-161412520	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
13	rs118093782	chr6:161412564-161412565	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
14	rs192760198	chr6:161412584-161412585	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
15	rs373585339	chr6:161412597-161412598	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
16	rs137869356	chr6:161412608-161412609	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
17	rs75587077	chr6:161412633-161412634	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
18	rs574191268	chr6:161412643-161412644	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
19	rs543109354	chr6:161412684-161412685	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
20	rs561885881	chr6:161412707-161412708	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
21	rs201449441	chr6:161412732-161412733	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
22	rs71913884	chr6:161412733-161412734	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
23	rs572182643	chr6:161412768-161412769	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs368064120	chr6:161412775-161412776	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs541001091	chr6:161412809-161412810	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
26	rs564395695	chr6:161412812-161412813	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
27	rs532833960	chr6:161412905-161412906	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs367947922	chr6:161412934-161412935	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs370613797	chr6:161412938-161412939	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs548649049	chr6:161412954-161412955	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs566178445	chr6:161412973-161412974	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
32	rs535214105	chr6:161412994-161412995	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs551836413	chr6:161413038-161413039	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs78823261	chr6:161413041-161413042	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs569609736	chr6:161413044-161413045	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs369151355	chr6:161413045-161413046	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs537306423	chr6:161413080-161413081	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs371606483	chr6:161413099-161413100	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs374317318	chr6:161413128-161413129	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs574054977	chr6:161413133-161413134	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs536771398	chr6:161413180-161413181	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs662541	chr6:161413211-161413212	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs539381316	chr6:161413221-161413222	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs572186997	chr6:161413244-161413245	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs541216477	chr6:161413268-161413269	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs564078817	chr6:161413272-161413273	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs371625824	chr6:161413275-161413276	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs543275467	chr6:161413279-161413280	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs559290424	chr6:161413282-161413283	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs562976075	chr6:161413328-161413329	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161411200-161414000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:161411200-161414600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:161411600-161412000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:161411600-161412000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:161411600-161412000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:161411600-161412000	Enhancers	Brain Germinal Matrix	brain
7	chr6:161411600-161412000	Enhancers	HSMM	muscle
8	chr6:161411600-161412200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:161411600-161412400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:161411600-161412600	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr6:161411600-161414000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:161411600-161414200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:161411600-161414400	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr6:161411800-161412000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:161411800-161412000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr6:161411800-161412000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
17	chr6:161411800-161412000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
18	chr6:161411800-161412000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr6:161411800-161412000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:161411800-161412000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr6:161411800-161412000	Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr6:161411800-161412000	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr6:161411800-161412000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr6:161411800-161412000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:161411800-161412000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:161411800-161412000	Enhancers	Adipose Nuclei	Adipose
27	chr6:161411800-161412000	Enhancers	Liver	Liver
28	chr6:161411800-161412000	Enhancers	Brain Anterior Caudate	brain
29	chr6:161411800-161412000	Enhancers	Brain Hippocampus Middle	brain
30	chr6:161411800-161412000	Enhancers	Duodenum Mucosa	Duodenum
31	chr6:161411800-161412000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr6:161411800-161412000	Enhancers	Fetal Heart	heart
33	chr6:161411800-161412000	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr6:161411800-161412000	Bivalent Enhancer	Dnd41	blood
35	chr6:161411800-161412000	Flanking Active TSS	HepG2	liver
36	chr6:161411800-161412000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
37	chr6:161411800-161412000	Flanking Active TSS	NHDF-Ad	bronchial
38	chr6:161411800-161412000	Flanking Active TSS	Osteobl	bone
39	chr6:161411800-161412200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr6:161411800-161412200	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr6:161411800-161412200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr6:161411800-161412200	Flanking Active TSS	Fetal Brain Female	brain
43	chr6:161411800-161412200	Flanking Active TSS	Fetal Intestine Small	intestine
44	chr6:161411800-161412200	Flanking Active TSS	A549	lung
45	chr6:161411800-161412200	Flanking Active TSS	HUVEC	blood vessel
46	chr6:161411800-161412400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:161411800-161412400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr6:161411800-161412600	Active TSS	Fetal Brain Male	brain
49	chr6:161411800-161413400	Active TSS	Fetal Lung	lung
50	chr6:161411800-161414000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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