Variant report

Variant	esv3363304
Chromosome Location	chr10:5931446-5933494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:613)
CpG islands
(count:611)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5931877-5932245	K562	blood:	n/a	n/a
2	ARID3A	chr10:5932049-5932198	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5931651-5931754	HepG2	liver:	n/a	n/a
4	ATF3	chr10:5931695-5932281	A549	lung:	n/a	chr10:5932023-5932032
5	BACH1	chr10:5931401-5931955	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:5932914-5932939	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr10:5931463-5932191	A549	lung:	n/a	chr10:5932161-5932170 chr10:5931971-5931980 chr10:5931889-5931898 chr10:5932151-5932164 chr10:5932126-5932139 chr10:5931916-5931929
8	BCLAF1	chr10:5931512-5932467	GM12878	blood:	n/a	chr10:5932161-5932170 chr10:5931971-5931980 chr10:5931889-5931898 chr10:5932151-5932164 chr10:5932126-5932139 chr10:5931916-5931929
9	BHLHE40	chr10:5931726-5931999	A549	lung:	n/a	chr10:5931974-5931990 chr10:5931975-5931991 chr10:5931892-5931908
10	BHLHE40	chr10:5932852-5933157	K562	blood:	n/a	n/a
11	BHLHE40	chr10:5931505-5932228	K562	blood:	n/a	chr10:5931974-5931990 chr10:5931536-5931552 chr10:5931975-5931991 chr10:5931892-5931908
12	BHLHE40	chr10:5931518-5932298	GM12878	blood:	n/a	chr10:5931974-5931990 chr10:5931536-5931552 chr10:5931975-5931991 chr10:5931892-5931908
13	BHLHE40	chr10:5931625-5932271	HepG2	liver:	n/a	chr10:5931974-5931990 chr10:5931975-5931991 chr10:5931892-5931908
14	BRCA1	chr10:5931646-5931837	HepG2	liver:	n/a	n/a
15	BRCA1	chr10:5931934-5932171	GM12878	blood:	n/a	n/a
16	BRCA1	chr10:5931803-5932228	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr10:5932063-5932196	HepG2	liver:	n/a	n/a
18	CBX3	chr10:5931531-5932061	K562	blood:	n/a	n/a
19	CCNT2	chr10:5930870-5932737	K562	blood:	n/a	chr10:5931902-5931911
20	CEBPB	chr10:5931966-5932138	K562	blood:	n/a	n/a
21	CEBPB	chr10:5932656-5932775	HepG2	liver:	n/a	n/a
22	CEBPB	chr10:5931867-5932047	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr10:5931955-5932135	HepG2	liver:	n/a	n/a
24	CEBPD	chr10:5931594-5932389	HepG2	liver:	n/a	n/a
25	CEBPZ	chr10:5933110-5933187	HepG2	liver:	n/a	n/a
26	CEBPZ	chr10:5931869-5932256	HepG2	liver:	n/a	n/a
27	CHD1	chr10:5932701-5932851	GM12878	blood:	n/a	n/a
28	CHD1	chr10:5931577-5931851	GM12878	blood:	n/a	n/a
29	CHD2	chr10:5931841-5932316	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr10:5932733-5932893	HepG2	liver:	n/a	n/a
31	CHD2	chr10:5931648-5932237	HepG2	liver:	n/a	n/a
32	CHD2	chr10:5930896-5932368	GM12878	blood:	n/a	n/a
33	CHD2	chr10:5931646-5932319	K562	blood:	n/a	n/a
34	CHD2	chr10:5931625-5932406	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr10:5931370-5932658	A549	lung:	n/a	n/a
36	CREB1	chr10:5931768-5932382	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr10:5931603-5932372	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr10:5931550-5932337	K562	blood:	n/a	n/a
39	CREB1	chr10:5931478-5932935	HepG2	liver:	n/a	n/a
40	CREB1	chr10:5931453-5932411	GM12878	blood:	n/a	n/a
41	CREB1	chr10:5931708-5932209	ECC-1	luminal epithelium:	n/a	n/a
42	CREB1	chr10:5931828-5932223	A549	lung:	n/a	n/a
43	CTCF	chr10:5930921-5931449	GM12878	blood:	n/a	n/a
44	CTCF	chr10:5932087-5932419	K562	blood:	n/a	chr10:5932131-5932144 chr10:5932131-5932144
45	CTCF	chr10:5932140-5932290	GM12872	blood:	n/a	n/a
46	CTCF	chr10:5932460-5932610	GM12865	blood:	n/a	n/a
47	CTCF	chr10:5931620-5931770	AG04449	skin:	n/a	n/a
48	CTCF	chr10:5932100-5932250	GM12865	blood:	n/a	chr10:5932131-5932144 chr10:5932131-5932144
49	CTCF	chr10:5932420-5932570	GM12873	blood:	n/a	n/a
50	CTCF	chr10:5932080-5932230	GM12871	blood:	n/a	chr10:5932131-5932144 chr10:5932131-5932144

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5932028-5932078	K562	blood:	n/a
2	chr10:5932028-5932078	K562	blood:	n/a
3	chr10:5931975-5932025	MCF-7	breast:	n/a
4	chr10:5932028-5932078	NHBE	bronchial:	n/a
5	chr10:5931975-5932025	Hela-S3	cervix:	n/a
6	chr10:5932028-5932078	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:5931975-5932025	Jurkat	blood:	n/a
8	chr10:5931970-5932020	ovcar-3	ovarian:	n/a
9	chr10:5932028-5932078	PrEC	prostate:	n/a
10	chr10:5932453-5932503	CMK	blood:	n/a
11	chr10:5932028-5932078	HCPEpiC	choroid plexus:	n/a
12	chr10:5932453-5932503	NHDF-neo	bronchial:	n/a
13	chr10:5932453-5932503	GM12891	blood:	n/a
14	chr10:5932028-5932078	SKMC	muscle:	n/a
15	chr10:5932529-5932579	SK-N-SH	brain:	n/a
16	chr10:5932453-5932503	MCF10A-Er-Src	breast:	n/a
17	chr10:5932529-5932579	SAEC	small airway:	n/a
18	chr10:5932028-5932078	GM19239	blood:	n/a
19	chr10:5931821-5931871	HMEC	breast:	n/a
20	chr10:5932529-5932579	AG10803	skin:	n/a
21	chr10:5931783-5931833	GM12891	blood:	n/a
22	chr10:5932453-5932503	H1-hESC	embryonic stem cell:	embryo
23	chr10:5931880-5931930	NHBE	bronchial:	n/a
24	chr10:5931821-5931871	ProgFib	skin:	n/a
25	chr10:5932043-5932093	AG04449	skin:	fetal
26	chr10:5931970-5932020	ECC-1	luminal epithelium:	n/a
27	chr10:5932453-5932503	U87	brain:	n/a
28	chr10:5931975-5932025	HMEC	breast:	n/a
29	chr10:5932028-5932078	HCF	heart:	n/a
30	chr10:5932700-5932750	SK-N-SH	brain:	n/a
31	chr10:5931970-5932020	H1-hESC	embryonic stem cell:	embryo
32	chr10:5931970-5932020	HRCEpiC	kidney:	n/a
33	chr10:5931783-5931833	HCT-116	colon:	n/a
34	chr10:5932453-5932503	AoSMC	blood vessel:	n/a
35	chr10:5932529-5932579	Hepatocyte	liver:	n/a
36	chr10:5931783-5931833	HRPEpiC	eye:	n/a
37	chr10:5931821-5931871	GM12892	blood:	n/a
38	chr10:5932700-5932750	HRPEpiC	eye:	n/a
39	chr10:5931783-5931833	SAEC	small airway:	n/a
40	chr10:5932700-5932750	AG10803	skin:	n/a
41	chr10:5932028-5932078	AG04450	lung:	fetal
42	chr10:5932043-5932093	GM06990	blood:	n/a
43	chr10:5931880-5931930	PFSK-1	brain:	n/a
44	chr10:5931821-5931871	CMK	blood:	n/a
45	chr10:5932028-5932078	HNPCEpiC	eye:	n/a
46	chr10:5932453-5932503	PrEC	prostate:	n/a
47	chr10:5932529-5932579	SK-N-MC	brain:	n/a
48	chr10:5931821-5931871	HCM	heart:	n/a
49	chr10:5932043-5932093	AG10803	skin:	n/a
50	chr10:5931970-5932020	NHBE	bronchial:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5725559..5728313-chr10:5930802..5933492,3	K562	blood:
2	chr10:5930398..5933295-chr10:6184026..6187985,3	K562	blood:
3	chr10:5725094..5729377-chr10:5927689..5933777,6	MCF-7	breast:
4	chr10:5933201..5936012-chr10:6019635..6021875,2	K562	blood:
5	chr10:5488345..5491486-chr10:5930515..5933192,3	MCF-7	breast:
6	chr10:5930925..5933506-chr10:6244058..6246915,2	MCF-7	breast:
7	chr10:5932395..5934386-chr10:6130743..6132352,2	K562	blood:
8	chr10:5853532..5857435-chr10:5928623..5934190,13	MCF-7	breast:
9	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:
10	chr10:5904346..5907644-chr10:5928919..5931742,3	MCF-7	breast:
11	chr10:5707177..5709381-chr10:5931479..5933432,3	MCF-7	breast:
12	chr10:5707419..5708953-chr10:5931052..5933501,2	MCF-7	breast:
13	chr10:5931081..5933467-chr10:5942750..5946622,4	MCF-7	breast:
14	chr10:5931600..5932308-chr17:37009547..37010442,2	HCT-116	colon:
15	chr10:5931810..5933817-chr10:6018457..6020176,2	MCF-7	breast:
16	chr10:5852595..5861125-chr10:5921136..5936216,31	MCF-7	breast:
17	chr10:5930440..5932910-chr10:5957697..5960803,4	MCF-7	breast:
18	chr10:5853439..5857708-chr10:5926443..5936823,24	K562	blood:
19	chr10:5931780..5932593-chr11:2720733..2721352,2	HCT-116	colon:
20	chr10:5931232..5931977-chr12:46383975..46384769,2	Hela-S3	cervix:
21	chr10:5836323..5837944-chr10:5932347..5934576,2	K562	blood:
22	chr10:5853820..5856785-chr10:5927225..5934067,15	K562	blood:

No data

Variant related genes	Relation type
ANKRD16	TF binding region
FBXO18	TF binding region
ANKRD16	CpG island
FBXO18	CpG island
ENSG00000134452	chromatin interactions
ENSG00000170525	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000269821	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000125691	chromatin interactions
ENSG00000240180	chromatin interactions
ENSG00000213994	chromatin interactions
ENSG00000139218	chromatin interactions
ENSG00000134470	chromatin interactions
ENSG00000134453	chromatin interactions
ENSG00000272764	chromatin interactions

Extended variants
information (count: 72 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:72 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs59772576	chr10:5931468-5931469	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs560672441	chr10:5931521-5931522	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs562860237	chr10:5931586-5931587	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs547611806	chr10:5931600-5931601	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs559491121	chr10:5931604-5931605	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs529819712	chr10:5931637-5931638	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs548164965	chr10:5931641-5931642	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs115355428	chr10:5931656-5931657	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs569682714	chr10:5931673-5931674	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs537719191	chr10:5931693-5931694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs375978123	chr10:5931739-5931740	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs572269472	chr10:5931783-5931784	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs571156665	chr10:5931789-5931790	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs534896779	chr10:5931849-5931850	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
15	rs553576700	chr10:5931869-5931870	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
16	rs568175490	chr10:5931874-5931875	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs535569402	chr10:5931877-5931878	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs373037352	chr10:5931911-5931912	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
19	rs116838509	chr10:5931939-5931940	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs575212860	chr10:5931963-5931964	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
21	rs546215804	chr10:5932018-5932019	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs367737877	chr10:5932066-5932067	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs577118836	chr10:5932090-5932091	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs140731596	chr10:5932100-5932101	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs559594721	chr10:5932158-5932159	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs2253422	chr10:5932187-5932188	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188143833	chr10:5932193-5932194	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs563398903	chr10:5932194-5932195	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs145906182	chr10:5932200-5932201	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs530409122	chr10:5932210-5932211	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs552190463	chr10:5932259-5932260	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs531634049	chr10:5932286-5932287	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs571053574	chr10:5932367-5932368	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
34	rs191098822	chr10:5932394-5932395	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
35	rs546757442	chr10:5932397-5932398	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs568338664	chr10:5932412-5932413	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs369781423	chr10:5932413-5932414	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs557021465	chr10:5932443-5932444	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs569375692	chr10:5932448-5932449	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs10905405	chr10:5932475-5932476	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576002252	chr10:5932477-5932478	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs375522978	chr10:5932487-5932488	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
43	rs10905406	chr10:5932491-5932492	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
44	rs541330902	chr10:5932625-5932626	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
45	rs565358882	chr10:5932655-5932656	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs553173438	chr10:5932662-5932663	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs574661096	chr10:5932701-5932702	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs111248081	chr10:5932707-5932708	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs189442789	chr10:5932738-5932739	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs563362188	chr10:5932752-5932753	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5930200-5932600	Active TSS	Fetal Muscle Trunk	muscle
2	chr10:5930400-5931800	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr10:5930400-5931800	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr10:5930400-5931800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr10:5930600-5932600	Active TSS	H1 Cell Line	embryonic stem cell
6	chr10:5930600-5932600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:5930600-5932600	Active TSS	Aorta	Aorta
8	chr10:5930600-5932800	Active TSS	Fetal Intestine Small	intestine
9	chr10:5930600-5933000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:5930600-5933000	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr10:5930600-5933000	Active TSS	GM12878-XiMat	blood
12	chr10:5930600-5933200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr10:5930600-5933200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr10:5930600-5933400	Active TSS	Ovary	ovary
15	chr10:5930600-5933600	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr10:5930800-5931800	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
17	chr10:5930800-5932600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:5930800-5932600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr10:5930800-5932600	Active TSS	Brain Anterior Caudate	brain
20	chr10:5930800-5932600	Active TSS	Brain Hippocampus Middle	brain
21	chr10:5930800-5932600	Active TSS	Brain Substantia Nigra	brain
22	chr10:5930800-5932600	Active TSS	Left Ventricle	heart
23	chr10:5930800-5932600	Active TSS	Placenta Amnion	Placenta Amnion
24	chr10:5930800-5932800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr10:5930800-5932800	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr10:5930800-5932800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
27	chr10:5930800-5932800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr10:5930800-5932800	Active TSS	Colon Smooth Muscle	Colon
29	chr10:5930800-5932800	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr10:5930800-5932800	Active TSS	Fetal Kidney	kidney
31	chr10:5930800-5932800	Active TSS	Fetal Stomach	stomach
32	chr10:5930800-5932800	Active TSS	Rectal Smooth Muscle	rectum
33	chr10:5930800-5932800	Active TSS	HSMMtube	muscle
34	chr10:5930800-5932800	Active TSS	Osteobl	bone
35	chr10:5930800-5933000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
36	chr10:5930800-5933000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr10:5930800-5933000	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr10:5930800-5933000	Active TSS	Small Intestine	intestine
39	chr10:5930800-5933000	Active TSS	A549	lung
40	chr10:5930800-5933200	Active TSS	H9 Cell Line	embryonic stem cell
41	chr10:5930800-5933200	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr10:5930800-5933400	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr10:5930800-5933400	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr10:5931000-5931600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:5931000-5932400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
46	chr10:5931000-5932600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr10:5931000-5932600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr10:5931000-5932600	Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr10:5931000-5932600	Active TSS	Primary B cells from peripheral blood	blood
50	chr10:5931000-5932600	Active TSS	Primary T cells from cord blood	blood

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