Variant report

Variant	esv3360468
Chromosome Location	chr10:5930971-5933519
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:797)
CpG islands
(count:611)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:797 , 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	chr10:5931651-5931754	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5932049-5932198	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5931877-5932245	K562	blood:	n/a	n/a
4	ATF3	chr10:5931695-5932281	A549	lung:	n/a	chr10:5932023-5932032
5	BACH1	chr10:5930890-5931185	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:5932914-5932939	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:5931401-5931955	H1-hESC	embryonic stem cell:	n/a	n/a
8	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
9	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
10	BHLHE40	chr10:5930389-5931229	HepG2	liver:	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	chr10:5930868-5931281	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:5931726-5931999	A549	lung:	n/a	chr10:5931974-5931990 chr10:5931975-5931991 chr10:5931892-5931908
14	BHLHE40	chr10:5931518-5932298	GM12878	blood:	n/a	chr10:5931974-5931990 chr10:5931536-5931552 chr10:5931975-5931991 chr10:5931892-5931908
15	BHLHE40	chr10:5931625-5932271	HepG2	liver:	n/a	chr10:5931974-5931990 chr10:5931975-5931991 chr10:5931892-5931908
16	BHLHE40	chr10:5932852-5933157	K562	blood:	n/a	n/a
17	BRCA1	chr10:5932063-5932196	HepG2	liver:	n/a	n/a
18	BRCA1	chr10:5931934-5932171	GM12878	blood:	n/a	n/a
19	BRCA1	chr10:5931646-5931837	HepG2	liver:	n/a	n/a
20	BRCA1	chr10:5931803-5932228	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr10:5931531-5932061	K562	blood:	n/a	n/a
22	CCNT2	chr10:5930870-5932737	K562	blood:	n/a	chr10:5931902-5931911
23	CEBPB	chr10:5932656-5932775	HepG2	liver:	n/a	n/a
24	CEBPB	chr10:5931955-5932135	HepG2	liver:	n/a	n/a
25	CEBPB	chr10:5931966-5932138	K562	blood:	n/a	n/a
26	CEBPB	chr10:5931867-5932047	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr10:5930844-5931237	HepG2	liver:	n/a	n/a
28	CEBPD	chr10:5931594-5932389	HepG2	liver:	n/a	n/a
29	CEBPZ	chr10:5933110-5933187	HepG2	liver:	n/a	n/a
30	CEBPZ	chr10:5931869-5932256	HepG2	liver:	n/a	n/a
31	CHD1	chr10:5931577-5931851	GM12878	blood:	n/a	n/a
32	CHD1	chr10:5932701-5932851	GM12878	blood:	n/a	n/a
33	CHD1	chr10:5931037-5931372	GM12878	blood:	n/a	n/a
34	CHD1	chr10:5930881-5931123	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr10:5931646-5932319	K562	blood:	n/a	n/a
36	CHD2	chr10:5930896-5932368	GM12878	blood:	n/a	n/a
37	CHD2	chr10:5931648-5932237	HepG2	liver:	n/a	n/a
38	CHD2	chr10:5932733-5932893	HepG2	liver:	n/a	n/a
39	CHD2	chr10:5931625-5932406	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr10:5931841-5932316	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr10:5931768-5932382	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr10:5931708-5932209	ECC-1	luminal epithelium:	n/a	n/a
43	CREB1	chr10:5931370-5932658	A549	lung:	n/a	n/a
44	CREB1	chr10:5931603-5932372	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr10:5931550-5932337	K562	blood:	n/a	n/a
46	CREB1	chr10:5931828-5932223	A549	lung:	n/a	n/a
47	CREB1	chr10:5931478-5932935	HepG2	liver:	n/a	n/a
48	CREB1	chr10:5931453-5932411	GM12878	blood:	n/a	n/a
49	CTCF	chr10:5931160-5931310	GM12868	blood:	n/a	n/a
50	CTCF	chr10:5931160-5931310	AG04449	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5931975-5932025	K562	blood:	n/a
2	chr10:5931975-5932025	K562	blood:	n/a
3	chr10:5931880-5931930	Jurkat	blood:	n/a
4	chr10:5932028-5932078	T-47D	breast:	n/a
5	chr10:5932043-5932093	PFSK-1	brain:	n/a
6	chr10:5932529-5932579	U87	brain:	n/a
7	chr10:5932028-5932078	BE2_C	brain:	n/a
8	chr10:5931783-5931833	SK-N-SH_RA	brain:	n/a
9	chr10:5932028-5932078	NB4	blood:	n/a
10	chr10:5931783-5931833	AG04450	lung:	fetal
11	chr10:5931975-5932025	A549	lung:	n/a
12	chr10:5932043-5932093	HUVEC	blood vessel:	n/a
13	chr10:5931975-5932025	GM12891	blood:	n/a
14	chr10:5932043-5932093	GM19239	blood:	n/a
15	chr10:5931975-5932025	SK-N-MC	brain:	n/a
16	chr10:5932453-5932503	SK-N-SH	brain:	n/a
17	chr10:5932028-5932078	RPTEC	kidney:	n/a
18	chr10:5932700-5932750	Caco-2	colon:	n/a
19	chr10:5932700-5932750	HRE	kidney:	n/a
20	chr10:5932453-5932503	ovcar-3	ovarian:	n/a
21	chr10:5931880-5931930	MCF10A-Er-Src	breast:	n/a
22	chr10:5931880-5931930	H1-hESC	embryonic stem cell:	embryo
23	chr10:5932043-5932093	ProgFib	skin:	n/a
24	chr10:5932700-5932750	LNCaP	prostate:	n/a
25	chr10:5932700-5932750	IMR90	lung:	fetal
26	chr10:5931970-5932020	GM12878	blood:	n/a
27	chr10:5931880-5931930	T-47D	breast:	n/a
28	chr10:5932453-5932503	AG04450	lung:	fetal
29	chr10:5931970-5932020	HEEpiC	esophagus:	n/a
30	chr10:5932700-5932750	HepG2	liver:	n/a
31	chr10:5932529-5932579	Hela-S3	cervix:	n/a
32	chr10:5931821-5931871	MCF-7	breast:	n/a
33	chr10:5931821-5931871	Hela-S3	cervix:	n/a
34	chr10:5932043-5932093	HL-60	blood:	n/a
35	chr10:5931783-5931833	HL-60	blood:	n/a
36	chr10:5931880-5931930	GM12892	blood:	n/a
37	chr10:5931970-5932020	NHDF-neo	bronchial:	n/a
38	chr10:5932043-5932093	U87	brain:	n/a
39	chr10:5931970-5932020	H1-hESC	embryonic stem cell:	embryo
40	chr10:5932700-5932750	HAEpiC	amniotic membrane:	n/a
41	chr10:5932529-5932579	Hepatocyte	liver:	n/a
42	chr10:5932028-5932078	AG04449	skin:	fetal
43	chr10:5932028-5932078	HCM	heart:	n/a
44	chr10:5931880-5931930	HNPCEpiC	eye:	n/a
45	chr10:5932028-5932078	SK-N-MC	brain:	n/a
46	chr10:5931783-5931833	HEEpiC	esophagus:	n/a
47	chr10:5931880-5931930	ProgFib	skin:	n/a
48	chr10:5932043-5932093	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:5932028-5932078	Caco-2	colon:	n/a
50	chr10:5932043-5932093	HEK293	kidney:	embryo

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5488345..5491486-chr10:5930515..5933192,3	MCF-7	breast:
2	chr10:5725559..5728313-chr10:5930802..5933492,3	K562	blood:
3	chr10:5930925..5933506-chr10:6244058..6246915,2	MCF-7	breast:
4	chr10:5929157..5931311-chr10:6018059..6019673,2	MCF-7	breast:
5	chr10:5852595..5861125-chr10:5921136..5936216,31	MCF-7	breast:
6	chr10:5932395..5934386-chr10:6130743..6132352,2	K562	blood:
7	chr10:5933201..5936012-chr10:6019635..6021875,2	K562	blood:
8	chr10:5853532..5857435-chr10:5928623..5934190,13	MCF-7	breast:
9	chr10:5725094..5729377-chr10:5927689..5933777,6	MCF-7	breast:
10	chr10:5836323..5837944-chr10:5932347..5934576,2	K562	blood:
11	chr10:5853820..5856785-chr10:5927225..5934067,15	K562	blood:
12	chr10:5931780..5932593-chr11:2720733..2721352,2	HCT-116	colon:
13	chr10:5707177..5709381-chr10:5931479..5933432,3	MCF-7	breast:
14	chr10:5931600..5932308-chr17:37009547..37010442,2	HCT-116	colon:
15	chr10:5853439..5857708-chr10:5926443..5936823,24	K562	blood:
16	chr10:5707419..5708953-chr10:5931052..5933501,2	MCF-7	breast:
17	chr10:5931081..5933467-chr10:5942750..5946622,4	MCF-7	breast:
18	chr10:5930398..5933295-chr10:6184026..6187985,3	K562	blood:
19	chr10:5931810..5933817-chr10:6018457..6020176,2	MCF-7	breast:
20	chr10:5930440..5932910-chr10:5957697..5960803,4	MCF-7	breast:
21	chr10:5904346..5907644-chr10:5928919..5931742,3	MCF-7	breast:
22	chr10:5931232..5931977-chr12:46383975..46384769,2	Hela-S3	cervix:
23	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:

No data

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

Extended variants
information (count: 100 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146872932	chr10:5930979-5930980	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs75887320	chr10:5930986-5930987	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs199918753	chr10:5930999-5931000	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs148317727	chr10:5931011-5931012	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs375597526	chr10:5931026-5931027	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs369565697	chr10:5931033-5931034	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs368134353	chr10:5931037-5931038	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs372526816	chr10:5931038-5931039	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs548256145	chr10:5931040-5931041	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs141477133	chr10:5931041-5931042	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs116345232	chr10:5931134-5931135	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs138291670	chr10:5931158-5931159	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs143874225	chr10:5931164-5931165	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs577386197	chr10:5931184-5931185	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs375219358	chr10:5931198-5931199	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs147314702	chr10:5931200-5931201	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs202185769	chr10:5931209-5931210	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
18	rs553174934	chr10:5931213-5931214	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
19	rs369543649	chr10:5931215-5931216	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
20	rs112569010	chr10:5931218-5931219	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
21	rs3750659	chr10:5931230-5931231	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541818307	chr10:5931305-5931306	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs563352325	chr10:5931339-5931340	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
24	rs192437556	chr10:5931348-5931349	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
25	rs543376199	chr10:5931381-5931382	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
26	rs565214354	chr10:5931392-5931393	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
27	rs183765907	chr10:5931423-5931424	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	rs568175490	chr10:5931874-5931875	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs535569402	chr10:5931877-5931878	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	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
46	rs116838509	chr10:5931939-5931940	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs575212860	chr10:5931963-5931964	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	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
49	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
50	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

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:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5929800-5931000	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr10:5929800-5931200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr10:5930000-5931000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
4	chr10:5930000-5931000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:5930000-5931000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
6	chr10:5930000-5931000	Flanking Active TSS	Brain Germinal Matrix	brain
7	chr10:5930000-5931000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr10:5930000-5931000	Flanking Active TSS	Duodenum Mucosa	Duodenum
9	chr10:5930000-5931000	Flanking Active TSS	NHEK	skin
10	chr10:5930000-5931000	Flanking Active TSS	NHLF	lung
11	chr10:5930000-5931200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
12	chr10:5930000-5931200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr10:5930200-5931000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:5930200-5931000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr10:5930200-5931000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr10:5930200-5931000	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr10:5930200-5931000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:5930200-5931000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:5930200-5931000	Flanking Active TSS	Brain Angular Gyrus	brain
20	chr10:5930200-5931000	Flanking Active TSS	Brain Cingulate Gyrus	brain
21	chr10:5930200-5931000	Flanking Active TSS	Fetal Brain Male	brain
22	chr10:5930200-5931000	Flanking Active TSS	Fetal Brain Female	brain
23	chr10:5930200-5931000	Flanking Active TSS	Fetal Intestine Large	intestine
24	chr10:5930200-5931000	Flanking Active TSS	Fetal Lung	lung
25	chr10:5930200-5931000	Flanking Active TSS	Right Ventricle	heart
26	chr10:5930200-5931000	Flanking Active TSS	NH-A	brain
27	chr10:5930200-5931000	Flanking Active TSS	NHDF-Ad	bronchial
28	chr10:5930200-5931200	Flanking Active TSS	Primary hematopoietic stem cells	blood
29	chr10:5930200-5931200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
30	chr10:5930200-5931200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:5930200-5931200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:5930200-5931200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:5930200-5931200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr10:5930200-5931200	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr10:5930200-5931200	Flanking Active TSS	Liver	Liver
36	chr10:5930200-5931200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr10:5930200-5931200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr10:5930200-5931200	Flanking Active TSS	HMEC	breast
39	chr10:5930200-5932600	Active TSS	Fetal Muscle Trunk	muscle
40	chr10:5930400-5931000	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr10:5930400-5931000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr10:5930400-5931000	Flanking Active TSS	Primary B cells from peripheral blood	blood
43	chr10:5930400-5931000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr10:5930400-5931000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr10:5930400-5931000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
46	chr10:5930400-5931000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr10:5930400-5931000	Flanking Active TSS	Fetal Muscle Leg	muscle
48	chr10:5930400-5931000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr10:5930400-5931000	Flanking Active TSS	Thymus	Thymus
50	chr10:5930400-5931000	Flanking Active TSS	HUVEC	blood vessel

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