Variant report

Variant	esv1850593
Chromosome Location	chr1:71444149-71514969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:466)
CpG islands
(count:855)
Chromatin interactive
region (count:49)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71510208-71510932	K562	blood:	n/a	n/a
2	ARID3A	chr1:71468699-71468724	K562	blood:	n/a	n/a
3	ARID3A	chr1:71460522-71460848	K562	blood:	n/a	n/a
4	ARID3A	chr1:71481128-71481217	K562	blood:	n/a	n/a
5	ARID3A	chr1:71472265-71472284	K562	blood:	n/a	n/a
6	ARID3A	chr1:71511965-71512135	K562	blood:	n/a	n/a
7	ARID3A	chr1:71508903-71509315	K562	blood:	n/a	n/a
8	ARID3A	chr1:71511378-71511609	K562	blood:	n/a	n/a
9	ATF1	chr1:71451500-71451902	K562	blood:	n/a	n/a
10	ATF1	chr1:71510574-71510921	K562	blood:	n/a	n/a
11	ATF1	chr1:71445230-71445327	K562	blood:	n/a	n/a
12	ATF3	chr1:71510507-71510912	K562	blood:	n/a	n/a
13	BACH1	chr1:71513504-71513540	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:71468156-71468161	K562	blood:	n/a	n/a
15	BHLHE40	chr1:71480894-71480941	K562	blood:	n/a	n/a
16	BHLHE40	chr1:71485053-71485253	K562	blood:	n/a	n/a
17	BHLHE40	chr1:71501191-71501340	K562	blood:	n/a	n/a
18	BHLHE40	chr1:71465554-71465707	K562	blood:	n/a	n/a
19	BHLHE40	chr1:71512038-71514051	K562	blood:	n/a	chr1:71513319-71513335 chr1:71513322-71513338 chr1:71513407-71513423 chr1:71513352-71513368 chr1:71513419-71513435
20	BHLHE40	chr1:71510716-71511619	K562	blood:	n/a	n/a
21	CBX3	chr1:71511945-71512532	K562	blood:	n/a	n/a
22	CBX3	chr1:71512656-71513704	K562	blood:	n/a	n/a
23	CCNT2	chr1:71510706-71510856	K562	blood:	n/a	n/a
24	CCNT2	chr1:71511971-71513807	K562	blood:	n/a	chr1:71513534-71513543 chr1:71512342-71512351
25	CCNT2	chr1:71474825-71475012	K562	blood:	n/a	n/a
26	CEBPB	chr1:71467353-71467636	A549	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
27	CEBPB	chr1:71467358-71467677	IMR90	lung:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
28	CEBPB	chr1:71467330-71467690	HepG2	liver:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
29	CEBPB	chr1:71504008-71504240	K562	blood:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
30	CEBPB	chr1:71503963-71504259	HepG2	liver:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
31	CEBPB	chr1:71458228-71458549	K562	blood:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
32	CEBPB	chr1:71508853-71508988	A549	lung:	n/a	n/a
33	CEBPB	chr1:71469996-71470196	K562	blood:	n/a	chr1:71470127-71470140 chr1:71470129-71470140
34	CEBPB	chr1:71467360-71467695	K562	blood:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
35	CEBPB	chr1:71477204-71477504	K562	blood:	n/a	chr1:71477360-71477371
36	CEBPB	chr1:71485706-71485857	A549	lung:	n/a	chr1:71485756-71485767
37	CEBPB	chr1:71477312-71477504	HepG2	liver:	n/a	chr1:71477360-71477371
38	CEBPB	chr1:71503962-71504242	IMR90	lung:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
39	CEBPB	chr1:71508298-71509085	K562	blood:	n/a	chr1:71509025-71509036 chr1:71508482-71508495 chr1:71509025-71509036 chr1:71509021-71509032
40	CEBPB	chr1:71512160-71512281	K562	blood:	n/a	n/a
41	CEBPB	chr1:71458240-71458524	HepG2	liver:	n/a	chr1:71458394-71458405 chr1:71458394-71458407
42	CEBPB	chr1:71485618-71485862	IMR90	lung:	n/a	chr1:71485756-71485767
43	CEBPB	chr1:71510612-71510924	K562	blood:	n/a	n/a
44	CEBPB	chr1:71467389-71467679	H1-hESC	embryonic stem cell:	n/a	chr1:71467516-71467527 chr1:71467518-71467529 chr1:71467516-71467529
45	CEBPB	chr1:71508723-71509023	K562	blood:	n/a	n/a
46	CEBPB	chr1:71444470-71444536	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr1:71508727-71509055	K562	blood:	n/a	chr1:71509025-71509036 chr1:71509025-71509036 chr1:71509021-71509032
48	CEBPB	chr1:71483442-71483555	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:71503735-71504291	K562	blood:	n/a	chr1:71504112-71504123 chr1:71504112-71504125 chr1:71504112-71504125 chr1:71504114-71504123 chr1:71504114-71504125
50	CEBPB	chr1:71513488-71513954	K562	blood:	n/a	chr1:71513897-71513910

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71511514-71511564	IMR90	lung:	fetal
2	chr1:71511514-71511564	IMR90	lung:	fetal
3	chr1:71514431-71514481	GM06990	blood:	n/a
4	chr1:71511514-71511564	BJ	skin:	n/a
5	chr1:71511514-71511564	NHDF-neo	bronchial:	n/a
6	chr1:71511514-71511564	PrEC	prostate:	n/a
7	chr1:71513114-71513164	ProgFib	skin:	n/a
8	chr1:71512973-71513023	Hepatocyte	liver:	n/a
9	chr1:71472738-71472788	Caco-2	colon:	n/a
10	chr1:71513789-71513839	AG09319	gingival:	n/a
11	chr1:71513726-71513776	HRPEpiC	eye:	n/a
12	chr1:71513494-71513544	SKMC	muscle:	n/a
13	chr1:71512485-71512535	ECC-1	luminal epithelium:	n/a
14	chr1:71513733-71513783	SK-N-MC	brain:	n/a
15	chr1:71512485-71512535	GM12892	blood:	n/a
16	chr1:71513494-71513544	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:71512485-71512535	HEK293	kidney:	embryo
18	chr1:71513114-71513164	GM12878	blood:	n/a
19	chr1:71513114-71513164	HEK293	kidney:	embryo
20	chr1:71513733-71513783	PANC-1	pancreas:	n/a
21	chr1:71513733-71513783	AG09309	skin:	n/a
22	chr1:71514431-71514481	H1-hESC	embryonic stem cell:	embryo
23	chr1:71513566-71513616	HAEpiC	amniotic membrane:	n/a
24	chr1:71511514-71511564	SK-N-SH	brain:	n/a
25	chr1:71513733-71513783	HCT-116	colon:	n/a
26	chr1:71510804-71510854	Hepatocyte	liver:	n/a
27	chr1:71513114-71513164	T-47D	breast:	n/a
28	chr1:71513626-71513676	AG04450	lung:	fetal
29	chr1:71513566-71513616	Caco-2	colon:	n/a
30	chr1:71513789-71513839	HNPCEpiC	eye:	n/a
31	chr1:71513114-71513164	IMR90	lung:	fetal
32	chr1:71510804-71510854	SK-N-SH	brain:	n/a
33	chr1:71514431-71514481	RPTEC	kidney:	n/a
34	chr1:71513494-71513544	AG10803	skin:	n/a
35	chr1:71513566-71513616	HNPCEpiC	eye:	n/a
36	chr1:71512973-71513023	K562	blood:	n/a
37	chr1:71514431-71514481	AG04449	skin:	fetal
38	chr1:71510804-71510854	Caco-2	colon:	n/a
39	chr1:71512485-71512535	MCF-7	breast:	n/a
40	chr1:71513114-71513164	HIPEpiC	eye:	n/a
41	chr1:71512485-71512535	Jurkat	blood:	n/a
42	chr1:71512973-71513023	ECC-1	luminal epithelium:	n/a
43	chr1:71513726-71513776	HepG2	liver:	n/a
44	chr1:71512100-71512150	ECC-1	luminal epithelium:	n/a
45	chr1:71510804-71510854	AG09309	skin:	n/a
46	chr1:71513726-71513776	BE2_C	brain:	n/a
47	chr1:71510804-71510854	A549	lung:	n/a
48	chr1:71512485-71512535	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:71512973-71513023	SK-N-MC	brain:	n/a
50	chr1:71512973-71513023	PrEC	prostate:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:71499849..71501736-chr1:71503385..71504973,2	K562	blood:
2	chr1:71496393..71498256-chr1:71498283..71500475,2	K562	blood:
3	chr1:71493469..71495950-chr1:71496070..71500224,3	K562	blood:
4	chr1:71499543..71503702-chr1:71511179..71513554,5	K562	blood:
5	chr1:71488156..71490050-chr1:71494544..71497230,2	K562	blood:
6	chr1:70876526..70879847-chr1:71510519..71513789,3	K562	blood:
7	chr1:71488156..71490050-chr1:71494544..71497230,2	K562	blood:
8	chr1:71498308..71501736-chr1:71503473..71506751,3	K562	blood:
9	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
10	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
11	chr1:71498308..71501736-chr1:71503473..71506751,3	K562	blood:
12	chr1:71240165..71242218-chr1:71510173..71512188,2	K562	blood:
13	chr1:71164353..71167028-chr1:71509072..71511419,2	K562	blood:
14	chr1:71423003..71424991-chr1:71446277..71448535,2	K562	blood:
15	chr1:71493019..71494900-chr1:71500523..71502505,2	K562	blood:
16	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
17	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
18	chr1:71492579..71496076-chr1:71511495..71513785,3	K562	blood:
19	chr1:71497365..71498885-chr1:71507254..71510170,2	K562	blood:
20	chr1:71467023..71468927-chr1:71512007..71514052,2	K562	blood:
21	chr1:71496393..71498256-chr1:71498283..71500475,2	K562	blood:
22	chr1:71493019..71494900-chr1:71500523..71502505,2	K562	blood:
23	chr1:71128661..71130608-chr1:71489552..71491952,2	K562	blood:
24	chr1:71373472..71375942-chr1:71510520..71512137,2	K562	blood:
25	chr1:71493469..71495950-chr1:71496070..71500224,3	K562	blood:
26	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
27	chr1:71470890..71473474-chr1:71500472..71503086,2	MCF-7	breast:
28	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
29	chr1:70978338..70980257-chr1:71510997..71512703,2	K562	blood:
30	chr1:71492429..71494900-chr1:71500523..71502933,2	K562	blood:
31	chr1:71511577..71513859-chr1:71544920..71548466,4	K562	blood:
32	chr1:71488605..71491550-chr1:71545533..71547496,2	K562	blood:
33	chr1:71492429..71494900-chr1:71500523..71502933,2	K562	blood:
34	chr1:71440403..71443013-chr1:71443324..71446288,2	K562	blood:
35	chr1:71443738..71447073-chr1:71448870..71451609,5	K562	blood:
36	chr1:70994251..70996830-chr1:71512472..71514167,2	MCF-7	breast:
37	chr1:71113661..71115986-chr1:71510232..71513062,3	K562	blood:
38	chr1:71217715..71220280-chr1:71509356..71511477,2	K562	blood:
39	chr1:71486485..71490048-chr1:71491402..71493576,3	K562	blood:
40	chr1:71499849..71501736-chr1:71503385..71504973,2	K562	blood:
41	chr1:71442791..71448002-chr1:71448870..71452211,5	K562	blood:
42	chr1:71509104..71511027-chr1:71511341..71513340,2	MCF-7	breast:
43	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
44	chr1:71032636..71034814-chr1:71507461..71509971,2	K562	blood:
45	chr1:71002710..71005624-chr1:71510534..71512998,2	K562	blood:
46	chr1:71486485..71490048-chr1:71491402..71493576,3	K562	blood:
47	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
48	chr1:71510894..71514340-chr1:71523075..71528309,6	K562	blood:
49	chr1:71497365..71498885-chr1:71507254..71510170,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-4	chr1:71514538-71514671	ENSG00000235079.1
2	lnc-ZRANB2-3	chr1:71471537-71472185	ENSG00000269933.1
3	lnc-ZRANB2-2	chr1:71472542-71473814	NONHSAT003875
4	lnc-CTH-14	chr1:71475926-71475982	l_71_chr1:71319635-71475982_testes
5	lnc-CTH-13	chr1:71489933-71490390	NONHSAT003876
6	lnc-CTH-14	chr1:71475401-71475924	l_71_chr1:71319635-71475982_testes
7	lnc-CTH-13	chr1:71489270-71489329	NONHSAT003876
8	lnc-CTH-14	chr1:71461328-71461385	l_71_chr1:71319635-71475982_testes
9	lnc-CTH-14	chr1:71500505-71500572	l_71_chr1:71319635-71475982_testes

No data

Variant related genes	Relation type
ZRANB2-AS1	TF binding region
ENSG00000269933	TF binding region
PTGER3	TF binding region
ZRANB2-AS1	CpG island
ENSG00000269933	CpG island
PTGER3	CpG island
ENSG00000229956	chromatin interactions
ENSG00000233020	chromatin interactions
ENSG00000050628	chromatin interactions
ENSG00000235079	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000132485	chromatin interactions
ENSG00000269933	chromatin interactions

Extended variants
information (count: 2610 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2610 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs516647	chr1:71444149-71444150	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572304435	chr1:71444182-71444183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147395281	chr1:71444213-71444214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559989121	chr1:71444229-71444230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190951373	chr1:71444244-71444245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528139665	chr1:71444280-71444281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574446093	chr1:71444298-71444299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183738522	chr1:71444300-71444301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs601934	chr1:71444355-71444356	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568016319	chr1:71444405-71444406	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532184079	chr1:71444427-71444428	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36014745	chr1:71444443-71444444	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373217707	chr1:71444467-71444468	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546113558	chr1:71444470-71444471	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564084813	chr1:71444547-71444548	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76055983	chr1:71444565-71444566	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113145953	chr1:71444568-71444569	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541667	chr1:71444634-71444635	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs530165470	chr1:71444651-71444652	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs550619558	chr1:71444682-71444683	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs549874246	chr1:71444686-71444687	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs569691831	chr1:71444687-71444688	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs74087117	chr1:71444704-71444705	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs148486836	chr1:71444751-71444752	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs558804422	chr1:71444764-71444765	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs187931616	chr1:71444769-71444770	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570185327	chr1:71444794-71444795	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs192146242	chr1:71444813-71444814	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555097442	chr1:71444874-71444875	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs537637091	chr1:71444887-71444888	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs559030652	chr1:71444888-71444889	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs548062128	chr1:71444951-71444952	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs567949921	chr1:71444959-71444960	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs34862739	chr1:71444988-71444989	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs77047153	chr1:71444999-71445000	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs185072013	chr1:71445017-71445018	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs557138467	chr1:71445052-71445053	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs576885000	chr1:71445084-71445085	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs145793575	chr1:71445088-71445089	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs370020204	chr1:71445089-71445090	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs3216529	chr1:71445090-71445091	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs560194342	chr1:71445110-71445111	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs559403552	chr1:71445111-71445112	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs11434745	chr1:71445183-71445184	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs397964913	chr1:71445184-71445185	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs528361790	chr1:71445188-71445189	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs150617346	chr1:71445214-71445215	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs139687567	chr1:71445235-71445236	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs116814550	chr1:71445244-71445245	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs549860132	chr1:71445247-71445248	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71430200-71444200	Weak transcription	Adipose Nuclei	Adipose
2	chr1:71441600-71444800	Enhancers	Fetal Brain Male	brain
3	chr1:71443200-71456800	Weak transcription	Gastric	stomach
4	chr1:71443600-71446000	Weak transcription	Pancreas	Pancrea
5	chr1:71444000-71444600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr1:71444000-71445600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:71444200-71444600	Enhancers	Fetal Heart	heart
8	chr1:71444200-71446200	Enhancers	Primary hematopoietic stem cells	blood
9	chr1:71444200-71446600	Enhancers	Adipose Nuclei	Adipose
10	chr1:71444200-71447000	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr1:71444400-71444600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:71444400-71444800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:71444400-71445400	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr1:71444600-71445200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr1:71444600-71446000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:71444600-71446600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr1:71444800-71445600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:71445000-71446200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr1:71445200-71445400	Enhancers	Colon Smooth Muscle	Colon
20	chr1:71445200-71446200	Enhancers	K562	blood
21	chr1:71445200-71464200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr1:71445600-71446200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:71446000-71446200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:71446000-71446200	Enhancers	Colon Smooth Muscle	Colon
25	chr1:71446000-71446600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:71446000-71446600	Enhancers	Pancreas	Pancrea
27	chr1:71446200-71450600	Weak transcription	K562	blood
28	chr1:71446600-71447200	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr1:71446600-71449200	Weak transcription	Adipose Nuclei	Adipose
30	chr1:71446600-71456200	Weak transcription	Pancreas	Pancrea
31	chr1:71447400-71448200	Enhancers	Aorta	Aorta
32	chr1:71448200-71456800	Weak transcription	Aorta	Aorta
33	chr1:71449200-71449800	Enhancers	Adipose Nuclei	Adipose
34	chr1:71449800-71451400	Weak transcription	Adipose Nuclei	Adipose
35	chr1:71450600-71451600	Enhancers	NHDF-Ad	bronchial
36	chr1:71450600-71452200	Enhancers	K562	blood
37	chr1:71451400-71451800	Enhancers	Adipose Nuclei	Adipose
38	chr1:71456200-71457200	Enhancers	Pancreas	Pancrea
39	chr1:71456800-71458000	Enhancers	Gastric	stomach
40	chr1:71456800-71458400	Enhancers	Aorta	Aorta
41	chr1:71457000-71457400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:71458000-71459400	Weak transcription	Gastric	stomach
43	chr1:71459200-71459400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr1:71459200-71460000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:71459400-71459600	Enhancers	Gastric	stomach
46	chr1:71459600-71460400	Enhancers	Left Ventricle	heart
47	chr1:71459800-71461000	Enhancers	Fetal Heart	heart
48	chr1:71460600-71461200	Enhancers	K562	blood
49	chr1:71461200-71461600	Weak transcription	K562	blood
50	chr1:71461600-71461800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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