Variant report

Variant	esv11181
Chromosome Location	chr3:49726377-49733587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:811)
CpG islands
(count:793)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:49726435-49726638	K562	blood:	n/a	n/a
2	ARID3A	chr3:49726762-49727051	HepG2	liver:	n/a	n/a
3	ATF1	chr3:49726441-49726642	K562	blood:	n/a	n/a
4	ATF2	chr3:49726771-49727184	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:49726826-49727192	GM12878	blood:	n/a	n/a
6	ATF2	chr3:49726715-49727287	GM12878	blood:	n/a	n/a
7	ATF3	chr3:49726774-49727187	A549	lung:	n/a	n/a
8	ATF3	chr3:49726743-49727206	A549	lung:	n/a	n/a
9	BATF	chr3:49726459-49727151	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:49726963-49727227	GM12878	blood:	n/a	chr3:49727192-49727205
11	BCL11A	chr3:49726800-49727197	GM12878	blood:	n/a	n/a
12	BCL3	chr3:49726646-49727262	A549	lung:	n/a	chr3:49727192-49727205
13	BCL3	chr3:49726720-49727192	A549	lung:	n/a	n/a
14	BCLAF1	chr3:49726739-49727289	GM12878	blood:	n/a	chr3:49727192-49727205
15	BCLAF1	chr3:49726698-49727308	GM12878	blood:	n/a	chr3:49727192-49727205
16	BCLAF1	chr3:49726861-49727288	K562	blood:	n/a	chr3:49727192-49727205
17	BHLHE40	chr3:49726433-49727116	K562	blood:	n/a	n/a
18	BHLHE40	chr3:49726769-49727171	HepG2	liver:	n/a	n/a
19	BHLHE40	chr3:49726769-49727129	GM12878	blood:	n/a	n/a
20	BRCA1	chr3:49726858-49727121	HepG2	liver:	n/a	n/a
21	CBX3	chr3:49727290-49728239	K562	blood:	n/a	n/a
22	CBX3	chr3:49726336-49727034	K562	blood:	n/a	n/a
23	CBX3	chr3:49725844-49727257	K562	blood:	n/a	n/a
24	CCNT2	chr3:49726862-49727206	K562	blood:	n/a	n/a
25	CEBPB	chr3:49726073-49726639	K562	blood:	n/a	chr3:49726131-49726142
26	CEBPB	chr3:49725936-49727036	K562	blood:	n/a	chr3:49726131-49726142
27	CEBPB	chr3:49727017-49727128	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:49726820-49727185	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr3:49726932-49727132	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr3:49725976-49726402	HepG2	liver:	n/a	chr3:49726131-49726142
31	CEBPB	chr3:49726303-49727240	GM12878	blood:	n/a	n/a
32	CEBPD	chr3:49727848-49728263	K562	blood:	n/a	n/a
33	CEBPD	chr3:49726779-49727094	HepG2	liver:	n/a	n/a
34	CEBPD	chr3:49726053-49727801	K562	blood:	n/a	chr3:49726130-49726141
35	CEBPD	chr3:49726024-49726402	HepG2	liver:	n/a	chr3:49726130-49726141
36	CHD1	chr3:49727259-49727450	GM12878	blood:	n/a	n/a
37	CHD1	chr3:49726958-49727160	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr3:49726620-49726904	GM12878	blood:	n/a	n/a
39	CHD2	chr3:49726601-49727189	K562	blood:	n/a	n/a
40	CHD2	chr3:49726690-49727463	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr3:49726841-49727189	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr3:49726766-49727203	GM12878	blood:	n/a	n/a
43	CHD2	chr3:49726742-49727165	HepG2	liver:	n/a	n/a
44	CREB1	chr3:49726722-49727287	A549	lung:	n/a	n/a
45	CREB1	chr3:49726892-49727279	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr3:49726600-49726750	HCT-116	colon:	n/a	n/a
47	CTCF	chr3:49726880-49727030	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr3:49726880-49727030	GM06990	blood:	n/a	n/a
49	CTCF	chr3:49726880-49727030	GM12875	blood:	n/a	n/a
50	CTCF	chr3:49726860-49727010	HPF	lung:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:49727222-49727272	BJ	skin:	n/a
2	chr3:49726922-49726972	GM12892	blood:	n/a
3	chr3:49727025-49727075	AG10803	skin:	n/a
4	chr3:49727322-49727372	ProgFib	skin:	n/a
5	chr3:49726899-49726949	SKMC	muscle:	n/a
6	chr3:49726912-49726962	NT2-D1	testis:	n/a
7	chr3:49727025-49727075	IMR90	lung:	fetal
8	chr3:49726922-49726972	HEK293	kidney:	embryo
9	chr3:49727037-49727087	H1-hESC	embryonic stem cell:	embryo
10	chr3:49726775-49726825	SAEC	small airway:	n/a
11	chr3:49726912-49726962	T-47D	breast:	n/a
12	chr3:49726912-49726962	AG04449	skin:	fetal
13	chr3:49726910-49726960	HRE	kidney:	n/a
14	chr3:49726928-49726978	HPAEpiC	pulmonary alveolar:	n/a
15	chr3:49727037-49727087	SK-N-SH_RA	brain:	n/a
16	chr3:49726922-49726972	NB4	blood:	n/a
17	chr3:49727322-49727372	NH-A	brain:	n/a
18	chr3:49726785-49726835	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:49727322-49727372	HMEC	breast:	n/a
20	chr3:49726775-49726825	HepG2	liver:	n/a
21	chr3:49726910-49726960	AG09309	skin:	n/a
22	chr3:49727222-49727272	GM12878	blood:	n/a
23	chr3:49726775-49726825	RPTEC	kidney:	n/a
24	chr3:49727322-49727372	MCF10A-Er-Src	breast:	n/a
25	chr3:49726443-49726493	HUVEC	blood vessel:	n/a
26	chr3:49726910-49726960	SK-N-SH_RA	brain:	n/a
27	chr3:49727025-49727075	NH-A	brain:	n/a
28	chr3:49726928-49726978	ovcar-3	ovarian:	n/a
29	chr3:49726785-49726835	NT2-D1	testis:	n/a
30	chr3:49726910-49726960	GM12891	blood:	n/a
31	chr3:49727322-49727372	Jurkat	blood:	n/a
32	chr3:49727322-49727372	PANC-1	pancreas:	n/a
33	chr3:49726785-49726835	Hela-S3	cervix:	n/a
34	chr3:49727037-49727087	HepG2	liver:	n/a
35	chr3:49726922-49726972	BE2_C	brain:	n/a
36	chr3:49727222-49727272	ovcar-3	ovarian:	n/a
37	chr3:49727037-49727087	AG10803	skin:	n/a
38	chr3:49726775-49726825	BE2_C	brain:	n/a
39	chr3:49726775-49726825	Caco-2	colon:	n/a
40	chr3:49727474-49727524	GM19239	blood:	n/a
41	chr3:49726899-49726949	IMR90	lung:	fetal
42	chr3:49727322-49727372	HAEpiC	amniotic membrane:	n/a
43	chr3:49726785-49726835	T-47D	breast:	n/a
44	chr3:49727025-49727075	HEEpiC	esophagus:	n/a
45	chr3:49727037-49727087	HCPEpiC	choroid plexus:	n/a
46	chr3:49726899-49726949	MCF-7	breast:	n/a
47	chr3:49726443-49726493	SK-N-SH_RA	brain:	n/a
48	chr3:49726785-49726835	HIPEpiC	eye:	n/a
49	chr3:49726785-49726835	K562	blood:	n/a
50	chr3:49727222-49727272	AG04449	skin:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49719547..49721441-chr3:49726309..49728909,2	K562	blood:
2	chr3:49724739..49727802-chr3:49735823..49739048,3	MCF-7	breast:
3	chr1:16964923..16974624-chr3:49722461..49732046,16	K562	blood:
4	chr3:49727014..49727624-chr9:137217199..137217737,2	HCT-116	colon:
5	chr3:49448668..49451033-chr3:49723995..49726731,2	MCF-7	breast:
6	chr3:49711727..49717769-chr3:49722772..49726950,7	K562	blood:
7	chr3:49710552..49715225-chr3:49718907..49727364,14	MCF-7	breast:
8	chr3:49709764..49714141-chr3:49724462..49728582,8	MCF-7	breast:
9	chr1:16970425..16971927-chr3:49726367..49727791,15	HCT-116	colon:
10	chr3:49715099..49716706-chr3:49727000..49728524,2	K562	blood:
11	chr1:16965534..16967536-chr3:49731368..49733406,2	MCF-7	breast:
12	chr1:16968902..16969901-chr3:49728593..49729113,2	MCF-7	breast:
13	chr1:16970648..16971367-chr3:49726608..49727129,5	MCF-7	breast:
14	chr3:49724349..49727675-chr3:49755739..49757510,3	MCF-7	breast:
15	chr1:16969549..16972758-chr3:49725610..49728945,8	K562	blood:
16	chr1:16970617..16971914-chr3:49726307..49727625,5	Hela-S3	cervix:
17	chr12:54674340..54674894-chr3:49726726..49727505,2	Hela-S3	cervix:
18	chr3:49724901..49726999-chr3:49761086..49763587,3	MCF-7	breast:
19	chr3:49722536..49724153-chr3:49724898..49727146,2	MCF-7	breast:
20	chr3:49727338..49730126-chr3:49733777..49735933,2	K562	blood:
21	chr3:49708866..49715375-chr3:49724746..49730407,6	K562	blood:
22	chr1:16840059..16842019-chr3:49726620..49728606,2	MCF-7	breast:
23	chr1:16970672..16971760-chr3:49726371..49727463,9	MCF-7	breast:
24	chr1:16968825..16972400-chr3:49724902..49730445,9	MCF-7	breast:
25	chr1:16967505..16970339-chr3:49729112..49731366,2	MCF-7	breast:
26	chr1:16969769..16972744-chr3:49724987..49728952,10	MCF-7	breast:
27	chr3:49725473..49727934-chr3:49733228..49735163,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNF123	TF binding region
MST1	TF binding region
ENSG00000259970	TF binding region
RNF123	CpG island
MST1	CpG island
ENSG00000259970	CpG island
ENSG00000135486	chromatin interactions
ENSG00000164068	chromatin interactions
ENSG00000176020	chromatin interactions
ENSG00000186301	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000164062	chromatin interactions
ENSG00000173540	chromatin interactions
ENSG00000215908	chromatin interactions
ENSG00000173531	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000261135	chromatin interactions

Extended variants
information (count: 292 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542468495	chr3:49726388-49726389	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs562180245	chr3:49726547-49726548	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs4052565	chr3:49726555-49726556	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs529392117	chr3:49726574-49726575	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs113477650	chr3:49726618-49726619	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs543690615	chr3:49726636-49726637	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
7	rs550931845	chr3:49726670-49726671	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
8	rs185599246	chr3:49726684-49726685	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
9	rs3872336	chr3:49726688-49726689	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
10	rs3872335	chr3:49726705-49726706	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
11	rs4052568	chr3:49726728-49726729	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs3872334	chr3:49726772-49726773	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs561759982	chr3:49726788-49726789	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs1815467	chr3:49726809-49726810	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs2087730	chr3:49726811-49726812	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs189910529	chr3:49726821-49726822	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs566825722	chr3:49726822-49726823	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs534084863	chr3:49726830-49726831	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs182125211	chr3:49726834-49726835	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
20	rs567325981	chr3:49726870-49726871	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
21	rs4052570	chr3:49726882-49726883	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
22	rs374143555	chr3:49726889-49726890	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs537569455	chr3:49726893-49726894	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs556105922	chr3:49726900-49726901	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
25	rs2329012	chr3:49726918-49726919	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
26	rs4052571	chr3:49726950-49726951	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs577751005	chr3:49726951-49726952	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs2933246	chr3:49726981-49726982	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs2329013	chr3:49726990-49726991	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs538929696	chr3:49727010-49727011	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs2329014	chr3:49727013-49727014	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs554070486	chr3:49727017-49727018	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs2329015	chr3:49727023-49727024	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs2876716	chr3:49727037-49727038	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs149050592	chr3:49727082-49727083	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs185420417	chr3:49727088-49727089	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs190051026	chr3:49727100-49727101	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs138638527	chr3:49727101-49727102	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs113519872	chr3:49727132-49727133	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs560956312	chr3:49727137-49727138	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs2329016	chr3:49727141-49727142	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs191964003	chr3:49727156-49727157	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs138168709	chr3:49727180-49727181	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs141735766	chr3:49727205-49727206	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs183827603	chr3:49727253-49727254	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs139314219	chr3:49727289-49727290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs533111295	chr3:49727322-49727323	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs551369129	chr3:49727332-49727333	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs560378087	chr3:49727370-49727371	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs188322715	chr3:49727378-49727379	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49721400-49726400	Weak transcription	Aorta	Aorta
2	chr3:49723400-49726400	Weak transcription	Lung	lung
3	chr3:49724400-49726400	Enhancers	Spleen	Spleen
4	chr3:49724600-49726400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr3:49724800-49726400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr3:49724800-49726400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:49724800-49726400	Enhancers	Pancreas	Pancrea
8	chr3:49724800-49726400	Weak transcription	Right Atrium	heart
9	chr3:49724800-49726400	Enhancers	Right Ventricle	heart
10	chr3:49724800-49726400	Weak transcription	NH-A	brain
11	chr3:49724800-49726600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr3:49724800-49726600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:49724800-49726600	Weak transcription	NHDF-Ad	bronchial
14	chr3:49725000-49726400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr3:49725000-49726400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr3:49725000-49726400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr3:49725000-49726600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr3:49725200-49726400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:49725200-49728400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr3:49725400-49726400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:49725400-49726800	Flanking Active TSS	Fetal Intestine Small	intestine
22	chr3:49725600-49726400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:49725600-49726800	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr3:49725600-49726800	Flanking Active TSS	Dnd41	blood
25	chr3:49725600-49727200	Active TSS	Liver	Liver
26	chr3:49725800-49726400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr3:49725800-49726800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
28	chr3:49726000-49726400	Enhancers	Primary B cells from cord blood	blood
29	chr3:49726000-49726400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr3:49726000-49726400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr3:49726000-49726400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr3:49726000-49726400	Enhancers	Fetal Brain Male	brain
33	chr3:49726000-49726400	Enhancers	Fetal Heart	heart
34	chr3:49726000-49726400	Enhancers	Placenta	Placenta
35	chr3:49726000-49726400	Bivalent Enhancer	Fetal Stomach	stomach
36	chr3:49726000-49726600	Enhancers	Placenta Amnion	Placenta Amnion
37	chr3:49726000-49726600	Flanking Active TSS	Hela-S3	cervix
38	chr3:49726000-49726800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:49726200-49726400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
40	chr3:49726200-49726400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr3:49726200-49726400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr3:49726200-49726400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:49726200-49726400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr3:49726200-49726400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr3:49726200-49726400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr3:49726200-49726400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr3:49726200-49726400	Enhancers	Primary B cells from peripheral blood	blood
48	chr3:49726200-49726400	Enhancers	Primary hematopoietic stem cells	blood
49	chr3:49726200-49726400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr3:49726200-49726400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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