Variant report

Variant	esv3406509
Chromosome Location	chr1:10697590-10700138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:490)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:55 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:10699434-10699676	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr1:10699506-10699568	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr1:10698280-10698430	HCPEpiC	choroid plexus:	n/a	n/a
4	CTCF	chr1:10699420-10699570	HRPEpiC	eye:	n/a	n/a
5	CTCF	chr1:10697630-10697654	LNCaP	prostate:	n/a	n/a
6	CTCF	chr1:10698720-10698870	AoAF	blood vessel:	n/a	n/a
7	CTCF	chr1:10698220-10698510	HA-sp	spinal cord:	n/a	n/a
8	CTCF	chr1:10698400-10698550	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr1:10698260-10698410	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr1:10699420-10699570	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr1:10699380-10699530	AG09319	gingival:	n/a	n/a
12	CTCF	chr1:10698120-10698270	HPF	lung:	n/a	n/a
13	CTCF	chr1:10699487-10699589	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:10700080-10700230	SK-N-SH_RA	brain:	n/a	chr1:10700209-10700222
15	CTCF	chr1:10699460-10699610	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr1:10699440-10699590	HCFaa	heart:	n/a	n/a
17	CTCF	chr1:10699360-10699510	HA-sp	spinal cord:	n/a	n/a
18	E2F6	chr1:10699339-10699954	H1-hESC	embryonic stem cell:	n/a	n/a
19	E2F6	chr1:10699361-10700329	H1-hESC	embryonic stem cell:	n/a	chr1:10700269-10700278
20	EP300	chr1:10699735-10702043	SK-N-SH	brain:	n/a	chr1:10701367-10701374
21	GABPA	chr1:10699190-10699882	H1-hESC	embryonic stem cell:	n/a	n/a
22	GABPA	chr1:10699302-10699992	H1-hESC	embryonic stem cell:	n/a	n/a
23	GABPA	chr1:10698518-10699036	H1-hESC	embryonic stem cell:	n/a	n/a
24	HMGN3	chr1:10698335-10698619	K562	blood:	n/a	n/a
25	HMGN3	chr1:10699578-10699775	K562	blood:	n/a	n/a
26	MAX	chr1:10698957-10700089	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAX	chr1:10699064-10700305	H1-hESC	embryonic stem cell:	n/a	chr1:10700152-10700162 chr1:10700270-10700280 chr1:10700153-10700163
28	MYC	chr1:10699652-10699666	MCF-7	breast:	n/a	n/a
29	MYC	chr1:10699668-10699696	MCF-7	breast:	n/a	n/a
30	MYC	chr1:10699737-10699747	MCF-7	breast:	n/a	n/a
31	MYC	chr1:10699834-10700178	H1-hESC	embryonic stem cell:	n/a	chr1:10700152-10700162 chr1:10700153-10700163
32	NFIC	chr1:10699916-10700866	SK-N-SH	brain:	n/a	n/a
33	NFIC	chr1:10700040-10700708	SK-N-SH	brain:	n/a	n/a
34	NFIC	chr1:10699951-10700862	ECC-1	luminal epithelium:	n/a	n/a
35	NFIC	chr1:10699879-10700774	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr1:10699131-10699134	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr1:10699808-10699836	MCF-7	breast:	n/a	n/a
38	POLR2A	chr1:10699725-10699800	MCF-7	breast:	n/a	n/a
39	POLR2A	chr1:10697704-10697747	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr1:10699973-10700684	SK-N-MC	brain:	n/a	n/a
41	POLR2A	chr1:10699674-10699740	MCF-7	breast:	n/a	n/a
42	POLR2A	chr1:10697419-10697657	GM12878	blood:	n/a	n/a
43	POLR2A	chr1:10699658-10699674	MCF-7	breast:	n/a	n/a
44	POLR2A	chr1:10697790-10697828	HUVEC	blood vessel:	n/a	n/a
45	RAD21	chr1:10699025-10699776	H1-hESC	embryonic stem cell:	n/a	n/a
46	RAD21	chr1:10699430-10699702	H1-hESC	embryonic stem cell:	n/a	n/a
47	RAD21	chr1:10699984-10700455	H1-hESC	embryonic stem cell:	n/a	chr1:10700212-10700224 chr1:10700207-10700226 chr1:10700210-10700223 chr1:10700212-10700222
48	RFX5	chr1:10699951-10699994	H1-hESC	embryonic stem cell:	n/a	n/a
49	RFX5	chr1:10698199-10698216	K562	blood:	n/a	n/a
50	SIN3A	chr1:10699405-10699676	H1-hESC	embryonic stem cell:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10697703-10697753	ProgFib	skin:	n/a
2	chr1:10699975-10700025	GM19239	blood:	n/a
3	chr1:10697703-10697753	ProgFib	skin:	n/a
4	chr1:10699975-10700025	GM19239	blood:	n/a
5	chr1:10699604-10699654	HIPEpiC	eye:	n/a
6	chr1:10697703-10697753	BJ	skin:	n/a
7	chr1:10698719-10698769	K562	blood:	n/a
8	chr1:10699975-10700025	ECC-1	luminal epithelium:	n/a
9	chr1:10699604-10699654	AG09319	gingival:	n/a
10	chr1:10699975-10700025	SK-N-SH_RA	brain:	n/a
11	chr1:10697703-10697753	HUVEC	blood vessel:	n/a
12	chr1:10699604-10699654	PFSK-1	brain:	n/a
13	chr1:10698313-10698363	NHBE	bronchial:	n/a
14	chr1:10697703-10697753	HRCEpiC	kidney:	n/a
15	chr1:10698794-10698844	GM12892	blood:	n/a
16	chr1:10697703-10697753	SAEC	small airway:	n/a
17	chr1:10698794-10698844	NH-A	brain:	n/a
18	chr1:10699958-10700008	AG09319	gingival:	n/a
19	chr1:10699831-10699881	NHDF-neo	bronchial:	n/a
20	chr1:10699604-10699654	HRPEpiC	eye:	n/a
21	chr1:10697703-10697753	HCM	heart:	n/a
22	chr1:10698719-10698769	AG04450	lung:	fetal
23	chr1:10698794-10698844	HMEC	breast:	n/a
24	chr1:10698794-10698844	AoSMC	blood vessel:	n/a
25	chr1:10698794-10698844	HIPEpiC	eye:	n/a
26	chr1:10698794-10698844	HepG2	liver:	n/a
27	chr1:10698719-10698769	BE2_C	brain:	n/a
28	chr1:10698313-10698363	IMR90	lung:	fetal
29	chr1:10698719-10698769	Jurkat	blood:	n/a
30	chr1:10698313-10698363	HIPEpiC	eye:	n/a
31	chr1:10697703-10697753	GM19239	blood:	n/a
32	chr1:10698719-10698769	SAEC	small airway:	n/a
33	chr1:10699831-10699881	AG04450	lung:	fetal
34	chr1:10699604-10699654	AG04450	lung:	fetal
35	chr1:10699958-10700008	MCF-7	breast:	n/a
36	chr1:10699604-10699654	CMK	blood:	n/a
37	chr1:10699958-10700008	SAEC	small airway:	n/a
38	chr1:10697703-10697753	Hepatocyte	liver:	n/a
39	chr1:10699831-10699881	PANC-1	pancreas:	n/a
40	chr1:10699958-10700008	NT2-D1	testis:	n/a
41	chr1:10698719-10698769	SK-N-MC	brain:	n/a
42	chr1:10699975-10700025	NB4	blood:	n/a
43	chr1:10698719-10698769	NB4	blood:	n/a
44	chr1:10698719-10698769	HRCEpiC	kidney:	n/a
45	chr1:10698313-10698363	AG09309	skin:	n/a
46	chr1:10698719-10698769	AoSMC	blood vessel:	n/a
47	chr1:10698794-10698844	NHBE	bronchial:	n/a
48	chr1:10697703-10697753	HepG2	liver:	n/a
49	chr1:10698719-10698769	GM06990	blood:	n/a
50	chr1:10699604-10699654	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:10698140..10700728-chr1:10703080..10705863,3	K562	blood:
2	chr1:10685500..10687497-chr1:10695365..10698289,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DFFA-4	chr1:10698772-10698820	NONHSAT000866

No data

Variant related genes	Relation type
CASZ1	TF binding region
ENSG00000272078	TF binding region
CASZ1	CpG island
ENSG00000272078	CpG island
ENSG00000130940	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533664463	chr1:10697616-10697617	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs12404480	chr1:10697619-10697620	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs566301546	chr1:10697632-10697633	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530400127	chr1:10697649-10697650	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs188185377	chr1:10697679-10697680	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551436928	chr1:10697692-10697693	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563284604	chr1:10697703-10697704	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs537056136	chr1:10697741-10697742	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs558972562	chr1:10697756-10697757	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139937925	chr1:10697771-10697772	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534482520	chr1:10697841-10697842	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142845529	chr1:10697842-10697843	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144310260	chr1:10697864-10697865	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199867187	chr1:10697879-10697880	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567186092	chr1:10697880-10697881	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567321963	chr1:10697915-10697916	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541717997	chr1:10697918-10697919	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538649088	chr1:10697925-10697926	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191609779	chr1:10697972-10697973	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182954626	chr1:10697996-10697997	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564178454	chr1:10698130-10698131	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528149862	chr1:10698132-10698133	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540361726	chr1:10698134-10698135	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs559975152	chr1:10698165-10698166	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575046161	chr1:10698169-10698170	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530366392	chr1:10698181-10698182	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187980089	chr1:10698191-10698192	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371126309	chr1:10698194-10698195	Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191369987	chr1:10698200-10698201	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs555684	chr1:10698218-10698219	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs546022463	chr1:10698223-10698224	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs148704981	chr1:10698224-10698225	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs373225643	chr1:10698239-10698240	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564213932	chr1:10698251-10698252	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs546365765	chr1:10698259-10698260	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552312055	chr1:10698287-10698288	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571252771	chr1:10698307-10698308	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs570852916	chr1:10698310-10698311	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs534779019	chr1:10698342-10698343	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553092606	chr1:10698353-10698354	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs2624879	chr1:10698363-10698364	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567866272	chr1:10698387-10698388	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs2765547	chr1:10698388-10698389	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs35742428	chr1:10698427-10698428	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2765546	chr1:10698432-10698433	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183510698	chr1:10698434-10698435	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs61776293	chr1:10698442-10698443	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs187800579	chr1:10698486-10698487	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539747065	chr1:10698537-10698538	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs557449944	chr1:10698574-10698575	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	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
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	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
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	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
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10632600-10698000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:10651600-10715800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:10660200-10697600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr1:10664400-10698000	Weak transcription	Primary B cells from cord blood	blood
5	chr1:10681200-10697600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:10685200-10699400	Weak transcription	Aorta	Aorta
7	chr1:10686200-10698000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:10687600-10698000	Weak transcription	Small Intestine	intestine
9	chr1:10691400-10698000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:10691600-10697600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr1:10691600-10703000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr1:10691600-10706000	Weak transcription	Dnd41	blood
13	chr1:10691800-10697800	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr1:10692000-10697800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:10692400-10699400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr1:10692600-10698400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:10693200-10699400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:10693600-10697600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:10693600-10698000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr1:10694200-10697800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:10694400-10699400	Weak transcription	Liver	Liver
22	chr1:10694600-10698400	Weak transcription	NHLF	lung
23	chr1:10694800-10697800	Enhancers	Stomach Mucosa	stomach
24	chr1:10695400-10698200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:10695800-10697600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:10695800-10697600	Strong transcription	Fetal Intestine Large	intestine
27	chr1:10695800-10697600	Weak transcription	Ovary	ovary
28	chr1:10695800-10700400	Strong transcription	Fetal Intestine Small	intestine
29	chr1:10696000-10699400	Weak transcription	Pancreas	Pancrea
30	chr1:10696000-10699600	Weak transcription	Fetal Heart	heart
31	chr1:10696200-10697600	Weak transcription	Fetal Lung	lung
32	chr1:10696200-10698200	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr1:10696200-10698400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr1:10696200-10698600	Weak transcription	Left Ventricle	heart
35	chr1:10696200-10704000	Weak transcription	HSMMtube	muscle
36	chr1:10696400-10697600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:10696400-10697600	Weak transcription	Spleen	Spleen
38	chr1:10696400-10698200	Weak transcription	Right Atrium	heart
39	chr1:10696400-10698200	Weak transcription	Right Ventricle	heart
40	chr1:10696400-10699600	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr1:10696600-10697600	Weak transcription	Esophagus	oesophagus
42	chr1:10696600-10698200	Weak transcription	Psoas Muscle	Psoas
43	chr1:10696600-10698600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:10696600-10698800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:10696600-10699400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr1:10696800-10698400	Enhancers	NHEK	skin
47	chr1:10697000-10697800	Enhancers	HMEC	breast
48	chr1:10697200-10697600	Strong transcription	Lung	lung
49	chr1:10697200-10698200	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr1:10697200-10698400	Enhancers	Skeletal Muscle Male	skeletal muscle

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