Variant report

Variant	esv3416925
Chromosome Location	chr2:32233648-32236796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:953)
CpG islands
(count:610)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:32234455-32234481	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:32236051-32236427	K562	blood:	n/a	n/a
3	ARID3A	chr2:32235863-32236622	HepG2	liver:	n/a	n/a
4	ATF2	chr2:32235670-32236986	GM12878	blood:	n/a	n/a
5	ATF2	chr2:32235792-32236431	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:32235767-32236669	GM12878	blood:	n/a	n/a
7	ATF2	chr2:32235777-32236419	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr2:32235747-32236709	A549	lung:	n/a	chr2:32236136-32236145
9	ATF3	chr2:32235765-32236438	A549	lung:	n/a	chr2:32236136-32236145
10	BACH1	chr2:32234364-32234644	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:32235944-32236363	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr2:32235950-32236424	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:32235922-32236337	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:32235877-32236380	GM12878	blood:	n/a	n/a
15	BCL3	chr2:32235745-32236359	GM12878	blood:	n/a	n/a
16	BCL3	chr2:32235739-32236800	A549	lung:	n/a	chr2:32236777-32236786
17	BCL3	chr2:32235789-32236721	A549	lung:	n/a	n/a
18	BCLAF1	chr2:32235738-32236601	GM12878	blood:	n/a	n/a
19	BCLAF1	chr2:32235768-32236717	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:32235743-32236409	K562	blood:	n/a	n/a
21	BHLHE40	chr2:32235845-32236530	K562	blood:	n/a	chr2:32235917-32235933
22	BHLHE40	chr2:32235852-32236509	HepG2	liver:	n/a	chr2:32235917-32235933
23	BHLHE40	chr2:32234606-32235014	GM12878	blood:	n/a	chr2:32234871-32234887 chr2:32234676-32234692
24	BHLHE40	chr2:32235706-32236770	GM12878	blood:	n/a	chr2:32235917-32235933
25	BHLHE40	chr2:32234559-32235055	K562	blood:	n/a	chr2:32234871-32234887 chr2:32234676-32234692
26	BRCA1	chr2:32235806-32236443	GM12878	blood:	n/a	n/a
27	BRCA1	chr2:32235853-32236603	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr2:32235899-32236261	HepG2	liver:	n/a	n/a
29	CBX3	chr2:32235944-32236413	K562	blood:	n/a	n/a
30	CBX3	chr2:32235781-32236759	HCT-116	colon:	n/a	n/a
31	CBX3	chr2:32235769-32236725	K562	blood:	n/a	n/a
32	CBX3	chr2:32233249-32233764	K562	blood:	n/a	n/a
33	CCNT2	chr2:32234582-32235329	K562	blood:	n/a	n/a
34	CCNT2	chr2:32235740-32236376	K562	blood:	n/a	chr2:32236171-32236180
35	CEBPB	chr2:32235920-32236459	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:32235803-32236711	GM12878	blood:	n/a	n/a
37	CEBPB	chr2:32235929-32236423	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:32235830-32236442	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr2:32236049-32236249	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:32235935-32236170	K562	blood:	n/a	n/a
41	CEBPB	chr2:32235964-32236230	HepG2	liver:	n/a	n/a
42	CEBPD	chr2:32235710-32236334	HepG2	liver:	n/a	n/a
43	CEBPD	chr2:32235792-32236451	K562	blood:	n/a	n/a
44	CEBPD	chr2:32235622-32236397	HepG2	liver:	n/a	n/a
45	CHD1	chr2:32234686-32235047	GM12878	blood:	n/a	n/a
46	CHD1	chr2:32235885-32236677	GM12878	blood:	n/a	chr2:32236137-32236147
47	CHD1	chr2:32235943-32236307	H1-hESC	embryonic stem cell:	n/a	chr2:32236137-32236147
48	CHD2	chr2:32235871-32236586	H1-hESC	embryonic stem cell:	n/a	chr2:32236137-32236147
49	CHD2	chr2:32234862-32234863	HepG2	liver:	n/a	n/a
50	CHD2	chr2:32234619-32234873	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:32236023-32236073	SK-N-MC	brain:	n/a
2	chr2:32235240-32235290	HNPCEpiC	eye:	n/a
3	chr2:32235240-32235290	ProgFib	skin:	n/a
4	chr2:32235760-32235810	HCT-116	colon:	n/a
5	chr2:32235925-32235975	GM12878	blood:	n/a
6	chr2:32235770-32235820	HUVEC	blood vessel:	n/a
7	chr2:32236000-32236050	AG09309	skin:	n/a
8	chr2:32235760-32235810	ProgFib	skin:	n/a
9	chr2:32234829-32234879	ovcar-3	ovarian:	n/a
10	chr2:32235760-32235810	HEEpiC	esophagus:	n/a
11	chr2:32235240-32235290	SK-N-SH_RA	brain:	n/a
12	chr2:32236023-32236073	HCPEpiC	choroid plexus:	n/a
13	chr2:32234977-32235027	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:32235770-32235820	HAEpiC	amniotic membrane:	n/a
15	chr2:32236000-32236050	GM12892	blood:	n/a
16	chr2:32236023-32236073	HUVEC	blood vessel:	n/a
17	chr2:32236000-32236050	H1-hESC	embryonic stem cell:	embryo
18	chr2:32235925-32235975	HRCEpiC	kidney:	n/a
19	chr2:32236000-32236050	SK-N-MC	brain:	n/a
20	chr2:32235770-32235820	K562	blood:	n/a
21	chr2:32235760-32235810	T-47D	breast:	n/a
22	chr2:32234977-32235027	LNCaP	prostate:	n/a
23	chr2:32236247-32236297	HCPEpiC	choroid plexus:	n/a
24	chr2:32236343-32236393	MCF10A-Er-Src	breast:	n/a
25	chr2:32235240-32235290	GM12892	blood:	n/a
26	chr2:32236343-32236393	RPTEC	kidney:	n/a
27	chr2:32236343-32236393	NB4	blood:	n/a
28	chr2:32234829-32234879	HepG2	liver:	n/a
29	chr2:32235760-32235810	NH-A	brain:	n/a
30	chr2:32236343-32236393	HCM	heart:	n/a
31	chr2:32236247-32236297	BJ	skin:	n/a
32	chr2:32235240-32235290	HL-60	blood:	n/a
33	chr2:32235925-32235975	HCT-116	colon:	n/a
34	chr2:32236023-32236073	BE2_C	brain:	n/a
35	chr2:32235240-32235290	HEEpiC	esophagus:	n/a
36	chr2:32236247-32236297	HL-60	blood:	n/a
37	chr2:32235760-32235810	HepG2	liver:	n/a
38	chr2:32236247-32236297	PrEC	prostate:	n/a
39	chr2:32235925-32235975	BE2_C	brain:	n/a
40	chr2:32235770-32235820	SAEC	small airway:	n/a
41	chr2:32234977-32235027	HCPEpiC	choroid plexus:	n/a
42	chr2:32236023-32236073	HAEpiC	amniotic membrane:	n/a
43	chr2:32235770-32235820	Hela-S3	cervix:	n/a
44	chr2:32236000-32236050	LNCaP	prostate:	n/a
45	chr2:32234977-32235027	HEK293	kidney:	embryo
46	chr2:32236023-32236073	HepG2	liver:	n/a
47	chr2:32235240-32235290	SK-N-SH	brain:	n/a
48	chr2:32234977-32235027	AoSMC	blood vessel:	n/a
49	chr2:32235925-32235975	SKMC	muscle:	n/a
50	chr2:32236247-32236297	HNPCEpiC	eye:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:32231133..32238127-chr2:32263164..32266706,7	MCF-7	breast:
2	chr2:32166637..32169522-chr2:32234606..32236345,2	K562	blood:
3	chr2:32236441..32237946-chr2:32298713..32301695,2	K562	blood:
4	chr2:32077309..32079033-chr2:32235796..32237678,2	K562	blood:
5	chr2:32233869..32235900-chr2:32286911..32289660,3	K562	blood:
6	chr2:32233185..32238105-chr2:32388775..32395245,11	K562	blood:
7	chr2:32234479..32235226-chr2:32264789..32265391,2	Hela-S3	cervix:
8	chr2:32235154..32237462-chr2:32390889..32392468,2	MCF-7	breast:
9	chr1:210547155..210547688-chr2:32235666..32236437,2	Hela-S3	cervix:
10	chr2:32233242..32236257-chr2:32247330..32249765,3	MCF-7	breast:
11	chr2:32234518..32235424-chr2:32390732..32391392,2	Hela-S3	cervix:
12	chr2:32235559..32236383-chr5:43121008..43121950,2	Hela-S3	cervix:
13	chr2:32233050..32238839-chr2:32262715..32266551,10	MCF-7	breast:
14	chr17:56063594..56066516-chr2:32234123..32236602,2	MCF-7	breast:
15	chr1:45285087..45285958-chr2:32235554..32236249,2	HCT-116	colon:
16	chr2:32234151..32237531-chr2:32262421..32266825,7	K562	blood:
17	chr2:32234641..32236375-chr2:32389314..32391737,5	MCF-7	breast:
18	chr2:32234599..32235496-chr21:36260941..36261595,2	Hela-S3	cervix:
19	chr2:32233309..32238481-chr2:32286150..32290599,7	MCF-7	breast:
20	chr1:227916225..227917863-chr2:32234372..32236417,2	MCF-7	breast:
21	chr2:32158032..32160777-chr2:32231295..32234289,2	K562	blood:
22	chr2:32232898..32237970-chr2:32287390..32290443,5	K562	blood:
23	chr2:32235889..32238860-chr2:32287017..32290574,4	MCF-7	breast:
24	chr2:32233077..32237611-chr2:32388376..32395245,10	K562	blood:
25	chr2:32231239..32234526-chr2:32234585..32239142,5	MCF-7	breast:
26	chr2:32234491..32236283-chr2:32581671..32583851,2	MCF-7	breast:
27	chr2:32210208..32213123-chr2:32231743..32234482,2	K562	blood:
28	chr2:32232071..32233742-chr2:32268777..32271589,2	MCF-7	breast:
29	chr2:32173570..32176188-chr2:32233280..32235054,2	K562	blood:
30	chr2:32233869..32239615-chr2:32259766..32267170,13	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271228	TF binding region
MEMO1	TF binding region
ENSG00000271228	CpG island
MEMO1	CpG island
ENSG00000162959	chromatin interactions
ENSG00000143740	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000162961	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000273165	chromatin interactions
ENSG00000136451	chromatin interactions
ENSG00000272716	chromatin interactions
ENSG00000021574	chromatin interactions
ENSG00000271228	chromatin interactions
ENSG00000159216	chromatin interactions
ENSG00000152683	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000115760	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568932269	chr2:32233659-32233660	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs537949999	chr2:32233662-32233663	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs557614874	chr2:32233669-32233670	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs111402818	chr2:32233692-32233693	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs572804509	chr2:32233700-32233701	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs185080582	chr2:32233765-32233766	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs554020599	chr2:32233768-32233769	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs574014058	chr2:32233774-32233775	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs376654173	chr2:32233801-32233802	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs556344776	chr2:32233817-32233818	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs190125259	chr2:32233872-32233873	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs533507568	chr2:32233878-32233879	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs371089385	chr2:32233934-32233935	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs143110025	chr2:32233941-32233942	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs117116645	chr2:32234011-32234012	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs367947743	chr2:32234058-32234059	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs200758744	chr2:32234074-32234075	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs527665874	chr2:32234097-32234098	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs148250584	chr2:32234113-32234114	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs141820864	chr2:32234153-32234154	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs146280937	chr2:32234165-32234166	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs550424857	chr2:32234181-32234182	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs138805243	chr2:32234250-32234251	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs181654260	chr2:32234268-32234269	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs531446193	chr2:32234313-32234314	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs551440098	chr2:32234334-32234335	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs571281618	chr2:32234348-32234349	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs552392993	chr2:32234432-32234433	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs370390954	chr2:32234439-32234440	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs533514790	chr2:32234455-32234456	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs553364648	chr2:32234482-32234483	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs373599536	chr2:32234531-32234532	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs567576466	chr2:32234540-32234541	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs536547977	chr2:32234556-32234557	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs367777290	chr2:32234558-32234559	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs556483016	chr2:32234635-32234636	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
37	rs576566697	chr2:32234638-32234639	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
38	rs141990155	chr2:32234648-32234649	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
39	rs875167	chr2:32234656-32234657	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572465034	chr2:32234686-32234687	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
41	rs541397709	chr2:32234724-32234725	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
42	rs875168	chr2:32234790-32234791	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	rs530164069	chr2:32234799-32234800	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	rs568899396	chr2:32234910-32234911	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs562674598	chr2:32234912-32234913	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs13012667	chr2:32234946-32234947	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs551306824	chr2:32235151-32235152	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs571285203	chr2:32235296-32235297	Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs527391541	chr2:32235363-32235364	Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs546939640	chr2:32235486-32235487	Weak transcription Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Neurocytoma	17123091	CNVD
hereditary spastic paraplegia	21659953	CNVD
Autosomal-dominant hereditary spastic paraplegia	17098887	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:32191600-32234200	Weak transcription	Lung	lung
2	chr2:32206600-32234000	Weak transcription	Stomach Mucosa	stomach
3	chr2:32223400-32234400	Weak transcription	Spleen	Spleen
4	chr2:32225800-32234200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:32229200-32234200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:32229200-32234200	Weak transcription	Esophagus	oesophagus
7	chr2:32230000-32233800	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr2:32230000-32233800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr2:32230400-32234000	Weak transcription	Psoas Muscle	Psoas
10	chr2:32230800-32234000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr2:32231000-32233800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr2:32231400-32233800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:32231400-32234000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr2:32231800-32234000	Enhancers	Primary B cells from peripheral blood	blood
15	chr2:32231800-32234000	Weak transcription	Ovary	ovary
16	chr2:32232000-32233800	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr2:32232000-32234200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:32232000-32234200	Weak transcription	Pancreas	Pancrea
19	chr2:32232200-32233800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr2:32232200-32233800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:32232200-32233800	Enhancers	Brain Hippocampus Middle	brain
22	chr2:32232200-32233800	Enhancers	Fetal Brain Male	brain
23	chr2:32232200-32233800	Enhancers	Fetal Lung	lung
24	chr2:32232200-32234000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr2:32232800-32233800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:32233000-32233800	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr2:32233000-32233800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:32233000-32233800	Enhancers	Brain Angular Gyrus	brain
29	chr2:32233000-32233800	Enhancers	Colon Smooth Muscle	Colon
30	chr2:32233000-32234200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr2:32233000-32234400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr2:32233200-32233800	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr2:32233200-32233800	Active TSS	Brain Anterior Caudate	brain
34	chr2:32233200-32233800	Enhancers	Brain Cingulate Gyrus	brain
35	chr2:32233200-32233800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr2:32233200-32233800	Enhancers	Fetal Heart	heart
37	chr2:32233200-32233800	Enhancers	Rectal Smooth Muscle	rectum
38	chr2:32233200-32234000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr2:32233200-32234000	Enhancers	Placenta	Placenta
40	chr2:32233200-32234200	Flanking Active TSS	HUVEC	blood vessel
41	chr2:32233200-32234400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:32233200-32234400	Enhancers	Small Intestine	intestine
43	chr2:32233200-32234400	Flanking Active TSS	Dnd41	blood
44	chr2:32233200-32234400	Flanking Active TSS	Hela-S3	cervix
45	chr2:32233200-32234600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr2:32233200-32236200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:32233200-32236200	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr2:32233400-32233800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr2:32233400-32233800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr2:32233400-32233800	Active TSS	Brain Germinal Matrix	brain

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