Variant report

Variant	esv3339024
Chromosome Location	chr2:32233873-32237321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:956)
CpG islands
(count:610)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:956 , 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	chr2:32235863-32236622	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:32234455-32234481	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:32236051-32236427	K562	blood:	n/a	n/a
4	ATF2	chr2:32235777-32236419	H1-hESC	embryonic stem cell:	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	chr2:32235670-32236986	GM12878	blood:	n/a	n/a
8	ATF3	chr2:32235765-32236438	A549	lung:	n/a	chr2:32236136-32236145
9	ATF3	chr2:32235747-32236709	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	chr2:32235877-32236380	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:32235922-32236337	GM12878	blood:	n/a	n/a
15	BCL3	chr2:32235739-32236800	A549	lung:	n/a	chr2:32236777-32236786
16	BCL3	chr2:32235789-32236721	A549	lung:	n/a	n/a
17	BCL3	chr2:32235745-32236359	GM12878	blood:	n/a	n/a
18	BCLAF1	chr2:32235743-32236409	K562	blood:	n/a	n/a
19	BCLAF1	chr2:32235738-32236601	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:32235768-32236717	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:32234559-32235055	K562	blood:	n/a	chr2:32234871-32234887 chr2:32234676-32234692
22	BHLHE40	chr2:32235845-32236530	K562	blood:	n/a	chr2:32235917-32235933
23	BHLHE40	chr2:32235852-32236509	HepG2	liver:	n/a	chr2:32235917-32235933
24	BHLHE40	chr2:32235706-32236770	GM12878	blood:	n/a	chr2:32235917-32235933
25	BHLHE40	chr2:32234606-32235014	GM12878	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	chr2:32235769-32236725	K562	blood:	n/a	n/a
31	CBX3	chr2:32235781-32236759	HCT-116	colon:	n/a	n/a
32	CCNT2	chr2:32235740-32236376	K562	blood:	n/a	chr2:32236171-32236180
33	CCNT2	chr2:32234582-32235329	K562	blood:	n/a	n/a
34	CEBPB	chr2:32235920-32236459	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:32236049-32236249	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:32235929-32236423	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:32235935-32236170	K562	blood:	n/a	n/a
38	CEBPB	chr2:32235964-32236230	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:32235830-32236442	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr2:32235803-32236711	GM12878	blood:	n/a	n/a
41	CEBPD	chr2:32235622-32236397	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	CHD1	chr2:32235943-32236307	H1-hESC	embryonic stem cell:	n/a	chr2:32236137-32236147
45	CHD1	chr2:32234686-32235047	GM12878	blood:	n/a	n/a
46	CHD1	chr2:32235885-32236677	GM12878	blood:	n/a	chr2:32236137-32236147
47	CHD2	chr2:32235506-32235523	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr2:32234862-32234863	HepG2	liver:	n/a	n/a
49	CHD2	chr2:32235764-32236430	K562	blood:	n/a	chr2:32236137-32236147
50	CHD2	chr2:32234359-32234369	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	AG04450	lung:	fetal
2	chr2:32236023-32236073	HUVEC	blood vessel:	n/a
3	chr2:32236023-32236073	GM06990	blood:	n/a
4	chr2:32235760-32235810	H1-hESC	embryonic stem cell:	embryo
5	chr2:32234977-32235027	RPTEC	kidney:	n/a
6	chr2:32234977-32235027	SK-N-SH_RA	brain:	n/a
7	chr2:32234977-32235027	AG09319	gingival:	n/a
8	chr2:32235240-32235290	HRE	kidney:	n/a
9	chr2:32236000-32236050	HRPEpiC	eye:	n/a
10	chr2:32234977-32235027	SK-N-SH	brain:	n/a
11	chr2:32235925-32235975	HCPEpiC	choroid plexus:	n/a
12	chr2:32234977-32235027	H1-hESC	embryonic stem cell:	embryo
13	chr2:32235240-32235290	NH-A	brain:	n/a
14	chr2:32235760-32235810	MCF-7	breast:	n/a
15	chr2:32234829-32234879	AG04450	lung:	fetal
16	chr2:32236343-32236393	MCF-7	breast:	n/a
17	chr2:32236343-32236393	AG10803	skin:	n/a
18	chr2:32234977-32235027	HNPCEpiC	eye:	n/a
19	chr2:32236023-32236073	H1-hESC	embryonic stem cell:	embryo
20	chr2:32236343-32236393	Hepatocyte	liver:	n/a
21	chr2:32234829-32234879	HUVEC	blood vessel:	n/a
22	chr2:32235770-32235820	AoSMC	blood vessel:	n/a
23	chr2:32235770-32235820	MCF10A-Er-Src	breast:	n/a
24	chr2:32235770-32235820	SKMC	muscle:	n/a
25	chr2:32236023-32236073	GM19239	blood:	n/a
26	chr2:32236343-32236393	GM12878	blood:	n/a
27	chr2:32235760-32235810	HCPEpiC	choroid plexus:	n/a
28	chr2:32236343-32236393	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:32234829-32234879	HRE	kidney:	n/a
30	chr2:32236343-32236393	SK-N-MC	brain:	n/a
31	chr2:32236023-32236073	ECC-1	luminal epithelium:	n/a
32	chr2:32236000-32236050	ECC-1	luminal epithelium:	n/a
33	chr2:32236000-32236050	GM12891	blood:	n/a
34	chr2:32236343-32236393	PFSK-1	brain:	n/a
35	chr2:32236343-32236393	HCT-116	colon:	n/a
36	chr2:32235240-32235290	CMK	blood:	n/a
37	chr2:32235770-32235820	PrEC	prostate:	n/a
38	chr2:32234829-32234879	HMEC	breast:	n/a
39	chr2:32236247-32236297	A549	lung:	n/a
40	chr2:32236343-32236393	ovcar-3	ovarian:	n/a
41	chr2:32235770-32235820	LNCaP	prostate:	n/a
42	chr2:32236023-32236073	Hepatocyte	liver:	n/a
43	chr2:32236023-32236073	NB4	blood:	n/a
44	chr2:32234829-32234879	Caco-2	colon:	n/a
45	chr2:32234977-32235027	NHDF-neo	bronchial:	n/a
46	chr2:32236343-32236393	H1-hESC	embryonic stem cell:	embryo
47	chr2:32235925-32235975	GM19239	blood:	n/a
48	chr2:32235240-32235290	K562	blood:	n/a
49	chr2:32236000-32236050	PFSK-1	brain:	n/a
50	chr2:32236000-32236050	SK-N-SH_RA	brain:	n/a

(count:29 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEMO1-2	chr2:32236986-32237125	NONHSAT069965

No data

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

Extended variants
information (count: 106 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	rs551306824	chr2:32235151-32235152	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs571285203	chr2:32235296-32235297	Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs527391541	chr2:32235363-32235364	Weak transcription Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs546939640	chr2:32235486-32235487	Weak transcription Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs566917124	chr2:32235567-32235568	Weak transcription Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs535881132	chr2:32235848-32235849	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs556797238	chr2:32235852-32235853	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
43	rs570277386	chr2:32235863-32235864	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
44	rs539190398	chr2:32235867-32235868	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
45	rs558896759	chr2:32235879-32235880	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
46	rs572526880	chr2:32235884-32235885	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
47	rs368306118	chr2:32235924-32235925	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
48	rs535120559	chr2:32235965-32235966	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
49	rs184759784	chr2:32235987-32235988	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
50	rs574871154	chr2:32236002-32236003	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 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:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr2:32230400-32234000	Weak transcription	Psoas Muscle	Psoas
8	chr2:32230800-32234000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr2:32231400-32234000	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr2:32231800-32234000	Enhancers	Primary B cells from peripheral blood	blood
11	chr2:32231800-32234000	Weak transcription	Ovary	ovary
12	chr2:32232000-32234200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:32232000-32234200	Weak transcription	Pancreas	Pancrea
14	chr2:32232200-32234000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr2:32233000-32234200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr2:32233000-32234400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:32233200-32234000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr2:32233200-32234000	Enhancers	Placenta	Placenta
19	chr2:32233200-32234200	Flanking Active TSS	HUVEC	blood vessel
20	chr2:32233200-32234400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:32233200-32234400	Enhancers	Small Intestine	intestine
22	chr2:32233200-32234400	Flanking Active TSS	Dnd41	blood
23	chr2:32233200-32234400	Flanking Active TSS	Hela-S3	cervix
24	chr2:32233200-32234600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr2:32233200-32236200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:32233200-32236200	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr2:32233400-32234000	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr2:32233400-32234000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr2:32233400-32234000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:32233400-32234000	Active TSS	HepG2	liver
31	chr2:32233400-32234200	Flanking Active TSS	NH-A	brain
32	chr2:32233400-32234400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:32233400-32234600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr2:32233400-32234600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:32233400-32234600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:32233400-32236200	Active TSS	Colonic Mucosa	Colon
37	chr2:32233400-32236200	Active TSS	HSMM	muscle
38	chr2:32233400-32236400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:32233400-32236600	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr2:32233400-32236600	Active TSS	Fetal Intestine Large	intestine
41	chr2:32233600-32234000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:32233600-32234000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:32233600-32234000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:32233600-32234000	Flanking Active TSS	Primary T cells from cord blood	blood
45	chr2:32233600-32234000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr2:32233600-32234000	Enhancers	Adipose Nuclei	Adipose
47	chr2:32233600-32234000	Flanking Active TSS	Fetal Intestine Small	intestine
48	chr2:32233600-32234000	Flanking Active TSS	Fetal Thymus	thymus
49	chr2:32233600-32234000	Weak transcription	Right Atrium	heart
50	chr2:32233600-32234000	Flanking Active TSS	K562	blood

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