Variant report

Variant	esv2763643
Chromosome Location	chr2:64219887-64281337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1392)
CpG islands
(count:856)
Chromatin interactive
region (count:77)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1392 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:64248789-64249124	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:64247140-64247364	K562	blood:	n/a	n/a
3	ARID3A	chr2:64247738-64248011	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:64244818-64245208	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:64246717-64247240	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:64276892-64277198	K562	blood:	n/a	n/a
7	ARID3A	chr2:64243103-64243351	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:64251091-64252414	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:64220314-64220775	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:64245796-64245820	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:64266414-64266496	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:64276870-64277217	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:64244923-64245775	K562	blood:	n/a	n/a
14	ATF1	chr2:64263235-64263755	K562	blood:	n/a	n/a
15	ATF1	chr2:64244916-64245238	K562	blood:	n/a	n/a
16	ATF2	chr2:64276728-64277390	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:64246751-64247350	GM12878	blood:	n/a	n/a
18	ATF2	chr2:64263443-64263842	GM12878	blood:	n/a	n/a
19	ATF2	chr2:64276843-64277276	GM12878	blood:	n/a	n/a
20	ATF3	chr2:64235736-64236132	K562	blood:	n/a	n/a
21	BACH1	chr2:64262983-64263126	K562	blood:	n/a	n/a
22	BACH1	chr2:64245937-64246983	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr2:64262683-64263046	GM12878	blood:	n/a	chr2:64262891-64262899
24	BATF	chr2:64263543-64263781	GM12878	blood:	n/a	chr2:64263663-64263672
25	BATF	chr2:64263481-64263763	GM12878	blood:	n/a	chr2:64263663-64263672
26	BCL11A	chr2:64263450-64263773	GM12878	blood:	n/a	n/a
27	BCLAF1	chr2:64276697-64277289	GM12878	blood:	n/a	n/a
28	BCLAF1	chr2:64276753-64277250	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:64245602-64245946	GM12878	blood:	n/a	n/a
30	BCLAF1	chr2:64246256-64246782	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:64240402-64240469	K562	blood:	n/a	n/a
32	BHLHE40	chr2:64246384-64246987	GM12878	blood:	n/a	chr2:64246503-64246519 chr2:64246529-64246545
33	BHLHE40	chr2:64246300-64247109	HepG2	liver:	n/a	chr2:64246503-64246519 chr2:64246529-64246545
34	BHLHE40	chr2:64262843-64263101	GM12878	blood:	n/a	chr2:64262992-64263001
35	BHLHE40	chr2:64247257-64247357	K562	blood:	n/a	n/a
36	BHLHE40	chr2:64245768-64245932	K562	blood:	n/a	n/a
37	BHLHE40	chr2:64263533-64263750	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:64246282-64246740	K562	blood:	n/a	chr2:64246503-64246519 chr2:64246529-64246545
39	BRCA1	chr2:64246690-64246918	GM12878	blood:	n/a	n/a
40	BRCA1	chr2:64250926-64251118	HepG2	liver:	n/a	n/a
41	BRCA1	chr2:64276845-64277202	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr2:64276821-64277109	HepG2	liver:	n/a	n/a
43	BRCA1	chr2:64246728-64246918	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr2:64246353-64246439	HepG2	liver:	n/a	n/a
45	CBX3	chr2:64223763-64224008	K562	blood:	n/a	n/a
46	CBX3	chr2:64243003-64243476	HCT-116	colon:	n/a	n/a
47	CCNT2	chr2:64245986-64246822	K562	blood:	n/a	chr2:64245987-64245996
48	CEBPB	chr2:64235036-64235240	HepG2	liver:	n/a	chr2:64235167-64235180
49	CEBPB	chr2:64235782-64236118	IMR90	lung:	n/a	chr2:64235943-64235954
50	CEBPB	chr2:64226199-64226478	MCF-7	breast:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:64246845-64246895	PrEC	prostate:	n/a
2	chr2:64255986-64256036	SK-N-MC	brain:	n/a
3	chr2:64246845-64246895	PrEC	prostate:	n/a
4	chr2:64255986-64256036	SK-N-MC	brain:	n/a
5	chr2:64246689-64246739	Caco-2	colon:	n/a
6	chr2:64246689-64246739	GM12891	blood:	n/a
7	chr2:64247030-64247080	MCF10A-Er-Src	breast:	n/a
8	chr2:64245000-64245050	NHDF-neo	bronchial:	n/a
9	chr2:64245679-64245729	H1-hESC	embryonic stem cell:	embryo
10	chr2:64250606-64250656	H1-hESC	embryonic stem cell:	embryo
11	chr2:64246058-64246108	HL-60	blood:	n/a
12	chr2:64245000-64245050	PANC-1	pancreas:	n/a
13	chr2:64245679-64245729	HCT-116	colon:	n/a
14	chr2:64245000-64245050	K562	blood:	n/a
15	chr2:64277748-64277798	HCT-116	colon:	n/a
16	chr2:64246689-64246739	GM12892	blood:	n/a
17	chr2:64246311-64246361	HepG2	liver:	n/a
18	chr2:64247030-64247080	T-47D	breast:	n/a
19	chr2:64247030-64247080	HUVEC	blood vessel:	n/a
20	chr2:64246311-64246361	NHDF-neo	bronchial:	n/a
21	chr2:64246058-64246108	H1-hESC	embryonic stem cell:	embryo
22	chr2:64246349-64246399	HCF	heart:	n/a
23	chr2:64245812-64245862	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:64246311-64246361	HCPEpiC	choroid plexus:	n/a
25	chr2:64245679-64245729	ovcar-3	ovarian:	n/a
26	chr2:64246689-64246739	NHBE	bronchial:	n/a
27	chr2:64245679-64245729	HCPEpiC	choroid plexus:	n/a
28	chr2:64246058-64246108	T-47D	breast:	n/a
29	chr2:64255986-64256036	AG09319	gingival:	n/a
30	chr2:64277748-64277798	SK-N-MC	brain:	n/a
31	chr2:64277748-64277798	ProgFib	skin:	n/a
32	chr2:64255986-64256036	HRCEpiC	kidney:	n/a
33	chr2:64246058-64246108	AoSMC	blood vessel:	n/a
34	chr2:64245679-64245729	NH-A	brain:	n/a
35	chr2:64245812-64245862	ProgFib	skin:	n/a
36	chr2:64245679-64245729	SK-N-SH	brain:	n/a
37	chr2:64246297-64246347	HCF	heart:	n/a
38	chr2:64245679-64245729	ECC-1	luminal epithelium:	n/a
39	chr2:64255986-64256036	HL-60	blood:	n/a
40	chr2:64250606-64250656	AG09309	skin:	n/a
41	chr2:64246349-64246399	NHBE	bronchial:	n/a
42	chr2:64247030-64247080	NB4	blood:	n/a
43	chr2:64246311-64246361	Jurkat	blood:	n/a
44	chr2:64250606-64250656	SAEC	small airway:	n/a
45	chr2:64246349-64246399	AoSMC	blood vessel:	n/a
46	chr2:64246349-64246399	SK-N-SH_RA	brain:	n/a
47	chr2:64245000-64245050	SK-N-SH	brain:	n/a
48	chr2:64246297-64246347	U87	brain:	n/a
49	chr2:64246297-64246347	HIPEpiC	eye:	n/a
50	chr2:64255986-64256036	Caco-2	colon:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:64252726..64254533-chr2:64259258..64261543,2	K562	blood:
2	chr2:64231679..64233311-chr2:64235934..64238452,2	K562	blood:
3	chr2:64276818..64280771-chr2:64542300..64544663,3	MCF-7	breast:
4	chr2:64267308..64269461-chr2:64274492..64276041,2	K562	blood:
5	chr2:64246318..64247877-chr2:64269595..64271484,2	MCF-7	breast:
6	chr2:64251335..64255008-chr2:64255786..64259305,3	MCF-7	breast:
7	chr2:64245315..64247719-chr2:64265223..64268057,2	MCF-7	breast:
8	chr2:64236322..64240765-chr2:64241571..64244633,4	K562	blood:
9	chr2:64233493..64235637-chr2:64236506..64238086,2	K562	blood:
10	chr2:64275467..64277323-chr2:64280220..64283208,2	MCF-7	breast:
11	chr2:64232589..64235192-chr2:64239355..64241006,2	MCF-7	breast:
12	chr2:64276505..64277378-chr2:64557911..64558603,2	MCF-7	breast:
13	chr2:64276548..64277184-chr2:64715251..64715769,2	MCF-7	breast:
14	chr2:64245996..64247858-chr2:64247865..64250150,3	K562	blood:
15	chr2:64252726..64254533-chr2:64259258..64261543,2	K562	blood:
16	chr2:64225373..64227940-chr2:64228601..64231174,2	K562	blood:
17	chr2:64276518..64277484-chr2:64554739..64555702,3	MCF-7	breast:
18	chr2:64256185..64258127-chr2:64260254..64262848,2	K562	blood:
19	chr2:64244952..64247462-chr2:64258343..64262786,4	K562	blood:
20	chr2:64242543..64244844-chr2:64248879..64250453,2	K562	blood:
21	chr2:64246663..64249169-chr2:64259470..64260972,2	K562	blood:
22	chr2:64226896..64229641-chr2:64246459..64249027,4	K562	blood:
23	chr2:64256991..64258692-chr2:64262523..64264445,2	MCF-7	breast:
24	chr2:64277797..64280331-chr2:64538007..64540114,2	MCF-7	breast:
25	chr2:64245248..64247097-chr2:64369855..64371570,2	MCF-7	breast:
26	chr2:64232589..64235192-chr2:64239355..64241006,2	MCF-7	breast:
27	chr2:64276729..64277524-chr2:64539541..64540065,3	MCF-7	breast:
28	chr2:64227637..64233066-chr2:64233431..64237218,6	K562	blood:
29	chr2:64234313..64237072-chr2:64243615..64245579,2	MCF-7	breast:
30	chr2:64276612..64277598-chr2:64539193..64540210,6	MCF-7	breast:
31	chr2:64233493..64235637-chr2:64236506..64238086,2	K562	blood:
32	chr2:64276558..64277405-chr2:64539242..64539763,2	K562	blood:
33	chr2:64243174..64244724-chr2:64244885..64246414,2	K562	blood:
34	chr2:64246663..64249169-chr2:64259470..64260972,2	K562	blood:
35	chr2:64115956..64116564-chr2:64250969..64251483,2	MCF-7	breast:
36	chr2:64253837..64255979-chr2:64263941..64266708,2	K562	blood:
37	chr2:64233493..64236244-chr2:64240747..64243613,2	K562	blood:
38	chr2:64256991..64258692-chr2:64262523..64264445,2	MCF-7	breast:
39	chr2:64246318..64247877-chr2:64269595..64271484,2	MCF-7	breast:
40	chr2:64237815..64239979-chr2:64245041..64246546,2	K562	blood:
41	chr2:64241763..64244810-chr2:64244833..64246626,3	K562	blood:
42	chr2:64276338..64277502-chr2:64554729..64555729,5	MCF-7	breast:
43	chr2:64238714..64243533-chr2:64243978..64248852,9	MCF-7	breast:
44	chr2:64233493..64236244-chr2:64240747..64243613,2	K562	blood:
45	chr2:64280836..64282865-chr2:64492384..64494313,2	MCF-7	breast:
46	chr2:64230028..64232949-chr2:64243748..64246264,2	MCF-7	breast:
47	chr2:64251335..64255008-chr2:64255786..64259305,3	MCF-7	breast:
48	chr2:64237815..64241189-chr2:64245046..64247385,4	K562	blood:
49	chr2:64238078..64240765-chr2:64241757..64244633,2	K562	blood:
50	chr2:64227637..64233066-chr2:64233431..64237218,6	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VPS54-3	chr2:64265719-64266380	refGeneNc_4218_NR_033837
2	lnc-VPS54-3	chr2:64269655-64269770	NONHSAT071084
3	lnc-VPS54-3	chr2:64265716-64266380	NONHSAT071084
4	lnc-VPS54-3	chr2:64272994-64273096	NONHSAT071084
5	lnc-VPS54-3	chr2:64272994-64273096	refGeneNc_4218_NR_033837
6	lnc-VPS54-3	chr2:64269655-64269770	refGeneNc_4218_NR_033837

No data

Variant related genes	Relation type
VPS54	TF binding region
VPS54	CpG island
ENSG00000143952	chromatin interactions
ENSG00000197329	chromatin interactions
ENSG00000101158	chromatin interactions
ENSG00000225889	chromatin interactions

Extended variants
information (count: 2283 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2283 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113638924	chr2:64219897-64219898	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573612136	chr2:64219904-64219905	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555051966	chr2:64219977-64219978	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186401218	chr2:64219989-64219990	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189247312	chr2:64220069-64220070	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143000893	chr2:64220088-64220089	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544515970	chr2:64220139-64220140	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181445938	chr2:64220187-64220188	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531954118	chr2:64220244-64220245	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs543611200	chr2:64220250-64220251	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs558088796	chr2:64220414-64220415	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs562215073	chr2:64220435-64220436	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs112924587	chr2:64220446-64220447	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs376407067	chr2:64220462-64220463	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs185737170	chr2:64220509-64220510	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs13034625	chr2:64220527-64220528	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs533136215	chr2:64220548-64220549	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs151077923	chr2:64220605-64220606	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs540073238	chr2:64220624-64220625	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs56155077	chr2:64220627-64220628	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs191038686	chr2:64220710-64220711	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555221560	chr2:64220743-64220744	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs141047606	chr2:64220770-64220771	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs534748657	chr2:64220775-64220776	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs553087477	chr2:64220844-64220845	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144600372	chr2:64220848-64220849	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs147186136	chr2:64220893-64220894	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs182931705	chr2:64220903-64220904	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs201903571	chr2:64220907-64220908	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544992635	chr2:64220908-64220909	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs147908458	chr2:64220910-64220911	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs576613311	chr2:64220934-64220935	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs79948778	chr2:64220943-64220944	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs544094162	chr2:64220970-64220971	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs141673653	chr2:64220977-64220978	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs186096057	chr2:64220984-64220985	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs541157241	chr2:64220989-64220990	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559396051	chr2:64221022-64221023	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs533173787	chr2:64221075-64221076	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs551443472	chr2:64221084-64221085	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs367625587	chr2:64221114-64221115	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs190996638	chr2:64221182-64221183	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs561923736	chr2:64221183-64221184	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs183446630	chr2:64221184-64221185	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs35960986	chr2:64221195-64221196	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs12615049	chr2:64221219-64221220	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs6708930	chr2:64221259-64221260	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs570817766	chr2:64221356-64221357	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533314941	chr2:64221408-64221409	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs538631291	chr2:64221421-64221422	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:64139800-64220600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr2:64154800-64242600	Weak transcription	Aorta	Aorta
3	chr2:64176000-64228000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:64185800-64245000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:64194000-64243200	Weak transcription	NHLF	lung
6	chr2:64198600-64228000	Weak transcription	Right Ventricle	heart
7	chr2:64202800-64232400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr2:64203200-64228400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr2:64203400-64228000	Weak transcription	Ovary	ovary
10	chr2:64203600-64221400	Weak transcription	HMEC	breast
11	chr2:64204200-64227600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:64205600-64220800	Weak transcription	Thymus	Thymus
13	chr2:64205600-64228000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:64209000-64229200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr2:64209400-64244800	Weak transcription	HSMM	muscle
16	chr2:64210200-64220400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr2:64210200-64221200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:64210200-64222000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:64210200-64243000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr2:64212600-64222200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr2:64212800-64228400	Weak transcription	NHEK	skin
22	chr2:64213000-64224200	Weak transcription	A549	lung
23	chr2:64213600-64222600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr2:64213800-64244600	Weak transcription	HUVEC	blood vessel
25	chr2:64216000-64222600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:64217200-64227800	Weak transcription	Left Ventricle	heart
27	chr2:64217400-64220600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr2:64217400-64221000	Weak transcription	Primary T cells from cord blood	blood
29	chr2:64217400-64221000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr2:64217600-64220400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:64217600-64222000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:64217800-64224000	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr2:64217800-64224200	Weak transcription	Fetal Lung	lung
34	chr2:64217800-64225400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:64218000-64220200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr2:64218000-64220600	Weak transcription	Dnd41	blood
37	chr2:64218600-64221600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:64218800-64224000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr2:64219200-64220200	Enhancers	HepG2	liver
40	chr2:64219200-64221200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr2:64219200-64224200	Weak transcription	Fetal Muscle Trunk	muscle
42	chr2:64219200-64227800	Weak transcription	Fetal Stomach	stomach
43	chr2:64219200-64237000	Weak transcription	Placenta	Placenta
44	chr2:64219400-64220600	Weak transcription	Liver	Liver
45	chr2:64219400-64220800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr2:64219400-64238400	Weak transcription	Gastric	stomach
47	chr2:64219600-64220600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr2:64219600-64221200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:64220200-64220800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:64220200-64221400	Flanking Active TSS	HepG2	liver

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