Variant report

Variant	nsv2731
Chromosome Location	chr2:54745069-54790057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2195)
CpG islands
(count:1403)
Chromatin interactive
region (count:75)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2195 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:54787543-54788287	K562	blood:	n/a	chr2:54788043-54788059
2	ARID3A	chr2:54787826-54787991	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:54772824-54773842	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:54786905-54787244	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:54749885-54750209	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:54773647-54774065	K562	blood:	n/a	n/a
7	ARID3A	chr2:54785301-54785649	K562	blood:	n/a	n/a
8	ARID3A	chr2:54749988-54750074	K562	blood:	n/a	n/a
9	ARID3A	chr2:54760107-54760390	K562	blood:	n/a	n/a
10	ARID3A	chr2:54783527-54783660	HepG2	liver:	n/a	chr2:54783540-54783556
11	ARID3A	chr2:54782387-54783044	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:54759531-54760565	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:54784486-54785845	HepG2	liver:	n/a	n/a
14	ATF1	chr2:54760172-54760428	K562	blood:	n/a	n/a
15	ATF2	chr2:54785238-54785758	GM12878	blood:	n/a	n/a
16	ATF2	chr2:54751729-54752304	GM12878	blood:	n/a	n/a
17	ATF2	chr2:54785261-54785785	GM12878	blood:	n/a	n/a
18	ATF2	chr2:54787243-54788162	GM12878	blood:	n/a	n/a
19	ATF2	chr2:54786871-54788216	GM12878	blood:	n/a	n/a
20	ATF2	chr2:54749783-54750154	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr2:54751708-54752194	GM12878	blood:	n/a	n/a
22	ATF2	chr2:54784655-54785065	GM12878	blood:	n/a	n/a
23	ATF2	chr2:54784684-54785977	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr2:54784622-54785202	GM12878	blood:	n/a	n/a
25	ATF2	chr2:54785181-54785839	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr2:54772755-54773367	A549	lung:	n/a	n/a
27	ATF3	chr2:54785346-54785646	H1-hESC	embryonic stem cell:	n/a	chr2:54785450-54785463 chr2:54785451-54785464 chr2:54785449-54785464 chr2:54785391-54785400
28	ATF3	chr2:54785233-54785601	K562	blood:	n/a	chr2:54785450-54785463 chr2:54785451-54785464 chr2:54785449-54785464 chr2:54785391-54785400
29	ATF3	chr2:54760064-54760598	A549	lung:	n/a	n/a
30	ATF3	chr2:54785008-54785719	K562	blood:	n/a	chr2:54785450-54785463 chr2:54785451-54785464 chr2:54785449-54785464 chr2:54785391-54785400 chr2:54785081-54785090
31	ATF3	chr2:54759950-54760632	A549	lung:	n/a	n/a
32	BACH1	chr2:54787645-54787845	K562	blood:	n/a	n/a
33	BACH1	chr2:54785265-54785613	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr2:54781038-54781292	GM12878	blood:	n/a	n/a
35	BATF	chr2:54751817-54752113	GM12878	blood:	n/a	chr2:54751986-54751997
36	BATF	chr2:54781019-54781328	GM12878	blood:	n/a	n/a
37	BATF	chr2:54751806-54752125	GM12878	blood:	n/a	chr2:54751986-54751997
38	BATF	chr2:54782543-54782877	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:54751839-54752175	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:54787356-54787995	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:54751845-54752086	GM12878	blood:	n/a	n/a
42	BCL3	chr2:54787316-54788096	A549	lung:	n/a	n/a
43	BCL3	chr2:54759505-54760628	A549	lung:	n/a	n/a
44	BCL3	chr2:54785330-54785936	A549	lung:	n/a	chr2:54785503-54785516 chr2:54785504-54785517 chr2:54785506-54785519
45	BCL3	chr2:54759384-54760772	A549	lung:	n/a	n/a
46	BCL3	chr2:54787294-54788086	GM12878	blood:	n/a	n/a
47	BCL3	chr2:54786590-54787725	A549	lung:	n/a	n/a
48	BCLAF1	chr2:54786739-54788179	GM12878	blood:	n/a	n/a
49	BCLAF1	chr2:54749808-54750237	GM12878	blood:	n/a	n/a
50	BCLAF1	chr2:54760320-54760571	GM12878	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:54789491-54789541	CMK	blood:	n/a
2	chr2:54783773-54783823	AG10803	skin:	n/a
3	chr2:54751507-54751557	ECC-1	luminal epithelium:	n/a
4	chr2:54785550-54785600	SAEC	small airway:	n/a
5	chr2:54783773-54783823	HL-60	blood:	n/a
6	chr2:54784402-54784452	BJ	skin:	n/a
7	chr2:54785178-54785228	A549	lung:	n/a
8	chr2:54785550-54785600	T-47D	breast:	n/a
9	chr2:54786148-54786198	K562	blood:	n/a
10	chr2:54783773-54783823	Jurkat	blood:	n/a
11	chr2:54785406-54785456	HCT-116	colon:	n/a
12	chr2:54760330-54760380	HRCEpiC	kidney:	n/a
13	chr2:54785795-54785845	HepG2	liver:	n/a
14	chr2:54753625-54753675	GM19239	blood:	n/a
15	chr2:54781750-54781800	SK-N-SH	brain:	n/a
16	chr2:54760330-54760380	HEEpiC	esophagus:	n/a
17	chr2:54781750-54781800	HRPEpiC	eye:	n/a
18	chr2:54785476-54785526	Jurkat	blood:	n/a
19	chr2:54785375-54785425	K562	blood:	n/a
20	chr2:54781750-54781800	GM12891	blood:	n/a
21	chr2:54754922-54754972	NHDF-neo	bronchial:	n/a
22	chr2:54773290-54773340	RPTEC	kidney:	n/a
23	chr2:54789491-54789541	GM19239	blood:	n/a
24	chr2:54773290-54773340	IMR90	lung:	fetal
25	chr2:54778016-54778066	AG10803	skin:	n/a
26	chr2:54789491-54789541	AG09319	gingival:	n/a
27	chr2:54773290-54773340	PrEC	prostate:	n/a
28	chr2:54753625-54753675	MCF10A-Er-Src	breast:	n/a
29	chr2:54754922-54754972	HL-60	blood:	n/a
30	chr2:54783773-54783823	Caco-2	colon:	n/a
31	chr2:54760330-54760380	HL-60	blood:	n/a
32	chr2:54785183-54785233	AG04449	skin:	fetal
33	chr2:54754922-54754972	Caco-2	colon:	n/a
34	chr2:54785375-54785425	MCF10A-Er-Src	breast:	n/a
35	chr2:54773290-54773340	ovcar-3	ovarian:	n/a
36	chr2:54784402-54784452	HCPEpiC	choroid plexus:	n/a
37	chr2:54784402-54784452	AG04449	skin:	fetal
38	chr2:54785550-54785600	HEEpiC	esophagus:	n/a
39	chr2:54785406-54785456	HCM	heart:	n/a
40	chr2:54773290-54773340	SKMC	muscle:	n/a
41	chr2:54785178-54785228	HRCEpiC	kidney:	n/a
42	chr2:54785473-54785523	ProgFib	skin:	n/a
43	chr2:54778016-54778066	HEK293	kidney:	embryo
44	chr2:54778016-54778066	ECC-1	luminal epithelium:	n/a
45	chr2:54785307-54785357	HNPCEpiC	eye:	n/a
46	chr2:54754901-54754951	SK-N-SH_RA	brain:	n/a
47	chr2:54785476-54785526	GM12891	blood:	n/a
48	chr2:54789491-54789541	ovcar-3	ovarian:	n/a
49	chr2:54786148-54786198	Hela-S3	cervix:	n/a
50	chr2:54789491-54789541	ProgFib	skin:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:54760402..54763033-chr2:54763448..54765136,2	MCF-7	breast:
2	chr2:54749018..54751873-chr2:54799647..54801248,2	MCF-7	breast:
3	chr2:54761132..54763342-chr2:54783145..54786144,3	MCF-7	breast:
4	chr2:54749588..54750503-chr2:54931523..54932509,5	K562	blood:
5	chr2:54783297..54785333-chr2:54809031..54810704,2	K562	blood:
6	chr2:54342843..54345092-chr2:54785975..54787644,2	K562	blood:
7	chr2:54777010..54778863-chr2:54780329..54781851,2	MCF-7	breast:
8	chr2:54749549..54750174-chr2:54888310..54888932,2	K562	blood:
9	chr2:54761029..54763821-chr2:54783036..54786331,4	K562	blood:
10	chr2:54771500..54773380-chr2:54779555..54782261,2	MCF-7	breast:
11	chr2:54749566..54750373-chr2:54884453..54885101,2	MCF-7	breast:
12	chr2:54748253..54750106-chr2:54930790..54932794,2	MCF-7	breast:
13	chr2:54197301..54199396-chr2:54783418..54785695,2	MCF-7	breast:
14	chr12:6445562..6446227-chr2:54787047..54787677,2	Hela-S3	cervix:
15	chr12:57913784..57914554-chr2:54784859..54785443,2	Hela-S3	cervix:
16	chr2:54758614..54760270-chr2:54799626..54801180,2	MCF-7	breast:
17	chr2:54751127..54751822-chr2:54884889..54885446,2	K562	blood:
18	chr2:54764431..54771229-chr2:54784220..54787609,7	MCF-7	breast:
19	chr2:54749551..54750475-chr2:54884374..54885088,3	K562	blood:
20	chr2:54764431..54771229-chr2:54784220..54787609,7	MCF-7	breast:
21	chr2:54764232..54766337-chr2:54769153..54772806,3	K562	blood:
22	chr2:54749132..54757147-chr2:54784492..54789269,9	MCF-7	breast:
23	chr2:54763693..54765544-chr2:54775882..54778958,3	MCF-7	breast:
24	chr2:54749977..54750495-chr2:54931192..54932037,2	MCF-7	breast:
25	chr2:54786715..54789713-chr2:54890702..54893003,2	K562	blood:
26	chr2:54789266..54791330-chr2:54815899..54818560,2	K562	blood:
27	chr2:54770128..54773516-chr2:54775238..54777528,3	MCF-7	breast:
28	chr2:54767756..54770528-chr2:54788177..54790066,2	MCF-7	breast:
29	chr2:54782515..54784267-chr2:54820223..54822640,2	MCF-7	breast:
30	chr2:54342378..54344218-chr2:54786110..54788365,2	MCF-7	breast:
31	chr2:54785770..54787299-chr2:54826149..54827905,2	K562	blood:
32	chr2:54757446..54759466-chr2:54767763..54770756,2	K562	blood:
33	chr2:54754602..54758699-chr2:54783105..54787010,4	MCF-7	breast:
34	chr2:54764181..54766561-chr2:54813594..54815881,2	K562	blood:
35	chr2:54763693..54765544-chr2:54775882..54778958,3	MCF-7	breast:
36	chr10:123734176..123734706-chr2:54786768..54787716,2	Hela-S3	cervix:
37	chr2:54770128..54773516-chr2:54775238..54777528,3	MCF-7	breast:
38	chr2:54767808..54771330-chr2:54771769..54776449,4	K562	blood:
39	chr2:54749911..54750650-chr2:54931167..54932344,3	MCF-7	breast:
40	chr2:54759200..54761130-chr2:54762739..54764614,2	K562	blood:
41	chr2:54752145..54754517-chr2:54758567..54761057,2	MCF-7	breast:
42	chr2:54749132..54757147-chr2:54784492..54789269,9	MCF-7	breast:
43	chr2:54752145..54754517-chr2:54758567..54761057,2	MCF-7	breast:
44	chr2:54341806..54344770-chr2:54784235..54787039,2	MCF-7	breast:
45	chr2:54754602..54758699-chr2:54783105..54787010,4	MCF-7	breast:
46	chr2:54772020..54776106-chr2:54782775..54785505,4	K562	blood:
47	chr2:54764232..54766337-chr2:54769153..54772806,3	K562	blood:
48	chr1:207500876..207501439-chr2:54787208..54788035,2	Hela-S3	cervix:
49	chr2:54761550..54763887-chr2:54765151..54767469,2	K562	blood:
50	chr2:54196354..54198285-chr2:54758115..54760291,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPYL6-2	chr2:54747467-54747602	ENSG00000228108.1
2	lnc-TSPYL6-2	chr2:54767736-54767834	ENSG00000228108.1
3	lnc-TSPYL6-3	chr2:54773608-54773814	ENSG00000234943.2
4	lnc-TSPYL6-2	chr2:54762177-54762275	ENSG00000228108.1
5	lnc-TSPYL6-3	chr2:54772505-54772674	ENSG00000234943.2

No data

Variant related genes	Relation type
ENSG00000234943	TF binding region
SPTBN1	TF binding region
RPL23AP32	TF binding region
ENSG00000228108	TF binding region
ENSG00000234943	CpG island
SPTBN1	CpG island
RPL23AP32	CpG island
ENSG00000228108	CpG island
ENSG00000228108	chromatin interactions
ENSG00000115306	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000068878	chromatin interactions
ENSG00000237887	chromatin interactions
ENSG00000214595	chromatin interactions
ENSG00000107672	chromatin interactions
ENSG00000166987	chromatin interactions
ENSG00000175197	chromatin interactions
ENSG00000234943	chromatin interactions
ENSG00000203875	chromatin interactions

Extended variants
information (count: 1699 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1699 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555698071	chr2:54745074-54745075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs71750543	chr2:54745084-54745085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35846594	chr2:54745098-54745099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76034766	chr2:54745102-54745103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs56381959	chr2:54745110-54745111	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs182195367	chr2:54745193-54745194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537322080	chr2:54745205-54745206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577646389	chr2:54745224-54745225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557328543	chr2:54745281-54745282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370993856	chr2:54745282-54745283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187405599	chr2:54745304-54745305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546066471	chr2:54745306-54745307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552897083	chr2:54745321-54745322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572857464	chr2:54745322-54745323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530152528	chr2:54745369-54745370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541577348	chr2:54745399-54745400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149204405	chr2:54745424-54745425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561698008	chr2:54745443-54745444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530455434	chr2:54745455-54745456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192244231	chr2:54745474-54745475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183459023	chr2:54745571-54745572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199676030	chr2:54745591-54745592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542518075	chr2:54745602-54745603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75811839	chr2:54745605-54745606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34275507	chr2:54745606-54745607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533446916	chr2:54745634-54745635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562399901	chr2:54745715-54745716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73934321	chr2:54745739-54745740	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs370628727	chr2:54745742-54745743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200678075	chr2:54745758-54745759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76655402	chr2:54745763-54745764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143056413	chr2:54745779-54745780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188464991	chr2:54745788-54745789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191771252	chr2:54745809-54745810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530776186	chr2:54745833-54745834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569222042	chr2:54745911-54745912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182412693	chr2:54745962-54745963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538283384	chr2:54745966-54745967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557289982	chr2:54745968-54745969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570716194	chr2:54745986-54745987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148226548	chr2:54745999-54746000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559884613	chr2:54746000-54746001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564375029	chr2:54746013-54746014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186946706	chr2:54746146-54746147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34632228	chr2:54746168-54746169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs397869717	chr2:54746169-54746170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572976990	chr2:54746235-54746236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4671946	chr2:54746290-54746291	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs555209261	chr2:54746293-54746294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35286812	chr2:54746330-54746331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
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
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
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54719000-54751800	Weak transcription	Aorta	Aorta
2	chr2:54730400-54747600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:54732800-54754800	Weak transcription	Fetal Intestine Small	intestine
4	chr2:54733600-54747000	Weak transcription	Gastric	stomach
5	chr2:54737000-54751400	Weak transcription	HUVEC	blood vessel
6	chr2:54737600-54753800	Weak transcription	Fetal Brain Male	brain
7	chr2:54738200-54746200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr2:54738200-54746400	Weak transcription	NHLF	lung
9	chr2:54738200-54748200	Weak transcription	Fetal Stomach	stomach
10	chr2:54738200-54751600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr2:54738400-54746200	Weak transcription	A549	lung
12	chr2:54738400-54751400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr2:54739400-54746400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:54740400-54746200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:54740400-54746200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:54740400-54746200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr2:54740400-54746200	Weak transcription	Right Atrium	heart
18	chr2:54740400-54746400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:54740400-54746400	Weak transcription	Psoas Muscle	Psoas
20	chr2:54740400-54747000	Weak transcription	Pancreas	Pancrea
21	chr2:54740400-54747800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr2:54740400-54751600	Weak transcription	Placenta	Placenta
23	chr2:54740400-54770200	Weak transcription	Esophagus	oesophagus
24	chr2:54740600-54745200	Weak transcription	Brain Hippocampus Middle	brain
25	chr2:54740600-54746200	Weak transcription	NHDF-Ad	bronchial
26	chr2:54740600-54746800	Weak transcription	Osteobl	bone
27	chr2:54740600-54747000	Weak transcription	Stomach Smooth Muscle	stomach
28	chr2:54740600-54749800	Weak transcription	HepG2	liver
29	chr2:54740600-54753400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:54740600-54761800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr2:54740800-54745800	Weak transcription	Brain Angular Gyrus	brain
32	chr2:54740800-54746400	Weak transcription	Brain Anterior Caudate	brain
33	chr2:54740800-54746400	Weak transcription	HSMM	muscle
34	chr2:54740800-54746800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr2:54740800-54747000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr2:54741000-54746200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr2:54741000-54748000	Weak transcription	Adipose Nuclei	Adipose
38	chr2:54742000-54747000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:54742400-54745200	Weak transcription	Brain Substantia Nigra	brain
40	chr2:54742400-54745200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr2:54742400-54747400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:54742400-54748000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr2:54742600-54746200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr2:54742600-54746600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:54742600-54746800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:54742600-54747800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr2:54742800-54750600	Weak transcription	Brain Germinal Matrix	brain
48	chr2:54743400-54748200	Enhancers	Fetal Heart	heart
49	chr2:54743600-54751600	Weak transcription	Fetal Muscle Trunk	muscle
50	chr2:54744000-54746600	Weak transcription	Placenta Amnion	Placenta Amnion

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