Variant report

Variant	nsv1007926
Chromosome Location	chr2:20350751-20393557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1179)
CpG islands
(count:429)
Chromatin interactive
region (count:76)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:20382099-20382453	K562	blood:	n/a	n/a
2	ARID3A	chr2:20383924-20384238	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:20386226-20386632	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:20377549-20377680	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:20356882-20357084	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:20372324-20372649	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:20379543-20379887	HepG2	liver:	n/a	n/a
8	ATF2	chr2:20350891-20351453	GM12878	blood:	n/a	n/a
9	ATF2	chr2:20356951-20357553	GM12878	blood:	n/a	n/a
10	ATF2	chr2:20350999-20351524	GM12878	blood:	n/a	n/a
11	ATF3	chr2:20379356-20379998	A549	lung:	n/a	n/a
12	ATF3	chr2:20381911-20382891	A549	lung:	n/a	n/a
13	ATF3	chr2:20386266-20386589	HepG2	liver:	n/a	n/a
14	ATF3	chr2:20386224-20386648	GM12878	blood:	n/a	n/a
15	ATF3	chr2:20386320-20386576	K562	blood:	n/a	n/a
16	BACH1	chr2:20391143-20391343	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr2:20351069-20351364	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:20351016-20351358	GM12878	blood:	n/a	n/a
19	BCL3	chr2:20366414-20366928	GM12878	blood:	n/a	n/a
20	BCL3	chr2:20351012-20351439	GM12878	blood:	n/a	n/a
21	BCL3	chr2:20377831-20378212	GM12878	blood:	n/a	n/a
22	BCL3	chr2:20364089-20366232	A549	lung:	n/a	n/a
23	BCL3	chr2:20379064-20380150	A549	lung:	n/a	chr2:20379666-20379679
24	BCLAF1	chr2:20350994-20351407	GM12878	blood:	n/a	n/a
25	BCLAF1	chr2:20350883-20351461	GM12878	blood:	n/a	n/a
26	BCLAF1	chr2:20365821-20366405	GM12878	blood:	n/a	chr2:20366229-20366238
27	BHLHE40	chr2:20372252-20372519	HepG2	liver:	n/a	chr2:20372393-20372409
28	BHLHE40	chr2:20351067-20351412	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:20357067-20357469	GM12878	blood:	n/a	n/a
30	BHLHE40	chr2:20364518-20364923	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:20386464-20386470	GM12878	blood:	n/a	n/a
32	BHLHE40	chr2:20386024-20386631	K562	blood:	n/a	n/a
33	BHLHE40	chr2:20377992-20378136	K562	blood:	n/a	n/a
34	BHLHE40	chr2:20365724-20365909	K562	blood:	n/a	n/a
35	BHLHE40	chr2:20382274-20382765	K562	blood:	n/a	n/a
36	BRCA1	chr2:20384009-20384010	HepG2	liver:	n/a	n/a
37	BRCA1	chr2:20377707-20377750	HepG2	liver:	n/a	n/a
38	CBX3	chr2:20386139-20386651	K562	blood:	n/a	n/a
39	CBX3	chr2:20364573-20364958	K562	blood:	n/a	n/a
40	CBX3	chr2:20382139-20382734	K562	blood:	n/a	n/a
41	CCNT2	chr2:20382326-20382550	K562	blood:	n/a	n/a
42	CEBPB	chr2:20379294-20380406	A549	lung:	n/a	chr2:20379649-20379660
43	CEBPB	chr2:20379473-20379811	Hela-S3	cervix:	n/a	chr2:20379649-20379660
44	CEBPB	chr2:20383911-20384251	Hela-S3	cervix:	n/a	chr2:20384073-20384084
45	CEBPB	chr2:20379403-20379985	A549	lung:	n/a	chr2:20379649-20379660
46	CEBPB	chr2:20383898-20384269	HepG2	liver:	n/a	chr2:20384073-20384084
47	CEBPB	chr2:20383824-20384312	MCF-7	breast:	n/a	chr2:20384073-20384084
48	CEBPB	chr2:20370603-20370743	HepG2	liver:	n/a	chr2:20370634-20370645
49	CEBPB	chr2:20379443-20379782	HepG2	liver:	n/a	chr2:20379649-20379660
50	CEBPB	chr2:20382359-20382605	Hela-S3	cervix:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:20371971-20372021	Jurkat	blood:	n/a
2	chr2:20387826-20387876	HUVEC	blood vessel:	n/a
3	chr2:20371971-20372021	Jurkat	blood:	n/a
4	chr2:20387826-20387876	HUVEC	blood vessel:	n/a
5	chr2:20366443-20366493	AG09319	gingival:	n/a
6	chr2:20371971-20372021	AG04450	lung:	fetal
7	chr2:20384285-20384335	HAEpiC	amniotic membrane:	n/a
8	chr2:20387826-20387876	HAEpiC	amniotic membrane:	n/a
9	chr2:20371971-20372021	GM19239	blood:	n/a
10	chr2:20384285-20384335	A549	lung:	n/a
11	chr2:20357306-20357356	IMR90	lung:	fetal
12	chr2:20357306-20357356	Caco-2	colon:	n/a
13	chr2:20384285-20384335	HRE	kidney:	n/a
14	chr2:20387826-20387876	Caco-2	colon:	n/a
15	chr2:20370392-20370442	SK-N-SH	brain:	n/a
16	chr2:20386466-20386516	HMEC	breast:	n/a
17	chr2:20366443-20366493	HL-60	blood:	n/a
18	chr2:20387826-20387876	AG04450	lung:	fetal
19	chr2:20366443-20366493	HCT-116	colon:	n/a
20	chr2:20370392-20370442	HRE	kidney:	n/a
21	chr2:20371971-20372021	AG09309	skin:	n/a
22	chr2:20386466-20386516	MCF-7	breast:	n/a
23	chr2:20387826-20387876	ProgFib	skin:	n/a
24	chr2:20387826-20387876	NHBE	bronchial:	n/a
25	chr2:20386466-20386516	ECC-1	luminal epithelium:	n/a
26	chr2:20384285-20384335	SK-N-SH_RA	brain:	n/a
27	chr2:20357306-20357356	NHDF-neo	bronchial:	n/a
28	chr2:20386466-20386516	Jurkat	blood:	n/a
29	chr2:20357306-20357356	NT2-D1	testis:	n/a
30	chr2:20370392-20370442	HAEpiC	amniotic membrane:	n/a
31	chr2:20386466-20386516	Hepatocyte	liver:	n/a
32	chr2:20357306-20357356	ovcar-3	ovarian:	n/a
33	chr2:20386466-20386516	PFSK-1	brain:	n/a
34	chr2:20366443-20366493	IMR90	lung:	fetal
35	chr2:20357306-20357356	HRPEpiC	eye:	n/a
36	chr2:20387826-20387876	SAEC	small airway:	n/a
37	chr2:20371971-20372021	ProgFib	skin:	n/a
38	chr2:20371971-20372021	ovcar-3	ovarian:	n/a
39	chr2:20371971-20372021	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:20357306-20357356	SAEC	small airway:	n/a
41	chr2:20370392-20370442	MCF10A-Er-Src	breast:	n/a
42	chr2:20366443-20366493	AG04450	lung:	fetal
43	chr2:20384285-20384335	SKMC	muscle:	n/a
44	chr2:20371971-20372021	NT2-D1	testis:	n/a
45	chr2:20366443-20366493	HMEC	breast:	n/a
46	chr2:20386466-20386516	GM19239	blood:	n/a
47	chr2:20387826-20387876	HCPEpiC	choroid plexus:	n/a
48	chr2:20371971-20372021	HepG2	liver:	n/a
49	chr2:20371971-20372021	ECC-1	luminal epithelium:	n/a
50	chr2:20371971-20372021	HEEpiC	esophagus:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:20374283..20377217-chr2:20380767..20383134,3	MCF-7	breast:
2	chr2:20364604..20368497-chr2:20376297..20379611,4	MCF-7	breast:
3	chr2:20306634..20307462-chr2:20390804..20391353,2	MCF-7	breast:
4	chr2:20347344..20349010-chr2:20367659..20370421,2	MCF-7	breast:
5	chr2:20339624..20342165-chr2:20377427..20379627,2	MCF-7	breast:
6	chr2:20368402..20370917-chr2:20372413..20374946,2	K562	blood:
7	chr2:20337465..20342202-chr2:20382545..20388364,6	MCF-7	breast:
8	chr2:20365445..20367731-chr2:20374746..20377053,2	MCF-7	breast:
9	chr2:20366533..20369508-chr2:20380029..20382114,2	MCF-7	breast:
10	chr2:20372315..20374998-chr2:20375202..20377674,2	MCF-7	breast:
11	chr2:20301825..20304525-chr2:20380174..20381913,2	MCF-7	breast:
12	chr2:20380124..20381774-chr2:20398168..20400030,2	MCF-7	breast:
13	chr2:20362106..20364188-chr2:20366369..20369040,2	MCF-7	breast:
14	chr2:20352822..20355874-chr2:20423290..20424865,3	MCF-7	breast:
15	chr2:20377278..20381105-chr2:20382551..20387503,5	K562	blood:
16	chr2:20335194..20335984-chr2:20390827..20391610,3	MCF-7	breast:
17	chr2:20339841..20342282-chr2:20379713..20382419,2	MCF-7	breast:
18	chr2:20368602..20370551-chr2:20379312..20381264,2	MCF-7	breast:
19	chr2:20248476..20251356-chr2:20368246..20369984,2	MCF-7	breast:
20	chr2:20357950..20360555-chr2:20362622..20364914,3	MCF-7	breast:
21	chr2:20307232..20308797-chr2:20378092..20380183,2	MCF-7	breast:
22	chr2:20383626..20385611-chr2:20385923..20390219,5	MCF-7	breast:
23	chr2:20375045..20377368-chr2:20378301..20380397,2	K562	blood:
24	chr2:20364604..20368497-chr2:20376297..20379611,4	MCF-7	breast:
25	chr2:20357663..20359639-chr2:20362711..20364978,2	K562	blood:
26	chr2:20101674..20103205-chr2:20369213..20371363,2	MCF-7	breast:
27	chr2:20362106..20364188-chr2:20366369..20369040,2	MCF-7	breast:
28	chr2:20359744..20361850-chr2:20371412..20373041,2	MCF-7	breast:
29	chr2:20366533..20369508-chr2:20380029..20382114,2	MCF-7	breast:
30	chr2:20348330..20350992-chr2:20378144..20381464,4	MCF-7	breast:
31	chr2:20338664..20345614-chr2:20377409..20381353,9	MCF-7	breast:
32	chr2:20368402..20370917-chr2:20372413..20374946,2	K562	blood:
33	chr2:20378964..20381641-chr2:20471495..20474271,2	MCF-7	breast:
34	chr2:20377278..20381105-chr2:20382551..20387503,5	K562	blood:
35	chr2:20386118..20389028-chr2:20389700..20391555,2	K562	blood:
36	chr2:20309325..20314922-chr2:20379425..20384303,7	MCF-7	breast:
37	chr2:20379159..20380103-chr2:20424857..20425621,3	MCF-7	breast:
38	chr2:20384920..20386704-chr2:20549838..20552413,2	MCF-7	breast:
39	chr2:20364675..20367244-chr2:20367416..20369596,2	K562	blood:
40	chr2:20335050..20336054-chr2:20390851..20391800,4	MCF-7	breast:
41	chr2:20251074..20253926-chr2:20378631..20381986,3	MCF-7	breast:
42	chr2:20364500..20366851-chr2:20367517..20369898,2	MCF-7	breast:
43	chr2:20304028..20306367-chr2:20390369..20392912,2	MCF-7	breast:
44	chr2:20357950..20360555-chr2:20362622..20364914,3	MCF-7	breast:
45	chr2:20364027..20368295-chr2:20377113..20381748,5	MCF-7	breast:
46	chr2:20348330..20350992-chr2:20378144..20381464,4	MCF-7	breast:
47	chr2:20369269..20371931-chr2:20376136..20379582,4	MCF-7	breast:
48	chr2:20342469..20346864-chr2:20382569..20386022,5	MCF-7	breast:
49	chr2:20343897..20346310-chr2:20367652..20370210,2	MCF-7	breast:
50	chr2:20369269..20371931-chr2:20376136..20379582,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHOB-11	chr2:20382137-20382704	NONHSAT069431
2	lnc-RHOB-12	chr2:20375107-20375397	NONHSAT069428
3	lnc-SDC1-1	chr2:20378877-20378886	NONHSAT069430
4	lnc-RHOB-11	chr2:20384172-20384343	NONHSAT069431
5	lnc-SDC1-1	chr2:20380060-20380264	NONHSAT069430

No data

Variant related genes	Relation type
RN7SL140P	TF binding region
ENSG00000213729	TF binding region
RNU6-961P	TF binding region
RN7SL140P	CpG island
ENSG00000213729	CpG island
RNU6-961P	CpG island
ENSG00000266059	chromatin interactions
ENSG00000234378	chromatin interactions
ENSG00000183891	chromatin interactions
ENSG00000068697	chromatin interactions
ENSG00000271991	chromatin interactions
ENSG00000200763	chromatin interactions
ENSG00000115884	chromatin interactions
ENSG00000055917	chromatin interactions
ENSG00000223734	chromatin interactions

Extended variants
information (count: 1805 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1805 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10495702	chr2:20350751-20350752	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555903763	chr2:20350753-20350754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184518567	chr2:20350761-20350762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542058117	chr2:20350776-20350777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10495703	chr2:20350783-20350784	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs141585230	chr2:20350784-20350785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34395910	chr2:20350787-20350788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201346507	chr2:20350861-20350862	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs563865924	chr2:20350876-20350877	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs17652660	chr2:20350892-20350893	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs80108612	chr2:20350927-20350928	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs577060383	chr2:20350978-20350979	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs7607854	chr2:20351003-20351004	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552821633	chr2:20351006-20351007	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs569435198	chr2:20351035-20351036	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs7564193	chr2:20351136-20351137	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551333693	chr2:20351175-20351176	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs188688658	chr2:20351191-20351192	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs549853567	chr2:20351197-20351198	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs145393041	chr2:20351203-20351204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377664398	chr2:20351217-20351218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533821496	chr2:20351229-20351230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73225798	chr2:20351232-20351233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs371123193	chr2:20351243-20351244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192830307	chr2:20351263-20351264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537342837	chr2:20351276-20351277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550419677	chr2:20351280-20351281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539104747	chr2:20351286-20351287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79567028	chr2:20351306-20351307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369828501	chr2:20351309-20351310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79490780	chr2:20351325-20351326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34471733	chr2:20351326-20351327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78063883	chr2:20351327-20351328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567126857	chr2:20351330-20351331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555940421	chr2:20351370-20351371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs977130	chr2:20351391-20351392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555457176	chr2:20351400-20351401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541649307	chr2:20351587-20351588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78704398	chr2:20351644-20351645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572223876	chr2:20351645-20351646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540643927	chr2:20351654-20351655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78656579	chr2:20351675-20351676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560482105	chr2:20351709-20351710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532663759	chr2:20351747-20351748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185005574	chr2:20351748-20351749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35720501	chr2:20351801-20351802	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531976293	chr2:20351805-20351806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370191974	chr2:20351827-20351828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs199543511	chr2:20351845-20351846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144004951	chr2:20351856-20351857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	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
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Medulloblastoma	22160402	CNVD
Schizophrenia	22118685	CNVD
Epilepsy	22118685	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	17908972	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	18765546	CNVD
Neuroblastoma	18281664	CNVD
Neuroblastoma	17289879	CNVD
Neuroblastoma	19738985	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20332200-20364400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:20345600-20356600	Weak transcription	Liver	Liver
3	chr2:20346000-20355600	Weak transcription	Esophagus	oesophagus
4	chr2:20346800-20352800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:20348000-20351200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:20348000-20351400	Enhancers	HSMM	muscle
7	chr2:20348200-20351200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr2:20348400-20351200	Enhancers	Fetal Lung	lung
9	chr2:20348400-20351400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:20348600-20351000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr2:20348600-20351200	Enhancers	Fetal Brain Female	brain
12	chr2:20348600-20351200	Enhancers	Fetal Muscle Leg	muscle
13	chr2:20348800-20351800	Enhancers	Fetal Brain Male	brain
14	chr2:20349000-20353000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr2:20349200-20351000	Enhancers	Stomach Mucosa	stomach
16	chr2:20349200-20351800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:20349400-20351200	Enhancers	NHDF-Ad	bronchial
18	chr2:20349400-20355400	Weak transcription	Fetal Intestine Small	intestine
19	chr2:20349600-20350800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:20349600-20350800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:20349600-20350800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr2:20349600-20350800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:20349600-20350800	Weak transcription	K562	blood
24	chr2:20349600-20351200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:20349600-20352000	Weak transcription	Brain Germinal Matrix	brain
26	chr2:20349600-20352400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr2:20349600-20352600	Weak transcription	NHEK	skin
28	chr2:20349600-20356600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr2:20349800-20350800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr2:20349800-20350800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr2:20349800-20350800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:20349800-20351000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:20349800-20351000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:20349800-20351000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:20349800-20351000	Weak transcription	Fetal Muscle Trunk	muscle
36	chr2:20349800-20351000	Weak transcription	Lung	lung
37	chr2:20349800-20351000	Enhancers	Osteobl	bone
38	chr2:20349800-20351400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr2:20349800-20351400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr2:20349800-20351400	Enhancers	HSMMtube	muscle
41	chr2:20349800-20351600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr2:20349800-20352400	Weak transcription	Placenta	Placenta
43	chr2:20349800-20353200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:20349800-20353400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:20349800-20355200	Weak transcription	Duodenum Mucosa	Duodenum
46	chr2:20349800-20355600	Weak transcription	Pancreas	Pancrea
47	chr2:20350000-20352600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:20350000-20352800	Weak transcription	HMEC	breast
49	chr2:20350400-20350800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr2:20350400-20350800	Enhancers	GM12878-XiMat	blood

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