Variant report

Variant	nsv875583
Chromosome Location	chr2:188395700-188521234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2236)
CpG islands
(count:488)
Chromatin interactive
region (count:88)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2236 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188411998-188413154	K562	blood:	n/a	n/a
2	ARID3A	chr2:188441711-188441904	K562	blood:	n/a	n/a
3	ARID3A	chr2:188417188-188419388	K562	blood:	n/a	n/a
4	ARID3A	chr2:188513230-188513415	K562	blood:	n/a	n/a
5	ARID3A	chr2:188405710-188407124	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:188414692-188415523	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:188439872-188439983	K562	blood:	n/a	n/a
8	ARID3A	chr2:188417779-188418437	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:188445260-188446786	K562	blood:	n/a	n/a
10	ARID3A	chr2:188410134-188410334	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:188411457-188411585	K562	blood:	n/a	n/a
12	ARID3A	chr2:188459686-188459815	K562	blood:	n/a	n/a
13	ARID3A	chr2:188445189-188446578	HepG2	liver:	n/a	n/a
14	ARID3A	chr2:188412186-188412528	HepG2	liver:	n/a	n/a
15	ARID3A	chr2:188416243-188416679	K562	blood:	n/a	n/a
16	ARID3A	chr2:188414115-188414413	HepG2	liver:	n/a	n/a
17	ATF1	chr2:188451755-188452052	K562	blood:	n/a	n/a
18	ATF1	chr2:188461274-188461426	K562	blood:	n/a	n/a
19	ATF1	chr2:188417828-188418218	K562	blood:	n/a	n/a
20	ATF1	chr2:188412101-188412457	K562	blood:	n/a	n/a
21	ATF3	chr2:188406218-188406907	A549	lung:	n/a	n/a
22	ATF3	chr2:188404393-188405200	HCT-116	colon:	n/a	chr2:188404612-188404623 chr2:188404614-188404622
23	ATF3	chr2:188445322-188445922	A549	lung:	n/a	n/a
24	ATF3	chr2:188412092-188412532	A549	lung:	n/a	n/a
25	ATF3	chr2:188406176-188407188	A549	lung:	n/a	n/a
26	ATF3	chr2:188445228-188445831	K562	blood:	n/a	n/a
27	ATF3	chr2:188412043-188412645	HCT-116	colon:	n/a	n/a
28	ATF3	chr2:188417772-188418260	K562	blood:	n/a	n/a
29	ATF3	chr2:188412011-188412662	HCT-116	colon:	n/a	n/a
30	ATF3	chr2:188412150-188412417	K562	blood:	n/a	n/a
31	ATF3	chr2:188412053-188412480	K562	blood:	n/a	n/a
32	BACH1	chr2:188395959-188396172	K562	blood:	n/a	n/a
33	BACH1	chr2:188417841-188418170	K562	blood:	n/a	n/a
34	BACH1	chr2:188407802-188407916	K562	blood:	n/a	n/a
35	BACH1	chr2:188445366-188445738	K562	blood:	n/a	n/a
36	BACH1	chr2:188411517-188411587	K562	blood:	n/a	n/a
37	BACH1	chr2:188412142-188412526	K562	blood:	n/a	n/a
38	BATF	chr2:188417919-188418121	GM12878	blood:	n/a	chr2:188418061-188418071 chr2:188418045-188418056 chr2:188418034-188418043 chr2:188418060-188418071
39	BATF	chr2:188417889-188418168	GM12878	blood:	n/a	chr2:188418061-188418071 chr2:188418045-188418056 chr2:188418034-188418043 chr2:188418060-188418071
40	BCL3	chr2:188408055-188408736	A549	lung:	n/a	n/a
41	BCL3	chr2:188411972-188412666	A549	lung:	n/a	n/a
42	BCL3	chr2:188409053-188409807	A549	lung:	n/a	chr2:188409532-188409539
43	BCL3	chr2:188406093-188406881	A549	lung:	n/a	n/a
44	BCL3	chr2:188417712-188418398	A549	lung:	n/a	n/a
45	BCL3	chr2:188405887-188407122	A549	lung:	n/a	n/a
46	BCLAF1	chr2:188418641-188419399	K562	blood:	n/a	n/a
47	BHLHE40	chr2:188406307-188406736	HepG2	liver:	n/a	n/a
48	BHLHE40	chr2:188417969-188418369	A549	lung:	n/a	n/a
49	BHLHE40	chr2:188441708-188441986	K562	blood:	n/a	n/a
50	BHLHE40	chr2:188406329-188406823	HepG2	liver:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188419087-188419137	BE2_C	brain:	n/a
2	chr2:188419933-188419983	HRPEpiC	eye:	n/a
3	chr2:188481707-188481757	GM12892	blood:	n/a
4	chr2:188419830-188419880	NHBE	bronchial:	n/a
5	chr2:188481707-188481757	HNPCEpiC	eye:	n/a
6	chr2:188406934-188406984	HUVEC	blood vessel:	n/a
7	chr2:188419830-188419880	CMK	blood:	n/a
8	chr2:188419087-188419137	NH-A	brain:	n/a
9	chr2:188419830-188419880	T-47D	breast:	n/a
10	chr2:188419830-188419880	HEK293	kidney:	embryo
11	chr2:188419087-188419137	AG09319	gingival:	n/a
12	chr2:188481707-188481757	HRPEpiC	eye:	n/a
13	chr2:188420266-188420316	PrEC	prostate:	n/a
14	chr2:188420266-188420316	LNCaP	prostate:	n/a
15	chr2:188419568-188419618	NT2-D1	testis:	n/a
16	chr2:188420266-188420316	HMEC	breast:	n/a
17	chr2:188419568-188419618	PrEC	prostate:	n/a
18	chr2:188406934-188406984	NHBE	bronchial:	n/a
19	chr2:188483530-188483580	HCM	heart:	n/a
20	chr2:188406934-188406984	ovcar-3	ovarian:	n/a
21	chr2:188406934-188406984	K562	blood:	n/a
22	chr2:188419568-188419618	GM12891	blood:	n/a
23	chr2:188406934-188406984	AG09319	gingival:	n/a
24	chr2:188481707-188481757	SK-N-SH_RA	brain:	n/a
25	chr2:188419933-188419983	GM12878	blood:	n/a
26	chr2:188420266-188420316	SK-N-MC	brain:	n/a
27	chr2:188420266-188420316	AG04449	skin:	fetal
28	chr2:188483530-188483580	HL-60	blood:	n/a
29	chr2:188419830-188419880	K562	blood:	n/a
30	chr2:188419568-188419618	HNPCEpiC	eye:	n/a
31	chr2:188419933-188419983	HEEpiC	esophagus:	n/a
32	chr2:188406934-188406984	HIPEpiC	eye:	n/a
33	chr2:188481707-188481757	HRE	kidney:	n/a
34	chr2:188419830-188419880	Hepatocyte	liver:	n/a
35	chr2:188420266-188420316	CMK	blood:	n/a
36	chr2:188419568-188419618	AG10803	skin:	n/a
37	chr2:188419568-188419618	NHBE	bronchial:	n/a
38	chr2:188419087-188419137	PFSK-1	brain:	n/a
39	chr2:188420266-188420316	NHBE	bronchial:	n/a
40	chr2:188419830-188419880	SK-N-SH	brain:	n/a
41	chr2:188419830-188419880	HUVEC	blood vessel:	n/a
42	chr2:188419933-188419983	NB4	blood:	n/a
43	chr2:188481707-188481757	HRCEpiC	kidney:	n/a
44	chr2:188419087-188419137	GM12891	blood:	n/a
45	chr2:188481707-188481757	PANC-1	pancreas:	n/a
46	chr2:188419933-188419983	NHBE	bronchial:	n/a
47	chr2:188483530-188483580	GM19239	blood:	n/a
48	chr2:188406934-188406984	NH-A	brain:	n/a
49	chr2:188481707-188481757	SK-N-MC	brain:	n/a
50	chr2:188419568-188419618	ProgFib	skin:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
2	chr2:188362271..188363016-chr2:188446864..188447543,2	MCF-7	breast:
3	chr2:188445739..188446515-chr2:188708197..188708735,2	MCF-7	breast:
4	chr2:188366744..188369184-chr2:188446137..188447850,2	K562	blood:
5	chr2:263068..264963-chr2:188441341..188443685,2	MCF-7	breast:
6	chr2:188443788..188447797-chr2:188450278..188454059,4	K562	blood:
7	chr2:188392650..188395033-chr2:188412614..188414418,2	K562	blood:
8	chr2:188366746..188369254-chr2:188412378..188414717,2	K562	blood:
9	chr2:188473165..188475172-chr2:188477640..188480014,2	K562	blood:
10	chr2:188393262..188398014-chr2:188414587..188419751,6	K562	blood:
11	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
12	chr2:188398970..188401688-chr2:188404214..188406089,3	K562	blood:
13	chr2:188404419..188406273-chr2:188410816..188412480,2	MCF-7	breast:
14	chr2:188412314..188413944-chr2:188414421..188417624,3	MCF-7	breast:
15	chr2:188412314..188413944-chr2:188414421..188417624,3	MCF-7	breast:
16	chr2:188430133..188432200-chr2:188438721..188440616,2	K562	blood:
17	chr2:188363922..188366266-chr2:188444694..188447033,35	MCF-7	breast:
18	chr2:188407472..188409911-chr2:188410680..188413536,3	MCF-7	breast:
19	chr2:188367231..188371096-chr2:188401019..188405423,6	K562	blood:
20	chr2:188395123..188398204-chr2:188399307..188403080,4	K562	blood:
21	chr2:188395046..188397968-chr2:188414786..188417959,4	K562	blood:
22	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
23	chr2:188410825..188412949-chr2:190475105..190477931,2	K562	blood:
24	chr2:188467603..188470192-chr2:188473529..188476139,3	K562	blood:
25	chr2:188445783..188446859-chr2:188707667..188708674,8	MCF-7	breast:
26	chr2:188440946..188443688-chr2:188443875..188445768,2	MCF-7	breast:
27	chr16:73088044..73089636-chr2:188441847..188444162,2	MCF-7	breast:
28	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
29	chr2:188389696..188391580-chr2:188402374..188405162,2	K562	blood:
30	chr2:188449920..188452608-chr2:188452638..188454975,2	K562	blood:
31	chr2:188407472..188409911-chr2:188410680..188413536,3	MCF-7	breast:
32	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
33	chr2:188382405..188385031-chr2:188403850..188405817,2	K562	blood:
34	chr2:188363929..188365341-chr2:188444758..188446502,16	K562	blood:
35	chr2:187749024..187750695-chr2:188416544..188418279,2	K562	blood:
36	chr2:188363780..188367877-chr2:188441342..188445875,5	MCF-7	breast:
37	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
38	chr2:188459276..188460160-chr2:189841055..189841647,2	MCF-7	breast:
39	chr2:188443788..188447797-chr2:188450278..188454059,4	K562	blood:
40	chr2:188408868..188410387-chr2:188412786..188414991,2	MCF-7	breast:
41	chr2:188361661..188363462-chr2:188407026..188409234,2	K562	blood:
42	chr2:188375111..188377616-chr2:188395627..188398222,2	K562	blood:
43	chr2:188363950..188366399-chr2:188445083..188446553,13	MCF-7	breast:
44	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
45	chr2:188440243..188443082-chr2:188444632..188448024,3	K562	blood:
46	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:
47	chr2:188398970..188401688-chr2:188404214..188406089,3	K562	blood:
48	chr2:188458841..188460185-chr2:189376734..189377597,3	MCF-7	breast:
49	chr2:188460269..188463083-chr2:188643990..188646491,2	K562	blood:
50	chr2:188411707..188414780-chr2:188445119..188447288,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM171B-1	chr2:188418876-188418918	ENSG00000224063.1
2	lnc-FAM171B-1	chr2:188419304-188419390	ENSG00000224063.1
3	lnc-FAM171B-1	chr2:188419003-188419120	ENSG00000224063.1

No data

Variant related genes	Relation type
TFPI	TF binding region
ENSG00000224063	TF binding region
TFPI	CpG island
ENSG00000224063	CpG island
ENSG00000224063	chromatin interactions
ENSG00000003436	chromatin interactions
ENSG00000143727	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000035115	chromatin interactions

Extended variants
information (count: 3752 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:3752 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16829090	chr2:188395700-188395701	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77589957	chr2:188395704-188395705	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560813319	chr2:188395812-188395813	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148663208	chr2:188395910-188395911	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549520218	chr2:188395953-188395954	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs141284255	chr2:188396038-188396039	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs538720635	chr2:188396090-188396091	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs564797029	chr2:188396109-188396110	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs150773659	chr2:188396162-188396163	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565648524	chr2:188396176-188396177	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs115056474	chr2:188396195-188396196	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs555318517	chr2:188396215-188396216	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs199517884	chr2:188396220-188396221	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs570687618	chr2:188396223-188396224	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576770361	chr2:188396226-188396227	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs199749246	chr2:188396253-188396254	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs537688309	chr2:188396273-188396274	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559184371	chr2:188396331-188396332	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs35935664	chr2:188396336-188396337	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566562056	chr2:188396351-188396352	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541492858	chr2:188396453-188396454	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559558521	chr2:188396460-188396461	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs574788276	chr2:188396545-188396546	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201409976	chr2:188396569-188396570	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs541779440	chr2:188396653-188396654	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs68040026	chr2:188396654-188396655	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548223375	chr2:188396703-188396704	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs560849695	chr2:188396714-188396715	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145468929	chr2:188396716-188396717	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549607891	chr2:188396721-188396722	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs534023967	chr2:188396774-188396775	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566529414	chr2:188396891-188396892	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547491645	chr2:188396899-188396900	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571490980	chr2:188396907-188396908	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs529704382	chr2:188396925-188396926	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533900505	chr2:188396934-188396935	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548203503	chr2:188396977-188396978	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs570402022	chr2:188396990-188396991	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs537723917	chr2:188397028-188397029	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs548880075	chr2:188397038-188397039	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559222848	chr2:188397040-188397041	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571044400	chr2:188397041-188397042	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs114282516	chr2:188397055-188397056	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553439617	chr2:188397056-188397057	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs114676835	chr2:188397078-188397079	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs552654796	chr2:188397090-188397091	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs34464802	chr2:188397102-188397103	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368785980	chr2:188397135-188397136	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs187741845	chr2:188397162-188397163	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192580303	chr2:188397209-188397210	Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1573 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188375200-188400000	Weak transcription	Duodenum Mucosa	Duodenum
2	chr2:188381800-188406000	Weak transcription	Small Intestine	intestine
3	chr2:188381800-188406600	Weak transcription	Aorta	Aorta
4	chr2:188385200-188397000	Weak transcription	Pancreas	Pancrea
5	chr2:188385200-188397200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:188385200-188397200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr2:188385200-188406000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr2:188385400-188396400	Weak transcription	Fetal Muscle Leg	muscle
9	chr2:188385400-188397000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:188385400-188397000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:188385400-188397000	Weak transcription	Fetal Stomach	stomach
12	chr2:188385400-188397200	Weak transcription	Fetal Intestine Small	intestine
13	chr2:188385400-188397600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr2:188385800-188397000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr2:188387000-188397000	Weak transcription	Lung	lung
16	chr2:188387000-188406000	Weak transcription	Fetal Intestine Large	intestine
17	chr2:188387200-188397000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr2:188387200-188398600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:188387200-188406000	Weak transcription	HSMMtube	muscle
20	chr2:188387600-188397000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:188390000-188398400	Genic enhancers	HepG2	liver
22	chr2:188391000-188398000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr2:188391800-188405800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr2:188392200-188402000	Weak transcription	Fetal Lung	lung
25	chr2:188392200-188413200	Weak transcription	Psoas Muscle	Psoas
26	chr2:188392400-188397000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr2:188392400-188397200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:188392400-188397200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:188392400-188397600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:188392400-188409200	Weak transcription	Ovary	ovary
31	chr2:188392600-188397200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr2:188393000-188404800	Weak transcription	NH-A	brain
33	chr2:188393000-188406200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr2:188393200-188397200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:188393400-188397400	Enhancers	Hela-S3	cervix
36	chr2:188393800-188396000	Enhancers	Liver	Liver
37	chr2:188394400-188397000	Enhancers	HUVEC	blood vessel
38	chr2:188394600-188396000	Enhancers	Muscle Satellite Cultured Cells	--
39	chr2:188394600-188396000	Enhancers	Osteobl	bone
40	chr2:188394600-188397000	Weak transcription	Placenta	Placenta
41	chr2:188394800-188396800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:188394800-188397000	Weak transcription	HSMM	muscle
43	chr2:188394800-188405800	Weak transcription	NHLF	lung
44	chr2:188394800-188408400	Weak transcription	K562	blood
45	chr2:188395000-188397000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:188395200-188399400	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr2:188395400-188395800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr2:188395400-188402800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:188395400-188405800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr2:188395600-188396000	Flanking Active TSS	A549	lung

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