Variant report

Variant	esv1851951
Chromosome Location	chr15:30043659-30178871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1495)
CpG islands
(count:1710)
Chromatin interactive
region (count:99)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:30113516-30113887	K562	blood:	n/a	n/a
2	ARID3A	chr15:30069116-30069923	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:30110302-30110578	K562	blood:	n/a	n/a
4	ARID3A	chr15:30117315-30117656	K562	blood:	n/a	n/a
5	ARID3A	chr15:30107113-30107341	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:30178838-30179138	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:30107571-30108231	K562	blood:	n/a	n/a
8	ARID3A	chr15:30113508-30113944	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:30115339-30115686	HepG2	liver:	n/a	n/a
10	ATF1	chr15:30113535-30113894	K562	blood:	n/a	n/a
11	ATF1	chr15:30117551-30117790	K562	blood:	n/a	n/a
12	ATF1	chr15:30067207-30067459	K562	blood:	n/a	n/a
13	ATF1	chr15:30135914-30136187	K562	blood:	n/a	n/a
14	ATF2	chr15:30113491-30113996	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr15:30113515-30113947	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr15:30113464-30113906	K562	blood:	n/a	n/a
17	ATF3	chr15:30113629-30113845	K562	blood:	n/a	n/a
18	ATF3	chr15:30107673-30107877	K562	blood:	n/a	n/a
19	BACH1	chr15:30113488-30115592	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:30047584-30047764	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:30112449-30113905	K562	blood:	n/a	n/a
22	BACH1	chr15:30050797-30051372	K562	blood:	n/a	n/a
23	BACH1	chr15:30107071-30108300	K562	blood:	n/a	n/a
24	BACH1	chr15:30081027-30081151	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr15:30076367-30076406	K562	blood:	n/a	n/a
26	BATF	chr15:30113602-30113834	GM12878	blood:	n/a	n/a
27	BCL3	chr15:30114340-30115772	A549	lung:	n/a	n/a
28	BHLHE40	chr15:30163662-30164025	K562	blood:	n/a	n/a
29	BHLHE40	chr15:30107187-30108283	K562	blood:	n/a	chr15:30107749-30107770
30	BHLHE40	chr15:30113612-30115724	HepG2	liver:	n/a	chr15:30114178-30114194 chr15:30113787-30113803 chr15:30113928-30113944
31	BHLHE40	chr15:30135982-30136182	K562	blood:	n/a	n/a
32	BHLHE40	chr15:30147906-30148026	K562	blood:	n/a	n/a
33	BHLHE40	chr15:30167283-30167521	K562	blood:	n/a	n/a
34	BHLHE40	chr15:30097981-30098805	K562	blood:	n/a	n/a
35	BHLHE40	chr15:30107401-30107939	A549	lung:	n/a	chr15:30107749-30107770
36	BHLHE40	chr15:30113347-30115139	K562	blood:	n/a	chr15:30114178-30114194 chr15:30113787-30113803 chr15:30113928-30113944
37	BHLHE40	chr15:30107613-30107955	HepG2	liver:	n/a	chr15:30107749-30107770
38	BRCA1	chr15:30114822-30115569	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr15:30122911-30123251	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr15:30157921-30158102	GM12878	blood:	n/a	n/a
41	BRCA1	chr15:30115035-30115474	HepG2	liver:	n/a	n/a
42	BRCA1	chr15:30114219-30114626	HepG2	liver:	n/a	n/a
43	BRCA1	chr15:30097342-30097553	HepG2	liver:	n/a	n/a
44	CCNT2	chr15:30113637-30115356	K562	blood:	n/a	n/a
45	CCNT2	chr15:30167280-30167543	K562	blood:	n/a	chr15:30167421-30167441
46	CCNT2	chr15:30117280-30117748	K562	blood:	n/a	n/a
47	CEBPB	chr15:30067063-30067462	IMR90	lung:	n/a	chr15:30067243-30067254
48	CEBPB	chr15:30097286-30097565	ECC-1	luminal epithelium:	n/a	chr15:30097393-30097406 chr15:30097393-30097404 chr15:30097395-30097406
49	CEBPB	chr15:30152307-30152855	IMR90	lung:	n/a	n/a
50	CEBPB	chr15:30097279-30097584	K562	blood:	n/a	chr15:30097393-30097406 chr15:30097393-30097404 chr15:30097395-30097406

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30163825-30163875	GM06990	blood:	n/a
2	chr15:30110856-30110906	AG04449	skin:	fetal
3	chr15:30163825-30163875	GM06990	blood:	n/a
4	chr15:30110856-30110906	AG04449	skin:	fetal
5	chr15:30163660-30163710	HL-60	blood:	n/a
6	chr15:30163726-30163776	NT2-D1	testis:	n/a
7	chr15:30106104-30106154	BJ	skin:	n/a
8	chr15:30117681-30117731	GM12891	blood:	n/a
9	chr15:30115147-30115197	HL-60	blood:	n/a
10	chr15:30049198-30049248	Caco-2	colon:	n/a
11	chr15:30163660-30163710	BJ	skin:	n/a
12	chr15:30163660-30163710	Caco-2	colon:	n/a
13	chr15:30163660-30163710	IMR90	lung:	fetal
14	chr15:30078357-30078407	BJ	skin:	n/a
15	chr15:30114871-30114921	GM19239	blood:	n/a
16	chr15:30163825-30163875	ProgFib	skin:	n/a
17	chr15:30114651-30114701	AG10803	skin:	n/a
18	chr15:30135976-30136026	HNPCEpiC	eye:	n/a
19	chr15:30115299-30115349	HepG2	liver:	n/a
20	chr15:30114816-30114866	CMK	blood:	n/a
21	chr15:30115149-30115199	HEK293	kidney:	embryo
22	chr15:30110856-30110906	GM12892	blood:	n/a
23	chr15:30113831-30113881	NT2-D1	testis:	n/a
24	chr15:30164845-30164895	HAEpiC	amniotic membrane:	n/a
25	chr15:30095720-30095770	T-47D	breast:	n/a
26	chr15:30113831-30113881	SK-N-SH	brain:	n/a
27	chr15:30114814-30114864	HUVEC	blood vessel:	n/a
28	chr15:30114651-30114701	HepG2	liver:	n/a
29	chr15:30098131-30098181	ECC-1	luminal epithelium:	n/a
30	chr15:30163825-30163875	AG09309	skin:	n/a
31	chr15:30114474-30114524	GM19239	blood:	n/a
32	chr15:30049198-30049248	NHBE	bronchial:	n/a
33	chr15:30114295-30114345	Hela-S3	cervix:	n/a
34	chr15:30113651-30113701	SK-N-MC	brain:	n/a
35	chr15:30095720-30095770	BE2_C	brain:	n/a
36	chr15:30114295-30114345	NHDF-neo	bronchial:	n/a
37	chr15:30114651-30114701	IMR90	lung:	fetal
38	chr15:30113651-30113701	SK-N-SH	brain:	n/a
39	chr15:30114871-30114921	BE2_C	brain:	n/a
40	chr15:30115147-30115197	NB4	blood:	n/a
41	chr15:30115149-30115199	HNPCEpiC	eye:	n/a
42	chr15:30049198-30049248	H1-hESC	embryonic stem cell:	embryo
43	chr15:30114912-30114962	HMEC	breast:	n/a
44	chr15:30163825-30163875	Jurkat	blood:	n/a
45	chr15:30114651-30114701	AG04449	skin:	fetal
46	chr15:30049198-30049248	HMEC	breast:	n/a
47	chr15:30115299-30115349	GM06990	blood:	n/a
48	chr15:30114474-30114524	GM06990	blood:	n/a
49	chr15:30114474-30114524	HCT-116	colon:	n/a
50	chr15:30114814-30114864	HEEpiC	esophagus:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:30082131..30086893-chr15:30112422..30116198,5	K562	blood:
2	chr15:30078003..30079594-chr15:30081264..30082897,2	K562	blood:
3	chr15:30157341..30159871-chr15:30168182..30170252,2	K562	blood:
4	chr15:30113090..30115260-chr15:30117657..30120039,3	MCF-7	breast:
5	chr15:30048520..30050804-chr15:30113395..30115611,2	MCF-7	breast:
6	chr15:30115117..30117286-chr15:30127029..30129725,2	K562	blood:
7	chr15:30055188..30057254-chr15:30065411..30067206,2	K562	blood:
8	chr15:30069062..30071900-chr15:30110638..30114646,3	K562	blood:
9	chr15:30116855..30119130-chr15:30151022..30153262,2	K562	blood:
10	chr15:30056869..30058668-chr15:30062635..30065302,2	MCF-7	breast:
11	chr15:30047903..30050810-chr15:30051700..30053369,2	K562	blood:
12	chr15:30113418..30114284-chr5:10249625..10250242,2	Hela-S3	cervix:
13	chr15:30088873..30091696-chr15:30091777..30093834,2	K562	blood:
14	chr1:52521763..52522611-chr15:30114227..30114914,2	Hela-S3	cervix:
15	chr15:30094465..30098543-chr15:30102930..30106302,5	K562	blood:
16	chr15:30066918..30068960-chr15:30070446..30071982,2	MCF-7	breast:
17	chr15:30089221..30092085-chr15:30112820..30114645,2	K562	blood:
18	chr15:30171448..30173034-chr15:30173407..30175865,2	K562	blood:
19	chr15:30095523..30098044-chr15:30106073..30108934,2	MCF-7	breast:
20	chr15:30063787..30066295-chr15:30068795..30070825,2	MCF-7	breast:
21	chr15:30099589..30102361-chr15:30114186..30117139,2	MCF-7	breast:
22	chr15:30091964..30094234-chr15:30103253..30105641,2	MCF-7	breast:
23	chr15:30111283..30113750-chr22:19879705..19881456,2	K562	blood:
24	chr15:30052065..30053802-chr15:30055280..30057234,2	K562	blood:
25	chr15:30033909..30035507-chr15:30113047..30114881,2	MCF-7	breast:
26	chr15:30066918..30068960-chr15:30070446..30071982,2	MCF-7	breast:
27	chr15:30117277..30119104-chr15:30123293..30126134,3	MCF-7	breast:
28	chr15:30072029..30073605-chr15:30114260..30117133,2	K562	blood:
29	chr15:30131583..30134243-chr15:30136228..30138609,2	K562	blood:
30	chr15:30131583..30134243-chr15:30136228..30138609,2	K562	blood:
31	chr15:30110373..30112075-chr15:30112692..30115321,2	MCF-7	breast:
32	chr15:30051900..30054307-chr15:30111477..30113324,2	K562	blood:
33	chr15:30086191..30088708-chr15:30102161..30104753,2	K562	blood:
34	chr15:30092733..30096489-chr15:30112182..30116476,4	K562	blood:
35	chr15:30115117..30117286-chr15:30127029..30129725,2	K562	blood:
36	chr15:30087643..30090373-chr15:30092334..30094638,2	K562	blood:
37	chr15:30042693..30044993-chr15:72522248..72524393,2	MCF-7	breast:
38	chr15:30103514..30110154-chr15:30110674..30116017,8	MCF-7	breast:
39	chr15:30091067..30092760-chr15:30104276..30106583,2	K562	blood:
40	chr15:30087643..30090373-chr15:30092334..30094638,2	K562	blood:
41	chr15:30054766..30057672-chr15:30112714..30114260,2	MCF-7	breast:
42	chr12:57913766..57914507-chr15:30113406..30114143,2	Hela-S3	cervix:
43	chr15:30082232..30084095-chr15:30112942..30115729,2	MCF-7	breast:
44	chr15:30162335..30165638-chr15:30172933..30175702,3	K562	blood:
45	chr15:30157341..30159871-chr15:30168182..30170252,2	K562	blood:
46	chr15:30079574..30082465-chr15:30085373..30086938,2	K562	blood:
47	chr15:30087602..30089110-chr15:30112846..30115488,2	K562	blood:
48	chr15:30104918..30110272-chr15:30111258..30116596,7	MCF-7	breast:
49	chr15:30122911..30125644-chr15:30126014..30127546,2	MCF-7	breast:
50	chr15:30056869..30058668-chr15:30062635..30065302,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA8J-2	chr15:30115425-30115571	XLOC_011197
2	lnc-GOLGA8J-2	chr15:30114834-30116284	ENSG00000259523.1
3	lnc-GOLGA8J-2	chr15:30117587-30117856	XLOC_011197

No data

Variant related genes	Relation type
ENSG00000259523	TF binding region
TJP1	TF binding region
ENSG00000259523	CpG island
TJP1	CpG island
ENSG00000166987	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000183617	chromatin interactions
ENSG00000089693	chromatin interactions
ENSG00000005955	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000259523	chromatin interactions
ENSG00000038274	chromatin interactions
ENSG00000117862	chromatin interactions
ENSG00000175197	chromatin interactions
ENSG00000134717	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000104067	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000204388	chromatin interactions

Extended variants
information (count: 5068 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:5068 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16955736	chr15:30043659-30043660	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182465644	chr15:30043675-30043676	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs186913752	chr15:30043685-30043686	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544077017	chr15:30043691-30043692	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs78519373	chr15:30043716-30043717	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542144636	chr15:30043727-30043728	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117481413	chr15:30043775-30043776	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555114373	chr15:30043838-30043839	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141799046	chr15:30043906-30043907	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537106506	chr15:30043930-30043931	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532876356	chr15:30043932-30043933	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557470660	chr15:30043934-30043935	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150576201	chr15:30043938-30043939	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140306292	chr15:30043954-30043955	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553375724	chr15:30043975-30043976	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573546131	chr15:30043998-30043999	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372968184	chr15:30044061-30044062	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562220002	chr15:30044062-30044063	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531140450	chr15:30044066-30044067	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs192118487	chr15:30044079-30044080	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564232319	chr15:30044111-30044112	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs8038593	chr15:30044113-30044114	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs8038737	chr15:30044174-30044175	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs8026437	chr15:30044228-30044229	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529104256	chr15:30044285-30044286	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199750785	chr15:30044304-30044305	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548874400	chr15:30044311-30044312	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200728984	chr15:30044319-30044320	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs78610970	chr15:30044324-30044325	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568702354	chr15:30044409-30044410	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs547739551	chr15:30044443-30044444	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs538091646	chr15:30044455-30044456	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs147386269	chr15:30044490-30044491	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs570960643	chr15:30044556-30044557	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs539566832	chr15:30044704-30044705	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs139542922	chr15:30044708-30044709	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs10162985	chr15:30044727-30044728	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs542503637	chr15:30044873-30044874	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs149895952	chr15:30044898-30044899	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs575882708	chr15:30044945-30044946	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs544821640	chr15:30044972-30044973	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs190555978	chr15:30044990-30044991	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs533016196	chr15:30045085-30045086	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs148758350	chr15:30045169-30045170	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559678773	chr15:30045196-30045197	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs528896368	chr15:30045241-30045242	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs114643870	chr15:30045292-30045293	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368430802	chr15:30045308-30045309	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs531391370	chr15:30045327-30045328	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538350635	chr15:30045347-30045348	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:157)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Schizophrenia	19197363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Mental retardation	17124404	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	19843651	CNVD
Schizophrenia	19843651	CNVD
Schizophrenia	23813976	CNVD
Cognitive impairment	21505072	CNVD
Epilepsy	20502679	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
Schizophrenia	20388499	CNVD
Autism	20841430	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Attention deficit hyperactivity disorder	22420046	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:3508 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30016600-30052000	Weak transcription	Spleen	Spleen
2	chr15:30016600-30068200	Weak transcription	Brain Germinal Matrix	brain
3	chr15:30017600-30048600	Weak transcription	Fetal Brain Male	brain
4	chr15:30018200-30052000	Weak transcription	Gastric	stomach
5	chr15:30021200-30061600	Weak transcription	Colonic Mucosa	Colon
6	chr15:30021400-30097200	Weak transcription	Aorta	Aorta
7	chr15:30025200-30065000	Weak transcription	Fetal Brain Female	brain
8	chr15:30026000-30051800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:30026000-30057600	Weak transcription	Esophagus	oesophagus
10	chr15:30028200-30047600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr15:30028200-30049200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr15:30029600-30048600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr15:30029800-30056000	Weak transcription	K562	blood
14	chr15:30030400-30060800	Weak transcription	Hela-S3	cervix
15	chr15:30030400-30067000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr15:30031600-30046200	Weak transcription	Fetal Kidney	kidney
17	chr15:30032800-30046400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr15:30033200-30046600	Weak transcription	NH-A	brain
19	chr15:30033200-30051800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr15:30033600-30049000	Weak transcription	HUVEC	blood vessel
21	chr15:30034200-30051400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr15:30034400-30048400	Weak transcription	Colon Smooth Muscle	Colon
23	chr15:30034400-30051800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr15:30034400-30051800	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr15:30034400-30057800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr15:30034800-30046400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr15:30034800-30052800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr15:30035000-30048400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr15:30035000-30048600	Weak transcription	Osteobl	bone
30	chr15:30035000-30048800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr15:30035000-30048800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr15:30035000-30053200	Weak transcription	Psoas Muscle	Psoas
33	chr15:30035200-30044600	Weak transcription	NHEK	skin
34	chr15:30035200-30045800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr15:30035400-30048800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr15:30035800-30046400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr15:30038800-30043800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:30039800-30044200	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr15:30041800-30048200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr15:30042000-30044400	Weak transcription	Liver	Liver
41	chr15:30042000-30045000	Weak transcription	Brain Hippocampus Middle	brain
42	chr15:30042000-30045200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr15:30042000-30045200	Weak transcription	HSMMtube	muscle
44	chr15:30042000-30045600	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr15:30042000-30045800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr15:30042000-30045800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr15:30042000-30046200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr15:30042000-30046200	Weak transcription	Brain Substantia Nigra	brain
49	chr15:30042000-30046200	Weak transcription	Fetal Lung	lung
50	chr15:30042000-30046400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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