Variant report

Variant	esv3409123
Chromosome Location	chr1:150121478-150123676
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:150123306-150124077	GM12878	blood:	n/a	n/a
2	ATF2	chr1:150123368-150124377	GM12878	blood:	n/a	n/a
3	BACH1	chr1:150122636-150122999	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:150121802-150122291	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:150121857-150122103	GM12878	blood:	n/a	chr1:150121977-150121988
6	BATF	chr1:150123538-150123846	GM12878	blood:	n/a	n/a
7	BCL3	chr1:150121674-150122140	GM12878	blood:	n/a	chr1:150121896-150121909 chr1:150121994-150122007 chr1:150121999-150122008
8	BCLAF1	chr1:150120699-150122572	GM12878	blood:	n/a	chr1:150122497-150122510 chr1:150122500-150122513 chr1:150121896-150121909 chr1:150122495-150122508 chr1:150121994-150122007 chr1:150122206-150122219 chr1:150122329-150122338 chr1:150121999-150122008 chr1:150122543-150122556 chr1:150122545-150122554 chr1:150122503-150122512
9	BCLAF1	chr1:150122894-150124323	GM12878	blood:	n/a	chr1:150123863-150123872
10	BCLAF1	chr1:150122973-150124359	GM12878	blood:	n/a	chr1:150123863-150123872
11	BCLAF1	chr1:150121253-150122324	GM12878	blood:	n/a	chr1:150121896-150121909 chr1:150121994-150122007 chr1:150122206-150122219 chr1:150121999-150122008
12	BHLHE40	chr1:150123558-150124210	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:150121684-150122397	GM12878	blood:	n/a	chr1:150121899-150121915
14	CCNT2	chr1:150121552-150122661	K562	blood:	n/a	chr1:150121998-150122007 chr1:150122210-150122219
15	CEBPB	chr1:150121042-150121853	GM12878	blood:	n/a	n/a
16	CHD1	chr1:150122234-150124524	GM12878	blood:	n/a	n/a
17	CHD1	chr1:150122789-150123205	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr1:150120708-150124616	IMR90	lung:	n/a	chr1:150122211-150122221
19	CHD1	chr1:150121326-150121854	GM12878	blood:	n/a	n/a
20	CHD2	chr1:150122268-150122294	K562	blood:	n/a	n/a
21	CHD2	chr1:150121694-150121789	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr1:150121432-150122332	GM12878	blood:	n/a	chr1:150122211-150122221
23	CHD2	chr1:150122904-150124212	GM12878	blood:	n/a	n/a
24	CHD2	chr1:150122845-150122847	K562	blood:	n/a	n/a
25	CHD2	chr1:150121948-150121984	K562	blood:	n/a	n/a
26	CREB1	chr1:150121476-150122569	HepG2	liver:	n/a	n/a
27	CREB1	chr1:150121878-150122436	GM12878	blood:	n/a	n/a
28	CREB1	chr1:150121798-150122605	A549	lung:	n/a	n/a
29	CTCF	chr1:150121700-150121850	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr1:150122263-150122293	GM19239	blood:	n/a	n/a
31	CTCF	chr1:150121680-150121830	BJ	skin:	n/a	n/a
32	CTCF	chr1:150123200-150123350	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr1:150122246-150122250	GM19239	blood:	n/a	n/a
34	CTCF	chr1:150122200-150122350	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr1:150121660-150121810	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr1:150122200-150122350	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr1:150122335-150122393	GM12878	blood:	n/a	n/a
38	CTCF	chr1:150121640-150121790	AG04449	skin:	n/a	n/a
39	E2F4	chr1:150123591-150123693	GM12878	blood:	n/a	n/a
40	E2F4	chr1:150121647-150122020	MCF10A-Er-Src	breast:	n/a	chr1:150121901-150121911 chr1:150121721-150121735 chr1:150121998-150122007
41	E2F6	chr1:150121473-150122411	A549	lung:	n/a	chr1:150122332-150122342 chr1:150122305-150122316 chr1:150121901-150121911 chr1:150121721-150121735 chr1:150121998-150122007
42	E2F6	chr1:150122139-150122484	A549	lung:	n/a	chr1:150122332-150122342 chr1:150122305-150122316
43	E2F6	chr1:150122613-150122912	K562	blood:	n/a	n/a
44	E2F6	chr1:150121624-150122566	K562	blood:	n/a	chr1:150122332-150122342 chr1:150122305-150122316 chr1:150121901-150121911 chr1:150121721-150121735 chr1:150121998-150122007 chr1:150122502-150122512
45	E2F6	chr1:150121632-150122511	K562	blood:	n/a	chr1:150122332-150122342 chr1:150122305-150122316 chr1:150121901-150121911 chr1:150121721-150121735 chr1:150121998-150122007
46	EBF1	chr1:150121707-150122327	GM12878	blood:	n/a	chr1:150121924-150121935
47	EBF1	chr1:150121730-150122136	GM12878	blood:	n/a	chr1:150121924-150121935
48	EGR1	chr1:150121860-150123071	K562	blood:	n/a	chr1:150121993-150122003 chr1:150121992-150122007 chr1:150122224-150122233 chr1:150122506-150122516 chr1:150121993-150122006 chr1:150121998-150122008 chr1:150121993-150122006 chr1:150121997-150122007
49	EGR1	chr1:150122582-150123015	K562	blood:	n/a	n/a
50	EGR1	chr1:150121297-150122894	MCF-7	breast:	n/a	chr1:150121993-150122003 chr1:150121992-150122007 chr1:150122224-150122233 chr1:150122506-150122516 chr1:150121993-150122006 chr1:150121998-150122008 chr1:150121993-150122006 chr1:150121997-150122007 chr1:150121724-150121734

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150123037-150123087	HIPEpiC	eye:	n/a
2	chr1:150123037-150123087	HIPEpiC	eye:	n/a
3	chr1:150121727-150121777	BE2_C	brain:	n/a
4	chr1:150123037-150123087	T-47D	breast:	n/a
5	chr1:150121727-150121777	HNPCEpiC	eye:	n/a
6	chr1:150121813-150121863	HUVEC	blood vessel:	n/a
7	chr1:150121725-150121775	Jurkat	blood:	n/a
8	chr1:150122500-150122550	HRPEpiC	eye:	n/a
9	chr1:150123037-150123087	PrEC	prostate:	n/a
10	chr1:150121441-150121491	ovcar-3	ovarian:	n/a
11	chr1:150122278-150122328	Hepatocyte	liver:	n/a
12	chr1:150123146-150123196	AG09309	skin:	n/a
13	chr1:150122500-150122550	NH-A	brain:	n/a
14	chr1:150121813-150121863	Hepatocyte	liver:	n/a
15	chr1:150123077-150123127	Jurkat	blood:	n/a
16	chr1:150123146-150123196	HRE	kidney:	n/a
17	chr1:150123037-150123087	MCF-7	breast:	n/a
18	chr1:150122500-150122550	HCF	heart:	n/a
19	chr1:150122690-150122740	GM06990	blood:	n/a
20	chr1:150122654-150122704	HRCEpiC	kidney:	n/a
21	chr1:150122690-150122740	HEK293	kidney:	embryo
22	chr1:150122690-150122740	ProgFib	skin:	n/a
23	chr1:150122654-150122704	HL-60	blood:	n/a
24	chr1:150122690-150122740	HCF	heart:	n/a
25	chr1:150121441-150121491	HUVEC	blood vessel:	n/a
26	chr1:150123037-150123087	HCT-116	colon:	n/a
27	chr1:150122690-150122740	Caco-2	colon:	n/a
28	chr1:150123077-150123127	IMR90	lung:	fetal
29	chr1:150123077-150123127	U87	brain:	n/a
30	chr1:150121441-150121491	LNCaP	prostate:	n/a
31	chr1:150122690-150122740	Hela-S3	cervix:	n/a
32	chr1:150121813-150121863	A549	lung:	n/a
33	chr1:150121725-150121775	AG09309	skin:	n/a
34	chr1:150122278-150122328	NB4	blood:	n/a
35	chr1:150123146-150123196	HRCEpiC	kidney:	n/a
36	chr1:150122654-150122704	NH-A	brain:	n/a
37	chr1:150122690-150122740	PANC-1	pancreas:	n/a
38	chr1:150121813-150121863	GM19239	blood:	n/a
39	chr1:150121813-150121863	AG10803	skin:	n/a
40	chr1:150123077-150123127	AG10803	skin:	n/a
41	chr1:150122500-150122550	Hepatocyte	liver:	n/a
42	chr1:150122690-150122740	NB4	blood:	n/a
43	chr1:150121441-150121491	NH-A	brain:	n/a
44	chr1:150122654-150122704	BJ	skin:	n/a
45	chr1:150123490-150123540	PFSK-1	brain:	n/a
46	chr1:150121725-150121775	HL-60	blood:	n/a
47	chr1:150121813-150121863	CMK	blood:	n/a
48	chr1:150121725-150121775	HCF	heart:	n/a
49	chr1:150121727-150121777	T-47D	breast:	n/a
50	chr1:150121725-150121775	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:149856777..149860438-chr1:150121197..150124713,4	K562	blood:
2	chr1:150038076..150040720-chr1:150121290..150124944,3	K562	blood:
3	chr1:150033546..150035301-chr1:150123056..150125109,2	K562	blood:
4	chr1:149858428..149861867-chr1:150121197..150123185,3	K562	blood:
5	chr1:150048782..150051113-chr1:150122010..150123547,2	MCF-7	breast:
6	chr1:150121160..150123717-chr1:150206817..150209674,5	MCF-7	breast:
7	chr1:150120783..150123550-chr1:150205612..150208208,2	K562	blood:
8	chr1:150047834..150051741-chr1:150120632..150125901,6	MCF-7	breast:
9	chr1:150120710..150123122-chr1:155106674..155108306,2	MCF-7	breast:
10	chr1:150121553..150123075-chr6:27798165..27799927,2	MCF-7	breast:
11	chr1:150063760..150067981-chr1:150120061..150123839,7	MCF-7	breast:
12	chr1:150121582..150124449-chr1:150206466..150208946,2	MCF-7	breast:
13	chr1:149855859..149860778-chr1:150121854..150124549,4	MCF-7	breast:
14	chr1:149858884..149861217-chr1:150120977..150123082,2	MCF-7	breast:
15	chr1:150121990..150123693-chr1:150240466..150243151,2	K562	blood:
16	chr1:150038270..150039782-chr1:150120828..150123212,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VPS45-1	chr1:150122827-150123248	NONHSAT006272

Variant related genes	Relation type
PLEKHO1	TF binding region
PLEKHO1	CpG island
ENSG00000136631	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000118292	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000222222	chromatin interactions
ENSG00000117362	chromatin interactions
ENSG00000143401	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000197914	chromatin interactions

Extended variants
information (count: 77 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:77 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76123009	chr1:150121546-150121547	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs587597916	chr1:150121654-150121655	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs587650442	chr1:150121737-150121738	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs587727879	chr1:150121765-150121766	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs587623389	chr1:150121769-150121770	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs111988509	chr1:150121826-150121827	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs587680782	chr1:150121864-150121865	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs587760172	chr1:150121869-150121870	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs192810588	chr1:150121894-150121895	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs76413654	chr1:150121929-150121930	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs587749421	chr1:150121971-150121972	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs587752942	chr1:150121995-150121996	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs369887217	chr1:150122066-150122067	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs372730107	chr1:150122072-150122073	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs587679792	chr1:150122074-150122075	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs587734903	chr1:150122099-150122100	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs587632720	chr1:150122110-150122111	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs587687723	chr1:150122120-150122121	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs587762656	chr1:150122177-150122178	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs185723031	chr1:150122178-150122179	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs76541931	chr1:150122269-150122270	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs76050098	chr1:150122344-150122345	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs189274971	chr1:150122369-150122370	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	mRNA abundance
24	rs587643363	chr1:150122425-150122426	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs587751164	chr1:150122468-150122469	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs4553237	chr1:150122493-150122494	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs183546410	chr1:150122523-150122524	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs587774051	chr1:150122567-150122568	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs587656132	chr1:150122573-150122574	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs587752536	chr1:150122580-150122581	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs587737670	chr1:150122594-150122595	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs587607178	chr1:150122653-150122654	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs111615125	chr1:150122655-150122656	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs587668584	chr1:150122699-150122700	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs587718138	chr1:150122710-150122711	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs142468019	chr1:150122739-150122740	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs188023024	chr1:150122754-150122755	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs587735025	chr1:150122760-150122761	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs587630731	chr1:150122800-150122801	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs111605530	chr1:150122801-150122802	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs116378235	chr1:150122847-150122848	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
42	rs7518016	chr1:150122890-150122891	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs587610187	chr1:150122934-150122935	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
44	rs587694668	chr1:150122935-150122936	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
45	rs587746366	chr1:150122978-150122979	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
46	rs146836012	chr1:150122981-150122982	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
47	rs587701293	chr1:150122984-150122985	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
48	rs587773662	chr1:150122987-150122988	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
49	rs587677216	chr1:150122992-150122993	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
50	rs587709591	chr1:150122995-150122996	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Schizophrenia	19805367	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150114800-150125200	Weak transcription	Hela-S3	cervix
2	chr1:150117200-150121600	Weak transcription	Gastric	stomach
3	chr1:150120200-150121800	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr1:150120200-150121800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:150120200-150123200	Active TSS	Stomach Smooth Muscle	stomach
6	chr1:150120200-150124000	Active TSS	GM12878-XiMat	blood
7	chr1:150120400-150121800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:150120600-150121600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
9	chr1:150120600-150121600	Flanking Active TSS	Fetal Muscle Leg	muscle
10	chr1:150120600-150121800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:150120600-150122000	Flanking Active TSS	Primary hematopoietic stem cells	blood
12	chr1:150120800-150121600	Flanking Active TSS	Rectal Smooth Muscle	rectum
13	chr1:150120800-150121600	Flanking Active TSS	HUVEC	blood vessel
14	chr1:150120800-150121800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr1:150120800-150121800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr1:150120800-150121800	Flanking Active TSS	Dnd41	blood
17	chr1:150120800-150121800	Flanking Active TSS	NH-A	brain
18	chr1:150120800-150122000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
19	chr1:150120800-150123400	Active TSS	Fetal Muscle Trunk	muscle
20	chr1:150120800-150124000	Active TSS	Aorta	Aorta
21	chr1:150120800-150124400	Active TSS	Brain Anterior Caudate	brain
22	chr1:150120800-150125200	Active TSS	Brain Hippocampus Middle	brain
23	chr1:150120800-150125200	Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr1:150121000-150121600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr1:150121000-150121600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
26	chr1:150121000-150121600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
27	chr1:150121000-150121600	Flanking Active TSS	Primary B cells from peripheral blood	blood
28	chr1:150121000-150121600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
29	chr1:150121000-150121600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr1:150121000-150121600	Active TSS	Brain Germinal Matrix	brain
31	chr1:150121000-150121600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr1:150121000-150121600	Flanking Active TSS	Fetal Lung	lung
33	chr1:150121000-150121600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr1:150121000-150121600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr1:150121000-150121800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr1:150121000-150121800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:150121000-150121800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:150121000-150121800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:150121000-150121800	Active TSS	Fetal Brain Male	brain
40	chr1:150121000-150121800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr1:150121000-150121800	Flanking Active TSS	HSMM	muscle
42	chr1:150121000-150122000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
43	chr1:150121000-150122800	Active TSS	Fetal Brain Female	brain
44	chr1:150121000-150123000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
45	chr1:150121000-150123200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:150121000-150123200	Active TSS	Fetal Stomach	stomach
47	chr1:150121000-150123600	Active TSS	HSMMtube	muscle
48	chr1:150121000-150124000	Active TSS	Right Atrium	heart
49	chr1:150121000-150124200	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr1:150121000-150124200	Active TSS	Fetal Kidney	kidney

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