Variant report

Variant	esv3436996
Chromosome Location	chr4:77132828-77137126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:734)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:77134821-77134936	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:77135103-77135106	K562	blood:	n/a	n/a
3	ATF2	chr4:77135144-77135604	GM12878	blood:	n/a	n/a
4	ATF2	chr4:77134734-77135673	GM12878	blood:	n/a	chr4:77134994-77135008
5	ATF3	chr4:77134686-77135221	K562	blood:	n/a	chr4:77135115-77135124 chr4:77134992-77135012
6	ATF3	chr4:77134916-77135200	HepG2	liver:	n/a	chr4:77135115-77135124 chr4:77134992-77135012
7	BACH1	chr4:77134734-77135491	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:77135163-77135728	GM12878	blood:	n/a	n/a
9	BCL3	chr4:77134914-77135665	GM12878	blood:	n/a	chr4:77135068-77135077 chr4:77135095-77135104 chr4:77135090-77135103 chr4:77135091-77135104
10	BCLAF1	chr4:77134596-77135577	GM12878	blood:	n/a	chr4:77135068-77135077 chr4:77135095-77135104 chr4:77134895-77134904 chr4:77135090-77135103 chr4:77135091-77135104
11	BHLHE40	chr4:77134007-77134275	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:77134513-77135596	HepG2	liver:	n/a	chr4:77135091-77135107 chr4:77135039-77135055
13	BHLHE40	chr4:77134601-77135471	GM12878	blood:	n/a	chr4:77135091-77135107 chr4:77135039-77135055
14	BHLHE40	chr4:77134311-77135641	K562	blood:	n/a	chr4:77135091-77135107 chr4:77135039-77135055
15	BRCA1	chr4:77135757-77136083	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr4:77134699-77134871	HepG2	liver:	n/a	n/a
17	BRCA1	chr4:77135217-77135417	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:77134577-77134997	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr4:77134923-77135397	K562	blood:	n/a	n/a
20	CCNT2	chr4:77134555-77135329	K562	blood:	n/a	n/a
21	CEBPB	chr4:77134917-77135522	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:77134936-77135087	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:77135202-77135587	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:77134936-77135513	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr4:77134897-77135545	HepG2	liver:	n/a	n/a
26	CEBPD	chr4:77134708-77135457	HepG2	liver:	n/a	n/a
27	CHD1	chr4:77134929-77134934	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:77134699-77135447	HepG2	liver:	n/a	n/a
29	CHD2	chr4:77134789-77135619	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr4:77134640-77135395	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr4:77134798-77135367	K562	blood:	n/a	n/a
32	CHD2	chr4:77134128-77135608	GM12878	blood:	n/a	n/a
33	CREB1	chr4:77134429-77135352	K562	blood:	n/a	n/a
34	CREB1	chr4:77134326-77135223	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr4:77134543-77135298	A549	lung:	n/a	n/a
36	CREB1	chr4:77134311-77135770	HepG2	liver:	n/a	n/a
37	CTBP2	chr4:77134544-77135705	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:77135260-77135410	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr4:77135520-77135670	GM12867	blood:	n/a	n/a
40	CTCF	chr4:77134840-77134990	GM12873	blood:	n/a	chr4:77134867-77134880
41	CTCF	chr4:77135140-77135290	GM12871	blood:	n/a	n/a
42	CTCF	chr4:77132740-77132890	HRE	kidney:	n/a	n/a
43	CTCF	chr4:77135300-77135450	GM12874	blood:	n/a	n/a
44	CTCF	chr4:77134760-77134910	GM12866	blood:	n/a	chr4:77134867-77134880
45	CTCF	chr4:77134660-77134810	AG04449	skin:	n/a	n/a
46	CTCF	chr4:77135280-77135430	HRE	kidney:	n/a	n/a
47	CTCF	chr4:77135321-77135381	GM12891	blood:	n/a	n/a
48	CTCF	chr4:77135280-77135430	HCT-116	colon:	n/a	n/a
49	CTCF	chr4:77134780-77134930	GM12867	blood:	n/a	chr4:77134867-77134880
50	CTCF	chr4:77134280-77134430	GM12872	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:77135186-77135236	CMK	blood:	n/a
2	chr4:77135351-77135401	NH-A	brain:	n/a
3	chr4:77135186-77135236	CMK	blood:	n/a
4	chr4:77135351-77135401	NH-A	brain:	n/a
5	chr4:77134319-77134369	GM19239	blood:	n/a
6	chr4:77133417-77133467	HEK293	kidney:	embryo
7	chr4:77134319-77134369	HEK293	kidney:	embryo
8	chr4:77135005-77135055	NT2-D1	testis:	n/a
9	chr4:77133417-77133467	U87	brain:	n/a
10	chr4:77135347-77135397	RPTEC	kidney:	n/a
11	chr4:77135186-77135236	HCM	heart:	n/a
12	chr4:77135005-77135055	NB4	blood:	n/a
13	chr4:77134319-77134369	LNCaP	prostate:	n/a
14	chr4:77135347-77135397	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:77134319-77134369	BJ	skin:	n/a
16	chr4:77135351-77135401	Jurkat	blood:	n/a
17	chr4:77135162-77135212	HAEpiC	amniotic membrane:	n/a
18	chr4:77135351-77135401	U87	brain:	n/a
19	chr4:77133417-77133467	AG04449	skin:	fetal
20	chr4:77134585-77134635	BE2_C	brain:	n/a
21	chr4:77135005-77135055	SK-N-SH_RA	brain:	n/a
22	chr4:77135351-77135401	NHDF-neo	bronchial:	n/a
23	chr4:77135162-77135212	CMK	blood:	n/a
24	chr4:77134585-77134635	NB4	blood:	n/a
25	chr4:77135347-77135397	IMR90	lung:	fetal
26	chr4:77135351-77135401	RPTEC	kidney:	n/a
27	chr4:77135351-77135401	HCPEpiC	choroid plexus:	n/a
28	chr4:77135347-77135397	HMEC	breast:	n/a
29	chr4:77135162-77135212	IMR90	lung:	fetal
30	chr4:77133417-77133467	CMK	blood:	n/a
31	chr4:77135162-77135212	AG09309	skin:	n/a
32	chr4:77135162-77135212	U87	brain:	n/a
33	chr4:77135347-77135397	HUVEC	blood vessel:	n/a
34	chr4:77135005-77135055	IMR90	lung:	fetal
35	chr4:77135506-77135556	SKMC	muscle:	n/a
36	chr4:77135005-77135055	HEK293	kidney:	embryo
37	chr4:77133417-77133467	MCF-7	breast:	n/a
38	chr4:77134585-77134635	Caco-2	colon:	n/a
39	chr4:77135506-77135556	ovcar-3	ovarian:	n/a
40	chr4:77135186-77135236	Hela-S3	cervix:	n/a
41	chr4:77134471-77134521	NH-A	brain:	n/a
42	chr4:77134319-77134369	GM06990	blood:	n/a
43	chr4:77135351-77135401	GM12892	blood:	n/a
44	chr4:77134585-77134635	NHBE	bronchial:	n/a
45	chr4:77135195-77135245	ECC-1	luminal epithelium:	n/a
46	chr4:77135506-77135556	HCM	heart:	n/a
47	chr4:77135005-77135055	HRPEpiC	eye:	n/a
48	chr4:77133417-77133467	IMR90	lung:	fetal
49	chr4:77135351-77135401	NB4	blood:	n/a
50	chr4:77134471-77134521	HMEC	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:77133278..77135557-chr4:77171656..77174471,3	MCF-7	breast:
2	chr4:77135441..77137897-chr4:77152068..77153830,2	K562	blood:
3	chr4:77136412..77137216-chr4:77157279..77157833,2	MCF-7	breast:
4	chr4:77066331..77070645-chr4:77133023..77136401,5	K562	blood:
5	chr19:34286957..34287458-chr4:77134764..77135364,2	Hela-S3	cervix:
6	chr4:77067778..77069460-chr4:77134577..77136401,2	K562	blood:
7	chr4:77133904..77135705-chr4:77183809..77185526,2	MCF-7	breast:
8	chr4:77132690..77134987-chr4:77135558..77138954,3	K562	blood:
9	chr4:77131893..77139465-chr4:77152630..77158664,14	MCF-7	breast:
10	chr4:77062870..77064723-chr4:77131850..77133606,2	K562	blood:
11	chr4:77132690..77134987-chr4:77135558..77138954,3	K562	blood:
12	chr1:147806653..147807174-chr4:77134889..77135788,2	Hela-S3	cervix:
13	chr4:77132958..77141575-chr4:77150872..77159587,22	MCF-7	breast:

No data

Variant related genes	Relation type
SCARB2	TF binding region
FAM47E	TF binding region
SCARB2	CpG island
FAM47E	CpG island
ENSG00000153885	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000189157	chromatin interactions
ENSG00000118804	chromatin interactions
ENSG00000138760	chromatin interactions
ENSG00000138750	chromatin interactions
ENSG00000272414	chromatin interactions

Extended variants
information (count: 154 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181626349	chr4:77132842-77132843	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs568219971	chr4:77132878-77132879	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570560454	chr4:77132882-77132883	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs539309448	chr4:77132896-77132897	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs556032236	chr4:77132904-77132905	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs373639797	chr4:77132925-77132926	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs139285404	chr4:77132939-77132940	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs367660915	chr4:77132983-77132984	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573809678	chr4:77132997-77132998	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555513146	chr4:77133014-77133015	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs79146874	chr4:77133048-77133049	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs12498327	chr4:77133079-77133080	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564661125	chr4:77133136-77133137	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs144108533	chr4:77133137-77133138	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544075039	chr4:77133147-77133148	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs76069026	chr4:77133175-77133176	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs529645955	chr4:77133436-77133437	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs143929519	chr4:77133444-77133445	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs79766965	chr4:77133453-77133454	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs561549449	chr4:77133454-77133455	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs527336164	chr4:77133455-77133456	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs35563881	chr4:77133494-77133495	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs372277205	chr4:77133540-77133541	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs148640739	chr4:77133579-77133580	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs570255470	chr4:77133587-77133588	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs142137870	chr4:77133601-77133602	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs549593856	chr4:77133634-77133635	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs556401126	chr4:77133644-77133645	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs185489947	chr4:77133729-77133730	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs555686076	chr4:77133766-77133767	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs151140286	chr4:77133783-77133784	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs34239901	chr4:77133825-77133826	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs190003806	chr4:77133861-77133862	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs139491858	chr4:77133880-77133881	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs558614260	chr4:77133886-77133887	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs578162432	chr4:77133915-77133916	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs548322638	chr4:77133956-77133957	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs566588077	chr4:77133957-77133958	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs145637377	chr4:77133998-77133999	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs371472445	chr4:77134012-77134013	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs34138525	chr4:77134105-77134106	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs563886207	chr4:77134112-77134113	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs574356481	chr4:77134122-77134123	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs575372109	chr4:77134162-77134163	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs201853080	chr4:77134210-77134211	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs201076199	chr4:77134212-77134213	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs555146289	chr4:77134273-77134274	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs527282041	chr4:77134274-77134275	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs78406257	chr4:77134284-77134285	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs201151829	chr4:77134288-77134289	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:77113200-77134000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:77113600-77134200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:77117000-77134000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:77121400-77133600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr4:77121400-77134000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:77122400-77133600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:77128400-77133200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr4:77128600-77133000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr4:77128800-77133400	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr4:77128800-77133600	Enhancers	Small Intestine	intestine
11	chr4:77129800-77133400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr4:77130200-77133000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:77130200-77133000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:77130200-77133000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:77130200-77133000	Weak transcription	A549	lung
16	chr4:77130200-77133200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr4:77130200-77133400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr4:77130200-77133400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr4:77130200-77133800	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr4:77130200-77133800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr4:77130800-77133600	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr4:77130800-77133800	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr4:77130800-77134000	Enhancers	Primary B cells from peripheral blood	blood
24	chr4:77130800-77134000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr4:77130800-77134800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr4:77131000-77133000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:77131000-77133200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr4:77131000-77133400	Flanking Active TSS	Brain Hippocampus Middle	brain
29	chr4:77131000-77133600	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr4:77131000-77134000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr4:77131000-77134600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr4:77131200-77133800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:77131200-77134200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr4:77131400-77133400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:77131400-77133800	Enhancers	Primary hematopoietic stem cells	blood
36	chr4:77131400-77134000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr4:77131400-77134000	Flanking Active TSS	Osteobl	bone
38	chr4:77131600-77133000	Enhancers	Placenta	Placenta
39	chr4:77131600-77133200	Flanking Active TSS	Fetal Brain Female	brain
40	chr4:77131600-77134200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:77131600-77134600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:77131600-77134600	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr4:77131600-77134600	Flanking Active TSS	Liver	Liver
44	chr4:77131800-77133400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:77131800-77134600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr4:77132200-77133200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:77132200-77133200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr4:77132200-77133200	Flanking Active TSS	NHLF	lung
49	chr4:77132200-77133400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
50	chr4:77132200-77133400	Enhancers	NHEK	skin

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