Variant report

Variant	esv3351978
Chromosome Location	chr4:15655904-15658002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:562)
CpG islands
(count:366)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:15656279-15656311	K562	blood:	n/a	n/a
2	ARID3A	chr4:15656094-15656275	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:15656835-15657458	HepG2	liver:	n/a	n/a
4	ATF2	chr4:15657010-15657526	GM12878	blood:	n/a	n/a
5	ATF2	chr4:15657001-15658061	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:15657485-15658011	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:15657062-15657456	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:15656933-15657194	H1-hESC	embryonic stem cell:	n/a	chr4:15657104-15657113 chr4:15657093-15657113
9	ATF3	chr4:15656930-15657240	K562	blood:	n/a	chr4:15657104-15657113 chr4:15657093-15657113
10	ATF3	chr4:15656938-15657188	HepG2	liver:	n/a	chr4:15657104-15657113 chr4:15657093-15657113
11	ATF3	chr4:15656919-15657169	GM12878	blood:	n/a	chr4:15657104-15657113 chr4:15657093-15657113
12	ATF3	chr4:15656876-15657324	GM12878	blood:	n/a	chr4:15657104-15657113 chr4:15657093-15657113
13	ATF3	chr4:15656703-15657116	A549	lung:	n/a	chr4:15657104-15657113 chr4:15656735-15656744 chr4:15657093-15657113
14	BACH1	chr4:15657161-15657824	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr4:15656632-15657493	A549	lung:	n/a	chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
16	BCL3	chr4:15656555-15657319	GM12878	blood:	n/a	chr4:15656617-15656630 chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
17	BCL3	chr4:15656616-15657467	A549	lung:	n/a	chr4:15656617-15656630 chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
18	BCLAF1	chr4:15657015-15657454	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:15656310-15657727	GM12878	blood:	n/a	chr4:15656617-15656630 chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
20	BHLHE40	chr4:15655504-15655947	K562	blood:	n/a	n/a
21	BHLHE40	chr4:15656735-15657421	HepG2	liver:	n/a	n/a
22	BHLHE40	chr4:15656503-15657452	GM12878	blood:	n/a	chr4:15656721-15656737 chr4:15656728-15656744 chr4:15656584-15656600 chr4:15656683-15656699
23	BHLHE40	chr4:15656620-15657421	K562	blood:	n/a	chr4:15656721-15656737 chr4:15656728-15656744 chr4:15656683-15656699
24	BRCA1	chr4:15657195-15657332	GM12878	blood:	n/a	n/a
25	BRCA1	chr4:15656910-15657042	HepG2	liver:	n/a	n/a
26	CBX3	chr4:15656980-15657909	K562	blood:	n/a	n/a
27	CCNT2	chr4:15656329-15658018	K562	blood:	n/a	chr4:15657746-15657755 chr4:15657603-15657612
28	CEBPB	chr4:15656886-15656890	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:15656726-15656865	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:15656366-15656432	HepG2	liver:	n/a	n/a
31	CEBPD	chr4:15656785-15657301	HepG2	liver:	n/a	n/a
32	CHD1	chr4:15656724-15656917	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr4:15657145-15658074	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr4:15656349-15657479	GM12878	blood:	n/a	n/a
35	CHD1	chr4:15655942-15656288	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr4:15656832-15657517	GM12878	blood:	n/a	n/a
37	CHD2	chr4:15656607-15657329	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr4:15657127-15657328	HepG2	liver:	n/a	n/a
39	CHD2	chr4:15656810-15657465	K562	blood:	n/a	n/a
40	CHD2	chr4:15656741-15657954	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr4:15656476-15657554	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr4:15656465-15656786	A549	lung:	n/a	n/a
43	CREB1	chr4:15655425-15655914	K562	blood:	n/a	n/a
44	CREB1	chr4:15656261-15657656	HepG2	liver:	n/a	n/a
45	CREB1	chr4:15656890-15657202	A549	lung:	n/a	n/a
46	CREB1	chr4:15655433-15655959	GM12878	blood:	n/a	n/a
47	CTCF	chr4:15657460-15657610	AG04449	skin:	n/a	n/a
48	CTCF	chr4:15656834-15657028	GM12892	blood:	n/a	chr4:15656990-15657003
49	CTCF	chr4:15656200-15656350	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr4:15656220-15656370	GM06990	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:15657820-15657870	HMEC	breast:	n/a
2	chr4:15657820-15657870	H1-hESC	embryonic stem cell:	embryo
3	chr4:15656832-15656882	GM12892	blood:	n/a
4	chr4:15657820-15657870	ProgFib	skin:	n/a
5	chr4:15656911-15656961	Hepatocyte	liver:	n/a
6	chr4:15656911-15656961	AG09319	gingival:	n/a
7	chr4:15657657-15657707	ProgFib	skin:	n/a
8	chr4:15656832-15656882	GM12891	blood:	n/a
9	chr4:15657657-15657707	AG04449	skin:	fetal
10	chr4:15657657-15657707	AG09309	skin:	n/a
11	chr4:15656832-15656882	AG04450	lung:	fetal
12	chr4:15656503-15656553	PANC-1	pancreas:	n/a
13	chr4:15656874-15656924	NT2-D1	testis:	n/a
14	chr4:15656874-15656924	HEEpiC	esophagus:	n/a
15	chr4:15656503-15656553	HMEC	breast:	n/a
16	chr4:15657657-15657707	HRPEpiC	eye:	n/a
17	chr4:15656911-15656961	NHBE	bronchial:	n/a
18	chr4:15656503-15656553	T-47D	breast:	n/a
19	chr4:15656832-15656882	HMEC	breast:	n/a
20	chr4:15656911-15656961	ovcar-3	ovarian:	n/a
21	chr4:15657657-15657707	IMR90	lung:	fetal
22	chr4:15656832-15656882	AG04449	skin:	fetal
23	chr4:15657820-15657870	Caco-2	colon:	n/a
24	chr4:15657657-15657707	LNCaP	prostate:	n/a
25	chr4:15657820-15657870	LNCaP	prostate:	n/a
26	chr4:15656874-15656924	AG09309	skin:	n/a
27	chr4:15657820-15657870	NB4	blood:	n/a
28	chr4:15656911-15656961	GM19239	blood:	n/a
29	chr4:15656911-15656961	A549	lung:	n/a
30	chr4:15656874-15656924	BE2_C	brain:	n/a
31	chr4:15656832-15656882	U87	brain:	n/a
32	chr4:15656832-15656882	ECC-1	luminal epithelium:	n/a
33	chr4:15656832-15656882	CMK	blood:	n/a
34	chr4:15656503-15656553	NT2-D1	testis:	n/a
35	chr4:15657820-15657870	PFSK-1	brain:	n/a
36	chr4:15656503-15656553	AG09319	gingival:	n/a
37	chr4:15656874-15656924	HNPCEpiC	eye:	n/a
38	chr4:15657820-15657870	GM06990	blood:	n/a
39	chr4:15656874-15656924	HCT-116	colon:	n/a
40	chr4:15656911-15656961	Hela-S3	cervix:	n/a
41	chr4:15656832-15656882	HCM	heart:	n/a
42	chr4:15656832-15656882	MCF10A-Er-Src	breast:	n/a
43	chr4:15656832-15656882	HAEpiC	amniotic membrane:	n/a
44	chr4:15656874-15656924	HRE	kidney:	n/a
45	chr4:15656503-15656553	GM12892	blood:	n/a
46	chr4:15657820-15657870	HAEpiC	amniotic membrane:	n/a
47	chr4:15656832-15656882	NB4	blood:	n/a
48	chr4:15656911-15656961	HEEpiC	esophagus:	n/a
49	chr4:15656832-15656882	T-47D	breast:	n/a
50	chr4:15656874-15656924	HIPEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15655590..15657245-chr4:15703796..15706264,2	K562	blood:
2	chr4:15650206..15660298-chr4:15677140..15687517,25	K562	blood:
3	chr4:15652080..15658606-chr4:15677363..15685579,17	MCF-7	breast:
4	chr4:15479740..15482605-chr4:15655501..15658427,3	MCF-7	breast:
5	chr4:15649396..15652390-chr4:15655110..15656784,2	MCF-7	breast:
6	chr4:15654963..15657954-chr4:15685988..15688544,3	MCF-7	breast:
7	chr15:72766669..72767169-chr4:15657562..15658305,2	HCT-116	colon:
8	chr4:15649873..15653235-chr4:15657425..15660766,3	MCF-7	breast:
9	chr4:15650281..15653257-chr4:15654255..15656394,2	K562	blood:
10	chr21:34601586..34602556-chr4:15656823..15657778,2	NB4	blood:
11	chr4:15002808..15006132-chr4:15656406..15658114,3	K562	blood:
12	chr4:15655671..15658131-chr4:15716646..15719360,2	MCF-7	breast:
13	chr4:15469326..15470996-chr4:15657243..15660173,2	MCF-7	breast:
14	chr4:15652688..15657004-chr4:15659488..15663550,8	K562	blood:
15	chr4:15655595..15658742-chr4:15680185..15687360,10	MCF-7	breast:
16	chr4:15656159..15658615-chr4:15712805..15714316,2	K562	blood:
17	chr12:122235040..122237798-chr4:15655451..15658367,2	MCF-7	breast:
18	chr4:15656218..15656918-chr7:45018290..45018877,2	Hela-S3	cervix:
19	chr4:15651703..15660794-chr4:15677607..15686235,25	K562	blood:
20	chr4:15654775..15659231-chr4:15659761..15666940,9	K562	blood:
21	chr4:15544533..15546139-chr4:15654596..15656765,2	K562	blood:

No data

Variant related genes	Relation type
FBXL5	TF binding region
FBXL5	CpG island
ENSG00000237765	chromatin interactions
ENSG00000136286	chromatin interactions
ENSG00000048342	chromatin interactions
ENSG00000247624	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000118564	chromatin interactions
ENSG00000109743	chromatin interactions
ENSG00000159110	chromatin interactions
ENSG00000272849	chromatin interactions
ENSG00000137449	chromatin interactions

Extended variants
information (count: 71 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577040964	chr4:15655918-15655919	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs545794705	chr4:15655948-15655949	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs559483435	chr4:15655966-15655967	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs192170260	chr4:15655990-15655991	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs111546450	chr4:15655995-15655996	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs372536742	chr4:15656035-15656036	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs144227506	chr4:15656038-15656039	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs4318643	chr4:15656042-15656043	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs368178319	chr4:15656049-15656050	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs550099065	chr4:15656078-15656079	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs537852233	chr4:15656104-15656105	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs182839999	chr4:15656184-15656185	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs539283581	chr4:15656203-15656204	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs73241198	chr4:15656212-15656213	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187743568	chr4:15656268-15656269	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs534929830	chr4:15656340-15656341	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs375424436	chr4:15656431-15656432	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs375254130	chr4:15656437-15656438	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs13135399	chr4:15656567-15656568	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs554754388	chr4:15656607-15656608	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs141324869	chr4:15656696-15656697	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs193239008	chr4:15656735-15656736	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs376438311	chr4:15656802-15656803	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs370880362	chr4:15656806-15656807	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs370870648	chr4:15656820-15656821	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs201406404	chr4:15656821-15656822	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs200927708	chr4:15656881-15656882	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs377684367	chr4:15656884-15656885	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs1127154	chr4:15656897-15656898	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs573065834	chr4:15656939-15656940	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs184805452	chr4:15657036-15657037	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs6846508	chr4:15657068-15657069	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs575768035	chr4:15657122-15657123	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs561865362	chr4:15657188-15657189	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs188835305	chr4:15657192-15657193	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs530187400	chr4:15657198-15657199	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs543566111	chr4:15657210-15657211	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs563683373	chr4:15657229-15657230	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs115294707	chr4:15657236-15657237	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs368598726	chr4:15657245-15657246	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs565995632	chr4:15657248-15657249	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs7688984	chr4:15657253-15657254	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs192167412	chr4:15657276-15657277	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs568332671	chr4:15657324-15657325	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs537135835	chr4:15657331-15657332	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs556806445	chr4:15657379-15657380	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs183843759	chr4:15657386-15657387	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs77355802	chr4:15657395-15657396	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs552942640	chr4:15657478-15657479	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs573126060	chr4:15657479-15657480	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Breast cancer	22522925	CNVD
Non-small cell lung cancer	21829676	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15642000-15656200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:15651800-15656200	Weak transcription	Spleen	Spleen
3	chr4:15652800-15656400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:15653400-15656000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:15653400-15656600	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr4:15653400-15657600	Active TSS	Right Atrium	heart
7	chr4:15653800-15657200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:15653800-15657200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr4:15653800-15657600	Active TSS	K562	blood
10	chr4:15654000-15656200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:15654000-15656400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:15654000-15657200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:15654200-15656000	Flanking Active TSS	Liver	Liver
14	chr4:15654200-15657000	Active TSS	HMEC	breast
15	chr4:15654200-15657200	Active TSS	Primary monocytes fromperipheralblood	blood
16	chr4:15654400-15656000	Flanking Active TSS	HUVEC	blood vessel
17	chr4:15654400-15656200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr4:15654400-15656200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr4:15654400-15656600	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr4:15654400-15657200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr4:15654400-15657400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:15654600-15656000	Flanking Active TSS	Fetal Brain Male	brain
23	chr4:15654600-15656000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
24	chr4:15654600-15656000	Flanking Active TSS	NH-A	brain
25	chr4:15654600-15656400	Flanking Active TSS	Primary T cells from cord blood	blood
26	chr4:15654600-15657200	Active TSS	Muscle Satellite Cultured Cells	--
27	chr4:15654600-15657200	Active TSS	NHEK	skin
28	chr4:15654600-15657200	Active TSS	NHLF	lung
29	chr4:15654600-15657600	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr4:15654600-15658000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:15654600-15658200	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr4:15654800-15656000	Flanking Active TSS	Fetal Kidney	kidney
33	chr4:15654800-15656200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr4:15654800-15656200	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr4:15654800-15656600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
36	chr4:15654800-15657200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:15654800-15657200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr4:15654800-15657200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr4:15654800-15657200	Active TSS	HSMM	muscle
40	chr4:15654800-15657200	Active TSS	NHDF-Ad	bronchial
41	chr4:15654800-15657400	Active TSS	Brain Hippocampus Middle	brain
42	chr4:15654800-15657600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:15654800-15657600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr4:15654800-15657600	Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr4:15654800-15657600	Active TSS	GM12878-XiMat	blood
46	chr4:15654800-15658000	Active TSS	Psoas Muscle	Psoas
47	chr4:15655000-15656000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr4:15655000-15656000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr4:15655000-15656000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr4:15655000-15656000	Flanking Active TSS	Fetal Heart	heart

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