Variant report

Variant	esv3326369
Chromosome Location	chr4:3074679-3077527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:923)
CpG islands
(count:794)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3076111-3076475	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:3077170-3077212	K562	blood:	n/a	n/a
3	ARID3A	chr4:3076229-3076487	K562	blood:	n/a	n/a
4	ATF2	chr4:3076827-3077509	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:3076902-3078066	GM12878	blood:	n/a	n/a
6	ATF2	chr4:3076989-3077471	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:3076817-3077785	GM12878	blood:	n/a	n/a
8	ATF3	chr4:3076216-3076521	K562	blood:	n/a	n/a
9	BACH1	chr4:3075553-3075747	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr4:3076054-3076689	GM12878	blood:	n/a	chr4:3076489-3076502
11	BCLAF1	chr4:3077412-3078618	GM12878	blood:	n/a	chr4:3077949-3077958
12	BCLAF1	chr4:3076783-3077366	GM12878	blood:	n/a	chr4:3077266-3077279
13	BCLAF1	chr4:3076808-3077331	GM12878	blood:	n/a	chr4:3077266-3077279
14	BCLAF1	chr4:3077356-3078153	GM12878	blood:	n/a	chr4:3077368-3077381 chr4:3077949-3077958 chr4:3077376-3077389
15	BHLHE40	chr4:3076077-3076488	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:3077027-3077031	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3076073-3076452	K562	blood:	n/a	n/a
18	BHLHE40	chr4:3077051-3077305	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:3075445-3075734	HepG2	liver:	n/a	chr4:3075553-3075569
20	BRCA1	chr4:3077033-3077221	GM12878	blood:	n/a	chr4:3077035-3077044
21	BRCA1	chr4:3076899-3077271	H1-hESC	embryonic stem cell:	n/a	chr4:3077035-3077044
22	BRCA1	chr4:3076919-3077192	HepG2	liver:	n/a	chr4:3077035-3077044
23	BRCA1	chr4:3075529-3075611	HepG2	liver:	n/a	n/a
24	BRCA1	chr4:3076971-3077283	Hela-S3	cervix:	n/a	chr4:3077035-3077044
25	BRCA1	chr4:3076111-3076456	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr4:3075980-3076356	K562	blood:	n/a	n/a
27	CCNT2	chr4:3075541-3075760	K562	blood:	n/a	n/a
28	CCNT2	chr4:3076883-3077031	K562	blood:	n/a	chr4:3076912-3076921
29	CCNT2	chr4:3076021-3076570	K562	blood:	n/a	n/a
30	CEBPB	chr4:3076324-3076352	K562	blood:	n/a	n/a
31	CEBPD	chr4:3076179-3076595	HepG2	liver:	n/a	n/a
32	CEBPD	chr4:3075411-3075813	HepG2	liver:	n/a	n/a
33	CEBPD	chr4:3076306-3076634	K562	blood:	n/a	n/a
34	CHD1	chr4:3076483-3076628	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr4:3076963-3078549	GM12878	blood:	n/a	chr4:3077381-3077391 chr4:3076978-3076988 chr4:3077035-3077044
36	CHD1	chr4:3076093-3076615	GM12878	blood:	n/a	n/a
37	CHD2	chr4:3076836-3077361	H1-hESC	embryonic stem cell:	n/a	chr4:3076978-3076988 chr4:3077035-3077044
38	CHD2	chr4:3075566-3075739	HepG2	liver:	n/a	n/a
39	CHD2	chr4:3076879-3077358	Hela-S3	cervix:	n/a	chr4:3076978-3076988 chr4:3077035-3077044
40	CHD2	chr4:3076057-3076609	GM12878	blood:	n/a	n/a
41	CHD2	chr4:3076851-3077329	K562	blood:	n/a	chr4:3076978-3076988 chr4:3077035-3077044
42	CHD2	chr4:3076043-3076492	K562	blood:	n/a	n/a
43	CHD2	chr4:3075519-3076592	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr4:3076812-3077389	HepG2	liver:	n/a	chr4:3076978-3076988 chr4:3077035-3077044
45	CHD2	chr4:3075532-3075705	GM12878	blood:	n/a	n/a
46	CHD2	chr4:3075615-3075711	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr4:3075465-3075643	K562	blood:	n/a	n/a
48	CHD2	chr4:3076842-3077600	GM12878	blood:	n/a	chr4:3077381-3077391 chr4:3076978-3076988 chr4:3077035-3077044
49	CHD2	chr4:3074781-3074873	GM12878	blood:	n/a	n/a
50	CHD2	chr4:3076106-3076573	HepG2	liver:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3076557-3076607	ECC-1	luminal epithelium:	n/a
2	chr4:3076557-3076607	ECC-1	luminal epithelium:	n/a
3	chr4:3075484-3075534	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:3075002-3075052	ovcar-3	ovarian:	n/a
5	chr4:3076334-3076384	H1-hESC	embryonic stem cell:	embryo
6	chr4:3075002-3075052	HCM	heart:	n/a
7	chr4:3076345-3076395	MCF10A-Er-Src	breast:	n/a
8	chr4:3076334-3076384	HCF	heart:	n/a
9	chr4:3075002-3075052	SK-N-SH	brain:	n/a
10	chr4:3076345-3076395	Hela-S3	cervix:	n/a
11	chr4:3076557-3076607	H1-hESC	embryonic stem cell:	embryo
12	chr4:3075655-3075705	GM12892	blood:	n/a
13	chr4:3076345-3076395	GM12878	blood:	n/a
14	chr4:3076345-3076395	AG04449	skin:	fetal
15	chr4:3075888-3075938	GM19239	blood:	n/a
16	chr4:3075484-3075534	K562	blood:	n/a
17	chr4:3075002-3075052	HCPEpiC	choroid plexus:	n/a
18	chr4:3075484-3075534	GM12878	blood:	n/a
19	chr4:3076334-3076384	ovcar-3	ovarian:	n/a
20	chr4:3075655-3075705	HCPEpiC	choroid plexus:	n/a
21	chr4:3075655-3075705	HEK293	kidney:	embryo
22	chr4:3076907-3076957	AG04449	skin:	fetal
23	chr4:3075888-3075938	PrEC	prostate:	n/a
24	chr4:3075002-3075052	SKMC	muscle:	n/a
25	chr4:3075893-3075943	U87	brain:	n/a
26	chr4:3076259-3076309	PrEC	prostate:	n/a
27	chr4:3075893-3075943	HRE	kidney:	n/a
28	chr4:3076557-3076607	U87	brain:	n/a
29	chr4:3075655-3075705	SK-N-MC	brain:	n/a
30	chr4:3076259-3076309	MCF10A-Er-Src	breast:	n/a
31	chr4:3076271-3076321	H1-hESC	embryonic stem cell:	embryo
32	chr4:3076418-3076468	AG09319	gingival:	n/a
33	chr4:3075893-3075943	RPTEC	kidney:	n/a
34	chr4:3076418-3076468	PrEC	prostate:	n/a
35	chr4:3076907-3076957	H1-hESC	embryonic stem cell:	embryo
36	chr4:3076259-3076309	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:3076557-3076607	MCF-7	breast:	n/a
38	chr4:3075893-3075943	HL-60	blood:	n/a
39	chr4:3076271-3076321	U87	brain:	n/a
40	chr4:3076907-3076957	NB4	blood:	n/a
41	chr4:3075893-3075943	K562	blood:	n/a
42	chr4:3076334-3076384	AoSMC	blood vessel:	n/a
43	chr4:3076907-3076957	AG10803	skin:	n/a
44	chr4:3076418-3076468	MCF-7	breast:	n/a
45	chr4:3076557-3076607	AoSMC	blood vessel:	n/a
46	chr4:3076259-3076309	NT2-D1	testis:	n/a
47	chr4:3076418-3076468	RPTEC	kidney:	n/a
48	chr4:3076271-3076321	HRPEpiC	eye:	n/a
49	chr4:3076907-3076957	HepG2	liver:	n/a
50	chr4:3076271-3076321	K562	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3076522..3079094-chr4:3136211..3138250,2	MCF-7	breast:
2	chr4:3076425..3077993-chr4:3087345..3089440,2	MCF-7	breast:
3	chr4:3076858..3078560-chr4:3090552..3093969,4	MCF-7	breast:
4	chr4:2935808..2938115-chr4:3076304..3078834,3	K562	blood:
5	chr4:3076735..3079040-chr4:3100560..3102807,2	K562	blood:
6	chr4:3076969..3077469-chr6:36853503..36854013,2	K562	blood:
7	chr17:16556241..16557924-chr4:3075466..3077603,2	MCF-7	breast:
8	chr4:3075973..3077923-chr4:3128614..3130547,2	MCF-7	breast:
9	chr4:3070733..3073155-chr4:3073597..3075559,3	K562	blood:
10	chr4:3068906..3071079-chr4:3073190..3075687,2	MCF-7	breast:
11	chr4:2468745..2470693-chr4:3075535..3077781,3	K562	blood:
12	chr4:2262471..2264332-chr4:3074788..3077577,2	MCF-7	breast:
13	chr4:3074016..3078502-chr4:3111809..3117809,7	MCF-7	breast:
14	chr4:3076560..3079556-chr4:3107118..3109310,3	MCF-7	breast:
15	chr4:3074885..3077461-chr4:3292207..3294882,2	MCF-7	breast:
16	chr4:2964356..2966158-chr4:3074837..3077632,2	K562	blood:
17	chr4:2935808..2937729-chr4:3076912..3078834,2	K562	blood:
18	chr4:3075638..3077191-chr4:3246487..3249347,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOP14-2	chr4:3076153-3076241	NONHSAT094847
2	lnc-NOP14-2	chr4:3076153-3076241	XLOC_003858

No data

Variant related genes	Relation type
HTT-AS	TF binding region
HTT	TF binding region
HTT-AS	CpG island
HTT	CpG island
ENSG00000087269	chromatin interactions
ENSG00000197566	chromatin interactions
ENSG00000125388	chromatin interactions
ENSG00000264765	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000197386	chromatin interactions
ENSG00000123933	chromatin interactions
ENSG00000188981	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000198663	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000063978	chromatin interactions

Extended variants
information (count: 113 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187490343	chr4:3074701-3074702	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs190418122	chr4:3074758-3074759	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs35655630	chr4:3074764-3074765	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs370050166	chr4:3074781-3074782	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs762855	chr4:3074795-3074796	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs117140887	chr4:3074826-3074827	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs58848332	chr4:3074831-3074832	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs188051804	chr4:3074952-3074953	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs9996199	chr4:3074965-3074966	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs115583116	chr4:3074993-3074994	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs570708202	chr4:3074996-3074997	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs539636569	chr4:3074998-3074999	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs556355543	chr4:3075092-3075093	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs76466316	chr4:3075103-3075104	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs547381510	chr4:3075136-3075137	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs544290719	chr4:3075150-3075151	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs535915512	chr4:3075185-3075186	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs555494747	chr4:3075193-3075194	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs192838728	chr4:3075249-3075250	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs184373234	chr4:3075264-3075265	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs558025663	chr4:3075277-3075278	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs577856773	chr4:3075281-3075282	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs543617606	chr4:3075284-3075285	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs187843805	chr4:3075296-3075297	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs114562181	chr4:3075312-3075313	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs143861513	chr4:3075394-3075395	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs541873881	chr4:3075498-3075499	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs368830030	chr4:3075503-3075504	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs527277424	chr4:3075507-3075508	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs115117610	chr4:3075541-3075542	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs564384178	chr4:3075563-3075564	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs533218574	chr4:3075583-3075584	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs28431418	chr4:3075588-3075589	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs398982	chr4:3075662-3075663	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs2857935	chr4:3075691-3075692	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs549435903	chr4:3075708-3075709	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs433069	chr4:3075731-3075732	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs28616835	chr4:3075736-3075737	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs398691	chr4:3075753-3075754	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs28441493	chr4:3075783-3075784	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs373236283	chr4:3075784-3075785	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs376165809	chr4:3075794-3075795	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs386868	chr4:3075858-3075859	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs2798300	chr4:3075861-3075862	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs35657303	chr4:3075890-3075891	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs398128	chr4:3075891-3075892	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs11933387	chr4:3075928-3075929	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs34514515	chr4:3075981-3075982	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs149624523	chr4:3076028-3076029	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs574508305	chr4:3076035-3076036	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3048200-3075200	Weak transcription	Right Atrium	heart
2	chr4:3049600-3074800	Weak transcription	Lung	lung
3	chr4:3058200-3075200	Weak transcription	Psoas Muscle	Psoas
4	chr4:3060800-3074800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr4:3061000-3074800	Weak transcription	Spleen	Spleen
6	chr4:3061600-3075000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:3062200-3075000	Weak transcription	Adipose Nuclei	Adipose
8	chr4:3063800-3075200	Weak transcription	Right Ventricle	heart
9	chr4:3064400-3075000	Weak transcription	Fetal Intestine Small	intestine
10	chr4:3064800-3074800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr4:3064800-3075000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr4:3068800-3075000	Weak transcription	Primary B cells from cord blood	blood
13	chr4:3069600-3075200	Weak transcription	Brain Hippocampus Middle	brain
14	chr4:3071800-3075000	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:3072200-3075200	Enhancers	Liver	Liver
16	chr4:3072800-3074800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:3072800-3075200	Weak transcription	Gastric	stomach
18	chr4:3073000-3074800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:3073000-3074800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr4:3073200-3075000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:3073400-3075000	Weak transcription	Osteobl	bone
22	chr4:3073600-3074800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr4:3073600-3075000	Weak transcription	HSMM	muscle
24	chr4:3073600-3075200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr4:3073600-3075400	Weak transcription	HSMMtube	muscle
26	chr4:3073800-3074800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr4:3073800-3075000	Weak transcription	NH-A	brain
28	chr4:3073800-3075200	Weak transcription	NHDF-Ad	bronchial
29	chr4:3074000-3074800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:3074000-3074800	Weak transcription	Placenta	Placenta
31	chr4:3074000-3075000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:3074000-3075200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:3074000-3075200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr4:3074000-3075200	Enhancers	Pancreas	Pancrea
35	chr4:3074000-3075200	Weak transcription	NHLF	lung
36	chr4:3074200-3075000	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr4:3074600-3074800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr4:3074600-3074800	Enhancers	HepG2	liver
39	chr4:3074600-3075000	Enhancers	Stomach Smooth Muscle	stomach
40	chr4:3074600-3075200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr4:3074800-3075000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
42	chr4:3074800-3075000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:3074800-3075000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr4:3074800-3075000	Enhancers	Primary hematopoietic stem cells	blood
45	chr4:3074800-3075000	Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr4:3074800-3075000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:3074800-3075000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:3074800-3075000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:3074800-3075000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:3074800-3075000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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