Variant report

Variant	esv3406922
Chromosome Location	chr5:79949421-79951969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:592)
CpG islands
(count:671)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:592 , 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	ATF2	chr5:79950660-79951227	GM12878	blood:	n/a	n/a
2	BCL3	chr5:79950396-79951073	GM12878	blood:	n/a	chr5:79950484-79950497 chr5:79950818-79950831 chr5:79950514-79950527
3	BCLAF1	chr5:79950418-79950889	GM12878	blood:	n/a	chr5:79950484-79950497 chr5:79950818-79950831 chr5:79950514-79950527
4	BHLHE40	chr5:79949407-79949795	K562	blood:	n/a	n/a
5	BHLHE40	chr5:79950439-79950717	K562	blood:	n/a	n/a
6	BHLHE40	chr5:79950441-79951336	GM12878	blood:	n/a	n/a
7	BRCA1	chr5:79950582-79950705	HepG2	liver:	n/a	n/a
8	CCNT2	chr5:79949448-79951322	K562	blood:	n/a	chr5:79950385-79950394 chr5:79950824-79950833 chr5:79950816-79950825
9	CEBPB	chr5:79950093-79951524	Hela-S3	cervix:	n/a	n/a
10	CEBPD	chr5:79950465-79950841	HepG2	liver:	n/a	n/a
11	CHD1	chr5:79950528-79951284	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr5:79950461-79951543	GM12878	blood:	n/a	n/a
13	CHD2	chr5:79950503-79951071	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr5:79950459-79950695	HepG2	liver:	n/a	n/a
15	CHD2	chr5:79950215-79951152	GM12878	blood:	n/a	chr5:79950383-79950393
16	CHD2	chr5:79950129-79951513	Hela-S3	cervix:	n/a	chr5:79950383-79950393
17	CHD2	chr5:79950502-79951063	K562	blood:	n/a	n/a
18	CREB1	chr5:79950157-79951197	HepG2	liver:	n/a	n/a
19	CTCF	chr5:79950520-79950670	HCT-116	colon:	n/a	n/a
20	CTCF	chr5:79950480-79950770	SAEC	small airway:	n/a	n/a
21	CTCF	chr5:79950718-79950722	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr5:79950700-79950850	A549	lung:	n/a	n/a
23	CTCF	chr5:79950566-79950809	A549	lung:	n/a	n/a
24	CTCF	chr5:79950520-79950670	HRE	kidney:	n/a	n/a
25	CTCF	chr5:79950556-79951047	K562	blood:	n/a	n/a
26	CTCF	chr5:79950580-79950730	GM12874	blood:	n/a	n/a
27	CTCF	chr5:79950640-79950790	NHEK	skin:	n/a	n/a
28	CTCF	chr5:79950493-79950534	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr5:79950580-79950730	GM12865	blood:	n/a	n/a
30	CTCF	chr5:79950661-79950781	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr5:79950541-79950808	GM19239	blood:	n/a	n/a
32	CTCF	chr5:79950620-79950770	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr5:79950676-79950729	Gliobla	brain:	n/a	n/a
34	CTCF	chr5:79950520-79950790	GM06990	blood:	n/a	n/a
35	CTCF	chr5:79950680-79950830	GM12866	blood:	n/a	n/a
36	CTCF	chr5:79950289-79950358	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:79950640-79950790	GM12867	blood:	n/a	n/a
38	CTCF	chr5:79950223-79950362	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr5:79950562-79950568	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:79950580-79950730	K562	blood:	n/a	n/a
41	CTCF	chr5:79950627-79950791	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:79950588-79950814	GM19240	blood:	n/a	n/a
43	CTCF	chr5:79950660-79950810	HCM	heart:	n/a	n/a
44	CTCF	chr5:79950559-79950811	Fibrobl	skin:	n/a	n/a
45	CTCF	chr5:79950640-79950790	GM12865	blood:	n/a	n/a
46	CTCF	chr5:79950548-79950554	GM13976	blood:	n/a	n/a
47	CTCF	chr5:79950620-79950770	HMF	breast:	n/a	n/a
48	CTCF	chr5:79950740-79950890	BE2_C	brain:	n/a	n/a
49	CTCF	chr5:79950640-79950790	GM12864	blood:	n/a	n/a
50	CTCF	chr5:79950600-79950750	SAEC	small airway:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79950976-79951026	GM12891	blood:	n/a
2	chr5:79950934-79950984	AG09319	gingival:	n/a
3	chr5:79950956-79951006	HepG2	liver:	n/a
4	chr5:79950508-79950558	HEK293	kidney:	embryo
5	chr5:79950815-79950865	PrEC	prostate:	n/a
6	chr5:79950075-79950125	CMK	blood:	n/a
7	chr5:79950508-79950558	GM12878	blood:	n/a
8	chr5:79950383-79950433	HL-60	blood:	n/a
9	chr5:79950120-79950170	NHBE	bronchial:	n/a
10	chr5:79950383-79950433	GM06990	blood:	n/a
11	chr5:79950956-79951006	Hepatocyte	liver:	n/a
12	chr5:79950075-79950125	HepG2	liver:	n/a
13	chr5:79951536-79951586	GM19239	blood:	n/a
14	chr5:79950075-79950125	PrEC	prostate:	n/a
15	chr5:79950075-79950125	AG10803	skin:	n/a
16	chr5:79950934-79950984	HRE	kidney:	n/a
17	chr5:79950501-79950551	PFSK-1	brain:	n/a
18	chr5:79950508-79950558	PFSK-1	brain:	n/a
19	chr5:79950611-79950661	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:79950976-79951026	PFSK-1	brain:	n/a
21	chr5:79950075-79950125	GM12892	blood:	n/a
22	chr5:79950815-79950865	HIPEpiC	eye:	n/a
23	chr5:79950934-79950984	AG04450	lung:	fetal
24	chr5:79950815-79950865	HMEC	breast:	n/a
25	chr5:79950976-79951026	AG10803	skin:	n/a
26	chr5:79950815-79950865	SKMC	muscle:	n/a
27	chr5:79950934-79950984	AG09309	skin:	n/a
28	chr5:79951536-79951586	HCM	heart:	n/a
29	chr5:79950976-79951026	HEK293	kidney:	embryo
30	chr5:79950383-79950433	HCT-116	colon:	n/a
31	chr5:79950956-79951006	HRE	kidney:	n/a
32	chr5:79950501-79950551	GM12878	blood:	n/a
33	chr5:79950976-79951026	PANC-1	pancreas:	n/a
34	chr5:79950383-79950433	ECC-1	luminal epithelium:	n/a
35	chr5:79950976-79951026	Hepatocyte	liver:	n/a
36	chr5:79950934-79950984	RPTEC	kidney:	n/a
37	chr5:79950934-79950984	HCPEpiC	choroid plexus:	n/a
38	chr5:79951536-79951586	AG10803	skin:	n/a
39	chr5:79950934-79950984	GM19239	blood:	n/a
40	chr5:79950956-79951006	HIPEpiC	eye:	n/a
41	chr5:79951536-79951586	IMR90	lung:	fetal
42	chr5:79950501-79950551	ProgFib	skin:	n/a
43	chr5:79950075-79950125	NB4	blood:	n/a
44	chr5:79950075-79950125	HCPEpiC	choroid plexus:	n/a
45	chr5:79950508-79950558	AG10803	skin:	n/a
46	chr5:79950120-79950170	SK-N-SH	brain:	n/a
47	chr5:79950815-79950865	GM12878	blood:	n/a
48	chr5:79950383-79950433	SK-N-SH	brain:	n/a
49	chr5:79950956-79951006	HUVEC	blood vessel:	n/a
50	chr5:79950508-79950558	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:85955785..85956525-chr5:79950777..79951467,2	NB4	blood:
2	chr5:79930876..79933489-chr5:79951399..79953527,2	K562	blood:
3	chr5:79918045..79920951-chr5:79949482..79951097,2	MCF-7	breast:
4	chr5:79950548..79951545-chr7:5569740..5570286,2	Hela-S3	cervix:
5	chr5:79950686..79951228-chr6:105850772..105851601,2	NB4	blood:
6	chr5:79781713..79786255-chr5:79948613..79954295,12	MCF-7	breast:
7	chr5:79950077..79950796-chr6:26199069..26200065,2	NB4	blood:
8	chr5:79950108..79951095-chr6:27860383..27860953,2	Hela-S3	cervix:
9	chr5:79950349..79951063-chrX:23685473..23686093,2	Hela-S3	cervix:
10	chr5:79702114..79706204-chr5:79947823..79953616,8	MCF-7	breast:
11	chr5:79782822..79786705-chr5:79948261..79952248,11	MCF-7	breast:
12	chr12:105379925..105380593-chr5:79950231..79951164,2	HCT-116	colon:
13	chr5:79773551..79776073-chr5:79951057..79953387,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM151B-3	chr5:79950971-79951398	NONHSAT102418

No data

Variant related genes	Relation type
MTRNR2L2	TF binding region
DHFR	TF binding region
MSH3	TF binding region
MTRNR2L2	CpG island
DHFR	CpG island
MSH3	CpG island
ENSG00000075624	chromatin interactions
ENSG00000249042	chromatin interactions
ENSG00000151131	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000251221	chromatin interactions
ENSG00000039319	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000085377	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000152380	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000123131	chromatin interactions

Extended variants
information (count: 143 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3822706	chr5:79949432-79949433	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs572617388	chr5:79949444-79949445	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs1677626	chr5:79949445-79949446	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs371303766	chr5:79949500-79949501	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs1478834	chr5:79949575-79949576	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs532287141	chr5:79949595-79949596	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs1478835	chr5:79949600-79949601	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs183332077	chr5:79949618-79949619	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs528941007	chr5:79949639-79949640	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs371219726	chr5:79949658-79949659	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs565636780	chr5:79949691-79949692	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs534709026	chr5:79949694-79949695	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs557857251	chr5:79949702-79949703	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs571040322	chr5:79949716-79949717	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs539629126	chr5:79949720-79949721	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs556862773	chr5:79949724-79949725	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs188843682	chr5:79949745-79949746	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs6151593	chr5:79949803-79949804	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs144847410	chr5:79949807-79949808	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs201745474	chr5:79949873-79949874	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs555346066	chr5:79949880-79949881	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs572081813	chr5:79949887-79949888	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs541144933	chr5:79949936-79949937	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs562836282	chr5:79949948-79949949	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs533184784	chr5:79949953-79949954	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs191745317	chr5:79949965-79949966	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs6151594	chr5:79949966-79949967	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs184211767	chr5:79949970-79949971	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs549250404	chr5:79950033-79950034	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs559411604	chr5:79950045-79950046	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs70991108	chr5:79950163-79950164	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs200822257	chr5:79950179-79950180	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs368073490	chr5:79950186-79950187	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs531484931	chr5:79950220-79950221	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs371588943	chr5:79950242-79950243	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs61736208	chr5:79950257-79950258	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs374922165	chr5:79950288-79950289	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs199586723	chr5:79950298-79950299	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs368748249	chr5:79950322-79950323	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs76613872	chr5:79950375-79950376	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs151182735	chr5:79950390-79950391	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
42	rs551488807	chr5:79950394-79950395	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
43	rs4326123	chr5:79950400-79950401	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs10168	chr5:79950403-79950404	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs4386720	chr5:79950439-79950440	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs540066105	chr5:79950458-79950459	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs550118288	chr5:79950470-79950471	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs569869247	chr5:79950481-79950482	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs535768731	chr5:79950489-79950490	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs555608568	chr5:79950490-79950491	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	17409424	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79919600-79949800	Weak transcription	Pancreas	Pancrea
2	chr5:79923600-79949800	Weak transcription	Brain Hippocampus Middle	brain
3	chr5:79924200-79949800	Weak transcription	Left Ventricle	heart
4	chr5:79925600-79949600	Weak transcription	HSMMtube	muscle
5	chr5:79929000-79949800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr5:79934200-79949600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr5:79937000-79950000	Weak transcription	Ovary	ovary
8	chr5:79937800-79949800	Weak transcription	Lung	lung
9	chr5:79937800-79949800	Weak transcription	Psoas Muscle	Psoas
10	chr5:79944800-79949600	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr5:79945600-79949800	Weak transcription	Brain Substantia Nigra	brain
12	chr5:79948600-79949600	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
13	chr5:79948600-79950200	Transcr. at gene 5' and 3'	Dnd41	blood
14	chr5:79948600-79951200	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr5:79948600-79952000	Active TSS	GM12878-XiMat	blood
16	chr5:79948800-79949600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr5:79948800-79949800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr5:79948800-79951400	Active TSS	Fetal Intestine Large	intestine
19	chr5:79949000-79949600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:79949000-79949600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:79949000-79949600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr5:79949000-79949600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr5:79949000-79949600	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr5:79949000-79949600	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr5:79949000-79949600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr5:79949000-79949600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr5:79949000-79949600	Enhancers	Adipose Nuclei	Adipose
28	chr5:79949000-79949600	Flanking Active TSS	Hela-S3	cervix
29	chr5:79949000-79949600	Flanking Active TSS	HMEC	breast
30	chr5:79949000-79949600	Flanking Active TSS	K562	blood
31	chr5:79949000-79949800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr5:79949000-79949800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
33	chr5:79949000-79949800	Flanking Active TSS	NHEK	skin
34	chr5:79949000-79950000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr5:79949000-79950000	Enhancers	Spleen	Spleen
36	chr5:79949000-79950200	Flanking Active TSS	Primary T cells from cord blood	blood
37	chr5:79949000-79950200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:79949000-79950200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr5:79949000-79950200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:79949000-79950200	Flanking Active TSS	Liver	Liver
41	chr5:79949000-79950200	Flanking Active TSS	Duodenum Mucosa	Duodenum
42	chr5:79949000-79950200	Flanking Active TSS	HUVEC	blood vessel
43	chr5:79949000-79951200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr5:79949000-79951200	Active TSS	Stomach Mucosa	stomach
45	chr5:79949000-79951400	Active TSS	H1 Cell Line	embryonic stem cell
46	chr5:79949000-79951400	Active TSS	H9 Cell Line	embryonic stem cell
47	chr5:79949000-79951400	Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr5:79949000-79951400	Active TSS	Fetal Intestine Small	intestine
49	chr5:79949000-79951600	Active TSS	A549	lung
50	chr5:79949200-79949600	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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