Variant report

Variant	esv32852
Chromosome Location	chr7:6745984-6746850
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6746508-6747088	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:6746582-6746922	K562	blood:	n/a	n/a
3	ATF3	chr7:6746344-6746860	A549	lung:	n/a	chr7:6746443-6746452
4	ATF3	chr7:6746455-6746774	K562	blood:	n/a	n/a
5	ATF3	chr7:6746338-6746843	A549	lung:	n/a	chr7:6746443-6746452
6	BCLAF1	chr7:6746183-6746931	GM12878	blood:	n/a	chr7:6746574-6746587 chr7:6746324-6746333 chr7:6746577-6746590 chr7:6746318-6746331 chr7:6746657-6746670
7	BHLHE40	chr7:6745621-6745991	K562	blood:	n/a	n/a
8	BHLHE40	chr7:6746435-6747008	K562	blood:	n/a	n/a
9	BHLHE40	chr7:6746430-6746875	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:6746299-6746907	HepG2	liver:	n/a	n/a
11	BRCA1	chr7:6745893-6746041	HepG2	liver:	n/a	n/a
12	BRCA1	chr7:6746551-6747053	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr7:6746365-6746883	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr7:6746338-6747069	GM12878	blood:	n/a	n/a
15	CBX3	chr7:6745362-6746144	K562	blood:	n/a	n/a
16	CBX3	chr7:6746385-6747206	K562	blood:	n/a	n/a
17	CBX3	chr7:6746593-6747092	K562	blood:	n/a	n/a
18	CCNT2	chr7:6746165-6746778	K562	blood:	n/a	n/a
19	CHD1	chr7:6746278-6746741	GM12878	blood:	n/a	n/a
20	CHD2	chr7:6745927-6746701	HepG2	liver:	n/a	n/a
21	CHD2	chr7:6746096-6747076	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr7:6745687-6746766	K562	blood:	n/a	n/a
23	CHD2	chr7:6745687-6747056	GM12878	blood:	n/a	n/a
24	CHD2	chr7:6746279-6746724	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr7:6745917-6746759	A549	lung:	n/a	chr7:6746010-6746023
26	CREB1	chr7:6746457-6746641	A549	lung:	n/a	n/a
27	CTCF	chr7:6746631-6746712	GM12878	blood:	n/a	n/a
28	CTCF	chr7:6746420-6746570	GM12875	blood:	n/a	n/a
29	CTCF	chr7:6746574-6746602	Fibrobl	skin:	n/a	n/a
30	CTCF	chr7:6746650-6746867	K562	blood:	n/a	n/a
31	CUX1	chr7:6746604-6746983	K562	blood:	n/a	n/a
32	E2F4	chr7:6746484-6746922	MCF10A-Er-Src	breast:	n/a	chr7:6746622-6746631 chr7:6746590-6746599 chr7:6746662-6746672
33	E2F6	chr7:6745848-6746758	K562	blood:	n/a	chr7:6746445-6746454 chr7:6746622-6746631 chr7:6746590-6746599 chr7:6746662-6746672 chr7:6746469-6746484
34	E2F6	chr7:6745570-6746947	K562	blood:	n/a	chr7:6746445-6746454 chr7:6746622-6746631 chr7:6746590-6746599 chr7:6746662-6746672 chr7:6746469-6746484
35	E2F6	chr7:6746321-6747010	A549	lung:	n/a	chr7:6746445-6746454 chr7:6746622-6746631 chr7:6746590-6746599 chr7:6746662-6746672 chr7:6746469-6746484
36	E2F6	chr7:6746458-6746781	K562	blood:	n/a	chr7:6746622-6746631 chr7:6746590-6746599 chr7:6746662-6746672 chr7:6746469-6746484
37	E2F6	chr7:6746349-6746844	H1-hESC	embryonic stem cell:	n/a	chr7:6746445-6746454 chr7:6746622-6746631 chr7:6746590-6746599 chr7:6746662-6746672 chr7:6746469-6746484
38	EBF1	chr7:6746339-6746678	GM12878	blood:	n/a	n/a
39	EBF1	chr7:6746462-6747018	GM12878	blood:	n/a	chr7:6746699-6746710
40	EGR1	chr7:6745830-6745988	GM12878	blood:	n/a	chr7:6745897-6745910 chr7:6745894-6745908 chr7:6745897-6745910 chr7:6745898-6745907 chr7:6745898-6745909
41	EGR1	chr7:6745451-6746045	K562	blood:	n/a	chr7:6745897-6745910 chr7:6745894-6745908 chr7:6745897-6745910 chr7:6745898-6745907 chr7:6745898-6745909
42	EGR1	chr7:6745487-6746021	K562	blood:	n/a	chr7:6745897-6745910 chr7:6745894-6745908 chr7:6745897-6745910 chr7:6745898-6745907 chr7:6745898-6745909
43	ELF1	chr7:6746202-6746847	K562	blood:	n/a	chr7:6746336-6746345 chr7:6746274-6746286 chr7:6746636-6746649 chr7:6746577-6746589
44	ELF1	chr7:6746406-6747008	A549	lung:	n/a	chr7:6746636-6746649 chr7:6746577-6746589
45	ELF1	chr7:6746279-6747099	MCF-7	breast:	n/a	chr7:6746336-6746345 chr7:6746636-6746649 chr7:6746577-6746589
46	ELF1	chr7:6746334-6746822	HepG2	liver:	n/a	chr7:6746336-6746345 chr7:6746636-6746649 chr7:6746577-6746589
47	ELF1	chr7:6746429-6746772	A549	lung:	n/a	chr7:6746636-6746649 chr7:6746577-6746589
48	ELF1	chr7:6746335-6747091	MCF-7	breast:	n/a	chr7:6746336-6746345 chr7:6746636-6746649 chr7:6746577-6746589
49	ELF1	chr7:6746269-6746854	HepG2	liver:	n/a	chr7:6746336-6746345 chr7:6746274-6746286 chr7:6746636-6746649 chr7:6746577-6746589
50	ELF1	chr7:6746312-6747019	K562	blood:	n/a	chr7:6746336-6746345 chr7:6746636-6746649 chr7:6746577-6746589

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6746688-6746738	HAEpiC	amniotic membrane:	n/a
2	chr7:6746688-6746738	HAEpiC	amniotic membrane:	n/a
3	chr7:6746715-6746765	HIPEpiC	eye:	n/a
4	chr7:6746208-6746258	U87	brain:	n/a
5	chr7:6746599-6746649	AG04449	skin:	fetal
6	chr7:6746837-6746887	AoSMC	blood vessel:	n/a
7	chr7:6746837-6746887	GM12892	blood:	n/a
8	chr7:6746580-6746630	HCF	heart:	n/a
9	chr7:6746208-6746258	NHBE	bronchial:	n/a
10	chr7:6746837-6746887	NB4	blood:	n/a
11	chr7:6746837-6746887	HEK293	kidney:	embryo
12	chr7:6746837-6746887	GM19239	blood:	n/a
13	chr7:6745969-6746019	A549	lung:	n/a
14	chr7:6746799-6746849	A549	lung:	n/a
15	chr7:6746208-6746258	HCT-116	colon:	n/a
16	chr7:6746688-6746738	HRE	kidney:	n/a
17	chr7:6746558-6746608	MCF10A-Er-Src	breast:	n/a
18	chr7:6746208-6746258	Caco-2	colon:	n/a
19	chr7:6746580-6746630	NB4	blood:	n/a
20	chr7:6746715-6746765	HAEpiC	amniotic membrane:	n/a
21	chr7:6746688-6746738	SKMC	muscle:	n/a
22	chr7:6746799-6746849	U87	brain:	n/a
23	chr7:6746650-6746700	HEEpiC	esophagus:	n/a
24	chr7:6746650-6746700	CMK	blood:	n/a
25	chr7:6746605-6746655	PANC-1	pancreas:	n/a
26	chr7:6746650-6746700	PFSK-1	brain:	n/a
27	chr7:6746837-6746887	HCPEpiC	choroid plexus:	n/a
28	chr7:6746688-6746738	HRPEpiC	eye:	n/a
29	chr7:6746599-6746649	MCF-7	breast:	n/a
30	chr7:6746580-6746630	ECC-1	luminal epithelium:	n/a
31	chr7:6745969-6746019	AG04449	skin:	fetal
32	chr7:6746599-6746649	SKMC	muscle:	n/a
33	chr7:6746208-6746258	PFSK-1	brain:	n/a
34	chr7:6746605-6746655	HRPEpiC	eye:	n/a
35	chr7:6746208-6746258	AG09319	gingival:	n/a
36	chr7:6746599-6746649	NB4	blood:	n/a
37	chr7:6746558-6746608	SK-N-MC	brain:	n/a
38	chr7:6746605-6746655	AoSMC	blood vessel:	n/a
39	chr7:6746715-6746765	T-47D	breast:	n/a
40	chr7:6746605-6746655	HAEpiC	amniotic membrane:	n/a
41	chr7:6746799-6746849	SKMC	muscle:	n/a
42	chr7:6746605-6746655	GM19239	blood:	n/a
43	chr7:6746650-6746700	SAEC	small airway:	n/a
44	chr7:6746580-6746630	NH-A	brain:	n/a
45	chr7:6745969-6746019	HEEpiC	esophagus:	n/a
46	chr7:6746799-6746849	Jurkat	blood:	n/a
47	chr7:6746558-6746608	GM06990	blood:	n/a
48	chr7:6745969-6746019	SK-N-SH_RA	brain:	n/a
49	chr7:6746837-6746887	MCF10A-Er-Src	breast:	n/a
50	chr7:6746688-6746738	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6676193..6679067-chr7:6744810..6746794,4	K562	blood:
2	chr7:6675962..6678642-chr7:6744432..6748032,4	MCF-7	breast:
3	chr7:6681243..6682856-chr7:6746246..6748831,2	K562	blood:
4	chr7:6746161..6747688-chr7:6768318..6771249,2	MCF-7	breast:
5	chr7:6700299..6703221-chr7:6744305..6746051,2	MCF-7	breast:
6	chr7:6744871..6747873-chr7:6767656..6771321,4	K562	blood:
7	chr12:7052777..7053414-chr7:6746050..6746651,2	Hela-S3	cervix:
8	chr7:6745463..6748475-chr7:6767656..6769994,3	K562	blood:
9	chr17:59484738..59486572-chr7:6745021..6746847,2	MCF-7	breast:
10	chr7:6628194..6631157-chr7:6744707..6746398,2	MCF-7	breast:
11	chr7:6745224..6747442-chr7:6767898..6770902,3	MCF-7	breast:
12	chr7:6729955..6731866-chr7:6746781..6748682,2	MCF-7	breast:
13	chr2:179315296..179317868-chr7:6745682..6748008,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-1	chr7:6746704-6748672	NONHSAT119061

Variant related genes	Relation type
ZNF12	TF binding region
PMS2CL	TF binding region
ZNF12	CpG island
PMS2CL	CpG island
ENSG00000111678	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000180228	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000204311	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000265245	chromatin interactions
ENSG00000232581	chromatin interactions

Extended variants
information (count: 42 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149743149	chr7:6745992-6745993	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs543298227	chr7:6746002-6746003	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs555312134	chr7:6746021-6746022	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs73331250	chr7:6746063-6746064	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540807993	chr7:6746076-6746077	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs13239758	chr7:6746098-6746099	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs577258555	chr7:6746108-6746109	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs544424817	chr7:6746113-6746114	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs562852666	chr7:6746117-6746118	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs530042907	chr7:6746160-6746161	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs55869731	chr7:6746205-6746206	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540993340	chr7:6746210-6746211	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs144461280	chr7:6746237-6746238	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs546760529	chr7:6746258-6746259	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs571395309	chr7:6746275-6746276	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs113323830	chr7:6746281-6746282	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs538724762	chr7:6746318-6746319	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs550408336	chr7:6746341-6746342	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs559286889	chr7:6746443-6746444	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs115110901	chr7:6746462-6746463	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs6952107	chr7:6746479-6746480	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs554633187	chr7:6746512-6746513	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs573562531	chr7:6746518-6746519	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs534264203	chr7:6746537-6746538	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs559102575	chr7:6746546-6746547	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs577367109	chr7:6746554-6746555	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs113306985	chr7:6746556-6746557	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs139423352	chr7:6746574-6746575	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs574461960	chr7:6746580-6746581	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs541802062	chr7:6746589-6746590	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs560152415	chr7:6746593-6746594	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs192947684	chr7:6746608-6746609	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs545084285	chr7:6746615-6746616	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs565046168	chr7:6746628-6746629	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs532218159	chr7:6746633-6746634	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs145146031	chr7:6746677-6746678	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs386709842	chr7:6746736-6746737	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs9639027	chr7:6746738-6746739	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs544831788	chr7:6746793-6746794	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
40	rs368520856	chr7:6746808-6746809	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
41	rs147577390	chr7:6746826-6746827	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
42	rs370000763	chr7:6746845-6746846	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6744400-6746000	Flanking Active TSS	Primary T cells from cord blood	blood
2	chr7:6744400-6746200	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr7:6744600-6747200	Active TSS	Right Ventricle	heart
4	chr7:6744800-6746000	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:6744800-6746800	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr7:6744800-6747200	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr7:6745000-6746000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:6745000-6746000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr7:6745000-6746200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr7:6745000-6746800	Active TSS	Stomach Mucosa	stomach
11	chr7:6745000-6746800	Active TSS	GM12878-XiMat	blood
12	chr7:6745000-6746800	Active TSS	HMEC	breast
13	chr7:6745000-6747000	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr7:6745000-6747000	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr7:6745000-6747000	Active TSS	Fetal Intestine Large	intestine
16	chr7:6745000-6747000	Active TSS	Stomach Smooth Muscle	stomach
17	chr7:6745000-6747200	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr7:6745000-6747200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:6745000-6747200	Active TSS	Colonic Mucosa	Colon
20	chr7:6745000-6747200	Active TSS	Fetal Kidney	kidney
21	chr7:6745000-6747200	Active TSS	Ovary	ovary
22	chr7:6745000-6747200	Active TSS	Right Atrium	heart
23	chr7:6745000-6747400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:6745000-6747600	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr7:6745200-6746000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
26	chr7:6745200-6746000	Flanking Active TSS	Fetal Muscle Leg	muscle
27	chr7:6745200-6746200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr7:6745200-6746200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr7:6745200-6746200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:6745200-6746800	Active TSS	Rectal Smooth Muscle	rectum
31	chr7:6745200-6746800	Active TSS	Hela-S3	cervix
32	chr7:6745200-6746800	Active TSS	HSMM	muscle
33	chr7:6745200-6746800	Active TSS	K562	blood
34	chr7:6745200-6747000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:6745200-6747000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:6745200-6747000	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr7:6745200-6747000	Active TSS	A549	lung
38	chr7:6745200-6747200	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr7:6745200-6747200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:6745200-6747200	Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr7:6745200-6747200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr7:6745200-6747200	Active TSS	Left Ventricle	heart
43	chr7:6745200-6747200	Active TSS	Psoas Muscle	Psoas
44	chr7:6745200-6747200	Active TSS	NHDF-Ad	bronchial
45	chr7:6745200-6747400	Flanking Active TSS	Primary B cells from cord blood	blood
46	chr7:6745200-6747400	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr7:6745200-6747400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr7:6745400-6746000	Flanking Active TSS	Primary B cells from peripheral blood	blood
49	chr7:6745400-6746000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr7:6745400-6746000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood

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