Variant report

Variant	nsv970482
Chromosome Location	chr7:56094574-56104957
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:639)
CpG islands
(count:244)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:56101409-56101825	K562	blood:	n/a	n/a
2	ARID3A	chr7:56096670-56097705	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:56101293-56102015	HepG2	liver:	n/a	n/a
4	ATF1	chr7:56101279-56101974	K562	blood:	n/a	n/a
5	ATF2	chr7:56101478-56102040	GM12878	blood:	n/a	n/a
6	ATF3	chr7:56101366-56101516	K562	blood:	n/a	n/a
7	ATF3	chr7:56101200-56101626	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr7:56101272-56101718	K562	blood:	n/a	n/a
9	ATF3	chr7:56101305-56101568	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:56101424-56101459	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr7:56101337-56101514	GM12878	blood:	n/a	n/a
12	BCL3	chr7:56101354-56101930	A549	lung:	n/a	n/a
13	BCL3	chr7:56101582-56102201	A549	lung:	n/a	n/a
14	BCLAF1	chr7:56101243-56102240	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:56101448-56102188	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:56101396-56101901	K562	blood:	n/a	n/a
17	BRCA1	chr7:56101608-56101783	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:56101667-56101947	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:56101712-56102171	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr7:56101296-56102148	Hela-S3	cervix:	n/a	n/a
21	CCNT2	chr7:56101589-56102119	K562	blood:	n/a	chr7:56101911-56101920
22	CEBPB	chr7:56101247-56101845	A549	lung:	n/a	chr7:56101424-56101435
23	CEBPB	chr7:56101321-56101558	HepG2	liver:	n/a	chr7:56101424-56101435
24	CEBPB	chr7:56101201-56101835	MCF-7	breast:	n/a	chr7:56101424-56101435
25	CEBPB	chr7:56101246-56101611	K562	blood:	n/a	chr7:56101424-56101435
26	CEBPB	chr7:56101276-56101653	HepG2	liver:	n/a	chr7:56101424-56101435
27	CEBPB	chr7:56096790-56097711	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:56101191-56101854	MCF-7	breast:	n/a	chr7:56101424-56101435
29	CEBPB	chr7:56101244-56102206	H1-hESC	embryonic stem cell:	n/a	chr7:56101424-56101435
30	CEBPB	chr7:56101227-56102110	HCT-116	colon:	n/a	chr7:56101424-56101435
31	CEBPB	chr7:56101193-56101727	ECC-1	luminal epithelium:	n/a	chr7:56101424-56101435
32	CEBPB	chr7:56101095-56102304	HCT-116	colon:	n/a	chr7:56101424-56101435
33	CEBPB	chr7:56101249-56101675	ECC-1	luminal epithelium:	n/a	chr7:56101424-56101435
34	CEBPB	chr7:56099334-56099931	HepG2	liver:	n/a	chr7:56099457-56099468
35	CEBPB	chr7:56097303-56097570	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:56101231-56102263	K562	blood:	n/a	chr7:56101424-56101435
37	CEBPB	chr7:56101231-56102158	IMR90	lung:	n/a	chr7:56101424-56101435
38	CEBPB	chr7:56101215-56101694	A549	lung:	n/a	chr7:56101424-56101435
39	CEBPB	chr7:56101226-56102067	A549	lung:	n/a	chr7:56101424-56101435
40	CEBPB	chr7:56099368-56099503	HepG2	liver:	n/a	chr7:56099457-56099468
41	CEBPB	chr7:56101244-56102229	HepG2	liver:	n/a	chr7:56101424-56101435
42	CEBPB	chr7:56101154-56101906	K562	blood:	n/a	chr7:56101424-56101435
43	CEBPB	chr7:56101235-56102206	HepG2	liver:	n/a	chr7:56101424-56101435
44	CEBPB	chr7:56101219-56102288	Hela-S3	cervix:	n/a	chr7:56101424-56101435
45	CEBPD	chr7:56101691-56102028	HepG2	liver:	n/a	n/a
46	CEBPD	chr7:56101281-56101584	HepG2	liver:	n/a	chr7:56101425-56101436 chr7:56101425-56101436
47	CEBPD	chr7:56101304-56101992	K562	blood:	n/a	chr7:56101425-56101436 chr7:56101425-56101436
48	CEBPD	chr7:56101597-56102148	HepG2	liver:	n/a	n/a
49	CEBPD	chr7:56101276-56102076	K562	blood:	n/a	chr7:56101425-56101436 chr7:56101425-56101436
50	CEBPZ	chr7:56101393-56101666	HepG2	liver:	n/a	chr7:56101425-56101436

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56101644-56101694	PANC-1	pancreas:	n/a
2	chr7:56101905-56101955	AG09319	gingival:	n/a
3	chr7:56101905-56101955	PANC-1	pancreas:	n/a
4	chr7:56101905-56101955	RPTEC	kidney:	n/a
5	chr7:56101998-56102048	MCF-7	breast:	n/a
6	chr7:56101998-56102048	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:56101998-56102048	IMR90	lung:	fetal
8	chr7:56101644-56101694	LNCaP	prostate:	n/a
9	chr7:56101644-56101694	HCM	heart:	n/a
10	chr7:56101644-56101694	GM12878	blood:	n/a
11	chr7:56101998-56102048	NHDF-neo	bronchial:	n/a
12	chr7:56101644-56101694	Hepatocyte	liver:	n/a
13	chr7:56101644-56101694	Jurkat	blood:	n/a
14	chr7:56101905-56101955	HCF	heart:	n/a
15	chr7:56101905-56101955	GM12878	blood:	n/a
16	chr7:56101644-56101694	AG04449	skin:	fetal
17	chr7:56097042-56097092	HRCEpiC	kidney:	n/a
18	chr7:56097042-56097092	HepG2	liver:	n/a
19	chr7:56101905-56101955	SK-N-SH_RA	brain:	n/a
20	chr7:56101905-56101955	K562	blood:	n/a
21	chr7:56101998-56102048	HepG2	liver:	n/a
22	chr7:56101905-56101955	GM12891	blood:	n/a
23	chr7:56101644-56101694	T-47D	breast:	n/a
24	chr7:56101644-56101694	ProgFib	skin:	n/a
25	chr7:56101905-56101955	LNCaP	prostate:	n/a
26	chr7:56101905-56101955	GM19239	blood:	n/a
27	chr7:56101905-56101955	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:56101998-56102048	GM12891	blood:	n/a
29	chr7:56097042-56097092	SK-N-SH_RA	brain:	n/a
30	chr7:56101998-56102048	HMEC	breast:	n/a
31	chr7:56097042-56097092	PANC-1	pancreas:	n/a
32	chr7:56101998-56102048	HCF	heart:	n/a
33	chr7:56101998-56102048	HNPCEpiC	eye:	n/a
34	chr7:56101905-56101955	MCF-7	breast:	n/a
35	chr7:56097042-56097092	ECC-1	luminal epithelium:	n/a
36	chr7:56101644-56101694	K562	blood:	n/a
37	chr7:56101905-56101955	HIPEpiC	eye:	n/a
38	chr7:56101644-56101694	HCF	heart:	n/a
39	chr7:56101644-56101694	ovcar-3	ovarian:	n/a
40	chr7:56101998-56102048	ovcar-3	ovarian:	n/a
41	chr7:56097042-56097092	HEK293	kidney:	embryo
42	chr7:56101644-56101694	SKMC	muscle:	n/a
43	chr7:56097042-56097092	HAEpiC	amniotic membrane:	n/a
44	chr7:56101905-56101955	HCT-116	colon:	n/a
45	chr7:56101905-56101955	HCM	heart:	n/a
46	chr7:56101644-56101694	IMR90	lung:	fetal
47	chr7:56101644-56101694	SK-N-SH	brain:	n/a
48	chr7:56097042-56097092	LNCaP	prostate:	n/a
49	chr7:56097042-56097092	HL-60	blood:	n/a
50	chr7:56097042-56097092	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:56095036..56098595-chr7:56117042..56120763,4	MCF-7	breast:
2	chr7:56092875..56095055-chr7:56099185..56100786,2	MCF-7	breast:
3	chr7:56092875..56095055-chr7:56099185..56100786,2	MCF-7	breast:
4	chr7:56093650..56095156-chr7:56099679..56101422,2	K562	blood:
5	chr7:56030925..56032633-chr7:56101899..56104592,2	K562	blood:
6	chr7:56095133..56098395-chr7:56099647..56103046,4	MCF-7	breast:
7	chr7:56095555..56097443-chr7:56098499..56101480,2	MCF-7	breast:
8	chr7:56100362..56103278-chr7:56116659..56119395,4	K562	blood:
9	chr7:56093650..56095156-chr7:56099679..56101422,2	K562	blood:
10	chr7:56100095..56103801-chr7:56117179..56120388,5	K562	blood:
11	chr7:56094252..56096504-chr7:56118049..56120713,2	MCF-7	breast:
12	chr7:56100273..56103332-chr7:56118092..56121325,5	MCF-7	breast:
13	chr7:56095555..56097443-chr7:56098499..56101480,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHKG1-2	chr7:56100827-56101187	NONHSAT120719
2	lnc-PHKG1-2	chr7:56101654-56101864	NONHSAT120719

No data

Variant related genes	Relation type
PSPH	TF binding region
PSPH	CpG island
ENSG00000146733	chromatin interactions
ENSG00000146731	chromatin interactions
ENSG00000146729	chromatin interactions

Extended variants
information (count: 417 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548010497	chr7:56094578-56094579	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs561821191	chr7:56094602-56094603	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs370299415	chr7:56094606-56094607	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs10259981	chr7:56094621-56094622	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs143751995	chr7:56094622-56094623	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs34319969	chr7:56094626-56094627	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs527726553	chr7:56094670-56094671	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552157627	chr7:56094678-56094679	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148131470	chr7:56094711-56094712	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553450191	chr7:56094758-56094759	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538571155	chr7:56094773-56094774	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs12113229	chr7:56094785-56094786	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs147984357	chr7:56094791-56094792	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568985206	chr7:56094839-56094840	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs199729188	chr7:56094842-56094843	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs554743544	chr7:56094847-56094848	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs113675476	chr7:56094853-56094854	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs35888472	chr7:56094903-56094904	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs564149675	chr7:56094904-56094905	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs67145608	chr7:56094905-56094906	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs533721844	chr7:56094909-56094910	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11322718	chr7:56094921-56094922	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189698235	chr7:56095085-56095086	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs146139044	chr7:56095108-56095109	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs75695345	chr7:56095113-56095114	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556705229	chr7:56095118-56095119	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs574976289	chr7:56095140-56095141	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541918413	chr7:56095141-56095142	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs181222710	chr7:56095151-56095152	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527791174	chr7:56095156-56095157	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs369528717	chr7:56095157-56095158	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545756326	chr7:56095167-56095168	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547008143	chr7:56095187-56095188	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139142927	chr7:56095194-56095195	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566788431	chr7:56095214-56095215	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532414255	chr7:56095254-56095255	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs142345747	chr7:56095293-56095294	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs35102510	chr7:56095381-56095382	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185973482	chr7:56095437-56095438	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs114425389	chr7:56095463-56095464	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548405713	chr7:56095466-56095467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs566530293	chr7:56095476-56095477	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs150545768	chr7:56095492-56095493	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs139505563	chr7:56095516-56095517	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs570390744	chr7:56095572-56095573	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs11445778	chr7:56095580-56095581	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538523670	chr7:56095589-56095590	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs372954930	chr7:56095607-56095608	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368957114	chr7:56095619-56095620	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs6962857	chr7:56095640-56095641	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Esophageal squamous carcinoma	21637470	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
small cell lung cancer	20016488	CNVD
Lung adenocarcinoma	21935476	CNVD
Cancer	20164919	CNVD
Gastric cancer	17229543	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56049200-56101600	Weak transcription	Small Intestine	intestine
2	chr7:56060600-56099600	Weak transcription	HUVEC	blood vessel
3	chr7:56063400-56096800	Weak transcription	NH-A	brain
4	chr7:56063600-56101000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:56063600-56101200	Weak transcription	NHLF	lung
6	chr7:56064400-56101400	Weak transcription	Gastric	stomach
7	chr7:56065000-56101400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr7:56065000-56101400	Weak transcription	Colonic Mucosa	Colon
9	chr7:56065400-56101400	Weak transcription	Fetal Brain Male	brain
10	chr7:56065800-56095800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr7:56067200-56101400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr7:56067400-56100800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr7:56067800-56099600	Weak transcription	K562	blood
14	chr7:56068200-56101200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr7:56075400-56101400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:56077800-56099600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr7:56077800-56100600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:56078200-56099800	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr7:56078200-56101200	Weak transcription	Colon Smooth Muscle	Colon
20	chr7:56081600-56097000	Weak transcription	Placenta	Placenta
21	chr7:56082200-56101200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr7:56082600-56101200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:56083600-56096800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr7:56086000-56100200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr7:56086400-56098400	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr7:56086800-56101200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr7:56087400-56101400	Weak transcription	Brain Germinal Matrix	brain
28	chr7:56087600-56101200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr7:56087600-56101400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr7:56087800-56097200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr7:56087800-56101400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:56088000-56095000	Weak transcription	Brain Cingulate Gyrus	brain
33	chr7:56088000-56101400	Weak transcription	Esophagus	oesophagus
34	chr7:56088000-56101600	Weak transcription	Lung	lung
35	chr7:56088600-56101600	Weak transcription	Spleen	Spleen
36	chr7:56088800-56095800	Weak transcription	Fetal Brain Female	brain
37	chr7:56088800-56096000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:56088800-56096600	Weak transcription	Thymus	Thymus
39	chr7:56088800-56096800	Weak transcription	Brain Hippocampus Middle	brain
40	chr7:56088800-56101400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:56088800-56101400	Weak transcription	Aorta	Aorta
42	chr7:56088800-56101400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr7:56089000-56095000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr7:56089000-56095000	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr7:56089000-56095200	Weak transcription	Fetal Muscle Trunk	muscle
46	chr7:56089000-56095600	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr7:56089000-56095600	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr7:56089000-56095800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:56089000-56096200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:56089000-56096200	Weak transcription	Fetal Thymus	thymus

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