Variant report

Variant	nsv528739
Chromosome Location	chr7:105318058-105346117
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:492)
CpG islands
(count:1039)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105343735-105344077	HepG2	liver:	n/a	n/a
2	ATF1	chr7:105319466-105319927	K562	blood:	n/a	n/a
3	ATF1	chr7:105331443-105331479	K562	blood:	n/a	n/a
4	ATF2	chr7:105332118-105332651	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:105328413-105328668	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:105318282-105318534	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:105319330-105319861	K562	blood:	n/a	n/a
8	BHLHE40	chr7:105321037-105321434	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:105332198-105332736	GM12878	blood:	n/a	n/a
10	BRCA1	chr7:105332084-105332491	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr7:105331855-105331918	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:105323174-105323470	A549	lung:	n/a	chr7:105323316-105323327
13	CEBPB	chr7:105320221-105320342	K562	blood:	n/a	chr7:105320283-105320294
14	CEBPB	chr7:105321103-105321314	K562	blood:	n/a	chr7:105321178-105321189
15	CEBPB	chr7:105323154-105323474	HepG2	liver:	n/a	chr7:105323316-105323327
16	CEBPB	chr7:105340015-105340392	HepG2	liver:	n/a	chr7:105340189-105340200
17	CEBPB	chr7:105323140-105323484	Hela-S3	cervix:	n/a	chr7:105323316-105323327
18	CEBPB	chr7:105321004-105321268	HepG2	liver:	n/a	chr7:105321178-105321189
19	CEBPB	chr7:105339533-105339747	A549	lung:	n/a	chr7:105339635-105339646
20	CEBPB	chr7:105320153-105320314	HepG2	liver:	n/a	chr7:105320283-105320294
21	CEBPB	chr7:105339587-105339786	H1-hESC	embryonic stem cell:	n/a	chr7:105339635-105339646
22	CEBPB	chr7:105339430-105339766	K562	blood:	n/a	chr7:105339635-105339646
23	CEBPB	chr7:105321060-105321278	H1-hESC	embryonic stem cell:	n/a	chr7:105321178-105321189
24	CEBPB	chr7:105320905-105321443	MCF-7	breast:	n/a	chr7:105321178-105321189
25	CEBPB	chr7:105343761-105343922	HepG2	liver:	n/a	chr7:105343864-105343875
26	CEBPB	chr7:105339550-105339800	HepG2	liver:	n/a	chr7:105339635-105339646
27	CEBPB	chr7:105339531-105339678	HepG2	liver:	n/a	chr7:105339635-105339646
28	CEBPB	chr7:105332264-105332637	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:105323161-105323431	H1-hESC	embryonic stem cell:	n/a	chr7:105323316-105323327
30	CEBPB	chr7:105332154-105332599	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:105332324-105332454	K562	blood:	n/a	n/a
32	CEBPB	chr7:105323149-105323485	IMR90	lung:	n/a	chr7:105323316-105323327
33	CEBPB	chr7:105339449-105339742	A549	lung:	n/a	chr7:105339635-105339646
34	CEBPB	chr7:105321010-105321358	HepG2	liver:	n/a	chr7:105321178-105321189
35	CEBPB	chr7:105339458-105339821	K562	blood:	n/a	chr7:105339635-105339646
36	CEBPB	chr7:105323154-105323468	K562	blood:	n/a	chr7:105323316-105323327
37	CEBPB	chr7:105339563-105339796	Hela-S3	cervix:	n/a	chr7:105339635-105339646
38	CEBPB	chr7:105340094-105340374	H1-hESC	embryonic stem cell:	n/a	chr7:105340189-105340200
39	CEBPB	chr7:105343706-105344024	HepG2	liver:	n/a	chr7:105343864-105343875
40	CEBPB	chr7:105332148-105332664	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:105320992-105321399	HepG2	liver:	n/a	chr7:105321178-105321189
42	CEBPB	chr7:105339528-105339696	K562	blood:	n/a	chr7:105339635-105339646
43	CEBPB	chr7:105320985-105321372	HepG2	liver:	n/a	chr7:105321178-105321189
44	CEBPB	chr7:105320836-105321521	MCF-7	breast:	n/a	chr7:105321178-105321189
45	CEBPD	chr7:105321056-105321262	HepG2	liver:	n/a	n/a
46	CEBPD	chr7:105320960-105321291	HepG2	liver:	n/a	n/a
47	CHD1	chr7:105331624-105332105	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr7:105323242-105323248	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr7:105331511-105331701	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr7:105332231-105332678	Hela-S3	cervix:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105319558-105319608	GM06990	blood:	n/a
2	chr7:105337735-105337785	LNCaP	prostate:	n/a
3	chr7:105319558-105319608	GM06990	blood:	n/a
4	chr7:105337735-105337785	LNCaP	prostate:	n/a
5	chr7:105331310-105331360	MCF10A-Er-Src	breast:	n/a
6	chr7:105339648-105339698	ECC-1	luminal epithelium:	n/a
7	chr7:105319615-105319665	HCM	heart:	n/a
8	chr7:105319558-105319608	HAEpiC	amniotic membrane:	n/a
9	chr7:105332220-105332270	MCF10A-Er-Src	breast:	n/a
10	chr7:105331310-105331360	HUVEC	blood vessel:	n/a
11	chr7:105320151-105320201	NHBE	bronchial:	n/a
12	chr7:105320396-105320446	NHDF-neo	bronchial:	n/a
13	chr7:105319558-105319608	MCF-7	breast:	n/a
14	chr7:105332311-105332361	PrEC	prostate:	n/a
15	chr7:105320396-105320446	HCT-116	colon:	n/a
16	chr7:105337724-105337774	HEEpiC	esophagus:	n/a
17	chr7:105332311-105332361	A549	lung:	n/a
18	chr7:105332279-105332329	ovcar-3	ovarian:	n/a
19	chr7:105332279-105332329	BE2_C	brain:	n/a
20	chr7:105320396-105320446	HEK293	kidney:	embryo
21	chr7:105332311-105332361	SAEC	small airway:	n/a
22	chr7:105331648-105331698	Hepatocyte	liver:	n/a
23	chr7:105319679-105319729	HCM	heart:	n/a
24	chr7:105332220-105332270	Hela-S3	cervix:	n/a
25	chr7:105339648-105339698	IMR90	lung:	fetal
26	chr7:105319615-105319665	BE2_C	brain:	n/a
27	chr7:105319615-105319665	ProgFib	skin:	n/a
28	chr7:105320396-105320446	ProgFib	skin:	n/a
29	chr7:105319819-105319869	U87	brain:	n/a
30	chr7:105319615-105319665	RPTEC	kidney:	n/a
31	chr7:105319679-105319729	SAEC	small airway:	n/a
32	chr7:105339648-105339698	SK-N-SH_RA	brain:	n/a
33	chr7:105337724-105337774	HAEpiC	amniotic membrane:	n/a
34	chr7:105319558-105319608	T-47D	breast:	n/a
35	chr7:105332220-105332270	ProgFib	skin:	n/a
36	chr7:105319486-105319536	AG10803	skin:	n/a
37	chr7:105319558-105319608	HIPEpiC	eye:	n/a
38	chr7:105320151-105320201	NHDF-neo	bronchial:	n/a
39	chr7:105319615-105319665	ECC-1	luminal epithelium:	n/a
40	chr7:105319819-105319869	ECC-1	luminal epithelium:	n/a
41	chr7:105331310-105331360	Hela-S3	cervix:	n/a
42	chr7:105320396-105320446	Caco-2	colon:	n/a
43	chr7:105319486-105319536	HRCEpiC	kidney:	n/a
44	chr7:105332279-105332329	NT2-D1	testis:	n/a
45	chr7:105331310-105331360	RPTEC	kidney:	n/a
46	chr7:105320151-105320201	GM12878	blood:	n/a
47	chr7:105319437-105319487	GM06990	blood:	n/a
48	chr7:105332311-105332361	HUVEC	blood vessel:	n/a
49	chr7:105319486-105319536	H1-hESC	embryonic stem cell:	embryo
50	chr7:105332311-105332361	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:105314687..105317812-chr7:105319787..105322529,3	K562	blood:
2	chr7:105320146..105323057-chr7:105327793..105330127,2	MCF-7	breast:
3	chr7:105336972..105340159-chr7:105343977..105346880,3	K562	blood:
4	chr7:105333638..105336603-chr7:105339254..105341591,2	K562	blood:
5	chr7:105297335..105297912-chr7:105341024..105341843,2	MCF-7	breast:
6	chr7:105292178..105293451-chr7:105341016..105341968,4	MCF-7	breast:
7	chr7:105310890..105312874-chr7:105328926..105331441,2	MCF-7	breast:
8	chr7:105292553..105293251-chr7:105341024..105341528,2	MCF-7	breast:
9	chr7:105326154..105327962-chr7:105331686..105333648,2	MCF-7	breast:
10	chr7:105319464..105322936-chr7:105325535..105328908,4	K562	blood:
11	chr7:105295635..105297294-chr7:105321836..105324476,2	K562	blood:
12	chr7:105304113..105306346-chr7:105332549..105334059,2	MCF-7	breast:
13	chr7:105336963..105338472-chr7:105345380..105347416,2	K562	blood:
14	chr7:105320146..105323057-chr7:105327793..105330127,2	MCF-7	breast:
15	chr7:105333638..105336603-chr7:105339254..105341591,2	K562	blood:
16	chr7:105336963..105338472-chr7:105345380..105347416,2	K562	blood:
17	chr7:105336972..105340159-chr7:105343977..105346880,3	K562	blood:
18	chr7:105312890..105314402-chr7:105328440..105330609,2	MCF-7	breast:

No data

Variant related genes	Relation type
ATXN7L1	TF binding region
ATXN7L1	CpG island
ENSG00000146776	chromatin interactions

Extended variants
information (count: 1134 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1134 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6942982	chr7:105318058-105318059	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs532759838	chr7:105318072-105318073	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs140288431	chr7:105318116-105318117	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs559921585	chr7:105318132-105318133	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs369641819	chr7:105318140-105318141	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs117879115	chr7:105318141-105318142	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs535246565	chr7:105318216-105318217	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs145390905	chr7:105318229-105318230	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs79564649	chr7:105318232-105318233	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs531404341	chr7:105318351-105318352	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs551420175	chr7:105318376-105318377	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs79799619	chr7:105318377-105318378	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs533912737	chr7:105318512-105318513	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs554111153	chr7:105318513-105318514	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs74423463	chr7:105318539-105318540	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs79298890	chr7:105318542-105318543	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs372206564	chr7:105318546-105318547	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs567585870	chr7:105318547-105318548	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs536934297	chr7:105318556-105318557	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs200110805	chr7:105318558-105318559	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs556941111	chr7:105318560-105318561	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs6947622	chr7:105318589-105318590	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375566978	chr7:105318593-105318594	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs539254004	chr7:105318651-105318652	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs116114806	chr7:105318658-105318659	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs577647825	chr7:105318686-105318687	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs539988032	chr7:105318720-105318721	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs374455151	chr7:105318754-105318755	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs560085415	chr7:105318761-105318762	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs573349960	chr7:105318827-105318828	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs141060519	chr7:105318845-105318846	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs150264484	chr7:105318859-105318860	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs562450196	chr7:105318876-105318877	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs531367936	chr7:105318891-105318892	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs540473749	chr7:105318894-105318895	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs185101638	chr7:105318898-105318899	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527767373	chr7:105318984-105318985	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs547612816	chr7:105319074-105319075	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs114647177	chr7:105319079-105319080	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536649435	chr7:105319089-105319090	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs550463832	chr7:105319095-105319096	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570386032	chr7:105319099-105319100	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539371276	chr7:105319111-105319112	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs138950942	chr7:105319117-105319118	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs112096347	chr7:105319118-105319119	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs561918045	chr7:105319122-105319123	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs533883793	chr7:105319131-105319132	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs142953147	chr7:105319146-105319147	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs573259617	chr7:105319188-105319189	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs542230221	chr7:105319203-105319204	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1241 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105280800-105319400	Weak transcription	Aorta	Aorta
2	chr7:105290400-105321800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:105302000-105319200	Weak transcription	Osteobl	bone
4	chr7:105302200-105319200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:105305600-105318400	Weak transcription	NHLF	lung
6	chr7:105306200-105319200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:105306200-105319400	Weak transcription	HSMMtube	muscle
8	chr7:105306200-105325200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:105306400-105319000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr7:105307800-105319200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:105311800-105319200	Weak transcription	HSMM	muscle
12	chr7:105313000-105318600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr7:105313200-105318200	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr7:105313400-105318200	Enhancers	Primary T cells from cord blood	blood
15	chr7:105314200-105320600	Weak transcription	HepG2	liver
16	chr7:105314400-105318200	Weak transcription	HUVEC	blood vessel
17	chr7:105314400-105318600	Weak transcription	Brain Hippocampus Middle	brain
18	chr7:105314400-105318800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr7:105314400-105319000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:105314600-105318200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:105314600-105318600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr7:105314600-105318600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:105314600-105318800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr7:105314600-105318800	Weak transcription	Small Intestine	intestine
25	chr7:105314600-105319400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:105315200-105318600	Weak transcription	Esophagus	oesophagus
27	chr7:105315200-105318800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:105315200-105318800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:105315200-105319400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:105315200-105320600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr7:105315200-105324200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:105315400-105318800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr7:105315800-105319400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr7:105315800-105319400	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr7:105315800-105319400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr7:105315800-105319800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr7:105315800-105320000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr7:105315800-105323200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr7:105316000-105318200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr7:105316000-105320000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr7:105316200-105318200	Enhancers	Adipose Nuclei	Adipose
42	chr7:105316200-105319800	Flanking Active TSS	Fetal Thymus	thymus
43	chr7:105316400-105318600	Enhancers	Brain Substantia Nigra	brain
44	chr7:105316400-105318600	Genic enhancers	Stomach Smooth Muscle	stomach
45	chr7:105316400-105318800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:105316400-105318800	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr7:105316400-105319200	Enhancers	Placenta	Placenta
48	chr7:105316400-105319200	Enhancers	Left Ventricle	heart
49	chr7:105316400-105319200	Enhancers	Lung	lung
50	chr7:105316400-105319200	Enhancers	Pancreas	Pancrea

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