Variant report

Variant	nsv538945
Chromosome Location	chr7:71715105-71794258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:166)
CpG islands
(count:245)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:166 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:71748535-71748603	K562	blood:	n/a	n/a
2	ATF2	chr7:71730568-71730921	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:71730494-71730993	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr7:71730295-71730461	K562	blood:	n/a	n/a
5	CEBPB	chr7:71721022-71721087	HepG2	liver:	n/a	chr7:71721064-71721077
6	CEBPB	chr7:71723021-71723355	HepG2	liver:	n/a	chr7:71723174-71723185
7	CEBPB	chr7:71757503-71757552	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:71723120-71723245	K562	blood:	n/a	chr7:71723174-71723185
9	CEBPB	chr7:71729286-71729372	HepG2	liver:	n/a	chr7:71729324-71729335
10	CEBPB	chr7:71752628-71752861	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:71723036-71723330	IMR90	lung:	n/a	chr7:71723174-71723185
12	CEBPB	chr7:71723050-71723323	A549	lung:	n/a	chr7:71723174-71723185
13	CHD2	chr7:71722105-71722245	K562	blood:	n/a	n/a
14	CTCF	chr7:71743584-71743805	K562	blood:	n/a	n/a
15	CTCF	chr7:71793302-71793397	GM20000	blood:	n/a	n/a
16	CTCF	chr7:71743620-71743770	K562	blood:	n/a	n/a
17	CTCF	chr7:71743607-71743811	K562	blood:	n/a	n/a
18	CTCF	chr7:71743683-71743758	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:71743635-71743787	LNCaP	prostate:	n/a	n/a
20	CTCF	chr7:71743564-71743842	K562	blood:	n/a	n/a
21	CTCF	chr7:71757145-71757475	K562	blood:	n/a	n/a
22	CTCF	chr7:71743673-71743779	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:71757176-71757389	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr7:71757201-71757385	K562	blood:	n/a	n/a
25	CTCF	chr7:71743651-71743794	K562	blood:	n/a	n/a
26	CTCF	chr7:71743583-71743846	K562	blood:	n/a	n/a
27	CTCF	chr7:71757240-71757390	HepG2	liver:	n/a	n/a
28	CTCF	chr7:71757129-71757479	K562	blood:	n/a	n/a
29	CTCF	chr7:71724171-71724188	GM13976	blood:	n/a	n/a
30	CTCF	chr7:71757081-71757531	HepG2	liver:	n/a	n/a
31	CTCF	chr7:71743653-71743785	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:71757220-71757370	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr7:71743651-71743781	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:71757122-71757466	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:71743600-71743750	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:71783680-71783830	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr7:71787236-71787266	GM20000	blood:	n/a	n/a
38	CTCF	chr7:71780518-71780619	GM10248	blood:	n/a	n/a
39	CTCF	chr7:71743660-71743810	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr7:71743690-71743750	LNCaP	prostate:	n/a	n/a
41	CTCF	chr7:71766720-71766870	HepG2	liver:	n/a	n/a
42	CTCF	chr7:71757188-71757402	HepG2	liver:	n/a	n/a
43	CTCF	chr7:71757062-71757428	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:71757278-71757315	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr7:71743632-71743795	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:71757154-71757437	K562	blood:	n/a	n/a
47	CTCF	chr7:71734401-71734427	Lung_OC	lung:	n/a	n/a
48	CTCF	chr7:71757020-71757472	K562	blood:	n/a	n/a
49	CTCF	chr7:71757239-71757361	HepG2	liver:	n/a	n/a
50	CTCF	chr7:71732549-71732587	MCF-7	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71747028-71747078	PFSK-1	brain:	n/a
2	chr7:71747028-71747078	PFSK-1	brain:	n/a
3	chr7:71747632-71747682	Hepatocyte	liver:	n/a
4	chr7:71744787-71744837	HNPCEpiC	eye:	n/a
5	chr7:71744787-71744837	ECC-1	luminal epithelium:	n/a
6	chr7:71747632-71747682	NT2-D1	testis:	n/a
7	chr7:71744787-71744837	HMEC	breast:	n/a
8	chr7:71747028-71747078	ECC-1	luminal epithelium:	n/a
9	chr7:71747632-71747682	NB4	blood:	n/a
10	chr7:71747028-71747078	Hela-S3	cervix:	n/a
11	chr7:71729065-71729115	LNCaP	prostate:	n/a
12	chr7:71747028-71747078	ProgFib	skin:	n/a
13	chr7:71729065-71729115	AG09309	skin:	n/a
14	chr7:71747028-71747078	GM12892	blood:	n/a
15	chr7:71744787-71744837	RPTEC	kidney:	n/a
16	chr7:71747632-71747682	H1-hESC	embryonic stem cell:	embryo
17	chr7:71729065-71729115	SK-N-MC	brain:	n/a
18	chr7:71747028-71747078	NB4	blood:	n/a
19	chr7:71747028-71747078	SK-N-SH	brain:	n/a
20	chr7:71744787-71744837	CMK	blood:	n/a
21	chr7:71747028-71747078	SAEC	small airway:	n/a
22	chr7:71744787-71744837	NHBE	bronchial:	n/a
23	chr7:71744787-71744837	BJ	skin:	n/a
24	chr7:71747028-71747078	MCF-7	breast:	n/a
25	chr7:71747632-71747682	ovcar-3	ovarian:	n/a
26	chr7:71744787-71744837	K562	blood:	n/a
27	chr7:71747028-71747078	SKMC	muscle:	n/a
28	chr7:71747632-71747682	RPTEC	kidney:	n/a
29	chr7:71744787-71744837	ProgFib	skin:	n/a
30	chr7:71747028-71747078	H1-hESC	embryonic stem cell:	embryo
31	chr7:71729065-71729115	HMEC	breast:	n/a
32	chr7:71729065-71729115	HAEpiC	amniotic membrane:	n/a
33	chr7:71747632-71747682	AG10803	skin:	n/a
34	chr7:71729065-71729115	NHBE	bronchial:	n/a
35	chr7:71744787-71744837	HL-60	blood:	n/a
36	chr7:71747028-71747078	HCM	heart:	n/a
37	chr7:71729065-71729115	AG04449	skin:	fetal
38	chr7:71744787-71744837	HRCEpiC	kidney:	n/a
39	chr7:71729065-71729115	SAEC	small airway:	n/a
40	chr7:71747632-71747682	IMR90	lung:	fetal
41	chr7:71747632-71747682	AG04450	lung:	fetal
42	chr7:71744787-71744837	GM12878	blood:	n/a
43	chr7:71744787-71744837	A549	lung:	n/a
44	chr7:71729065-71729115	Jurkat	blood:	n/a
45	chr7:71744787-71744837	HIPEpiC	eye:	n/a
46	chr7:71747632-71747682	SK-N-SH_RA	brain:	n/a
47	chr7:71747028-71747078	HAEpiC	amniotic membrane:	n/a
48	chr7:71747028-71747078	HRCEpiC	kidney:	n/a
49	chr7:71744787-71744837	SK-N-SH	brain:	n/a
50	chr7:71747632-71747682	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:71765415..71767059-chr7:71769100..71770926,2	K562	blood:
2	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
3	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
4	chr7:71789897..71791400-chr7:71794472..71797210,2	K562	blood:
5	chr7:71765415..71767059-chr7:71769100..71770926,2	K562	blood:
6	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:
7	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
8	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
9	chr7:71730756..71733410-chr7:71737455..71739236,2	K562	blood:
10	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:
11	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:
12	chr7:71730756..71733410-chr7:71737455..71739236,2	K562	blood:
13	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:

No data

Variant related genes	Relation type
CALN1	TF binding region
CALN1	CpG island

Extended variants
information (count: 3756 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3756 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17503801	chr7:71715202-71715203	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182636189	chr7:71715208-71715209	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142228481	chr7:71715214-71715215	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559907077	chr7:71715219-71715220	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62464863	chr7:71715263-71715264	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs371438239	chr7:71715370-71715371	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561463272	chr7:71715379-71715380	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531982971	chr7:71715434-71715435	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139064594	chr7:71715451-71715452	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112107255	chr7:71715468-71715469	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571743088	chr7:71715498-71715499	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373781217	chr7:71715508-71715509	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6963187	chr7:71715532-71715533	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs77518222	chr7:71715548-71715549	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143997114	chr7:71715550-71715551	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565944029	chr7:71715556-71715557	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553768615	chr7:71715582-71715583	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539332229	chr7:71715586-71715587	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35564490	chr7:71715588-71715589	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10253308	chr7:71715594-71715595	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs555284424	chr7:71715612-71715613	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573487961	chr7:71715618-71715619	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532169	chr7:71715628-71715629	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs555960692	chr7:71715637-71715638	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146440877	chr7:71715653-71715654	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112575984	chr7:71715682-71715683	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553678353	chr7:71715705-71715706	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571993350	chr7:71715714-71715715	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188005642	chr7:71715716-71715717	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561601662	chr7:71715727-71715728	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111916116	chr7:71715771-71715772	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142137625	chr7:71715785-71715786	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151192674	chr7:71715800-71715801	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565489508	chr7:71715801-71715802	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74721693	chr7:71715805-71715806	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs36024687	chr7:71715848-71715849	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs117007641	chr7:71715873-71715874	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572206492	chr7:71715916-71715917	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368633803	chr7:71715923-71715924	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140335577	chr7:71715950-71715951	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190947896	chr7:71715955-71715956	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372038692	chr7:71715993-71715994	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555897573	chr7:71715995-71715996	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372039975	chr7:71716058-71716059	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542337488	chr7:71716077-71716078	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145286117	chr7:71716092-71716093	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183593903	chr7:71716136-71716137	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536759	chr7:71716138-71716139	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs542671636	chr7:71716139-71716140	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13239080	chr7:71716159-71716160	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71709000-71731000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:71712600-71717800	ZNF genes & repeats	Fetal Thymus	thymus
3	chr7:71712800-71717200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:71714200-71716800	Strong transcription	Thymus	Thymus
5	chr7:71714800-71716800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:71715400-71716400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:71716800-71722000	Weak transcription	Thymus	Thymus
8	chr7:71717200-71719000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:71717800-71722000	Strong transcription	Fetal Thymus	thymus
10	chr7:71718000-71720200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:71719000-71720000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:71720000-71722200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:71720200-71730200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:71721400-71734600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr7:71721600-71722000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr7:71721800-71722000	Enhancers	Adipose Nuclei	Adipose
17	chr7:71721800-71727200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:71722000-71722400	ZNF genes & repeats	Fetal Thymus	thymus
19	chr7:71722000-71722400	Genic enhancers	Thymus	Thymus
20	chr7:71722200-71722600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:71722200-71722800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
22	chr7:71722200-71723200	Weak transcription	Adipose Nuclei	Adipose
23	chr7:71722400-71723600	Strong transcription	Fetal Thymus	thymus
24	chr7:71722400-71725000	Weak transcription	Thymus	Thymus
25	chr7:71722600-71723000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:71722800-71735200	Weak transcription	Primary hematopoietic stem cells	blood
27	chr7:71723000-71729800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:71723200-71723600	Enhancers	Adipose Nuclei	Adipose
29	chr7:71723600-71724800	Weak transcription	Fetal Thymus	thymus
30	chr7:71724800-71726600	Genic enhancers	Fetal Thymus	thymus
31	chr7:71725000-71725400	Genic enhancers	Thymus	Thymus
32	chr7:71725400-71726000	Enhancers	Thymus	Thymus
33	chr7:71726000-71727200	Genic enhancers	Thymus	Thymus
34	chr7:71726600-71729000	Strong transcription	Fetal Thymus	thymus
35	chr7:71727200-71728200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:71727200-71728400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:71727200-71728600	Weak transcription	Thymus	Thymus
38	chr7:71727400-71728200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:71727400-71728400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr7:71727600-71728200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:71727800-71728000	Enhancers	H9 Cell Line	embryonic stem cell
42	chr7:71727800-71728200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:71727800-71728200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:71728000-71728200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr7:71728000-71728200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:71728000-71731400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr7:71728200-71730000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr7:71728200-71730000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr7:71728200-71730000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr7:71728200-71730200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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