Variant report

Variant	nsv888695
Chromosome Location	chr7:87328502-87430669
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:123)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:87427172-87427417	K562	blood:	n/a	n/a
2	ARID3A	chr7:87344877-87345209	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:87427122-87427505	HepG2	liver:	n/a	n/a
4	BACH1	chr7:87413791-87414062	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr7:87426712-87427072	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:87427248-87427485	K562	blood:	n/a	n/a
7	BHLHE40	chr7:87427223-87427414	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:87418945-87418977	A549	lung:	n/a	n/a
9	CEBPB	chr7:87331709-87332044	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:87364431-87364547	A549	lung:	n/a	n/a
11	CEBPB	chr7:87425705-87425986	IMR90	lung:	n/a	chr7:87425839-87425850
12	CEBPB	chr7:87344845-87345227	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:87404033-87404360	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:87425774-87425968	A549	lung:	n/a	chr7:87425839-87425850
15	CEBPB	chr7:87364726-87365098	MCF-7	breast:	n/a	n/a
16	CEBPB	chr7:87364675-87365040	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:87425722-87425992	HepG2	liver:	n/a	chr7:87425839-87425850
18	CEBPB	chr7:87364663-87365101	MCF-7	breast:	n/a	n/a
19	CEBPB	chr7:87368675-87368893	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:87344904-87345088	HepG2	liver:	n/a	n/a
21	CHD1	chr7:87369019-87369088	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr7:87427331-87427436	GM12878	blood:	n/a	n/a
23	CHD2	chr7:87376699-87376953	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr7:87427260-87427410	RPTEC	kidney:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
25	CTCF	chr7:87362425-87362551	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr7:87427240-87427390	HRE	kidney:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
27	CTCF	chr7:87413800-87413950	BJ	skin:	n/a	n/a
28	CTCF	chr7:87427007-87427581	HCT-116	colon:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
29	CTCF	chr7:87413860-87414010	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr7:87427148-87427437	ECC-1	luminal epithelium:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
31	CTCF	chr7:87376700-87376850	GM12873	blood:	n/a	n/a
32	CTCF	chr7:87427240-87427390	SK-N-SH_RA	brain:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
33	CTCF	chr7:87427260-87427410	WERI-Rb-1	eye:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
34	CTCF	chr7:87413759-87413988	GM12878	blood:	n/a	n/a
35	CTCF	chr7:87427220-87427370	MCF-7	breast:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
36	CTCF	chr7:87413820-87413970	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr7:87376680-87376830	GM06990	blood:	n/a	n/a
38	CTCF	chr7:87376773-87376794	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr7:87376733-87376871	GM12891	blood:	n/a	n/a
40	CTCF	chr7:87353464-87353531	ProgFib	skin:	n/a	n/a
41	CTCF	chr7:87427260-87427410	HRPEpiC	eye:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
42	CTCF	chr7:87427200-87427350	Caco-2	colon:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
43	CTCF	chr7:87413820-87413970	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr7:87427240-87427390	BJ	skin:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
45	CTCF	chr7:87376720-87376870	GM12868	blood:	n/a	n/a
46	CTCF	chr7:87404401-87404537	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr7:87427205-87427419	GM10266	blood:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
48	CTCF	chr7:87427260-87427410	HEK293	kidney:	n/a	chr7:87427305-87427323 chr7:87427307-87427328 chr7:87427306-87427322
49	CTCF	chr7:87376717-87376890	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:87376680-87376830	HepG2	liver:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87329407-87329457	PFSK-1	brain:	n/a
2	chr7:87329407-87329457	PFSK-1	brain:	n/a
3	chr7:87343956-87344006	PrEC	prostate:	n/a
4	chr7:87343956-87344006	HAEpiC	amniotic membrane:	n/a
5	chr7:87329407-87329457	Caco-2	colon:	n/a
6	chr7:87343956-87344006	NB4	blood:	n/a
7	chr7:87343956-87344006	HMEC	breast:	n/a
8	chr7:87329407-87329457	HL-60	blood:	n/a
9	chr7:87343956-87344006	NHDF-neo	bronchial:	n/a
10	chr7:87343956-87344006	PFSK-1	brain:	n/a
11	chr7:87343956-87344006	HEK293	kidney:	embryo
12	chr7:87329407-87329457	Hela-S3	cervix:	n/a
13	chr7:87329407-87329457	U87	brain:	n/a
14	chr7:87329407-87329457	MCF10A-Er-Src	breast:	n/a
15	chr7:87343956-87344006	AG10803	skin:	n/a
16	chr7:87329407-87329457	HCM	heart:	n/a
17	chr7:87329407-87329457	GM12878	blood:	n/a
18	chr7:87329407-87329457	NH-A	brain:	n/a
19	chr7:87329407-87329457	HIPEpiC	eye:	n/a
20	chr7:87343956-87344006	IMR90	lung:	fetal
21	chr7:87343956-87344006	SK-N-SH	brain:	n/a
22	chr7:87343956-87344006	ECC-1	luminal epithelium:	n/a
23	chr7:87329407-87329457	NHDF-neo	bronchial:	n/a
24	chr7:87343956-87344006	K562	blood:	n/a
25	chr7:87343956-87344006	HCM	heart:	n/a
26	chr7:87329407-87329457	MCF-7	breast:	n/a
27	chr7:87343956-87344006	H1-hESC	embryonic stem cell:	embryo
28	chr7:87343956-87344006	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:87329407-87329457	HCT-116	colon:	n/a
30	chr7:87329407-87329457	GM19239	blood:	n/a
31	chr7:87329407-87329457	HRPEpiC	eye:	n/a
32	chr7:87343956-87344006	NT2-D1	testis:	n/a
33	chr7:87329407-87329457	AG10803	skin:	n/a
34	chr7:87343956-87344006	ovcar-3	ovarian:	n/a
35	chr7:87329407-87329457	AoSMC	blood vessel:	n/a
36	chr7:87329407-87329457	IMR90	lung:	fetal
37	chr7:87343956-87344006	T-47D	breast:	n/a
38	chr7:87343956-87344006	Hepatocyte	liver:	n/a
39	chr7:87329407-87329457	NHBE	bronchial:	n/a
40	chr7:87329407-87329457	HEK293	kidney:	embryo
41	chr7:87343956-87344006	BJ	skin:	n/a
42	chr7:87343956-87344006	GM12878	blood:	n/a
43	chr7:87329407-87329457	BE2_C	brain:	n/a
44	chr7:87329407-87329457	HEEpiC	esophagus:	n/a
45	chr7:87329407-87329457	SKMC	muscle:	n/a
46	chr7:87343956-87344006	U87	brain:	n/a
47	chr7:87343956-87344006	HNPCEpiC	eye:	n/a
48	chr7:87329407-87329457	SK-N-SH_RA	brain:	n/a
49	chr7:87329407-87329457	ECC-1	luminal epithelium:	n/a
50	chr7:87343956-87344006	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:87425772..87428458-chr7:87515194..87517899,2	K562	blood:
2	chr7:87425415..87428269-chr7:87430526..87432099,2	MCF-7	breast:
3	chr7:87426500..87427788-chr7:87515992..87516871,4	MCF-7	breast:
4	chr7:87427188..87427812-chr7:87516197..87516849,2	MCF-7	breast:
5	chr7:87327238..87329747-chr7:87397840..87399665,2	MCF-7	breast:
6	chr7:87429183..87429817-chr7:87515965..87516800,2	K562	blood:
7	chr7:87392119..87394274-chr7:87504265..87506461,2	MCF-7	breast:
8	chr7:87364971..87366565-chr7:87368760..87371193,2	MCF-7	breast:
9	chr7:87426827..87427351-chr7:87798790..87799475,2	K562	blood:
10	chr7:87426880..87428200-chr7:87740409..87741499,6	K562	blood:
11	chr7:87413447..87414027-chr7:87740900..87741405,2	MCF-7	breast:
12	chr7:87425415..87428269-chr7:87430526..87432099,2	MCF-7	breast:
13	chr7:87391516..87395464-chr7:87395726..87398529,3	MCF-7	breast:
14	chr7:87427067..87428110-chr7:87740458..87741372,5	MCF-7	breast:
15	chr7:87391516..87395464-chr7:87395726..87398529,3	MCF-7	breast:
16	chr7:87265939..87267557-chr7:87351505..87353964,2	MCF-7	breast:
17	chr7:87413764..87415269-chr7:87503904..87505851,2	K562	blood:
18	chr7:87364971..87366565-chr7:87368760..87371193,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCB4-2	chr7:87342477-87342611	NONHSAT121839
2	lnc-ABCB4-2	chr7:87342478-87342570	NONHSAT121836
3	lnc-ABCB4-2	chr7:87342478-87342728	NONHSAT121843
4	lnc-RUNDC3B-2	chr7:87329737-87329866	NONHSAT121842
5	lnc-ABCB4-2	chr7:87342478-87342570	NONHSAT121838
6	lnc-ABCB4-2	chr7:87342478-87342570	NONHSAT121837

No data

Variant related genes	Relation type
RUNDC3B	TF binding region
ABCB1	TF binding region
RUNDC3B	CpG island
ABCB1	CpG island
ENSG00000006634	chromatin interactions
ENSG00000075303	chromatin interactions
ENSG00000105784	chromatin interactions

Extended variants
information (count: 2713 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2713 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs267601613	chr7:87329760-87329761	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs139503670	chr7:87329764-87329765	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs545413671	chr7:87329769-87329770	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs74986278	chr7:87329800-87329801	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs563701368	chr7:87329802-87329803	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs531310295	chr7:87329833-87329834	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs551522997	chr7:87331613-87331614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372794501	chr7:87331615-87331616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147260009	chr7:87331630-87331631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570020695	chr7:87331638-87331639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537300392	chr7:87331645-87331646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11508500	chr7:87331680-87331681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139486091	chr7:87331707-87331708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542480785	chr7:87331772-87331773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143151264	chr7:87331777-87331778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191649210	chr7:87331830-87331831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572934423	chr7:87331847-87331848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577784285	chr7:87331855-87331856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146703753	chr7:87331856-87331857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10278483	chr7:87331965-87331966	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs114680828	chr7:87332012-87332013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542956831	chr7:87332100-87332101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369275703	chr7:87332140-87332141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75061094	chr7:87332239-87332240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564831987	chr7:87332273-87332274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541036076	chr7:87332377-87332378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530180063	chr7:87332644-87332645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557091659	chr7:87332668-87332669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575553191	chr7:87332669-87332670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542444062	chr7:87332682-87332683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17146782	chr7:87332697-87332698	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145818951	chr7:87332728-87332729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73706904	chr7:87332773-87332774	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs374472635	chr7:87332813-87332814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60723608	chr7:87332839-87332840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533151343	chr7:87332851-87332852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545138095	chr7:87332853-87332854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182696633	chr7:87332972-87332973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201768076	chr7:87332997-87332998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74650504	chr7:87333003-87333004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77999176	chr7:87333004-87333005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74340831	chr7:87333005-87333006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79150205	chr7:87333006-87333007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531162024	chr7:87333047-87333048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548370048	chr7:87333065-87333066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74670569	chr7:87333071-87333072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567096407	chr7:87333113-87333114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71562766	chr7:87333176-87333177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367631868	chr7:87333201-87333202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71117549	chr7:87333227-87333228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	22341455	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Pancreatic cancer	17952125	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myxofibrosarcoma	20639860	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87331600-87332200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:87331800-87332200	Enhancers	HMEC	breast
3	chr7:87331800-87332400	Enhancers	NHEK	skin
4	chr7:87332000-87332400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:87332000-87332400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:87332600-87332800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr7:87332600-87360000	Weak transcription	Liver	Liver
8	chr7:87338400-87339000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:87338400-87339000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr7:87338400-87339000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:87338400-87339200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:87338600-87338800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:87338600-87339000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr7:87338600-87339000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:87338800-87339000	Enhancers	HUVEC	blood vessel
16	chr7:87339000-87341200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:87339000-87342600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:87339200-87340800	Weak transcription	HUVEC	blood vessel
19	chr7:87340800-87341000	Enhancers	HUVEC	blood vessel
20	chr7:87341000-87341800	Flanking Active TSS	HUVEC	blood vessel
21	chr7:87341000-87342800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:87341200-87341600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:87341200-87343000	Enhancers	Muscle Satellite Cultured Cells	--
24	chr7:87341600-87341800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:87341600-87342600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:87341800-87342000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:87341800-87342200	Active TSS	HUVEC	blood vessel
28	chr7:87342000-87342200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:87342200-87342400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:87342200-87342800	Flanking Active TSS	HUVEC	blood vessel
31	chr7:87342400-87342800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:87342400-87342800	Enhancers	Primary hematopoietic stem cells	blood
33	chr7:87342400-87342800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:87342600-87343000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:87342600-87343000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr7:87342800-87343000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:87342800-87343000	Enhancers	HUVEC	blood vessel
38	chr7:87345400-87345800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:87358600-87359000	Enhancers	Placenta	Placenta
40	chr7:87359000-87362800	Weak transcription	Placenta	Placenta
41	chr7:87360000-87360200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:87360200-87364400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:87362800-87363200	Enhancers	Placenta	Placenta
44	chr7:87363200-87364400	Weak transcription	Placenta	Placenta
45	chr7:87364400-87364800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:87364600-87364800	Enhancers	Placenta	Placenta
47	chr7:87364600-87365000	Enhancers	HMEC	breast
48	chr7:87364600-87365000	Enhancers	HUVEC	blood vessel
49	chr7:87368000-87368800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:87368000-87369400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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