Variant report

Variant	nsv464364
Chromosome Location	chr7:10904752-10988866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1210)
CpG islands
(count:1039)
Chromatin interactive
region (count:54)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:10980830-10981145	K562	blood:	n/a	n/a
2	ARID3A	chr7:10929010-10929223	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:10979737-10980496	K562	blood:	n/a	n/a
4	ARID3A	chr7:10979327-10980859	HepG2	liver:	n/a	n/a
5	ATF2	chr7:10948088-10948631	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:10948090-10948701	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:10979531-10980462	GM12878	blood:	n/a	n/a
8	ATF2	chr7:10979521-10980319	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:10979354-10980570	GM12878	blood:	n/a	n/a
10	ATF2	chr7:10928900-10929340	GM12878	blood:	n/a	n/a
11	ATF3	chr7:10948157-10948481	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:10979518-10980525	A549	lung:	n/a	n/a
13	ATF3	chr7:10979536-10980170	A549	lung:	n/a	n/a
14	BACH1	chr7:10978379-10978666	K562	blood:	n/a	n/a
15	BCL11A	chr7:10980077-10980487	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:10980137-10980408	GM12878	blood:	n/a	n/a
17	BCL3	chr7:10979371-10980456	A549	lung:	n/a	n/a
18	BCLAF1	chr7:10979550-10980503	K562	blood:	n/a	n/a
19	BCLAF1	chr7:10979265-10980538	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:10979519-10980461	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:10979879-10980434	A549	lung:	n/a	n/a
22	BHLHE40	chr7:10979553-10980980	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:10979238-10981040	K562	blood:	n/a	n/a
24	BHLHE40	chr7:10979924-10980273	HepG2	liver:	n/a	n/a
25	BHLHE40	chr7:10929005-10929271	GM12878	blood:	n/a	n/a
26	BRCA1	chr7:10979598-10980714	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr7:10979532-10980042	HepG2	liver:	n/a	n/a
28	BRCA1	chr7:10979566-10980034	GM12878	blood:	n/a	n/a
29	CBX3	chr7:10980143-10980434	K562	blood:	n/a	n/a
30	CBX3	chr7:10951230-10951678	K562	blood:	n/a	n/a
31	CBX3	chr7:10979335-10980544	K562	blood:	n/a	n/a
32	CCNT2	chr7:10970572-10970825	K562	blood:	n/a	n/a
33	CCNT2	chr7:10979501-10980529	K562	blood:	n/a	n/a
34	CEBPB	chr7:10945946-10946181	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:10979415-10980113	K562	blood:	n/a	n/a
36	CEBPB	chr7:10943996-10944124	K562	blood:	n/a	n/a
37	CEBPB	chr7:10979163-10979275	HepG2	liver:	n/a	chr7:10979232-10979243
38	CEBPB	chr7:10945928-10946066	K562	blood:	n/a	n/a
39	CEBPB	chr7:10979027-10979228	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:10980143-10980487	K562	blood:	n/a	n/a
41	CEBPB	chr7:10970988-10971102	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:10979668-10980444	K562	blood:	n/a	n/a
43	CEBPB	chr7:10979073-10979419	HepG2	liver:	n/a	chr7:10979232-10979243
44	CEBPB	chr7:10979391-10980369	GM12878	blood:	n/a	n/a
45	CEBPB	chr7:10971542-10971570	K562	blood:	n/a	n/a
46	CEBPB	chr7:10978966-10980509	Hela-S3	cervix:	n/a	chr7:10979232-10979243
47	CEBPB	chr7:10950556-10950747	HepG2	liver:	n/a	n/a
48	CEBPD	chr7:10980093-10980398	HepG2	liver:	n/a	n/a
49	CEBPD	chr7:10979452-10980415	HepG2	liver:	n/a	n/a
50	CEBPZ	chr7:10987055-10987078	HepG2	liver:	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	chr7:10971841-10971891	NH-A	brain:	n/a
2	chr7:10976748-10976798	GM12891	blood:	n/a
3	chr7:10971841-10971891	NH-A	brain:	n/a
4	chr7:10976748-10976798	GM12891	blood:	n/a
5	chr7:10980008-10980058	HRPEpiC	eye:	n/a
6	chr7:10979772-10979822	BE2_C	brain:	n/a
7	chr7:10979772-10979822	HCM	heart:	n/a
8	chr7:10974404-10974454	ProgFib	skin:	n/a
9	chr7:10979847-10979897	BE2_C	brain:	n/a
10	chr7:10979899-10979949	SK-N-SH	brain:	n/a
11	chr7:10974404-10974454	HMEC	breast:	n/a
12	chr7:10979772-10979822	NHDF-neo	bronchial:	n/a
13	chr7:10979341-10979391	CMK	blood:	n/a
14	chr7:10980278-10980328	H1-hESC	embryonic stem cell:	embryo
15	chr7:10979586-10979636	AG09319	gingival:	n/a
16	chr7:10979341-10979391	HRE	kidney:	n/a
17	chr7:10979997-10980047	HCT-116	colon:	n/a
18	chr7:10979772-10979822	HMEC	breast:	n/a
19	chr7:10980008-10980058	CMK	blood:	n/a
20	chr7:10980318-10980368	SK-N-SH	brain:	n/a
21	chr7:10980278-10980328	NHBE	bronchial:	n/a
22	chr7:10974404-10974454	BJ	skin:	n/a
23	chr7:10980278-10980328	SK-N-SH_RA	brain:	n/a
24	chr7:10979247-10979297	NH-A	brain:	n/a
25	chr7:10979847-10979897	ECC-1	luminal epithelium:	n/a
26	chr7:10979341-10979391	SKMC	muscle:	n/a
27	chr7:10979341-10979391	HNPCEpiC	eye:	n/a
28	chr7:10980278-10980328	U87	brain:	n/a
29	chr7:10980944-10980994	BJ	skin:	n/a
30	chr7:10974404-10974454	T-47D	breast:	n/a
31	chr7:10979997-10980047	HIPEpiC	eye:	n/a
32	chr7:10980008-10980058	H1-hESC	embryonic stem cell:	embryo
33	chr7:10971841-10971891	GM12878	blood:	n/a
34	chr7:10979956-10980006	PFSK-1	brain:	n/a
35	chr7:10980278-10980328	HEK293	kidney:	embryo
36	chr7:10980008-10980058	NT2-D1	testis:	n/a
37	chr7:10979341-10979391	ovcar-3	ovarian:	n/a
38	chr7:10979772-10979822	HCF	heart:	n/a
39	chr7:10979341-10979391	HIPEpiC	eye:	n/a
40	chr7:10980008-10980058	U87	brain:	n/a
41	chr7:10976748-10976798	AG09309	skin:	n/a
42	chr7:10979913-10979963	RPTEC	kidney:	n/a
43	chr7:10979247-10979297	PrEC	prostate:	n/a
44	chr7:10980318-10980368	HUVEC	blood vessel:	n/a
45	chr7:10979847-10979897	GM12891	blood:	n/a
46	chr7:10979772-10979822	PFSK-1	brain:	n/a
47	chr7:10976748-10976798	HRPEpiC	eye:	n/a
48	chr7:10971841-10971891	SK-N-SH_RA	brain:	n/a
49	chr7:10979247-10979297	HIPEpiC	eye:	n/a
50	chr7:10979772-10979822	PrEC	prostate:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:10975492..10977726-chr7:10981592..10983238,2	MCF-7	breast:
2	chr15:41694166..41694806-chr7:10979376..10980136,2	Hela-S3	cervix:
3	chr7:10962204..10964945-chr7:11012202..11014539,2	MCF-7	breast:
4	chr7:10952784..10957510-chr7:10959357..10962973,4	MCF-7	breast:
5	chr7:10960377..10963595-chr7:10978264..10982254,4	MCF-7	breast:
6	chr3:156391482..156392232-chr7:10979248..10979918,2	HCT-116	colon:
7	chr7:10903152..10905363-chr7:10907278..10909562,2	K562	blood:
8	chr7:10982115..10983687-chr7:11012566..11014511,2	MCF-7	breast:
9	chr7:10985009..10987966-chr7:11011919..11013774,2	MCF-7	breast:
10	chr7:10903152..10905363-chr7:10907278..10909562,2	K562	blood:
11	chr3:12882526..12883455-chr7:10979276..10980108,2	Hela-S3	cervix:
12	chr7:10978313..10981160-chr7:11099563..11101890,2	K562	blood:
13	chr7:10966685..10968984-chr7:10971328..10972857,2	K562	blood:
14	chr7:10676395..10677225-chr7:10928650..10929592,2	K562	blood:
15	chr7:10978242..10981238-chr7:11011671..11015550,7	MCF-7	breast:
16	chr7:10972604..10974747-chr7:11013678..11015868,2	K562	blood:
17	chr3:119182037..119182735-chr7:10979846..10980807,2	Hela-S3	cervix:
18	chr2:97481562..97482123-chr7:10979299..10980019,2	Hela-S3	cervix:
19	chr7:10950431..10952397-chr7:10957935..10960206,2	K562	blood:
20	chr7:10958230..10961956-chr7:10970091..10974620,4	K562	blood:
21	chr7:10970436..10972192-chr7:11007402..11009320,2	K562	blood:
22	chr7:10976808..10978708-chr7:10978899..10981503,2	MCF-7	breast:
23	chr7:10929007..10929956-chr7:11380303..11381142,3	MCF-7	breast:
24	chr7:10971957..10975609-chr7:11018033..11021117,4	K562	blood:
25	chr7:10976808..10978708-chr7:10978899..10981503,2	MCF-7	breast:
26	chr7:10909984..10911612-chr7:10912737..10914507,2	K562	blood:
27	chr7:10978101..10982429-chr7:11011509..11017731,20	K562	blood:
28	chr7:10958230..10961956-chr7:10970091..10974620,4	K562	blood:
29	chr7:10975906..10982429-chr7:11007978..11018673,26	K562	blood:
30	chr7:10747761..10748702-chr7:10928662..10929453,2	MCF-7	breast:
31	chr7:10956497..10958710-chr7:10978302..10980650,2	K562	blood:
32	chr7:10955950..10957997-chr7:10978214..10979802,2	K562	blood:
33	chr7:10932953..10935447-chr7:10974620..10977431,2	K562	blood:
34	chr7:10979872..10980668-chr7:40173740..40174309,2	Hela-S3	cervix:
35	chr7:10966685..10968984-chr7:10971328..10972857,2	K562	blood:
36	chr7:10908452..10910556-chr7:11019934..11022818,2	K562	blood:
37	chr7:10975492..10977726-chr7:10981592..10983238,2	MCF-7	breast:
38	chr7:10909984..10911612-chr7:10912737..10914507,2	K562	blood:
39	chr7:10903863..10905750-chr7:10907380..10909562,2	K562	blood:
40	chr22:44350679..44351402-chr7:10979367..10979964,2	HCT-116	colon:
41	chr7:10977305..10982144-chr7:11011875..11016071,10	MCF-7	breast:
42	chr7:10988102..10989982-chr7:10992834..10996627,3	MCF-7	breast:
43	chr7:10952784..10957510-chr7:10959357..10962973,4	MCF-7	breast:
44	chr7:10903863..10905750-chr7:10907380..10909562,2	K562	blood:
45	chr7:10972604..10974203-chr7:11013490..11015178,2	K562	blood:
46	chr7:10910112..10911906-chr7:10912737..10915573,2	K562	blood:
47	chr7:10950431..10952397-chr7:10957935..10960206,2	K562	blood:
48	chr7:10947517..10950005-chr7:10956259..10958787,2	K562	blood:
49	chr7:10932953..10935447-chr7:10974620..10977431,2	K562	blood:
50	chr7:10972277..10974447-chr7:11011761..11013440,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF14-5	chr7:10980050-10980362	ENSG00000271185.1

No data

Variant related genes	Relation type
NDUFA4	TF binding region
ENSG00000271185	TF binding region
ENSG00000201774	TF binding region
NDUFA4	CpG island
ENSG00000271185	CpG island
ENSG00000201774	CpG island
ENSG00000144713	chromatin interactions
ENSG00000100347	chromatin interactions
ENSG00000163659	chromatin interactions
ENSG00000271185	chromatin interactions
ENSG00000168763	chromatin interactions
ENSG00000106443	chromatin interactions
ENSG00000137806	chromatin interactions
ENSG00000189043	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000168303	chromatin interactions
ENSG00000176142	chromatin interactions
ENSG00000243926	chromatin interactions

Extended variants
information (count: 2468 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2468 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536854607	chr7:10910008-10910009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532760578	chr7:10910016-10910017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549833745	chr7:10910020-10910021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569915592	chr7:10910058-10910059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572212308	chr7:10910069-10910070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367777595	chr7:10910129-10910130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372015389	chr7:10910134-10910135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34937574	chr7:10910192-10910193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549117190	chr7:10910196-10910197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566189670	chr7:10910219-10910220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186510534	chr7:10910222-10910223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558282596	chr7:10910235-10910236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139430026	chr7:10910240-10910241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190870198	chr7:10910299-10910300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375260625	chr7:10910377-10910378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144061616	chr7:10910386-10910387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541189636	chr7:10910413-10910414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182579616	chr7:10910418-10910419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553490660	chr7:10910466-10910467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6961139	chr7:10910482-10910483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187256660	chr7:10910490-10910491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540772806	chr7:10910526-10910527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191086255	chr7:10910603-10910604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147304260	chr7:10910623-10910624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140869435	chr7:10910709-10910710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183513949	chr7:10910751-10910752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563454116	chr7:10910782-10910783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529148374	chr7:10910788-10910789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374827310	chr7:10913004-10913005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536257983	chr7:10913068-10913069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552964709	chr7:10913075-10913076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181574199	chr7:10913101-10913102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545368223	chr7:10913184-10913185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558549557	chr7:10913222-10913223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574388136	chr7:10913241-10913242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184690225	chr7:10913254-10913255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561453176	chr7:10913341-10913342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530089934	chr7:10913343-10913344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540238928	chr7:10913347-10913348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530674073	chr7:10913351-10913352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11976325	chr7:10913387-10913388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560164158	chr7:10913392-10913393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35450332	chr7:10913402-10913403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552488919	chr7:10913421-10913422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189663088	chr7:10913423-10913424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561707359	chr7:10913424-10913425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572167693	chr7:10913445-10913446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550489905	chr7:10913447-10913448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531955945	chr7:10913457-10913458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548448133	chr7:10913458-10913459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:10910000-10910800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr7:10910400-10910800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr7:10913000-10913200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:10913200-10914200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:10914200-10915200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:10927800-10929200	Enhancers	Primary T cells from cord blood	blood
7	chr7:10928000-10929000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:10928000-10929200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr7:10928000-10929200	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr7:10928200-10928400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:10928200-10928400	Active TSS	Monocytes-CD14+_RO01746	blood
12	chr7:10928200-10928600	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr7:10928200-10928800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr7:10928200-10929000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr7:10928200-10929200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr7:10928200-10929200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr7:10928200-10929400	Enhancers	Primary B cells from peripheral blood	blood
18	chr7:10928200-10929400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr7:10928200-10929400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:10928400-10928600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr7:10928400-10928800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr7:10928400-10928800	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr7:10928400-10928800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr7:10928400-10928800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr7:10928400-10928800	Enhancers	Fetal Thymus	thymus
26	chr7:10928400-10929000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr7:10928400-10929000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:10928400-10929000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:10928400-10929200	Enhancers	Primary T cells fromperipheralblood	blood
30	chr7:10928600-10929000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr7:10928600-10929000	Enhancers	Primary hematopoietic stem cells	blood
32	chr7:10928600-10929000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr7:10928600-10929000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr7:10928600-10929000	Enhancers	Liver	Liver
35	chr7:10928600-10929000	Enhancers	Brain Hippocampus Middle	brain
36	chr7:10928600-10929000	Enhancers	Dnd41	blood
37	chr7:10928600-10929000	Enhancers	GM12878-XiMat	blood
38	chr7:10928600-10929000	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr7:10928600-10929200	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr7:10928600-10929200	Enhancers	Spleen	Spleen
41	chr7:10928800-10929000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:10928800-10929000	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr7:10928800-10929200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr7:10928800-10929200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr7:10928800-10929200	Enhancers	Brain Angular Gyrus	brain
46	chr7:10928800-10929200	Enhancers	Brain Anterior Caudate	brain
47	chr7:10928800-10929200	Enhancers	Brain Substantia Nigra	brain
48	chr7:10929000-10929200	Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr7:10929000-10929200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:10929200-10933400	Weak transcription	Primary monocytes fromperipheralblood	blood

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