Variant report

Variant	nsv887758
Chromosome Location	chr7:16632561-16668034
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:16659418-16660055	GM12878	blood:	n/a	n/a
2	ATF2	chr7:16659358-16660122	GM12878	blood:	n/a	n/a
3	BATF	chr7:16659469-16659761	GM12878	blood:	n/a	n/a
4	BATF	chr7:16659523-16660147	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:16659534-16660048	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:16659644-16659769	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:16666939-16667139	A549	lung:	n/a	n/a
8	CCNT2	chr7:16635375-16635535	K562	blood:	n/a	n/a
9	CEBPB	chr7:16666957-16667117	MCF-7	breast:	n/a	n/a
10	CEBPB	chr7:16666796-16667297	A549	lung:	n/a	n/a
11	CEBPB	chr7:16666878-16667210	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:16666921-16667173	A549	lung:	n/a	n/a
13	CEBPB	chr7:16650703-16650797	K562	blood:	n/a	chr7:16650748-16650759
14	CEBPB	chr7:16650623-16650860	HepG2	liver:	n/a	chr7:16650748-16650759
15	CEBPB	chr7:16666869-16667219	IMR90	lung:	n/a	n/a
16	CREB1	chr7:16659499-16660035	GM12878	blood:	n/a	n/a
17	CREB1	chr7:16659571-16660080	GM12878	blood:	n/a	n/a
18	CTCF	chr7:16643880-16644030	HMEC	breast:	n/a	n/a
19	CTCF	chr7:16643733-16643986	SK-N-SH_RA	brain:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
20	CTCF	chr7:16643604-16644127	HCT-116	colon:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
21	CTCF	chr7:16643840-16643990	HCT-116	colon:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
22	CTCF	chr7:16643722-16644010	GM12878	blood:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
23	CTCF	chr7:16643860-16644010	HCM	heart:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
24	CTCF	chr7:16643807-16643958	Medullo	brain:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
25	CTCF	chr7:16643713-16643993	IMR90	lung:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
26	CTCF	chr7:16643780-16643930	AG04450	lung:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
27	CTCF	chr7:16643760-16643910	HAc	cerebellar:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
28	CTCF	chr7:16643740-16643890	GM12874	blood:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
29	CTCF	chr7:16643840-16643990	HFF-Myc	foreskin:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
30	CTCF	chr7:16643740-16643890	HCFaa	heart:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
31	CTCF	chr7:16643780-16643930	SK-N-SH_RA	brain:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
32	CTCF	chr7:16643740-16643890	GM12869	blood:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
33	CTCF	chr7:16643740-16643890	HPF	lung:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
34	CTCF	chr7:16643820-16643970	HMF	breast:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
35	CTCF	chr7:16643820-16643970	HBMEC	blood vessel:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
36	CTCF	chr7:16643800-16643950	BE2_C	brain:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
37	CTCF	chr7:16643900-16644050	HVMF	connective:	n/a	n/a
38	CTCF	chr7:16643813-16643853	ProgFib	skin:	n/a	n/a
39	CTCF	chr7:16643763-16644081	MCF-7	breast:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
40	CTCF	chr7:16643720-16643870	HEK293	kidney:	n/a	n/a
41	CTCF	chr7:16643800-16643950	HMF	breast:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
42	CTCF	chr7:16643626-16644150	MCF-7	breast:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
43	CTCF	chr7:16643791-16643940	GM12878	blood:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
44	CTCF	chr7:16643820-16643970	Hela-S3	cervix:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
45	CTCF	chr7:16643820-16643970	HPF	lung:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
46	CTCF	chr7:16643720-16643870	GM12871	blood:	n/a	n/a
47	CTCF	chr7:16643740-16643890	GM12868	blood:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
48	CTCF	chr7:16643840-16643990	GM12865	blood:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
49	CTCF	chr7:16643710-16644034	K562	blood:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879
50	CTCF	chr7:16643820-16643970	HRPEpiC	eye:	n/a	chr7:16643864-16643877 chr7:16643863-16643884 chr7:16643861-16643879

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16656054-16656104	HRPEpiC	eye:	n/a
2	chr7:16637638-16637688	BJ	skin:	n/a
3	chr7:16639517-16639567	HCPEpiC	choroid plexus:	n/a
4	chr7:16637638-16637688	HIPEpiC	eye:	n/a
5	chr7:16637638-16637688	HCM	heart:	n/a
6	chr7:16656054-16656104	HMEC	breast:	n/a
7	chr7:16639517-16639567	SKMC	muscle:	n/a
8	chr7:16639517-16639567	HIPEpiC	eye:	n/a
9	chr7:16639517-16639567	NB4	blood:	n/a
10	chr7:16639517-16639567	AoSMC	blood vessel:	n/a
11	chr7:16637638-16637688	Hela-S3	cervix:	n/a
12	chr7:16637638-16637688	HEEpiC	esophagus:	n/a
13	chr7:16656054-16656104	SK-N-MC	brain:	n/a
14	chr7:16639517-16639567	Hela-S3	cervix:	n/a
15	chr7:16637638-16637688	SKMC	muscle:	n/a
16	chr7:16637638-16637688	Caco-2	colon:	n/a
17	chr7:16637638-16637688	PrEC	prostate:	n/a
18	chr7:16637638-16637688	ovcar-3	ovarian:	n/a
19	chr7:16639517-16639567	MCF10A-Er-Src	breast:	n/a
20	chr7:16656054-16656104	AG10803	skin:	n/a
21	chr7:16639517-16639567	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:16656054-16656104	Hepatocyte	liver:	n/a
23	chr7:16656054-16656104	LNCaP	prostate:	n/a
24	chr7:16639517-16639567	HepG2	liver:	n/a
25	chr7:16637638-16637688	BE2_C	brain:	n/a
26	chr7:16639517-16639567	BJ	skin:	n/a
27	chr7:16656054-16656104	MCF-7	breast:	n/a
28	chr7:16637638-16637688	HCPEpiC	choroid plexus:	n/a
29	chr7:16637638-16637688	Hepatocyte	liver:	n/a
30	chr7:16656054-16656104	PFSK-1	brain:	n/a
31	chr7:16656054-16656104	HCPEpiC	choroid plexus:	n/a
32	chr7:16637638-16637688	AG04449	skin:	fetal
33	chr7:16637638-16637688	MCF-7	breast:	n/a
34	chr7:16639517-16639567	A549	lung:	n/a
35	chr7:16656054-16656104	BE2_C	brain:	n/a
36	chr7:16639517-16639567	GM06990	blood:	n/a
37	chr7:16656054-16656104	K562	blood:	n/a
38	chr7:16639517-16639567	AG04449	skin:	fetal
39	chr7:16637638-16637688	A549	lung:	n/a
40	chr7:16639517-16639567	SK-N-SH	brain:	n/a
41	chr7:16656054-16656104	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:16637638-16637688	HRCEpiC	kidney:	n/a
43	chr7:16639517-16639567	HNPCEpiC	eye:	n/a
44	chr7:16637638-16637688	AG09319	gingival:	n/a
45	chr7:16637638-16637688	HEK293	kidney:	embryo
46	chr7:16656054-16656104	SAEC	small airway:	n/a
47	chr7:16637638-16637688	ProgFib	skin:	n/a
48	chr7:16639517-16639567	GM19239	blood:	n/a
49	chr7:16639517-16639567	HRE	kidney:	n/a
50	chr7:16639517-16639567	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:16643475..16644221-chr7:16957387..16958014,2	MCF-7	breast:
2	chr7:16641415..16643036-chr7:16685793..16687476,2	MCF-7	breast:
3	chr7:16650532..16652095-chr7:16654625..16656401,2	K562	blood:
4	chr7:16637135..16639582-chr7:16641679..16644005,2	K562	blood:
5	chr7:16664063..16666801-chr7:16668158..16671236,3	K562	blood:
6	chr7:16433382..16436329-chr7:16629318..16633087,3	K562	blood:
7	chr7:16635320..16637285-chr7:16647888..16649843,2	K562	blood:
8	chr7:16667727..16670675-chr7:16700899..16703274,2	K562	blood:
9	chr7:16647541..16650601-chr7:16652797..16655866,3	K562	blood:
10	chr7:16635320..16637285-chr7:16647888..16649843,2	K562	blood:
11	chr7:16637135..16639582-chr7:16641679..16644005,2	K562	blood:
12	chr7:16663926..16665720-chr7:16685466..16687345,2	K562	blood:
13	chr7:16642756..16644444-chr7:16668487..16671282,2	K562	blood:
14	chr7:16661782..16663449-chr7:16681609..16684213,2	K562	blood:
15	chr7:16659196..16661017-chr7:16698458..16700775,2	K562	blood:
16	chr7:16640696..16642517-chr7:16685710..16687291,2	MCF-7	breast:
17	chr7:16644986..16647948-chr7:16650301..16653215,3	K562	blood:
18	chr7:16473934..16476388-chr7:16667166..16670049,2	K562	blood:
19	chr7:16644986..16647948-chr7:16650301..16653215,3	K562	blood:
20	chr7:16649613..16652124-chr7:16656843..16659640,2	K562	blood:
21	chr7:16647541..16650601-chr7:16652797..16655866,3	K562	blood:
22	chr7:16652156..16654551-chr7:16658497..16660099,2	K562	blood:
23	chr7:16644705..16646601-chr7:16684304..16687284,2	MCF-7	breast:
24	chr7:16642489..16644865-chr7:16673141..16675282,2	K562	blood:
25	chr7:16655192..16657272-chr7:16805854..16808580,2	MCF-7	breast:
26	chr7:16639597..16641925-chr7:16642837..16645779,2	K562	blood:
27	chr7:16639597..16641925-chr7:16642837..16645779,2	K562	blood:
28	chr7:16653579..16656411-chr7:16684734..16687056,2	MCF-7	breast:
29	chr7:16652156..16654551-chr7:16658497..16660099,2	K562	blood:
30	chr7:16649613..16652124-chr7:16656843..16659640,2	K562	blood:
31	chr7:16646853..16650643-chr7:16684954..16687917,3	MCF-7	breast:
32	chr7:16662487..16665291-chr7:16666130..16668303,2	K562	blood:
33	chr7:16650532..16652095-chr7:16654625..16656401,2	K562	blood:
34	chr7:16662487..16665291-chr7:16666130..16668303,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKMY2-2	chr7:16633253-16633849	ENSG00000272361.1

Variant related genes	Relation type
ENSG00000272361	TF binding region
ENSG00000272361	CpG island
ENSG00000106524	chromatin interactions
ENSG00000136261	chromatin interactions

Extended variants
information (count: 1561 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1561 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs506875	chr7:16632561-16632562	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551158783	chr7:16632565-16632566	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs535470346	chr7:16632587-16632588	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs369176777	chr7:16632632-16632633	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs559794182	chr7:16632648-16632649	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs186482846	chr7:16632655-16632656	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs530646914	chr7:16632737-16632738	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs149110272	chr7:16632789-16632790	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs190867457	chr7:16632812-16632813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556955967	chr7:16632816-16632817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12531923	chr7:16632840-16632841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182313145	chr7:16632862-16632863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546533371	chr7:16632891-16632892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186280992	chr7:16632899-16632900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143251670	chr7:16632910-16632911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190745749	chr7:16632913-16632914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375713616	chr7:16632914-16632915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12531944	chr7:16632935-16632936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148294402	chr7:16632937-16632938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140482457	chr7:16632939-16632940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149145900	chr7:16632959-16632960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372941139	chr7:16632966-16632967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61191063	chr7:16632977-16632978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112757491	chr7:16632981-16632982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs398003797	chr7:16633003-16633004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376414498	chr7:16633012-16633013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374745739	chr7:16633014-16633015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377460350	chr7:16633015-16633016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573320423	chr7:16633082-16633083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10231984	chr7:16633089-16633090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183407392	chr7:16633095-16633096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187903468	chr7:16633096-16633097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192200423	chr7:16633110-16633111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532613873	chr7:16633111-16633112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138280770	chr7:16633112-16633113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372048593	chr7:16633114-16633115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538271374	chr7:16633122-16633123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13437773	chr7:16633153-16633154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34563911	chr7:16633156-16633157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111343240	chr7:16633159-16633160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372794267	chr7:16633180-16633181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147333861	chr7:16633190-16633191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528487678	chr7:16633192-16633193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143001506	chr7:16633215-16633216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35067827	chr7:16633249-16633250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150666329	chr7:16633252-16633253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531982861	chr7:16633275-16633276	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs138960101	chr7:16633296-16633297	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs75593119	chr7:16633320-16633321	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs10247772	chr7:16633321-16633322	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16622200-16635000	Weak transcription	K562	blood
2	chr7:16624000-16645600	Weak transcription	Gastric	stomach
3	chr7:16626000-16638000	Weak transcription	Fetal Stomach	stomach
4	chr7:16626400-16639400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:16626600-16637800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:16627000-16637800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr7:16627400-16633800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr7:16627600-16635200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:16627800-16633800	Weak transcription	Osteobl	bone
10	chr7:16627800-16637800	Weak transcription	Fetal Muscle Leg	muscle
11	chr7:16627800-16639400	Weak transcription	Brain Germinal Matrix	brain
12	chr7:16627800-16640200	Weak transcription	Fetal Brain Female	brain
13	chr7:16627800-16640200	Weak transcription	Right Ventricle	heart
14	chr7:16627800-16654200	Weak transcription	Brain Angular Gyrus	brain
15	chr7:16628000-16637800	Weak transcription	Adipose Nuclei	Adipose
16	chr7:16628200-16639000	Weak transcription	Left Ventricle	heart
17	chr7:16628400-16639000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr7:16629400-16634200	Weak transcription	Pancreas	Pancrea
19	chr7:16629600-16642400	Weak transcription	Fetal Brain Male	brain
20	chr7:16629800-16638800	Weak transcription	Aorta	Aorta
21	chr7:16630000-16638000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr7:16630400-16633800	Weak transcription	Hela-S3	cervix
23	chr7:16630400-16634000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr7:16630400-16638000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:16630400-16640600	Weak transcription	A549	lung
26	chr7:16630400-16643000	Weak transcription	HUVEC	blood vessel
27	chr7:16630600-16637800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr7:16630600-16637800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr7:16630600-16639400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr7:16630600-16640800	Weak transcription	Fetal Heart	heart
31	chr7:16630800-16638400	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:16630800-16643000	Weak transcription	Thymus	Thymus
33	chr7:16631000-16633600	Weak transcription	Stomach Mucosa	stomach
34	chr7:16631200-16634000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:16631200-16635000	Weak transcription	Fetal Intestine Small	intestine
36	chr7:16632000-16638000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:16632200-16632800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:16632200-16633600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr7:16632200-16640200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr7:16632400-16634000	Weak transcription	Fetal Intestine Large	intestine
41	chr7:16632400-16637800	Weak transcription	Stomach Smooth Muscle	stomach
42	chr7:16632400-16638200	Weak transcription	Psoas Muscle	Psoas
43	chr7:16632400-16639200	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr7:16632600-16639400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:16632600-16643200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr7:16632800-16633600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:16633600-16634200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr7:16633600-16634400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:16633600-16634400	Enhancers	Stomach Mucosa	stomach
50	chr7:16633600-16634600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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