Variant report

Variant	nsv1023297
Chromosome Location	chr7:17570370-17671038
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1088)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:17639920-17640241	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17658089-17658641	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:17570705-17570973	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:17582050-17582722	HepG2	liver:	n/a	n/a
5	ATF1	chr7:17639533-17639733	K562	blood:	n/a	n/a
6	ATF3	chr7:17598348-17598968	A549	lung:	n/a	n/a
7	ATF3	chr7:17598333-17599109	A549	lung:	n/a	n/a
8	BATF	chr7:17586358-17586636	GM12878	blood:	n/a	chr7:17586494-17586505 chr7:17586523-17586532
9	BCL3	chr7:17598337-17599111	A549	lung:	n/a	n/a
10	BCL3	chr7:17598160-17599399	A549	lung:	n/a	chr7:17598247-17598256
11	BCL3	chr7:17597307-17597887	A549	lung:	n/a	n/a
12	BHLHE40	chr7:17651388-17651657	HepG2	liver:	n/a	n/a
13	BHLHE40	chr7:17639603-17639687	HepG2	liver:	n/a	n/a
14	BHLHE40	chr7:17586327-17586569	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:17640010-17640130	HepG2	liver:	n/a	n/a
16	BHLHE40	chr7:17570680-17570977	GM12878	blood:	n/a	n/a
17	BRCA1	chr7:17638505-17638954	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr7:17639276-17640418	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr7:17572366-17573261	HCT-116	colon:	n/a	n/a
20	CBX3	chr7:17572488-17573127	HCT-116	colon:	n/a	n/a
21	CEBPB	chr7:17572381-17573224	HCT-116	colon:	n/a	chr7:17572855-17572868
22	CEBPB	chr7:17639318-17640395	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:17586081-17586691	Hela-S3	cervix:	n/a	chr7:17586613-17586624 chr7:17586613-17586626 chr7:17586613-17586626
24	CEBPB	chr7:17647770-17648418	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:17572434-17573078	IMR90	lung:	n/a	chr7:17572855-17572868
26	CEBPB	chr7:17639869-17640297	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:17635217-17635512	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:17628420-17628522	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:17604355-17604602	HepG2	liver:	n/a	chr7:17604492-17604503
30	CEBPB	chr7:17658023-17658624	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:17596241-17596381	A549	lung:	n/a	n/a
32	CEBPB	chr7:17604308-17604693	IMR90	lung:	n/a	chr7:17604492-17604503
33	CEBPB	chr7:17596998-17597659	IMR90	lung:	n/a	chr7:17597278-17597289 chr7:17597111-17597124 chr7:17597111-17597122
34	CEBPB	chr7:17582319-17582618	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:17574012-17574303	A549	lung:	n/a	chr7:17574146-17574157
36	CEBPB	chr7:17656136-17656334	HepG2	liver:	n/a	chr7:17656236-17656247
37	CEBPB	chr7:17597063-17597136	HepG2	liver:	n/a	chr7:17597111-17597124 chr7:17597111-17597122
38	CEBPB	chr7:17600249-17600430	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:17648031-17648547	MCF-7	breast:	n/a	n/a
40	CEBPB	chr7:17598370-17598901	A549	lung:	n/a	n/a
41	CEBPB	chr7:17572428-17572917	A549	lung:	n/a	chr7:17572855-17572868
42	CEBPB	chr7:17586151-17586765	IMR90	lung:	n/a	chr7:17586613-17586624 chr7:17586613-17586626 chr7:17586613-17586626
43	CEBPB	chr7:17598274-17599125	A549	lung:	n/a	n/a
44	CEBPB	chr7:17572424-17573031	Hela-S3	cervix:	n/a	chr7:17572855-17572868
45	CEBPB	chr7:17586096-17586561	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:17619815-17620008	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:17657965-17658571	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:17639801-17640370	MCF-7	breast:	n/a	n/a
49	CEBPB	chr7:17600169-17600496	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:17658878-17659339	Hela-S3	cervix:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17598458-17598508	NH-A	brain:	n/a
2	chr7:17585471-17585521	HRCEpiC	kidney:	n/a
3	chr7:17598458-17598508	MCF10A-Er-Src	breast:	n/a
4	chr7:17582718-17582768	GM12891	blood:	n/a
5	chr7:17582718-17582768	HMEC	breast:	n/a
6	chr7:17598458-17598508	SK-N-SH_RA	brain:	n/a
7	chr7:17598458-17598508	AG04449	skin:	fetal
8	chr7:17582718-17582768	IMR90	lung:	fetal
9	chr7:17598458-17598508	HepG2	liver:	n/a
10	chr7:17585471-17585521	HepG2	liver:	n/a
11	chr7:17585471-17585521	ProgFib	skin:	n/a
12	chr7:17585471-17585521	HL-60	blood:	n/a
13	chr7:17598458-17598508	IMR90	lung:	fetal
14	chr7:17598458-17598508	GM12891	blood:	n/a
15	chr7:17582718-17582768	SK-N-MC	brain:	n/a
16	chr7:17582718-17582768	NB4	blood:	n/a
17	chr7:17585471-17585521	MCF10A-Er-Src	breast:	n/a
18	chr7:17582718-17582768	A549	lung:	n/a
19	chr7:17585471-17585521	SKMC	muscle:	n/a
20	chr7:17598458-17598508	AoSMC	blood vessel:	n/a
21	chr7:17598458-17598508	HNPCEpiC	eye:	n/a
22	chr7:17585471-17585521	SK-N-SH_RA	brain:	n/a
23	chr7:17585471-17585521	NHDF-neo	bronchial:	n/a
24	chr7:17582718-17582768	HepG2	liver:	n/a
25	chr7:17582718-17582768	HCT-116	colon:	n/a
26	chr7:17582718-17582768	HEK293	kidney:	embryo
27	chr7:17598458-17598508	PrEC	prostate:	n/a
28	chr7:17582718-17582768	NT2-D1	testis:	n/a
29	chr7:17598458-17598508	GM12878	blood:	n/a
30	chr7:17585471-17585521	HCM	heart:	n/a
31	chr7:17585471-17585521	K562	blood:	n/a
32	chr7:17582718-17582768	HRPEpiC	eye:	n/a
33	chr7:17585471-17585521	HMEC	breast:	n/a
34	chr7:17598458-17598508	K562	blood:	n/a
35	chr7:17598458-17598508	PFSK-1	brain:	n/a
36	chr7:17582718-17582768	HEEpiC	esophagus:	n/a
37	chr7:17585471-17585521	NHBE	bronchial:	n/a
38	chr7:17585471-17585521	SK-N-MC	brain:	n/a
39	chr7:17598458-17598508	MCF-7	breast:	n/a
40	chr7:17582718-17582768	NHBE	bronchial:	n/a
41	chr7:17582718-17582768	CMK	blood:	n/a
42	chr7:17582718-17582768	GM06990	blood:	n/a
43	chr7:17598458-17598508	GM19239	blood:	n/a
44	chr7:17582718-17582768	H1-hESC	embryonic stem cell:	embryo
45	chr7:17598458-17598508	T-47D	breast:	n/a
46	chr7:17585471-17585521	HRPEpiC	eye:	n/a
47	chr7:17585471-17585521	PANC-1	pancreas:	n/a
48	chr7:17598458-17598508	Hepatocyte	liver:	n/a
49	chr7:17585471-17585521	Hepatocyte	liver:	n/a
50	chr7:17598458-17598508	HL-60	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:17344294..17345014-chr7:17570513..17571272,2	MCF-7	breast:
2	chr21:43784659..43785489-chr7:17669385..17670101,2	MCF-7	breast:
3	chr7:17595637..17596623-chr7:17657831..17658483,2	MCF-7	breast:
4	chr7:17579664..17581435-chr7:17584339..17586742,2	K562	blood:
5	chr7:17657830..17658417-chr7:17668431..17669006,2	MCF-7	breast:
6	chr7:17657830..17658417-chr7:17668431..17669006,2	MCF-7	breast:
7	chr7:17662491..17664335-chr7:17674964..17676646,2	K562	blood:
8	chr7:17595637..17596623-chr7:17657831..17658483,2	MCF-7	breast:
9	chr7:17661017..17663957-chr7:17664042..17665980,2	MCF-7	breast:
10	chr7:17342140..17343219-chr7:17570441..17571204,3	MCF-7	breast:
11	chr7:17337629..17339397-chr7:17596553..17598570,2	MCF-7	breast:
12	chr7:17661017..17663957-chr7:17664042..17665980,2	MCF-7	breast:
13	chr18:3406071..3406571-chr7:17665685..17666459,2	MCF-7	breast:
14	chr7:17514240..17514759-chr7:17570395..17571281,2	MCF-7	breast:
15	chr7:16974533..16976554-chr7:17579096..17580960,2	K562	blood:
16	chr7:17102519..17103019-chr7:17570516..17571366,2	MCF-7	breast:
17	chr7:17579664..17581435-chr7:17584339..17586742,2	K562	blood:
18	chr7:17585475..17587800-chr7:17685188..17687624,2	MCF-7	breast:
19	chr7:17566122..17568059-chr7:17569390..17571113,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX13-3	chr7:17619972-17620082	NONHSAT119341
2	lnc-SNX13-1	chr7:17598376-17598533	ENSG00000226598

No data

Variant related genes	Relation type
ENSG00000226598	TF binding region
ENSG00000226598	CpG island
ENSG00000237773	chromatin interactions
ENSG00000106546	chromatin interactions

Extended variants
information (count: 5024 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:5024 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545578752	chr7:17570376-17570377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs895844	chr7:17570408-17570409	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549559326	chr7:17570409-17570410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs75351879	chr7:17570463-17570464	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs73075167	chr7:17570479-17570480	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536280341	chr7:17570484-17570485	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs10274365	chr7:17570495-17570496	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs555229092	chr7:17570558-17570559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs6971877	chr7:17570569-17570570	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs79831021	chr7:17570578-17570579	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs555944268	chr7:17570582-17570583	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs2389754	chr7:17570591-17570592	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs2389753	chr7:17570594-17570595	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs183346843	chr7:17570608-17570609	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs185763325	chr7:17570609-17570610	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs542677966	chr7:17570619-17570620	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs369213168	chr7:17570623-17570624	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs202203611	chr7:17570641-17570642	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs199506159	chr7:17570644-17570645	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs149279190	chr7:17570666-17570667	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs76929790	chr7:17570694-17570695	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs398066661	chr7:17570698-17570699	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs571103124	chr7:17570728-17570729	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs532088588	chr7:17570746-17570747	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs528244837	chr7:17570763-17570764	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144429165	chr7:17570775-17570776	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs565887109	chr7:17570791-17570792	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs548094446	chr7:17570887-17570888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139475333	chr7:17570911-17570912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532474751	chr7:17570923-17570924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17137816	chr7:17570957-17570958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17707288	chr7:17570971-17570972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536239131	chr7:17570977-17570978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145273769	chr7:17571052-17571053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10229888	chr7:17571110-17571111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537757664	chr7:17571134-17571135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1448649	chr7:17571140-17571141	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs115437618	chr7:17571173-17571174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147218923	chr7:17571174-17571175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553813319	chr7:17571182-17571183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112430487	chr7:17571183-17571184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144397819	chr7:17571238-17571239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552942999	chr7:17571268-17571269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552983795	chr7:17571292-17571293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554606208	chr7:17571302-17571303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566452322	chr7:17571306-17571307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573531982	chr7:17571332-17571333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536011911	chr7:17571375-17571376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190944712	chr7:17571379-17571380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76633003	chr7:17571392-17571393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Sezary syndrome	18413736	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17561800-17572400	Weak transcription	HSMMtube	muscle
2	chr7:17564400-17570400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:17564400-17573000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:17564600-17570800	Weak transcription	Stomach Mucosa	stomach
5	chr7:17564800-17572200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:17564800-17572200	Weak transcription	NHEK	skin
7	chr7:17565000-17571200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:17565000-17572200	Weak transcription	NHLF	lung
9	chr7:17565400-17572600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:17565800-17571200	Weak transcription	Hela-S3	cervix
11	chr7:17568400-17571200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr7:17568400-17571200	Weak transcription	HMEC	breast
13	chr7:17568400-17573000	Enhancers	Osteobl	bone
14	chr7:17569000-17571400	Weak transcription	HSMM	muscle
15	chr7:17569400-17570800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:17569600-17570800	Enhancers	NH-A	brain
17	chr7:17569800-17570400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:17569800-17570600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:17569800-17570800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:17569800-17570800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:17569800-17572600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:17569800-17573000	Enhancers	NHDF-Ad	bronchial
23	chr7:17570000-17570400	Enhancers	Liver	Liver
24	chr7:17570000-17570600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr7:17570000-17570600	Enhancers	Ovary	ovary
26	chr7:17570200-17570800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr7:17570200-17572200	Weak transcription	Small Intestine	intestine
28	chr7:17570200-17575800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:17570400-17570600	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr7:17570400-17570800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:17570400-17570800	Flanking Active TSS	Liver	Liver
32	chr7:17570400-17571800	Enhancers	Duodenum Mucosa	Duodenum
33	chr7:17570600-17571200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr7:17570600-17572200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:17570800-17571600	Enhancers	Liver	Liver
36	chr7:17570800-17571600	Weak transcription	NH-A	brain
37	chr7:17570800-17572200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:17570800-17572200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:17570800-17572400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:17570800-17573200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr7:17570800-17573400	Enhancers	Stomach Mucosa	stomach
42	chr7:17571000-17571200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:17571000-17571400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:17571200-17571400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr7:17571200-17571400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr7:17571200-17571800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr7:17571200-17571800	Enhancers	HUVEC	blood vessel
48	chr7:17571200-17572200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:17571200-17573000	Enhancers	Primary hematopoietic stem cells	blood
50	chr7:17571200-17573400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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