Variant report

Variant	nsv1031163
Chromosome Location	chr7:17707971-17733754
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	ARID3A	chr7:17720492-17720803	K562	blood:	n/a	n/a
2	ARID3A	chr7:17720541-17720883	HepG2	liver:	n/a	n/a
3	ATF1	chr7:17714261-17714461	K562	blood:	n/a	n/a
4	ATF1	chr7:17729747-17729995	K562	blood:	n/a	n/a
5	ATF1	chr7:17724862-17725125	K562	blood:	n/a	n/a
6	BCL3	chr7:17719409-17720099	A549	lung:	n/a	chr7:17719888-17719897 chr7:17719765-17719774
7	BCL3	chr7:17719467-17720248	A549	lung:	n/a	chr7:17719888-17719897 chr7:17719765-17719774
8	BHLHE40	chr7:17729759-17729967	K562	blood:	n/a	n/a
9	BHLHE40	chr7:17719711-17719835	GM12878	blood:	n/a	n/a
10	BRCA1	chr7:17729210-17729955	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr7:17720466-17720857	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:17719749-17719961	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:17716968-17717319	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:17729900-17729901	K562	blood:	n/a	n/a
15	CEBPB	chr7:17713763-17714147	MCF-7	breast:	n/a	n/a
16	CEBPB	chr7:17719713-17720056	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:17713926-17713965	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:17729626-17730082	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:17729733-17729807	A549	lung:	n/a	n/a
20	CEBPB	chr7:17719644-17720156	A549	lung:	n/a	n/a
21	CEBPB	chr7:17729119-17729470	MCF-7	breast:	n/a	n/a
22	CEBPB	chr7:17713895-17713992	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:17719682-17720262	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:17719700-17720404	A549	lung:	n/a	n/a
25	CEBPB	chr7:17729128-17730076	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr7:17719497-17720367	A549	lung:	n/a	n/a
27	CHD2	chr7:17729215-17730058	Hela-S3	cervix:	n/a	n/a
28	CREB1	chr7:17719588-17719931	A549	lung:	n/a	n/a
29	CTCF	chr7:17720560-17720710	GM12864	blood:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
30	CTCF	chr7:17720640-17720790	NB4	blood:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
31	CTCF	chr7:17720600-17720750	AG10803	skin:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
32	CTCF	chr7:17720540-17720690	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr7:17720640-17720790	RPTEC	kidney:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
34	CTCF	chr7:17720583-17720779	Kidney_OC	kidney:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
35	CTCF	chr7:17720560-17720809	A549	lung:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
36	CTCF	chr7:17720452-17720904	MCF-7	breast:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
37	CTCF	chr7:17720414-17721049	HCT-116	colon:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
38	CTCF	chr7:17720800-17720950	HRE	kidney:	n/a	n/a
39	CTCF	chr7:17720600-17720750	AG09319	gingival:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
40	CTCF	chr7:17719915-17721119	A549	lung:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
41	CTCF	chr7:17720580-17720730	HBMEC	blood vessel:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
42	CTCF	chr7:17720580-17720730	HepG2	liver:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
43	CTCF	chr7:17720620-17720770	AoAF	blood vessel:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
44	CTCF	chr7:17720533-17720732	ECC-1	luminal epithelium:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
45	CTCF	chr7:17720840-17720990	GM12875	blood:	n/a	n/a
46	CTCF	chr7:17727980-17728130	GM12871	blood:	n/a	n/a
47	CTCF	chr7:17720620-17720770	AG09319	gingival:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
48	CTCF	chr7:17720660-17720810	HPF	lung:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
49	CTCF	chr7:17720620-17720770	AG10803	skin:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698
50	CTCF	chr7:17720620-17720770	Caco-2	colon:	n/a	chr7:17720681-17720697 chr7:17720684-17720691 chr7:17720682-17720703 chr7:17720680-17720698

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17730027-17730077	ovcar-3	ovarian:	n/a
2	chr7:17730027-17730077	GM12891	blood:	n/a
3	chr7:17730027-17730077	HCPEpiC	choroid plexus:	n/a
4	chr7:17730027-17730077	MCF10A-Er-Src	breast:	n/a
5	chr7:17720468-17720518	GM12891	blood:	n/a
6	chr7:17720468-17720518	H1-hESC	embryonic stem cell:	embryo
7	chr7:17720468-17720518	NHBE	bronchial:	n/a
8	chr7:17730027-17730077	GM06990	blood:	n/a
9	chr7:17730027-17730077	U87	brain:	n/a
10	chr7:17730027-17730077	HAEpiC	amniotic membrane:	n/a
11	chr7:17730027-17730077	ECC-1	luminal epithelium:	n/a
12	chr7:17730027-17730077	NHBE	bronchial:	n/a
13	chr7:17720468-17720518	GM12892	blood:	n/a
14	chr7:17720468-17720518	IMR90	lung:	fetal
15	chr7:17730027-17730077	RPTEC	kidney:	n/a
16	chr7:17730027-17730077	NH-A	brain:	n/a
17	chr7:17720468-17720518	GM06990	blood:	n/a
18	chr7:17720468-17720518	GM19239	blood:	n/a
19	chr7:17730027-17730077	Hepatocyte	liver:	n/a
20	chr7:17720468-17720518	GM12878	blood:	n/a
21	chr7:17720468-17720518	AG09319	gingival:	n/a
22	chr7:17720468-17720518	SK-N-MC	brain:	n/a
23	chr7:17720468-17720518	A549	lung:	n/a
24	chr7:17720468-17720518	SK-N-SH_RA	brain:	n/a
25	chr7:17730027-17730077	HepG2	liver:	n/a
26	chr7:17720468-17720518	HCF	heart:	n/a
27	chr7:17720468-17720518	U87	brain:	n/a
28	chr7:17720468-17720518	HRPEpiC	eye:	n/a
29	chr7:17730027-17730077	Jurkat	blood:	n/a
30	chr7:17720468-17720518	NT2-D1	testis:	n/a
31	chr7:17730027-17730077	K562	blood:	n/a
32	chr7:17720468-17720518	SK-N-SH	brain:	n/a
33	chr7:17730027-17730077	HCF	heart:	n/a
34	chr7:17730027-17730077	GM19239	blood:	n/a
35	chr7:17720468-17720518	NHDF-neo	bronchial:	n/a
36	chr7:17730027-17730077	HRPEpiC	eye:	n/a
37	chr7:17720468-17720518	HCM	heart:	n/a
38	chr7:17730027-17730077	AG09309	skin:	n/a
39	chr7:17730027-17730077	HUVEC	blood vessel:	n/a
40	chr7:17720468-17720518	HIPEpiC	eye:	n/a
41	chr7:17730027-17730077	SK-N-SH	brain:	n/a
42	chr7:17720468-17720518	SAEC	small airway:	n/a
43	chr7:17730027-17730077	Caco-2	colon:	n/a
44	chr7:17720468-17720518	K562	blood:	n/a
45	chr7:17720468-17720518	PrEC	prostate:	n/a
46	chr7:17730027-17730077	MCF-7	breast:	n/a
47	chr7:17720468-17720518	HAEpiC	amniotic membrane:	n/a
48	chr7:17730027-17730077	BJ	skin:	n/a
49	chr7:17720468-17720518	HRCEpiC	kidney:	n/a
50	chr7:17720468-17720518	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:17702578..17704543-chr7:17713221..17714766,2	MCF-7	breast:
2	chr7:17720091..17721114-chr7:17746094..17746756,4	MCF-7	breast:
3	chr7:17709533..17711370-chr7:17717501..17719526,2	MCF-7	breast:
4	chr7:17728037..17729747-chr7:17732682..17734758,2	MCF-7	breast:
5	chr17:59488041..59490128-chr7:17728518..17731177,2	MCF-7	breast:
6	chr7:17712355..17715598-chr7:17735050..17738524,3	MCF-7	breast:
7	chr7:17728037..17729747-chr7:17732682..17734758,2	MCF-7	breast:
8	chr7:17720220..17720870-chr7:20637924..20638671,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX13-3	chr7:17719080-17719218	NONHSAT119341
2	lnc-AHR-3	chr7:17720085-17720283	XLOC_005999
3	lnc-AHR-3	chr7:17719173-17719246	XLOC_005999

Variant related genes	Relation type
ENSG00000228675	TF binding region
ENSG00000228675	CpG island
ENSG00000267280	chromatin interactions
ENSG00000228675	chromatin interactions
ENSG00000187013	chromatin interactions
SPIN4	miRNA target sites

Extended variants
information (count: 1266 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544020246	chr7:17707997-17707998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559153950	chr7:17708002-17708003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75115168	chr7:17708003-17708004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532105995	chr7:17708016-17708017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577516258	chr7:17708034-17708035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145195536	chr7:17708036-17708037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183292993	chr7:17708092-17708093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551741273	chr7:17708097-17708098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559605571	chr7:17708098-17708099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568528719	chr7:17708149-17708150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530088330	chr7:17708175-17708176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538129523	chr7:17708179-17708180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540971564	chr7:17708182-17708183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10273343	chr7:17708246-17708247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs10243677	chr7:17708264-17708265	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187772518	chr7:17708317-17708318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144435714	chr7:17708334-17708335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72304939	chr7:17708335-17708336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56666535	chr7:17708336-17708337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564694652	chr7:17708339-17708340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6976334	chr7:17708354-17708355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs371631876	chr7:17708365-17708366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547054835	chr7:17708369-17708370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565673824	chr7:17708375-17708376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200581972	chr7:17708407-17708408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs55677320	chr7:17708408-17708409	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs539971420	chr7:17708410-17708411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs58948716	chr7:17708419-17708420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs202105853	chr7:17708420-17708421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10276616	chr7:17708465-17708466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs149207012	chr7:17708506-17708507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559314403	chr7:17708511-17708512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74469756	chr7:17708512-17708513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535264654	chr7:17708513-17708514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553408747	chr7:17708537-17708538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115289621	chr7:17708544-17708545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542199275	chr7:17708563-17708564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs386710839	chr7:17708652-17708653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183631687	chr7:17708653-17708654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543285069	chr7:17708654-17708655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574693826	chr7:17708664-17708665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79667333	chr7:17708708-17708709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73302012	chr7:17708745-17708746	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114110176	chr7:17708759-17708760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116642318	chr7:17708771-17708772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559389374	chr7:17708779-17708780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10233355	chr7:17708788-17708789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548269429	chr7:17708806-17708807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372416509	chr7:17708861-17708862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569642597	chr7:17708881-17708882	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
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17702800-17713800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:17703600-17708800	Weak transcription	NHEK	skin
3	chr7:17703600-17713000	Weak transcription	HMEC	breast
4	chr7:17708800-17709400	Enhancers	NHEK	skin
5	chr7:17708800-17711000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:17709400-17713200	Weak transcription	NHEK	skin
7	chr7:17710000-17710200	Enhancers	Placenta	Placenta
8	chr7:17711000-17711200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:17711200-17713400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:17711800-17713400	Weak transcription	Placenta	Placenta
11	chr7:17712600-17715400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:17713000-17722000	Enhancers	HMEC	breast
13	chr7:17713200-17716000	Enhancers	NHEK	skin
14	chr7:17713400-17713800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:17713400-17715200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr7:17713400-17715200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:17713400-17715200	Enhancers	Placenta	Placenta
18	chr7:17713600-17714000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:17713600-17714600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:17713600-17715000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:17713600-17715800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:17713800-17714000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:17713800-17714000	Enhancers	Brain Cingulate Gyrus	brain
24	chr7:17713800-17714000	Enhancers	NHDF-Ad	bronchial
25	chr7:17713800-17714200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:17713800-17714200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr7:17713800-17714200	Enhancers	Fetal Kidney	kidney
28	chr7:17713800-17714400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:17713800-17714600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr7:17714000-17715400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:17714000-17719000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:17714000-17720800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr7:17714200-17716200	Weak transcription	NHDF-Ad	bronchial
34	chr7:17714200-17719400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr7:17714400-17715200	Enhancers	Placenta Amnion	Placenta Amnion
36	chr7:17714400-17719200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:17714600-17717400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:17714600-17717600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr7:17715200-17717400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:17715200-17717400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr7:17715200-17718400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr7:17715200-17719200	Weak transcription	Placenta	Placenta
43	chr7:17715400-17717200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:17715400-17718200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:17715600-17717200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:17715800-17717200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:17716000-17717000	Weak transcription	NHEK	skin
48	chr7:17716200-17719400	Enhancers	NHDF-Ad	bronchial
49	chr7:17716400-17719200	Enhancers	HSMM	muscle
50	chr7:17716400-17723400	Enhancers	NHLF	lung

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