Variant report

Variant	nsv516692
Chromosome Location	chr7:13875122-13907827
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	chr7:13889765-13890070	K562	blood:	n/a	n/a
2	ATF1	chr7:13900658-13900844	K562	blood:	n/a	n/a
3	ATF1	chr7:13889729-13890161	K562	blood:	n/a	n/a
4	ATF3	chr7:13889705-13890029	K562	blood:	n/a	n/a
5	BACH1	chr7:13889847-13890003	H1-hESC	embryonic stem cell:	n/a	chr7:13889889-13889903
6	BHLHE40	chr7:13889782-13890158	K562	blood:	n/a	n/a
7	CBX3	chr7:13889755-13890146	K562	blood:	n/a	n/a
8	CBX3	chr7:13889571-13890520	HCT-116	colon:	n/a	n/a
9	CBX3	chr7:13889637-13890195	K562	blood:	n/a	n/a
10	CBX3	chr7:13889630-13890509	HCT-116	colon:	n/a	n/a
11	CCNT2	chr7:13889753-13890143	K562	blood:	n/a	n/a
12	CEBPB	chr7:13880948-13881315	HepG2	liver:	n/a	chr7:13881124-13881135
13	CEBPB	chr7:13886140-13886336	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:13886123-13886339	K562	blood:	n/a	n/a
15	CEBPB	chr7:13900625-13900913	A549	lung:	n/a	n/a
16	CEBPB	chr7:13880970-13881205	A549	lung:	n/a	chr7:13881124-13881135
17	CEBPB	chr7:13881008-13881269	K562	blood:	n/a	chr7:13881124-13881135
18	CEBPB	chr7:13889742-13890398	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:13886050-13886429	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:13886155-13886335	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:13900136-13900404	K562	blood:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
22	CEBPB	chr7:13903095-13903310	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:13880992-13881274	H1-hESC	embryonic stem cell:	n/a	chr7:13881124-13881135
24	CEBPB	chr7:13891431-13891773	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:13900168-13900410	H1-hESC	embryonic stem cell:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
26	CEBPB	chr7:13899934-13900452	IMR90	lung:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
27	CEBPB	chr7:13889794-13890080	K562	blood:	n/a	n/a
28	CEBPB	chr7:13903094-13903302	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:13900159-13900379	HepG2	liver:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
30	CEBPB	chr7:13886138-13886375	A549	lung:	n/a	n/a
31	CEBPB	chr7:13903039-13903324	K562	blood:	n/a	n/a
32	CEBPB	chr7:13900060-13900418	A549	lung:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
33	CEBPB	chr7:13880963-13881277	IMR90	lung:	n/a	chr7:13881124-13881135
34	CTCF	chr7:13903080-13903230	K562	blood:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
35	CTCF	chr7:13877865-13877940	Lung_OC	lung:	n/a	n/a
36	CTCF	chr7:13903080-13903230	HCT-116	colon:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
37	CTCF	chr7:13904400-13904550	Caco-2	colon:	n/a	chr7:13904451-13904472 chr7:13904449-13904467
38	CTCF	chr7:13902994-13903303	GM12878	blood:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
39	CTCF	chr7:13903000-13903150	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr7:13903160-13903310	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr7:13903100-13903250	BJ	skin:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
42	CTCF	chr7:13903160-13903310	HMF	breast:	n/a	n/a
43	CTCF	chr7:13903080-13903230	Caco-2	colon:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
44	CTCF	chr7:13888927-13888929	K562	blood:	n/a	n/a
45	CTCF	chr7:13902960-13903110	HVMF	connective:	n/a	n/a
46	CTCF	chr7:13889820-13890234	K562	blood:	n/a	chr7:13889868-13889886 chr7:13889863-13889884
47	CTCF	chr7:13902987-13903317	K562	blood:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
48	CTCF	chr7:13902980-13903270	BE2_C	brain:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
49	CTCF	chr7:13902960-13903254	H1-hESC	embryonic stem cell:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
50	CTCF	chr7:13903080-13903217	K562	blood:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13889871-13889921	HepG2	liver:	n/a
2	chr7:13889871-13889921	GM06990	blood:	n/a
3	chr7:13889871-13889921	HAEpiC	amniotic membrane:	n/a
4	chr7:13889871-13889921	HCPEpiC	choroid plexus:	n/a
5	chr7:13889871-13889921	AG04449	skin:	fetal
6	chr7:13889871-13889921	A549	lung:	n/a
7	chr7:13889871-13889921	H1-hESC	embryonic stem cell:	embryo
8	chr7:13889871-13889921	GM19239	blood:	n/a
9	chr7:13889871-13889921	AoSMC	blood vessel:	n/a
10	chr7:13889871-13889921	LNCaP	prostate:	n/a
11	chr7:13889871-13889921	U87	brain:	n/a
12	chr7:13889871-13889921	ECC-1	luminal epithelium:	n/a
13	chr7:13889871-13889921	HCT-116	colon:	n/a
14	chr7:13889871-13889921	HL-60	blood:	n/a
15	chr7:13889871-13889921	Hepatocyte	liver:	n/a
16	chr7:13889871-13889921	K562	blood:	n/a
17	chr7:13889871-13889921	SAEC	small airway:	n/a
18	chr7:13889871-13889921	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:13889871-13889921	GM12892	blood:	n/a
20	chr7:13889871-13889921	AG10803	skin:	n/a
21	chr7:13889871-13889921	HRCEpiC	kidney:	n/a
22	chr7:13889871-13889921	MCF-7	breast:	n/a
23	chr7:13889871-13889921	RPTEC	kidney:	n/a
24	chr7:13889871-13889921	PFSK-1	brain:	n/a
25	chr7:13889871-13889921	GM12891	blood:	n/a
26	chr7:13889871-13889921	CMK	blood:	n/a
27	chr7:13889871-13889921	HNPCEpiC	eye:	n/a
28	chr7:13889871-13889921	HRPEpiC	eye:	n/a
29	chr7:13889871-13889921	GM12878	blood:	n/a
30	chr7:13889871-13889921	Hela-S3	cervix:	n/a
31	chr7:13889871-13889921	ovcar-3	ovarian:	n/a
32	chr7:13889871-13889921	BE2_C	brain:	n/a
33	chr7:13889871-13889921	HMEC	breast:	n/a
34	chr7:13889871-13889921	SK-N-SH_RA	brain:	n/a
35	chr7:13889871-13889921	NHBE	bronchial:	n/a
36	chr7:13889871-13889921	AG09319	gingival:	n/a
37	chr7:13889871-13889921	HRE	kidney:	n/a
38	chr7:13889871-13889921	T-47D	breast:	n/a
39	chr7:13889871-13889921	NHDF-neo	bronchial:	n/a
40	chr7:13889871-13889921	HEK293	kidney:	embryo
41	chr7:13889871-13889921	HUVEC	blood vessel:	n/a
42	chr7:13889871-13889921	IMR90	lung:	fetal
43	chr7:13889871-13889921	AG09309	skin:	n/a
44	chr7:13889871-13889921	NH-A	brain:	n/a
45	chr7:13889871-13889921	NB4	blood:	n/a
46	chr7:13889871-13889921	MCF10A-Er-Src	breast:	n/a
47	chr7:13889871-13889921	ProgFib	skin:	n/a
48	chr7:13889871-13889921	BJ	skin:	n/a
49	chr7:13889871-13889921	SKMC	muscle:	n/a
50	chr7:13889871-13889921	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
2	chr7:13894294..13896373-chr7:13930641..13933578,2	K562	blood:
3	chr7:13898559..13901034-chr7:13906643..13908176,2	K562	blood:
4	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
5	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
6	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
7	chr7:13869026..13872125-chr7:13876719..13879737,3	K562	blood:
8	chr7:13888536..13892464-chr7:13896702..13899784,3	K562	blood:
9	chr7:13888923..13892464-chr7:13896702..13899775,3	K562	blood:
10	chr7:13882109..13884330-chr7:14031307..14033942,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETV1-1	chr7:13898560-13898650	XLOC_006359
2	lnc-ETV1-1	chr7:13893980-13894247	XLOC_006359

Variant related genes	Relation type
ENSG00000224330	TF binding region
ENSG00000213875	TF binding region
ENSG00000224330	CpG island
ENSG00000213875	CpG island
ENSG00000224330	chromatin interactions

Extended variants
information (count: 1321 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1321 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs757904	chr7:13875122-13875123	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537453343	chr7:13875124-13875125	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370005922	chr7:13875170-13875171	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56239184	chr7:13875191-13875192	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148873654	chr7:13875247-13875248	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142640228	chr7:13875267-13875268	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs115181592	chr7:13875284-13875285	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs10486069	chr7:13875291-13875292	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs544812162	chr7:13875311-13875312	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs191457434	chr7:13875339-13875340	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs183601735	chr7:13875364-13875365	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs200371135	chr7:13875392-13875393	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs544197740	chr7:13875403-13875404	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs375968567	chr7:13875408-13875409	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs560505357	chr7:13875422-13875423	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs529951991	chr7:13875423-13875424	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs546459669	chr7:13875428-13875429	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs566355426	chr7:13875429-13875430	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs190462679	chr7:13875439-13875440	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs377629469	chr7:13875490-13875491	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs551633413	chr7:13875498-13875499	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs10236940	chr7:13875502-13875503	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs537111559	chr7:13875525-13875526	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs561881931	chr7:13875550-13875551	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs557343408	chr7:13875554-13875555	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs182239284	chr7:13875569-13875570	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs185292179	chr7:13875606-13875607	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs150996932	chr7:13875706-13875707	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs527518250	chr7:13875744-13875745	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs553687066	chr7:13875758-13875759	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs56362231	chr7:13875821-13875822	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs573519593	chr7:13875844-13875845	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs372838598	chr7:13875845-13875846	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs367762277	chr7:13875867-13875868	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs545579490	chr7:13875876-13875877	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs558837359	chr7:13875901-13875902	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575306557	chr7:13875910-13875911	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs543937346	chr7:13875927-13875928	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs190239008	chr7:13875941-13875942	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs10251265	chr7:13875957-13875958	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs181330227	chr7:13875973-13875974	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs560002501	chr7:13875998-13875999	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs140886448	chr7:13876003-13876004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533258851	chr7:13876022-13876023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550158466	chr7:13876052-13876053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552360953	chr7:13876059-13876060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569904706	chr7:13876064-13876065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146305108	chr7:13876075-13876076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10281229	chr7:13876094-13876095	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs147882480	chr7:13876126-13876127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	21298110	CNVD
Glioblastoma multiforme	22122801	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17079440	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13873000-13875200	Enhancers	H1 Cell Line	embryonic stem cell
2	chr7:13873200-13876000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:13873200-13876600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:13873200-13877000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr7:13873400-13875400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr7:13873400-13875400	Enhancers	Fetal Heart	heart
7	chr7:13873400-13875600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr7:13873400-13877400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:13873600-13875400	Enhancers	HSMMtube	muscle
10	chr7:13873600-13875600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:13873600-13876000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:13873600-13876600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:13873600-13877000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:13873800-13875600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:13874000-13875400	Enhancers	Fetal Brain Female	brain
16	chr7:13874000-13876400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr7:13874000-13876400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:13874000-13876600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:13874200-13875200	Weak transcription	Fetal Muscle Leg	muscle
20	chr7:13874800-13875600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr7:13874800-13876000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr7:13875000-13875400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:13875000-13875600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:13875000-13876000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:13875000-13877000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:13875200-13875600	Enhancers	Fetal Muscle Leg	muscle
27	chr7:13875200-13876000	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr7:13876000-13876200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr7:13876000-13877000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:13876000-13878200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:13876000-13881400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:13876200-13876400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr7:13876400-13880600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:13876600-13880400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr7:13877000-13878400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr7:13877000-13881400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr7:13878200-13879200	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr7:13879200-13879400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr7:13879400-13879600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr7:13879600-13881000	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr7:13880400-13882400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr7:13880600-13881200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:13880800-13882200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:13881000-13889400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr7:13881400-13881800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:13881400-13881800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:13884600-13885000	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr7:13884800-13885000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:13885000-13885600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:13885000-13889800	Weak transcription	Rectal Mucosa Donor 31	rectum

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