Variant report

Variant	nsv605881
Chromosome Location	chr7:3213851-3258801
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:623)
CpG islands
(count:793)
Chromatin interactive
region (count:27)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3221006-3221355	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3234233-3234865	HepG2	liver:	n/a	n/a
3	ATF2	chr7:3234272-3234806	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:3234177-3234810	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:3240149-3240409	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:3234182-3234735	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr7:3234202-3234797	A549	lung:	n/a	n/a
8	BCL3	chr7:3220998-3221446	GM12878	blood:	n/a	n/a
9	BCL3	chr7:3221093-3221491	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:3216612-3216813	K562	blood:	n/a	n/a
11	CEBPB	chr7:3254435-3254556	A549	lung:	n/a	n/a
12	CEBPB	chr7:3253624-3254014	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr7:3255533-3256206	MCF-7	breast:	n/a	n/a
14	CEBPB	chr7:3234293-3234711	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:3234396-3234625	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:3253725-3254035	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:3253683-3254028	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:3234374-3234541	K562	blood:	n/a	n/a
19	CEBPB	chr7:3220965-3221379	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:3253678-3254005	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:3255447-3256238	MCF-7	breast:	n/a	n/a
22	CEBPB	chr7:3253682-3253924	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:3221076-3221267	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:3258481-3258795	HepG2	liver:	n/a	chr7:3258619-3258630
25	CEBPB	chr7:3234205-3234712	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:3253677-3254027	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:3253684-3254018	A549	lung:	n/a	n/a
28	CEBPB	chr7:3253766-3254022	K562	blood:	n/a	n/a
29	CEBPB	chr7:3234300-3234711	A549	lung:	n/a	n/a
30	CEBPB	chr7:3234098-3234698	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:3231891-3232043	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:3253649-3254023	A549	lung:	n/a	n/a
33	CEBPB	chr7:3215918-3216112	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:3234322-3234665	A549	lung:	n/a	n/a
35	CEBPB	chr7:3255708-3255979	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:3253634-3254152	A549	lung:	n/a	n/a
37	CEBPB	chr7:3253762-3253885	HepG2	liver:	n/a	n/a
38	CHD2	chr7:3221032-3221442	HepG2	liver:	n/a	n/a
39	CHD2	chr7:3234357-3234596	HepG2	liver:	n/a	n/a
40	CHD2	chr7:3243911-3244232	K562	blood:	n/a	n/a
41	CTBP2	chr7:3234305-3234912	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr7:3234480-3234630	GM12872	blood:	n/a	n/a
43	CTCF	chr7:3240208-3240469	HUVEC	blood vessel:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
44	CTCF	chr7:3240156-3240411	HepG2	liver:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
45	CTCF	chr7:3240216-3240406	MCF-7	breast:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
46	CTCF	chr7:3240240-3240390	GM12873	blood:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
47	CTCF	chr7:3240052-3240575	MCF-7	breast:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
48	CTCF	chr7:3240280-3240430	HRE	kidney:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
49	CTCF	chr7:3234380-3234530	GM12868	blood:	n/a	n/a
50	CTCF	chr7:3234220-3234370	NHEK	skin:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3214289-3214339	GM19239	blood:	n/a
2	chr7:3221373-3221423	SKMC	muscle:	n/a
3	chr7:3221150-3221200	RPTEC	kidney:	n/a
4	chr7:3221228-3221278	HEEpiC	esophagus:	n/a
5	chr7:3215287-3215337	CMK	blood:	n/a
6	chr7:3215543-3215593	SK-N-SH_RA	brain:	n/a
7	chr7:3221373-3221423	NHBE	bronchial:	n/a
8	chr7:3221150-3221200	NHBE	bronchial:	n/a
9	chr7:3227262-3227312	HRE	kidney:	n/a
10	chr7:3221150-3221200	HepG2	liver:	n/a
11	chr7:3256369-3256419	Hepatocyte	liver:	n/a
12	chr7:3221150-3221200	NHDF-neo	bronchial:	n/a
13	chr7:3258347-3258397	PrEC	prostate:	n/a
14	chr7:3215287-3215337	ECC-1	luminal epithelium:	n/a
15	chr7:3256369-3256419	SK-N-SH_RA	brain:	n/a
16	chr7:3227332-3227382	HRCEpiC	kidney:	n/a
17	chr7:3221228-3221278	HepG2	liver:	n/a
18	chr7:3258347-3258397	HL-60	blood:	n/a
19	chr7:3234697-3234747	SK-N-SH	brain:	n/a
20	chr7:3227262-3227312	HCM	heart:	n/a
21	chr7:3221228-3221278	SKMC	muscle:	n/a
22	chr7:3221228-3221278	GM12892	blood:	n/a
23	chr7:3256369-3256419	AG09309	skin:	n/a
24	chr7:3227332-3227382	A549	lung:	n/a
25	chr7:3214289-3214339	ovcar-3	ovarian:	n/a
26	chr7:3227277-3227327	GM12878	blood:	n/a
27	chr7:3215287-3215337	HUVEC	blood vessel:	n/a
28	chr7:3256369-3256419	Hela-S3	cervix:	n/a
29	chr7:3221228-3221278	HMEC	breast:	n/a
30	chr7:3221150-3221200	HCT-116	colon:	n/a
31	chr7:3221373-3221423	HRPEpiC	eye:	n/a
32	chr7:3256369-3256419	SAEC	small airway:	n/a
33	chr7:3214400-3214450	HCPEpiC	choroid plexus:	n/a
34	chr7:3256369-3256419	ProgFib	skin:	n/a
35	chr7:3227332-3227382	AG09309	skin:	n/a
36	chr7:3256369-3256419	HIPEpiC	eye:	n/a
37	chr7:3256369-3256419	HepG2	liver:	n/a
38	chr7:3227277-3227327	CMK	blood:	n/a
39	chr7:3258347-3258397	HRPEpiC	eye:	n/a
40	chr7:3234697-3234747	SK-N-SH_RA	brain:	n/a
41	chr7:3221150-3221200	ProgFib	skin:	n/a
42	chr7:3227332-3227382	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:3221228-3221278	HCT-116	colon:	n/a
44	chr7:3256369-3256419	SK-N-SH	brain:	n/a
45	chr7:3221373-3221423	H1-hESC	embryonic stem cell:	embryo
46	chr7:3215287-3215337	HAEpiC	amniotic membrane:	n/a
47	chr7:3221150-3221200	Caco-2	colon:	n/a
48	chr7:3215287-3215337	Caco-2	colon:	n/a
49	chr7:3227262-3227312	ProgFib	skin:	n/a
50	chr7:3221373-3221423	SAEC	small airway:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:
2	chr7:3240198..3242825-chr7:3445733..3447901,2	K562	blood:
3	chr7:3254376..3256017-chr7:3281440..3283827,2	MCF-7	breast:
4	chr7:3227729..3230209-chr7:3232264..3234725,2	MCF-7	breast:
5	chr7:3128837..3129871-chr7:3239803..3240577,4	MCF-7	breast:
6	chr7:2912750..2915143-chr7:3228683..3231010,3	MCF-7	breast:
7	chr7:3251471..3253553-chr7:3281258..3284246,2	MCF-7	breast:
8	chr7:3256947..3259532-chr7:3270807..3273199,2	MCF-7	breast:
9	chr7:3253620..3255788-chr7:3339992..3342861,2	MCF-7	breast:
10	chr7:3255932..3258041-chr7:3261586..3263750,2	MCF-7	breast:
11	chr7:2921568..2923869-chr7:3228214..3231115,2	MCF-7	breast:
12	chr7:3254337..3257238-chr7:3340637..3342323,2	MCF-7	breast:
13	chr7:2926249..2926927-chr7:3240062..3240775,2	MCF-7	breast:
14	chr7:3227729..3230209-chr7:3232264..3234725,2	MCF-7	breast:
15	chr7:3210617..3212945-chr7:3214732..3216839,2	K562	blood:
16	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:
17	chr7:2915975..2917721-chr7:3231286..3232804,2	MCF-7	breast:
18	chr7:3249846..3250536-chr7:3341685..3342449,3	MCF-7	breast:
19	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
20	chr7:3104998..3105685-chr7:3239854..3240733,2	MCF-7	breast:
21	chr7:3255245..3256305-chr7:3283809..3284534,3	MCF-7	breast:
22	chr7:3210592..3212478-chr7:3220599..3222530,2	K562	blood:
23	chr7:3255775..3258559-chr7:3276222..3279313,3	MCF-7	breast:
24	chr7:3255528..3257837-chr7:3259945..3262892,2	MCF-7	breast:
25	chr7:2926533..2927268-chr7:3239915..3240463,3	MCF-7	breast:
26	chr7:3254030..3256348-chr7:3338235..3340171,2	MCF-7	breast:
27	chr7:3254572..3259584-chr7:3282203..3284323,4	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091801.1.1-1	chr7:3214230-3214287	XLOC_006339
2	lnc-AC091801.1.1-4	chr7:3242576-3242787	XLOC_006342
3	lnc-AC091801.1.1-4	chr7:3243575-3243666	XLOC_006342
4	lnc-AC091801.1.1-2	chr7:3234354-3234428	XLOC_006340
5	lnc-AC091801.1.1-2	chr7:3233737-3234256	XLOC_006340
6	lnc-AC091801.1.1-1	chr7:3214230-3214287	NONHSAT118844

No data

Variant related genes	Relation type
ENSG00000217455	TF binding region
ENSG00000231892	TF binding region
ENSG00000217455	CpG island
ENSG00000231892	CpG island
ENSG00000146555	chromatin interactions
ENSG00000236708	chromatin interactions
HIPK3	miRNA target sites

Extended variants
information (count: 2574 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2574 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1525549	chr7:3213851-3213852	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577743842	chr7:3213856-3213857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540521293	chr7:3213860-3213861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560438938	chr7:3213868-3213869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529077461	chr7:3213877-3213878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549165829	chr7:3213883-3213884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148281802	chr7:3213897-3213898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531050119	chr7:3213902-3213903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373339276	chr7:3213903-3213904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59959021	chr7:3213913-3213914	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs186568208	chr7:3213917-3213918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189034406	chr7:3213955-3213956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1525550	chr7:3214048-3214049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs567198877	chr7:3214053-3214054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535625283	chr7:3214075-3214076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180828627	chr7:3214113-3214114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185420110	chr7:3214130-3214131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575211911	chr7:3214138-3214139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367960712	chr7:3214160-3214161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs398085541	chr7:3214167-3214168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369915327	chr7:3214168-3214169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191019098	chr7:3214173-3214174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182047026	chr7:3214210-3214211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577705188	chr7:3214213-3214214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76308080	chr7:3214236-3214237	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs185925787	chr7:3214241-3214242	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs573889195	chr7:3214345-3214346	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376451196	chr7:3214356-3214357	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs370155725	chr7:3214390-3214391	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs562726768	chr7:3214476-3214477	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs569259697	chr7:3214505-3214506	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs4722523	chr7:3214521-3214522	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550644699	chr7:3214523-3214524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs191861460	chr7:3214548-3214549	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs141311145	chr7:3214576-3214577	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs546592444	chr7:3214588-3214589	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs76280540	chr7:3214647-3214648	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs536159072	chr7:3214683-3214684	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs549280190	chr7:3214691-3214692	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs182843650	chr7:3214703-3214704	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs373754102	chr7:3214710-3214711	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542252078	chr7:3214781-3214782	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs538483132	chr7:3214787-3214788	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs557885951	chr7:3214800-3214801	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs74819760	chr7:3214895-3214896	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533730146	chr7:3214900-3214901	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs527836406	chr7:3214901-3214902	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs188336703	chr7:3214921-3214922	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs542887285	chr7:3214945-3214946	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs191331830	chr7:3215002-3215003	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3205200-3221000	Weak transcription	Right Atrium	heart
2	chr7:3208400-3215200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:3208400-3215400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:3208600-3216200	Weak transcription	Pancreas	Pancrea
5	chr7:3211800-3215200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:3211800-3216200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr7:3212000-3214200	Weak transcription	Fetal Brain Male	brain
8	chr7:3213000-3215400	Weak transcription	HepG2	liver
9	chr7:3213600-3214000	Enhancers	Fetal Heart	heart
10	chr7:3214800-3216400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:3215000-3216800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr7:3215200-3215400	Bivalent Enhancer	Fetal Stomach	stomach
13	chr7:3215200-3215600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr7:3215200-3215800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:3215200-3216400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:3215200-3216400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:3215200-3216600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr7:3215200-3216600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr7:3215200-3216800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:3215200-3216800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:3215400-3215800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:3215400-3216400	Enhancers	HepG2	liver
23	chr7:3215400-3216600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:3215400-3216600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr7:3215600-3219000	Weak transcription	Fetal Brain Male	brain
26	chr7:3215800-3216200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:3215800-3220200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:3216000-3216600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:3216200-3216400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:3216200-3216600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr7:3216200-3216600	Enhancers	Pancreas	Pancrea
32	chr7:3216200-3216800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:3216400-3218400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:3216400-3218400	Weak transcription	HepG2	liver
35	chr7:3216400-3218800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:3216400-3219800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:3216600-3220400	Weak transcription	Pancreas	Pancrea
38	chr7:3216800-3218600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:3216800-3232600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr7:3218400-3218800	Enhancers	HepG2	liver
41	chr7:3218600-3219400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:3218800-3219000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:3218800-3219600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:3218800-3219600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr7:3218800-3219800	Flanking Active TSS	HepG2	liver
46	chr7:3219000-3219200	Enhancers	Fetal Brain Male	brain
47	chr7:3219200-3220200	Weak transcription	Fetal Brain Male	brain
48	chr7:3219600-3223800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr7:3219800-3220400	Enhancers	HepG2	liver
50	chr7:3220200-3220600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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