Variant report

Variant	nsv530553
Chromosome Location	chr7:3629504-3736851
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	chr7:3635039-3635334	HepG2	liver:	n/a	chr7:3635139-3635155
2	BACH1	chr7:3657589-3657734	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:3713169-3713470	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:3731377-3731827	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:3636895-3637153	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:3721967-3722323	HepG2	liver:	n/a	n/a
7	CCNT2	chr7:3662206-3662335	K562	blood:	n/a	n/a
8	CEBPB	chr7:3631970-3632335	MCF-7	breast:	n/a	n/a
9	CEBPB	chr7:3722260-3722580	HepG2	liver:	n/a	chr7:3722426-3722437
10	CEBPB	chr7:3689750-3690087	Hela-S3	cervix:	n/a	chr7:3689906-3689917
11	CEBPB	chr7:3633609-3634015	HepG2	liver:	n/a	chr7:3633893-3633904
12	CEBPB	chr7:3722392-3722443	IMR90	lung:	n/a	chr7:3722426-3722437
13	CEBPB	chr7:3735439-3735877	K562	blood:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
14	CEBPB	chr7:3689754-3690077	K562	blood:	n/a	chr7:3689906-3689917
15	CEBPB	chr7:3669099-3669481	MCF-7	breast:	n/a	chr7:3669297-3669308
16	CEBPB	chr7:3732825-3733006	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:3735387-3735863	HepG2	liver:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
18	CEBPB	chr7:3735440-3735874	A549	lung:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
19	CEBPB	chr7:3689730-3690095	IMR90	lung:	n/a	chr7:3689906-3689917
20	CEBPB	chr7:3632072-3632263	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:3633614-3633989	K562	blood:	n/a	chr7:3633893-3633904
22	CEBPB	chr7:3632070-3632192	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:3689783-3689977	H1-hESC	embryonic stem cell:	n/a	chr7:3689906-3689917
24	CEBPB	chr7:3735419-3735759	H1-hESC	embryonic stem cell:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
25	CEBPB	chr7:3631968-3632350	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:3633733-3634004	A549	lung:	n/a	chr7:3633893-3633904
27	CEBPB	chr7:3669159-3669429	HepG2	liver:	n/a	chr7:3669297-3669308
28	CEBPB	chr7:3632006-3632301	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:3689739-3690076	HepG2	liver:	n/a	chr7:3689906-3689917
30	CEBPB	chr7:3689734-3690090	A549	lung:	n/a	chr7:3689906-3689917
31	CEBPB	chr7:3632048-3632246	A549	lung:	n/a	n/a
32	CEBPB	chr7:3722310-3722477	HepG2	liver:	n/a	chr7:3722426-3722437
33	CEBPB	chr7:3689713-3690022	MCF-7	breast:	n/a	chr7:3689906-3689917
34	CEBPB	chr7:3666847-3666953	HepG2	liver:	n/a	n/a
35	CHD2	chr7:3723200-3723390	HepG2	liver:	n/a	n/a
36	CHD2	chr7:3713229-3713285	HepG2	liver:	n/a	n/a
37	CTCF	chr7:3735360-3735510	GM12864	blood:	n/a	chr7:3735433-3735451
38	CTCF	chr7:3632512-3632664	MCF-7	breast:	n/a	chr7:3632557-3632575 chr7:3632559-3632572
39	CTCF	chr7:3713106-3713493	A549	lung:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
40	CTCF	chr7:3735360-3735510	HPAF	blood vessel:	n/a	chr7:3735433-3735451
41	CTCF	chr7:3713240-3713390	A549	lung:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
42	CTCF	chr7:3713280-3713430	HEEpiC	esophagus:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
43	CTCF	chr7:3735260-3735410	HCFaa	heart:	n/a	n/a
44	CTCF	chr7:3689000-3689150	A549	lung:	n/a	n/a
45	CTCF	chr7:3735332-3735549	Spleen_OC	spleen:	n/a	chr7:3735433-3735451
46	CTCF	chr7:3713240-3713390	GM12865	blood:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
47	CTCF	chr7:3735360-3735510	HCPEpiC	choroid plexus:	n/a	chr7:3735433-3735451
48	CTCF	chr7:3713260-3713410	HRPEpiC	eye:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
49	CTCF	chr7:3713220-3713370	GM12869	blood:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358
50	CTCF	chr7:3713280-3713430	HPF	lung:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3727166-3727216	CMK	blood:	n/a
2	chr7:3710628-3710678	Caco-2	colon:	n/a
3	chr7:3727166-3727216	CMK	blood:	n/a
4	chr7:3710628-3710678	Caco-2	colon:	n/a
5	chr7:3691268-3691318	GM12878	blood:	n/a
6	chr7:3632395-3632445	SAEC	small airway:	n/a
7	chr7:3727166-3727216	AG09319	gingival:	n/a
8	chr7:3727166-3727216	HMEC	breast:	n/a
9	chr7:3632395-3632445	GM06990	blood:	n/a
10	chr7:3723660-3723710	HAEpiC	amniotic membrane:	n/a
11	chr7:3723660-3723710	ProgFib	skin:	n/a
12	chr7:3710628-3710678	HRPEpiC	eye:	n/a
13	chr7:3723660-3723710	HRCEpiC	kidney:	n/a
14	chr7:3691268-3691318	HCF	heart:	n/a
15	chr7:3710628-3710678	HCM	heart:	n/a
16	chr7:3632395-3632445	AG09309	skin:	n/a
17	chr7:3727166-3727216	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:3723660-3723710	Hela-S3	cervix:	n/a
19	chr7:3691268-3691318	AG10803	skin:	n/a
20	chr7:3632395-3632445	HCPEpiC	choroid plexus:	n/a
21	chr7:3723660-3723710	Jurkat	blood:	n/a
22	chr7:3727166-3727216	HEK293	kidney:	embryo
23	chr7:3727189-3727239	ProgFib	skin:	n/a
24	chr7:3710628-3710678	HepG2	liver:	n/a
25	chr7:3727189-3727239	BJ	skin:	n/a
26	chr7:3727189-3727239	AG09319	gingival:	n/a
27	chr7:3713348-3713398	SK-N-SH_RA	brain:	n/a
28	chr7:3710628-3710678	ovcar-3	ovarian:	n/a
29	chr7:3691268-3691318	MCF10A-Er-Src	breast:	n/a
30	chr7:3710628-3710678	T-47D	breast:	n/a
31	chr7:3727166-3727216	SK-N-SH	brain:	n/a
32	chr7:3723660-3723710	H1-hESC	embryonic stem cell:	embryo
33	chr7:3727166-3727216	AG10803	skin:	n/a
34	chr7:3713348-3713398	HEEpiC	esophagus:	n/a
35	chr7:3727166-3727216	NHDF-neo	bronchial:	n/a
36	chr7:3727166-3727216	HUVEC	blood vessel:	n/a
37	chr7:3710628-3710678	AG09309	skin:	n/a
38	chr7:3632395-3632445	T-47D	breast:	n/a
39	chr7:3727166-3727216	NHBE	bronchial:	n/a
40	chr7:3713348-3713398	SK-N-MC	brain:	n/a
41	chr7:3710628-3710678	HL-60	blood:	n/a
42	chr7:3710628-3710678	HEEpiC	esophagus:	n/a
43	chr7:3727166-3727216	U87	brain:	n/a
44	chr7:3727166-3727216	AG09309	skin:	n/a
45	chr7:3723660-3723710	AG09309	skin:	n/a
46	chr7:3713348-3713398	HUVEC	blood vessel:	n/a
47	chr7:3713348-3713398	NT2-D1	testis:	n/a
48	chr7:3710628-3710678	HCF	heart:	n/a
49	chr7:3632395-3632445	GM19239	blood:	n/a
50	chr7:3632395-3632445	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
2	chr7:3681955..3684927-chr7:3685128..3688064,3	K562	blood:
3	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
4	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:
5	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
6	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
7	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
8	chr7:3521755..3523053-chr7:3688631..3689551,7	MCF-7	breast:
9	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:
10	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
11	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:
12	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
13	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
14	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
15	chr7:3610768..3613073-chr7:3628327..3630622,2	MCF-7	breast:
16	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
17	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
18	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
19	chr4:37757943..37758649-chr7:3694176..3695010,2	MCF-7	breast:
20	chr7:3522949..3523470-chr7:3687761..3688597,2	MCF-7	breast:
21	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
22	chr7:3734945..3735889-chr7:3936899..3937757,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091801.1.1-7	chr7:3682447-3682983	ENSG00000236510.1
2	lnc-AC091801.1.1-7	chr7:3683098-3683416	ENSG00000236510.1

Variant related genes	Relation type
ENSG00000236510	TF binding region
ENSG00000236510	CpG island
ENSG00000236510	chromatin interactions

Extended variants
information (count: 6758 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6758 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185560177	chr7:3629508-3629509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532135722	chr7:3629509-3629510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535970191	chr7:3629517-3629518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117010132	chr7:3629521-3629522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189514247	chr7:3629534-3629535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572430246	chr7:3629540-3629541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546206969	chr7:3629548-3629549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138864036	chr7:3629557-3629558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369896169	chr7:3629563-3629564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564516854	chr7:3629581-3629582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112226006	chr7:3629628-3629629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536951983	chr7:3629639-3629640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181447458	chr7:3629652-3629653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576716991	chr7:3629664-3629665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539198874	chr7:3629667-3629668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184716024	chr7:3629688-3629689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572083453	chr7:3629696-3629697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150813227	chr7:3629704-3629705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560928764	chr7:3629712-3629713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113072833	chr7:3629713-3629714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79813546	chr7:3629751-3629752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144383486	chr7:3629762-3629763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368239445	chr7:3629787-3629788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112480960	chr7:3629791-3629792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532197395	chr7:3629803-3629804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144821654	chr7:3629837-3629838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569453563	chr7:3629838-3629839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147379857	chr7:3629849-3629850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111925171	chr7:3629900-3629901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567657164	chr7:3629920-3629921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147289623	chr7:3629928-3629929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374171693	chr7:3629933-3629934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371181525	chr7:3629954-3629955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375720524	chr7:3629955-3629956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76498805	chr7:3629972-3629973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550508843	chr7:3629980-3629981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369015835	chr7:3629994-3629995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570334243	chr7:3629997-3629998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188644708	chr7:3630004-3630005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559178179	chr7:3630010-3630011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181388233	chr7:3630014-3630015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13438448	chr7:3630039-3630040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13438449	chr7:3630046-3630047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186456152	chr7:3630076-3630077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554320604	chr7:3630102-3630103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574389182	chr7:3630149-3630150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117141990	chr7:3630174-3630175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372986299	chr7:3630196-3630197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377517258	chr7:3630205-3630206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559014523	chr7:3630233-3630234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3617600-3630400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:3625600-3630800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:3625600-3631000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:3625800-3630600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr7:3625800-3630800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:3625800-3631000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr7:3625800-3631200	Weak transcription	Stomach Mucosa	stomach
8	chr7:3625800-3631400	Weak transcription	Brain Germinal Matrix	brain
9	chr7:3625800-3631600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:3625800-3632200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:3625800-3632600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr7:3626000-3631000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:3626000-3631000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr7:3626600-3630400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr7:3626600-3630800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr7:3626600-3632200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:3626800-3631000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:3627400-3631000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:3628600-3629600	Enhancers	Pancreas	Pancrea
20	chr7:3629000-3629800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:3629000-3630000	Enhancers	NHEK	skin
22	chr7:3629200-3629800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:3629400-3629600	Enhancers	Colon Smooth Muscle	Colon
24	chr7:3629400-3629800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:3629600-3632200	Weak transcription	Colon Smooth Muscle	Colon
26	chr7:3629600-3632200	Weak transcription	Pancreas	Pancrea
27	chr7:3630400-3630600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:3630400-3633400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr7:3630600-3631000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:3630600-3632800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr7:3630800-3632800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr7:3630800-3633200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:3630800-3633400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr7:3630800-3633400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr7:3631000-3631200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:3631000-3631200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:3631000-3632200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:3631000-3632400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr7:3631000-3632800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:3631000-3632800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr7:3631000-3633200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:3631200-3631600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:3631200-3632200	Enhancers	Stomach Mucosa	stomach
44	chr7:3631200-3636000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:3631400-3631600	Enhancers	Brain Germinal Matrix	brain
46	chr7:3631400-3631600	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:3631600-3632000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr7:3631600-3632000	Weak transcription	Brain Germinal Matrix	brain
49	chr7:3631600-3632000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr7:3631600-3632800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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