Variant report

Variant	nsv538680
Chromosome Location	chr7:3616095-3753563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:861)
CpG islands
(count:428)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	chr7:3713169-3713470	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:3731377-3731827	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:3657589-3657734	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:3621741-3622079	GM12878	blood:	n/a	n/a
6	BATF	chr7:3636895-3637153	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:3621641-3621866	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:3621621-3622000	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:3721967-3722323	HepG2	liver:	n/a	n/a
10	CBX3	chr7:3618108-3618346	K562	blood:	n/a	n/a
11	CCNT2	chr7:3662206-3662335	K562	blood:	n/a	n/a
12	CEBPB	chr7:3689739-3690076	HepG2	liver:	n/a	chr7:3689906-3689917
13	CEBPB	chr7:3735387-3735863	HepG2	liver:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
14	CEBPB	chr7:3750311-3750526	K562	blood:	n/a	chr7:3750408-3750425
15	CEBPB	chr7:3689754-3690077	K562	blood:	n/a	chr7:3689906-3689917
16	CEBPB	chr7:3722392-3722443	IMR90	lung:	n/a	chr7:3722426-3722437
17	CEBPB	chr7:3633609-3634015	HepG2	liver:	n/a	chr7:3633893-3633904
18	CEBPB	chr7:3689750-3690087	Hela-S3	cervix:	n/a	chr7:3689906-3689917
19	CEBPB	chr7:3689730-3690095	IMR90	lung:	n/a	chr7:3689906-3689917
20	CEBPB	chr7:3669159-3669429	HepG2	liver:	n/a	chr7:3669297-3669308
21	CEBPB	chr7:3625582-3625840	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:3735419-3735759	H1-hESC	embryonic stem cell:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
23	CEBPB	chr7:3619257-3619600	MCF-7	breast:	n/a	n/a
24	CEBPB	chr7:3633614-3633989	K562	blood:	n/a	chr7:3633893-3633904
25	CEBPB	chr7:3750144-3750719	MCF-7	breast:	n/a	chr7:3750408-3750425
26	CEBPB	chr7:3735440-3735874	A549	lung:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
27	CEBPB	chr7:3750353-3750572	IMR90	lung:	n/a	chr7:3750408-3750425
28	CEBPB	chr7:3632070-3632192	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:3732825-3733006	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:3631970-3632335	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:3632006-3632301	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:3666847-3666953	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:3689713-3690022	MCF-7	breast:	n/a	chr7:3689906-3689917
34	CEBPB	chr7:3689783-3689977	H1-hESC	embryonic stem cell:	n/a	chr7:3689906-3689917
35	CEBPB	chr7:3722310-3722477	HepG2	liver:	n/a	chr7:3722426-3722437
36	CEBPB	chr7:3632072-3632263	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:3750088-3750627	MCF-7	breast:	n/a	chr7:3750408-3750425
38	CEBPB	chr7:3669099-3669481	MCF-7	breast:	n/a	chr7:3669297-3669308
39	CEBPB	chr7:3722260-3722580	HepG2	liver:	n/a	chr7:3722426-3722437
40	CEBPB	chr7:3735439-3735877	K562	blood:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
41	CEBPB	chr7:3633733-3634004	A549	lung:	n/a	chr7:3633893-3633904
42	CEBPB	chr7:3750202-3750546	Hela-S3	cervix:	n/a	chr7:3750408-3750425
43	CEBPB	chr7:3631968-3632350	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:3689734-3690090	A549	lung:	n/a	chr7:3689906-3689917
45	CEBPB	chr7:3632048-3632246	A549	lung:	n/a	n/a
46	CHD2	chr7:3723200-3723390	HepG2	liver:	n/a	n/a
47	CHD2	chr7:3713229-3713285	HepG2	liver:	n/a	n/a
48	CTCF	chr7:3735395-3735496	Kidney_OC	kidney:	n/a	chr7:3735433-3735451
49	CTCF	chr7:3705321-3705415	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:3713260-3713410	HMF	breast:	n/a	chr7:3713345-3713363 chr7:3713347-3713360 chr7:3713346-3713362 chr7:3713348-3713358

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3727166-3727216	NH-A	brain:	n/a
2	chr7:3727166-3727216	NH-A	brain:	n/a
3	chr7:3713348-3713398	HNPCEpiC	eye:	n/a
4	chr7:3691268-3691318	BE2_C	brain:	n/a
5	chr7:3727189-3727239	MCF-7	breast:	n/a
6	chr7:3727189-3727239	SAEC	small airway:	n/a
7	chr7:3632395-3632445	Jurkat	blood:	n/a
8	chr7:3713348-3713398	GM19239	blood:	n/a
9	chr7:3723660-3723710	Caco-2	colon:	n/a
10	chr7:3691268-3691318	ProgFib	skin:	n/a
11	chr7:3727189-3727239	PFSK-1	brain:	n/a
12	chr7:3713348-3713398	GM12878	blood:	n/a
13	chr7:3632395-3632445	A549	lung:	n/a
14	chr7:3727189-3727239	GM12878	blood:	n/a
15	chr7:3713348-3713398	SK-N-SH	brain:	n/a
16	chr7:3723660-3723710	SK-N-MC	brain:	n/a
17	chr7:3691268-3691318	K562	blood:	n/a
18	chr7:3727189-3727239	U87	brain:	n/a
19	chr7:3727166-3727216	NHBE	bronchial:	n/a
20	chr7:3632395-3632445	Hela-S3	cervix:	n/a
21	chr7:3710628-3710678	HUVEC	blood vessel:	n/a
22	chr7:3691268-3691318	HCT-116	colon:	n/a
23	chr7:3727166-3727216	HCF	heart:	n/a
24	chr7:3713348-3713398	HEEpiC	esophagus:	n/a
25	chr7:3632395-3632445	Hepatocyte	liver:	n/a
26	chr7:3727166-3727216	ECC-1	luminal epithelium:	n/a
27	chr7:3632395-3632445	PrEC	prostate:	n/a
28	chr7:3727166-3727216	NHDF-neo	bronchial:	n/a
29	chr7:3727166-3727216	GM06990	blood:	n/a
30	chr7:3713348-3713398	HAEpiC	amniotic membrane:	n/a
31	chr7:3710628-3710678	LNCaP	prostate:	n/a
32	chr7:3723660-3723710	RPTEC	kidney:	n/a
33	chr7:3691268-3691318	HRE	kidney:	n/a
34	chr7:3713348-3713398	NB4	blood:	n/a
35	chr7:3691268-3691318	LNCaP	prostate:	n/a
36	chr7:3723660-3723710	HRCEpiC	kidney:	n/a
37	chr7:3723660-3723710	HAEpiC	amniotic membrane:	n/a
38	chr7:3691268-3691318	CMK	blood:	n/a
39	chr7:3632395-3632445	HepG2	liver:	n/a
40	chr7:3727166-3727216	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:3710628-3710678	HEEpiC	esophagus:	n/a
42	chr7:3727166-3727216	ProgFib	skin:	n/a
43	chr7:3723660-3723710	HepG2	liver:	n/a
44	chr7:3691268-3691318	NHDF-neo	bronchial:	n/a
45	chr7:3691268-3691318	HUVEC	blood vessel:	n/a
46	chr7:3723660-3723710	HIPEpiC	eye:	n/a
47	chr7:3713348-3713398	H1-hESC	embryonic stem cell:	embryo
48	chr7:3691268-3691318	HMEC	breast:	n/a
49	chr7:3713348-3713398	CMK	blood:	n/a
50	chr7:3632395-3632445	Caco-2	colon:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
2	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
3	chr7:3734945..3735889-chr7:3936899..3937757,3	MCF-7	breast:
4	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
5	chr7:3750817..3752407-chr7:3752998..3754553,2	K562	blood:
6	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
7	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
8	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
9	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
10	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
11	chr7:3609002..3610756-chr7:3616407..3619133,2	MCF-7	breast:
12	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
13	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:
14	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:
15	chr7:3624042..3625672-chr7:3626577..3628999,2	MCF-7	breast:
16	chr7:3624042..3625672-chr7:3626577..3628999,2	MCF-7	breast:
17	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
18	chr7:3681955..3684927-chr7:3685128..3688064,3	K562	blood:
19	chr4:37757943..37758649-chr7:3694176..3695010,2	MCF-7	breast:
20	chr7:3610768..3613073-chr7:3628327..3630622,2	MCF-7	breast:
21	chr7:3750817..3752407-chr7:3752998..3754553,2	K562	blood:
22	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
23	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
24	chr7:3522949..3523470-chr7:3687761..3688597,2	MCF-7	breast:
25	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:
26	chr7:3521755..3523053-chr7:3688631..3689551,7	MCF-7	breast:
27	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
28	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 8629 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:8629 , 50 per page) page: 1 2 3 4 5 6 7 ... 173

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556774077	chr7:3616102-3616103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563854820	chr7:3616106-3616107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189596214	chr7:3616116-3616117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538797166	chr7:3616197-3616198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77508946	chr7:3616205-3616206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543342069	chr7:3616261-3616262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10275784	chr7:3616286-3616287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193061499	chr7:3616287-3616288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs118061544	chr7:3616288-3616289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573517157	chr7:3616294-3616295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546478920	chr7:3616298-3616299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544105137	chr7:3616317-3616318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184796434	chr7:3616324-3616325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532743314	chr7:3616370-3616371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12540209	chr7:3616379-3616380	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs371616438	chr7:3616397-3616398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189529886	chr7:3616403-3616404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559401992	chr7:3616423-3616424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528147534	chr7:3616442-3616443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548184119	chr7:3616458-3616459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567949248	chr7:3616465-3616466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530743413	chr7:3616487-3616488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181445959	chr7:3616492-3616493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146912554	chr7:3616504-3616505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527643990	chr7:3616511-3616512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186269860	chr7:3616559-3616560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117085344	chr7:3616560-3616561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566178525	chr7:3616608-3616609	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10263702	chr7:3616613-3616614	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189529516	chr7:3616614-3616615	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554974052	chr7:3616641-3616642	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181527131	chr7:3616642-3616643	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534678876	chr7:3616667-3616668	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557695727	chr7:3616671-3616672	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546758434	chr7:3616686-3616687	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577565556	chr7:3616709-3616710	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138943990	chr7:3616714-3616715	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185860023	chr7:3616748-3616749	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369302538	chr7:3616760-3616761	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572929070	chr7:3616764-3616765	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541544231	chr7:3616765-3616766	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532019515	chr7:3616779-3616780	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561762984	chr7:3616805-3616806	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530420039	chr7:3616812-3616813	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550111013	chr7:3616815-3616816	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190911291	chr7:3616824-3616825	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533032699	chr7:3616858-3616859	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568633872	chr7:3616859-3616860	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182623926	chr7:3616869-3616870	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114201285	chr7:3616913-3616914	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3600600-3616600	Weak transcription	Gastric	stomach
2	chr7:3612400-3617000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:3613200-3625200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:3614400-3616400	Enhancers	HepG2	liver
5	chr7:3614400-3616600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:3614400-3617000	Enhancers	Stomach Mucosa	stomach
7	chr7:3615800-3617200	Enhancers	Pancreas	Pancrea
8	chr7:3616600-3617000	ZNF genes & repeats	Gastric	stomach
9	chr7:3616600-3617200	ZNF genes & repeats	Aorta	Aorta
10	chr7:3616600-3617600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:3617000-3619200	Weak transcription	Stomach Mucosa	stomach
12	chr7:3617200-3620400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:3617200-3622600	Weak transcription	Pancreas	Pancrea
14	chr7:3617400-3618200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr7:3617400-3622600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:3617600-3630400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:3618800-3619000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:3619200-3619800	Enhancers	Stomach Mucosa	stomach
19	chr7:3619600-3621400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:3619800-3622800	Weak transcription	Stomach Mucosa	stomach
21	chr7:3620400-3620800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr7:3620400-3625000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:3621400-3621600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:3621400-3621600	Enhancers	Gastric	stomach
25	chr7:3621600-3622600	Weak transcription	Gastric	stomach
26	chr7:3621600-3625200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:3621800-3622800	Enhancers	Fetal Stomach	stomach
28	chr7:3622400-3622800	Enhancers	Fetal Lung	lung
29	chr7:3622600-3622800	Enhancers	Gastric	stomach
30	chr7:3622600-3623200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:3622600-3624000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:3622600-3624200	Enhancers	Pancreas	Pancrea
33	chr7:3622800-3623200	Weak transcription	Gastric	stomach
34	chr7:3622800-3625000	Enhancers	Stomach Mucosa	stomach
35	chr7:3623200-3623600	Enhancers	Gastric	stomach
36	chr7:3623800-3624000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr7:3623800-3624000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:3624000-3624600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr7:3624000-3624600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr7:3624000-3625000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:3624000-3626600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr7:3624200-3628600	Weak transcription	Pancreas	Pancrea
43	chr7:3624600-3625800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:3624600-3625800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:3624600-3626600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr7:3624800-3625200	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:3624800-3625600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr7:3624800-3625800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr7:3625000-3626000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:3625000-3626000	Enhancers	HUES6 Cell Line	embryonic stem cell

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