Variant report

Variant	nsv1016930
Chromosome Location	chr7:3627295-3705057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:354)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

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	BATF	chr7:3636895-3637153	GM12878	blood:	n/a	n/a
4	CCNT2	chr7:3662206-3662335	K562	blood:	n/a	n/a
5	CEBPB	chr7:3631968-3632350	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:3633614-3633989	K562	blood:	n/a	chr7:3633893-3633904
7	CEBPB	chr7:3689754-3690077	K562	blood:	n/a	chr7:3689906-3689917
8	CEBPB	chr7:3632048-3632246	A549	lung:	n/a	n/a
9	CEBPB	chr7:3689783-3689977	H1-hESC	embryonic stem cell:	n/a	chr7:3689906-3689917
10	CEBPB	chr7:3632070-3632192	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:3632072-3632263	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:3689713-3690022	MCF-7	breast:	n/a	chr7:3689906-3689917
13	CEBPB	chr7:3689734-3690090	A549	lung:	n/a	chr7:3689906-3689917
14	CEBPB	chr7:3669159-3669429	HepG2	liver:	n/a	chr7:3669297-3669308
15	CEBPB	chr7:3631970-3632335	MCF-7	breast:	n/a	n/a
16	CEBPB	chr7:3633733-3634004	A549	lung:	n/a	chr7:3633893-3633904
17	CEBPB	chr7:3632006-3632301	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:3689739-3690076	HepG2	liver:	n/a	chr7:3689906-3689917
19	CEBPB	chr7:3633609-3634015	HepG2	liver:	n/a	chr7:3633893-3633904
20	CEBPB	chr7:3689750-3690087	Hela-S3	cervix:	n/a	chr7:3689906-3689917
21	CEBPB	chr7:3689730-3690095	IMR90	lung:	n/a	chr7:3689906-3689917
22	CEBPB	chr7:3669099-3669481	MCF-7	breast:	n/a	chr7:3669297-3669308
23	CEBPB	chr7:3666847-3666953	HepG2	liver:	n/a	n/a
24	CTCF	chr7:3688920-3689070	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr7:3632482-3632721	MCF-7	breast:	n/a	chr7:3632557-3632575 chr7:3632559-3632572
26	CTCF	chr7:3688940-3689090	GM12864	blood:	n/a	n/a
27	CTCF	chr7:3688964-3689119	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:3688946-3689159	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:3632480-3632630	HCPEpiC	choroid plexus:	n/a	chr7:3632557-3632575 chr7:3632559-3632572
30	CTCF	chr7:3688980-3689130	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr7:3688959-3689147	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:3688940-3689090	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr7:3689000-3689150	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr7:3688960-3689110	HVMF	connective:	n/a	n/a
35	CTCF	chr7:3689005-3689109	Medullo	brain:	n/a	n/a
36	CTCF	chr7:3688976-3689151	A549	lung:	n/a	n/a
37	CTCF	chr7:3632516-3632670	HepG2	liver:	n/a	chr7:3632557-3632575 chr7:3632559-3632572
38	CTCF	chr7:3688940-3689090	HAc	cerebellar:	n/a	n/a
39	CTCF	chr7:3630487-3630528	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr7:3688960-3689110	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:3632526-3632701	Pancreas_OC	pancreas:	n/a	chr7:3632557-3632575 chr7:3632559-3632572
42	CTCF	chr7:3632380-3632530	HRE	kidney:	n/a	n/a
43	CTCF	chr7:3655957-3656050	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:3688920-3689070	AG04449	skin:	n/a	n/a
45	CTCF	chr7:3632560-3632710	HPF	lung:	n/a	n/a
46	CTCF	chr7:3688948-3689071	GM12878	blood:	n/a	n/a
47	CTCF	chr7:3688940-3689090	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr7:3632540-3632690	A549	lung:	n/a	chr7:3632557-3632575 chr7:3632559-3632572
49	CTCF	chr7:3688920-3689070	HAc	cerebellar:	n/a	n/a
50	CTCF	chr7:3632392-3632784	MCF-7	breast:	n/a	chr7:3632557-3632575 chr7:3632559-3632572

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3691268-3691318	MCF10A-Er-Src	breast:	n/a
2	chr7:3691268-3691318	PANC-1	pancreas:	n/a
3	chr7:3691268-3691318	NB4	blood:	n/a
4	chr7:3691268-3691318	GM06990	blood:	n/a
5	chr7:3691268-3691318	GM12878	blood:	n/a
6	chr7:3691268-3691318	NHDF-neo	bronchial:	n/a
7	chr7:3691268-3691318	IMR90	lung:	fetal
8	chr7:3691268-3691318	ProgFib	skin:	n/a
9	chr7:3691268-3691318	AG10803	skin:	n/a
10	chr7:3632395-3632445	NB4	blood:	n/a
11	chr7:3632395-3632445	AoSMC	blood vessel:	n/a
12	chr7:3632395-3632445	IMR90	lung:	fetal
13	chr7:3691268-3691318	Jurkat	blood:	n/a
14	chr7:3632395-3632445	HL-60	blood:	n/a
15	chr7:3691268-3691318	HIPEpiC	eye:	n/a
16	chr7:3632395-3632445	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:3632395-3632445	GM19239	blood:	n/a
18	chr7:3632395-3632445	HCPEpiC	choroid plexus:	n/a
19	chr7:3691268-3691318	CMK	blood:	n/a
20	chr7:3632395-3632445	AG04450	lung:	fetal
21	chr7:3632395-3632445	ECC-1	luminal epithelium:	n/a
22	chr7:3691268-3691318	PFSK-1	brain:	n/a
23	chr7:3691268-3691318	HEK293	kidney:	embryo
24	chr7:3632395-3632445	HAEpiC	amniotic membrane:	n/a
25	chr7:3691268-3691318	AG04449	skin:	fetal
26	chr7:3632395-3632445	RPTEC	kidney:	n/a
27	chr7:3691268-3691318	AG09309	skin:	n/a
28	chr7:3632395-3632445	SK-N-SH	brain:	n/a
29	chr7:3691268-3691318	HCT-116	colon:	n/a
30	chr7:3691268-3691318	H1-hESC	embryonic stem cell:	embryo
31	chr7:3691268-3691318	U87	brain:	n/a
32	chr7:3691268-3691318	SKMC	muscle:	n/a
33	chr7:3691268-3691318	T-47D	breast:	n/a
34	chr7:3632395-3632445	BJ	skin:	n/a
35	chr7:3691268-3691318	MCF-7	breast:	n/a
36	chr7:3691268-3691318	Hepatocyte	liver:	n/a
37	chr7:3632395-3632445	MCF10A-Er-Src	breast:	n/a
38	chr7:3691268-3691318	HRPEpiC	eye:	n/a
39	chr7:3632395-3632445	HEEpiC	esophagus:	n/a
40	chr7:3632395-3632445	AG10803	skin:	n/a
41	chr7:3632395-3632445	GM12878	blood:	n/a
42	chr7:3691268-3691318	GM12892	blood:	n/a
43	chr7:3691268-3691318	HepG2	liver:	n/a
44	chr7:3691268-3691318	SK-N-SH_RA	brain:	n/a
45	chr7:3632395-3632445	Jurkat	blood:	n/a
46	chr7:3632395-3632445	NT2-D1	testis:	n/a
47	chr7:3691268-3691318	SK-N-MC	brain:	n/a
48	chr7:3632395-3632445	A549	lung:	n/a
49	chr7:3632395-3632445	AG04449	skin:	fetal
50	chr7:3632395-3632445	SKMC	muscle:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:
2	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
3	chr7:3522949..3523470-chr7:3687761..3688597,2	MCF-7	breast:
4	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
5	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
6	chr7:3681955..3684927-chr7:3685128..3688064,3	K562	blood:
7	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
8	chr7:3624042..3625672-chr7:3626577..3628999,2	MCF-7	breast:
9	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
10	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
11	chr4:37757943..37758649-chr7:3694176..3695010,2	MCF-7	breast:
12	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
13	chr7:3521755..3523053-chr7:3688631..3689551,7	MCF-7	breast:
14	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
15	chr7:3610768..3613073-chr7:3628327..3630622,2	MCF-7	breast:
16	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
17	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 4869 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4869 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78367920	chr7:3627308-3627309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548875201	chr7:3627312-3627313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568627524	chr7:3627313-3627314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183403480	chr7:3627320-3627321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376902781	chr7:3627360-3627361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7797872	chr7:3627370-3627371	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs12700996	chr7:3627391-3627392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs148573304	chr7:3627398-3627399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552595342	chr7:3627425-3627426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188767004	chr7:3627438-3627439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535065216	chr7:3627441-3627442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555648627	chr7:3627469-3627470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116595904	chr7:3627476-3627477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74929201	chr7:3627530-3627531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557975583	chr7:3627541-3627542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373821953	chr7:3627572-3627573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577460711	chr7:3627594-3627595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192180269	chr7:3627596-3627597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183855077	chr7:3627605-3627606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528503421	chr7:3627641-3627642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541832033	chr7:3627645-3627646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373032266	chr7:3627660-3627661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188581745	chr7:3627668-3627669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191086758	chr7:3627681-3627682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183773769	chr7:3627683-3627684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376233674	chr7:3627685-3627686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568135062	chr7:3627736-3627737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190339656	chr7:3627785-3627786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112314520	chr7:3627796-3627797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2614967	chr7:3627799-3627800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs117512981	chr7:3627810-3627811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151079929	chr7:3627834-3627835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2705606	chr7:3627841-3627842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs535941527	chr7:3627846-3627847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114020407	chr7:3627849-3627850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182518454	chr7:3627865-3627866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186672387	chr7:3627909-3627910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577922966	chr7:3627921-3627922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190139987	chr7:3627924-3627925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181658514	chr7:3627971-3627972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139861921	chr7:3627983-3627984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542245115	chr7:3627997-3627998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577141098	chr7:3628009-3628010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75621015	chr7:3628027-3628028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575792533	chr7:3628051-3628052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185555516	chr7:3628055-3628056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536839560	chr7:3628063-3628064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369776013	chr7:3628072-3628073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144344511	chr7:3628112-3628113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564396349	chr7:3628137-3628138	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:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3617600-3630400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:3624200-3628600	Weak transcription	Pancreas	Pancrea
3	chr7:3625000-3627400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:3625600-3630800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:3625600-3631000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:3625800-3630600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr7:3625800-3630800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:3625800-3631000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:3625800-3631200	Weak transcription	Stomach Mucosa	stomach
10	chr7:3625800-3631400	Weak transcription	Brain Germinal Matrix	brain
11	chr7:3625800-3631600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:3625800-3632200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:3625800-3632600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr7:3626000-3631000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:3626000-3631000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:3626600-3630400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr7:3626600-3630800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:3626600-3632200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:3626800-3631000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:3627400-3631000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:3628600-3629600	Enhancers	Pancreas	Pancrea
22	chr7:3629000-3629800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:3629000-3630000	Enhancers	NHEK	skin
24	chr7:3629200-3629800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:3629400-3629600	Enhancers	Colon Smooth Muscle	Colon
26	chr7:3629400-3629800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:3629600-3632200	Weak transcription	Colon Smooth Muscle	Colon
28	chr7:3629600-3632200	Weak transcription	Pancreas	Pancrea
29	chr7:3630400-3630600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:3630400-3633400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr7:3630600-3631000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:3630600-3632800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:3630800-3632800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr7:3630800-3633200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr7:3630800-3633400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:3630800-3633400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:3631000-3631200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr7:3631000-3631200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:3631000-3632200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:3631000-3632400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr7:3631000-3632800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:3631000-3632800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:3631000-3633200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:3631200-3631600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr7:3631200-3632200	Enhancers	Stomach Mucosa	stomach
46	chr7:3631200-3636000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:3631400-3631600	Enhancers	Brain Germinal Matrix	brain
48	chr7:3631400-3631600	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr7:3631600-3632000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:3631600-3632000	Weak transcription	Brain Germinal Matrix	brain

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