Variant report

Variant	nsv1030082
Chromosome Location	chr7:3941203-3986403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:335)
CpG islands
(count:305)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:3961793-3962131	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr7:3961803-3962230	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:3971600-3971798	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:3961926-3962237	K562	blood:	n/a	n/a
5	BACH1	chr7:3983186-3983373	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:3982338-3982740	H1-hESC	embryonic stem cell:	n/a	chr7:3982547-3982561
7	BACH1	chr7:3961708-3962300	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr7:3954072-3954381	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:3962019-3962205	K562	blood:	n/a	n/a
10	BRCA1	chr7:3946900-3946914	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:3954115-3954365	HepG2	liver:	n/a	chr7:3954269-3954282 chr7:3954269-3954280
12	CEBPB	chr7:3954137-3954374	HepG2	liver:	n/a	chr7:3954269-3954282 chr7:3954269-3954280
13	CEBPB	chr7:3982039-3982244	HepG2	liver:	n/a	chr7:3982167-3982178 chr7:3982167-3982180
14	CEBPB	chr7:3954007-3954455	HepG2	liver:	n/a	chr7:3954269-3954282 chr7:3954269-3954280 chr7:3954007-3954020
15	CEBPB	chr7:3982139-3982260	K562	blood:	n/a	chr7:3982167-3982178 chr7:3982167-3982180
16	CEBPB	chr7:3954017-3954465	HepG2	liver:	n/a	chr7:3954269-3954282 chr7:3954269-3954280
17	CREB1	chr7:3961826-3962190	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr7:3948840-3948990	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr7:3961960-3962110	K562	blood:	n/a	chr7:3962091-3962107
20	CTCF	chr7:3962060-3962210	HCM	heart:	n/a	chr7:3962091-3962107
21	CTCF	chr7:3961973-3962167	MCF-7	breast:	n/a	chr7:3962091-3962107
22	CTCF	chr7:3961973-3962209	LNCaP	prostate:	n/a	chr7:3962091-3962107
23	CTCF	chr7:3961983-3962162	MCF-7	breast:	n/a	chr7:3962091-3962107
24	CTCF	chr7:3962020-3962170	GM12869	blood:	n/a	chr7:3962091-3962107
25	CTCF	chr7:3962040-3962190	Hela-S3	cervix:	n/a	chr7:3962091-3962107
26	CTCF	chr7:3962020-3962170	HRPEpiC	eye:	n/a	chr7:3962091-3962107
27	CTCF	chr7:3962040-3962190	HepG2	liver:	n/a	chr7:3962091-3962107
28	CTCF	chr7:3962052-3962124	GM19239	blood:	n/a	chr7:3962091-3962107
29	CTCF	chr7:3961980-3962130	HL-60	blood:	n/a	chr7:3962091-3962107
30	CTCF	chr7:3962000-3962150	SAEC	small airway:	n/a	chr7:3962091-3962107
31	CTCF	chr7:3961979-3962234	HUVEC	blood vessel:	n/a	chr7:3962091-3962107
32	CTCF	chr7:3962020-3962170	MCF-7	breast:	n/a	chr7:3962091-3962107
33	CTCF	chr7:3963440-3963590	GM12869	blood:	n/a	n/a
34	CTCF	chr7:3962020-3962170	AG09319	gingival:	n/a	chr7:3962091-3962107
35	CTCF	chr7:3974420-3974570	WI-38	lung:	n/a	n/a
36	CTCF	chr7:3961980-3962130	WERI-Rb-1	eye:	n/a	chr7:3962091-3962107
37	CTCF	chr7:3962000-3962150	AG10803	skin:	n/a	chr7:3962091-3962107
38	CTCF	chr7:3961980-3962130	Caco-2	colon:	n/a	chr7:3962091-3962107
39	CTCF	chr7:3961980-3962130	HCPEpiC	choroid plexus:	n/a	chr7:3962091-3962107
40	CTCF	chr7:3985355-3985391	Lung_OC	lung:	n/a	n/a
41	CTCF	chr7:3962020-3962170	HMF	breast:	n/a	chr7:3962091-3962107
42	CTCF	chr7:3962000-3962150	HAc	cerebellar:	n/a	chr7:3962091-3962107
43	CTCF	chr7:3962060-3962210	HRE	kidney:	n/a	chr7:3962091-3962107
44	CTCF	chr7:3962100-3962250	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr7:3957720-3957870	GM12864	blood:	n/a	n/a
46	CTCF	chr7:3961992-3962193	K562	blood:	n/a	chr7:3962091-3962107
47	CTCF	chr7:3962000-3962150	HPF	lung:	n/a	chr7:3962091-3962107
48	CTCF	chr7:3962020-3962170	BE2_C	brain:	n/a	chr7:3962091-3962107
49	CTCF	chr7:3962000-3962150	Hela-S3	cervix:	n/a	chr7:3962091-3962107
50	CTCF	chr7:3962040-3962190	HCT-116	colon:	n/a	chr7:3962091-3962107

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3948024-3948074	HRPEpiC	eye:	n/a
2	chr7:3947798-3947848	AG09319	gingival:	n/a
3	chr7:3982778-3982828	PFSK-1	brain:	n/a
4	chr7:3967516-3967566	AG04449	skin:	fetal
5	chr7:3947798-3947848	PrEC	prostate:	n/a
6	chr7:3962202-3962252	HNPCEpiC	eye:	n/a
7	chr7:3947798-3947848	PANC-1	pancreas:	n/a
8	chr7:3947798-3947848	AoSMC	blood vessel:	n/a
9	chr7:3948024-3948074	H1-hESC	embryonic stem cell:	embryo
10	chr7:3967516-3967566	HCM	heart:	n/a
11	chr7:3962202-3962252	GM19239	blood:	n/a
12	chr7:3967516-3967566	NHBE	bronchial:	n/a
13	chr7:3962202-3962252	GM06990	blood:	n/a
14	chr7:3948024-3948074	RPTEC	kidney:	n/a
15	chr7:3962202-3962252	HL-60	blood:	n/a
16	chr7:3967516-3967566	HIPEpiC	eye:	n/a
17	chr7:3948024-3948074	HEK293	kidney:	embryo
18	chr7:3947798-3947848	HRPEpiC	eye:	n/a
19	chr7:3948024-3948074	ProgFib	skin:	n/a
20	chr7:3982778-3982828	HepG2	liver:	n/a
21	chr7:3962202-3962252	HIPEpiC	eye:	n/a
22	chr7:3948024-3948074	HCM	heart:	n/a
23	chr7:3982778-3982828	HUVEC	blood vessel:	n/a
24	chr7:3948024-3948074	HUVEC	blood vessel:	n/a
25	chr7:3982778-3982828	HNPCEpiC	eye:	n/a
26	chr7:3948024-3948074	NT2-D1	testis:	n/a
27	chr7:3947798-3947848	SKMC	muscle:	n/a
28	chr7:3962202-3962252	GM12892	blood:	n/a
29	chr7:3947798-3947848	HepG2	liver:	n/a
30	chr7:3948024-3948074	U87	brain:	n/a
31	chr7:3948024-3948074	HCPEpiC	choroid plexus:	n/a
32	chr7:3982778-3982828	NHBE	bronchial:	n/a
33	chr7:3967516-3967566	PrEC	prostate:	n/a
34	chr7:3982778-3982828	MCF10A-Er-Src	breast:	n/a
35	chr7:3947798-3947848	HCPEpiC	choroid plexus:	n/a
36	chr7:3962202-3962252	RPTEC	kidney:	n/a
37	chr7:3967516-3967566	SK-N-SH_RA	brain:	n/a
38	chr7:3982778-3982828	HCPEpiC	choroid plexus:	n/a
39	chr7:3962202-3962252	H1-hESC	embryonic stem cell:	embryo
40	chr7:3947798-3947848	BJ	skin:	n/a
41	chr7:3982778-3982828	AG10803	skin:	n/a
42	chr7:3947798-3947848	HNPCEpiC	eye:	n/a
43	chr7:3967516-3967566	SKMC	muscle:	n/a
44	chr7:3967516-3967566	AoSMC	blood vessel:	n/a
45	chr7:3947798-3947848	GM12892	blood:	n/a
46	chr7:3962202-3962252	HRE	kidney:	n/a
47	chr7:3967516-3967566	MCF10A-Er-Src	breast:	n/a
48	chr7:3982778-3982828	HL-60	blood:	n/a
49	chr7:3948024-3948074	HRE	kidney:	n/a
50	chr7:3967516-3967566	SK-N-SH	brain:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3945929..3947531-chr7:3955821..3957556,2	K562	blood:
2	chr7:3970889..3972517-chr7:3996007..3997736,2	K562	blood:
3	chr7:3974845..3976476-chr7:3981172..3983741,2	K562	blood:
4	chr7:3978680..3980412-chr7:3980890..3982919,2	MCF-7	breast:
5	chr7:3958497..3961306-chr7:3966157..3968851,3	K562	blood:
6	chr7:3959798..3963581-chr7:3965288..3967967,3	MCF-7	breast:
7	chr7:3963610..3965143-chr7:3967284..3969432,2	MCF-7	breast:
8	chr7:3945929..3947531-chr7:3955821..3957556,2	K562	blood:
9	chr7:3978680..3980412-chr7:3980890..3982919,2	MCF-7	breast:
10	chr7:3953782..3957860-chr7:3959035..3961864,3	K562	blood:
11	chr7:3958497..3961306-chr7:3967336..3968851,2	K562	blood:
12	chr7:3959798..3963581-chr7:3965288..3967967,3	MCF-7	breast:
13	chr7:3937855..3940563-chr7:3945183..3947294,2	MCF-7	breast:
14	chr7:3978447..3980634-chr7:4022956..4025748,2	K562	blood:
15	chr7:3947932..3950368-chr7:3952794..3955461,2	MCF-7	breast:
16	chr7:3947932..3950368-chr7:3952794..3955461,2	MCF-7	breast:
17	chr7:3965980..3968136-chr7:4044962..4047552,2	K562	blood:
18	chr7:3974845..3976476-chr7:3981172..3983741,2	K562	blood:
19	chr7:3953782..3957860-chr7:3959035..3961864,3	K562	blood:
20	chr7:3959768..3961980-chr7:3963709..3965719,2	K562	blood:
21	chr7:3959768..3961980-chr7:3963709..3965719,2	K562	blood:
22	chr10:76875421..76878006-chr7:3960727..3962572,2	MCF-7	breast:
23	chr7:3963610..3965143-chr7:3967284..3969432,2	MCF-7	breast:
24	chr7:3958497..3961306-chr7:3967336..3968851,2	K562	blood:
25	chr7:3966955..3968724-chr7:3970667..3972517,2	MCF-7	breast:
26	chr7:3958497..3961306-chr7:3966157..3968851,3	K562	blood:
27	chr7:3976851..3979067-chr7:3985021..3987722,2	K562	blood:
28	chr7:3961683..3962198-chr7:4031551..4032127,2	MCF-7	breast:
29	chr7:3973154..3974793-chr7:3987448..3990268,2	K562	blood:
30	chr7:3931415..3933843-chr7:3939844..3942061,2	MCF-7	breast:
31	chr7:3976851..3979067-chr7:3985021..3987722,2	K562	blood:
32	chr7:3966955..3968724-chr7:3970667..3972517,2	MCF-7	breast:

No data

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island

Extended variants
information (count: 2504 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2504 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10245389	chr7:3941203-3941204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532949604	chr7:3941219-3941220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74513596	chr7:3941246-3941247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185580486	chr7:3941275-3941276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188799821	chr7:3941277-3941278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551118955	chr7:3941284-3941285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529316174	chr7:3941287-3941288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549095950	chr7:3941310-3941311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145069645	chr7:3941317-3941318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562368900	chr7:3941339-3941340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537926711	chr7:3941370-3941371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529577935	chr7:3941371-3941372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147556704	chr7:3941372-3941373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541199540	chr7:3941381-3941382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76992655	chr7:3941391-3941392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10479835	chr7:3941435-3941436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs559498620	chr7:3941437-3941438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180775581	chr7:3941440-3941441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370177505	chr7:3941461-3941462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185489596	chr7:3941471-3941472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536279548	chr7:3941508-3941509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141932975	chr7:3941517-3941518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191928872	chr7:3941522-3941523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61080392	chr7:3941535-3941536	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs113101172	chr7:3941547-3941548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10258950	chr7:3941562-3941563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs540808204	chr7:3941566-3941567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560875569	chr7:3941591-3941592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150171379	chr7:3941602-3941603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145596905	chr7:3941604-3941605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373532267	chr7:3941656-3941657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562694700	chr7:3941658-3941659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112058179	chr7:3941659-3941660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569653024	chr7:3941663-3941664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148878028	chr7:3941664-3941665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551498310	chr7:3941689-3941690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10245891	chr7:3941732-3941733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533763381	chr7:3941745-3941746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143550452	chr7:3941771-3941772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567520342	chr7:3941772-3941773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534891711	chr7:3941805-3941806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575969706	chr7:3941848-3941849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536127027	chr7:3941899-3941900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556126309	chr7:3941906-3941907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7783415	chr7:3941919-3941920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs138907924	chr7:3941948-3941949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558714182	chr7:3941969-3941970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572155572	chr7:3941976-3941977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375613524	chr7:3941990-3941991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182223112	chr7:3941992-3941993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Ependymoma	20639864	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3901200-3959600	Weak transcription	Pancreas	Pancrea
2	chr7:3906800-3949000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3936800-3974200	Weak transcription	Aorta	Aorta
4	chr7:3937800-3943400	Weak transcription	Psoas Muscle	Psoas
5	chr7:3939600-3947600	Weak transcription	Brain Substantia Nigra	brain
6	chr7:3940200-3943400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr7:3940600-3953800	Weak transcription	Fetal Brain Male	brain
8	chr7:3942800-3944000	Weak transcription	Fetal Muscle Trunk	muscle
9	chr7:3943400-3943600	Enhancers	Psoas Muscle	Psoas
10	chr7:3943400-3943600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr7:3944000-3944200	Enhancers	Fetal Muscle Trunk	muscle
12	chr7:3944200-3948000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr7:3946400-3948800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:3947000-3947200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:3947200-3951600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:3947400-3948200	Enhancers	Fetal Lung	lung
17	chr7:3947600-3947800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:3947600-3947800	Enhancers	Brain Substantia Nigra	brain
19	chr7:3947800-3948000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:3947800-3948000	Enhancers	Brain Hippocampus Middle	brain
21	chr7:3947800-3948200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:3947800-3948600	Weak transcription	Brain Substantia Nigra	brain
23	chr7:3947800-3949800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:3948000-3949000	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:3948000-3949200	Enhancers	Fetal Muscle Trunk	muscle
26	chr7:3948000-3950600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:3948200-3949000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:3948200-3951400	Weak transcription	Fetal Lung	lung
29	chr7:3948200-3955000	Weak transcription	Spleen	Spleen
30	chr7:3948600-3950000	Enhancers	Brain Substantia Nigra	brain
31	chr7:3948800-3949400	Enhancers	Fetal Muscle Leg	muscle
32	chr7:3948800-3949800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr7:3948800-3950000	Enhancers	Brain Cingulate Gyrus	brain
34	chr7:3948800-3950200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:3948800-3950600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:3948800-3951000	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr7:3948800-3953000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr7:3949000-3949200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:3949000-3949200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:3949000-3949600	Enhancers	Brain Angular Gyrus	brain
41	chr7:3949000-3949800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:3949000-3950000	Enhancers	Brain Anterior Caudate	brain
43	chr7:3949000-3950400	Enhancers	Brain Germinal Matrix	brain
44	chr7:3949000-3950400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:3949000-3951000	Enhancers	Brain Hippocampus Middle	brain
46	chr7:3949000-3951200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:3949200-3950600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:3949200-3950600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr7:3949200-3952200	Weak transcription	Fetal Muscle Trunk	muscle
50	chr7:3949600-3950000	Weak transcription	Brain Angular Gyrus	brain

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