Variant report

Variant	nsv538946
Chromosome Location	chr7:71803570-71854572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:71823147-71823309	K562	blood:	n/a	n/a
2	BRCA1	chr7:71814539-71814706	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:71822928-71823201	HepG2	liver:	n/a	chr7:71823032-71823043
4	CEBPB	chr7:71822855-71823202	K562	blood:	n/a	chr7:71823032-71823043
5	CEBPB	chr7:71826938-71827321	K562	blood:	n/a	n/a
6	CEBPB	chr7:71826906-71827200	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:71828035-71828140	A549	lung:	n/a	n/a
8	CEBPB	chr7:71826949-71827134	A549	lung:	n/a	n/a
9	CTCF	chr7:71837180-71837330	GM12864	blood:	n/a	n/a
10	CTCF	chr7:71812459-71812480	GM12892	blood:	n/a	n/a
11	CTCF	chr7:71812460-71812538	GM12891	blood:	n/a	n/a
12	CTCF	chr7:71809065-71809124	LNCaP	prostate:	n/a	n/a
13	CTCF	chr7:71812471-71812495	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr7:71812471-71812495	MCF-7	breast:	n/a	n/a
15	CTCF	chr7:71812432-71812542	MCF-7	breast:	n/a	n/a
16	CTCF	chr7:71812376-71812555	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:71812459-71812496	ProgFib	skin:	n/a	n/a
18	CTCF	chr7:71812458-71812549	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:71804716-71804800	GM20000	blood:	n/a	n/a
20	CTCF	chr7:71812417-71812455	MCF-7	breast:	n/a	n/a
21	CUX1	chr7:71818593-71818598	K562	blood:	n/a	n/a
22	E2F4	chr7:71828051-71828227	MCF10A-Er-Src	breast:	n/a	n/a
23	GABPA	chr7:71803226-71803657	MCF-7	breast:	n/a	n/a
24	GATA3	chr7:71825067-71825218	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr7:71837283-71837705	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr7:71839664-71839736	SH-SY5Y	brain:	n/a	n/a
27	IRF1	chr7:71828478-71828705	K562	blood:	n/a	chr7:71828613-71828630 chr7:71828612-71828625 chr7:71828612-71828625 chr7:71828612-71828625 chr7:71828614-71828624 chr7:71828611-71828625 chr7:71828610-71828624 chr7:71828614-71828625 chr7:71828615-71828626
28	IRF1	chr7:71828515-71828799	K562	blood:	n/a	chr7:71828613-71828630 chr7:71828612-71828625 chr7:71828612-71828625 chr7:71828612-71828625 chr7:71828614-71828624 chr7:71828611-71828625 chr7:71828610-71828624 chr7:71828614-71828625 chr7:71828615-71828626
29	JUN	chr7:71813495-71813540	H1-hESC	embryonic stem cell:	n/a	n/a
30	JUND	chr7:71822984-71823138	K562	blood:	n/a	n/a
31	JUND	chr7:71822147-71822154	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAFF	chr7:71851184-71851490	K562	blood:	n/a	chr7:71851333-71851351
33	MAFF	chr7:71817490-71817690	HepG2	liver:	n/a	n/a
34	MAFF	chr7:71851176-71851485	HepG2	liver:	n/a	chr7:71851333-71851351
35	MAFK	chr7:71851244-71851479	H1-hESC	embryonic stem cell:	n/a	chr7:71851335-71851350
36	MAFK	chr7:71851198-71851486	HepG2	liver:	n/a	chr7:71851335-71851350
37	MAFK	chr7:71817477-71817717	HepG2	liver:	n/a	n/a
38	MAFK	chr7:71851257-71851517	K562	blood:	n/a	chr7:71851335-71851350
39	MAFK	chr7:71851167-71851504	HepG2	liver:	n/a	chr7:71851335-71851350
40	MAFK	chr7:71817513-71817677	HepG2	liver:	n/a	n/a
41	MAFK	chr7:71851165-71851499	IMR90	lung:	n/a	chr7:71851335-71851350
42	MXI1	chr7:71829482-71829531	GM12878	blood:	n/a	n/a
43	MYC	chr7:71812333-71812601	MCF-7	breast:	n/a	n/a
44	MYC	chr7:71812357-71812624	MCF-7	breast:	n/a	n/a
45	MYC	chr7:71812387-71812564	MCF-7	breast:	n/a	n/a
46	MYC	chr7:71812458-71812495	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr7:71854363-71854445	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr7:71809182-71809325	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr7:71812360-71812495	Gliobla	brain:	n/a	n/a
50	POLR2A	chr7:71825351-71825413	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71806067-71806117	A549	lung:	n/a
2	chr7:71806067-71806117	HRPEpiC	eye:	n/a
3	chr7:71806067-71806117	SKMC	muscle:	n/a
4	chr7:71806067-71806117	HRCEpiC	kidney:	n/a
5	chr7:71806067-71806117	LNCaP	prostate:	n/a
6	chr7:71806067-71806117	IMR90	lung:	fetal
7	chr7:71806067-71806117	NB4	blood:	n/a
8	chr7:71806067-71806117	GM06990	blood:	n/a
9	chr7:71806067-71806117	Hela-S3	cervix:	n/a
10	chr7:71806067-71806117	AG04449	skin:	fetal
11	chr7:71806067-71806117	T-47D	breast:	n/a
12	chr7:71806067-71806117	SAEC	small airway:	n/a
13	chr7:71806067-71806117	HCT-116	colon:	n/a
14	chr7:71806067-71806117	H1-hESC	embryonic stem cell:	embryo
15	chr7:71806067-71806117	NHBE	bronchial:	n/a
16	chr7:71806067-71806117	NT2-D1	testis:	n/a
17	chr7:71806067-71806117	Caco-2	colon:	n/a
18	chr7:71806067-71806117	HCF	heart:	n/a
19	chr7:71806067-71806117	HL-60	blood:	n/a
20	chr7:71806067-71806117	K562	blood:	n/a
21	chr7:71806067-71806117	Jurkat	blood:	n/a
22	chr7:71806067-71806117	SK-N-SH_RA	brain:	n/a
23	chr7:71806067-71806117	Hepatocyte	liver:	n/a
24	chr7:71806067-71806117	SK-N-SH	brain:	n/a
25	chr7:71806067-71806117	GM12878	blood:	n/a
26	chr7:71806067-71806117	NH-A	brain:	n/a
27	chr7:71806067-71806117	BJ	skin:	n/a
28	chr7:71806067-71806117	U87	brain:	n/a
29	chr7:71806067-71806117	GM19239	blood:	n/a
30	chr7:71806067-71806117	ECC-1	luminal epithelium:	n/a
31	chr7:71806067-71806117	HIPEpiC	eye:	n/a
32	chr7:71806067-71806117	RPTEC	kidney:	n/a
33	chr7:71806067-71806117	NHDF-neo	bronchial:	n/a
34	chr7:71806067-71806117	PrEC	prostate:	n/a
35	chr7:71806067-71806117	PFSK-1	brain:	n/a
36	chr7:71806067-71806117	ovcar-3	ovarian:	n/a
37	chr7:71806067-71806117	BE2_C	brain:	n/a
38	chr7:71806067-71806117	PANC-1	pancreas:	n/a
39	chr7:71806067-71806117	HepG2	liver:	n/a
40	chr7:71806067-71806117	MCF-7	breast:	n/a
41	chr7:71806067-71806117	ProgFib	skin:	n/a
42	chr7:71806067-71806117	AG09319	gingival:	n/a
43	chr7:71806067-71806117	HCPEpiC	choroid plexus:	n/a
44	chr7:71806067-71806117	GM12891	blood:	n/a
45	chr7:71806067-71806117	HCM	heart:	n/a
46	chr7:71806067-71806117	SK-N-MC	brain:	n/a
47	chr7:71806067-71806117	AG10803	skin:	n/a
48	chr7:71806067-71806117	HEK293	kidney:	embryo
49	chr7:71806067-71806117	HEEpiC	esophagus:	n/a
50	chr7:71806067-71806117	MCF10A-Er-Src	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:71806092..71808807-chr7:71850228..71852499,2	K562	blood:
2	chr7:71804343..71806702-chr7:71808239..71810092,2	K562	blood:
3	chr7:71838948..71841718-chr7:71841980..71845073,3	K562	blood:
4	chr7:71835115..71837488-chr7:71840184..71842880,2	K562	blood:
5	chr7:71810202..71812135-chr7:71814451..71816672,2	K562	blood:
6	chr7:71800589..71802149-chr7:71805434..71807505,2	K562	blood:
7	chr7:71851405..71854103-chr7:71858001..71860587,2	MCF-7	breast:
8	chr7:71835115..71837488-chr7:71840184..71842880,2	K562	blood:
9	chr7:71804343..71806702-chr7:71808239..71810092,2	K562	blood:
10	chr7:71806092..71808807-chr7:71850228..71852499,2	K562	blood:
11	chr3:149645275..149646111-chr7:71851509..71852107,2	MCF-7	breast:
12	chr7:71810202..71812135-chr7:71814451..71816672,2	K562	blood:
13	chr7:71838948..71841718-chr7:71841980..71845073,3	K562	blood:

No data

Variant related genes	Relation type
CALN1	TF binding region
CALN1	CpG island
ENSG00000183166	chromatin interactions

Extended variants
information (count: 678 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377615544	chr7:71803572-71803573	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs186049491	chr7:71803573-71803574	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs530611601	chr7:71803590-71803591	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs544444108	chr7:71803643-71803644	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs562772916	chr7:71803648-71803649	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs13307517	chr7:71803683-71803684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs533071390	chr7:71803698-71803699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551532195	chr7:71803728-71803729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111754045	chr7:71803751-71803752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114464919	chr7:71803761-71803762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75829232	chr7:71803839-71803840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575946391	chr7:71803888-71803889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113269740	chr7:71803889-71803890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537821507	chr7:71803963-71803964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555904525	chr7:71803985-71803986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371814033	chr7:71804000-71804001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190792485	chr7:71804036-71804037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538990022	chr7:71804041-71804042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182273923	chr7:71804050-71804051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377295012	chr7:71804073-71804074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572715937	chr7:71804084-71804085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543251451	chr7:71804086-71804087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528448377	chr7:71804092-71804093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576480647	chr7:71804107-71804108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543784829	chr7:71804115-71804116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187237031	chr7:71804151-71804152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115002890	chr7:71804152-71804153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545015863	chr7:71804162-71804163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12539798	chr7:71804170-71804171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560027888	chr7:71804173-71804174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376414660	chr7:71804202-71804203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191167256	chr7:71804217-71804218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548383978	chr7:71804301-71804302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147767019	chr7:71804325-71804326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372744742	chr7:71804330-71804331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377132227	chr7:71804384-71804385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549726254	chr7:71804422-71804423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571198822	chr7:71804438-71804439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141141676	chr7:71804541-71804542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546667841	chr7:71804567-71804568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568586718	chr7:71804601-71804602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71515107	chr7:71804660-71804661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554465033	chr7:71804677-71804678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566379109	chr7:71804698-71804699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537202780	chr7:71804703-71804704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557541607	chr7:71804726-71804727	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs555216260	chr7:71804738-71804739	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs571124893	chr7:71804787-71804788	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs182948983	chr7:71804832-71804833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543600837	chr7:71804844-71804845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Williams Syndrome	16773131	CNVD
Breast cancer	16417655	CNVD
Rheumatoid arthritis	21728841	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Williams Syndrome	16617304	CNVD
Williams Syndrome	20206275	CNVD
Williams Syndrome	16199537	CNVD
Williams Syndrome	18923514	CNVD
Williams Syndrome	20970697	CNVD
Williams-beuren syndrome	20926892	CNVD
Williams-beuren syndrome	21808859	CNVD
periventricular nodular heterotopia	20648244	CNVD
Williams Syndrome	20425783	CNVD
Williams-beuren syndrome	22226172	CNVD
Williams-beuren syndrome	18923513	CNVD
Williams-beuren syndrome	17565757	CNVD
Williams-beuren syndrome	18787571	CNVD
Williams Syndrome	22241247	CNVD
Autism	21686962	CNVD
Autism	20970697	CNVD
Epilepsy	22118685	CNVD
Epilepsy	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21686962	CNVD
Schizophrenia	22118685	CNVD
Williams-beuren syndrome	18337728	CNVD
language delay	21686962	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
Mental retardation	16773131	CNVD
Colorectal cancer	19455253	CNVD
Williams-beuren syndrome	16971481	CNVD
Idiopathic infantile hypercalcaemia	20466674	CNVD
Williams Syndrome	18308711	CNVD
Williams Syndrome	19255058	CNVD
Williams Syndrome	18924169	CNVD
Williams Syndrome	21939500	CNVD
Williams Syndrome	20425784	CNVD
Williams Syndrome	22241097	CNVD
Williams Syndrome	19176822	CNVD
Williams Syndrome	17505701	CNVD
Supravalvular aortic stenosis	19844261	CNVD
Williams Syndrome	16760918	CNVD
Williams-beuren syndrome	18452001	CNVD
Williams-beuren syndrome	19880526	CNVD
Autism	17666889	CNVD
speech delay	17666889	CNVD
Metanephric adenoma	20802469	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71803000-71803600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
2	chr7:71803000-71803600	Bivalent Enhancer	Fetal Brain Male	brain
3	chr7:71803000-71803600	Enhancers	Pancreas	Pancrea
4	chr7:71803000-71812800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:71803400-71803600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:71803400-71803600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:71803400-71803600	Bivalent Enhancer	Fetal Thymus	thymus
8	chr7:71803400-71803600	Active TSS	Thymus	Thymus
9	chr7:71803600-71807000	Weak transcription	Thymus	Thymus
10	chr7:71803600-71807400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:71803600-71808200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:71807000-71807600	Enhancers	Thymus	Thymus
13	chr7:71807200-71810800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:71807400-71807800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:71808000-71808200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr7:71808000-71810400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:71808200-71808800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr7:71808200-71809000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:71808200-71809000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr7:71808400-71809000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:71808600-71809200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:71808600-71809400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr7:71808600-71809400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:71808600-71809600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:71808600-71809600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr7:71808600-71809800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr7:71808800-71809000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr7:71808800-71809000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:71809000-71813400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr7:71809200-71813800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:71809600-71813200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr7:71809600-71813600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:71809800-71810200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr7:71810200-71810400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr7:71810400-71813400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr7:71810400-71813800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr7:71812800-71813400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:71813200-71813400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr7:71813200-71814200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:71813400-71814000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:71813400-71814200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:71813400-71814600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr7:71813600-71814200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr7:71813600-71814400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:71813800-71814000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr7:71813800-71814000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:71814000-71814400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr7:71814000-71814400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:71814200-71814800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr7:71814400-71814800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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