Variant report

Variant	nsv888278
Chromosome Location	chr7:64048473-64139463
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1447)
CpG islands
(count:856)
Chromatin interactive
region (count:19)
LncRNA
region (count:33)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1447 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:64126331-64126433	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:64090841-64091296	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:64085518-64085801	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:64085532-64085845	K562	blood:	n/a	n/a
5	ARID3A	chr7:64087022-64087310	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:64082157-64082263	K562	blood:	n/a	n/a
7	ATF1	chr7:64079602-64079802	K562	blood:	n/a	n/a
8	ATF1	chr7:64126244-64126581	K562	blood:	n/a	n/a
9	ATF2	chr7:64126148-64126755	GM12878	blood:	n/a	n/a
10	ATF2	chr7:64129018-64129462	GM12878	blood:	n/a	n/a
11	BACH1	chr7:64126554-64126563	K562	blood:	n/a	n/a
12	BACH1	chr7:64111281-64111597	K562	blood:	n/a	n/a
13	BATF	chr7:64086454-64086733	GM12878	blood:	n/a	n/a
14	BATF	chr7:64129056-64129326	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:64126417-64126836	GM12878	blood:	n/a	n/a
16	BCLAF1	chr7:64126744-64127203	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:64111281-64111651	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:64126241-64126572	K562	blood:	n/a	n/a
19	BHLHE40	chr7:64086181-64086649	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:64090919-64091317	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:64126247-64126744	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:64114553-64114722	K562	blood:	n/a	n/a
23	BHLHE40	chr7:64111277-64111654	K562	blood:	n/a	n/a
24	BRCA1	chr7:64111281-64111647	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:64126528-64126665	HepG2	liver:	n/a	n/a
26	BRCA1	chr7:64111281-64111656	GM12878	blood:	n/a	n/a
27	BRCA1	chr7:64126297-64126616	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr7:64126174-64126859	K562	blood:	n/a	n/a
29	CCNT2	chr7:64126367-64126575	K562	blood:	n/a	n/a
30	CEBPB	chr7:64117378-64117570	K562	blood:	n/a	n/a
31	CEBPB	chr7:64119843-64120108	A549	lung:	n/a	n/a
32	CEBPB	chr7:64073938-64075089	A549	lung:	n/a	n/a
33	CEBPB	chr7:64064514-64064738	K562	blood:	n/a	chr7:64064632-64064643
34	CEBPB	chr7:64059756-64060129	K562	blood:	n/a	n/a
35	CEBPB	chr7:64126225-64126697	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:64096087-64096609	IMR90	lung:	n/a	chr7:64096259-64096270
37	CEBPB	chr7:64079487-64079851	K562	blood:	n/a	n/a
38	CEBPB	chr7:64097160-64097419	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:64101085-64101259	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr7:64097057-64097707	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:64063838-64064250	HepG2	liver:	n/a	chr7:64064053-64064064
42	CEBPB	chr7:64098067-64099109	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:64079528-64079817	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:64097099-64097460	A549	lung:	n/a	n/a
45	CEBPB	chr7:64095075-64095363	IMR90	lung:	n/a	chr7:64095206-64095217
46	CEBPB	chr7:64104062-64104228	K562	blood:	n/a	n/a
47	CEBPB	chr7:64072154-64072613	MCF-7	breast:	n/a	chr7:64072406-64072417
48	CEBPB	chr7:64111281-64112440	A549	lung:	n/a	n/a
49	CEBPB	chr7:64093712-64094175	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:64093640-64094200	MCF-7	breast:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64138755-64138805	NHBE	bronchial:	n/a
2	chr7:64125557-64125607	NH-A	brain:	n/a
3	chr7:64138755-64138805	NHBE	bronchial:	n/a
4	chr7:64125557-64125607	NH-A	brain:	n/a
5	chr7:64126140-64126190	HL-60	blood:	n/a
6	chr7:64127516-64127566	U87	brain:	n/a
7	chr7:64125557-64125607	Hela-S3	cervix:	n/a
8	chr7:64126532-64126582	PANC-1	pancreas:	n/a
9	chr7:64126779-64126829	NB4	blood:	n/a
10	chr7:64126456-64126506	SK-N-MC	brain:	n/a
11	chr7:64126532-64126582	AoSMC	blood vessel:	n/a
12	chr7:64126742-64126792	PANC-1	pancreas:	n/a
13	chr7:64126456-64126506	H1-hESC	embryonic stem cell:	embryo
14	chr7:64126944-64126994	HIPEpiC	eye:	n/a
15	chr7:64138755-64138805	MCF-7	breast:	n/a
16	chr7:64126809-64126859	HepG2	liver:	n/a
17	chr7:64126532-64126582	HRE	kidney:	n/a
18	chr7:64126456-64126506	SK-N-SH_RA	brain:	n/a
19	chr7:64129143-64129193	GM12891	blood:	n/a
20	chr7:64126742-64126792	LNCaP	prostate:	n/a
21	chr7:64126140-64126190	MCF-7	breast:	n/a
22	chr7:64125401-64125451	H1-hESC	embryonic stem cell:	embryo
23	chr7:64125580-64125630	K562	blood:	n/a
24	chr7:64129143-64129193	SK-N-SH	brain:	n/a
25	chr7:64126944-64126994	GM12891	blood:	n/a
26	chr7:64126532-64126582	LNCaP	prostate:	n/a
27	chr7:64126809-64126859	AG04449	skin:	fetal
28	chr7:64125580-64125630	Hepatocyte	liver:	n/a
29	chr7:64129143-64129193	Jurkat	blood:	n/a
30	chr7:64126779-64126829	GM19239	blood:	n/a
31	chr7:64126456-64126506	HIPEpiC	eye:	n/a
32	chr7:64125557-64125607	SK-N-SH	brain:	n/a
33	chr7:64126470-64126520	GM12878	blood:	n/a
34	chr7:64138755-64138805	AG10803	skin:	n/a
35	chr7:64126944-64126994	H1-hESC	embryonic stem cell:	embryo
36	chr7:64125557-64125607	AG09319	gingival:	n/a
37	chr7:64126779-64126829	CMK	blood:	n/a
38	chr7:64126944-64126994	SAEC	small airway:	n/a
39	chr7:64126779-64126829	HRPEpiC	eye:	n/a
40	chr7:64125401-64125451	MCF-7	breast:	n/a
41	chr7:64126456-64126506	ECC-1	luminal epithelium:	n/a
42	chr7:64127516-64127566	HRPEpiC	eye:	n/a
43	chr7:64126140-64126190	GM06990	blood:	n/a
44	chr7:64126532-64126582	NB4	blood:	n/a
45	chr7:64126456-64126506	HEEpiC	esophagus:	n/a
46	chr7:64126809-64126859	HIPEpiC	eye:	n/a
47	chr7:64138755-64138805	NT2-D1	testis:	n/a
48	chr7:64126944-64126994	AoSMC	blood vessel:	n/a
49	chr7:64125580-64125630	RPTEC	kidney:	n/a
50	chr7:64127516-64127566	AG09319	gingival:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:64130443..64133428-chr7:64253798..64256248,4	MCF-7	breast:
2	chr7:64059458..64060477-chr7:64099321..64100139,7	MCF-7	breast:
3	chr7:64059558..64060118-chr7:64071550..64072484,4	MCF-7	breast:
4	chr7:64133042..64135869-chr7:64139508..64142679,3	K562	blood:
5	chr7:63774283..63776835-chr7:64075332..64078268,2	MCF-7	breast:
6	chr7:64059389..64060099-chr7:64099412..64099918,2	MCF-7	breast:
7	chr7:64133042..64135798-chr7:64140855..64142679,2	K562	blood:
8	chr7:64099496..64100069-chr7:64350429..64351249,2	MCF-7	breast:
9	chr7:64059458..64060477-chr7:64099321..64100040,3	MCF-7	breast:
10	chr7:64059389..64060099-chr7:64099412..64099918,2	MCF-7	breast:
11	chr7:64059458..64060477-chr7:64099321..64100139,7	MCF-7	breast:
12	chr7:64115402..64117141-chr7:64125488..64128451,2	MCF-7	breast:
13	chr7:64059558..64060118-chr7:64071550..64072484,4	MCF-7	breast:
14	chr7:64059458..64060477-chr7:64099321..64100040,3	MCF-7	breast:
15	chr7:64125646..64128378-chr7:64129230..64132337,4	K562	blood:
16	chr7:64126083..64128264-chr7:64130876..64132561,2	K562	blood:
17	chr7:64126311..64128257-chr7:64129298..64130838,2	MCF-7	breast:
18	chr19:23941209..23941866-chr7:64126456..64127217,2	Hela-S3	cervix:
19	chr7:64096183..64096701-chr8:43095392..43095917,3	MCF-7	breast:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF107-1	chr7:64115544-64115592	XLOC_006128
2	lnc-ZNF107-2	chr7:64072804-64073166	XLOC_006126
3	lnc-ZNF138-3	chr7:64129415-64129556	NR_104148
4	lnc-ZNF138-3	chr7:64126461-64126663	NR_104149
5	lnc-ZNF107-2	chr7:64071556-64071580	NONHSAT121030
6	lnc-ZNF680-14	chr7:64139332-64139425	NONHSAT121037
7	lnc-ZNF107-2	chr7:64072804-64072950	NONHSAT121032
8	lnc-ZNF107-2	chr7:64080388-64080834	NONHSAT121030
9	lnc-ZNF107-2	chr7:64072128-64072225	XLOC_006126
10	lnc-ZNF107-2	chr7:64073798-64074198	XLOC_006126
11	lnc-ZNF107-2	chr7:64074198-64074708	NONHSAT121033
12	lnc-ZNF107-1	chr7:64115544-64116152	XLOC_006128
13	lnc-ZNF107-1	chr7:64103412-64103809	XLOC_006128
14	lnc-ZNF107-2	chr7:64074527-64074708	NONHSAT121030
15	lnc-ZNF107-2	chr7:64072804-64072950	NONHSAT121029
16	lnc-ZNF107-2	chr7:64074877-64078967	NONHSAT121025
17	lnc-ZNF107-3	chr7:64064186-64064418	NONHSAT121028
18	lnc-ZNF107-2	chr7:64068567-64068736	NONHSAT121029
19	lnc-ZNF107-2	chr7:64074877-64075201	NONHSAT121032
20	lnc-ZNF107-3	chr7:64060773-64060819	NONHSAT121028
21	lnc-ZNF107-2	chr7:64074877-64075201	NONHSAT121029
22	lnc-ZNF107-2	chr7:64060037-64060160	NONHSAT121025
23	lnc-ZNF107-1	chr7:64115544-64116147	NONHSAT121036
24	lnc-ZNF107-3	chr7:64063937-64064007	NONHSAT121028
25	lnc-ZNF107-2	chr7:64072804-64072950	NONHSAT121030
26	lnc-ZNF138-3	chr7:64126461-64126663	NR_104148
27	lnc-ZNF107-1	chr7:64112335-64112385	NONHSAT121036
28	lnc-ZNF107-1	chr7:64103960-64104051	XLOC_006128
29	lnc-ZNF107-1	chr7:64115771-64116285	XLOC_006128
30	lnc-ZNF107-2	chr7:64072165-64072225	NONHSAT121032
31	lnc-ZNF107-2	chr7:64074877-64074966	NONHSAT121030
32	lnc-ZNF107-3	chr7:64063683-64063783	NONHSAT121028
33	lnc-ZNF107-2	chr7:64074877-64075201	NONHSAT121033

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6839-5p	chr7:64139447-64139468	MIMAT0027580

No data

Variant related genes	Relation type
ZNF107	TF binding region
ZNF107	CpG island
ENSG00000189316	chromatin interactions
ENSG00000234444	chromatin interactions
ENSG00000196172	chromatin interactions
ENSG00000196247	chromatin interactions
ENSG00000197008	chromatin interactions
SHC1	miRNA target sites

Extended variants
information (count: 2861 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2861 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6460169	chr7:64048473-64048474	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571148596	chr7:64048557-64048558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552007709	chr7:64048581-64048582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562553886	chr7:64048592-64048593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143180068	chr7:64048607-64048608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185344796	chr7:64048651-64048652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201233788	chr7:64048707-64048708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568409179	chr7:64048731-64048732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534061134	chr7:64048732-64048733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547648378	chr7:64048735-64048736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570678127	chr7:64048740-64048741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561519322	chr7:64048743-64048744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375398209	chr7:64048752-64048753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556386728	chr7:64048770-64048771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576442145	chr7:64048786-64048787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535522040	chr7:64048789-64048790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542312003	chr7:64048801-64048802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555339825	chr7:64048814-64048815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572438943	chr7:64048821-64048822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369992510	chr7:64048846-64048847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138734042	chr7:64048857-64048858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564410846	chr7:64048873-64048874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531168550	chr7:64048883-64048884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551264764	chr7:64048886-64048887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564808709	chr7:64048901-64048902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543953202	chr7:64048902-64048903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562482113	chr7:64048911-64048912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189718403	chr7:64048921-64048922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547902549	chr7:64048935-64048936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527495067	chr7:64048936-64048937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547309474	chr7:64048941-64048942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs180704036	chr7:64048971-64048972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185925121	chr7:64048980-64048981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536389677	chr7:64048990-64048991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550285262	chr7:64048995-64048996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201975559	chr7:64048996-64048997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192507237	chr7:64049080-64049081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528685488	chr7:64049129-64049130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570098527	chr7:64049152-64049153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10264743	chr7:64049155-64049156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs113224919	chr7:64049196-64049197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572130124	chr7:64049220-64049221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534653155	chr7:64049250-64049251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56956695	chr7:64049254-64049255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370999243	chr7:64049275-64049276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141854193	chr7:64049290-64049291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78339363	chr7:64049316-64049317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80229260	chr7:64049341-64049342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148046991	chr7:64049401-64049402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535306257	chr7:64049427-64049428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:885 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64039400-64064000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:64046000-64059400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:64051400-64051600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:64051600-64051800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:64051800-64054600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:64054600-64054800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:64055000-64055600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:64059000-64065800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:64059200-64076200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr7:64059400-64059600	Weak transcription	Fetal Brain Female	brain
11	chr7:64059400-64076400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:64059600-64060600	Enhancers	Placenta	Placenta
13	chr7:64059600-64067400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr7:64059800-64063800	Weak transcription	Fetal Brain Female	brain
15	chr7:64060600-64064200	Weak transcription	Placenta	Placenta
16	chr7:64062600-64062800	Enhancers	Fetal Heart	heart
17	chr7:64062800-64077400	Weak transcription	Fetal Heart	heart
18	chr7:64063200-64064800	Weak transcription	Fetal Stomach	stomach
19	chr7:64064000-64064600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr7:64064200-64065400	Enhancers	Placenta	Placenta
21	chr7:64064600-64068400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr7:64064800-64065400	Strong transcription	Fetal Stomach	stomach
23	chr7:64065400-64069400	Weak transcription	Placenta	Placenta
24	chr7:64065400-64076800	Weak transcription	Fetal Stomach	stomach
25	chr7:64065800-64066000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:64066000-64066200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:64066200-64073000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:64068400-64069200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr7:64068400-64073200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr7:64069200-64075200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:64069400-64075800	Enhancers	Placenta	Placenta
32	chr7:64072400-64073600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
33	chr7:64073200-64073600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:64075400-64079400	Weak transcription	Brain Substantia Nigra	brain
35	chr7:64076400-64077400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:64079200-64081200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:64079400-64079600	Enhancers	Brain Substantia Nigra	brain
38	chr7:64079400-64080200	ZNF genes & repeats	Brain Angular Gyrus	brain
39	chr7:64086000-64086400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:64086600-64087800	Enhancers	HepG2	liver
41	chr7:64087000-64087200	Enhancers	Liver	Liver
42	chr7:64087400-64089000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr7:64087800-64089000	Weak transcription	HepG2	liver
44	chr7:64088200-64089400	Enhancers	Placenta	Placenta
45	chr7:64088800-64089400	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr7:64089000-64089600	Enhancers	Liver	Liver
47	chr7:64089000-64090200	Enhancers	HepG2	liver
48	chr7:64089000-64091000	Enhancers	Brain Substantia Nigra	brain
49	chr7:64089200-64089400	Enhancers	Brain Hippocampus Middle	brain
50	chr7:64089400-64097200	Weak transcription	Placenta	Placenta

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