Variant report

Variant	nsv1018050
Chromosome Location	chr7:70320604-70594940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:758)
CpG islands
(count:798)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:70473461-70473667	K562	blood:	n/a	n/a
2	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70321901-70322317	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70359196-70359849	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:70384908-70384986	K562	blood:	n/a	n/a
7	BACH1	chr7:70578379-70578450	K562	blood:	n/a	n/a
8	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr7:70359245-70359587	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr7:70470205-70470386	K562	blood:	n/a	n/a
11	BHLHE40	chr7:70482560-70482896	K562	blood:	n/a	n/a
12	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
13	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
14	BHLHE40	chr7:70498977-70499038	K562	blood:	n/a	n/a
15	CBX3	chr7:70538895-70539134	K562	blood:	n/a	n/a
16	CBX3	chr7:70515518-70515757	K562	blood:	n/a	n/a
17	CBX3	chr7:70482488-70483015	K562	blood:	n/a	n/a
18	CCNT2	chr7:70543176-70543345	K562	blood:	n/a	n/a
19	CEBPB	chr7:70488397-70488574	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:70520536-70520878	MCF-7	breast:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
21	CEBPB	chr7:70520490-70520869	K562	blood:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
22	CEBPB	chr7:70528607-70528917	IMR90	lung:	n/a	chr7:70528754-70528765
23	CEBPB	chr7:70426400-70426506	A549	lung:	n/a	n/a
24	CEBPB	chr7:70520499-70520875	HepG2	liver:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
25	CEBPB	chr7:70536265-70536412	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:70528604-70528901	A549	lung:	n/a	chr7:70528754-70528765
27	CEBPB	chr7:70518584-70518708	A549	lung:	n/a	n/a
28	CEBPB	chr7:70443503-70443748	HepG2	liver:	n/a	chr7:70443649-70443660 chr7:70443597-70443608
29	CEBPB	chr7:70477923-70478050	HepG2	liver:	n/a	chr7:70477953-70477964
30	CEBPB	chr7:70473682-70474054	K562	blood:	n/a	n/a
31	CEBPB	chr7:70388372-70388507	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr7:70518557-70518568	K562	blood:	n/a	n/a
33	CEBPB	chr7:70491156-70491389	HepG2	liver:	n/a	chr7:70491297-70491308
34	CEBPB	chr7:70473715-70474044	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:70520567-70520872	H1-hESC	embryonic stem cell:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
36	CEBPB	chr7:70582974-70583308	HepG2	liver:	n/a	chr7:70583233-70583242 chr7:70583231-70583242 chr7:70583012-70583025
37	CEBPB	chr7:70473679-70474025	MCF-7	breast:	n/a	n/a
38	CEBPB	chr7:70528617-70528925	HepG2	liver:	n/a	chr7:70528754-70528765
39	CEBPB	chr7:70520499-70520883	A549	lung:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
40	CEBPB	chr7:70473685-70474059	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:70477784-70478010	H1-hESC	embryonic stem cell:	n/a	chr7:70477953-70477964
42	CEBPB	chr7:70520515-70520867	IMR90	lung:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
43	CEBPB	chr7:70473695-70474052	A549	lung:	n/a	n/a
44	CEBPB	chr7:70583176-70583266	K562	blood:	n/a	chr7:70583233-70583242 chr7:70583231-70583242
45	CEBPB	chr7:70528739-70528775	H1-hESC	embryonic stem cell:	n/a	chr7:70528754-70528765
46	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
47	CEBPB	chr7:70477839-70478111	IMR90	lung:	n/a	chr7:70477953-70477964
48	CEBPB	chr7:70536360-70536397	K562	blood:	n/a	n/a
49	CEBPB	chr7:70528726-70528794	K562	blood:	n/a	chr7:70528754-70528765
50	CEBPB	chr7:70520613-70520780	K562	blood:	n/a	chr7:70520680-70520691 chr7:70520691-70520702

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70543320-70543370	MCF-7	breast:	n/a
2	chr7:70577170-70577220	BE2_C	brain:	n/a
3	chr7:70482891-70482941	IMR90	lung:	fetal
4	chr7:70543490-70543540	AoSMC	blood vessel:	n/a
5	chr7:70482891-70482941	HEEpiC	esophagus:	n/a
6	chr7:70543320-70543370	MCF-7	breast:	n/a
7	chr7:70577170-70577220	BE2_C	brain:	n/a
8	chr7:70482891-70482941	IMR90	lung:	fetal
9	chr7:70543490-70543540	AoSMC	blood vessel:	n/a
10	chr7:70482891-70482941	HEEpiC	esophagus:	n/a
11	chr7:70543079-70543129	K562	blood:	n/a
12	chr7:70543490-70543540	U87	brain:	n/a
13	chr7:70543079-70543129	HCPEpiC	choroid plexus:	n/a
14	chr7:70482891-70482941	SAEC	small airway:	n/a
15	chr7:70561125-70561175	BE2_C	brain:	n/a
16	chr7:70322401-70322451	HCPEpiC	choroid plexus:	n/a
17	chr7:70417419-70417469	HNPCEpiC	eye:	n/a
18	chr7:70577170-70577220	SK-N-MC	brain:	n/a
19	chr7:70543800-70543850	Hepatocyte	liver:	n/a
20	chr7:70482771-70482821	GM12892	blood:	n/a
21	chr7:70543079-70543129	HNPCEpiC	eye:	n/a
22	chr7:70482771-70482821	K562	blood:	n/a
23	chr7:70359655-70359705	HL-60	blood:	n/a
24	chr7:70592898-70592948	HCF	heart:	n/a
25	chr7:70543079-70543129	HAEpiC	amniotic membrane:	n/a
26	chr7:70543079-70543129	HCT-116	colon:	n/a
27	chr7:70577170-70577220	MCF10A-Er-Src	breast:	n/a
28	chr7:70417419-70417469	AG09319	gingival:	n/a
29	chr7:70322401-70322451	H1-hESC	embryonic stem cell:	embryo
30	chr7:70417419-70417469	AoSMC	blood vessel:	n/a
31	chr7:70359655-70359705	HRE	kidney:	n/a
32	chr7:70359655-70359705	HAEpiC	amniotic membrane:	n/a
33	chr7:70322401-70322451	RPTEC	kidney:	n/a
34	chr7:70322401-70322451	HCF	heart:	n/a
35	chr7:70543320-70543370	HCT-116	colon:	n/a
36	chr7:70543320-70543370	Hela-S3	cervix:	n/a
37	chr7:70417419-70417469	HEK293	kidney:	embryo
38	chr7:70592898-70592948	H1-hESC	embryonic stem cell:	embryo
39	chr7:70482891-70482941	ovcar-3	ovarian:	n/a
40	chr7:70322401-70322451	PrEC	prostate:	n/a
41	chr7:70543079-70543129	AG09309	skin:	n/a
42	chr7:70543490-70543540	HCT-116	colon:	n/a
43	chr7:70561125-70561175	HL-60	blood:	n/a
44	chr7:70543079-70543129	SK-N-MC	brain:	n/a
45	chr7:70543605-70543655	GM06990	blood:	n/a
46	chr7:70543320-70543370	NHBE	bronchial:	n/a
47	chr7:70592898-70592948	SK-N-SH	brain:	n/a
48	chr7:70543490-70543540	HIPEpiC	eye:	n/a
49	chr7:70322401-70322451	IMR90	lung:	fetal
50	chr7:70592898-70592948	HIPEpiC	eye:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
2	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
3	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
4	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
5	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
6	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
7	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
8	chr7:70574285..70576318-chr7:70581134..70583277,2	K562	blood:
9	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
10	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
11	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
12	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
13	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
14	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
15	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
16	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
17	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
18	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
19	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
20	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
21	chr7:70574285..70576318-chr7:70581134..70583277,2	K562	blood:
22	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:

No data

Variant related genes	Relation type
WBSCR17	TF binding region
WBSCR17	CpG island

Extended variants
information (count: 7451 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7451 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138690658	chr7:70320632-70320633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542306279	chr7:70320645-70320646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141717290	chr7:70320656-70320657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551576427	chr7:70320694-70320695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113304053	chr7:70320702-70320703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374335063	chr7:70320703-70320704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs59979363	chr7:70320715-70320716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190423848	chr7:70320725-70320726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112020896	chr7:70320768-70320769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533226322	chr7:70320777-70320778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6971253	chr7:70320787-70320788	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs144039674	chr7:70320802-70320803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568556281	chr7:70320812-70320813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143873616	chr7:70320817-70320818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549684676	chr7:70320859-70320860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537498353	chr7:70320871-70320872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375820854	chr7:70320945-70320946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538438731	chr7:70320948-70320949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556838477	chr7:70320984-70320985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550651454	chr7:70320993-70320994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148600367	chr7:70320994-70320995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182585983	chr7:70320996-70320997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563959663	chr7:70320999-70321000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188502073	chr7:70321013-70321014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370119190	chr7:70321044-70321045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540250517	chr7:70321058-70321059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555237250	chr7:70321070-70321071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541605516	chr7:70321078-70321079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573636493	chr7:70321089-70321090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191952893	chr7:70321098-70321099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71531724	chr7:70321102-70321103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562293540	chr7:70321134-70321135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552529716	chr7:70321162-70321163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs66984746	chr7:70321182-70321183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137862558	chr7:70321183-70321184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183326474	chr7:70321200-70321201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs151318616	chr7:70321204-70321205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189076485	chr7:70321207-70321208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192342835	chr7:70321214-70321215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140168835	chr7:70321278-70321279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2204624	chr7:70321339-70321340	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532002595	chr7:70321343-70321344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550498814	chr7:70321344-70321345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145590250	chr7:70321352-70321353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539256475	chr7:70321402-70321403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551166913	chr7:70321413-70321414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566607637	chr7:70321416-70321417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113794614	chr7:70321419-70321420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533533154	chr7:70321455-70321456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371276218	chr7:70321477-70321478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
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
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70315000-70321600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:70316800-70321600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr7:70320400-70321200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:70320600-70321600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:70320600-70321800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:70321200-70323600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:70321400-70322000	Enhancers	Fetal Muscle Trunk	muscle
8	chr7:70321400-70322200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr7:70321400-70322800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:70321400-70325000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:70321600-70322000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:70321600-70322000	Enhancers	Placenta	Placenta
13	chr7:70321600-70322000	Bivalent Enhancer	Fetal Stomach	stomach
14	chr7:70321600-70322400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:70321600-70323400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:70321600-70323400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr7:70321600-70323600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:70321800-70322800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:70322000-70322200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:70322000-70322800	Enhancers	Fetal Stomach	stomach
21	chr7:70322200-70322800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr7:70322200-70322800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr7:70322200-70323400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:70322400-70322800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr7:70322400-70322800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:70322800-70323000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:70322800-70323400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:70322800-70323400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr7:70322800-70323600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr7:70322800-70323600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:70323000-70323400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:70323400-70323800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr7:70323400-70323800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:70323400-70324200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
35	chr7:70323600-70324400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
36	chr7:70323600-70325000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
37	chr7:70323600-70325000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr7:70323800-70324200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
39	chr7:70323800-70324600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:70323800-70324800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr7:70333600-70333800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:70333800-70335600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:70334200-70334800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:70335600-70335800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:70335600-70335800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:70335800-70349000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:70336600-70337000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
48	chr7:70337400-70338000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr7:70337800-70338400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr7:70346600-70347200	Enhancers	Fetal Stomach	stomach

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