Variant report

Variant	nsv1034945
Chromosome Location	chr7:121843701-121933166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:121857139-121857576	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:121859375-121859662	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:121878353-121878599	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:121878401-121879106	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr7:121857242-121857575	MCF-7	breast:	n/a	chr7:121857346-121857357
6	CEBPB	chr7:121916234-121916474	HepG2	liver:	n/a	chr7:121916366-121916377
7	CEBPB	chr7:121857184-121857556	HepG2	liver:	n/a	chr7:121857346-121857357
8	CEBPB	chr7:121916863-121916995	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:121857154-121857575	HepG2	liver:	n/a	chr7:121857346-121857357
10	CEBPB	chr7:121857247-121857462	HepG2	liver:	n/a	chr7:121857346-121857357
11	CEBPB	chr7:121857162-121857556	Hela-S3	cervix:	n/a	chr7:121857346-121857357
12	CEBPB	chr7:121865021-121865376	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:121865062-121865220	A549	lung:	n/a	n/a
14	CEBPB	chr7:121865049-121865361	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:121857212-121857507	A549	lung:	n/a	chr7:121857346-121857357
16	CEBPB	chr7:121865125-121865328	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:121908189-121908361	HepG2	liver:	n/a	chr7:121908287-121908298
18	CEBPB	chr7:121857173-121857477	HepG2	liver:	n/a	chr7:121857346-121857357
19	CEBPB	chr7:121896413-121896572	K562	blood:	n/a	n/a
20	CEBPB	chr7:121897595-121897817	HepG2	liver:	n/a	chr7:121897726-121897737
21	CEBPB	chr7:121857128-121857582	MCF-7	breast:	n/a	chr7:121857346-121857357
22	CEBPB	chr7:121865066-121865289	K562	blood:	n/a	n/a
23	CHD2	chr7:121878882-121879118	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr7:121859372-121859661	K562	blood:	n/a	chr7:121859504-121859525
25	CTCF	chr7:121859320-121859470	HVMF	connective:	n/a	n/a
26	CTCF	chr7:121859460-121859610	HCM	heart:	n/a	chr7:121859504-121859525
27	CTCF	chr7:121859380-121859530	HA-sp	spinal cord:	n/a	chr7:121859504-121859525
28	CTCF	chr7:121859435-121859553	GM20000	blood:	n/a	chr7:121859504-121859525
29	CTCF	chr7:121930618-121930890	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:121859358-121859591	SK-N-SH_RA	brain:	n/a	chr7:121859504-121859525
31	CTCF	chr7:121859480-121859630	HRE	kidney:	n/a	chr7:121859504-121859525
32	CTCF	chr7:121859420-121859570	HUVEC	blood vessel:	n/a	chr7:121859504-121859525
33	CTCF	chr7:121859400-121859550	AG04449	skin:	n/a	chr7:121859504-121859525
34	CTCF	chr7:121859152-121859931	SK-N-SH	brain:	n/a	chr7:121859504-121859525
35	CTCF	chr7:121859420-121859570	GM12872	blood:	n/a	chr7:121859504-121859525
36	CTCF	chr7:121899180-121899330	NB4	blood:	n/a	n/a
37	CTCF	chr7:121859420-121859570	HPF	lung:	n/a	chr7:121859504-121859525
38	CTCF	chr7:121859383-121859581	SK-N-SH_RA	brain:	n/a	chr7:121859504-121859525
39	CTCF	chr7:121859460-121859610	AG10803	skin:	n/a	chr7:121859504-121859525
40	CTCF	chr7:121924740-121924890	HepG2	liver:	n/a	n/a
41	CTCF	chr7:121859372-121859602	ECC-1	luminal epithelium:	n/a	chr7:121859504-121859525
42	CTCF	chr7:121859400-121859550	GM12873	blood:	n/a	chr7:121859504-121859525
43	CTCF	chr7:121859460-121859610	GM12869	blood:	n/a	chr7:121859504-121859525
44	CTCF	chr7:121859408-121859619	GM10266	blood:	n/a	chr7:121859504-121859525
45	CTCF	chr7:121859380-121859530	Hela-S3	cervix:	n/a	chr7:121859504-121859525
46	CTCF	chr7:121859480-121859630	GM12871	blood:	n/a	chr7:121859504-121859525
47	CTCF	chr7:121859440-121859590	BJ	skin:	n/a	chr7:121859504-121859525
48	CTCF	chr7:121859440-121859590	AG04450	lung:	n/a	chr7:121859504-121859525
49	CTCF	chr7:121859420-121859570	HL-60	blood:	n/a	chr7:121859504-121859525
50	CTCF	chr7:121859398-121859651	A549	lung:	n/a	chr7:121859504-121859525

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121900908-121900958	MCF10A-Er-Src	breast:	n/a
2	chr7:121878634-121878684	IMR90	lung:	fetal
3	chr7:121900908-121900958	BJ	skin:	n/a
4	chr7:121900908-121900958	HCM	heart:	n/a
5	chr7:121878634-121878684	ECC-1	luminal epithelium:	n/a
6	chr7:121900908-121900958	Hela-S3	cervix:	n/a
7	chr7:121900908-121900958	RPTEC	kidney:	n/a
8	chr7:121895636-121895686	NH-A	brain:	n/a
9	chr7:121895636-121895686	LNCaP	prostate:	n/a
10	chr7:121878634-121878684	ProgFib	skin:	n/a
11	chr7:121878634-121878684	GM12892	blood:	n/a
12	chr7:121900908-121900958	SK-N-MC	brain:	n/a
13	chr7:121878634-121878684	NB4	blood:	n/a
14	chr7:121878634-121878684	HCM	heart:	n/a
15	chr7:121878634-121878684	ovcar-3	ovarian:	n/a
16	chr7:121878634-121878684	HCF	heart:	n/a
17	chr7:121895636-121895686	ECC-1	luminal epithelium:	n/a
18	chr7:121878634-121878684	CMK	blood:	n/a
19	chr7:121878634-121878684	A549	lung:	n/a
20	chr7:121895636-121895686	HMEC	breast:	n/a
21	chr7:121895636-121895686	HRE	kidney:	n/a
22	chr7:121878634-121878684	SK-N-MC	brain:	n/a
23	chr7:121878634-121878684	GM12891	blood:	n/a
24	chr7:121900908-121900958	HCPEpiC	choroid plexus:	n/a
25	chr7:121878634-121878684	MCF10A-Er-Src	breast:	n/a
26	chr7:121895636-121895686	NHBE	bronchial:	n/a
27	chr7:121895636-121895686	RPTEC	kidney:	n/a
28	chr7:121900908-121900958	CMK	blood:	n/a
29	chr7:121895636-121895686	HCF	heart:	n/a
30	chr7:121878634-121878684	NHBE	bronchial:	n/a
31	chr7:121878634-121878684	SAEC	small airway:	n/a
32	chr7:121895636-121895686	Caco-2	colon:	n/a
33	chr7:121900908-121900958	NH-A	brain:	n/a
34	chr7:121900908-121900958	SK-N-SH_RA	brain:	n/a
35	chr7:121878634-121878684	H1-hESC	embryonic stem cell:	embryo
36	chr7:121878634-121878684	HEEpiC	esophagus:	n/a
37	chr7:121895636-121895686	GM12891	blood:	n/a
38	chr7:121878634-121878684	PrEC	prostate:	n/a
39	chr7:121878634-121878684	Jurkat	blood:	n/a
40	chr7:121895636-121895686	CMK	blood:	n/a
41	chr7:121878634-121878684	HCT-116	colon:	n/a
42	chr7:121900908-121900958	HMEC	breast:	n/a
43	chr7:121900908-121900958	LNCaP	prostate:	n/a
44	chr7:121900908-121900958	HRE	kidney:	n/a
45	chr7:121895636-121895686	NB4	blood:	n/a
46	chr7:121900908-121900958	AG10803	skin:	n/a
47	chr7:121895636-121895686	HEEpiC	esophagus:	n/a
48	chr7:121900908-121900958	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:121900908-121900958	HEK293	kidney:	embryo
50	chr7:121895636-121895686	SK-N-MC	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:121859014..121859979-chr7:122172471..122173393,3	MCF-7	breast:
2	chr11:116367060..116367872-chr7:121915708..121916412,2	MCF-7	breast:
3	chr7:121858437..121859375-chr7:122168762..122169335,2	MCF-7	breast:
4	chr7:121859190..121860364-chr7:122168361..122169672,5	MCF-7	breast:
5	chr7:121856928..121858928-chr7:122169140..122170961,2	MCF-7	breast:
6	chr7:121889359..121891616-chr7:121898116..121900388,2	K562	blood:
7	chr7:121859583..121860476-chr7:122165216..122166173,2	MCF-7	breast:
8	chr7:121889359..121891616-chr7:121898116..121900388,2	K562	blood:
9	chr7:121927994..121930149-chr7:121934147..121936454,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRZ1-1	chr7:121857023-121857082	XLOC_006220
2	lnc-PTPRZ1-1	chr7:121856401-121856516	XLOC_006220
3	lnc-PTPRZ1-1	chr7:121858196-121858491	XLOC_006220
4	lnc-PTPRZ1-11	chr7:121897939-121898595	NONHSAT123025
5	lnc-PTPRZ1-11	chr7:121904455-121904728	NONHSAT123025
6	lnc-PTPRZ1-10	chr7:121874585-121874957	NONHSAT123024

No data

Variant related genes	Relation type
ENSG00000213302	TF binding region
ENSG00000234418	TF binding region
ENSG00000213302	CpG island
ENSG00000234418	CpG island

Extended variants
information (count: 1712 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565408602	chr7:121843781-121843782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186195649	chr7:121843784-121843785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532147087	chr7:121843788-121843789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547673172	chr7:121843824-121843825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142543563	chr7:121843848-121843849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560527659	chr7:121843878-121843879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544532244	chr7:121843900-121843901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs284367	chr7:121843905-121843906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs546369069	chr7:121843910-121843911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560204555	chr7:121843940-121843941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532161916	chr7:121843942-121843943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552371081	chr7:121843972-121843973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112742448	chr7:121843987-121843988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538116524	chr7:121843988-121843989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140809498	chr7:121844009-121844010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190715855	chr7:121844025-121844026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529715520	chr7:121844032-121844033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144550175	chr7:121844099-121844100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546532674	chr7:121844153-121844154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553144056	chr7:121844159-121844160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573305817	chr7:121844172-121844173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538819914	chr7:121844199-121844200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373679905	chr7:121844204-121844205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575464204	chr7:121844235-121844236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147843944	chr7:121844243-121844244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570035284	chr7:121844285-121844286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574055259	chr7:121844362-121844363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540228473	chr7:121844365-121844366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113636151	chr7:121844515-121844516	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs566484883	chr7:121844631-121844632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142375458	chr7:121844656-121844657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552275892	chr7:121844660-121844661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34958481	chr7:121844669-121844670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562669232	chr7:121844673-121844674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62474309	chr7:121844681-121844682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548462975	chr7:121844708-121844709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181320935	chr7:121844750-121844751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569126512	chr7:121844783-121844784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs36009316	chr7:121844835-121844836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375429159	chr7:121844844-121844845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536223247	chr7:121844890-121844891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546985547	chr7:121844922-121844923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566784411	chr7:121845084-121845085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369644072	chr7:121845089-121845090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185463567	chr7:121845140-121845141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538024965	chr7:121845151-121845152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558675821	chr7:121845245-121845246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190516342	chr7:121845266-121845267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182744976	chr7:121845289-121845290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6953415	chr7:121845291-121845292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121839600-121845800	Weak transcription	Fetal Heart	heart
2	chr7:121843000-121844400	Weak transcription	Left Ventricle	heart
3	chr7:121844400-121844600	ZNF genes & repeats	Left Ventricle	heart
4	chr7:121844600-121847000	Weak transcription	Left Ventricle	heart
5	chr7:121845200-121845400	Weak transcription	Brain Hippocampus Middle	brain
6	chr7:121845600-121847000	Weak transcription	Psoas Muscle	Psoas
7	chr7:121847000-121847400	ZNF genes & repeats	Psoas Muscle	Psoas
8	chr7:121847200-121847400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:121852800-121853200	Enhancers	HUVEC	blood vessel
10	chr7:121856800-121858000	Enhancers	Liver	Liver
11	chr7:121857200-121857800	Enhancers	HepG2	liver
12	chr7:121865000-121868800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:121865800-121867000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:121868200-121868600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:121868200-121869000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:121877400-121877600	Enhancers	Hela-S3	cervix
17	chr7:121877600-121878000	Flanking Active TSS	Hela-S3	cervix
18	chr7:121877800-121878600	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr7:121877800-121878800	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr7:121878000-121879000	Active TSS	Hela-S3	cervix
21	chr7:121878200-121878800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr7:121878200-121878800	Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr7:121878200-121878800	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr7:121878200-121878800	Active TSS	HepG2	liver
25	chr7:121878200-121879000	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr7:121878200-121879000	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr7:121878200-121879000	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr7:121878200-121879200	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr7:121878600-121879000	Active TSS	H1 Cell Line	embryonic stem cell
30	chr7:121878600-121879000	Active TSS	H9 Cell Line	embryonic stem cell
31	chr7:121878600-121879000	Active TSS	Placenta	Placenta
32	chr7:121879000-121879200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr7:121879000-121894800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr7:121889800-121895200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:121893600-121894000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:121893600-121894200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr7:121893800-121894400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr7:121894000-121894200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr7:121894000-121894200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr7:121894000-121895000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr7:121894200-121894600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr7:121894200-121894800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:121894200-121895200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr7:121894400-121894800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:121894600-121895400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:121894800-121895400	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:121894800-121896400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr7:121894800-121896800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr7:121895000-121895400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:121895000-121896000	Enhancers	H9 Cell Line	embryonic stem cell

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