Variant report

Variant	esv3384970
Chromosome Location	chr7:152789043-152858746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:152831055-152831178	K562	blood:	n/a	n/a
2	BRCA1	chr7:152799042-152799048	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr7:152803896-152804125	HepG2	liver:	n/a	n/a
4	CEBPB	chr7:152803932-152804127	K562	blood:	n/a	n/a
5	CEBPB	chr7:152850025-152850417	Hela-S3	cervix:	n/a	chr7:152850048-152850059
6	CEBPB	chr7:152850149-152850438	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr7:152827676-152827697	HepG2	liver:	n/a	chr7:152827682-152827693
8	CEBPB	chr7:152810473-152810663	K562	blood:	n/a	n/a
9	CEBPB	chr7:152827562-152827720	K562	blood:	n/a	chr7:152827682-152827693
10	CEBPB	chr7:152850019-152850414	HepG2	liver:	n/a	chr7:152850048-152850059
11	CEBPB	chr7:152850225-152850399	K562	blood:	n/a	n/a
12	CEBPB	chr7:152810354-152810738	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:152850796-152850999	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr7:152810361-152810535	HepG2	liver:	n/a	n/a
15	CTCF	chr7:152801260-152801410	MCF-7	breast:	n/a	n/a
16	CTCF	chr7:152819460-152819610	K562	blood:	n/a	n/a
17	CTCF	chr7:152810340-152810490	GM12864	blood:	n/a	n/a
18	CTCF	chr7:152810420-152810570	GM12871	blood:	n/a	n/a
19	CTCF	chr7:152810360-152810510	HCT-116	colon:	n/a	n/a
20	CTCF	chr7:152819469-152819537	Gliobla	brain:	n/a	n/a
21	CTCF	chr7:152810360-152810510	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:152819500-152819650	HCT-116	colon:	n/a	n/a
23	CTCF	chr7:152810440-152810590	GM12873	blood:	n/a	n/a
24	CTCF	chr7:152810368-152810533	Gliobla	brain:	n/a	n/a
25	CTCF	chr7:152819456-152819560	LNCaP	prostate:	n/a	n/a
26	CTCF	chr7:152810341-152810559	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:152819394-152819638	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:152810253-152810571	K562	blood:	n/a	n/a
29	CTCF	chr7:152819460-152819610	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:152819397-152819618	K562	blood:	n/a	n/a
31	CTCF	chr7:152790006-152790047	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:152810420-152810570	GM12865	blood:	n/a	n/a
33	CTCF	chr7:152810400-152810550	GM12871	blood:	n/a	n/a
34	CTCF	chr7:152810448-152810468	GM19239	blood:	n/a	n/a
35	CTCF	chr7:152810420-152810570	HEK293	kidney:	n/a	n/a
36	CTCF	chr7:152810420-152810570	K562	blood:	n/a	n/a
37	CTCF	chr7:152810420-152810570	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:152810402-152810504	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:152801250-152801282	Hela-S3	cervix:	n/a	chr7:152801253-152801263 chr7:152801250-152801271
40	CTCF	chr7:152810360-152810510	K562	blood:	n/a	n/a
41	CTCF	chr7:152810500-152810650	GM12872	blood:	n/a	n/a
42	CTCF	chr7:152819435-152819633	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:152819420-152819570	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:152810343-152810562	LNCaP	prostate:	n/a	n/a
45	CTCF	chr7:152819480-152819630	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr7:152810380-152810530	GM12866	blood:	n/a	n/a
47	CTCF	chr7:152810276-152810678	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr7:152819444-152819622	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:152819345-152819625	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr7:152810360-152810510	GM12872	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:152855213-152855263	HRCEpiC	kidney:	n/a
2	chr7:152855213-152855263	IMR90	lung:	fetal
3	chr7:152855213-152855263	HL-60	blood:	n/a
4	chr7:152855213-152855263	GM06990	blood:	n/a
5	chr7:152841676-152841726	HCPEpiC	choroid plexus:	n/a
6	chr7:152841676-152841726	SK-N-SH_RA	brain:	n/a
7	chr7:152855213-152855263	RPTEC	kidney:	n/a
8	chr7:152855213-152855263	Hela-S3	cervix:	n/a
9	chr7:152841676-152841726	NH-A	brain:	n/a
10	chr7:152842263-152842313	GM12892	blood:	n/a
11	chr7:152855213-152855263	HRE	kidney:	n/a
12	chr7:152855213-152855263	A549	lung:	n/a
13	chr7:152855213-152855263	AG09319	gingival:	n/a
14	chr7:152855213-152855263	HCT-116	colon:	n/a
15	chr7:152841676-152841726	HRPEpiC	eye:	n/a
16	chr7:152841676-152841726	PFSK-1	brain:	n/a
17	chr7:152842263-152842313	HRPEpiC	eye:	n/a
18	chr7:152855213-152855263	AG09309	skin:	n/a
19	chr7:152842263-152842313	ProgFib	skin:	n/a
20	chr7:152842263-152842313	HRE	kidney:	n/a
21	chr7:152855213-152855263	MCF10A-Er-Src	breast:	n/a
22	chr7:152842263-152842313	K562	blood:	n/a
23	chr7:152841676-152841726	HRE	kidney:	n/a
24	chr7:152841676-152841726	GM12891	blood:	n/a
25	chr7:152855213-152855263	HAEpiC	amniotic membrane:	n/a
26	chr7:152841676-152841726	IMR90	lung:	fetal
27	chr7:152841676-152841726	RPTEC	kidney:	n/a
28	chr7:152842263-152842313	ovcar-3	ovarian:	n/a
29	chr7:152842263-152842313	HEK293	kidney:	embryo
30	chr7:152841676-152841726	MCF-7	breast:	n/a
31	chr7:152841676-152841726	NHBE	bronchial:	n/a
32	chr7:152855213-152855263	HIPEpiC	eye:	n/a
33	chr7:152855213-152855263	HRPEpiC	eye:	n/a
34	chr7:152855213-152855263	PrEC	prostate:	n/a
35	chr7:152841676-152841726	HCT-116	colon:	n/a
36	chr7:152855213-152855263	NHDF-neo	bronchial:	n/a
37	chr7:152855213-152855263	GM12878	blood:	n/a
38	chr7:152842263-152842313	CMK	blood:	n/a
39	chr7:152841676-152841726	ovcar-3	ovarian:	n/a
40	chr7:152841676-152841726	AG04449	skin:	fetal
41	chr7:152841676-152841726	T-47D	breast:	n/a
42	chr7:152842263-152842313	HRCEpiC	kidney:	n/a
43	chr7:152842263-152842313	GM19239	blood:	n/a
44	chr7:152855213-152855263	PANC-1	pancreas:	n/a
45	chr7:152855213-152855263	SK-N-SH_RA	brain:	n/a
46	chr7:152842263-152842313	GM06990	blood:	n/a
47	chr7:152842263-152842313	Caco-2	colon:	n/a
48	chr7:152842263-152842313	HUVEC	blood vessel:	n/a
49	chr7:152842263-152842313	SK-N-MC	brain:	n/a
50	chr7:152855213-152855263	HMEC	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:152793146..152798996-chr7:152800502..152805868,6	K562	blood:
2	chr7:152810422..152812239-chr7:153097689..153099428,2	K562	blood:
3	chr7:152567221..152568854-chr7:152821734..152824144,2	K562	blood:
4	chr7:152853415..152855713-chr7:153110034..153111649,2	K562	blood:
5	chr7:152793146..152798996-chr7:152800502..152805868,6	K562	blood:
6	chr21:15652023..15652746-chr7:152811109..152812098,2	MCF-7	breast:
7	chr3:64251465..64252412-chr7:152789423..152790423,2	MCF-7	breast:
8	chr11:75863959..75864459-chr7:152795919..152796557,2	MCF-7	breast:
9	chr7:152786648..152788875-chr7:152810703..152813051,2	K562	blood:
10	chr7:152788621..152790562-chr7:153104603..153106199,2	K562	blood:
11	chr7:152778420..152780194-chr7:152788675..152790497,2	K562	blood:
12	chr7:152616673..152619076-chr7:152800039..152802738,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XRCC2-11	chr7:152841398-152841673	NONHSAT124290

No data

Variant related genes	Relation type
ENSG00000224104	TF binding region
ENSG00000224104	CpG island
ENSG00000234722	chromatin interactions

Extended variants
information (count: 1609 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1609 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528085898	chr7:152789046-152789047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190505065	chr7:152789064-152789065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180916774	chr7:152789073-152789074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556890451	chr7:152789103-152789104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575052503	chr7:152789110-152789111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35477318	chr7:152789114-152789115	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs559882834	chr7:152789116-152789117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528500931	chr7:152789131-152789132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557283994	chr7:152789221-152789222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367920892	chr7:152789231-152789232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371765654	chr7:152789244-152789245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540243230	chr7:152789266-152789267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562088743	chr7:152789294-152789295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183620350	chr7:152789302-152789303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551015607	chr7:152789314-152789315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569356184	chr7:152789348-152789349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35552323	chr7:152789393-152789394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs398086268	chr7:152789394-152789395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368946832	chr7:152789414-152789415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188873219	chr7:152789435-152789436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114381668	chr7:152789447-152789448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567152683	chr7:152789454-152789455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534628043	chr7:152789486-152789487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78418947	chr7:152789488-152789489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71543516	chr7:152789500-152789501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs73489236	chr7:152789535-152789536	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs187100971	chr7:152789579-152789580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575137305	chr7:152789590-152789591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79425587	chr7:152789604-152789605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571256838	chr7:152789649-152789650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557659232	chr7:152789650-152789651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572826376	chr7:152789704-152789705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540489640	chr7:152789707-152789708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561951071	chr7:152789720-152789721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142513302	chr7:152789725-152789726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375842600	chr7:152789798-152789799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544424950	chr7:152789815-152789816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562959404	chr7:152789816-152789817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538550284	chr7:152789845-152789846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533598132	chr7:152789858-152789859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551980396	chr7:152789865-152789866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs151105680	chr7:152789895-152789896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9691825	chr7:152789938-152789939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7797939	chr7:152789939-152789940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71537386	chr7:152789961-152789962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528007358	chr7:152789992-152789993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542059033	chr7:152789997-152789998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558145111	chr7:152790000-152790001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573110623	chr7:152790013-152790014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549611648	chr7:152790021-152790022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Wilms tumour	21544195	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:152782400-152792400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr7:152788800-152789200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:152788800-152789200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:152789200-152808400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:152808000-152808400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:152808400-152808600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:152810600-152811600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr7:152810600-152811800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:152810800-152811400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr7:152811000-152811400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:152825600-152825800	ZNF genes & repeats	Pancreas	Pancrea
12	chr7:152825800-152829800	Weak transcription	Pancreas	Pancrea
13	chr7:152826800-152828000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:152826800-152828200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:152826800-152828400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:152827000-152827400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:152827000-152827600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr7:152827000-152828000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr7:152827000-152828200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:152827400-152827800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:152827800-152828000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:152827800-152828000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:152828000-152829800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:152829800-152830000	ZNF genes & repeats	Pancreas	Pancrea
25	chr7:152829800-152830200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:152835000-152837800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:152836400-152836600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:152836600-152838000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:152849000-152849800	ZNF genes & repeats	Placenta	Placenta
30	chr7:152849800-152852000	Weak transcription	Placenta	Placenta
31	chr7:152850200-152850400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:152850400-152854600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr7:152852000-152853200	Enhancers	Placenta	Placenta
34	chr7:152854200-152854600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:152854400-152854600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:152854400-152855800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr7:152854600-152855200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:152854600-152855600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:152854600-152855600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:152854600-152855800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr7:152854600-152855800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr7:152854600-152856000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:152854600-152856000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:152854800-152855800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:152855000-152855800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:152855600-152856200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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