Variant report

Variant	nsv889142
Chromosome Location	chr7:124958806-125068580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:413)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:125036847-125037232	K562	blood:	n/a	n/a
2	ATF1	chr7:125036628-125037136	K562	blood:	n/a	n/a
3	ATF2	chr7:124995766-124996416	GM12878	blood:	n/a	n/a
4	ATF2	chr7:124995927-124996331	GM12878	blood:	n/a	n/a
5	ATF3	chr7:125036857-125037111	K562	blood:	n/a	n/a
6	BATF	chr7:124996009-124996436	GM12878	blood:	n/a	n/a
7	BATF	chr7:124996043-124996381	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:124995894-124996370	GM12878	blood:	n/a	n/a
9	BCL3	chr7:124995875-124996328	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:125052988-125053632	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:124995944-124996351	GM12878	blood:	n/a	n/a
12	CEBPB	chr7:124970621-124970919	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:125013215-125013415	HepG2	liver:	n/a	chr7:125013342-125013353 chr7:125013340-125013353 chr7:125013340-125013351 chr7:125013340-125013353 chr7:125013340-125013353
14	CEBPB	chr7:124989938-124990049	A549	lung:	n/a	chr7:124990012-124990025
15	CEBPB	chr7:124971430-124971613	H1-hESC	embryonic stem cell:	n/a	chr7:124971556-124971569 chr7:124971558-124971569 chr7:124971556-124971569
16	CEBPB	chr7:124988349-124988457	K562	blood:	n/a	n/a
17	CEBPB	chr7:124970724-124970817	A549	lung:	n/a	n/a
18	CEBPB	chr7:125021399-125021663	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:125010917-125011228	HepG2	liver:	n/a	chr7:125011072-125011083
20	CEBPB	chr7:124988292-124988456	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:125013289-125013418	K562	blood:	n/a	chr7:125013342-125013353 chr7:125013340-125013353 chr7:125013340-125013351 chr7:125013340-125013353 chr7:125013340-125013353
22	CEBPB	chr7:125010980-125011205	A549	lung:	n/a	chr7:125011072-125011083
23	CEBPD	chr7:125036863-125037248	K562	blood:	n/a	n/a
24	CHD1	chr7:124976970-124977013	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr7:124996022-124996326	GM12878	blood:	n/a	n/a
26	CHD2	chr7:125053474-125053659	GM12878	blood:	n/a	n/a
27	CREB1	chr7:125063828-125064124	GM12878	blood:	n/a	n/a
28	CTCF	chr7:125023516-125023631	HepG2	liver:	n/a	n/a
29	CTCF	chr7:125023480-125023630	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr7:125023500-125023650	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr7:125023540-125023690	HMF	breast:	n/a	n/a
32	CTCF	chr7:125023480-125023630	HCT-116	colon:	n/a	n/a
33	CTCF	chr7:125023484-125023649	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr7:125023500-125023650	BE2_C	brain:	n/a	n/a
35	CTCF	chr7:125023420-125023570	GM12873	blood:	n/a	n/a
36	CTCF	chr7:125023480-125023630	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr7:125023480-125023630	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:125023489-125023615	GM10248	blood:	n/a	n/a
39	CTCF	chr7:125023462-125023650	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:125023440-125023590	K562	blood:	n/a	n/a
41	CTCF	chr7:125023480-125023630	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr7:125023520-125023670	RPTEC	kidney:	n/a	n/a
43	CTCF	chr7:125023500-125023650	GM12874	blood:	n/a	n/a
44	CTCF	chr7:125023460-125023610	GM12869	blood:	n/a	n/a
45	CTCF	chr7:125023537-125023631	GM10266	blood:	n/a	n/a
46	CTCF	chr7:124977520-124977670	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr7:125023200-125023350	GM06990	blood:	n/a	n/a
48	CTCF	chr7:125023440-125023590	GM12873	blood:	n/a	n/a
49	CTCF	chr7:125023460-125023610	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr7:125023380-125023530	NHEK	skin:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr7:124979372..124981820-chr7:124985278..124987442,3	K562	blood:
2	chr7:124656588..124658906-chr7:124962987..124965229,2	K562	blood:
3	chr7:125003566..125005765-chr7:125027328..125029861,2	K562	blood:
4	chr7:124965414..124966985-chr7:125006930..125009873,2	K562	blood:
5	chr7:125044926..125048888-chr7:125049294..125054485,5	K562	blood:
6	chr7:124965414..124966985-chr7:125006930..125009873,2	K562	blood:
7	chr3:108533640..108534622-chr7:125014752..125015433,2	MCF-7	breast:
8	chr6:38756306..38758851-chr7:124960777..124963063,2	MCF-7	breast:
9	chr7:125037857..125040245-chr7:125044740..125047619,2	K562	blood:
10	chr7:125044926..125048888-chr7:125049294..125054485,5	K562	blood:
11	chr7:123483979..123486169-chr7:125020238..125022477,2	K562	blood:
12	chr7:125023517..125024026-chr7:125310752..125311652,2	MCF-7	breast:
13	chr7:125014089..125016137-chr7:125017840..125020682,3	K562	blood:
14	chr7:125003566..125005765-chr7:125027328..125029861,2	K562	blood:
15	chr7:125014089..125016137-chr7:125017840..125020682,3	K562	blood:
16	chr7:124699558..124701618-chr7:125055753..125057701,2	K562	blood:
17	chr7:124980320..124982022-chr7:124985560..124987145,2	K562	blood:
18	chr7:124558834..124561175-chr7:124980135..124981921,2	K562	blood:
19	chr7:125037857..125040245-chr7:125044740..125047619,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-5	chr7:125019112-125019375	NR_110188
2	lnc-SPAM1-5	chr7:124975307-124975469	NONHSAT123102
3	lnc-SPAM1-5	chr7:124969736-124969801	NONHSAT123102
4	lnc-SPAM1-5	chr7:125003489-125003570	NR_110188
5	lnc-SPAM1-8	chr7:124985023-124985431	NONHSAT123106
6	lnc-SPAM1-5	chr7:124970311-124970457	ENSG00000237764.2
7	lnc-SPAM1-5	chr7:124975307-124975469	ENSG00000237764.2
8	lnc-SPAM1-5	chr7:124975307-124975469	NR_110188
9	lnc-SPAM1-5	chr7:124987179-124987261	NR_110188
10	lnc-SPAM1-5	chr7:124987179-124987261	ENSG00000237764.2
11	lnc-SPAM1-5	chr7:125003489-125003570	NONHSAT123102
12	lnc-SPAM1-5	chr7:125019112-125019375	ENSG00000237764.2
13	lnc-SPAM1-5	chr7:124987179-124987261	NONHSAT123102
14	lnc-SPAM1-5	chr7:124970311-124970457	NR_110188
15	lnc-SPAM1-5	chr7:125003489-125003570	ENSG00000237764.2
16	lnc-SPAM1-5	chr7:124969736-124969801	NR_110188
17	lnc-SPAM1-5	chr7:125019112-125019375	NONHSAT123102
18	lnc-SPAM1-9	chr7:124985879-124986251	NONHSAT123107
19	lnc-SPAM1-5	chr7:124970311-124970457	NONHSAT123102
20	lnc-SPAM1-5	chr7:124969736-124969801	ENSG00000237764.2

No data

Variant related genes	Relation type
ENSG00000227869	TF binding region
ENSG00000227847	TF binding region
ENSG00000234071	TF binding region
ENSG00000106302	chromatin interactions
ENSG00000227847	chromatin interactions

Extended variants
information (count: 3131 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3131 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6973477	chr7:124958806-124958807	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73719368	chr7:124958846-124958847	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs577968931	chr7:124958852-124958853	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs367852638	chr7:124958878-124958879	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs148353531	chr7:124958909-124958910	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs34158324	chr7:124958916-124958917	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs563532418	chr7:124958953-124958954	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs573895056	chr7:124958970-124958971	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs73442580	chr7:124958971-124958972	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs567518194	chr7:124958988-124958989	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs536064887	chr7:124959002-124959003	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs6973838	chr7:124959006-124959007	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs199742404	chr7:124959011-124959012	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs376181168	chr7:124959016-124959017	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs140730126	chr7:124959017-124959018	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs367661020	chr7:124959018-124959019	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs535943896	chr7:124959022-124959023	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs76421582	chr7:124959030-124959031	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs116453877	chr7:124959051-124959052	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs566530115	chr7:124959052-124959053	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs569988374	chr7:124959063-124959064	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs546390649	chr7:124959137-124959138	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs375412919	chr7:124959190-124959191	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs73442581	chr7:124959215-124959216	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549199818	chr7:124959284-124959285	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs566257296	chr7:124959305-124959306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs73442583	chr7:124959308-124959309	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs558188014	chr7:124959397-124959398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs34190978	chr7:124959412-124959413	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs137890012	chr7:124959421-124959422	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs537406650	chr7:124959424-124959425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs186667401	chr7:124959446-124959447	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs574008553	chr7:124959457-124959458	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs542925082	chr7:124959475-124959476	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs552931795	chr7:124959483-124959484	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs572991172	chr7:124959491-124959492	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs544779907	chr7:124959521-124959522	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs143460601	chr7:124959557-124959558	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs74505900	chr7:124959577-124959578	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs543834197	chr7:124959578-124959579	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs560531363	chr7:124959643-124959644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs144352298	chr7:124959649-124959650	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs368152308	chr7:124959650-124959651	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs75204438	chr7:124959655-124959656	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs71160747	chr7:124959684-124959685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs6150339	chr7:124959685-124959686	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs529587438	chr7:124959713-124959714	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs147217394	chr7:124959725-124959726	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs118113215	chr7:124959740-124959741	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs10235219	chr7:124959808-124959809	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

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
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124958400-124962000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:124959800-124960200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:124960000-124960200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:124962000-124984400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:124974400-124974600	Enhancers	Pancreas	Pancrea
6	chr7:124975200-124977200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:124975200-124977600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:124975400-124976800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:124975400-124977600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr7:124975600-124975800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr7:124975600-124975800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr7:124975600-124976400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:124975600-124976600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr7:124975600-124977400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:124975800-124976600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr7:124975800-124976800	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:124976600-124977200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:124976800-124977200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr7:124977200-124978000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr7:124979000-124979200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:124985800-124986400	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr7:124987000-124988200	Enhancers	HUVEC	blood vessel
23	chr7:124995000-124996000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:124995600-124999400	Enhancers	HUVEC	blood vessel
25	chr7:124995800-124996800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:124995800-124999000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr7:124996000-124996200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:124996000-124996600	Enhancers	NH-A	brain
29	chr7:124996000-124997000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:124996400-124997600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:124996600-124997000	Weak transcription	NH-A	brain
32	chr7:124996800-124997800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:124997000-124997200	Enhancers	NH-A	brain
34	chr7:124997000-124999000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:124997200-125003800	Weak transcription	NH-A	brain
36	chr7:124997400-124999000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr7:124997600-124998400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr7:124997800-124998000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:125003800-125004400	Enhancers	NH-A	brain
40	chr7:125004800-125005000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:125015400-125016400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr7:125015400-125017000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:125015800-125017200	Enhancers	Brain Germinal Matrix	brain
44	chr7:125021400-125023800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:125023800-125028000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:125028000-125029000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:125029000-125031000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:125031000-125031200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr7:125031000-125031400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:125031200-125032400	Enhancers	HUVEC	blood vessel

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