Variant report

Variant	esv993870
Chromosome Location	chr7:128292907-128295065
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:58)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:58 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr7:128293288-128293860	K562	blood:	n/a	n/a
2	CEBPB	chr7:128293514-128293858	K562	blood:	n/a	n/a
3	CEBPB	chr7:128293555-128293810	K562	blood:	n/a	n/a
4	CTCF	chr7:128293320-128293470	A549	lung:	n/a	n/a
5	CTCF	chr7:128293360-128293510	K562	blood:	n/a	n/a
6	CTCF	chr7:128293320-128293470	GM12868	blood:	n/a	n/a
7	CTCF	chr7:128293221-128293533	K562	blood:	n/a	n/a
8	CTCF	chr7:128293220-128293370	HepG2	liver:	n/a	n/a
9	CTCF	chr7:128293106-128293632	K562	blood:	n/a	n/a
10	CTCF	chr7:128293340-128293490	HEK293	kidney:	n/a	n/a
11	CTCF	chr7:128293360-128293510	RPTEC	kidney:	n/a	n/a
12	CTCF	chr7:128293211-128293584	K562	blood:	n/a	n/a
13	CTCF	chr7:128293280-128293430	K562	blood:	n/a	n/a
14	CTCF	chr7:128293260-128293410	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr7:128293380-128293530	MCF-7	breast:	n/a	n/a
16	CTCF	chr7:128293220-128293370	SAEC	small airway:	n/a	n/a
17	CTCF	chr7:128293360-128293510	HMF	breast:	n/a	n/a
18	CTCF	chr7:128293360-128293510	HCPEpiC	choroid plexus:	n/a	n/a
19	FOSL2	chr7:128293364-128293949	HepG2	liver:	n/a	n/a
20	FOSL2	chr7:128293160-128294053	HepG2	liver:	n/a	chr7:128294013-128294022
21	FOSL2	chr7:128294059-128294309	HepG2	liver:	n/a	n/a
22	HEY1	chr7:128293172-128294048	K562	blood:	n/a	n/a
23	HEY1	chr7:128293176-128294007	K562	blood:	n/a	n/a
24	HEY1	chr7:128293707-128293983	HepG2	liver:	n/a	n/a
25	HEY1	chr7:128293321-128293526	HepG2	liver:	n/a	n/a
26	HEY1	chr7:128293177-128294000	HepG2	liver:	n/a	n/a
27	JUND	chr7:128293732-128293909	HepG2	liver:	n/a	n/a
28	JUND	chr7:128293273-128293977	HepG2	liver:	n/a	n/a
29	NR2F2	chr7:128293255-128293948	K562	blood:	n/a	n/a
30	NR2F2	chr7:128293511-128293871	K562	blood:	n/a	n/a
31	POLR2A	chr7:128293469-128293706	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:128293614-128293908	HepG2	liver:	n/a	n/a
33	POLR2A	chr7:128293346-128294143	GM12878	blood:	n/a	n/a
34	POLR2A	chr7:128293209-128293421	K562	blood:	n/a	n/a
35	POLR2A	chr7:128293607-128294261	GM12878	blood:	n/a	n/a
36	POLR2A	chr7:128294045-128294245	K562	blood:	n/a	n/a
37	POLR2A	chr7:128293994-128294028	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr7:128293532-128293947	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr7:128294509-128294859	K562	blood:	n/a	n/a
40	POLR2A	chr7:128294692-128294896	K562	blood:	n/a	n/a
41	POLR2A	chr7:128293666-128293993	HepG2	liver:	n/a	n/a
42	POU2F2	chr7:128293571-128294016	GM12878	blood:	n/a	n/a
43	RXRA	chr7:128293301-128293905	HepG2	liver:	n/a	n/a
44	RXRA	chr7:128293316-128293866	HepG2	liver:	n/a	n/a
45	SIN3AK20	chr7:128293737-128293969	HepG2	liver:	n/a	n/a
46	SIN3AK20	chr7:128293338-128293573	HepG2	liver:	n/a	n/a
47	SP1	chr7:128293419-128293772	K562	blood:	n/a	n/a
48	SP1	chr7:128293289-128293927	HepG2	liver:	n/a	n/a
49	SPI1	chr7:128293690-128293888	K562	blood:	n/a	n/a
50	SPI1	chr7:128293719-128293933	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128293588-128293638	Caco-2	colon:	n/a
2	chr7:128292968-128293018	A549	lung:	n/a
3	chr7:128294083-128294133	HIPEpiC	eye:	n/a
4	chr7:128294083-128294133	AG09319	gingival:	n/a
5	chr7:128294794-128294844	SK-N-MC	brain:	n/a
6	chr7:128294794-128294844	MCF10A-Er-Src	breast:	n/a
7	chr7:128294794-128294844	GM12891	blood:	n/a
8	chr7:128294083-128294133	SAEC	small airway:	n/a
9	chr7:128292968-128293018	HCPEpiC	choroid plexus:	n/a
10	chr7:128293756-128293806	T-47D	breast:	n/a
11	chr7:128293588-128293638	PrEC	prostate:	n/a
12	chr7:128294405-128294455	SK-N-SH_RA	brain:	n/a
13	chr7:128294794-128294844	GM19239	blood:	n/a
14	chr7:128292968-128293018	U87	brain:	n/a
15	chr7:128294794-128294844	PFSK-1	brain:	n/a
16	chr7:128293588-128293638	K562	blood:	n/a
17	chr7:128294794-128294844	HepG2	liver:	n/a
18	chr7:128292968-128293018	SK-N-SH	brain:	n/a
19	chr7:128293588-128293638	BJ	skin:	n/a
20	chr7:128294405-128294455	AG04449	skin:	fetal
21	chr7:128294405-128294455	AG09319	gingival:	n/a
22	chr7:128294405-128294455	H1-hESC	embryonic stem cell:	embryo
23	chr7:128293588-128293638	ProgFib	skin:	n/a
24	chr7:128294405-128294455	ECC-1	luminal epithelium:	n/a
25	chr7:128294083-128294133	GM12892	blood:	n/a
26	chr7:128293756-128293806	PANC-1	pancreas:	n/a
27	chr7:128293588-128293638	IMR90	lung:	fetal
28	chr7:128294083-128294133	LNCaP	prostate:	n/a
29	chr7:128294794-128294844	Jurkat	blood:	n/a
30	chr7:128293756-128293806	GM06990	blood:	n/a
31	chr7:128294083-128294133	AoSMC	blood vessel:	n/a
32	chr7:128293756-128293806	SKMC	muscle:	n/a
33	chr7:128293588-128293638	HCPEpiC	choroid plexus:	n/a
34	chr7:128293588-128293638	HEK293	kidney:	embryo
35	chr7:128293756-128293806	BE2_C	brain:	n/a
36	chr7:128294083-128294133	NHBE	bronchial:	n/a
37	chr7:128293588-128293638	RPTEC	kidney:	n/a
38	chr7:128294083-128294133	NH-A	brain:	n/a
39	chr7:128294794-128294844	GM12878	blood:	n/a
40	chr7:128294083-128294133	AG04450	lung:	fetal
41	chr7:128292968-128293018	HEEpiC	esophagus:	n/a
42	chr7:128293756-128293806	AG04449	skin:	fetal
43	chr7:128292968-128293018	GM12892	blood:	n/a
44	chr7:128294083-128294133	PrEC	prostate:	n/a
45	chr7:128294794-128294844	AG09309	skin:	n/a
46	chr7:128294083-128294133	T-47D	breast:	n/a
47	chr7:128294083-128294133	GM12891	blood:	n/a
48	chr7:128294083-128294133	BJ	skin:	n/a
49	chr7:128294083-128294133	RPTEC	kidney:	n/a
50	chr7:128292968-128293018	AoSMC	blood vessel:	n/a

No data

Variant related genes	Relation type
ENSG00000243679	TF binding region
ENSG00000229413	TF binding region
ENSG00000230715	TF binding region
ENSG00000243679	CpG island
ENSG00000229413	CpG island
ENSG00000230715	CpG island

Extended variants
information (count: 116 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:116 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560112830	chr7:128292912-128292913	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527435441	chr7:128292937-128292938	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548812447	chr7:128292938-128292939	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369878897	chr7:128292944-128292945	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567393383	chr7:128292946-128292947	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537542325	chr7:128292980-128292981	Strong transcription Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
7	rs373385237	chr7:128292981-128292982	Strong transcription Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
8	rs549391268	chr7:128292991-128292992	Strong transcription Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
9	rs570894383	chr7:128293001-128293002	Strong transcription Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
10	rs181425771	chr7:128293009-128293010	Strong transcription Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
11	rs186363005	chr7:128293010-128293011	Strong transcription Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
12	rs3213981	chr7:128293013-128293014	Strong transcription Weak transcription	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs536892837	chr7:128293017-128293018	Strong transcription Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
14	rs554861810	chr7:128293034-128293035	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3213980	chr7:128293035-128293036	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543918272	chr7:128293047-128293048	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559010861	chr7:128293090-128293091	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189690763	chr7:128293099-128293100	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545327324	chr7:128293106-128293107	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs375714803	chr7:128293112-128293113	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs560352933	chr7:128293148-128293149	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs527579883	chr7:128293159-128293160	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs542850839	chr7:128293160-128293161	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs3213979	chr7:128293187-128293188	Strong transcription Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs531338499	chr7:128293191-128293192	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs374126403	chr7:128293202-128293203	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs549430342	chr7:128293221-128293222	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs570931233	chr7:128293232-128293233	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531932814	chr7:128293257-128293258	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs3213978	chr7:128293258-128293259	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566412052	chr7:128293259-128293260	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs536523900	chr7:128293262-128293263	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs368301720	chr7:128293266-128293267	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs371303034	chr7:128293276-128293277	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs34960471	chr7:128293294-128293295	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs374312911	chr7:128293302-128293303	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs199826580	chr7:128293344-128293345	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs570231667	chr7:128293379-128293380	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs537566548	chr7:128293516-128293517	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs559046976	chr7:128293519-128293520	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs180930427	chr7:128293520-128293521	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs573294269	chr7:128293531-128293532	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs185979294	chr7:128293562-128293563	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs150942915	chr7:128293583-128293584	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs553086961	chr7:128293619-128293620	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs572330643	chr7:128293654-128293655	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs542539704	chr7:128293680-128293681	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs191005735	chr7:128293713-128293714	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs539141252	chr7:128293714-128293715	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs6973327	chr7:128293715-128293716	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	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
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128239200-128296400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:128249600-128293400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr7:128249600-128295200	Weak transcription	NH-A	brain
4	chr7:128249600-128297600	Weak transcription	HUVEC	blood vessel
5	chr7:128249600-128308400	Weak transcription	HSMM	muscle
6	chr7:128249600-128312200	Weak transcription	Psoas Muscle	Psoas
7	chr7:128249600-128319600	Weak transcription	NHLF	lung
8	chr7:128260000-128296400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr7:128260400-128300600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:128262200-128293200	Weak transcription	Brain Germinal Matrix	brain
11	chr7:128272200-128300000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:128272400-128293200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:128274200-128296400	Weak transcription	Colonic Mucosa	Colon
14	chr7:128275600-128295000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:128279600-128296200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr7:128279800-128293000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr7:128279800-128293600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr7:128279800-128296400	Weak transcription	Brain Angular Gyrus	brain
19	chr7:128279800-128300000	Weak transcription	Dnd41	blood
20	chr7:128279800-128301400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr7:128281200-128293200	Weak transcription	Ovary	ovary
22	chr7:128282400-128295400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr7:128282400-128301400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:128282400-128312400	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:128282600-128300000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:128284000-128304800	Weak transcription	Primary T cells from cord blood	blood
27	chr7:128284200-128294600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:128284200-128301400	Weak transcription	Fetal Lung	lung
29	chr7:128284200-128313200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr7:128284400-128294400	Weak transcription	Small Intestine	intestine
31	chr7:128284400-128299200	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr7:128284400-128313200	Weak transcription	Colon Smooth Muscle	Colon
33	chr7:128285600-128293400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:128285800-128296000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr7:128286400-128298400	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr7:128287400-128301400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr7:128288400-128294400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr7:128288800-128296200	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr7:128289000-128301400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:128290000-128295000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:128290000-128295000	Strong transcription	Liver	Liver
42	chr7:128290000-128295200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:128290600-128294200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:128290600-128294600	Strong transcription	Fetal Brain Female	brain
45	chr7:128290600-128295000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:128290600-128295000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr7:128290600-128295000	Strong transcription	Pancreas	Pancrea
48	chr7:128290600-128295400	Strong transcription	Fetal Intestine Small	intestine
49	chr7:128290600-128295800	Strong transcription	Fetal Stomach	stomach
50	chr7:128290800-128293400	Strong transcription	HUES6 Cell Line	embryonic stem cell

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