Variant report

Variant	esv16529
Chromosome Location	chr7:150249312-150312843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:732)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:150267732-150267822	K562	blood:	n/a	n/a
2	CBX3	chr7:150256834-150257112	K562	blood:	n/a	n/a
3	CBX3	chr7:150256848-150257143	K562	blood:	n/a	n/a
4	CEBPB	chr7:150262477-150262657	K562	blood:	n/a	chr7:150262534-150262545
5	CEBPB	chr7:150262475-150262594	Hela-S3	cervix:	n/a	chr7:150262534-150262545
6	CEBPB	chr7:150262403-150262688	A549	lung:	n/a	chr7:150262534-150262545
7	CEBPB	chr7:150268399-150268473	K562	blood:	n/a	n/a
8	CEBPB	chr7:150262346-150262711	K562	blood:	n/a	chr7:150262534-150262545
9	CEBPB	chr7:150262385-150262720	HepG2	liver:	n/a	chr7:150262534-150262545
10	CEBPB	chr7:150262354-150262705	K562	blood:	n/a	chr7:150262534-150262545
11	CEBPB	chr7:150262392-150262657	IMR90	lung:	n/a	chr7:150262534-150262545
12	CEBPB	chr7:150262381-150262701	H1-hESC	embryonic stem cell:	n/a	chr7:150262534-150262545
13	CTCF	chr7:150252478-150252552	Lung_OC	lung:	n/a	n/a
14	CTCF	chr7:150265874-150265958	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr7:150265880-150266030	GM12875	blood:	n/a	n/a
16	CTCF	chr7:150257660-150257810	SAEC	small airway:	n/a	n/a
17	CTCF	chr7:150266502-150266593	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr7:150293420-150293457	Lung_OC	lung:	n/a	n/a
19	CTCF	chr7:150284180-150284330	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr7:150265891-150266001	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr7:150284260-150284410	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr7:150256454-150256532	GM20000	blood:	n/a	n/a
23	CTCF	chr7:150268549-150268584	Lung_OC	lung:	n/a	n/a
24	CTCF	chr7:150265920-150266070	GM12865	blood:	n/a	n/a
25	CTCF	chr7:150265953-150265983	GM12878	blood:	n/a	n/a
26	CTCF	chr7:150257660-150257810	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr7:150256510-150256563	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr7:150299328-150299415	Pancreas_OC	pancreas:	n/a	n/a
29	EBF1	chr7:150265699-150265895	GM12878	blood:	n/a	chr7:150265796-150265807
30	EBF1	chr7:150254264-150254411	GM12878	blood:	n/a	n/a
31	EP300	chr7:150256101-150256183	K562	blood:	n/a	n/a
32	FOS	chr7:150283869-150284242	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr7:150260963-150261435	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr7:150259824-150260877	HUVEC	blood vessel:	n/a	n/a
35	FOS	chr7:150283906-150284146	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr7:150283869-150284188	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr7:150263827-150263902	MCF10A-Er-Src	breast:	n/a	chr7:150263864-150263872 chr7:150263862-150263874 chr7:150263864-150263871 chr7:150263863-150263873 chr7:150263863-150263872
38	FOS	chr7:150263803-150264462	HUVEC	blood vessel:	n/a	chr7:150263864-150263872 chr7:150263862-150263874 chr7:150263864-150263871 chr7:150263863-150263873 chr7:150263863-150263872
39	FOS	chr7:150283200-150284769	HUVEC	blood vessel:	n/a	n/a
40	FOXA1	chr7:150277002-150277416	HepG2	liver:	n/a	n/a
41	FOXA2	chr7:150277023-150277346	A549	lung:	n/a	n/a
42	FOXA2	chr7:150294473-150294994	A549	lung:	n/a	n/a
43	FOXA2	chr7:150276888-150277417	A549	lung:	n/a	n/a
44	FOXA2	chr7:150302944-150303317	A549	lung:	n/a	n/a
45	GATA2	chr7:150259735-150260740	HUVEC	blood vessel:	n/a	n/a
46	GATA2	chr7:150283414-150285023	HUVEC	blood vessel:	n/a	n/a
47	GATA2	chr7:150253524-150254182	HUVEC	blood vessel:	n/a	chr7:150253997-150254011
48	GATA2	chr7:150292481-150292745	HUVEC	blood vessel:	n/a	n/a
49	IRF1	chr7:150266789-150266889	K562	blood:	n/a	n/a
50	IRF1	chr7:150266696-150266954	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150253908-150253958	LNCaP	prostate:	n/a
2	chr7:150270224-150270274	GM12891	blood:	n/a
3	chr7:150264767-150264817	BJ	skin:	n/a
4	chr7:150263324-150263374	NHBE	bronchial:	n/a
5	chr7:150263087-150263137	NB4	blood:	n/a
6	chr7:150270224-150270274	HCM	heart:	n/a
7	chr7:150269315-150269365	HNPCEpiC	eye:	n/a
8	chr7:150254026-150254076	H1-hESC	embryonic stem cell:	embryo
9	chr7:150270224-150270274	ProgFib	skin:	n/a
10	chr7:150264987-150265037	GM06990	blood:	n/a
11	chr7:150264284-150264334	SK-N-SH_RA	brain:	n/a
12	chr7:150263324-150263374	HCM	heart:	n/a
13	chr7:150264284-150264334	T-47D	breast:	n/a
14	chr7:150253908-150253958	HNPCEpiC	eye:	n/a
15	chr7:150263324-150263374	PANC-1	pancreas:	n/a
16	chr7:150253908-150253958	HepG2	liver:	n/a
17	chr7:150253908-150253958	IMR90	lung:	fetal
18	chr7:150264284-150264334	HCT-116	colon:	n/a
19	chr7:150269315-150269365	MCF10A-Er-Src	breast:	n/a
20	chr7:150264284-150264334	SAEC	small airway:	n/a
21	chr7:150264767-150264817	IMR90	lung:	fetal
22	chr7:150264311-150264361	HRCEpiC	kidney:	n/a
23	chr7:150263322-150263372	NHBE	bronchial:	n/a
24	chr7:150263324-150263374	A549	lung:	n/a
25	chr7:150264311-150264361	H1-hESC	embryonic stem cell:	embryo
26	chr7:150263324-150263374	GM12891	blood:	n/a
27	chr7:150269315-150269365	IMR90	lung:	fetal
28	chr7:150270224-150270274	SK-N-MC	brain:	n/a
29	chr7:150262075-150262125	NH-A	brain:	n/a
30	chr7:150264284-150264334	AG04449	skin:	fetal
31	chr7:150263322-150263372	K562	blood:	n/a
32	chr7:150262075-150262125	U87	brain:	n/a
33	chr7:150264311-150264361	ProgFib	skin:	n/a
34	chr7:150264987-150265037	HCF	heart:	n/a
35	chr7:150270224-150270274	SK-N-SH_RA	brain:	n/a
36	chr7:150253908-150253958	NH-A	brain:	n/a
37	chr7:150263324-150263374	AG10803	skin:	n/a
38	chr7:150264284-150264334	Hela-S3	cervix:	n/a
39	chr7:150264767-150264817	SKMC	muscle:	n/a
40	chr7:150254026-150254076	MCF-7	breast:	n/a
41	chr7:150253908-150253958	NHBE	bronchial:	n/a
42	chr7:150253908-150253958	HEK293	kidney:	embryo
43	chr7:150254026-150254076	GM12878	blood:	n/a
44	chr7:150263087-150263137	PANC-1	pancreas:	n/a
45	chr7:150253908-150253958	MCF-7	breast:	n/a
46	chr7:150263087-150263137	AG09319	gingival:	n/a
47	chr7:150262075-150262125	NHDF-neo	bronchial:	n/a
48	chr7:150264311-150264361	PrEC	prostate:	n/a
49	chr7:150262075-150262125	Hepatocyte	liver:	n/a
50	chr7:150254026-150254076	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:150232590..150235233-chr7:150277857..150280710,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GIMAP7-1	chr7:150270658-150271040	NONHSAT124144
2	lnc-GIMAP6-1	chr7:150300649-150301732	NONHSAT124145

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GIMAP4	hsa-miR-146a-5p	chr7:150270870-150270892

Variant related genes	Relation type
ENSG00000271568	TF binding region
ENSG00000232361	TF binding region
GIMAP4	TF binding region
ENSG00000271568	CpG island
ENSG00000232361	CpG island
GIMAP4	CpG island

Extended variants
information (count: 3325 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3325 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142385989	chr7:150249323-150249324	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs2140140	chr7:150249354-150249355	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs571306671	chr7:150249364-150249365	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs2373807	chr7:150249370-150249371	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs147936166	chr7:150249375-150249376	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs2373808	chr7:150249391-150249392	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs141841065	chr7:150249421-150249422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs12535647	chr7:150249440-150249441	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs573390169	chr7:150249441-150249442	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs193209303	chr7:150249455-150249456	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs2373809	chr7:150249465-150249466	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs114327886	chr7:150249479-150249480	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs185751638	chr7:150249484-150249485	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs2373810	chr7:150249492-150249493	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs529980613	chr7:150249494-150249495	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs147124709	chr7:150249497-150249498	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs10237569	chr7:150249527-150249528	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs532224687	chr7:150249549-150249550	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs551959531	chr7:150249550-150249551	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs552769481	chr7:150249573-150249574	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs138291415	chr7:150249574-150249575	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558076347	chr7:150249609-150249610	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs189431208	chr7:150249623-150249624	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs75373621	chr7:150249691-150249692	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs567579836	chr7:150249720-150249721	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs10238055	chr7:150249729-150249730	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs535187157	chr7:150249741-150249742	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs10238068	chr7:150249758-150249759	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs567050214	chr7:150249807-150249808	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs145240765	chr7:150249812-150249813	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs368870127	chr7:150249815-150249816	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs559210798	chr7:150249833-150249834	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs568190653	chr7:150249839-150249840	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs575383945	chr7:150249848-150249849	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs142317044	chr7:150249881-150249882	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs79302273	chr7:150249912-150249913	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs28763707	chr7:150249934-150249935	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs12538768	chr7:150250000-150250001	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs75340638	chr7:150250017-150250018	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150195038	chr7:150250048-150250049	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12538773	chr7:150250055-150250056	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs573222507	chr7:150250076-150250077	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192459919	chr7:150250084-150250085	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184083403	chr7:150250086-150250087	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536926572	chr7:150250094-150250095	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550828498	chr7:150250102-150250103	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371281020	chr7:150250158-150250159	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567640641	chr7:150250223-150250224	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530085906	chr7:150250228-150250229	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138768387	chr7:150250235-150250236	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	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
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Adrenocortical carcinoma	18281524	CNVD

Chromatin state (count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150247600-150253000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:150247800-150249400	Weak transcription	Primary T cells from cord blood	blood
3	chr7:150247800-150251600	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr7:150248000-150254000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr7:150248200-150249400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr7:150248200-150253400	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr7:150248400-150250000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:150248400-150250600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:150248400-150254000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr7:150249000-150250400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
11	chr7:150249000-150254800	Weak transcription	Pancreas	Pancrea
12	chr7:150249200-150249400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:150249200-150249800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
14	chr7:150249200-150250000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr7:150249400-150249600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:150249400-150250000	Enhancers	Primary T cells from cord blood	blood
17	chr7:150249400-150250400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr7:150249600-150250600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:150249800-150253400	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr7:150250400-150251000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr7:150250400-150252400	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr7:150250600-150250800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:150250600-150251000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr7:150250800-150254000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr7:150251000-150252800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr7:150251000-150254200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr7:150251600-150251800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr7:150251600-150252400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
29	chr7:150251800-150252800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr7:150252400-150252600	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr7:150252400-150252800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr7:150252600-150253600	Enhancers	Primary T cells from cord blood	blood
33	chr7:150252600-150254000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:150252600-150254200	Enhancers	Primary T cells fromperipheralblood	blood
35	chr7:150252600-150254200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr7:150252600-150254200	Enhancers	Dnd41	blood
37	chr7:150252600-150255400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr7:150252800-150253400	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr7:150252800-150254000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr7:150252800-150254000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr7:150252800-150254200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:150253000-150253400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr7:150253000-150254000	Enhancers	Primary hematopoietic stem cells	blood
44	chr7:150253000-150254000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr7:150253200-150253400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:150253400-150253600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:150253400-150253800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr7:150253400-150254000	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr7:150253400-150254000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr7:150253400-150254000	Enhancers	Fetal Thymus	thymus

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