Variant report

Variant	esv2108072
Chromosome Location	chr7:38282936-38302893
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:87)
CpG islands
(count:305)
Chromatin interactive
region (count:1)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:87 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38298340-38298378	K562	blood:	n/a	n/a
2	ATF1	chr7:38285866-38286066	K562	blood:	n/a	n/a
3	ATF1	chr7:38285408-38285488	K562	blood:	n/a	n/a
4	ATF1	chr7:38298851-38299117	K562	blood:	n/a	n/a
5	ATF1	chr7:38296748-38296967	K562	blood:	n/a	n/a
6	ATF2	chr7:38289493-38289850	GM12878	blood:	n/a	n/a
7	BATF	chr7:38289510-38289833	GM12878	blood:	n/a	n/a
8	BATF	chr7:38289507-38289847	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:38289452-38289744	GM12878	blood:	n/a	chr7:38289640-38289649
10	BCL11A	chr7:38289442-38289823	GM12878	blood:	n/a	chr7:38289640-38289649
11	CEBPB	chr7:38282956-38283330	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:38282969-38283326	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
14	CEBPB	chr7:38282957-38283270	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:38282943-38283333	K562	blood:	n/a	n/a
16	CEBPB	chr7:38282932-38283307	K562	blood:	n/a	chr7:38282939-38282951
17	CEBPB	chr7:38285344-38285395	K562	blood:	n/a	n/a
18	CEBPB	chr7:38282963-38283206	MCF-7	breast:	n/a	n/a
19	CEBPB	chr7:38282957-38283329	A549	lung:	n/a	n/a
20	CEBPB	chr7:38282958-38283308	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr7:38298899-38298986	ProgFib	skin:	n/a	n/a
22	CTCF	chr7:38299457-38299550	Lung_OC	lung:	n/a	n/a
23	CTCF	chr7:38288542-38288588	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr7:38300410-38300476	Fibrobl	skin:	n/a	n/a
25	CTCF	chr7:38292997-38293033	Lung_OC	lung:	n/a	n/a
26	E2F4	chr7:38295337-38295499	MCF10A-Er-Src	breast:	n/a	n/a
27	EP300	chr7:38296707-38296986	K562	blood:	n/a	n/a
28	FOS	chr7:38283120-38283200	MCF10A-Er-Src	breast:	n/a	n/a
29	GATA3	chr7:38295488-38295652	SH-SY5Y	brain:	n/a	n/a
30	IRF1	chr7:38295253-38295287	K562	blood:	n/a	n/a
31	IRF4	chr7:38289363-38289945	GM12878	blood:	n/a	n/a
32	IRF4	chr7:38289425-38289865	GM12878	blood:	n/a	n/a
33	JUND	chr7:38301252-38301322	K562	blood:	n/a	n/a
34	JUND	chr7:38296695-38297059	K562	blood:	n/a	n/a
35	MAFF	chr7:38282987-38283208	HepG2	liver:	n/a	n/a
36	MAFF	chr7:38282947-38283201	K562	blood:	n/a	n/a
37	MAFK	chr7:38282973-38283227	HepG2	liver:	n/a	n/a
38	MAFK	chr7:38283013-38283216	IMR90	lung:	n/a	n/a
39	MAFK	chr7:38302721-38302861	HepG2	liver:	n/a	n/a
40	MAFK	chr7:38282955-38283216	HepG2	liver:	n/a	n/a
41	MAFK	chr7:38282954-38283133	Hela-S3	cervix:	n/a	n/a
42	MAFK	chr7:38282926-38283126	K562	blood:	n/a	n/a
43	MAX	chr7:38296352-38297047	NB4	blood:	n/a	n/a
44	MAX	chr7:38298232-38298389	NB4	blood:	n/a	n/a
45	MAX	chr7:38282983-38283292	NB4	blood:	n/a	n/a
46	MYC	chr7:38296645-38296965	NB4	blood:	n/a	n/a
47	MYC	chr7:38298360-38298420	NB4	blood:	n/a	n/a
48	MYC	chr7:38283076-38283297	NB4	blood:	n/a	n/a
49	NFYB	chr7:38287843-38288025	GM12878	blood:	n/a	n/a
50	POLR2A	chr7:38296900-38297402	HL-60	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38298908-38298958	HL-60	blood:	n/a
2	chr7:38298908-38298958	AG09319	gingival:	n/a
3	chr7:38298908-38298958	PrEC	prostate:	n/a
4	chr7:38296393-38296443	CMK	blood:	n/a
5	chr7:38294113-38294163	ovcar-3	ovarian:	n/a
6	chr7:38298908-38298958	SAEC	small airway:	n/a
7	chr7:38298966-38299016	AG09309	skin:	n/a
8	chr7:38296393-38296443	HCT-116	colon:	n/a
9	chr7:38299481-38299531	HNPCEpiC	eye:	n/a
10	chr7:38296393-38296443	Jurkat	blood:	n/a
11	chr7:38299481-38299531	CMK	blood:	n/a
12	chr7:38298966-38299016	AG09319	gingival:	n/a
13	chr7:38299481-38299531	HCF	heart:	n/a
14	chr7:38296393-38296443	AG04450	lung:	fetal
15	chr7:38296393-38296443	HCPEpiC	choroid plexus:	n/a
16	chr7:38294113-38294163	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:38298966-38299016	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:38298966-38299016	ovcar-3	ovarian:	n/a
19	chr7:38298908-38298958	NHBE	bronchial:	n/a
20	chr7:38294113-38294163	HEEpiC	esophagus:	n/a
21	chr7:38296393-38296443	SAEC	small airway:	n/a
22	chr7:38294113-38294163	NH-A	brain:	n/a
23	chr7:38296393-38296443	H1-hESC	embryonic stem cell:	embryo
24	chr7:38298966-38299016	HMEC	breast:	n/a
25	chr7:38298966-38299016	HCM	heart:	n/a
26	chr7:38294113-38294163	PFSK-1	brain:	n/a
27	chr7:38296393-38296443	NT2-D1	testis:	n/a
28	chr7:38298966-38299016	T-47D	breast:	n/a
29	chr7:38299481-38299531	MCF-7	breast:	n/a
30	chr7:38298966-38299016	MCF10A-Er-Src	breast:	n/a
31	chr7:38296393-38296443	Hepatocyte	liver:	n/a
32	chr7:38294113-38294163	IMR90	lung:	fetal
33	chr7:38294113-38294163	CMK	blood:	n/a
34	chr7:38299481-38299531	T-47D	breast:	n/a
35	chr7:38299481-38299531	NHDF-neo	bronchial:	n/a
36	chr7:38299481-38299531	AG09309	skin:	n/a
37	chr7:38298908-38298958	HCT-116	colon:	n/a
38	chr7:38298966-38299016	HCF	heart:	n/a
39	chr7:38298966-38299016	NHDF-neo	bronchial:	n/a
40	chr7:38298908-38298958	AoSMC	blood vessel:	n/a
41	chr7:38296393-38296443	ovcar-3	ovarian:	n/a
42	chr7:38294113-38294163	ProgFib	skin:	n/a
43	chr7:38298966-38299016	Hepatocyte	liver:	n/a
44	chr7:38296393-38296443	PrEC	prostate:	n/a
45	chr7:38298908-38298958	AG04450	lung:	fetal
46	chr7:38294113-38294163	HCT-116	colon:	n/a
47	chr7:38298908-38298958	HNPCEpiC	eye:	n/a
48	chr7:38294113-38294163	A549	lung:	n/a
49	chr7:38298966-38299016	NHBE	bronchial:	n/a
50	chr7:38298966-38299016	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:38301028..38303453-chr7:38304151..38306717,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
2	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120162
3	lnc-AMPH-10	chr7:38292981-38293028	NONHSAT120161
4	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120167
5	lnc-AMPH-10	chr7:38293236-38293239	NONHSAT120162
6	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120161
7	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120166
8	lnc-AMPH-10	chr7:38292981-38293025	NONHSAT120162
9	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167

No data

Variant related genes	Relation type
TRGC2	TF binding region
TRGJP2	TF binding region
TRGJ2	TF binding region
TRGC2	CpG island
TRGJP2	CpG island
TRGJ2	CpG island
ENSG00000211689	chromatin interactions

Extended variants
information (count: 1102 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75606174	chr7:38282939-38282940	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553965101	chr7:38282953-38282954	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547490461	chr7:38282954-38282955	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539169764	chr7:38282983-38282984	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371465914	chr7:38282998-38282999	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116201729	chr7:38283010-38283011	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs201802544	chr7:38283039-38283040	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs200525596	chr7:38283044-38283045	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs117280648	chr7:38283071-38283072	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs558475067	chr7:38283096-38283097	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs112506139	chr7:38283098-38283099	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs114289133	chr7:38283119-38283120	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs575241487	chr7:38283130-38283131	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs370560802	chr7:38283154-38283155	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs544471230	chr7:38283163-38283164	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs144742191	chr7:38283178-38283179	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs140016816	chr7:38283179-38283180	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs145339632	chr7:38283181-38283182	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs536728668	chr7:38283199-38283200	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs35500372	chr7:38283204-38283205	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs190722367	chr7:38283206-38283207	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs545888021	chr7:38283228-38283229	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs146918730	chr7:38283229-38283230	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs182510298	chr7:38283234-38283235	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs73360743	chr7:38283240-38283241	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs531352250	chr7:38283263-38283264	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs548234033	chr7:38283268-38283269	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs200499674	chr7:38283289-38283290	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555140437	chr7:38283341-38283342	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs140032288	chr7:38283343-38283344	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs567463443	chr7:38283346-38283347	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs538040821	chr7:38283356-38283357	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs116966570	chr7:38283365-38283366	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs113685022	chr7:38283372-38283373	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs188305070	chr7:38283391-38283392	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs192788270	chr7:38283428-38283429	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs376378702	chr7:38283438-38283439	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs556380258	chr7:38283471-38283472	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538716259	chr7:38283516-38283517	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs577872626	chr7:38283545-38283546	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs201703683	chr7:38283553-38283554	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs199709880	chr7:38283558-38283559	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs200870232	chr7:38283562-38283563	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs201860959	chr7:38283618-38283619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34670819	chr7:38283621-38283622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199977830	chr7:38283622-38283623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201300150	chr7:38283626-38283627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201496046	chr7:38283633-38283634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35849318	chr7:38283644-38283645	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs568884651	chr7:38283658-38283659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD
Neuroblastoma	19536264	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38273800-38292200	Weak transcription	Thymus	Thymus
2	chr7:38273800-38305400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr7:38276800-38285800	Weak transcription	Primary T cells from cord blood	blood
4	chr7:38276800-38295600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:38277600-38284200	Weak transcription	Fetal Thymus	thymus
6	chr7:38277600-38292600	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr7:38277600-38292600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr7:38278000-38290800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr7:38278200-38287600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr7:38280800-38284000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr7:38281200-38287200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr7:38281800-38284000	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr7:38282000-38283000	Strong transcription	Dnd41	blood
14	chr7:38282400-38283200	Strong transcription	Primary T killer memory cells from peripheral blood	blood
15	chr7:38282600-38283200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:38282600-38283200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr7:38282600-38283600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr7:38282800-38283000	Enhancers	K562	blood
19	chr7:38282800-38283000	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr7:38282800-38283400	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr7:38282800-38284200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:38283000-38283200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr7:38283000-38283800	Weak transcription	Dnd41	blood
24	chr7:38283000-38284400	Weak transcription	K562	blood
25	chr7:38283200-38283600	Active TSS	Monocytes-CD14+_RO01746	blood
26	chr7:38283200-38285400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr7:38283200-38287800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr7:38283400-38286800	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr7:38283600-38289200	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr7:38283800-38289400	Strong transcription	Dnd41	blood
31	chr7:38284000-38284200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr7:38284000-38285600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr7:38284200-38285000	Strong transcription	Fetal Thymus	thymus
34	chr7:38284200-38285800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:38284200-38287000	Genic enhancers	Primary T cells fromperipheralblood	blood
36	chr7:38284400-38284800	Enhancers	K562	blood
37	chr7:38285000-38287600	Weak transcription	Fetal Thymus	thymus
38	chr7:38285400-38286400	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr7:38285600-38286800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr7:38285800-38286000	Strong transcription	Primary T cells from cord blood	blood
41	chr7:38285800-38287000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:38286000-38286600	Weak transcription	Primary T cells from cord blood	blood
43	chr7:38286400-38287600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr7:38286600-38288200	Strong transcription	Primary T cells from cord blood	blood
45	chr7:38286800-38287000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr7:38286800-38288200	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr7:38287000-38287800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:38287000-38288000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr7:38287000-38288200	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
50	chr7:38287200-38288200	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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