Variant report

Variant	esv17064
Chromosome Location	chr7:38285259-38311187
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:99)
CpG islands
(count:427)
Chromatin interactive
region (count:2)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:99 , 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	chr7:38296748-38296967	K562	blood:	n/a	n/a
4	ATF1	chr7:38298851-38299117	K562	blood:	n/a	n/a
5	ATF1	chr7:38285408-38285488	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	BATF	chr7:38305616-38305913	GM12878	blood:	n/a	n/a
10	BATF	chr7:38305659-38305874	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:38305612-38305832	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38289452-38289744	GM12878	blood:	n/a	chr7:38289640-38289649
13	BCL11A	chr7:38289442-38289823	GM12878	blood:	n/a	chr7:38289640-38289649
14	BCL11A	chr7:38305548-38305926	GM12878	blood:	n/a	n/a
15	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
16	CEBPB	chr7:38285344-38285395	K562	blood:	n/a	n/a
17	CTCF	chr7:38299457-38299550	Lung_OC	lung:	n/a	n/a
18	CTCF	chr7:38300410-38300476	Fibrobl	skin:	n/a	n/a
19	CTCF	chr7:38292997-38293033	Lung_OC	lung:	n/a	n/a
20	CTCF	chr7:38298899-38298986	ProgFib	skin:	n/a	n/a
21	CTCF	chr7:38306007-38306040	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:38288542-38288588	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr7:38310342-38310394	Fibrobl	skin:	n/a	n/a
24	E2F4	chr7:38295337-38295499	MCF10A-Er-Src	breast:	n/a	n/a
25	EP300	chr7:38296707-38296986	K562	blood:	n/a	n/a
26	FOXA1	chr7:38304239-38304536	T-47D	breast:	n/a	n/a
27	FOXA1	chr7:38304288-38304517	T-47D	breast:	n/a	n/a
28	GATA3	chr7:38304203-38304546	MCF-7	breast:	n/a	n/a
29	GATA3	chr7:38304227-38304563	MCF-7	breast:	n/a	n/a
30	GATA3	chr7:38304251-38304532	T-47D	breast:	n/a	n/a
31	GATA3	chr7:38304239-38304527	T-47D	breast:	n/a	n/a
32	GATA3	chr7:38310582-38310988	MCF-7	breast:	n/a	n/a
33	GATA3	chr7:38295488-38295652	SH-SY5Y	brain:	n/a	n/a
34	HDAC2	chr7:38304352-38304545	MCF-7	breast:	n/a	n/a
35	IRF1	chr7:38295253-38295287	K562	blood:	n/a	n/a
36	IRF4	chr7:38305469-38305934	GM12878	blood:	n/a	n/a
37	IRF4	chr7:38289363-38289945	GM12878	blood:	n/a	n/a
38	IRF4	chr7:38289425-38289865	GM12878	blood:	n/a	n/a
39	IRF4	chr7:38305531-38305897	GM12878	blood:	n/a	n/a
40	JUN	chr7:38309698-38309924	HepG2	liver:	n/a	chr7:38309739-38309752 chr7:38309743-38309752
41	JUND	chr7:38296695-38297059	K562	blood:	n/a	n/a
42	JUND	chr7:38301252-38301322	K562	blood:	n/a	n/a
43	JUND	chr7:38309560-38309931	HepG2	liver:	n/a	chr7:38309743-38309752
44	MAFK	chr7:38302721-38302861	HepG2	liver:	n/a	n/a
45	MAX	chr7:38296352-38297047	NB4	blood:	n/a	n/a
46	MAX	chr7:38298232-38298389	NB4	blood:	n/a	n/a
47	MYC	chr7:38298360-38298420	NB4	blood:	n/a	n/a
48	MYC	chr7:38296645-38296965	NB4	blood:	n/a	n/a
49	MYC	chr7:38309590-38309606	MCF-7	breast:	n/a	n/a
50	NFYB	chr7:38287843-38288025	GM12878	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38303957-38304007	MCF-7	breast:	n/a
2	chr7:38298908-38298958	HAEpiC	amniotic membrane:	n/a
3	chr7:38299481-38299531	H1-hESC	embryonic stem cell:	embryo
4	chr7:38309984-38310034	K562	blood:	n/a
5	chr7:38309984-38310034	NHBE	bronchial:	n/a
6	chr7:38296393-38296443	AG09319	gingival:	n/a
7	chr7:38298908-38298958	HEEpiC	esophagus:	n/a
8	chr7:38309984-38310034	ovcar-3	ovarian:	n/a
9	chr7:38309984-38310034	BE2_C	brain:	n/a
10	chr7:38296393-38296443	ProgFib	skin:	n/a
11	chr7:38298908-38298958	ECC-1	luminal epithelium:	n/a
12	chr7:38296393-38296443	NH-A	brain:	n/a
13	chr7:38299481-38299531	K562	blood:	n/a
14	chr7:38298966-38299016	CMK	blood:	n/a
15	chr7:38309984-38310034	RPTEC	kidney:	n/a
16	chr7:38294113-38294163	SK-N-SH	brain:	n/a
17	chr7:38298966-38299016	HRPEpiC	eye:	n/a
18	chr7:38294113-38294163	HepG2	liver:	n/a
19	chr7:38294113-38294163	HRPEpiC	eye:	n/a
20	chr7:38298908-38298958	SK-N-SH_RA	brain:	n/a
21	chr7:38298966-38299016	RPTEC	kidney:	n/a
22	chr7:38298966-38299016	HUVEC	blood vessel:	n/a
23	chr7:38299481-38299531	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:38298908-38298958	ProgFib	skin:	n/a
25	chr7:38309984-38310034	NHDF-neo	bronchial:	n/a
26	chr7:38298908-38298958	GM12892	blood:	n/a
27	chr7:38296393-38296443	CMK	blood:	n/a
28	chr7:38299481-38299531	SK-N-SH	brain:	n/a
29	chr7:38309984-38310034	PrEC	prostate:	n/a
30	chr7:38298966-38299016	HNPCEpiC	eye:	n/a
31	chr7:38298908-38298958	AG09309	skin:	n/a
32	chr7:38299481-38299531	IMR90	lung:	fetal
33	chr7:38309984-38310034	U87	brain:	n/a
34	chr7:38298966-38299016	HIPEpiC	eye:	n/a
35	chr7:38296393-38296443	HEEpiC	esophagus:	n/a
36	chr7:38294113-38294163	Jurkat	blood:	n/a
37	chr7:38309984-38310034	PFSK-1	brain:	n/a
38	chr7:38298966-38299016	HEEpiC	esophagus:	n/a
39	chr7:38294113-38294163	GM19239	blood:	n/a
40	chr7:38296393-38296443	GM19239	blood:	n/a
41	chr7:38298966-38299016	U87	brain:	n/a
42	chr7:38298908-38298958	AG10803	skin:	n/a
43	chr7:38299481-38299531	HCF	heart:	n/a
44	chr7:38309984-38310034	GM06990	blood:	n/a
45	chr7:38303957-38304007	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:38303957-38304007	HRPEpiC	eye:	n/a
47	chr7:38309984-38310034	SK-N-SH_RA	brain:	n/a
48	chr7:38296393-38296443	HIPEpiC	eye:	n/a
49	chr7:38303957-38304007	HEEpiC	esophagus:	n/a
50	chr7:38303957-38304007	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:38309718..38312267-chr7:38320422..38323270,2	MCF-7	breast:
2	chr7:38301028..38303453-chr7:38304151..38306717,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-10	chr7:38293236-38293239	NONHSAT120162
2	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120161
3	lnc-AMPH-10	chr7:38308874-38309749	ucscGeneNc_uc003tgm_1
4	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120167
5	lnc-AMPH-10	chr7:38310790-38310903	ucscGeneNc_uc003tgm_1
6	lnc-AMPH-9	chr7:38305937-38306406	ucscGeneNc_uc003tgl_1
7	lnc-AMPH-10	chr7:38292981-38293028	NONHSAT120161
8	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
9	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120169
10	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167
11	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120166
12	lnc-AMPH-10	chr7:38292981-38293025	NONHSAT120162
13	lnc-AMPH-10	chr7:38310012-38310298	ucscGeneNc_uc003tgm_1
14	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120162
15	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120170

No data

Variant related genes	Relation type
TRGC2	TF binding region
TRGC1	TF binding region
TRGJP2	TF binding region
TRGJ2	TF binding region
TRGJ1	TF binding region
TRGC2	CpG island
TRGC1	CpG island
TRGJP2	CpG island
TRGJ2	CpG island
TRGJ1	CpG island
ENSG00000211689	chromatin interactions

Extended variants
information (count: 1372 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74610681	chr7:38285266-38285267	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74450386	chr7:38285267-38285268	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181394449	chr7:38285287-38285288	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536037286	chr7:38285288-38285289	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71546637	chr7:38285298-38285299	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116184590	chr7:38285308-38285309	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs71309097	chr7:38285310-38285311	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116074599	chr7:38285317-38285318	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71210566	chr7:38285328-38285329	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386712301	chr7:38285354-38285355	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs386712302	chr7:38285362-38285363	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386712303	chr7:38285375-38285376	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs67716508	chr7:38285376-38285377	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs116689366	chr7:38285387-38285388	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71309100	chr7:38285419-38285420	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548652602	chr7:38285423-38285424	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145938267	chr7:38285439-38285440	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386712304	chr7:38285476-38285477	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186031119	chr7:38285498-38285499	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570170333	chr7:38285499-38285500	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556861954	chr7:38285504-38285505	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62443344	chr7:38285513-38285514	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549729487	chr7:38285530-38285531	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542795582	chr7:38285541-38285542	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71309102	chr7:38285568-38285569	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111703645	chr7:38285586-38285587	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559327965	chr7:38285598-38285599	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35841647	chr7:38285601-38285602	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6949717	chr7:38285602-38285603	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113794270	chr7:38285621-38285622	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564438873	chr7:38285625-38285626	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533385300	chr7:38285645-38285646	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188357187	chr7:38285646-38285647	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556745825	chr7:38285647-38285648	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114032090	chr7:38285673-38285674	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200639665	chr7:38285685-38285686	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571449876	chr7:38285707-38285708	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181840050	chr7:38285732-38285733	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549552181	chr7:38285733-38285734	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs118176739	chr7:38285739-38285740	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146577144	chr7:38285763-38285764	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186448360	chr7:38285780-38285781	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201616743	chr7:38285784-38285785	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200134164	chr7:38285805-38285806	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200627156	chr7:38285810-38285811	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557586055	chr7:38285846-38285847	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570885892	chr7:38285865-38285866	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150836798	chr7:38285896-38285897	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201943672	chr7:38285908-38285909	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536630291	chr7:38285911-38285912	Weak transcription Strong transcription Genic enhancers Enhancers	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:146 , 50 per page) page: 1 2 3

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	chr7:38277600-38292600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr7:38277600-38292600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr7:38278000-38290800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr7:38278200-38287600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr7:38281200-38287200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:38283200-38285400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr7:38283200-38287800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr7:38283400-38286800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:38283600-38289200	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr7:38283800-38289400	Strong transcription	Dnd41	blood
15	chr7:38284000-38285600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr7:38284200-38285800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:38284200-38287000	Genic enhancers	Primary T cells fromperipheralblood	blood
18	chr7:38285000-38287600	Weak transcription	Fetal Thymus	thymus
19	chr7:38285400-38286400	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr7:38285600-38286800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr7:38285800-38286000	Strong transcription	Primary T cells from cord blood	blood
22	chr7:38285800-38287000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:38286000-38286600	Weak transcription	Primary T cells from cord blood	blood
24	chr7:38286400-38287600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr7:38286600-38288200	Strong transcription	Primary T cells from cord blood	blood
26	chr7:38286800-38287000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr7:38286800-38288200	Strong transcription	Primary neutrophils fromperipheralblood	blood
28	chr7:38287000-38287800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:38287000-38288000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr7:38287000-38288200	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
31	chr7:38287200-38288200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr7:38287400-38288000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:38287600-38288000	Strong transcription	Fetal Thymus	thymus
34	chr7:38287600-38288200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr7:38287600-38288200	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr7:38287800-38288200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr7:38287800-38288200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:38288000-38288200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr7:38288000-38296200	Weak transcription	Fetal Thymus	thymus
40	chr7:38288200-38289000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr7:38288200-38289200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:38288200-38290400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr7:38288200-38290400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr7:38288200-38292600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr7:38288200-38292600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr7:38288200-38295600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr7:38288200-38297000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr7:38288200-38311200	Weak transcription	Primary T cells from cord blood	blood
49	chr7:38289000-38293600	Active TSS	Primary T cells fromperipheralblood	blood
50	chr7:38289200-38290000	Enhancers	Monocytes-CD14+_RO01746	blood

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