Variant report

Variant	nsv1034617
Chromosome Location	chr7:38391353-38415389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1475)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1475 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38414156-38414377	K562	blood:	n/a	n/a
2	ATF2	chr7:38409406-38409844	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:38409481-38409625	K562	blood:	n/a	n/a
4	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
5	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
6	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
7	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
8	BATF	chr7:38414007-38414347	GM12878	blood:	n/a	n/a
9	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
10	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
11	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
12	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
13	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
14	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
15	BATF	chr7:38407600-38408059	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:38407578-38407819	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
18	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
20	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
21	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
22	BCLAF1	chr7:38407679-38408065	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
24	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
25	BHLHE40	chr7:38409540-38409919	HepG2	liver:	n/a	n/a
26	BHLHE40	chr7:38409538-38409840	K562	blood:	n/a	n/a
27	BHLHE40	chr7:38409415-38409953	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:38407782-38408093	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:38407780-38408107	K562	blood:	n/a	n/a
30	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
31	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:38408981-38409171	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr7:38409444-38409763	K562	blood:	n/a	n/a
34	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
35	CBX3	chr7:38407677-38408137	K562	blood:	n/a	n/a
36	CBX3	chr7:38407763-38408208	HCT-116	colon:	n/a	n/a
37	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
38	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
39	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
41	CEBPB	chr7:38407812-38408095	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
43	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
44	CHD1	chr7:38407239-38407391	GM12878	blood:	n/a	n/a
45	CHD2	chr7:38407933-38408048	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
47	CHD2	chr7:38403060-38403224	GM12878	blood:	n/a	n/a
48	CHD2	chr7:38407932-38408134	GM12878	blood:	n/a	n/a
49	CHD2	chr7:38407042-38407413	GM12878	blood:	n/a	n/a
50	CREB1	chr7:38409482-38409731	A549	lung:	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	chr7:38398836-38398886	SKMC	muscle:	n/a
2	chr7:38398839-38398889	MCF10A-Er-Src	breast:	n/a
3	chr7:38409725-38409775	SK-N-MC	brain:	n/a
4	chr7:38403507-38403557	AG04449	skin:	fetal
5	chr7:38408106-38408156	HRPEpiC	eye:	n/a
6	chr7:38409725-38409775	Hela-S3	cervix:	n/a
7	chr7:38398839-38398889	HEK293	kidney:	embryo
8	chr7:38398836-38398886	PANC-1	pancreas:	n/a
9	chr7:38398839-38398889	SAEC	small airway:	n/a
10	chr7:38403507-38403557	GM12878	blood:	n/a
11	chr7:38403507-38403557	PFSK-1	brain:	n/a
12	chr7:38398839-38398889	Caco-2	colon:	n/a
13	chr7:38408106-38408156	MCF10A-Er-Src	breast:	n/a
14	chr7:38408106-38408156	HEK293	kidney:	embryo
15	chr7:38398836-38398886	HRCEpiC	kidney:	n/a
16	chr7:38408106-38408156	AG04450	lung:	fetal
17	chr7:38398836-38398886	K562	blood:	n/a
18	chr7:38408106-38408156	BJ	skin:	n/a
19	chr7:38403507-38403557	SK-N-SH_RA	brain:	n/a
20	chr7:38408106-38408156	SK-N-MC	brain:	n/a
21	chr7:38398839-38398889	Hepatocyte	liver:	n/a
22	chr7:38403507-38403557	HCT-116	colon:	n/a
23	chr7:38398839-38398889	HepG2	liver:	n/a
24	chr7:38398836-38398886	GM12891	blood:	n/a
25	chr7:38408106-38408156	HIPEpiC	eye:	n/a
26	chr7:38403507-38403557	HRE	kidney:	n/a
27	chr7:38409725-38409775	T-47D	breast:	n/a
28	chr7:38403507-38403557	HMEC	breast:	n/a
29	chr7:38408106-38408156	GM06990	blood:	n/a
30	chr7:38409725-38409775	Jurkat	blood:	n/a
31	chr7:38398839-38398889	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:38408106-38408156	HCPEpiC	choroid plexus:	n/a
33	chr7:38403507-38403557	SAEC	small airway:	n/a
34	chr7:38398836-38398886	Caco-2	colon:	n/a
35	chr7:38403507-38403557	IMR90	lung:	fetal
36	chr7:38408106-38408156	NHDF-neo	bronchial:	n/a
37	chr7:38398839-38398889	AG09309	skin:	n/a
38	chr7:38398839-38398889	HNPCEpiC	eye:	n/a
39	chr7:38398836-38398886	HEK293	kidney:	embryo
40	chr7:38409725-38409775	HCM	heart:	n/a
41	chr7:38398839-38398889	HUVEC	blood vessel:	n/a
42	chr7:38409725-38409775	HAEpiC	amniotic membrane:	n/a
43	chr7:38408106-38408156	U87	brain:	n/a
44	chr7:38398836-38398886	HAEpiC	amniotic membrane:	n/a
45	chr7:38409725-38409775	SK-N-SH_RA	brain:	n/a
46	chr7:38408106-38408156	HRE	kidney:	n/a
47	chr7:38398836-38398886	MCF-7	breast:	n/a
48	chr7:38398839-38398889	HIPEpiC	eye:	n/a
49	chr7:38409725-38409775	HMEC	breast:	n/a
50	chr7:38408106-38408156	BE2_C	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
2	chr7:38415288..38417406-chr7:38417942..38420287,3	K562	blood:
3	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
4	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
5	chr7:38413282..38415935-chr7:38416823..38418449,3	K562	blood:
6	chr7:38409691..38411244-chr7:38417623..38419459,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-1	chr7:38407614-38407746	XLOC_006412
2	lnc-AMPH-1	chr7:38407246-38407494	XLOC_006412
3	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
4	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
5	lnc-STARD3NL-1	chr7:38415158-38418238	NONHSAT120179
6	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
7	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
8	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
9	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
10	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
11	lnc-STARD3NL-1	chr7:38415158-38418238	ENSG00000250924

No data

Variant related genes	Relation type
TRGV2	TF binding region
TRGV5	TF binding region
TRGV1	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV2	CpG island
TRGV5	CpG island
TRGV1	CpG island
TRGV4	CpG island
TRGV3	CpG island
ENSG00000249978	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000226212	chromatin interactions
FAM120C	miRNA target sites

Extended variants
information (count: 1354 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1354 , 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	rs373356485	chr7:38391369-38391370	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs58353432	chr7:38391439-38391440	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575597383	chr7:38391468-38391469	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544545557	chr7:38391474-38391475	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561661606	chr7:38391487-38391488	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574914572	chr7:38391516-38391517	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374153854	chr7:38391543-38391544	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201897035	chr7:38391544-38391545	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs3999879	chr7:38391547-38391548	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs564185776	chr7:38391557-38391558	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567160886	chr7:38391575-38391576	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529808258	chr7:38391578-38391579	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188724516	chr7:38391590-38391591	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531350952	chr7:38391627-38391628	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs548168768	chr7:38391636-38391637	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs2735131	chr7:38391669-38391670	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs7804460	chr7:38391687-38391688	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs547229041	chr7:38391688-38391689	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs180750785	chr7:38391711-38391712	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs3999880	chr7:38391778-38391779	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs558642943	chr7:38391787-38391788	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs13308897	chr7:38391808-38391809	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs4478467	chr7:38391815-38391816	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs558314338	chr7:38391817-38391818	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs2540189	chr7:38391833-38391834	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs13308903	chr7:38391841-38391842	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs143575278	chr7:38391845-38391846	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs147892860	chr7:38391846-38391847	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs13308908	chr7:38391867-38391868	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs577538598	chr7:38391873-38391874	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs185197411	chr7:38391889-38391890	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs2735130	chr7:38391904-38391905	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs367873055	chr7:38391968-38391969	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs112637583	chr7:38391975-38391976	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs531184453	chr7:38392007-38392008	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs372448292	chr7:38392037-38392038	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs548212619	chr7:38392055-38392056	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs561824095	chr7:38392057-38392058	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375469312	chr7:38392058-38392059	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs76201257	chr7:38392060-38392061	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs373526216	chr7:38392093-38392094	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs117147011	chr7:38392105-38392106	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs141664601	chr7:38392112-38392113	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs556660898	chr7:38392127-38392128	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs58534760	chr7:38392144-38392145	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs552231077	chr7:38392178-38392179	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs191856510	chr7:38392182-38392183	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs141859018	chr7:38392203-38392204	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs60962561	chr7:38392222-38392223	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs57619846	chr7:38392232-38392233	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:82)

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
lymphocytic leukemia	21291569	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
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
2	chr7:38388800-38391800	Active TSS	Primary T cells fromperipheralblood	blood
3	chr7:38388800-38394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:38389200-38392800	Active TSS	GM12878-XiMat	blood
5	chr7:38389600-38391400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
6	chr7:38389600-38391600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr7:38389600-38392800	Weak transcription	Spleen	Spleen
8	chr7:38389600-38413800	Weak transcription	K562	blood
9	chr7:38390600-38391400	Weak transcription	Primary T cells from cord blood	blood
10	chr7:38390600-38391400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:38390600-38391400	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr7:38390600-38392600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr7:38390600-38392800	Weak transcription	Primary B cells from cord blood	blood
14	chr7:38390600-38392800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr7:38390600-38392800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:38390600-38393400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr7:38390600-38393600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr7:38390600-38394600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr7:38390800-38391800	Weak transcription	Fetal Thymus	thymus
20	chr7:38390800-38392800	Weak transcription	Thymus	Thymus
21	chr7:38391000-38392800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr7:38391200-38391400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr7:38391200-38391400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:38391200-38391400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr7:38391200-38391400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr7:38391200-38391600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:38391200-38391600	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr7:38391200-38391600	Flanking Active TSS	Dnd41	blood
29	chr7:38391200-38394200	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr7:38391400-38391600	Enhancers	Primary T cells from cord blood	blood
31	chr7:38391400-38391600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr7:38391400-38391600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:38391400-38391600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:38391400-38392600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr7:38391400-38393400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr7:38391400-38396600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr7:38391600-38391800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr7:38391600-38391800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:38391600-38391800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr7:38391600-38392200	Weak transcription	Primary T cells from cord blood	blood
41	chr7:38391600-38392400	Enhancers	Primary hematopoietic stem cells	blood
42	chr7:38391600-38392800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr7:38391600-38392800	Active TSS	Dnd41	blood
44	chr7:38391600-38393200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr7:38391800-38392000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr7:38391800-38392000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr7:38391800-38392000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:38391800-38392000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:38391800-38392000	Enhancers	Fetal Thymus	thymus
50	chr7:38392000-38392200	Enhancers	Primary T cells fromperipheralblood	blood

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