Variant report

Variant	esv3514179
Chromosome Location	chr7:38396936-38406188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
2	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
3	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
4	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
5	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
6	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
7	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
8	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
11	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
12	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
13	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
14	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
15	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
16	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
17	CHD2	chr7:38403060-38403224	GM12878	blood:	n/a	n/a
18	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
19	CTCF	chr7:38402990-38403471	K562	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
20	CTCF	chr7:38403140-38403290	HCFaa	heart:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
21	CTCF	chr7:38403058-38403361	GM12891	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
22	CTCF	chr7:38403040-38403190	HCT-116	colon:	n/a	n/a
23	CTCF	chr7:38403020-38403170	GM12869	blood:	n/a	n/a
24	CTCF	chr7:38398680-38398830	AG09309	skin:	n/a	n/a
25	CTCF	chr7:38398595-38399049	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
26	CTCF	chr7:38398716-38399000	MCF-7	breast:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
27	CTCF	chr7:38398681-38399005	MCF-7	breast:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
28	CTCF	chr7:38398700-38398850	HCM	heart:	n/a	n/a
29	CTCF	chr7:38398741-38398858	HepG2	liver:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
30	CTCF	chr7:38398680-38398830	BE2_C	brain:	n/a	n/a
31	CTCF	chr7:38403079-38403338	GM10248	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
32	CTCF	chr7:38403060-38403342	ProgFib	skin:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
33	CTCF	chr7:38403120-38403270	GM12868	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
34	CTCF	chr7:38398680-38398830	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr7:38398641-38399052	GM19238	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
36	CTCF	chr7:38398703-38399012	GM10248	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
37	CTCF	chr7:38403060-38403210	GM12870	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
38	CTCF	chr7:38403100-38403250	HA-sp	spinal cord:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
39	CTCF	chr7:38402990-38403342	H1-hESC	embryonic stem cell:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
40	CTCF	chr7:38403140-38403290	HCPEpiC	choroid plexus:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
41	CTCF	chr7:38403120-38403270	A549	lung:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
42	CTCF	chr7:38398680-38398830	HFF	foreskin:	n/a	n/a
43	CTCF	chr7:38403140-38403290	Hela-S3	cervix:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
44	CTCF	chr7:38398671-38399165	GM19240	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
45	CTCF	chr7:38403120-38403270	K562	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
46	CTCF	chr7:38402400-38402690	GM12867	blood:	n/a	n/a
47	CTCF	chr7:38403085-38403322	HepG2	liver:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
48	CTCF	chr7:38403062-38403413	Spleen_OC	spleen:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
49	CTCF	chr7:38398731-38398990	LNCaP	prostate:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
50	CTCF	chr7:38403112-38403327	SK-N-SH_RA	brain:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38398839-38398889	NT2-D1	testis:	n/a
2	chr7:38398839-38398889	PANC-1	pancreas:	n/a
3	chr7:38398836-38398886	HepG2	liver:	n/a
4	chr7:38403507-38403557	HUVEC	blood vessel:	n/a
5	chr7:38403507-38403557	AG04450	lung:	fetal
6	chr7:38398836-38398886	Hela-S3	cervix:	n/a
7	chr7:38398839-38398889	HRCEpiC	kidney:	n/a
8	chr7:38403507-38403557	NT2-D1	testis:	n/a
9	chr7:38398839-38398889	T-47D	breast:	n/a
10	chr7:38398839-38398889	LNCaP	prostate:	n/a
11	chr7:38398839-38398889	AG09319	gingival:	n/a
12	chr7:38398836-38398886	HRE	kidney:	n/a
13	chr7:38403507-38403557	Hela-S3	cervix:	n/a
14	chr7:38403507-38403557	T-47D	breast:	n/a
15	chr7:38398836-38398886	AG10803	skin:	n/a
16	chr7:38403507-38403557	A549	lung:	n/a
17	chr7:38403507-38403557	GM06990	blood:	n/a
18	chr7:38398836-38398886	NH-A	brain:	n/a
19	chr7:38398836-38398886	NT2-D1	testis:	n/a
20	chr7:38398836-38398886	GM12891	blood:	n/a
21	chr7:38403507-38403557	AG09309	skin:	n/a
22	chr7:38398836-38398886	PrEC	prostate:	n/a
23	chr7:38398836-38398886	HCT-116	colon:	n/a
24	chr7:38398836-38398886	HRCEpiC	kidney:	n/a
25	chr7:38403507-38403557	GM12892	blood:	n/a
26	chr7:38398836-38398886	BJ	skin:	n/a
27	chr7:38398839-38398889	GM12878	blood:	n/a
28	chr7:38398839-38398889	GM12892	blood:	n/a
29	chr7:38398836-38398886	H1-hESC	embryonic stem cell:	embryo
30	chr7:38403507-38403557	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:38403507-38403557	SAEC	small airway:	n/a
32	chr7:38398839-38398889	CMK	blood:	n/a
33	chr7:38403507-38403557	NB4	blood:	n/a
34	chr7:38403507-38403557	BJ	skin:	n/a
35	chr7:38398839-38398889	IMR90	lung:	fetal
36	chr7:38403507-38403557	HRPEpiC	eye:	n/a
37	chr7:38398839-38398889	HCF	heart:	n/a
38	chr7:38403507-38403557	PANC-1	pancreas:	n/a
39	chr7:38398839-38398889	SKMC	muscle:	n/a
40	chr7:38398839-38398889	BE2_C	brain:	n/a
41	chr7:38398839-38398889	A549	lung:	n/a
42	chr7:38403507-38403557	NHBE	bronchial:	n/a
43	chr7:38398836-38398886	A549	lung:	n/a
44	chr7:38403507-38403557	HEEpiC	esophagus:	n/a
45	chr7:38398836-38398886	BE2_C	brain:	n/a
46	chr7:38398836-38398886	CMK	blood:	n/a
47	chr7:38403507-38403557	HRE	kidney:	n/a
48	chr7:38403507-38403557	NH-A	brain:	n/a
49	chr7:38398836-38398886	HCPEpiC	choroid plexus:	n/a
50	chr7:38403507-38403557	AG10803	skin:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
2	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
3	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
4	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
5	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182

Variant related genes	Relation type
TRGV4	TF binding region
TRGV3	TF binding region
TRGV2	TF binding region
TRGV4	CpG island
TRGV3	CpG island
TRGV2	CpG island

Extended variants
information (count: 624 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113797958	chr7:38396946-38396947	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550472583	chr7:38396955-38396956	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79365750	chr7:38396973-38396974	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181725399	chr7:38396983-38396984	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548665011	chr7:38396993-38396994	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565477517	chr7:38396996-38396997	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186530285	chr7:38397033-38397034	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11970890	chr7:38397036-38397037	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs114108178	chr7:38397037-38397038	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11974172	chr7:38397051-38397052	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111351534	chr7:38397064-38397065	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573861485	chr7:38397099-38397100	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542892341	chr7:38397103-38397104	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191289305	chr7:38397151-38397152	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114729880	chr7:38397152-38397153	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182763547	chr7:38397154-38397155	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115842861	chr7:38397162-38397163	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142320161	chr7:38397167-38397168	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs151282870	chr7:38397207-38397208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112471946	chr7:38397211-38397212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529436287	chr7:38397212-38397213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116143086	chr7:38397220-38397221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78079501	chr7:38397225-38397226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11981038	chr7:38397253-38397254	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs112690438	chr7:38397288-38397289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551468347	chr7:38397312-38397313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117979029	chr7:38397322-38397323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117521773	chr7:38397339-38397340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs560071966	chr7:38397345-38397346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370773490	chr7:38397355-38397356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567608274	chr7:38397412-38397413	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs67312387	chr7:38397435-38397436	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs200469325	chr7:38397488-38397489	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs373903446	chr7:38397533-38397534	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs146622310	chr7:38397545-38397546	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs370622373	chr7:38397551-38397552	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs553158895	chr7:38397555-38397556	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs141436760	chr7:38397576-38397577	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs190773221	chr7:38397588-38397589	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs145094370	chr7:38397589-38397590	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs558259641	chr7:38397599-38397600	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs552418331	chr7:38397635-38397636	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs183265066	chr7:38397653-38397654	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs563350399	chr7:38397696-38397697	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs116737724	chr7:38397702-38397703	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs62445012	chr7:38397709-38397710	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs143493761	chr7:38397755-38397756	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs374727111	chr7:38397756-38397757	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs528715790	chr7:38397792-38397793	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs370983159	chr7:38397867-38397868	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

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:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
2	chr7:38389600-38413800	Weak transcription	K562	blood
3	chr7:38392400-38398200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr7:38393800-38398000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr7:38394000-38397000	Weak transcription	Primary B cells from cord blood	blood
6	chr7:38394000-38397400	Weak transcription	Thymus	Thymus
7	chr7:38394200-38397600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr7:38394400-38397000	Enhancers	Dnd41	blood
9	chr7:38394400-38397800	Weak transcription	GM12878-XiMat	blood
10	chr7:38394400-38398200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:38394400-38402200	Weak transcription	Spleen	Spleen
12	chr7:38394600-38397600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr7:38395000-38398200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr7:38395000-38400000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:38395200-38398200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:38395600-38397800	Weak transcription	Fetal Thymus	thymus
17	chr7:38395800-38397400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:38396000-38397800	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr7:38396200-38397200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr7:38396200-38397600	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr7:38396200-38397800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr7:38396400-38398000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr7:38396400-38398200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr7:38396600-38397000	Active TSS	Primary T cells from cord blood	blood
25	chr7:38396600-38397200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr7:38396600-38397200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:38396600-38397600	Enhancers	Primary T cells fromperipheralblood	blood
28	chr7:38396800-38397800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr7:38396800-38398000	Weak transcription	Fetal Stomach	stomach
30	chr7:38397000-38397200	Enhancers	Primary B cells from cord blood	blood
31	chr7:38397000-38397200	Flanking Active TSS	Primary T cells from cord blood	blood
32	chr7:38397000-38397200	Flanking Active TSS	Dnd41	blood
33	chr7:38397200-38397600	Weak transcription	Primary B cells from cord blood	blood
34	chr7:38397200-38397600	Enhancers	Dnd41	blood
35	chr7:38397200-38397800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr7:38397200-38398000	Weak transcription	Primary T cells from cord blood	blood
37	chr7:38397200-38398000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr7:38397200-38398200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr7:38397400-38398000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:38397400-38402800	Active TSS	Thymus	Thymus
41	chr7:38397600-38398000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
42	chr7:38397600-38398000	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr7:38397600-38398200	Enhancers	Primary B cells from cord blood	blood
44	chr7:38397600-38398200	Enhancers	Primary B cells from peripheral blood	blood
45	chr7:38397600-38398600	Flanking Active TSS	Dnd41	blood
46	chr7:38397600-38399200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr7:38397600-38399200	Enhancers	HUVEC	blood vessel
48	chr7:38397600-38403600	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr7:38397800-38398000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:38397800-38398000	Enhancers	Fetal Thymus	thymus

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