Variant report

Variant	esv1825425
Chromosome Location	chr7:38457144-38507180
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	ARID3A	chr7:38473572-38473788	HepG2	liver:	n/a	n/a
2	ATF1	chr7:38500375-38500379	K562	blood:	n/a	n/a
3	ATF1	chr7:38504585-38504659	K562	blood:	n/a	n/a
4	BATF	chr7:38466929-38467217	GM12878	blood:	n/a	n/a
5	CEBPB	chr7:38474784-38474995	K562	blood:	n/a	chr7:38474831-38474842 chr7:38474831-38474844 chr7:38474833-38474842
6	CEBPB	chr7:38474713-38474921	HepG2	liver:	n/a	chr7:38474831-38474842 chr7:38474831-38474844 chr7:38474833-38474842
7	CEBPB	chr7:38486001-38486124	HepG2	liver:	n/a	n/a
8	CTCF	chr7:38473660-38473810	AG09309	skin:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
9	CTCF	chr7:38464820-38464970	GM12873	blood:	n/a	n/a
10	CTCF	chr7:38473626-38473812	LNCaP	prostate:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
11	CTCF	chr7:38491500-38491733	HepG2	liver:	n/a	chr7:38491617-38491638
12	CTCF	chr7:38473640-38473790	HRPEpiC	eye:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
13	CTCF	chr7:38473660-38473810	SK-N-SH_RA	brain:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
14	CTCF	chr7:38473580-38473730	AoAF	blood vessel:	n/a	n/a
15	CTCF	chr7:38473620-38473770	HA-sp	spinal cord:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
16	CTCF	chr7:38491490-38491732	A549	lung:	n/a	chr7:38491617-38491638
17	CTCF	chr7:38464400-38464550	AG09309	skin:	n/a	n/a
18	CTCF	chr7:38464600-38464750	SAEC	small airway:	n/a	n/a
19	CTCF	chr7:38473700-38473850	HBMEC	blood vessel:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
20	CTCF	chr7:38473741-38473788	GM12891	blood:	n/a	n/a
21	CTCF	chr7:38473640-38473790	AoAF	blood vessel:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
22	CTCF	chr7:38467660-38467810	AG10803	skin:	n/a	n/a
23	CTCF	chr7:38473651-38473821	Fibrobl	skin:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
24	CTCF	chr7:38491572-38491733	ProgFib	skin:	n/a	chr7:38491617-38491638
25	CTCF	chr7:38491600-38491750	MCF-7	breast:	n/a	chr7:38491617-38491638
26	CTCF	chr7:38473620-38473770	HCPEpiC	choroid plexus:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
27	CTCF	chr7:38491580-38491730	GM12865	blood:	n/a	chr7:38491617-38491638
28	CTCF	chr7:38473613-38473841	H1-hESC	embryonic stem cell:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
29	CTCF	chr7:38491540-38491690	HFF	foreskin:	n/a	chr7:38491617-38491638
30	CTCF	chr7:38473640-38473790	HCT-116	colon:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
31	CTCF	chr7:38473663-38473824	A549	lung:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
32	CTCF	chr7:38473612-38473801	GM12878	blood:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
33	CTCF	chr7:38464440-38464590	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr7:38473560-38473710	HCM	heart:	n/a	n/a
35	CTCF	chr7:38464600-38464750	HFF	foreskin:	n/a	n/a
36	CTCF	chr7:38473652-38473785	Pancreas_OC	pancreas:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
37	CTCF	chr7:38464460-38464610	BE2_C	brain:	n/a	n/a
38	CTCF	chr7:38473640-38473790	GM12871	blood:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
39	CTCF	chr7:38491560-38491710	HAc	cerebellar:	n/a	chr7:38491617-38491638
40	CTCF	chr7:38473800-38473950	HCM	heart:	n/a	n/a
41	CTCF	chr7:38473700-38473850	HMEC	breast:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
42	CTCF	chr7:38473594-38473997	K562	blood:	n/a	chr7:38473726-38473735 chr7:38473723-38473741
43	CTCF	chr7:38473728-38473787	GM19238	blood:	n/a	n/a
44	CTCF	chr7:38491140-38491290	HCM	heart:	n/a	n/a
45	CTCF	chr7:38464460-38464610	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr7:38491520-38491670	NHEK	skin:	n/a	chr7:38491617-38491638
47	CTCF	chr7:38491520-38491670	HPF	lung:	n/a	chr7:38491617-38491638
48	CTCF	chr7:38496142-38496207	ProgFib	skin:	n/a	n/a
49	CTCF	chr7:38491480-38491630	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr7:38473680-38473816	H1-hESC	embryonic stem cell:	n/a	chr7:38473726-38473735 chr7:38473723-38473741

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38468944-38468994	HCT-116	colon:	n/a
2	chr7:38468944-38468994	AG04450	lung:	fetal
3	chr7:38468944-38468994	HCT-116	colon:	n/a
4	chr7:38468944-38468994	AG04450	lung:	fetal
5	chr7:38504420-38504470	RPTEC	kidney:	n/a
6	chr7:38470088-38470138	HAEpiC	amniotic membrane:	n/a
7	chr7:38468985-38469035	HIPEpiC	eye:	n/a
8	chr7:38470088-38470138	AG09319	gingival:	n/a
9	chr7:38470088-38470138	U87	brain:	n/a
10	chr7:38468985-38469035	IMR90	lung:	fetal
11	chr7:38470121-38470171	HepG2	liver:	n/a
12	chr7:38492620-38492670	GM19239	blood:	n/a
13	chr7:38492620-38492670	ovcar-3	ovarian:	n/a
14	chr7:38492620-38492670	SK-N-SH_RA	brain:	n/a
15	chr7:38468944-38468994	PFSK-1	brain:	n/a
16	chr7:38504420-38504470	NH-A	brain:	n/a
17	chr7:38468944-38468994	HL-60	blood:	n/a
18	chr7:38468985-38469035	HEEpiC	esophagus:	n/a
19	chr7:38492620-38492670	NHDF-neo	bronchial:	n/a
20	chr7:38468985-38469035	PrEC	prostate:	n/a
21	chr7:38505101-38505151	NB4	blood:	n/a
22	chr7:38468944-38468994	HRE	kidney:	n/a
23	chr7:38504420-38504470	Hela-S3	cervix:	n/a
24	chr7:38469273-38469323	PFSK-1	brain:	n/a
25	chr7:38504420-38504470	HCPEpiC	choroid plexus:	n/a
26	chr7:38492620-38492670	Jurkat	blood:	n/a
27	chr7:38469054-38469104	GM06990	blood:	n/a
28	chr7:38469108-38469158	AG04450	lung:	fetal
29	chr7:38492620-38492670	MCF10A-Er-Src	breast:	n/a
30	chr7:38469108-38469158	LNCaP	prostate:	n/a
31	chr7:38468985-38469035	GM19239	blood:	n/a
32	chr7:38504420-38504470	Hepatocyte	liver:	n/a
33	chr7:38468985-38469035	Hepatocyte	liver:	n/a
34	chr7:38469108-38469158	AG10803	skin:	n/a
35	chr7:38469108-38469158	NB4	blood:	n/a
36	chr7:38469273-38469323	IMR90	lung:	fetal
37	chr7:38505101-38505151	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:38468985-38469035	NHDF-neo	bronchial:	n/a
39	chr7:38468985-38469035	H1-hESC	embryonic stem cell:	embryo
40	chr7:38468985-38469035	HL-60	blood:	n/a
41	chr7:38505101-38505151	HRCEpiC	kidney:	n/a
42	chr7:38470121-38470171	SK-N-SH_RA	brain:	n/a
43	chr7:38470121-38470171	PrEC	prostate:	n/a
44	chr7:38468944-38468994	H1-hESC	embryonic stem cell:	embryo
45	chr7:38469273-38469323	HEEpiC	esophagus:	n/a
46	chr7:38470121-38470171	SK-N-MC	brain:	n/a
47	chr7:38505101-38505151	Caco-2	colon:	n/a
48	chr7:38505101-38505151	SK-N-SH_RA	brain:	n/a
49	chr7:38469108-38469158	AoSMC	blood vessel:	n/a
50	chr7:38469054-38469104	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:38491211..38492331-chr7:38671592..38672516,5	MCF-7	breast:
2	chr7:38491273..38492093-chr7:38671152..38672318,4	MCF-7	breast:
3	chr7:38494078..38495935-chr7:38691855..38693892,2	MCF-7	breast:
4	chr7:38489919..38492334-chr7:38492644..38495218,2	K562	blood:
5	chr7:38489919..38492334-chr7:38492644..38495218,2	K562	blood:
6	chr7:38443727..38445487-chr7:38463169..38464997,2	MCF-7	breast:
7	chr7:38473622..38474218-chr7:38787900..38788567,2	MCF-7	breast:
8	chr7:38466807..38469075-chr7:38472266..38473848,2	MCF-7	breast:
9	chr7:38473424..38474293-chr7:38699841..38700536,2	MCF-7	breast:

Variant related genes	Relation type
AMPH	TF binding region
AMPH	CpG island
ENSG00000078053	chromatin interactions

Extended variants
information (count: 2067 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2067 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2270294	chr7:38457144-38457145	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149870533	chr7:38457162-38457163	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs73348881	chr7:38457192-38457193	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs567929050	chr7:38457215-38457216	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs35694535	chr7:38457218-38457219	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs554089082	chr7:38457242-38457243	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs111784215	chr7:38457255-38457256	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs577246973	chr7:38457304-38457305	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs539636283	chr7:38457305-38457306	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs556345269	chr7:38457308-38457309	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs113552937	chr7:38457325-38457326	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs188993939	chr7:38457341-38457342	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs372641364	chr7:38457356-38457357	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs558887615	chr7:38457371-38457372	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs201353173	chr7:38457381-38457382	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs377750480	chr7:38457388-38457389	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs199995985	chr7:38457389-38457390	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs202236524	chr7:38457409-38457410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368760883	chr7:38457414-38457415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201059599	chr7:38457454-38457455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140860940	chr7:38457465-38457466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373071104	chr7:38457481-38457482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199697871	chr7:38457488-38457489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200519832	chr7:38457491-38457492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150091535	chr7:38457534-38457535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201987021	chr7:38457572-38457573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540264095	chr7:38457612-38457613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10247761	chr7:38457688-38457689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532712440	chr7:38457732-38457733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367578504	chr7:38457760-38457761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552456377	chr7:38457850-38457851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145976868	chr7:38457910-38457911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76047876	chr7:38457917-38457918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562901050	chr7:38457919-38457920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541005030	chr7:38457927-38457928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200023257	chr7:38457931-38457932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374515361	chr7:38457945-38457946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6970953	chr7:38457957-38457958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs193116896	chr7:38457987-38457988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75776951	chr7:38458042-38458043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146415706	chr7:38458065-38458066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559113532	chr7:38458066-38458067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs55851043	chr7:38458097-38458098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547457968	chr7:38458152-38458153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570463156	chr7:38458344-38458345	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs560432527	chr7:38458373-38458374	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs541490282	chr7:38458489-38458490	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs539701410	chr7:38458507-38458508	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs116494451	chr7:38458530-38458531	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs535667109	chr7:38458546-38458547	Enhancers Weak transcription	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
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38431600-38489000	Weak transcription	Brain Angular Gyrus	brain
2	chr7:38439000-38483000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:38444000-38468600	Weak transcription	Fetal Stomach	stomach
4	chr7:38444800-38467600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:38449400-38458000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:38450000-38457200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:38451000-38460400	Weak transcription	Aorta	Aorta
8	chr7:38455400-38467400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:38456200-38481400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:38456600-38457400	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr7:38456600-38457400	Weak transcription	Pancreas	Pancrea
12	chr7:38457000-38457400	ZNF genes & repeats	Fetal Brain Female	brain
13	chr7:38457200-38457400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:38457400-38457600	Enhancers	Pancreas	Pancrea
15	chr7:38457400-38460200	Weak transcription	Fetal Brain Female	brain
16	chr7:38457400-38479600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr7:38458000-38459000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:38458800-38459400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr7:38459000-38462200	Weak transcription	Fetal Brain Male	brain
20	chr7:38459000-38473400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:38459200-38459400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:38459200-38470400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:38460400-38460600	ZNF genes & repeats	Aorta	Aorta
24	chr7:38460600-38467400	Weak transcription	Aorta	Aorta
25	chr7:38460600-38468600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:38461800-38462000	Enhancers	Primary T cells from cord blood	blood
27	chr7:38462000-38463200	Weak transcription	Primary T cells from cord blood	blood
28	chr7:38462200-38462600	Enhancers	Fetal Brain Male	brain
29	chr7:38462600-38464800	Weak transcription	Fetal Brain Male	brain
30	chr7:38463200-38466200	Enhancers	Primary T cells from cord blood	blood
31	chr7:38463400-38467600	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr7:38463400-38468400	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr7:38463600-38464000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:38463600-38467800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr7:38463800-38465400	ZNF genes & repeats	Primary B cells from peripheral blood	blood
36	chr7:38463800-38467400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:38463800-38467600	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr7:38463800-38467800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr7:38464000-38464400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr7:38464200-38466200	Enhancers	Primary B cells from cord blood	blood
41	chr7:38464200-38467800	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr7:38464400-38465400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr7:38464400-38466400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr7:38464400-38467800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr7:38464600-38465400	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr7:38464600-38465600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr7:38464800-38465000	Enhancers	Fetal Thymus	thymus
48	chr7:38464800-38465200	Enhancers	Primary T cells fromperipheralblood	blood
49	chr7:38464800-38465400	Enhancers	Fetal Brain Male	brain
50	chr7:38464800-38465600	Enhancers	HUVEC	blood vessel

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