Variant report

Variant	nsv879702
Chromosome Location	chr4:107065718-107175191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:107122500-107122908	K562	blood:	n/a	chr4:107122543-107122559 chr4:107122542-107122558
2	ARID3A	chr4:107158658-107158673	K562	blood:	n/a	n/a
3	ARID3A	chr4:107122568-107122875	HepG2	liver:	n/a	n/a
4	ATF2	chr4:107160021-107160295	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:107132367-107132419	K562	blood:	n/a	n/a
6	BCL3	chr4:107129042-107129310	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:107159962-107160052	HepG2	liver:	n/a	n/a
8	CBX3	chr4:107083312-107083858	K562	blood:	n/a	n/a
9	CEBPB	chr4:107096804-107097116	IMR90	lung:	n/a	chr4:107096936-107096947
10	CEBPB	chr4:107113405-107113567	K562	blood:	n/a	n/a
11	CEBPB	chr4:107116003-107116285	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:107171708-107171998	K562	blood:	n/a	chr4:107171819-107171830
13	CEBPB	chr4:107082153-107082403	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:107123436-107123705	HepG2	liver:	n/a	chr4:107123585-107123596
15	CEBPB	chr4:107130236-107130498	HepG2	liver:	n/a	chr4:107130336-107130349
16	CEBPB	chr4:107083323-107083504	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:107171675-107171952	IMR90	lung:	n/a	chr4:107171819-107171830
18	CEBPB	chr4:107068526-107068578	HepG2	liver:	n/a	chr4:107068539-107068550
19	CEBPB	chr4:107123476-107123689	K562	blood:	n/a	chr4:107123585-107123596
20	CEBPB	chr4:107130258-107130471	K562	blood:	n/a	chr4:107130336-107130349
21	CEBPB	chr4:107130226-107130488	Hela-S3	cervix:	n/a	chr4:107130336-107130349
22	CEBPB	chr4:107130215-107130494	IMR90	lung:	n/a	chr4:107130336-107130349
23	CEBPB	chr4:107096846-107097088	HepG2	liver:	n/a	chr4:107096936-107096947
24	CEBPB	chr4:107171749-107171973	HepG2	liver:	n/a	chr4:107171819-107171830
25	CEBPB	chr4:107130249-107130501	A549	lung:	n/a	chr4:107130336-107130349
26	CTCF	chr4:107160088-107160261	GM10266	blood:	n/a	n/a
27	CTCF	chr4:107122660-107122810	HRE	kidney:	n/a	n/a
28	CTCF	chr4:107160006-107160371	IMR90	lung:	n/a	n/a
29	CTCF	chr4:107160160-107160310	HRE	kidney:	n/a	n/a
30	CTCF	chr4:107160070-107160284	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr4:107160083-107160250	A549	lung:	n/a	n/a
32	CTCF	chr4:107160160-107160310	GM12878	blood:	n/a	n/a
33	CTCF	chr4:107160120-107160270	GM12865	blood:	n/a	n/a
34	CTCF	chr4:107122643-107122806	GM13976	blood:	n/a	n/a
35	CTCF	chr4:107160100-107160250	GM12872	blood:	n/a	n/a
36	CTCF	chr4:107160060-107160210	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr4:107160047-107160307	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:107160120-107160270	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr4:107166882-107166914	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr4:107122620-107122770	GM12871	blood:	n/a	n/a
41	CTCF	chr4:107122592-107122861	Medullo	brain:	n/a	n/a
42	CTCF	chr4:107160078-107160251	GM19240	blood:	n/a	n/a
43	CTCF	chr4:107160140-107160290	HMF	breast:	n/a	n/a
44	CTCF	chr4:107122680-107122830	NHEK	skin:	n/a	n/a
45	CTCF	chr4:107122618-107122842	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr4:107160059-107160447	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:107160080-107160230	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr4:107160140-107160290	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr4:107160140-107160290	GM12864	blood:	n/a	n/a
50	CTCF	chr4:107122653-107122812	GM13977	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:107130107-107130157	SK-N-SH	brain:	n/a
2	chr4:107130107-107130157	MCF-7	breast:	n/a
3	chr4:107130107-107130157	HepG2	liver:	n/a
4	chr4:107130107-107130157	HRPEpiC	eye:	n/a
5	chr4:107130107-107130157	NB4	blood:	n/a
6	chr4:107130107-107130157	NT2-D1	testis:	n/a
7	chr4:107130107-107130157	SAEC	small airway:	n/a
8	chr4:107130107-107130157	PANC-1	pancreas:	n/a
9	chr4:107130107-107130157	LNCaP	prostate:	n/a
10	chr4:107130107-107130157	HCPEpiC	choroid plexus:	n/a
11	chr4:107130107-107130157	HNPCEpiC	eye:	n/a
12	chr4:107130107-107130157	HMEC	breast:	n/a
13	chr4:107130107-107130157	Hela-S3	cervix:	n/a
14	chr4:107130107-107130157	HCF	heart:	n/a
15	chr4:107130107-107130157	AG09309	skin:	n/a
16	chr4:107130107-107130157	HCT-116	colon:	n/a
17	chr4:107130107-107130157	HIPEpiC	eye:	n/a
18	chr4:107130107-107130157	HAEpiC	amniotic membrane:	n/a
19	chr4:107130107-107130157	SK-N-MC	brain:	n/a
20	chr4:107130107-107130157	NHBE	bronchial:	n/a
21	chr4:107130107-107130157	HCM	heart:	n/a
22	chr4:107130107-107130157	AG04450	lung:	fetal
23	chr4:107130107-107130157	MCF10A-Er-Src	breast:	n/a
24	chr4:107130107-107130157	T-47D	breast:	n/a
25	chr4:107130107-107130157	HUVEC	blood vessel:	n/a
26	chr4:107130107-107130157	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:107130107-107130157	GM12891	blood:	n/a
28	chr4:107130107-107130157	AG09319	gingival:	n/a
29	chr4:107130107-107130157	Jurkat	blood:	n/a
30	chr4:107130107-107130157	ECC-1	luminal epithelium:	n/a
31	chr4:107130107-107130157	A549	lung:	n/a
32	chr4:107130107-107130157	RPTEC	kidney:	n/a
33	chr4:107130107-107130157	CMK	blood:	n/a
34	chr4:107130107-107130157	HRCEpiC	kidney:	n/a
35	chr4:107130107-107130157	BE2_C	brain:	n/a
36	chr4:107130107-107130157	PrEC	prostate:	n/a
37	chr4:107130107-107130157	Hepatocyte	liver:	n/a
38	chr4:107130107-107130157	NH-A	brain:	n/a
39	chr4:107130107-107130157	U87	brain:	n/a
40	chr4:107130107-107130157	K562	blood:	n/a
41	chr4:107130107-107130157	ovcar-3	ovarian:	n/a
42	chr4:107130107-107130157	ProgFib	skin:	n/a
43	chr4:107130107-107130157	SK-N-SH_RA	brain:	n/a
44	chr4:107130107-107130157	HRE	kidney:	n/a
45	chr4:107130107-107130157	SKMC	muscle:	n/a
46	chr4:107130107-107130157	H1-hESC	embryonic stem cell:	embryo
47	chr4:107130107-107130157	AG10803	skin:	n/a
48	chr4:107130107-107130157	GM19239	blood:	n/a
49	chr4:107130107-107130157	PFSK-1	brain:	n/a
50	chr4:107130107-107130157	HEEpiC	esophagus:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:107057719..107060245-chr4:107065228..107066927,2	K562	blood:
2	chr4:107129508..107131492-chr4:107132634..107135593,2	MCF-7	breast:
3	chr4:107164698..107166859-chr4:107230939..107233039,2	K562	blood:
4	chr4:107144706..107146969-chr4:107150712..107153683,3	K562	blood:
5	chr4:107142111..107144318-chr4:107145536..107147639,2	K562	blood:
6	chr4:107157087..107158697-chr4:107236510..107238674,2	MCF-7	breast:
7	chr4:106875594..106876144-chr4:107122239..107122877,2	MCF-7	breast:
8	chr4:107160677..107162898-chr4:107235492..107237232,2	MCF-7	breast:
9	chr4:107142111..107144318-chr4:107145536..107147639,2	K562	blood:
10	chr2:88990302..88991116-chr4:107159175..107159797,2	MCF-7	breast:
11	chr4:107116810..107118888-chr4:107121036..107122571,2	K562	blood:
12	chr4:107129974..107132069-chr4:107132979..107135565,2	MCF-7	breast:
13	chr4:107116810..107118888-chr4:107121036..107122571,2	K562	blood:

No data

Variant related genes	Relation type
TBCK	TF binding region
TBCK	CpG island
ENSG00000145348	chromatin interactions
ENSG00000164022	chromatin interactions

Extended variants
information (count: 3716 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3716 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11736518	chr4:107065718-107065719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184092440	chr4:107065724-107065725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547127715	chr4:107065800-107065801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375733797	chr4:107065801-107065802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140308559	chr4:107065888-107065889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112049738	chr4:107065901-107065902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376581069	chr4:107065908-107065909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370572683	chr4:107065930-107065931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186938940	chr4:107065946-107065947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541951595	chr4:107065949-107065950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561308929	chr4:107065974-107065975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571729141	chr4:107065976-107065977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541319403	chr4:107065978-107065979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367582941	chr4:107065995-107065996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370366349	chr4:107066001-107066002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112335958	chr4:107066009-107066010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551142052	chr4:107066052-107066053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374880585	chr4:107066080-107066081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559668773	chr4:107066094-107066095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533705986	chr4:107066095-107066096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543651352	chr4:107066123-107066124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563947245	chr4:107066124-107066125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529328351	chr4:107066137-107066138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549500730	chr4:107066160-107066161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139449857	chr4:107066161-107066162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34322527	chr4:107066177-107066178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6810877	chr4:107066199-107066200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs551834894	chr4:107066205-107066206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376371380	chr4:107066297-107066298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371910120	chr4:107066310-107066311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143943598	chr4:107066341-107066342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191430009	chr4:107066342-107066343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374733816	chr4:107066343-107066344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556078329	chr4:107066352-107066353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569842850	chr4:107066376-107066377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62321371	chr4:107066382-107066383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555057206	chr4:107066448-107066449	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs571840879	chr4:107066487-107066488	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs540599588	chr4:107066569-107066570	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs557375288	chr4:107066588-107066589	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs578180241	chr4:107066613-107066614	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542927010	chr4:107066674-107066675	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544104675	chr4:107066753-107066754	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559709105	chr4:107066772-107066773	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563683978	chr4:107066773-107066774	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75267087	chr4:107066781-107066782	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543111244	chr4:107066783-107066784	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559870456	chr4:107066830-107066831	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529032532	chr4:107066869-107066870	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528625891	chr4:107066920-107066921	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107035600-107083200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:107037600-107066400	Weak transcription	Fetal Kidney	kidney
3	chr4:107037800-107077400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:107038000-107112000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr4:107053600-107067600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr4:107053800-107070000	Weak transcription	Brain Hippocampus Middle	brain
7	chr4:107053800-107080000	Weak transcription	Right Ventricle	heart
8	chr4:107053800-107083400	Weak transcription	HSMM	muscle
9	chr4:107053800-107083800	Weak transcription	Left Ventricle	heart
10	chr4:107053800-107101600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr4:107054000-107066400	Weak transcription	Liver	Liver
12	chr4:107054000-107067000	Weak transcription	Fetal Lung	lung
13	chr4:107054000-107067000	Weak transcription	Fetal Muscle Leg	muscle
14	chr4:107054000-107067800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr4:107054000-107070000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr4:107054000-107070400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:107054000-107074400	Weak transcription	HepG2	liver
18	chr4:107054000-107076800	Weak transcription	Fetal Muscle Trunk	muscle
19	chr4:107054000-107077000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:107054000-107077000	Weak transcription	Fetal Intestine Large	intestine
21	chr4:107054000-107077400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:107054000-107077400	Weak transcription	Aorta	Aorta
23	chr4:107054000-107077400	Weak transcription	Fetal Stomach	stomach
24	chr4:107054000-107077400	Weak transcription	Lung	lung
25	chr4:107054000-107081600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr4:107054000-107083200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:107054000-107083400	Weak transcription	Pancreas	Pancrea
28	chr4:107054000-107091000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr4:107054000-107113600	Weak transcription	Brain Anterior Caudate	brain
30	chr4:107054200-107065800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr4:107054200-107070000	Weak transcription	Adipose Nuclei	Adipose
32	chr4:107054200-107083400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr4:107054600-107074400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:107056000-107066600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:107056000-107067200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr4:107056000-107067200	Weak transcription	Primary T cells from cord blood	blood
37	chr4:107056200-107067200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:107056200-107077000	Weak transcription	Ovary	ovary
39	chr4:107056200-107083400	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr4:107057800-107069800	Weak transcription	Primary B cells from cord blood	blood
41	chr4:107062200-107071200	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr4:107063000-107070000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:107063600-107067600	Weak transcription	Fetal Brain Male	brain
44	chr4:107064200-107070400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:107064400-107069600	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr4:107065000-107065800	Strong transcription	Primary B cells from peripheral blood	blood
47	chr4:107065000-107083400	Weak transcription	Brain Germinal Matrix	brain
48	chr4:107065800-107066600	Weak transcription	Primary B cells from peripheral blood	blood
49	chr4:107065800-107067600	Weak transcription	Psoas Muscle	Psoas
50	chr4:107066400-107067000	Strong transcription	Liver	Liver

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