Variant report

Variant	nsv879703
Chromosome Location	chr4:107082926-107163128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:551)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:107158658-107158673	K562	blood:	n/a	n/a
2	ARID3A	chr4:107122500-107122908	K562	blood:	n/a	chr4:107122543-107122559 chr4:107122542-107122558
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	chr4:107123436-107123705	HepG2	liver:	n/a	chr4:107123585-107123596
10	CEBPB	chr4:107116003-107116285	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:107130226-107130488	Hela-S3	cervix:	n/a	chr4:107130336-107130349
12	CEBPB	chr4:107096804-107097116	IMR90	lung:	n/a	chr4:107096936-107096947
13	CEBPB	chr4:107130236-107130498	HepG2	liver:	n/a	chr4:107130336-107130349
14	CEBPB	chr4:107123476-107123689	K562	blood:	n/a	chr4:107123585-107123596
15	CEBPB	chr4:107083323-107083504	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:107096846-107097088	HepG2	liver:	n/a	chr4:107096936-107096947
17	CEBPB	chr4:107130215-107130494	IMR90	lung:	n/a	chr4:107130336-107130349
18	CEBPB	chr4:107130258-107130471	K562	blood:	n/a	chr4:107130336-107130349
19	CEBPB	chr4:107130249-107130501	A549	lung:	n/a	chr4:107130336-107130349
20	CEBPB	chr4:107113405-107113567	K562	blood:	n/a	n/a
21	CTCF	chr4:107122700-107122850	HAc	cerebellar:	n/a	n/a
22	CTCF	chr4:107114260-107114410	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:107149828-107149842	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr4:107160100-107160250	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr4:107160100-107160232	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr4:107122520-107122670	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:107160140-107160290	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr4:107160120-107160270	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr4:107160380-107160530	GM12868	blood:	n/a	n/a
30	CTCF	chr4:107159965-107160380	K562	blood:	n/a	n/a
31	CTCF	chr4:107160160-107160310	BE2_C	brain:	n/a	n/a
32	CTCF	chr4:107160100-107160250	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr4:107122640-107122790	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr4:107122660-107122810	GM12873	blood:	n/a	n/a
35	CTCF	chr4:107122680-107122830	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr4:107122720-107122870	WI-38	lung:	n/a	n/a
37	CTCF	chr4:107160160-107160310	K562	blood:	n/a	n/a
38	CTCF	chr4:107160026-107160402	K562	blood:	n/a	n/a
39	CTCF	chr4:107122640-107122790	HMF	breast:	n/a	n/a
40	CTCF	chr4:107122600-107122750	HRE	kidney:	n/a	n/a
41	CTCF	chr4:107160100-107160250	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr4:107122640-107122790	AG09319	gingival:	n/a	n/a
43	CTCF	chr4:107122560-107122710	HCT-116	colon:	n/a	n/a
44	CTCF	chr4:107160160-107160310	HVMF	connective:	n/a	n/a
45	CTCF	chr4:107160120-107160270	GM06990	blood:	n/a	n/a
46	CTCF	chr4:107160100-107160250	Caco-2	colon:	n/a	n/a
47	CTCF	chr4:107160120-107160270	NHEK	skin:	n/a	n/a
48	CTCF	chr4:107160088-107160283	HepG2	liver:	n/a	n/a
49	CTCF	chr4:107122660-107122810	HPF	lung:	n/a	n/a
50	CTCF	chr4:107160046-107160302	Kidney_OC	kidney:	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	ProgFib	skin:	n/a
2	chr4:107130107-107130157	HEK293	kidney:	embryo
3	chr4:107130107-107130157	NHBE	bronchial:	n/a
4	chr4:107130107-107130157	HMEC	breast:	n/a
5	chr4:107130107-107130157	GM06990	blood:	n/a
6	chr4:107130107-107130157	AG09319	gingival:	n/a
7	chr4:107130107-107130157	PFSK-1	brain:	n/a
8	chr4:107130107-107130157	AoSMC	blood vessel:	n/a
9	chr4:107130107-107130157	BJ	skin:	n/a
10	chr4:107130107-107130157	PANC-1	pancreas:	n/a
11	chr4:107130107-107130157	K562	blood:	n/a
12	chr4:107130107-107130157	A549	lung:	n/a
13	chr4:107130107-107130157	AG04449	skin:	fetal
14	chr4:107130107-107130157	HEEpiC	esophagus:	n/a
15	chr4:107130107-107130157	SK-N-MC	brain:	n/a
16	chr4:107130107-107130157	RPTEC	kidney:	n/a
17	chr4:107130107-107130157	GM19239	blood:	n/a
18	chr4:107130107-107130157	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:107130107-107130157	SAEC	small airway:	n/a
20	chr4:107130107-107130157	HCF	heart:	n/a
21	chr4:107130107-107130157	H1-hESC	embryonic stem cell:	embryo
22	chr4:107130107-107130157	Jurkat	blood:	n/a
23	chr4:107130107-107130157	IMR90	lung:	fetal
24	chr4:107130107-107130157	CMK	blood:	n/a
25	chr4:107130107-107130157	HRCEpiC	kidney:	n/a
26	chr4:107130107-107130157	AG10803	skin:	n/a
27	chr4:107130107-107130157	BE2_C	brain:	n/a
28	chr4:107130107-107130157	HL-60	blood:	n/a
29	chr4:107130107-107130157	Caco-2	colon:	n/a
30	chr4:107130107-107130157	HRPEpiC	eye:	n/a
31	chr4:107130107-107130157	HAEpiC	amniotic membrane:	n/a
32	chr4:107130107-107130157	AG04450	lung:	fetal
33	chr4:107130107-107130157	ECC-1	luminal epithelium:	n/a
34	chr4:107130107-107130157	NH-A	brain:	n/a
35	chr4:107130107-107130157	GM12878	blood:	n/a
36	chr4:107130107-107130157	HCM	heart:	n/a
37	chr4:107130107-107130157	NT2-D1	testis:	n/a
38	chr4:107130107-107130157	Hepatocyte	liver:	n/a
39	chr4:107130107-107130157	SK-N-SH	brain:	n/a
40	chr4:107130107-107130157	GM12892	blood:	n/a
41	chr4:107130107-107130157	ovcar-3	ovarian:	n/a
42	chr4:107130107-107130157	LNCaP	prostate:	n/a
43	chr4:107130107-107130157	HepG2	liver:	n/a
44	chr4:107130107-107130157	MCF-7	breast:	n/a
45	chr4:107130107-107130157	NB4	blood:	n/a
46	chr4:107130107-107130157	HNPCEpiC	eye:	n/a
47	chr4:107130107-107130157	T-47D	breast:	n/a
48	chr4:107130107-107130157	HCPEpiC	choroid plexus:	n/a
49	chr4:107130107-107130157	SKMC	muscle:	n/a
50	chr4:107130107-107130157	Hela-S3	cervix:	n/a

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

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

No data

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

Extended variants
information (count: 2743 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2743 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4597909	chr4:107082926-107082927	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148791823	chr4:107082934-107082935	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552258672	chr4:107082964-107082965	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141753975	chr4:107083017-107083018	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563154400	chr4:107083029-107083030	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189980452	chr4:107083146-107083147	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528950764	chr4:107083168-107083169	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112051284	chr4:107083202-107083203	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569882988	chr4:107083250-107083251	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28848568	chr4:107083274-107083275	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528061174	chr4:107083284-107083285	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182260570	chr4:107083307-107083308	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536709183	chr4:107083318-107083319	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537743988	chr4:107083331-107083332	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72968432	chr4:107083497-107083498	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs567777653	chr4:107083510-107083511	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536722158	chr4:107083530-107083531	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146009328	chr4:107083582-107083583	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12646263	chr4:107083746-107083747	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs138349532	chr4:107083747-107083748	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10027207	chr4:107083779-107083780	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs149241123	chr4:107083782-107083783	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143461230	chr4:107083790-107083791	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs137895761	chr4:107083809-107083810	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10017707	chr4:107083918-107083919	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs189244555	chr4:107083949-107083950	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559174200	chr4:107083958-107083959	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142423388	chr4:107083978-107083979	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191965591	chr4:107084093-107084094	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564883290	chr4:107084097-107084098	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145973389	chr4:107084105-107084106	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78553662	chr4:107084207-107084208	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183885012	chr4:107084219-107084220	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370436958	chr4:107084253-107084254	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555444947	chr4:107084277-107084278	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13328056	chr4:107084288-107084289	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148703073	chr4:107084291-107084292	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547209048	chr4:107084317-107084318	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566845826	chr4:107084318-107084319	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12647078	chr4:107084333-107084334	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs558491337	chr4:107084459-107084460	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575259654	chr4:107084463-107084464	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141282539	chr4:107084497-107084498	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35802113	chr4:107084571-107084572	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556823287	chr4:107084591-107084592	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573919616	chr4:107084611-107084612	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34089033	chr4:107084612-107084613	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35653321	chr4:107084671-107084672	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72968436	chr4:107084734-107084735	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs188429689	chr4:107084739-107084740	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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

Chromatin state (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107035600-107083200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:107038000-107112000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr4:107053800-107083400	Weak transcription	HSMM	muscle
4	chr4:107053800-107083800	Weak transcription	Left Ventricle	heart
5	chr4:107053800-107101600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr4:107054000-107083200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:107054000-107083400	Weak transcription	Pancreas	Pancrea
8	chr4:107054000-107091000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr4:107054000-107113600	Weak transcription	Brain Anterior Caudate	brain
10	chr4:107054200-107083400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:107056200-107083400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr4:107065000-107083400	Weak transcription	Brain Germinal Matrix	brain
13	chr4:107066400-107151200	Weak transcription	Colon Smooth Muscle	Colon
14	chr4:107067400-107083600	Weak transcription	Fetal Kidney	kidney
15	chr4:107068600-107083200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:107068600-107083600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:107070200-107083200	Weak transcription	Brain Hippocampus Middle	brain
18	chr4:107070200-107083400	Weak transcription	Fetal Muscle Leg	muscle
19	chr4:107070400-107083200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr4:107070600-107084200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr4:107071400-107083000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr4:107071800-107176400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr4:107072000-107083000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:107072200-107083400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr4:107073000-107086800	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr4:107073400-107083000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:107074200-107114400	Weak transcription	NHDF-Ad	bronchial
28	chr4:107074400-107083400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:107074600-107111800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr4:107075200-107091000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr4:107075400-107083200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr4:107075800-107114000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr4:107075800-107118200	Weak transcription	Brain Substantia Nigra	brain
34	chr4:107075800-107129600	Weak transcription	Spleen	Spleen
35	chr4:107076000-107083800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr4:107076400-107083600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr4:107076400-107114200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr4:107076800-107083600	Weak transcription	Thymus	Thymus
39	chr4:107077000-107089600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr4:107077600-107083400	Weak transcription	Esophagus	oesophagus
41	chr4:107077800-107083000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr4:107077800-107083200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:107077800-107083200	Weak transcription	Fetal Lung	lung
44	chr4:107078000-107083200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr4:107078000-107083400	Weak transcription	Gastric	stomach
46	chr4:107078000-107083600	Weak transcription	Dnd41	blood
47	chr4:107078000-107083800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:107078000-107107800	Weak transcription	HSMMtube	muscle
49	chr4:107078200-107083200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr4:107078200-107116000	Weak transcription	Colonic Mucosa	Colon

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