Variant report

Variant	esv3517788
Chromosome Location	chr4:751652-754800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:73)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:73 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr4:754456-754736	K562	blood:	n/a	n/a
2	CTCF	chr4:754580-754730	WERI-Rb-1	eye:	n/a	n/a
3	CTCF	chr4:753720-753870	HBMEC	blood vessel:	n/a	n/a
4	E2F6	chr4:753669-754012	H1-hESC	embryonic stem cell:	n/a	n/a
5	E2F6	chr4:753649-754094	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr4:753711-753871	K562	blood:	n/a	n/a
7	HMGN3	chr4:754479-754630	K562	blood:	n/a	n/a
8	JUND	chr4:753525-753646	HepG2	liver:	n/a	n/a
9	JUND	chr4:753010-753169	HepG2	liver:	n/a	n/a
10	JUND	chr4:753441-753551	H1-hESC	embryonic stem cell:	n/a	n/a
11	JUND	chr4:752012-752612	H1-hESC	embryonic stem cell:	n/a	n/a
12	JUND	chr4:752012-752518	H1-hESC	embryonic stem cell:	n/a	n/a
13	JUND	chr4:752692-752851	HepG2	liver:	n/a	n/a
14	JUND	chr4:753667-753858	H1-hESC	embryonic stem cell:	n/a	n/a
15	JUND	chr4:753635-753883	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr4:753759-753909	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr4:753753-754077	K562	blood:	n/a	n/a
18	POLR2A	chr4:754404-754761	K562	blood:	n/a	n/a
19	POLR2A	chr4:753793-753927	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr4:754578-755005	GM12878	blood:	n/a	n/a
21	POLR2A	chr4:754068-754963	U87	brain:	n/a	n/a
22	POLR2A	chr4:751524-752111	K562	blood:	n/a	n/a
23	POLR2A	chr4:754105-761557	K562	blood:	n/a	n/a
24	POLR2A	chr4:754604-754845	HCT-116	colon:	n/a	n/a
25	POLR2A	chr4:751985-752055	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr4:751989-751994	MCF-7	breast:	n/a	n/a
27	POLR2A	chr4:754693-754717	MCF-7	breast:	n/a	n/a
28	POLR2A	chr4:752566-752842	GM12891	blood:	n/a	n/a
29	POLR2A	chr4:754068-754979	U87	brain:	n/a	n/a
30	POLR2A	chr4:753809-754048	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr4:753831-753839	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr4:754238-754341	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr4:754677-754689	HepG2	liver:	n/a	n/a
34	POLR2A	chr4:752034-752490	K562	blood:	n/a	n/a
35	POLR2A	chr4:754358-754373	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr4:754168-754307	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr4:753019-754283	K562	blood:	n/a	n/a
38	POLR2A	chr4:752060-752124	MCF-7	breast:	n/a	n/a
39	POLR2A	chr4:753760-754183	MCF-7	breast:	n/a	n/a
40	POLR2A	chr4:753868-753893	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr4:754275-761413	MCF-7	breast:	n/a	n/a
42	POLR2A	chr4:753719-754252	U87	brain:	n/a	n/a
43	POLR2A	chr4:754591-758949	HepG2	liver:	n/a	n/a
44	POLR2A	chr4:754446-754704	GM12878	blood:	n/a	n/a
45	POLR2A	chr4:752893-753160	GM12891	blood:	n/a	n/a
46	POLR2A	chr4:751986-752417	K562	blood:	n/a	n/a
47	POLR2A	chr4:753789-754734	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:753739-764687	K562	blood:	n/a	n/a
49	POLR2A	chr4:753802-754258	HepG2	liver:	n/a	n/a
50	POLR2A	chr4:752140-752159	MCF-7	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:753903-753953	H1-hESC	embryonic stem cell:	embryo
2	chr4:753903-753953	H1-hESC	embryonic stem cell:	embryo
3	chr4:754410-754460	T-47D	breast:	n/a
4	chr4:754410-754460	NT2-D1	testis:	n/a
5	chr4:754733-754783	A549	lung:	n/a
6	chr4:754410-754460	HCM	heart:	n/a
7	chr4:754410-754460	MCF10A-Er-Src	breast:	n/a
8	chr4:754733-754783	SKMC	muscle:	n/a
9	chr4:754410-754460	GM12891	blood:	n/a
10	chr4:753903-753953	IMR90	lung:	fetal
11	chr4:754410-754460	GM12878	blood:	n/a
12	chr4:754733-754783	ECC-1	luminal epithelium:	n/a
13	chr4:754410-754460	HCT-116	colon:	n/a
14	chr4:754733-754783	HCPEpiC	choroid plexus:	n/a
15	chr4:753903-753953	ovcar-3	ovarian:	n/a
16	chr4:754410-754460	Hepatocyte	liver:	n/a
17	chr4:754410-754460	HUVEC	blood vessel:	n/a
18	chr4:753903-753953	ECC-1	luminal epithelium:	n/a
19	chr4:753903-753953	AG04450	lung:	fetal
20	chr4:754410-754460	K562	blood:	n/a
21	chr4:753903-753953	HEEpiC	esophagus:	n/a
22	chr4:754410-754460	RPTEC	kidney:	n/a
23	chr4:754733-754783	U87	brain:	n/a
24	chr4:754410-754460	HMEC	breast:	n/a
25	chr4:753903-753953	GM19239	blood:	n/a
26	chr4:754410-754460	PANC-1	pancreas:	n/a
27	chr4:754733-754783	HepG2	liver:	n/a
28	chr4:753903-753953	PrEC	prostate:	n/a
29	chr4:753903-753953	CMK	blood:	n/a
30	chr4:754410-754460	ECC-1	luminal epithelium:	n/a
31	chr4:753903-753953	NB4	blood:	n/a
32	chr4:753903-753953	K562	blood:	n/a
33	chr4:754733-754783	AoSMC	blood vessel:	n/a
34	chr4:754733-754783	HIPEpiC	eye:	n/a
35	chr4:754410-754460	PFSK-1	brain:	n/a
36	chr4:753903-753953	HCF	heart:	n/a
37	chr4:754410-754460	SK-N-MC	brain:	n/a
38	chr4:753903-753953	SAEC	small airway:	n/a
39	chr4:754410-754460	AG09309	skin:	n/a
40	chr4:754733-754783	SK-N-MC	brain:	n/a
41	chr4:754410-754460	IMR90	lung:	fetal
42	chr4:753903-753953	SK-N-MC	brain:	n/a
43	chr4:754733-754783	HEK293	kidney:	embryo
44	chr4:754410-754460	HepG2	liver:	n/a
45	chr4:753903-753953	RPTEC	kidney:	n/a
46	chr4:754733-754783	HEEpiC	esophagus:	n/a
47	chr4:753903-753953	PFSK-1	brain:	n/a
48	chr4:753903-753953	Hepatocyte	liver:	n/a
49	chr4:754410-754460	HAEpiC	amniotic membrane:	n/a
50	chr4:753903-753953	AG10803	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:741902..744115-chr4:754225..756300,2	MCF-7	breast:
2	chr4:658116..660628-chr4:754612..756376,2	K562	blood:
3	chr4:754637..757120-chr4:925087..927511,3	MCF-7	breast:
4	chr4:593904..597020-chr4:753917..757326,3	MCF-7	breast:
5	chr4:749591..753567-chr4:753955..757140,4	MCF-7	breast:
6	chr4:745562..749408-chr4:752726..755779,3	MCF-7	breast:
7	chr4:666788..669425-chr4:753705..755956,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPLX1-8	chr4:751179-751731	expRegAs_chr4_73_-
2	lnc-CPLX1-4	chr4:753969-754335	predAs_ge08_PCGF3_2

No data

Variant related genes	Relation type
ENSG00000272588	TF binding region
ENSG00000272588	CpG island
ENSG00000215375	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000178950	chromatin interactions
ENSG00000133256	chromatin interactions
ENSG00000127419	chromatin interactions
ENSG00000272588	chromatin interactions

Extended variants
information (count: 213 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:213 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555772008	chr4:751675-751676	Weak transcription Strong transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs536765905	chr4:751683-751684	Weak transcription Strong transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs574009285	chr4:751685-751686	Weak transcription Strong transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs534669109	chr4:751722-751723	Weak transcription Strong transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs553064125	chr4:751736-751737	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs542465522	chr4:751754-751755	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577671779	chr4:751797-751798	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs142984892	chr4:751828-751829	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs554676470	chr4:751832-751833	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs557166373	chr4:751865-751866	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs575336827	chr4:751878-751879	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs374141047	chr4:751886-751887	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573476600	chr4:751888-751889	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560998551	chr4:751910-751911	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs528106976	chr4:751911-751912	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs62294067	chr4:751946-751947	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551003779	chr4:751975-751976	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs71166830	chr4:751976-751977	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs61081270	chr4:751980-751981	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs564975997	chr4:752016-752017	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs532294484	chr4:752033-752034	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs550689276	chr4:752040-752041	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570266694	chr4:752043-752044	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530991936	chr4:752048-752049	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs367761464	chr4:752058-752059	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs115035109	chr4:752064-752065	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs185262575	chr4:752072-752073	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545953125	chr4:752101-752102	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534703288	chr4:752103-752104	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs73058469	chr4:752132-752133	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs571304389	chr4:752133-752134	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs141046548	chr4:752140-752141	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs557157721	chr4:752149-752150	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs183997536	chr4:752156-752157	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs55955900	chr4:752166-752167	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11248038	chr4:752170-752171	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs371921557	chr4:752176-752177	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs111545929	chr4:752183-752184	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs573128340	chr4:752204-752205	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs540531500	chr4:752209-752210	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs146236395	chr4:752227-752228	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs564917454	chr4:752235-752236	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532130936	chr4:752244-752245	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs375179194	chr4:752257-752258	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs544326120	chr4:752265-752266	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs59438465	chr4:752276-752277	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs62294068	chr4:752277-752278	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs372039136	chr4:752299-752300	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs71604319	chr4:752314-752315	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs191430616	chr4:752329-752330	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:702200-754800	Weak transcription	Hela-S3	cervix
2	chr4:727000-767600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:728600-755800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr4:728600-763400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr4:729000-754600	Weak transcription	Fetal Kidney	kidney
6	chr4:729000-762600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr4:729600-753800	Weak transcription	Psoas Muscle	Psoas
8	chr4:729600-760800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr4:733600-753800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:736600-752000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:741400-751800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:741400-752000	Strong transcription	Fetal Intestine Small	intestine
13	chr4:741400-752400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:741400-752400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:741400-752800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:741400-752800	Strong transcription	Fetal Thymus	thymus
17	chr4:741600-752400	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr4:741600-752400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:741600-752400	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr4:741600-752800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:741800-751800	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:742600-751800	Strong transcription	Placenta	Placenta
23	chr4:742600-754400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:742600-763600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr4:742800-754200	Weak transcription	Colon Smooth Muscle	Colon
26	chr4:742800-756200	Weak transcription	Stomach Mucosa	stomach
27	chr4:742800-764000	Weak transcription	Small Intestine	intestine
28	chr4:744200-754800	Weak transcription	NHEK	skin
29	chr4:744400-752200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr4:744400-753800	Weak transcription	A549	lung
31	chr4:744400-763400	Weak transcription	Right Atrium	heart
32	chr4:744600-753800	Weak transcription	HUVEC	blood vessel
33	chr4:744600-754000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr4:745400-754800	Weak transcription	NHDF-Ad	bronchial
35	chr4:745600-752800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr4:745800-752400	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr4:746000-753800	Weak transcription	Fetal Heart	heart
38	chr4:746000-753800	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr4:746000-754400	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr4:746000-773800	Weak transcription	Fetal Brain Male	brain
41	chr4:746200-752400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:746200-754400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr4:746200-758600	Weak transcription	Brain Anterior Caudate	brain
44	chr4:746600-752000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:746800-752400	Strong transcription	Fetal Muscle Leg	muscle
46	chr4:747000-752600	Strong transcription	Fetal Muscle Trunk	muscle
47	chr4:747000-753800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr4:747000-754400	Weak transcription	Primary hematopoietic stem cells	blood
49	chr4:747000-756400	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr4:747200-754400	Weak transcription	Primary T helper cells PMA-I stimulated	--

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