Variant report

Variant	esv1822873
Chromosome Location	chr4:119542500-119577466
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	chr4:119546600-119546871	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:119547576-119547749	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:119576461-119576486	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:119550987-119551186	K562	blood:	n/a	n/a
5	CBX3	chr4:119550881-119551228	K562	blood:	n/a	n/a
6	CEBPB	chr4:119566666-119567031	K562	blood:	n/a	n/a
7	CEBPB	chr4:119550980-119551187	A549	lung:	n/a	n/a
8	CEBPB	chr4:119550798-119551230	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:119550892-119551149	K562	blood:	n/a	n/a
10	CEBPB	chr4:119550959-119551180	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:119550971-119551171	K562	blood:	n/a	n/a
12	CEBPB	chr4:119563765-119563790	HepG2	liver:	n/a	chr4:119563768-119563779 chr4:119563767-119563780
13	CEBPB	chr4:119544384-119544591	K562	blood:	n/a	n/a
14	CEBPB	chr4:119575027-119575397	K562	blood:	n/a	n/a
15	CEBPD	chr4:119574979-119575474	K562	blood:	n/a	n/a
16	CEBPD	chr4:119570052-119570409	K562	blood:	n/a	n/a
17	CTCF	chr4:119550880-119551030	SAEC	small airway:	n/a	n/a
18	CTCF	chr4:119550980-119551130	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr4:119550809-119551060	IMR90	lung:	n/a	n/a
20	CTCF	chr4:119550900-119551050	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr4:119552010-119552146	MCF-7	breast:	n/a	chr4:119552043-119552061
22	CTCF	chr4:119554627-119554944	K562	blood:	n/a	n/a
23	CTCF	chr4:119552275-119552357	HepG2	liver:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
24	CTCF	chr4:119552220-119552370	WERI-Rb-1	eye:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
25	CTCF	chr4:119552340-119552490	SK-N-SH_RA	brain:	n/a	chr4:119552363-119552376
26	CTCF	chr4:119550940-119551090	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:119550880-119551030	AG04449	skin:	n/a	n/a
28	CTCF	chr4:119550900-119551050	AG09309	skin:	n/a	n/a
29	CTCF	chr4:119552053-119552118	Gliobla	brain:	n/a	n/a
30	CTCF	chr4:119550900-119551050	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr4:119550880-119551030	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr4:119550900-119551050	K562	blood:	n/a	n/a
33	CTCF	chr4:119551865-119552362	K562	blood:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552043-119552061 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
34	CTCF	chr4:119552263-119552357	K562	blood:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
35	CTCF	chr4:119552033-119552120	GM19240	blood:	n/a	chr4:119552043-119552061
36	CTCF	chr4:119552018-119552130	K562	blood:	n/a	chr4:119552043-119552061
37	CTCF	chr4:119550980-119551130	HEK293	kidney:	n/a	n/a
38	CTCF	chr4:119550928-119551068	Gliobla	brain:	n/a	n/a
39	CTCF	chr4:119552289-119552291	GM19240	blood:	n/a	n/a
40	CTCF	chr4:119552008-119552151	MCF-7	breast:	n/a	chr4:119552043-119552061
41	CTCF	chr4:119550900-119551050	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr4:119550920-119551070	HCM	heart:	n/a	n/a
43	CTCF	chr4:119550920-119551070	HMEC	breast:	n/a	n/a
44	CTCF	chr4:119550980-119551130	HFF	foreskin:	n/a	n/a
45	CTCF	chr4:119550804-119551100	K562	blood:	n/a	n/a
46	CTCF	chr4:119556321-119556513	K562	blood:	n/a	chr4:119556484-119556497
47	CTCF	chr4:119550920-119551070	GM12865	blood:	n/a	n/a
48	CTCF	chr4:119552420-119552570	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:119550900-119551050	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr4:119552212-119552370	MCF-7	breast:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119556601-119556651	HNPCEpiC	eye:	n/a
2	chr4:119554219-119554269	Hela-S3	cervix:	n/a
3	chr4:119550632-119550682	SAEC	small airway:	n/a
4	chr4:119554219-119554269	SK-N-SH_RA	brain:	n/a
5	chr4:119555395-119555445	BJ	skin:	n/a
6	chr4:119555556-119555606	U87	brain:	n/a
7	chr4:119556601-119556651	SAEC	small airway:	n/a
8	chr4:119554219-119554269	Hepatocyte	liver:	n/a
9	chr4:119554219-119554269	GM12891	blood:	n/a
10	chr4:119555556-119555606	BE2_C	brain:	n/a
11	chr4:119555556-119555606	GM12892	blood:	n/a
12	chr4:119555556-119555606	Jurkat	blood:	n/a
13	chr4:119550632-119550682	LNCaP	prostate:	n/a
14	chr4:119553015-119553065	NHBE	bronchial:	n/a
15	chr4:119555395-119555445	MCF10A-Er-Src	breast:	n/a
16	chr4:119554219-119554269	IMR90	lung:	fetal
17	chr4:119557464-119557514	ovcar-3	ovarian:	n/a
18	chr4:119556601-119556651	HCPEpiC	choroid plexus:	n/a
19	chr4:119554219-119554269	HNPCEpiC	eye:	n/a
20	chr4:119554219-119554269	SK-N-SH	brain:	n/a
21	chr4:119556601-119556651	HepG2	liver:	n/a
22	chr4:119555556-119555606	HepG2	liver:	n/a
23	chr4:119555395-119555445	RPTEC	kidney:	n/a
24	chr4:119555395-119555445	HEEpiC	esophagus:	n/a
25	chr4:119556601-119556651	Jurkat	blood:	n/a
26	chr4:119554219-119554269	HL-60	blood:	n/a
27	chr4:119554219-119554269	HRE	kidney:	n/a
28	chr4:119556601-119556651	AG09319	gingival:	n/a
29	chr4:119557464-119557514	MCF10A-Er-Src	breast:	n/a
30	chr4:119554219-119554269	K562	blood:	n/a
31	chr4:119550632-119550682	GM19239	blood:	n/a
32	chr4:119556601-119556651	AG09309	skin:	n/a
33	chr4:119557464-119557514	Jurkat	blood:	n/a
34	chr4:119557464-119557514	H1-hESC	embryonic stem cell:	embryo
35	chr4:119556601-119556651	HEK293	kidney:	embryo
36	chr4:119550632-119550682	HCF	heart:	n/a
37	chr4:119550632-119550682	T-47D	breast:	n/a
38	chr4:119555556-119555606	Hela-S3	cervix:	n/a
39	chr4:119557464-119557514	HUVEC	blood vessel:	n/a
40	chr4:119555556-119555606	HCF	heart:	n/a
41	chr4:119557464-119557514	LNCaP	prostate:	n/a
42	chr4:119554219-119554269	GM19239	blood:	n/a
43	chr4:119553015-119553065	U87	brain:	n/a
44	chr4:119555556-119555606	SK-N-MC	brain:	n/a
45	chr4:119555556-119555606	NT2-D1	testis:	n/a
46	chr4:119553015-119553065	GM06990	blood:	n/a
47	chr4:119555556-119555606	SKMC	muscle:	n/a
48	chr4:119554219-119554269	HAEpiC	amniotic membrane:	n/a
49	chr4:119553015-119553065	MCF10A-Er-Src	breast:	n/a
50	chr4:119553015-119553065	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:119200131..119202202-chr4:119563480..119565428,2	K562	blood:

Variant related genes	Relation type
ENSG00000251155	TF binding region
CICP16	TF binding region
ENSG00000225892	TF binding region
ENSG00000251155	CpG island
CICP16	CpG island
ENSG00000225892	CpG island
ENSG00000269893	chromatin interactions

Extended variants
information (count: 849 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:849 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571720278	chr4:119542513-119542514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4104027	chr4:119542554-119542555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534234808	chr4:119542581-119542582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1844340	chr4:119542640-119542641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370297839	chr4:119542684-119542685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143163124	chr4:119542727-119542728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183720766	chr4:119542731-119542732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116412545	chr4:119542732-119542733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1844339	chr4:119542752-119542753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556842428	chr4:119542753-119542754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62326249	chr4:119542827-119542828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111470637	chr4:119543178-119543179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545624069	chr4:119543781-119543782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558844719	chr4:119543883-119543884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200310032	chr4:119543886-119543887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577322093	chr4:119543887-119543888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549904709	chr4:119543915-119543916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201402837	chr4:119543968-119543969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539914739	chr4:119544255-119544256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559734264	chr4:119544263-119544264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573337889	chr4:119544302-119544303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542239517	chr4:119544359-119544360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111402548	chr4:119544398-119544399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142203834	chr4:119544449-119544450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562850655	chr4:119544509-119544510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199721548	chr4:119544511-119544512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531462607	chr4:119544544-119544545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544472532	chr4:119544593-119544594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188437257	chr4:119544594-119544595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527800989	chr4:119544653-119544654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547945555	chr4:119544679-119544680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375253141	chr4:119544752-119544753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567740189	chr4:119544795-119544796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113593408	chr4:119544814-119544815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536697588	chr4:119544866-119544867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549897354	chr4:119544867-119544868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570339151	chr4:119544958-119544959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577757464	chr4:119544963-119544964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538916521	chr4:119544968-119544969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192695961	chr4:119544988-119544989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138185570	chr4:119545019-119545020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572271955	chr4:119545023-119545024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534875797	chr4:119545027-119545028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200350836	chr4:119545173-119545174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201293994	chr4:119545406-119545407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62326250	chr4:119545476-119545477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553480968	chr4:119545674-119545675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573400958	chr4:119545704-119545705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542650438	chr4:119545732-119545733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562296571	chr4:119545739-119545740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119513400-119551400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr4:119513400-119554000	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:119513400-119554800	Weak transcription	Ovary	ovary
4	chr4:119513400-119557200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:119513600-119549200	Weak transcription	Esophagus	oesophagus
6	chr4:119513600-119550400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:119513600-119551000	Weak transcription	Pancreas	Pancrea
8	chr4:119513600-119551600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:119513600-119552400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:119513600-119552400	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr4:119513600-119552400	Weak transcription	Fetal Brain Female	brain
12	chr4:119513600-119552400	Weak transcription	Lung	lung
13	chr4:119513600-119552400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr4:119513600-119554000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:119513600-119555800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr4:119513600-119559200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr4:119513800-119551200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr4:119513800-119552400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:119513800-119555000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr4:119513800-119556000	Weak transcription	Fetal Lung	lung
21	chr4:119518400-119552600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr4:119518800-119557000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr4:119519000-119549600	Weak transcription	Brain Anterior Caudate	brain
24	chr4:119519400-119552400	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr4:119519600-119551200	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr4:119519600-119552400	Weak transcription	Brain Angular Gyrus	brain
27	chr4:119519800-119552600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr4:119519800-119559000	Weak transcription	Brain Hippocampus Middle	brain
29	chr4:119520400-119551200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr4:119520600-119549200	Weak transcription	Spleen	Spleen
31	chr4:119520600-119550400	Weak transcription	Gastric	stomach
32	chr4:119520600-119550400	Weak transcription	Thymus	Thymus
33	chr4:119520600-119552200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr4:119520600-119552200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:119520600-119552400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr4:119520800-119551000	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr4:119520800-119552200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr4:119520800-119552400	Weak transcription	Right Ventricle	heart
39	chr4:119521000-119550000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr4:119521000-119550400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:119521000-119550400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:119521200-119550200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr4:119521200-119551200	Weak transcription	Adipose Nuclei	Adipose
44	chr4:119521200-119551600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:119521200-119552400	Weak transcription	Placenta	Placenta
46	chr4:119522600-119551600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:119526000-119556200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:119527200-119552200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr4:119527400-119544200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr4:119527400-119550200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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