Variant report

Variant	nsv966369
Chromosome Location	chr4:119539088-119559938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:427)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

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	chr4:119550987-119551186	K562	blood:	n/a	n/a
4	CBX3	chr4:119550881-119551228	K562	blood:	n/a	n/a
5	CEBPB	chr4:119550980-119551187	A549	lung:	n/a	n/a
6	CEBPB	chr4:119541445-119541681	K562	blood:	n/a	chr4:119541607-119541618
7	CEBPB	chr4:119544384-119544591	K562	blood:	n/a	n/a
8	CEBPB	chr4:119550892-119551149	K562	blood:	n/a	n/a
9	CEBPB	chr4:119550959-119551180	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:119550971-119551171	K562	blood:	n/a	n/a
11	CEBPB	chr4:119550798-119551230	IMR90	lung:	n/a	n/a
12	CTCF	chr4:119550928-119551068	Gliobla	brain:	n/a	n/a
13	CTCF	chr4:119550933-119551054	NHEK	skin:	n/a	n/a
14	CTCF	chr4:119550804-119551100	K562	blood:	n/a	n/a
15	CTCF	chr4:119552016-119552122	GM12892	blood:	n/a	chr4:119552043-119552061
16	CTCF	chr4:119550900-119551050	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr4:119550900-119551050	AG04449	skin:	n/a	n/a
18	CTCF	chr4:119550880-119551030	HPF	lung:	n/a	n/a
19	CTCF	chr4:119550900-119551050	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr4:119552036-119552135	MCF-7	breast:	n/a	chr4:119552043-119552061
21	CTCF	chr4:119550940-119551090	NB4	blood:	n/a	n/a
22	CTCF	chr4:119552033-119552120	GM19240	blood:	n/a	chr4:119552043-119552061
23	CTCF	chr4:119552054-119552112	GM19238	blood:	n/a	n/a
24	CTCF	chr4:119550920-119551070	HRE	kidney:	n/a	n/a
25	CTCF	chr4:119550880-119551030	AG09319	gingival:	n/a	n/a
26	CTCF	chr4:119550940-119551090	HAc	cerebellar:	n/a	n/a
27	CTCF	chr4:119552053-119552118	Gliobla	brain:	n/a	n/a
28	CTCF	chr4:119550900-119551050	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr4:119550980-119551130	HEK293	kidney:	n/a	n/a
30	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
31	CTCF	chr4:119550900-119551050	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr4:119550880-119551030	SAEC	small airway:	n/a	n/a
33	CTCF	chr4:119550940-119551090	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr4:119550560-119550710	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr4:119552340-119552490	SK-N-SH_RA	brain:	n/a	chr4:119552363-119552376
36	CTCF	chr4:119550900-119551050	HMF	breast:	n/a	n/a
37	CTCF	chr4:119550978-119551014	HepG2	liver:	n/a	n/a
38	CTCF	chr4:119550900-119551050	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr4:119550900-119551050	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr4:119556321-119556513	K562	blood:	n/a	chr4:119556484-119556497
41	CTCF	chr4:119552053-119552116	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:119552225-119552340	GM12891	blood:	n/a	chr4:119552304-119552317 chr4:119552305-119552315 chr4:119552302-119552320 chr4:119552297-119552318 chr4:119552308-119552317
43	CTCF	chr4:119550900-119551050	BJ	skin:	n/a	n/a
44	CTCF	chr4:119550940-119551090	HCM	heart:	n/a	n/a
45	CTCF	chr4:119550940-119551090	HCT-116	colon:	n/a	n/a
46	CTCF	chr4:119550894-119551051	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr4:119552008-119552151	MCF-7	breast:	n/a	chr4:119552043-119552061
48	CTCF	chr4:119550685-119551203	K562	blood:	n/a	n/a
49	CTCF	chr4:119550980-119551130	HCFaa	heart:	n/a	n/a
50	CTCF	chr4:119550920-119551070	RPTEC	kidney:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119554219-119554269	U87	brain:	n/a
2	chr4:119555556-119555606	NB4	blood:	n/a
3	chr4:119555556-119555606	HIPEpiC	eye:	n/a
4	chr4:119550632-119550682	RPTEC	kidney:	n/a
5	chr4:119550632-119550682	NT2-D1	testis:	n/a
6	chr4:119553015-119553065	K562	blood:	n/a
7	chr4:119554219-119554269	Jurkat	blood:	n/a
8	chr4:119550632-119550682	HCPEpiC	choroid plexus:	n/a
9	chr4:119554219-119554269	NH-A	brain:	n/a
10	chr4:119553015-119553065	GM06990	blood:	n/a
11	chr4:119557464-119557514	Hela-S3	cervix:	n/a
12	chr4:119554219-119554269	GM06990	blood:	n/a
13	chr4:119557464-119557514	T-47D	breast:	n/a
14	chr4:119556601-119556651	MCF10A-Er-Src	breast:	n/a
15	chr4:119554219-119554269	PANC-1	pancreas:	n/a
16	chr4:119553015-119553065	Hepatocyte	liver:	n/a
17	chr4:119557464-119557514	HEK293	kidney:	embryo
18	chr4:119553015-119553065	HAEpiC	amniotic membrane:	n/a
19	chr4:119556601-119556651	HRE	kidney:	n/a
20	chr4:119554219-119554269	HMEC	breast:	n/a
21	chr4:119554219-119554269	NB4	blood:	n/a
22	chr4:119555395-119555445	HRCEpiC	kidney:	n/a
23	chr4:119550632-119550682	GM12892	blood:	n/a
24	chr4:119555556-119555606	IMR90	lung:	fetal
25	chr4:119550632-119550682	NHDF-neo	bronchial:	n/a
26	chr4:119555395-119555445	AG04449	skin:	fetal
27	chr4:119555556-119555606	GM12891	blood:	n/a
28	chr4:119557464-119557514	PrEC	prostate:	n/a
29	chr4:119555556-119555606	HUVEC	blood vessel:	n/a
30	chr4:119550632-119550682	NH-A	brain:	n/a
31	chr4:119557464-119557514	NT2-D1	testis:	n/a
32	chr4:119553015-119553065	PFSK-1	brain:	n/a
33	chr4:119555556-119555606	MCF10A-Er-Src	breast:	n/a
34	chr4:119554219-119554269	BE2_C	brain:	n/a
35	chr4:119556601-119556651	U87	brain:	n/a
36	chr4:119556601-119556651	AG09319	gingival:	n/a
37	chr4:119555395-119555445	SK-N-MC	brain:	n/a
38	chr4:119553015-119553065	SAEC	small airway:	n/a
39	chr4:119557464-119557514	Jurkat	blood:	n/a
40	chr4:119555556-119555606	SK-N-SH_RA	brain:	n/a
41	chr4:119555395-119555445	HepG2	liver:	n/a
42	chr4:119554219-119554269	GM12878	blood:	n/a
43	chr4:119554219-119554269	HCF	heart:	n/a
44	chr4:119550632-119550682	HCM	heart:	n/a
45	chr4:119554219-119554269	AG10803	skin:	n/a
46	chr4:119555395-119555445	NHBE	bronchial:	n/a
47	chr4:119555395-119555445	HL-60	blood:	n/a
48	chr4:119557464-119557514	NB4	blood:	n/a
49	chr4:119554219-119554269	HUVEC	blood vessel:	n/a
50	chr4:119556601-119556651	Hepatocyte	liver:	n/a

No data

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL14-1	chr4:119541987-119541991	XLOC_003663
2	lnc-METTL14-1	chr4:119541480-119541765	XLOC_003663
3	lnc-METTL14-2	chr4:119539321-119539356	XLOC_003662
4	lnc-METTL14-2	chr4:119539320-119539356	NONHSAT097987
5	lnc-METTL14-1	chr4:119541479-119541765	NONHSAT097989
6	lnc-METTL14-1	chr4:119541986-119541991	NONHSAT097989

No data

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
PPM1D	miRNA target sites

Extended variants
information (count: 813 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:813 , 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	rs201781757	chr4:119539284-119539285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183079646	chr4:119539344-119539345	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs111381971	chr4:119539460-119539461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112659334	chr4:119539661-119539662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201736021	chr4:119539882-119539883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563049740	chr4:119539961-119539962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200105699	chr4:119540123-119540124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200847885	chr4:119540146-119540147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374712619	chr4:119540212-119540213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377663152	chr4:119540338-119540339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530539218	chr4:119540408-119540409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541378073	chr4:119540422-119540423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112977429	chr4:119540441-119540442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544261278	chr4:119540475-119540476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564009754	chr4:119540525-119540526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532970002	chr4:119540684-119540685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546184752	chr4:119540685-119540686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187774800	chr4:119540718-119540719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112673789	chr4:119540720-119540721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566471939	chr4:119540732-119540733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79582964	chr4:119540795-119540796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529112293	chr4:119540809-119540810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548770571	chr4:119540881-119540882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569007382	chr4:119540897-119540898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375789638	chr4:119540975-119540976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555257720	chr4:119541069-119541070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537971149	chr4:119541112-119541113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558268222	chr4:119541130-119541131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367799228	chr4:119541149-119541150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534224223	chr4:119541155-119541156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200416353	chr4:119541278-119541279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554164845	chr4:119541357-119541358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372023210	chr4:119541417-119541418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574387995	chr4:119541473-119541474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543312721	chr4:119541501-119541502	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs556494491	chr4:119541513-119541514	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs370472435	chr4:119541538-119541539	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs576609685	chr4:119541724-119541725	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs376954054	chr4:119541735-119541736	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs545249781	chr4:119541743-119541744	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs369447761	chr4:119541755-119541756	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs373675661	chr4:119541913-119541914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375781132	chr4:119541965-119541966	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564252901	chr4:119541972-119541973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532854979	chr4:119541975-119541976	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547567791	chr4:119541995-119541996	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539852043	chr4:119542105-119542106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559674589	chr4:119542112-119542113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370030919	chr4:119542180-119542181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549227449	chr4:119542182-119542183	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	21293372	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

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	chr4:119513600-119539200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:119513600-119549200	Weak transcription	Esophagus	oesophagus
7	chr4:119513600-119550400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:119513600-119551000	Weak transcription	Pancreas	Pancrea
9	chr4:119513600-119551600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr4:119513600-119552400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:119513600-119552400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr4:119513600-119552400	Weak transcription	Fetal Brain Female	brain
13	chr4:119513600-119552400	Weak transcription	Lung	lung
14	chr4:119513600-119552400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr4:119513600-119554000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:119513600-119555800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr4:119513600-119559200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:119513800-119551200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr4:119513800-119552400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:119513800-119555000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:119513800-119556000	Weak transcription	Fetal Lung	lung
22	chr4:119518400-119552600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:119518800-119557000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:119519000-119549600	Weak transcription	Brain Anterior Caudate	brain
25	chr4:119519400-119552400	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr4:119519600-119551200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr4:119519600-119552400	Weak transcription	Brain Angular Gyrus	brain
28	chr4:119519800-119552600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr4:119519800-119559000	Weak transcription	Brain Hippocampus Middle	brain
30	chr4:119520400-119551200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr4:119520600-119549200	Weak transcription	Spleen	Spleen
32	chr4:119520600-119550400	Weak transcription	Gastric	stomach
33	chr4:119520600-119550400	Weak transcription	Thymus	Thymus
34	chr4:119520600-119552200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:119520600-119552200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:119520600-119552400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr4:119520800-119551000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr4:119520800-119552200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr4:119520800-119552400	Weak transcription	Right Ventricle	heart
40	chr4:119521000-119550000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr4:119521000-119550400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:119521000-119550400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:119521200-119550200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr4:119521200-119551200	Weak transcription	Adipose Nuclei	Adipose
45	chr4:119521200-119551600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:119521200-119552400	Weak transcription	Placenta	Placenta
47	chr4:119522600-119551600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:119526000-119556200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:119526200-119541000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr4:119527200-119540600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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