Variant report

Variant	rs58227539
Chromosome Location	chr4:671887-671888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:113)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:113 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POU2F2	chr4:671744-672116	GM12891	blood:	n/a	n/a
2	EP300	chr4:671770-672103	GM12878	blood:	n/a	n/a
3	HEY1	chr4:671442-672059	HepG2	liver:	n/a	n/a
4	MXI1	chr4:671656-672087	HepG2	liver:	n/a	n/a
5	POLR2A	chr4:667464-672151	GM12878	blood:	n/a	n/a
6	POLR2A	chr4:671745-672063	Gliobla	brain:	n/a	n/a
7	RFX5	chr4:671778-672059	HepG2	liver:	n/a	n/a
8	POLR2A	chr4:671717-672121	GM12878	blood:	n/a	n/a
9	POLR2A	chr4:667656-672822	GM19099	blood:	n/a	n/a
10	EGR1	chr4:671767-672004	K562	blood:	n/a	n/a
11	POLR2A	chr4:667899-673815	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr4:670412-673685	HepG2	liver:	n/a	n/a
13	POU2F2	chr4:671789-672148	GM12878	blood:	n/a	n/a
14	EGR1	chr4:671434-672410	HCT-116	colon:	n/a	chr4:672267-672280
15	POLR2A	chr4:671038-672322	HepG2	liver:	n/a	n/a
16	MAX	chr4:671630-672095	HepG2	liver:	n/a	n/a
17	MYC	chr4:671863-671985	HepG2	liver:	n/a	n/a
18	POLR2A	chr4:667908-672199	GM12878	blood:	n/a	n/a
19	MAZ	chr4:671713-671913	HepG2	liver:	n/a	n/a
20	MAX	chr4:671600-672148	ECC-1	luminal epithelium:	n/a	n/a
21	POLR2A	chr4:671714-672101	HepG2	liver:	n/a	n/a
22	POLR2A	chr4:671628-672151	GM12892	blood:	n/a	n/a
23	POLR2A	chr4:667840-672164	SK-N-MC	brain:	n/a	n/a
24	NRF1	chr4:671736-672076	GM12878	blood:	n/a	n/a
25	POLR2A	chr4:671679-672221	HUVEC	blood vessel:	n/a	n/a
26	MBD4	chr4:671705-672208	HepG2	liver:	n/a	n/a
27	FOXA2	chr4:671740-672047	HepG2	liver:	n/a	n/a
28	POLR2A	chr4:670859-672125	SK-N-SH	brain:	n/a	n/a
29	POLR2A	chr4:671603-672231	ECC-1	luminal epithelium:	n/a	n/a
30	POU2F2	chr4:671656-672138	GM12878	blood:	n/a	n/a
31	SP1	chr4:671743-672144	GM12878	blood:	n/a	n/a
32	POLR2A	chr4:671735-672060	A549	lung:	n/a	n/a
33	POLR2A	chr4:670984-672143	HCT-116	colon:	n/a	n/a
34	TCF3	chr4:671650-672052	GM12878	blood:	n/a	n/a
35	POLR2A	chr4:669705-672344	ECC-1	luminal epithelium:	n/a	n/a
36	EGR1	chr4:671628-672173	ECC-1	luminal epithelium:	n/a	n/a
37	BHLHE40	chr4:671777-672089	GM12878	blood:	n/a	n/a
38	POLR2A	chr4:670373-673590	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr4:671861-672025	GM19239	blood:	n/a	n/a
40	MAX	chr4:671759-672057	GM12878	blood:	n/a	n/a
41	MYC	chr4:671755-672000	MCF10A-Er-Src	breast:	n/a	n/a
42	MAX	chr4:671524-672466	HepG2	liver:	n/a	chr4:671595-671605
43	FOSL2	chr4:671361-672084	HepG2	liver:	n/a	chr4:671632-671642 chr4:671632-671642
44	POLR2A	chr4:671768-672151	GM12891	blood:	n/a	n/a
45	POLR2A	chr4:671805-672062	HepG2	liver:	n/a	n/a
46	POLR2A	chr4:671779-672130	GM12891	blood:	n/a	n/a
47	POLR2A	chr4:670962-672143	HepG2	liver:	n/a	n/a
48	POLR2A	chr4:671395-672100	GM12878	blood:	n/a	n/a
49	NFATC1	chr4:671738-672239	GM12878	blood:	n/a	n/a
50	POLR2A	chr4:667550-672298	GM15510	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:671851-671901	GM12891	blood:	n/a
2	chr4:671851-671901	NHDF-neo	bronchial:	n/a
3	chr4:671851-671901	HRPEpiC	eye:	n/a
4	chr4:671851-671901	GM12892	blood:	n/a
5	chr4:671851-671901	HEEpiC	esophagus:	n/a
6	chr4:671851-671901	T-47D	breast:	n/a
7	chr4:671851-671901	HIPEpiC	eye:	n/a
8	chr4:671851-671901	BJ	skin:	n/a
9	chr4:671851-671901	HRE	kidney:	n/a
10	chr4:671851-671901	MCF10A-Er-Src	breast:	n/a
11	chr4:671851-671901	AG09309	skin:	n/a
12	chr4:671851-671901	PANC-1	pancreas:	n/a
13	chr4:671851-671901	AoSMC	blood vessel:	n/a
14	chr4:671851-671901	AG04449	skin:	fetal
15	chr4:671851-671901	NB4	blood:	n/a
16	chr4:671851-671901	RPTEC	kidney:	n/a
17	chr4:671851-671901	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:671851-671901	Hela-S3	cervix:	n/a
19	chr4:671851-671901	HNPCEpiC	eye:	n/a
20	chr4:671851-671901	NH-A	brain:	n/a
21	chr4:671851-671901	NHBE	bronchial:	n/a
22	chr4:671851-671901	ProgFib	skin:	n/a
23	chr4:671851-671901	HUVEC	blood vessel:	n/a
24	chr4:671851-671901	Caco-2	colon:	n/a
25	chr4:671851-671901	LNCaP	prostate:	n/a
26	chr4:671851-671901	HEK293	kidney:	embryo
27	chr4:671851-671901	GM19239	blood:	n/a
28	chr4:671851-671901	GM12878	blood:	n/a
29	chr4:671851-671901	IMR90	lung:	fetal
30	chr4:671851-671901	BE2_C	brain:	n/a
31	chr4:671851-671901	HRCEpiC	kidney:	n/a
32	chr4:671851-671901	K562	blood:	n/a
33	chr4:671851-671901	AG04450	lung:	fetal
34	chr4:671851-671901	HL-60	blood:	n/a
35	chr4:671851-671901	HepG2	liver:	n/a
36	chr4:671851-671901	SK-N-MC	brain:	n/a
37	chr4:671851-671901	PrEC	prostate:	n/a
38	chr4:671851-671901	NT2-D1	testis:	n/a
39	chr4:671851-671901	H1-hESC	embryonic stem cell:	embryo
40	chr4:671851-671901	U87	brain:	n/a
41	chr4:671851-671901	Hepatocyte	liver:	n/a
42	chr4:671851-671901	ovcar-3	ovarian:	n/a
43	chr4:671851-671901	SK-N-SH	brain:	n/a
44	chr4:671851-671901	HCPEpiC	choroid plexus:	n/a
45	chr4:671851-671901	Jurkat	blood:	n/a
46	chr4:671851-671901	ECC-1	luminal epithelium:	n/a
47	chr4:671851-671901	CMK	blood:	n/a
48	chr4:671851-671901	HCT-116	colon:	n/a
49	chr4:671851-671901	SK-N-SH_RA	brain:	n/a
50	chr4:671851-671901	HMEC	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:669988..672792-chr4:681146..683044,2	K562	blood:
2	chr4:491399..494814-chr4:670516..673656,5	K562	blood:
3	chr4:671080..676330-chr4:771868..776883,7	K562	blood:

No data

Variant related genes	Relation type
ATP5I	TF binding region
MYL5	TF binding region
MYL5	CpG island
ATP5I	CpG island
ENSG00000169026	Chromatin interaction
ENSG00000182903	Chromatin interaction
ENSG00000249592	Chromatin interaction
ENSG00000174227	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10027549	1.00[ASN][1000 genomes]
rs10030136	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1135375	1.00[ASN][1000 genomes]
rs28470912	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28483373	1.00[ASN][1000 genomes]
rs28488910	1.00[ASN][1000 genomes]
rs28525003	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28568555	1.00[ASN][1000 genomes]
rs28569875	1.00[ASN][1000 genomes]
rs28573204	1.00[ASN][1000 genomes]
rs28583078	1.00[ASN][1000 genomes]
rs28630797	1.00[ASN][1000 genomes]
rs28742266	1.00[ASN][1000 genomes]
rs28742899	1.00[ASN][1000 genomes]
rs3864130	1.00[ASN][1000 genomes]
rs3864131	1.00[ASN][1000 genomes]
rs3891250	1.00[ASN][1000 genomes]
rs4463020	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4518182	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60316402	1.00[ASN][1000 genomes]
rs71602496	1.00[ASN][1000 genomes]
rs73056602	1.00[ASN][1000 genomes]
rs73058406	1.00[ASN][1000 genomes]
rs7436737	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9985747	0.81[EUR][1000 genomes]
rs9991613	1.00[ASN][1000 genomes]
rs9992641	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv2830422	chr4:72247-681939	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv931097	chr4:72447-683874	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv878245	chr4:509178-694613	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
9	nsv878246	chr4:592507-696848	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
12	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
14	nsv593206	chr4:625962-735150	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
15	nsv878248	chr4:645300-685993	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
16	nsv878249	chr4:649639-691026	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
17	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
18	nsv829834	chr4:665477-775524	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
19	nsv10413	chr4:667204-684301	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv593208	chr4:668000-682233	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
21	nsv878250	chr4:668567-683842	Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv878251	chr4:669857-683842	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
23	nsv878252	chr4:669857-685993	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
24	esv3389909	chr4:670502-673300	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs58227539	RP11-1191J2.2	cis	Thyroid	GTEx
rs58227539	RP11-1191J2.2	cis	lung	GTEx
rs58227539	MFSD7	cis	Esophagus Muscularis	GTEx
rs58227539	RP11-1191J2.2	cis	Nerve Tibial	GTEx

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:668800-674400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:669000-672200	Enhancers	Spleen	Spleen
3	chr4:669200-672000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:669200-672600	Enhancers	Esophagus	oesophagus
5	chr4:669200-672600	Enhancers	Fetal Intestine Large	intestine
6	chr4:669200-673000	Enhancers	Pancreas	Pancrea
7	chr4:669200-674200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:669200-674400	Weak transcription	Fetal Lung	lung
9	chr4:669400-672200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:669400-672800	Enhancers	Duodenum Mucosa	Duodenum
11	chr4:669400-674000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:669400-674200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr4:669400-674200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr4:669400-674200	Weak transcription	NH-A	brain
15	chr4:669400-674400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr4:669400-674400	Weak transcription	Ovary	ovary
17	chr4:669400-674400	Weak transcription	Right Atrium	heart
18	chr4:669400-674600	Enhancers	Placenta	Placenta
19	chr4:669400-674600	Weak transcription	HUVEC	blood vessel
20	chr4:669600-673800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr4:669600-674000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr4:669600-674000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr4:669600-674000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr4:669600-674000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr4:669600-674000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr4:669600-674200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr4:669600-674200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr4:669600-674200	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr4:669600-674200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr4:669600-674200	Weak transcription	Osteobl	bone
31	chr4:669600-674400	Weak transcription	Primary T cells from cord blood	blood
32	chr4:669600-674400	Weak transcription	NHLF	lung
33	chr4:669600-674600	Weak transcription	Left Ventricle	heart
34	chr4:669600-674600	Weak transcription	Small Intestine	intestine
35	chr4:669800-672600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:669800-674000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:669800-674200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:669800-674200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:669800-674200	Weak transcription	Brain Hippocampus Middle	brain
40	chr4:669800-674600	Weak transcription	Brain Anterior Caudate	brain
41	chr4:669800-674600	Weak transcription	Brain Substantia Nigra	brain
42	chr4:670000-673000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:670000-673000	Weak transcription	Right Ventricle	heart
44	chr4:670000-674000	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr4:670000-674000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr4:670000-674000	Weak transcription	Lung	lung
47	chr4:670000-674200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr4:670000-674600	Weak transcription	Liver	Liver
49	chr4:670200-673600	Weak transcription	Dnd41	blood
50	chr4:670200-674000	Weak transcription	Primary T helper cells PMA-I stimulated	--

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