Variant report

Variant	rs150620
Chromosome Location	chr5:37300605-37300606
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:37299270..37301087-chr5:37332798..37335148,2	K562	blood:
2	chr5:37300122..37302180-chr5:37303244..37306127,2	K562	blood:

Variant related genes	Relation type
ENSG00000113569	Chromatin interaction

Extended variants
information (count: 110 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10056350	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10941328	0.92[YRI][hapmap];1.00[AMR][1000 genomes]
rs10941335	1.00[AMR][1000 genomes]
rs10941342	1.00[AMR][1000 genomes]
rs125684	0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13176630	1.00[AMR][1000 genomes]
rs150619	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs150622	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1589115	1.00[AMR][1000 genomes]
rs177811	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1829291	1.00[AMR][1000 genomes]
rs2056872	1.00[ASW][hapmap];0.86[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];1.00[AMR][1000 genomes]
rs216372	0.92[AFR][1000 genomes]
rs216373	0.92[YRI][hapmap];0.91[AFR][1000 genomes]
rs216374	0.88[AFR][1000 genomes]
rs216375	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216376	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216378	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216379	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216381	1.00[AFR][1000 genomes]
rs216382	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216384	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216391	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216397	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216399	1.00[ASW][hapmap];1.00[LWK][hapmap];0.93[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216400	1.00[ASW][hapmap];0.86[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs216401	1.00[ASW][hapmap];0.86[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2176477	1.00[AMR][1000 genomes]
rs217773	0.92[AFR][1000 genomes]
rs217774	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217775	1.00[ASW][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217779	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217782	0.92[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217783	0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217784	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217785	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217786	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217791	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217792	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217796	0.85[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217798	0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217800	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217801	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217815	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217816	0.96[AFR][1000 genomes]
rs217824	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217839	0.92[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217852	1.00[ASW][hapmap];0.86[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217853	0.91[AFR][1000 genomes]
rs217854	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs217855	0.84[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2366173	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2548041	1.00[ASW][hapmap];0.86[LWK][hapmap];0.86[MKK][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2886592	1.00[ASW][hapmap];0.86[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];1.00[AMR][1000 genomes]
rs4298274	0.86[MKK][hapmap];0.84[YRI][hapmap];1.00[AMR][1000 genomes]
rs4869500	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4869502	0.92[YRI][hapmap];1.00[AMR][1000 genomes]
rs4869510	0.84[YRI][hapmap];1.00[AMR][1000 genomes]
rs53429	1.00[ASW][hapmap];0.86[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55848769	1.00[AMR][1000 genomes]
rs56401	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56402	1.00[ASW][hapmap];0.86[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs594478	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59948566	1.00[AMR][1000 genomes]
rs61739227	0.85[AFR][1000 genomes]
rs6451315	0.92[YRI][hapmap];1.00[AMR][1000 genomes]
rs6889826	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6890019	0.92[YRI][hapmap];1.00[AMR][1000 genomes]
rs73749012	1.00[AMR][1000 genomes]
rs73749051	1.00[AMR][1000 genomes]
rs73750958	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73750959	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7706007	0.85[AFR][1000 genomes]
rs7710108	1.00[AMR][1000 genomes]
rs7715310	0.92[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7723593	0.81[AFR][1000 genomes]
rs7729149	1.00[AMR][1000 genomes]
rs9292654	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525478	chr5:36804225-37349895	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	esv1793961	chr5:36866835-37361728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv530225	chr5:36886635-37331912	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv1024051	chr5:36899712-37303001	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv537725	chr5:36899712-37303001	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	nsv534064	chr5:37054962-37586210	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
8	nsv881511	chr5:37088627-37552852	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
9	nsv597823	chr5:37111565-37430365	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
10	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
11	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
12	nsv1025988	chr5:37115142-37586211	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
13	nsv537727	chr5:37115142-37586211	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
14	nsv830265	chr5:37152221-37312233	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
15	nsv530227	chr5:37157106-37571999	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
16	nsv880406	chr5:37173930-37345270	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
17	nsv880839	chr5:37173930-37465126	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
18	nsv948741	chr5:37179341-37582164	Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
19	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
20	nsv597824	chr5:37206621-37409579	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
21	nsv597825	chr5:37206621-37430365	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
22	nsv881512	chr5:37239240-37364693	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
23	nsv880817	chr5:37239240-37465126	Weak transcription Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
24	nsv881492	chr5:37239240-37543121	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
25	nsv880444	chr5:37239240-37556926	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
26	nsv1015983	chr5:37240827-37666601	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
27	nsv1021284	chr5:37264275-37630188	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
28	nsv1029088	chr5:37285576-37604945	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS 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
29	nsv597844	chr5:37287836-37567851	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
30	nsv881076	chr5:37294473-37479198	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs150620	FCER2	trans	lymphoblastoid	seeQTL
rs150620	BCL11A	trans	lymphoblastoid	seeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37287800-37304600	Weak transcription	Fetal Heart	heart
2	chr5:37288200-37320000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:37288800-37301200	Weak transcription	Colonic Mucosa	Colon
4	chr5:37289000-37369200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr5:37289400-37310600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:37289800-37323600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:37291400-37301200	Weak transcription	NHLF	lung
8	chr5:37291600-37300800	Weak transcription	Pancreas	Pancrea
9	chr5:37292600-37301200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:37294400-37310800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:37296400-37306400	Strong transcription	Fetal Brain Female	brain
12	chr5:37296400-37307600	Strong transcription	Brain Germinal Matrix	brain
13	chr5:37296400-37308000	Strong transcription	Fetal Muscle Leg	muscle
14	chr5:37296400-37365400	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr5:37296400-37369000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr5:37296600-37305800	Strong transcription	Fetal Kidney	kidney
17	chr5:37296600-37308000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr5:37296600-37318600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr5:37296800-37306600	Strong transcription	Colon Smooth Muscle	Colon
20	chr5:37296800-37307400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:37296800-37307600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr5:37296800-37307800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr5:37296800-37308000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr5:37296800-37308000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:37296800-37308000	Strong transcription	Primary B cells from peripheral blood	blood
26	chr5:37296800-37308000	Strong transcription	Hela-S3	cervix
27	chr5:37296800-37311000	Strong transcription	H9 Cell Line	embryonic stem cell
28	chr5:37296800-37316600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:37296800-37316800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr5:37296800-37318400	Strong transcription	Fetal Muscle Trunk	muscle
31	chr5:37296800-37320200	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr5:37296800-37321600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr5:37296800-37353200	Strong transcription	Fetal Thymus	thymus
34	chr5:37296800-37358400	Strong transcription	Placenta	Placenta
35	chr5:37296800-37358600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr5:37296800-37358600	Strong transcription	Liver	Liver
37	chr5:37296800-37359000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:37296800-37359800	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr5:37296800-37359800	Strong transcription	Fetal Intestine Large	intestine
40	chr5:37296800-37360000	Strong transcription	Adipose Nuclei	Adipose
41	chr5:37296800-37364600	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr5:37296800-37364600	Strong transcription	Dnd41	blood
43	chr5:37296800-37365600	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr5:37297000-37306400	Strong transcription	Ovary	ovary
45	chr5:37297000-37307600	Strong transcription	Osteobl	bone
46	chr5:37297000-37307800	Strong transcription	Lung	lung
47	chr5:37297000-37308000	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr5:37297000-37308000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:37297000-37308000	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr5:37297000-37308000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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