Variant report

Variant	rs768220
Chromosome Location	chr5:37289789-37289790
allele	A/C/G/T
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	POLR2A	chr5:37289609-37290489	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr5:37289652-37289852	HepG2	liver:	n/a	n/a
3	POLR2A	chr5:37289260-37291474	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:37288508..37291349-chr5:37291892..37294572,2	K562	blood:

Variant related genes	Relation type
ENSG00000270558	TF binding region
ENSG00000113569	Chromatin interaction

Extended variants
information (count: 144 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs10037680	1.00[EUR][1000 genomes]
rs10038960	0.91[AMR][1000 genomes]
rs10051872	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10053828	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10054453	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10069026	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10070367	1.00[AMR][1000 genomes]
rs10072236	0.82[AMR][1000 genomes]
rs10077748	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10077819	1.00[EUR][1000 genomes]
rs10085007	1.00[EUR][1000 genomes]
rs10214352	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10440646	0.82[AMR][1000 genomes]
rs10472286	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10491332	1.00[EUR][1000 genomes]
rs11739318	1.00[EUR][1000 genomes]
rs11742290	1.00[EUR][1000 genomes]
rs11949254	1.00[EUR][1000 genomes]
rs11949707	0.82[AMR][1000 genomes]
rs11953538	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11955258	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12109225	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12186464	1.00[EUR][1000 genomes]
rs12523118	1.00[EUR][1000 genomes]
rs12656455	1.00[EUR][1000 genomes]
rs13160250	1.00[EUR][1000 genomes]
rs13166616	1.00[EUR][1000 genomes]
rs13175777	1.00[EUR][1000 genomes]
rs13355660	1.00[EUR][1000 genomes]
rs13356505	0.82[AMR][1000 genomes]
rs13359358	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13359981	1.00[EUR][1000 genomes]
rs1554969	1.00[EUR][1000 genomes]
rs16903584	1.00[EUR][1000 genomes]
rs16903585	1.00[EUR][1000 genomes]
rs16903599	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16903615	1.00[EUR][1000 genomes]
rs2056869	1.00[EUR][1000 genomes]
rs2142324	1.00[EUR][1000 genomes]
rs2366166	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2366172	1.00[EUR][1000 genomes]
rs2366175	1.00[EUR][1000 genomes]
rs28555070	1.00[EUR][1000 genomes]
rs28609469	0.91[AMR][1000 genomes]
rs34871356	1.00[EUR][1000 genomes]
rs4074950	1.00[EUR][1000 genomes]
rs4242249	1.00[EUR][1000 genomes]
rs4242250	1.00[EUR][1000 genomes]
rs4334908	1.00[EUR][1000 genomes]
rs4370304	1.00[EUR][1000 genomes]
rs4395662	1.00[EUR][1000 genomes]
rs4407651	1.00[EUR][1000 genomes]
rs4407652	1.00[EUR][1000 genomes]
rs4418127	1.00[EUR][1000 genomes]
rs4449561	1.00[EUR][1000 genomes]
rs4470784	1.00[EUR][1000 genomes]
rs4499858	1.00[EUR][1000 genomes]
rs4607372	1.00[EUR][1000 genomes]
rs4869431	1.00[EUR][1000 genomes]
rs4869432	1.00[EUR][1000 genomes]
rs4869434	1.00[EUR][1000 genomes]
rs4869506	1.00[EUR][1000 genomes]
rs4869508	1.00[EUR][1000 genomes]
rs58701977	0.84[AMR][1000 genomes]
rs59176360	1.00[EUR][1000 genomes]
rs59468995	1.00[EUR][1000 genomes]
rs59833929	1.00[EUR][1000 genomes]
rs60063938	1.00[EUR][1000 genomes]
rs60979839	1.00[EUR][1000 genomes]
rs61154857	1.00[EUR][1000 genomes]
rs6451316	1.00[EUR][1000 genomes]
rs6451317	1.00[EUR][1000 genomes]
rs6451318	1.00[EUR][1000 genomes]
rs6860757	1.00[EUR][1000 genomes]
rs6868163	1.00[EUR][1000 genomes]
rs6868843	1.00[EUR][1000 genomes]
rs6869205	1.00[EUR][1000 genomes]
rs6871254	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6871258	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6876447	1.00[EUR][1000 genomes]
rs6878453	0.82[AMR][1000 genomes]
rs6878728	0.91[AMR][1000 genomes]
rs6887309	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6893151	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6895753	1.00[EUR][1000 genomes]
rs6898035	1.00[EUR][1000 genomes]
rs6898900	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73068464	1.00[EUR][1000 genomes]
rs73068483	1.00[EUR][1000 genomes]
rs7702750	1.00[EUR][1000 genomes]
rs7702907	1.00[EUR][1000 genomes]
rs7703638	1.00[EUR][1000 genomes]
rs7703670	1.00[EUR][1000 genomes]
rs7704548	1.00[EUR][1000 genomes]
rs7709224	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7712722	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7714241	1.00[EUR][1000 genomes]
rs7724308	1.00[EUR][1000 genomes]
rs7724686	1.00[EUR][1000 genomes]
rs7725018	1.00[EUR][1000 genomes]
rs7725049	1.00[EUR][1000 genomes]
rs7727356	1.00[EUR][1000 genomes]
rs7728794	0.91[AMR][1000 genomes]
rs7728893	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7729506	1.00[EUR][1000 genomes]
rs7730242	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7732929	1.00[EUR][1000 genomes]
rs7733418	1.00[EUR][1000 genomes]
rs7735454	1.00[EUR][1000 genomes]
rs7736469	1.00[EUR][1000 genomes]
rs8180378	1.00[EUR][1000 genomes]
rs9292650	0.82[AMR][1000 genomes]
rs971785	1.00[EUR][1000 genomes]
rs974432	1.00[EUR][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	nsv328371	chr5:37288871-37294107	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37282400-37290400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:37284600-37290200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr5:37285400-37297000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:37285600-37298000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr5:37286000-37290200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr5:37286000-37290200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:37286000-37290600	Weak transcription	Primary T cells from cord blood	blood
8	chr5:37286200-37290000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:37286200-37290200	Weak transcription	Adipose Nuclei	Adipose
10	chr5:37287000-37290200	Weak transcription	Fetal Kidney	kidney
11	chr5:37287000-37290200	Weak transcription	Fetal Stomach	stomach
12	chr5:37287000-37290400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:37287000-37296800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr5:37287000-37298800	Weak transcription	Fetal Brain Male	brain
15	chr5:37287200-37296800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr5:37287200-37297400	Weak transcription	Brain Cingulate Gyrus	brain
17	chr5:37287400-37289800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr5:37287400-37291200	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr5:37287400-37296400	Weak transcription	Brain Germinal Matrix	brain
20	chr5:37287600-37290400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr5:37287600-37290600	Weak transcription	Fetal Intestine Large	intestine
22	chr5:37287600-37290600	Weak transcription	NH-A	brain
23	chr5:37287600-37290800	Weak transcription	Brain Hippocampus Middle	brain
24	chr5:37287800-37290200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr5:37287800-37297600	Weak transcription	Aorta	Aorta
26	chr5:37287800-37304600	Weak transcription	Fetal Heart	heart
27	chr5:37288000-37290200	Weak transcription	HepG2	liver
28	chr5:37288000-37291000	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr5:37288000-37298800	Weak transcription	Brain Angular Gyrus	brain
30	chr5:37288200-37289800	Weak transcription	Stomach Smooth Muscle	stomach
31	chr5:37288200-37289800	Weak transcription	Osteobl	bone
32	chr5:37288200-37290000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:37288200-37290200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr5:37288200-37290400	Weak transcription	Fetal Brain Female	brain
35	chr5:37288200-37290400	Weak transcription	HUVEC	blood vessel
36	chr5:37288200-37290600	Weak transcription	NHLF	lung
37	chr5:37288200-37295400	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr5:37288200-37320000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:37288400-37290000	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr5:37288400-37290200	Weak transcription	Ovary	ovary
41	chr5:37288400-37290400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr5:37288400-37291400	Weak transcription	Fetal Intestine Small	intestine
43	chr5:37288400-37294800	Strong transcription	Dnd41	blood
44	chr5:37288600-37290200	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr5:37288600-37290600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr5:37288600-37292800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr5:37288800-37290400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr5:37288800-37290600	Weak transcription	Esophagus	oesophagus
49	chr5:37288800-37290800	Weak transcription	Primary hematopoietic stem cells	blood
50	chr5:37288800-37290800	Weak transcription	Duodenum Mucosa	Duodenum

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