Variant report

Variant	rs7923023
Chromosome Location	chr10:28571860-28571861
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No data

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:28571848-28571898	GM12878	blood:	n/a
2	chr10:28571848-28571898	MCF10A-Er-Src	breast:	n/a
3	chr10:28571848-28571898	HRCEpiC	kidney:	n/a
4	chr10:28571848-28571898	Caco-2	colon:	n/a
5	chr10:28571848-28571898	T-47D	breast:	n/a
6	chr10:28571848-28571898	BE2_C	brain:	n/a
7	chr10:28571848-28571898	HCT-116	colon:	n/a
8	chr10:28571848-28571898	HCF	heart:	n/a
9	chr10:28571848-28571898	SK-N-MC	brain:	n/a
10	chr10:28571848-28571898	IMR90	lung:	fetal
11	chr10:28571848-28571898	GM12891	blood:	n/a
12	chr10:28571848-28571898	HMEC	breast:	n/a
13	chr10:28571848-28571898	HEEpiC	esophagus:	n/a
14	chr10:28571848-28571898	HAEpiC	amniotic membrane:	n/a
15	chr10:28571848-28571898	Jurkat	blood:	n/a
16	chr10:28571848-28571898	AG04449	skin:	fetal
17	chr10:28571848-28571898	SK-N-SH	brain:	n/a
18	chr10:28571848-28571898	HCPEpiC	choroid plexus:	n/a
19	chr10:28571848-28571898	AG04450	lung:	fetal
20	chr10:28571848-28571898	ECC-1	luminal epithelium:	n/a
21	chr10:28571848-28571898	AG10803	skin:	n/a
22	chr10:28571848-28571898	HIPEpiC	eye:	n/a
23	chr10:28571848-28571898	NHDF-neo	bronchial:	n/a
24	chr10:28571848-28571898	AG09319	gingival:	n/a
25	chr10:28571848-28571898	HepG2	liver:	n/a
26	chr10:28571848-28571898	HRE	kidney:	n/a
27	chr10:28571848-28571898	GM19239	blood:	n/a
28	chr10:28571848-28571898	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:28571848-28571898	BJ	skin:	n/a
30	chr10:28571848-28571898	NH-A	brain:	n/a
31	chr10:28571848-28571898	Hela-S3	cervix:	n/a
32	chr10:28571848-28571898	AoSMC	blood vessel:	n/a
33	chr10:28571848-28571898	HNPCEpiC	eye:	n/a
34	chr10:28571848-28571898	LNCaP	prostate:	n/a
35	chr10:28571848-28571898	SAEC	small airway:	n/a
36	chr10:28571848-28571898	NT2-D1	testis:	n/a
37	chr10:28571848-28571898	HRPEpiC	eye:	n/a
38	chr10:28571848-28571898	PrEC	prostate:	n/a
39	chr10:28571848-28571898	SKMC	muscle:	n/a
40	chr10:28571848-28571898	PFSK-1	brain:	n/a
41	chr10:28571848-28571898	CMK	blood:	n/a
42	chr10:28571848-28571898	Hepatocyte	liver:	n/a
43	chr10:28571848-28571898	K562	blood:	n/a
44	chr10:28571848-28571898	ovcar-3	ovarian:	n/a
45	chr10:28571848-28571898	HUVEC	blood vessel:	n/a
46	chr10:28571848-28571898	ProgFib	skin:	n/a
47	chr10:28571848-28571898	H1-hESC	embryonic stem cell:	embryo
48	chr10:28571848-28571898	AG09309	skin:	n/a
49	chr10:28571848-28571898	HCM	heart:	n/a
50	chr10:28571848-28571898	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr10:28571543..28573303-chr10:28575111..28577967,2	MCF-7	breast:
2	chr10:28567822..28570184-chr10:28571377..28572911,2	MCF-7	breast:
3	chr10:28570371..28575406-chr10:28590076..28593528,7	MCF-7	breast:

No data

Variant related genes	Relation type
MPP7	CpG island
ENSG00000150054	Chromatin interaction

Extended variants
information (count: 131 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs10763652	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs10763653	1.00[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs10826426	1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs10826427	0.84[ASN][1000 genomes]
rs10826428	1.00[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs10826429	0.84[ASN][1000 genomes]
rs10826430	0.83[ASN][1000 genomes]
rs10826431	0.87[ASN][1000 genomes]
rs10826438	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10826439	0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006921	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs11006924	0.84[ASN][1000 genomes]
rs11006930	0.84[ASN][1000 genomes]
rs11006931	1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs11006932	0.82[ASW][hapmap];0.81[CEU][hapmap]
rs11006935	0.82[ASW][hapmap];0.87[CEU][hapmap];0.86[MEX][hapmap];0.83[AMR][1000 genomes]
rs11006936	0.83[AMR][1000 genomes]
rs11006940	1.00[CHB][hapmap];0.90[CHD][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs11006948	0.93[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11006952	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs11006953	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11006971	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11006972	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006974	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006975	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006976	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006977	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006979	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006980	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006981	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006982	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11007002	1.00[AFR][1000 genomes]
rs11813709	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11814117	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12243871	0.84[ASN][1000 genomes]
rs12243947	0.84[ASN][1000 genomes]
rs12247867	0.84[ASN][1000 genomes]
rs12258617	0.84[ASN][1000 genomes]
rs12258912	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12263084	0.83[ASN][1000 genomes]
rs12263807	0.84[ASN][1000 genomes]
rs12264931	0.84[ASN][1000 genomes]
rs12355677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12356457	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12357214	0.84[ASN][1000 genomes]
rs12357236	0.84[ASN][1000 genomes]
rs12357385	1.00[ASW][hapmap];0.81[CEU][hapmap];1.00[AFR][1000 genomes]
rs12357685	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12358399	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12358648	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12359569	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12359994	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1840877	1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs1840879	0.84[ASN][1000 genomes]
rs2100614	1.00[YRI][hapmap]
rs2607548	0.81[CEU][hapmap];1.00[YRI][hapmap]
rs2801845	0.81[CEU][hapmap]
rs2985524	0.81[CEU][hapmap]
rs2985525	0.80[CEU][hapmap]
rs2985529	0.81[CEU][hapmap]
rs2985530	0.81[CEU][hapmap]
rs2985533	0.81[CEU][hapmap]
rs2997203	0.81[CEU][hapmap]
rs3847384	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs41406248	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4747617	0.81[CEU][hapmap]
rs55654850	0.87[ASN][1000 genomes]
rs58057536	0.87[ASN][1000 genomes]
rs61845919	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61845921	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61845936	0.99[ASN][1000 genomes]
rs61845938	1.00[AFR][1000 genomes]
rs6481511	0.83[ASN][1000 genomes]
rs6481513	1.00[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs6481514	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs7070142	0.83[ASN][1000 genomes]
rs7071331	0.81[ASN][1000 genomes]
rs7072588	0.84[ASN][1000 genomes]
rs7072854	1.00[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs7073107	0.80[CEU][hapmap];0.83[AMR][1000 genomes]
rs7078271	0.87[CEU][hapmap];0.83[AMR][1000 genomes]
rs7078842	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7081371	1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs7084650	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7084702	0.84[ASN][1000 genomes]
rs7084878	1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs7085924	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7086267	0.84[ASN][1000 genomes]
rs7086807	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7086943	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7090006	0.81[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs7090735	0.87[ASN][1000 genomes]
rs7091031	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7091331	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7092706	0.87[ASN][1000 genomes]
rs7094807	0.83[ASN][1000 genomes]
rs7097351	0.84[ASN][1000 genomes]
rs7100335	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7100582	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7100619	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7100983	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7101006	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73608074	0.84[ASN][1000 genomes]
rs74129024	0.83[AMR][1000 genomes]
rs7893685	1.00[CHB][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs7893733	0.83[ASN][1000 genomes]
rs7893878	0.83[ASN][1000 genomes]
rs7893935	0.81[ASN][1000 genomes]
rs7903957	0.81[CEU][hapmap]
rs7914949	0.81[CEU][hapmap]
rs7916525	0.82[ASW][hapmap];0.87[CEU][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes]
rs9664773	1.00[CHB][hapmap];0.90[CHD][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1040916	chr10:28558982-28579141	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
6	nsv466856	chr10:28562647-28571860	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv470929	chr10:28562647-28571860	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv550285	chr10:28562647-28571860	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv818752	chr10:28562647-28571860	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv437663	chr10:28562647-28585496	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1036270	chr10:28563995-28574327	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv1045247	chr10:28563995-28574624	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv1039546	chr10:28563995-28579141	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
14	esv2421445	chr10:28564207-28571860	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	esv3693051	chr10:28564732-28571860	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	nsv818753	chr10:28564732-28571860	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	nsv515548	chr10:28564732-28579969	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
18	esv12765	chr10:28564737-28573369	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
19	nsv818754	chr10:28567807-28571860	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7923023	ARHGAP12	cis	parietal	SCAN

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28550400-28582600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr10:28564000-28573200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr10:28564200-28573200	Weak transcription	Primary T cells from cord blood	blood
4	chr10:28564800-28572800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr10:28564800-28573000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr10:28566800-28573000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr10:28568400-28573200	Weak transcription	Right Ventricle	heart
8	chr10:28569000-28578400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr10:28569400-28572400	Enhancers	Colon Smooth Muscle	Colon
10	chr10:28569600-28572000	Enhancers	Aorta	Aorta
11	chr10:28570400-28572200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr10:28570400-28573200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr10:28570800-28572400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr10:28571000-28572000	Enhancers	Psoas Muscle	Psoas
15	chr10:28571000-28580200	Weak transcription	Lung	lung
16	chr10:28571200-28572400	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr10:28571400-28572000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr10:28571400-28572000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr10:28571400-28573000	Weak transcription	Fetal Heart	heart
20	chr10:28571400-28573200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr10:28571400-28573200	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr10:28571400-28573200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr10:28571400-28573400	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr10:28571400-28578200	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr10:28571400-28584600	Weak transcription	Fetal Intestine Small	intestine
26	chr10:28571600-28572000	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr10:28571600-28572800	Weak transcription	HepG2	liver
28	chr10:28571600-28573000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr10:28571600-28575400	Weak transcription	HSMMtube	muscle
30	chr10:28571600-28580200	Weak transcription	Esophagus	oesophagus
31	chr10:28571600-28580200	Weak transcription	Left Ventricle	heart
32	chr10:28571600-28583800	Weak transcription	Fetal Muscle Leg	muscle
33	chr10:28571800-28572400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr10:28571800-28572800	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr10:28571800-28573000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:28571800-28573200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr10:28571800-28573200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr10:28571800-28573400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr10:28571800-28573400	Weak transcription	Fetal Intestine Large	intestine
40	chr10:28571800-28574200	Weak transcription	Pancreas	Pancrea
41	chr10:28571800-28575400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr10:28571800-28580200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:28571800-28587800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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