Variant report

Variant	rs6826764
Chromosome Location	chr4:10030794-10030795
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:10028896..10030894-chr4:10122706..10125313,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-5	chr4:10030642-10030924	NONHSAT095152

Extended variants
information (count: 125 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10004571	0.83[ASN][1000 genomes]
rs10006397	1.00[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10016075	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs10018663	0.85[EUR][1000 genomes]
rs10018666	0.85[EUR][1000 genomes]
rs10022499	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes]
rs10023068	0.91[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs10033088	0.81[ASN][1000 genomes]
rs10516196	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs10516197	0.95[CHB][hapmap];0.80[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs10939650	0.91[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap]
rs12499734	0.95[CHB][hapmap];0.80[CHD][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs12642537	0.87[ASN][1000 genomes]
rs13106922	0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs13113006	0.83[JPT][hapmap]
rs13114106	0.94[ASN][1000 genomes]
rs13122112	0.95[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs13125476	0.84[CHB][hapmap];0.83[JPT][hapmap]
rs13129697	0.90[JPT][hapmap]
rs13132625	0.86[JPT][hapmap]
rs13135351	0.95[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs13139970	0.80[JPT][hapmap]
rs13142273	0.81[JPT][hapmap]
rs13144899	0.85[JPT][hapmap]
rs13148476	0.95[ASN][1000 genomes]
rs13151331	0.86[JPT][hapmap]
rs16891285	0.86[JPT][hapmap]
rs16891489	0.85[JPT][hapmap]
rs16892419	0.95[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs16892420	0.95[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs16892449	0.87[ASN][1000 genomes]
rs16892474	0.91[CHB][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs16892475	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs16892493	0.95[CHB][hapmap];0.80[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2240723	0.95[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs2276963	0.94[ASN][1000 genomes]
rs28730480	0.83[EUR][1000 genomes]
rs35201034	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs35249656	0.87[ASN][1000 genomes]
rs35334203	0.87[ASN][1000 genomes]
rs35782952	0.87[ASN][1000 genomes]
rs36036984	0.87[ASN][1000 genomes]
rs3756231	0.83[CHB][hapmap]
rs3756233	0.93[ASN][1000 genomes]
rs3756234	0.94[ASN][1000 genomes]
rs3775939	0.95[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs3775941	0.95[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs3775942	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs3775944	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3796829	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs3796835	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3796838	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3822250	0.95[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs4312756	0.86[JPT][hapmap]
rs4333184	0.86[JPT][hapmap]
rs4364264	0.85[JPT][hapmap]
rs4467565	0.85[JPT][hapmap]
rs4608811	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4697701	0.86[JPT][hapmap]
rs55668232	0.87[ASN][1000 genomes]
rs57897925	0.84[ASN][1000 genomes]
rs59234705	0.95[ASN][1000 genomes]
rs6812851	0.83[ASN][1000 genomes]
rs6813650	0.82[ASN][1000 genomes]
rs6820616	0.95[ASN][1000 genomes]
rs6820756	0.82[ASN][1000 genomes]
rs6821843	0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs6822023	0.82[ASN][1000 genomes]
rs6834555	0.83[ASN][1000 genomes]
rs6837659	0.84[ASN][1000 genomes]
rs6846692	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6853437	0.91[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.86[TSI][hapmap];0.84[EUR][1000 genomes]
rs6856396	0.90[CEU][hapmap]
rs714871	0.83[ASN][1000 genomes]
rs714873	0.87[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs733175	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7349721	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs751092	0.85[EUR][1000 genomes]
rs7657096	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs7663032	0.86[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap]
rs7664225	0.81[ASN][1000 genomes]
rs7666545	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7669090	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7675964	0.86[JPT][hapmap]
rs7678211	0.83[ASN][1000 genomes]
rs7685958	0.87[ASN][1000 genomes]
rs9291640	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs9291641	0.85[EUR][1000 genomes]
rs9291642	0.86[CEU][hapmap]
rs938558	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer 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 miRNA	74 gene(s)	inside rSNPs	diseases
2	nsv530090	chr4:9383695-10165033	Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	nsv1014216	chr4:9713612-10223836	Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
4	nsv1010249	chr4:9716101-10086188	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv878681	chr4:9802853-10397327	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
6	nsv997941	chr4:9805223-10493388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
7	nsv1008649	chr4:9805223-10589802	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	nsv1000587	chr4:9805223-10610752	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
9	nsv537022	chr4:9805223-10610752	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription 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 miRNA	56 gene(s)	inside rSNPs	diseases
10	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
11	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
12	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
13	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
14	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
15	esv2763339	chr4:9858426-10056376	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv537026	chr4:9903566-10262258	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
17	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
18	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription 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 miRNA	58 gene(s)	inside rSNPs	diseases
19	esv2752052	chr4:9911872-10313111	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
20	nsv878688	chr4:9915850-10038112	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
22	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
23	nsv532706	chr4:9948018-10451450	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
24	nsv1013022	chr4:9961220-10230042	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
25	nsv537028	chr4:9961220-10230042	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
26	nsv537029	chr4:9961220-10262258	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
27	nsv878691	chr4:9966477-10418078	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
28	nsv1013487	chr4:9972011-10320963	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
29	nsv829857	chr4:9982514-10155835	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
30	nsv469621	chr4:9987670-10142287	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
31	nsv482719	chr4:9987670-10142287	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
32	nsv1008067	chr4:10004664-10262258	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
33	nsv537030	chr4:10004664-10262258	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS 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 miRNA	47 gene(s)	inside rSNPs	diseases
34	nsv593691	chr4:10013173-10050141	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
35	nsv869057	chr4:10013411-10875454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6826764	SLC2A9	cis	parietal	SCAN

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10021400-10032000	Weak transcription	HSMMtube	muscle
2	chr4:10021600-10035200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:10021800-10032000	Weak transcription	Fetal Heart	heart
4	chr4:10024000-10032400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr4:10024200-10033400	Weak transcription	Fetal Intestine Large	intestine
6	chr4:10024400-10032800	Weak transcription	Brain Anterior Caudate	brain
7	chr4:10025200-10032600	Weak transcription	Spleen	Spleen
8	chr4:10025800-10034200	Weak transcription	Colonic Mucosa	Colon
9	chr4:10026000-10032200	Weak transcription	Right Ventricle	heart
10	chr4:10026000-10032400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:10026000-10032400	Weak transcription	Pancreas	Pancrea
12	chr4:10027000-10033000	Weak transcription	Lung	lung
13	chr4:10027800-10031000	Enhancers	HepG2	liver
14	chr4:10027800-10032400	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr4:10027800-10032400	Weak transcription	Liver	Liver
16	chr4:10027800-10032400	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr4:10029600-10031000	Enhancers	A549	lung
18	chr4:10029800-10031200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr4:10029800-10032400	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr4:10030000-10030800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
21	chr4:10030000-10031000	Enhancers	Right Atrium	heart
22	chr4:10030200-10030800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:10030200-10030800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr4:10030200-10030800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr4:10030200-10030800	Enhancers	NHLF	lung
26	chr4:10030200-10031000	Enhancers	Fetal Muscle Trunk	muscle
27	chr4:10030200-10031000	Enhancers	HMEC	breast
28	chr4:10030200-10031200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:10030200-10031200	Enhancers	NHEK	skin
30	chr4:10030200-10034200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:10030400-10030800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:10030400-10030800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:10030400-10030800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr4:10030400-10030800	Enhancers	Fetal Stomach	stomach
35	chr4:10030400-10030800	Enhancers	Left Ventricle	heart
36	chr4:10030400-10030800	Enhancers	HSMM	muscle
37	chr4:10030400-10031000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:10030400-10031000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:10030400-10031000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:10030400-10031000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:10030400-10031000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:10030400-10031000	Enhancers	Esophagus	oesophagus
43	chr4:10030400-10031000	Enhancers	Placenta	Placenta
44	chr4:10030400-10031000	Enhancers	Ovary	ovary
45	chr4:10030400-10031000	Enhancers	Psoas Muscle	Psoas
46	chr4:10030400-10031400	Enhancers	Fetal Muscle Leg	muscle
47	chr4:10030600-10030800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:10030600-10030800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:10030600-10030800	Enhancers	Adipose Nuclei	Adipose
50	chr4:10030600-10030800	Enhancers	Osteobl	bone

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