Variant report

Variant	rs4608811
Chromosome Location	chr4:10049675-10049676
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 130 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10004571	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10006397	1.00[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10016075	0.91[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.89[TSI][hapmap]
rs10022499	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs10023068	0.91[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.89[TSI][hapmap]
rs10033088	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs10516196	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs10516197	0.95[CHB][hapmap];0.81[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs10939650	0.91[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap]
rs10939679	0.89[ASN][1000 genomes]
rs10939680	0.89[ASN][1000 genomes]
rs10939681	0.85[ASN][1000 genomes]
rs12108388	0.89[ASN][1000 genomes]
rs12499734	0.95[CHB][hapmap];0.81[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs12642537	0.92[ASN][1000 genomes]
rs13106922	0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs13112782	0.89[ASN][1000 genomes]
rs13113006	0.83[JPT][hapmap]
rs13114106	0.83[ASN][1000 genomes]
rs13122112	0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs13125476	0.84[CHB][hapmap];0.83[JPT][hapmap]
rs13127630	0.89[ASN][1000 genomes]
rs13129697	0.90[JPT][hapmap]
rs13132625	0.85[JPT][hapmap]
rs13135351	0.95[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs13142273	0.81[JPT][hapmap]
rs13144899	0.85[JPT][hapmap]
rs13148476	0.84[ASN][1000 genomes]
rs13151331	0.85[JPT][hapmap]
rs16891285	0.85[JPT][hapmap]
rs16891489	0.85[JPT][hapmap]
rs16892419	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs16892420	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs16892449	0.92[ASN][1000 genomes]
rs16892474	0.91[CHB][hapmap];0.81[JPT][hapmap];0.92[ASN][1000 genomes]
rs16892475	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs16892493	0.95[CHB][hapmap];0.81[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs2240723	0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs2276963	0.83[ASN][1000 genomes]
rs28730480	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35201034	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs35249656	0.92[ASN][1000 genomes]
rs35334203	0.92[ASN][1000 genomes]
rs35782952	0.92[ASN][1000 genomes]
rs36036984	0.92[ASN][1000 genomes]
rs3756231	0.83[CHB][hapmap]
rs3756233	0.82[ASN][1000 genomes]
rs3756234	0.83[ASN][1000 genomes]
rs3775939	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs3775941	0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs3775942	0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs3775944	0.85[EUR][1000 genomes]
rs3796829	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs3822250	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs4312756	0.85[JPT][hapmap]
rs4333184	0.85[JPT][hapmap]
rs4364264	0.85[JPT][hapmap]
rs4467565	0.84[JPT][hapmap]
rs4549382	0.83[ASN][1000 genomes]
rs4697701	0.85[JPT][hapmap]
rs55668232	0.92[ASN][1000 genomes]
rs57897925	0.95[ASN][1000 genomes]
rs59234705	0.84[ASN][1000 genomes]
rs6812851	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6813650	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6820616	0.84[ASN][1000 genomes]
rs6820756	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6821843	0.95[CHB][hapmap];0.94[ASN][1000 genomes]
rs6822023	0.92[ASN][1000 genomes]
rs6826764	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.97[MKK][hapmap];0.93[TSI][hapmap];0.89[YRI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6834555	0.93[ASN][1000 genomes]
rs6837659	0.95[ASN][1000 genomes]
rs6846692	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6853437	0.91[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.86[TSI][hapmap]
rs6856396	0.90[CEU][hapmap]
rs714871	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs714873	0.87[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs733175	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7349721	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7657096	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs7659924	0.89[ASN][1000 genomes]
rs7663032	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap]
rs7664225	0.91[ASN][1000 genomes]
rs7669090	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7675964	0.85[JPT][hapmap]
rs7677430	0.88[ASN][1000 genomes]
rs7678211	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7678346	0.89[ASN][1000 genomes]
rs7683832	0.89[ASN][1000 genomes]
rs7685958	0.92[ASN][1000 genomes]
rs9291640	0.91[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.89[TSI][hapmap]
rs9291642	0.86[CEU][hapmap]
rs938558	0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:37 , 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	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	nsv537031	chr4:10040713-10262258	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS 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
36	nsv997936	chr4:10040713-11009045	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
37	nsv878692	chr4:10042160-10099333	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4608811	SLC2A9	cis	parietal	SCAN

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10035200-10065600	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr4:10035400-10065200	Weak transcription	Right Ventricle	heart
3	chr4:10035800-10068400	Weak transcription	Aorta	Aorta
4	chr4:10036200-10049800	Weak transcription	Lung	lung
5	chr4:10037000-10052400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:10037000-10056000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr4:10041000-10065000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr4:10042000-10050000	Weak transcription	Pancreas	Pancrea
9	chr4:10044600-10064800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr4:10044800-10056800	Weak transcription	Psoas Muscle	Psoas
11	chr4:10044800-10058800	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr4:10045200-10051200	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr4:10046800-10051800	Enhancers	Fetal Intestine Small	intestine
14	chr4:10046800-10053600	Enhancers	Fetal Intestine Large	intestine
15	chr4:10047400-10051000	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr4:10048000-10050000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:10048200-10065400	Weak transcription	Primary B cells from peripheral blood	blood
18	chr4:10048400-10051000	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr4:10048600-10049800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:10048600-10050000	Weak transcription	HMEC	breast
21	chr4:10048800-10049800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:10048800-10049800	Weak transcription	NHEK	skin
23	chr4:10048800-10051400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:10049000-10049800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:10049000-10050000	Weak transcription	Right Atrium	heart
26	chr4:10049000-10050400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr4:10049000-10050600	Weak transcription	Primary T cells from cord blood	blood
28	chr4:10049200-10050200	Weak transcription	HepG2	liver
29	chr4:10049400-10050000	Enhancers	Primary hematopoietic stem cells	blood
30	chr4:10049400-10050000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:10049600-10049800	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr4:10049600-10050000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr4:10049600-10050000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr4:10049600-10050000	Enhancers	Adipose Nuclei	Adipose
35	chr4:10049600-10050200	Enhancers	Primary T cells fromperipheralblood	blood

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