Variant report

Variant	rs12509955
Chromosome Location	chr4:10024303-10024304
allele	C/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	NR3C1	chr4:10023916-10024388	A549	lung:	n/a	chr4:10024183-10024200 chr4:10024179-10024205 chr4:10024179-10024205 chr4:10024185-10024199 chr4:10024179-10024205 chr4:10024183-10024201
2	CTCF	chr4:10024200-10024350	SAEC	small airway:	n/a	n/a
3	MYC	chr4:10023991-10024422	MCF10A-Er-Src	breast:	n/a	chr4:10024397-10024404 chr4:10024396-10024405 chr4:10024387-10024403
4	NR3C1	chr4:10023957-10024467	A549	lung:	n/a	chr4:10024183-10024200 chr4:10024179-10024205 chr4:10024179-10024205 chr4:10024185-10024199 chr4:10024179-10024205 chr4:10024183-10024201
5	NR3C1	chr4:10023946-10024372	A549	lung:	n/a	chr4:10024183-10024200 chr4:10024179-10024205 chr4:10024179-10024205 chr4:10024185-10024199 chr4:10024179-10024205 chr4:10024183-10024201

No.	Distal block	Cell Line	Cell type
1	chr4:10020622..10022306-chr4:10022841..10025006,2	MCF-7	breast:
2	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
3	chr4:10019661..10022849-chr4:10023062..10025452,3	K562	blood:

Variant related genes	Relation type
SLC2A9	TF binding region
ENSG00000109667	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10009493	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs10020887	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs10022911	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap]
rs10516194	1.00[CHB][hapmap]
rs1071988	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10939723	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap]
rs11721682	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs11722229	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11723439	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs11735668	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs11942223	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12498742	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12507606	1.00[JPT][hapmap]
rs13111638	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.80[EUR][1000 genomes]
rs13113918	1.00[CHD][hapmap]
rs13125209	1.00[JPT][hapmap]
rs13125646	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13131257	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13145758	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16868246	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16890979	0.87[CHD][hapmap];1.00[JPT][hapmap]
rs17198547	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap]
rs17251963	1.00[CHB][hapmap];0.88[CHD][hapmap]
rs17385112	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs17389602	1.00[CHB][hapmap]
rs4144	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4385059	1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap]
rs4428284	0.80[EUR][1000 genomes]
rs4475146	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4481233	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs4484299	1.00[ASN][1000 genomes]
rs4637402	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4639073	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4640669	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap]
rs4697700	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4697714	0.86[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap]
rs4697913	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4697933	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs4697939	1.00[CHB][hapmap]
rs5028843	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs62288518	0.89[ASN][1000 genomes]
rs6449173	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6449213	1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap]
rs6827401	1.00[CHB][hapmap]
rs6827946	1.00[CHB][hapmap]
rs6832439	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs6838021	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6855911	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs6856396	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs734553	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs737267	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs7376960	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7377625	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7439210	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7442295	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7663044	1.00[ASN][1000 genomes]
rs7669607	1.00[CHB][hapmap];0.87[CHD][hapmap];0.81[MEX][hapmap]
rs7670751	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs7671266	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7680126	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7696092	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs874432	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9291642	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs929575	0.80[CEU][hapmap]
rs938552	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs938554	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs938555	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs938564	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9991278	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap]
rs9998811	1.00[CHB][hapmap];1.00[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

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10020200-10024600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr4:10021000-10024800	Enhancers	Lung	lung
3	chr4:10021200-10025600	Enhancers	Primary B cells from cord blood	blood
4	chr4:10021200-10025800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr4:10021200-10026400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr4:10021200-10027400	Enhancers	Right Atrium	heart
7	chr4:10021400-10024800	Enhancers	Left Ventricle	heart
8	chr4:10021400-10025200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:10021400-10025200	Weak transcription	NH-A	brain
10	chr4:10021400-10026200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr4:10021400-10026200	Enhancers	Adipose Nuclei	Adipose
12	chr4:10021400-10026400	Enhancers	Fetal Muscle Leg	muscle
13	chr4:10021400-10029600	Weak transcription	A549	lung
14	chr4:10021400-10032000	Weak transcription	HSMMtube	muscle
15	chr4:10021600-10025200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr4:10021600-10026000	Enhancers	Right Ventricle	heart
17	chr4:10021600-10026000	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr4:10021600-10035200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:10021800-10032000	Weak transcription	Fetal Heart	heart
20	chr4:10022200-10025000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:10022200-10025200	Enhancers	Spleen	Spleen
22	chr4:10022200-10025400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr4:10022600-10024800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr4:10022600-10024800	Enhancers	Fetal Thymus	thymus
25	chr4:10022600-10025000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:10022600-10025800	Enhancers	Primary B cells from peripheral blood	blood
27	chr4:10022800-10024400	Enhancers	Brain Hippocampus Middle	brain
28	chr4:10023000-10026000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:10023000-10026000	Enhancers	Fetal Muscle Trunk	muscle
30	chr4:10023000-10026000	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr4:10023000-10026400	Enhancers	Placenta	Placenta
32	chr4:10023000-10030400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr4:10023200-10024400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr4:10023200-10025200	Weak transcription	Colonic Mucosa	Colon
35	chr4:10023200-10025800	Enhancers	Esophagus	oesophagus
36	chr4:10023200-10025800	Weak transcription	HSMM	muscle
37	chr4:10023200-10027400	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr4:10023400-10024600	Enhancers	Brain Substantia Nigra	brain
39	chr4:10023400-10025600	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr4:10023400-10026000	Enhancers	Liver	Liver
41	chr4:10023400-10026200	Enhancers	HMEC	breast
42	chr4:10023400-10027400	Enhancers	HepG2	liver
43	chr4:10023400-10027800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr4:10023600-10025200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:10023600-10026000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:10023600-10026000	Enhancers	NHEK	skin
47	chr4:10023600-10026200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:10023600-10026600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:10023800-10024400	Enhancers	Brain Anterior Caudate	brain
50	chr4:10024000-10024800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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