Variant report

Variant	rs9393683
Chromosome Location	chr6:26066198-26066199
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26062306..26067668-chr6:27858950..27863759,6	K562	blood:
2	chr6:26056669..26057216-chr6:26065836..26066480,2	K562	blood:
3	chr6:26052762..26068184-chr6:26093226..26113078,68	MCF-7	breast:
4	chr6:26065865..26066777-chr6:26097220..26098413,14	MCF-7	breast:
5	chr6:26064369..26067224-chr6:27113844..27115420,2	K562	blood:
6	chr6:26064765..26066287-chr6:27085154..27087707,2	K562	blood:
7	chr6:26062306..26067668-chr6:27858950..27863363,5	K562	blood:
8	chr6:26065834..26066684-chr6:26097254..26098120,4	MCF-7	breast:
9	chr6:26062694..26067901-chr6:26153847..26159350,8	MCF-7	breast:
10	chr6:26064133..26067139-chr6:26087188..26090926,6	MCF-7	breast:
11	chr6:26065328..26067963-chr6:26073996..26076276,2	MCF-7	breast:
12	chr6:26065547..26067255-chr6:26183017..26185475,2	MCF-7	breast:
13	chr6:26064512..26067179-chr6:26122089..26125460,6	MCF-7	breast:
14	chr6:26065500..26066266-chr6:26096170..26096872,2	K562	blood:
15	chr6:26063980..26067080-chr6:26097095..26099465,41	K562	blood:
16	chr20:9893278..9893949-chr6:26066133..26066755,2	MCF-7	breast:
17	chr6:26064740..26067843-chr6:26069105..26072811,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000187837	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000197697	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000010704	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000197061	Chromatin interaction
ENSG00000187475	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000196331	Chromatin interaction

Extended variants
information (count: 99 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1061482	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10807006	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10807007	0.85[CHB][hapmap];0.93[JPT][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1130000	0.81[CEU][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap]
rs1436306	0.90[CHD][hapmap];0.80[JPT][hapmap];0.80[MEX][hapmap]
rs1436309	0.87[JPT][hapmap];0.85[YRI][hapmap];0.80[ASN][1000 genomes]
rs1436310	0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs1539183	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1541987	0.90[CHD][hapmap];0.80[JPT][hapmap];0.80[MEX][hapmap]
rs1800702	0.96[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1865760	0.88[MEX][hapmap]
rs1971509	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2006736	0.96[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2013063	0.81[CEU][hapmap];0.84[MEX][hapmap];0.86[TSI][hapmap]
rs2032443	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2032445	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2032449	0.92[CEU][hapmap];0.89[AMR][1000 genomes]
rs2032450	0.81[CEU][hapmap]
rs2051544	0.89[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2071297	0.88[MEX][hapmap]
rs2071298	0.88[MEX][hapmap]
rs2071299	0.88[MEX][hapmap]
rs2071301	0.84[MEX][hapmap]
rs2157050	0.88[CEU][hapmap];0.86[GIH][hapmap];0.93[LWK][hapmap];0.91[MEX][hapmap];0.88[TSI][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs2328903	0.80[MEX][hapmap]
rs2328905	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2794719	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2794720	0.96[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2858993	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2876694	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3752419	0.89[ASW][hapmap];0.92[CEU][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.84[MKK][hapmap];0.97[TSI][hapmap];0.87[AMR][1000 genomes]
rs3752420	0.89[ASW][hapmap];0.92[CEU][hapmap];0.95[GIH][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.89[AMR][1000 genomes]
rs3752421	0.88[MEX][hapmap]
rs3799371	0.88[MEX][hapmap]
rs4529296	0.96[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6910174	0.88[MEX][hapmap]
rs6928717	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6938083	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6938233	0.88[MEX][hapmap]
rs6942196	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7738854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7753253	1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7770139	0.88[MEX][hapmap]
rs7772312	0.96[CEU][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9295681	0.80[JPT][hapmap]
rs9295684	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295685	0.92[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9295686	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9295687	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9295688	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9348704	0.83[ASN][1000 genomes]
rs9348706	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9356991	0.88[MEX][hapmap]
rs9356998	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9358896	0.80[MEX][hapmap]
rs9358902	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9358903	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358904	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9358905	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9366634	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9366636	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9379818	1.00[ASW][hapmap];0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.93[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.98[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9379819	0.84[CHB][hapmap];0.93[JPT][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9379820	0.96[CEU][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9379821	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9379823	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9379825	0.96[CEU][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9393681	0.88[CEU][hapmap];0.97[CHD][hapmap];0.93[JPT][hapmap];0.97[LWK][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9393684	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9461230	0.92[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9467646	0.80[MEX][hapmap]
rs9467647	0.80[JPT][hapmap]
rs9467656	0.83[CEU][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.85[ASN][1000 genomes]
rs9467658	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9467662	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs9467663	0.86[AMR][1000 genomes]
rs9467672	0.96[CEU][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription 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 miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv432857	chr6:25957109-26072445	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	451 gene(s)	inside rSNPs	diseases
8	nsv1015627	chr6:25973495-26100483	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
9	nsv538164	chr6:25973495-26100483	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
10	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
11	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
12	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
13	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
14	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
15	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
16	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
17	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
18	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
19	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
20	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
21	nsv1026692	chr6:26027408-26067081	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	363 gene(s)	inside rSNPs	diseases
22	esv3692889	chr6:26064510-26066198	Weak transcription Enhancers	Chromatin interactive region	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs9393683	HIST1H3B	cis	cerebellum	SCAN
rs9393683	HIST1H2AA	cis	parietal	SCAN
rs9393683	U91328.19	cis	Muscle Skeletal	GTEx
rs9393683	HIST1H2BC	cis	cerebellum	SCAN
rs9393683	BTN3A2	cis	cerebellum	SCAN
rs9393683	HIST1H3H	cis	parietal	SCAN
rs9393683	HIST1H2AH	cis	parietal	SCAN
rs9393683	HIST1H1C	cis	parietal	SCAN

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26057600-26066400	Weak transcription	NH-A	brain
2	chr6:26058800-26066400	Weak transcription	K562	blood
3	chr6:26060200-26066400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr6:26061000-26066400	Weak transcription	Stomach Mucosa	stomach
5	chr6:26063000-26067800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr6:26064800-26066400	Weak transcription	Fetal Intestine Large	intestine
7	chr6:26065200-26066200	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr6:26065200-26066400	Weak transcription	HepG2	liver
9	chr6:26065200-26066600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:26065200-26066600	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr6:26065200-26066800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:26065400-26066600	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr6:26065600-26066800	Enhancers	Dnd41	blood
14	chr6:26065800-26066600	Enhancers	Primary B cells from cord blood	blood
15	chr6:26066000-26066400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr6:26066000-26066600	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr6:26066000-26066600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr6:26066000-26066600	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr6:26066000-26066600	Enhancers	Fetal Lung	lung
20	chr6:26066000-26066800	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr6:26066000-26066800	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr6:26066000-26066800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:26066000-26066800	Enhancers	Colon Smooth Muscle	Colon
24	chr6:26066000-26066800	Enhancers	Hela-S3	cervix
25	chr6:26066000-26067000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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