Variant report

Variant	rs16891378
Chromosome Location	chr6:26188864-26188865
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:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26187375..26189880-chr6:27097420..27103446,8	K562	blood:
2	chr6:26026488..26028214-chr6:26187877..26190582,2	MCF-7	breast:
3	chr6:26187666..26189518-chr6:27113172..27116022,2	K562	blood:
4	chr6:26188276..26190980-chr6:26381179..26383865,2	K562	blood:
5	chr2:61764894..61765613-chr6:26188425..26189321,2	HCT-116	colon:
6	chr2:182705814..182707685-chr6:26186197..26188947,2	MCF-7	breast:
7	chr6:26187831..26190328-chr6:26520761..26523308,3	K562	blood:
8	chr20:45985042..45987861-chr6:26187518..26190404,2	MCF-7	breast:
9	chr6:26186794..26189358-chr6:31620269..31622161,2	K562	blood:
10	chr20:45946934..45948721-chr6:26187460..26189377,3	MCF-7	breast:
11	chr5:180659417..180661225-chr6:26188646..26190614,2	K562	blood:
12	chr6:26187875..26189403-chr6:27797113..27800006,2	MCF-7	breast:
13	chr6:26187687..26190163-chr6:27098059..27101507,5	K562	blood:
14	chr6:26187662..26190884-chr6:27112568..27116666,4	MCF-7	breast:
15	chr6:26054932..26056773-chr6:26188728..26190968,2	MCF-7	breast:
16	chr1:11968160..11968907-chr6:26188819..26189353,2	HCT-116	colon:
17	chr6:26187257..26192079-chr6:27098954..27103250,7	MCF-7	breast:
18	chr6:26187432..26189405-chr7:158620973..158622710,2	MCF-7	breast:
19	chr6:26032288..26035408-chr6:26183846..26189517,7	MCF-7	breast:
20	chr14:75745269..75745936-chr6:26188512..26189248,2	HCT-116	colon:
21	chr6:26187760..26190799-chr6:26518890..26523308,5	K562	blood:
22	chr6:26187507..26190261-chr6:27099153..27102365,6	MCF-7	breast:
23	chr6:26185337..26188954-chr6:26593847..26597178,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000197914	Chromatin interaction
ENSG00000117868	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000170345	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000267882	Chromatin interaction
ENSG00000082898	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000124508	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000146063	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000187837	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10452600	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10484436	1.00[ASW][hapmap];0.93[CHD][hapmap];0.85[LWK][hapmap];0.92[MEX][hapmap];0.80[MKK][hapmap];0.96[TSI][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11751812	0.85[JPT][hapmap]
rs11753131	1.00[ASW][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.85[LWK][hapmap];0.92[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11753625	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11753655	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11754744	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11755210	0.82[CEU][hapmap];0.85[JPT][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11755943	0.90[ASW][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.92[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11757394	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11757754	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11758351	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11759904	1.00[ASW][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.88[LWK][hapmap];0.92[MEX][hapmap];0.96[TSI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1341759	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16891375	0.85[JPT][hapmap]
rs16891397	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16891401	1.00[CEU][hapmap];0.86[JPT][hapmap];0.81[YRI][hapmap];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16891405	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16891407	0.85[JPT][hapmap]
rs16891443	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891446	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891455	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891456	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891466	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891467	1.00[ASW][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.85[LWK][hapmap];0.92[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17598927	1.00[CEU][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.86[JPT][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1997768	0.90[ASW][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.92[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2022448	0.88[ASW][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2050948	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2050950	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2069018	0.90[ASW][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2069019	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2069020	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2143345	1.00[ASW][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.88[LWK][hapmap];0.92[MEX][hapmap];0.87[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2143346	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2143347	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2183948	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3734530	1.00[CEU][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs3734533	0.86[CHD][hapmap]
rs3757135	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs41266801	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs41266807	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4496782	0.82[CHD][hapmap]
rs55643278	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55815656	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55848726	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56186759	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56220351	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56398712	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6906367	0.82[CHD][hapmap];0.87[GIH][hapmap]
rs9379831	0.82[LWK][hapmap]

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	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	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
17	nsv518431	chr6:26148311-26211368	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
18	nsv526456	chr6:26148311-26211368	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
19	nsv883490	chr6:26172219-26231608	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	316 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs16891378	HIST1H3F	cis	cerebellum	SCAN
rs16891378	HIST1H3D	cis	parietal	SCAN
rs16891378	HIST1H2AE	cis	multi-tissue	Pritchard
rs16891378	HIST1H2BG	cis	multi-tissue	Pritchard
rs16891378	HIST1H4F	cis	parietal	SCAN
rs16891378	HIST1H3E	cis	parietal	SCAN
rs16891378	HIST1H4F	cis	cerebellum	SCAN
rs16891378	HIST1H1D	cis	cerebellum	SCAN
rs16891378	HIST1H2AE	cis	lymphoblastoid	seeQTL
rs16891378	HIST1H3E	cis	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26182000-26193000	Weak transcription	Dnd41	blood
2	chr6:26187400-26189400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:26187800-26189600	Flanking Active TSS	Fetal Thymus	thymus
4	chr6:26188000-26189400	Active TSS	H9 Cell Line	embryonic stem cell
5	chr6:26188000-26189400	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr6:26188000-26189400	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr6:26188000-26189400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:26188000-26189400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:26188000-26189600	Active TSS	H1 Cell Line	embryonic stem cell
10	chr6:26188000-26189600	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr6:26188000-26189600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:26188000-26189600	Active TSS	A549	lung
13	chr6:26188000-26189800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr6:26188000-26189800	Active TSS	Fetal Brain Female	brain
15	chr6:26188000-26189800	Active TSS	Fetal Kidney	kidney
16	chr6:26188200-26189000	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:26188200-26189000	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr6:26188200-26189000	Flanking Active TSS	Primary T cells from cord blood	blood
19	chr6:26188200-26189000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
20	chr6:26188200-26189000	Enhancers	Spleen	Spleen
21	chr6:26188200-26189200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr6:26188200-26189200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
23	chr6:26188200-26189200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:26188200-26189200	Flanking Active TSS	HUVEC	blood vessel
25	chr6:26188200-26189400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:26188200-26189400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:26188200-26189400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:26188200-26189400	Active TSS	Colonic Mucosa	Colon
29	chr6:26188200-26189600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:26188200-26189600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:26188200-26189600	Flanking Active TSS	Primary hematopoietic stem cells	blood
32	chr6:26188200-26189600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr6:26188200-26189600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr6:26188200-26189600	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr6:26188200-26189600	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr6:26188200-26189600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr6:26188200-26189600	Active TSS	Fetal Lung	lung
38	chr6:26188200-26189600	Flanking Active TSS	NHEK	skin
39	chr6:26188200-26189600	Active TSS	Osteobl	bone
40	chr6:26188200-26189800	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr6:26188200-26189800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr6:26188200-26190000	Active TSS	Rectal Smooth Muscle	rectum
43	chr6:26188400-26189000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:26188400-26189000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
45	chr6:26188400-26189000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr6:26188400-26189000	Active TSS	Pancreas	Pancrea
47	chr6:26188400-26189000	Flanking Active TSS	NH-A	brain
48	chr6:26188400-26189400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr6:26188400-26189400	Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr6:26188400-26189400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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