Variant report

Variant	rs16891467
Chromosome Location	chr6:26235966-26235967
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:26233034-26244857	K562	blood:	n/a	n/a
2	ARID3A	chr6:26235860-26235970	K562	blood:	n/a	n/a
3	MAFK	chr6:26235947-26236006	K562	blood:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:24719968..24721731-chr6:26234799..26237042,2	K562	blood:
2	chr6:26031185..26034143-chr6:26233658..26236359,2	MCF-7	breast:
3	chr6:26231234..26236589-chr6:27099738..27104932,8	K562	blood:
4	chr17:56736343..56738004-chr6:26233634..26236262,2	MCF-7	breast:
5	chr6:26020523..26023508-chr6:26233779..26236758,2	MCF-7	breast:
6	chr15:74753352..74756015-chr6:26233514..26236458,2	K562	blood:
7	chr3:28388905..28390597-chr6:26234908..26237633,2	K562	blood:
8	chr6:26234528..26236146-chr6:26520612..26523386,2	K562	blood:
9	chr6:26233781..26236628-chr6:27113286..27115220,2	K562	blood:
10	chr16:2009340..2011468-chr6:26233811..26235989,2	MCF-7	breast:

No data

Variant related genes	Relation type
HIST1H4F	TF binding region
HIST1H1D	TF binding region
ENSG00000137259	Chromatin interaction
ENSG00000163512	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000138629	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000247240	Chromatin interaction
ENSG00000112308	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000140990	Chromatin interaction
ENSG00000196787	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10452600	1.00[ASW][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.85[LWK][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10484436	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11753131	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11753625	0.88[EUR][1000 genomes]
rs11753655	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11754744	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11755210	0.86[CHB][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11755943	0.90[ASW][hapmap];1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11757394	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11757754	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11758351	0.82[ASW][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.80[LWK][hapmap];0.93[MEX][hapmap];0.96[TSI][hapmap];0.82[YRI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11759720	0.85[CHD][hapmap]
rs11759904	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341759	1.00[ASW][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.85[LWK][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16891378	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]
rs16891397	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16891401	0.89[CHB][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16891405	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891443	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891446	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891455	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891456	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891466	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891474	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16891481	0.89[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17598927	0.89[CHB][hapmap];0.93[CHD][hapmap];0.96[TSI][hapmap];0.86[EUR][1000 genomes]
rs1997768	0.90[ASW][hapmap];1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2022448	0.88[ASW][hapmap];0.85[CEU][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.96[LWK][hapmap];0.92[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2050948	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2050950	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2069018	0.90[ASW][hapmap];0.85[CEU][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.96[LWK][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2069019	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2069020	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2143345	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2143346	1.00[ASW][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.85[LWK][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2143347	0.89[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.96[TSI][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2183948	0.87[EUR][1000 genomes]
rs3734530	0.88[CHB][hapmap]
rs3734533	0.93[CHD][hapmap];0.81[GIH][hapmap];0.80[LWK][hapmap]
rs3757135	1.00[ASW][hapmap];0.89[CHB][hapmap];0.86[CHD][hapmap];0.82[GIH][hapmap];0.81[LWK][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs41266801	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs41266807	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55643278	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55815656	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55848726	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56186759	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56220351	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56398712	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 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	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
13	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
14	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
15	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
16	nsv1021294	chr6:26190316-26246784	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	309 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs16891467	HIST1H3E	cis	parietal	SCAN
rs16891467	HIST1H2AE	cis	lymphoblastoid	seeQTL
rs16891467	HIST1H2BJ	cis	lymphoblastoid	seeQTL
rs16891467	HIST1H3F	cis	cerebellum	SCAN
rs16891467	HIST1H2BF	cis	parietal	SCAN
rs16891467	HIST1H3E	cis	cerebellum	SCAN
rs16891467	HIST1H1D	cis	cerebellum	SCAN
rs16891467	HIST1H4F	cis	cerebellum	SCAN
rs16891467	HIST1H2AE	cis	multi-tissue	Pritchard
rs16891467	ZNF187	cis	parietal	SCAN
rs16891467	HIST1H2BG	cis	multi-tissue	Pritchard
rs16891467	HIST1H4F	cis	parietal	SCAN
rs16891467	TNFRSF1A	trans	parietal	SCAN

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26231200-26236000	Active TSS	Thymus	Thymus
2	chr6:26232400-26236000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr6:26233000-26236000	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr6:26233000-26236000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:26233200-26236000	Active TSS	Fetal Kidney	kidney
6	chr6:26233200-26236000	Active TSS	A549	lung
7	chr6:26233600-26236000	Active TSS	H1 Cell Line	embryonic stem cell
8	chr6:26234200-26236000	Active TSS	Fetal Thymus	thymus
9	chr6:26234800-26236200	Active TSS	K562	blood
10	chr6:26235200-26236000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr6:26235200-26236800	Weak transcription	Spleen	Spleen
12	chr6:26235400-26236000	Flanking Active TSS	Primary B cells from cord blood	blood
13	chr6:26235400-26236000	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr6:26235400-26236200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:26235400-26240000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:26235400-26240000	Weak transcription	Placenta	Placenta
17	chr6:26235400-26240400	Weak transcription	Esophagus	oesophagus
18	chr6:26235600-26236000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr6:26235600-26236000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr6:26235600-26236000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr6:26235600-26236000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr6:26235600-26236000	Flanking Active TSS	Primary T cells from cord blood	blood
23	chr6:26235600-26236000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:26235600-26236000	Flanking Active TSS	Brain Germinal Matrix	brain
25	chr6:26235600-26236000	Bivalent Enhancer	Colon Smooth Muscle	Colon
26	chr6:26235600-26236000	Enhancers	Stomach Mucosa	stomach
27	chr6:26235600-26236200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr6:26235600-26236400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr6:26235800-26236000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:26235800-26236000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:26235800-26236000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:26235800-26236000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr6:26235800-26236000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr6:26235800-26236000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr6:26235800-26236000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr6:26235800-26236000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr6:26235800-26236000	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr6:26235800-26236000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr6:26235800-26236000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:26235800-26236000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:26235800-26236000	Flanking Active TSS	Dnd41	blood
42	chr6:26235800-26236000	Flanking Active TSS	GM12878-XiMat	blood
43	chr6:26235800-26236000	Bivalent Enhancer	HepG2	liver
44	chr6:26235800-26236000	Enhancers	NHEK	skin
45	chr6:26235800-26236200	Enhancers	Primary B cells from peripheral blood	blood
46	chr6:26235800-26236200	Enhancers	Primary T cells fromperipheralblood	blood
47	chr6:26235800-26236200	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr6:26235800-26236200	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr6:26235800-26236200	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr6:26235800-26236200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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