Variant report

Variant	rs7756117
Chromosome Location	chr6:26046565-26046566
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:26043180-26046720	GM12892	blood:	n/a	n/a
2	NFIC	chr6:26043271-26046700	GM12878	blood:	n/a	n/a
3	FOXA1	chr6:26046143-26046670	HepG2	liver:	n/a	n/a
4	KAT2A	chr6:26045530-26046601	GM12878	blood:	n/a	n/a
5	MXI1	chr6:26043247-26046992	IMR90	lung:	n/a	n/a
6	FOXM1	chr6:26045075-26046600	GM12878	blood:	n/a	n/a
7	POLR2A	chr6:26043122-26046798	SK-N-SH	brain:	n/a	n/a
8	POLR2A	chr6:26043135-26046646	HUVEC	blood vessel:	n/a	n/a
9	POLR2A	chr6:26043226-26046775	U87	brain:	n/a	n/a
10	POLR2A	chr6:26043081-26046720	GM12892	blood:	n/a	n/a
11	POLR2A	chr6:26043204-26046824	GM12878	blood:	n/a	n/a
12	FOXA1	chr6:26046209-26046672	HepG2	liver:	n/a	n/a
13	POLR2A	chr6:26043051-26046692	U87	brain:	n/a	n/a
14	CEBPB	chr6:26045355-26046608	Hela-S3	cervix:	n/a	chr6:26045517-26045525
15	POLR2A	chr6:26045360-26046640	GM12878	blood:	n/a	n/a
16	NFATC1	chr6:26044958-26046598	GM12878	blood:	n/a	n/a
17	ELF1	chr6:26046303-26046591	HepG2	liver:	n/a	n/a
18	POLR2A	chr6:26043191-26046694	HUVEC	blood vessel:	n/a	n/a
19	EP300	chr6:26045324-26046663	HepG2	liver:	n/a	n/a
20	USF2	chr6:26045403-26046593	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr6:26043157-26046775	U87	brain:	n/a	n/a
22	SIN3AK20	chr6:26045374-26046641	SK-N-SH	brain:	n/a	n/a
23	BCLAF1	chr6:26045089-26046690	GM12878	blood:	n/a	n/a
24	ZBTB33	chr6:26045365-26046616	A549	lung:	n/a	n/a
25	MYBL2	chr6:26043120-26046769	HepG2	liver:	n/a	n/a
26	ZEB1	chr6:26043228-26046771	HepG2	liver:	n/a	chr6:26043391-26043399
27	RELA	chr6:26045067-26046604	GM12878	blood:	n/a	n/a
28	POLR2A	chr6:26046329-26046591	Gliobla	brain:	n/a	n/a
29	JUND	chr6:26046451-26046728	HepG2	liver:	n/a	n/a
30	FOXA1	chr6:26046065-26046806	HepG2	liver:	n/a	n/a
31	POLR2A	chr6:26043056-26046727	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr6:26043249-26046673	GM12891	blood:	n/a	n/a
33	FOXM1	chr6:26045131-26046573	GM12878	blood:	n/a	n/a
34	POLR2A	chr6:26045196-26046659	GM12892	blood:	n/a	n/a
35	NFIC	chr6:26044963-26046667	HepG2	liver:	n/a	n/a
36	BCLAF1	chr6:26043220-26046641	GM12878	blood:	n/a	chr6:26043387-26043396
37	FOXA2	chr6:26046087-26046671	HepG2	liver:	n/a	n/a
38	ZBTB33	chr6:26043270-26046780	SK-N-SH	brain:	n/a	n/a
39	RUNX3	chr6:26044701-26046624	GM12878	blood:	n/a	n/a
40	POLR2A	chr6:26044999-26046684	SK-N-SH	brain:	n/a	n/a
41	POLR2A	chr6:26045234-26046622	GM10847	blood:	n/a	n/a
42	POLR2A	chr6:26043179-26046830	PANC-1	pancreas:	n/a	n/a
43	RELA	chr6:26045183-26046605	GM18951	blood:	n/a	n/a
44	CREB1	chr6:26043258-26046731	HepG2	liver:	n/a	n/a
45	FOXA1	chr6:26046218-26046698	HepG2	liver:	n/a	n/a
46	MBD4	chr6:26045141-26046666	HepG2	liver:	n/a	n/a
47	POLR2A	chr6:26043263-26046700	GM12891	blood:	n/a	n/a
48	POLR2A	chr6:26043047-26046763	GM12892	blood:	n/a	n/a
49	POLR2A	chr6:26043046-26046705	HepG2	liver:	n/a	n/a
50	NFIC	chr6:26044997-26046858	HepG2	liver:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26044671..26047980-chr6:26183838..26186075,3	MCF-7	breast:
2	chr6:26044692..26047309-chr6:27838299..27842021,15	MCF-7	breast:
3	chr6:26044049..26046588-chr6:26248373..26251129,2	MCF-7	breast:
4	chr17:56708294..56710638-chr6:26044705..26047582,3	MCF-7	breast:
5	chr6:26045666..26048095-chr6:26203965..26208002,5	MCF-7	breast:
6	chr6:26045293..26047313-chr6:35435617..35437589,2	MCF-7	breast:
7	chr6:26044526..26047786-chr6:27838310..27841317,7	MCF-7	breast:
8	chr6:26041051..26050922-chr6:26154916..26161227,19	MCF-7	breast:
9	chr6:26044121..26047112-chr6:27113025..27116157,4	MCF-7	breast:
10	chr6:26043872..26047495-chr6:26122651..26127553,11	MCF-7	breast:
11	chr6:26043570..26047536-chr6:26215421..26218540,6	MCF-7	breast:

No data

Variant related genes	Relation type
HIST1H2BB	TF binding region
ENSG00000182572	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000197697	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000198558	Chromatin interaction
ENSG00000198755	Chromatin interaction
ENSG00000198518	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000256316	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000187990	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10425	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs115810	0.88[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs1165201	0.83[CHD][hapmap]
rs12346	0.92[CEU][hapmap];0.92[CHD][hapmap];0.81[GIH][hapmap];0.81[EUR][1000 genomes]
rs129129	0.86[CHB][hapmap];0.87[CHD][hapmap]
rs1540275	0.96[CEU][hapmap];0.86[CHB][hapmap];0.96[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1540276	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1935235	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs198810	0.84[CHD][hapmap];0.84[GIH][hapmap]
rs198815	0.86[JPT][hapmap]
rs198820	0.84[CHD][hapmap];0.84[GIH][hapmap]
rs198845	0.92[CHD][hapmap];0.84[GIH][hapmap]
rs198848	0.91[CHD][hapmap];0.84[GIH][hapmap]
rs198852	0.92[CHD][hapmap];0.84[GIH][hapmap]
rs198853	0.92[CEU][hapmap];0.96[CHD][hapmap];0.84[GIH][hapmap];0.82[MEX][hapmap];0.80[TSI][hapmap]
rs199737	0.86[CHB][hapmap]
rs199739	0.86[CHB][hapmap]
rs199741	0.86[CHB][hapmap];0.83[CHD][hapmap]
rs199750	0.92[CEU][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs199751	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs199752	0.92[CEU][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs199753	0.88[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs199754	0.83[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.88[ASN][1000 genomes]
rs199755	0.91[ASN][1000 genomes]
rs2032447	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2213284	0.96[CEU][hapmap];0.96[CHD][hapmap];0.91[GIH][hapmap];0.88[JPT][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2230655	0.96[CEU][hapmap];0.86[CHB][hapmap];0.96[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34413295	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3752416	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs428469	0.86[CHB][hapmap]
rs4401650	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs442601	0.86[CHB][hapmap]
rs537581	0.83[CHD][hapmap]
rs599444	0.83[CHD][hapmap]
rs6901039	0.88[CEU][hapmap];0.86[CHB][hapmap];0.96[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6922788	0.86[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6942072	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7760848	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs807212	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs807214	0.88[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs9295683	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9356995	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9358901	1.00[CEU][hapmap];0.88[CHB][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9379822	0.91[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9467664	0.96[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs7756117	HIST1H1T	cis	multi-tissue	Pritchard
rs7756117	HIST1H2BD	cis	multi-tissue	Pritchard
rs7756117	HIST1H4I	cis	cerebellum	SCAN
rs7756117	HIST1H2AJ	cis	parietal	SCAN
rs7756117	ZNF187	cis	parietal	SCAN
rs7756117	HIST1H2AA	cis	parietal	SCAN
rs7756117	HIST1H2BB	cis	parietal	SCAN

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26034400-26048200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:26043000-26046600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:26043200-26046600	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr6:26043200-26046600	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr6:26043200-26046600	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr6:26043200-26046800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:26043400-26046600	Active TSS	H9 Cell Line	embryonic stem cell
8	chr6:26043400-26046600	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr6:26043400-26046600	Active TSS	A549	lung
10	chr6:26043400-26046600	Flanking Active TSS	NHEK	skin
11	chr6:26043800-26046600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:26044200-26046600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:26044200-26046600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:26044200-26046600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:26044200-26046600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
16	chr6:26044200-26046600	Flanking Active TSS	HMEC	breast
17	chr6:26044200-26046800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr6:26044600-26054800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:26044600-26055000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:26045000-26046600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr6:26045600-26046600	Flanking Active TSS	Fetal Thymus	thymus
22	chr6:26045600-26046600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr6:26045600-26046600	Enhancers	Spleen	Spleen
24	chr6:26045800-26046600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
25	chr6:26045800-26046600	Flanking Active TSS	Dnd41	blood
26	chr6:26045800-26046600	Flanking Active TSS	GM12878-XiMat	blood
27	chr6:26045800-26046600	Flanking Active TSS	HUVEC	blood vessel
28	chr6:26045800-26054600	Weak transcription	Ovary	ovary
29	chr6:26046000-26046600	Enhancers	Primary B cells from peripheral blood	blood
30	chr6:26046000-26046600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr6:26046000-26046600	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr6:26046000-26046600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr6:26046000-26046600	Enhancers	Placenta	Placenta
34	chr6:26046000-26046600	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr6:26046000-26046600	Flanking Active TSS	Hela-S3	cervix
36	chr6:26046000-26046600	Flanking Active TSS	HepG2	liver
37	chr6:26046000-26046800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr6:26046000-26047000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:26046000-26047800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr6:26046200-26046600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:26046200-26046600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr6:26046200-26046600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr6:26046200-26046600	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr6:26046200-26046600	Enhancers	Primary T cells from cord blood	blood
45	chr6:26046200-26046600	Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr6:26046200-26046600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr6:26046200-26046600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr6:26046200-26046600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:26046200-26046600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:26046200-26046600	Active TSS	Duodenum Mucosa	Duodenum

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