Variant report

Variant	rs6558535
Chromosome Location	chr8:1710632-1710633
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr8:1704744-1714404	K562	blood:	n/a	n/a
2	ZMIZ1	chr8:1710590-1711442	K562	blood:	n/a	n/a
3	POLR2A	chr8:1706662-1711460	PBDE	blood:	n/a	n/a
4	CEBPD	chr8:1710617-1711471	K562	blood:	n/a	n/a
5	MAFK	chr8:1710598-1710937	K562	blood:	n/a	n/a
6	JUND	chr8:1710619-1711579	GM12878	blood:	n/a	chr8:1711473-1711482
7	CEBPD	chr8:1710593-1711130	K562	blood:	n/a	n/a
8	POLR2A	chr8:1710516-1711069	K562	blood:	n/a	n/a
9	GATA1	chr8:1709786-1711444	PBDE	blood:	n/a	n/a
10	FOXA2	chr8:1710338-1710741	A549	lung:	n/a	n/a
11	UBTF	chr8:1710564-1711505	K562	blood:	n/a	n/a
12	POLR2A	chr8:1710578-1711501	MCF10A-Er-Src	breast:	n/a	n/a
13	POLR2A	chr8:1710507-1711559	IMR90	lung:	n/a	n/a
14	JUND	chr8:1710569-1711542	K562	blood:	n/a	chr8:1711473-1711482
15	TAL1	chr8:1710516-1711189	K562	blood:	n/a	n/a
16	RCOR1	chr8:1710531-1711439	K562	blood:	n/a	n/a
17	CCNT2	chr8:1710544-1710966	K562	blood:	n/a	n/a
18	POLR2A	chr8:1710550-1712748	K562	blood:	n/a	n/a
19	NR2F2	chr8:1710451-1711068	K562	blood:	n/a	n/a
20	EP300	chr8:1710493-1711402	K562	blood:	n/a	n/a
21	POLR2A	chr8:1710548-1711600	K562	blood:	n/a	n/a
22	GATA1	chr8:1710553-1711563	K562	blood:	n/a	n/a
23	POLR2A	chr8:1710542-1711622	K562	blood:	n/a	n/a
24	POLR2A	chr8:1710507-1712994	K562	blood:	n/a	n/a
25	TEAD4	chr8:1710499-1711083	K562	blood:	n/a	n/a
26	IRF1	chr8:1710597-1711425	K562	blood:	n/a	n/a
27	MAZ	chr8:1710575-1713059	K562	blood:	n/a	chr8:1712674-1712693 chr8:1712679-1712688 chr8:1712678-1712689 chr8:1712448-1712457

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:1708066..1710813-chr8:1745165..1747310,2	MCF-7	breast:
2	chr8:1702392..1708895-chr8:1709221..1714010,17	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERICH1-7	chr8:1710247-1711094	ENSG00000253982.1
2	lnc-ERICH1-7	chr8:1710156-1711094	ENSG00000253982.1
3	lnc-ERICH1-7	chr8:1709431-1711094	NONHSAT124680
4	lnc-ERICH1-7	chr8:1709431-1711094	NONHSAT124681

No data

Variant related genes	Relation type
CLN8	TF binding region
ENSG00000182372	Chromatin interaction

Extended variants
information (count: 115 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10087654	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10095548	0.81[ASN][1000 genomes]
rs10095696	0.81[ASN][1000 genomes]
rs10097891	0.88[ASN][1000 genomes]
rs10100341	0.86[ASN][1000 genomes]
rs10102731	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10105317	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10106153	0.92[ASN][1000 genomes]
rs10109098	0.81[ASN][1000 genomes]
rs10113471	0.86[ASN][1000 genomes]
rs10481354	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11136421	0.87[ASN][1000 genomes]
rs11136422	0.87[ASN][1000 genomes]
rs11136424	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11778824	0.84[ASN][1000 genomes]
rs12335115	0.92[ASN][1000 genomes]
rs12674711	0.89[ASN][1000 genomes]
rs13251071	0.87[ASN][1000 genomes]
rs13256424	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13261755	0.88[ASN][1000 genomes]
rs13282161	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13540	0.98[ASN][1000 genomes]
rs2293977	0.95[ASN][1000 genomes]
rs28376731	0.93[ASN][1000 genomes]
rs2957085	0.87[ASN][1000 genomes]
rs2977197	0.86[ASN][1000 genomes]
rs35062922	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3812477	0.84[ASN][1000 genomes]
rs4242538	0.88[ASN][1000 genomes]
rs4370560	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4372027	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4595147	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4639549	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4875806	0.92[ASN][1000 genomes]
rs4875889	0.86[ASN][1000 genomes]
rs4875957	0.92[ASN][1000 genomes]
rs4875958	0.92[ASN][1000 genomes]
rs4876133	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6558518	0.90[ASN][1000 genomes]
rs6558520	0.91[ASN][1000 genomes]
rs6558521	0.88[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6558522	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6558523	0.92[ASN][1000 genomes]
rs6558524	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6558525	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6558526	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6558527	0.92[ASN][1000 genomes]
rs6558528	0.91[ASN][1000 genomes]
rs6558530	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6558531	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6558532	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6558533	0.99[ASN][1000 genomes]
rs6558534	1.00[ASN][1000 genomes]
rs6981804	0.92[ASN][1000 genomes]
rs6982516	0.93[ASN][1000 genomes]
rs6984632	0.89[ASN][1000 genomes]
rs6986102	0.91[ASN][1000 genomes]
rs6991773	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6991783	0.86[ASN][1000 genomes]
rs6993706	0.92[ASN][1000 genomes]
rs7000162	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7001282	0.92[ASN][1000 genomes]
rs7005592	0.92[ASN][1000 genomes]
rs7005699	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7008465	0.87[ASN][1000 genomes]
rs7014327	0.86[ASN][1000 genomes]
rs7014823	0.86[ASN][1000 genomes]
rs7015858	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs71499040	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs730377	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs730379	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7341635	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7459507	0.89[ASN][1000 genomes]
rs7460230	0.88[ASN][1000 genomes]
rs7460287	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7460365	0.91[ASN][1000 genomes]
rs7460866	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7460972	0.98[ASN][1000 genomes]
rs7461159	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7461259	0.88[ASN][1000 genomes]
rs7461600	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7463876	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7463879	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7465178	0.91[ASN][1000 genomes]
rs7818406	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7822816	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7827009	0.85[ASN][1000 genomes]
rs7827285	0.85[ASN][1000 genomes]
rs7828950	0.97[ASN][1000 genomes]
rs7838456	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7842425	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7844748	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7846610	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9022	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[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	nsv889697	chr8:1238564-1861971	Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1031375	chr8:1320657-1722050	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv889704	chr8:1563904-1965389	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv889707	chr8:1581839-1920461	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv889708	chr8:1581839-1965389	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv889709	chr8:1581839-1965389	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv889711	chr8:1591412-1904157	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv889712	chr8:1591412-2337777	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv889714	chr8:1616718-1965389	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv934075	chr8:1626857-1736355	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv1034490	chr8:1654716-1782467	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
12	nsv609527	chr8:1681733-1753497	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer 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	8 gene(s)	inside rSNPs	diseases
13	nsv870096	chr8:1682851-1767342	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
14	nsv465274	chr8:1685064-1728292	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv609528	chr8:1685064-1728292	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	nsv532892	chr8:1687433-1839578	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers 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 miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
17	esv2755149	chr8:1689290-1755281	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer 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	8 gene(s)	inside rSNPs	diseases
18	nsv465275	chr8:1697086-1768004	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
19	nsv609529	chr8:1697086-1768004	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
20	nsv465276	chr8:1701432-1777571	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
21	nsv609530	chr8:1701432-1777571	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs6558535	CTD-2336O2.1	cis	Thyroid	GTEx
rs6558535	CTD-2336O2.1	cis	lung	GTEx
rs6558535	CTD-2336O2.1	cis	Esophagus Muscularis	GTEx
rs6558535	CTD-2336O2.1	cis	Artery Tibial	GTEx
rs6558535	CTD-2336O2.1	cis	Adipose Subcutaneous	GTEx
rs6558535	CTD-2336O2.1	cis	Muscle Skeletal	GTEx
rs6558535	CTD-2336O2.1	cis	Nerve Tibial	GTEx

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1704000-1710800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr8:1707400-1710800	Enhancers	Fetal Thymus	thymus
3	chr8:1707800-1710800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:1707800-1710800	Weak transcription	Right Ventricle	heart
5	chr8:1708400-1710800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:1708400-1710800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:1708600-1710800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:1709000-1710800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:1709000-1710800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr8:1709000-1710800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr8:1709200-1710800	Weak transcription	Pancreas	Pancrea
12	chr8:1710000-1710800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:1710200-1710800	Enhancers	Primary T cells fromperipheralblood	blood
14	chr8:1710200-1710800	Enhancers	Fetal Muscle Leg	muscle
15	chr8:1710400-1710800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:1710400-1710800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr8:1710400-1710800	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr8:1710400-1710800	Enhancers	Left Ventricle	heart
19	chr8:1710400-1711200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
20	chr8:1710400-1711200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:1710400-1711200	Transcr. at gene 5' and 3'	A549	lung
22	chr8:1710400-1711400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:1710400-1712200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr8:1710600-1710800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:1710600-1710800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:1710600-1710800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr8:1710600-1710800	Enhancers	Primary B cells from cord blood	blood
28	chr8:1710600-1710800	Enhancers	Primary B cells from peripheral blood	blood
29	chr8:1710600-1710800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr8:1710600-1710800	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr8:1710600-1710800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr8:1710600-1710800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr8:1710600-1710800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr8:1710600-1710800	Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr8:1710600-1710800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr8:1710600-1710800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr8:1710600-1710800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr8:1710600-1710800	Enhancers	Brain Angular Gyrus	brain
39	chr8:1710600-1710800	Active TSS	Brain Anterior Caudate	brain
40	chr8:1710600-1710800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr8:1710600-1710800	Enhancers	Colon Smooth Muscle	Colon
42	chr8:1710600-1710800	Enhancers	Duodenum Mucosa	Duodenum
43	chr8:1710600-1710800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr8:1710600-1710800	Weak transcription	Esophagus	oesophagus
45	chr8:1710600-1710800	Enhancers	Fetal Brain Male	brain
46	chr8:1710600-1710800	Enhancers	Fetal Heart	heart
47	chr8:1710600-1710800	Flanking Active TSS	Fetal Intestine Large	intestine
48	chr8:1710600-1710800	Enhancers	Fetal Intestine Small	intestine
49	chr8:1710600-1710800	Flanking Active TSS	Fetal Lung	lung
50	chr8:1710600-1710800	Enhancers	Placenta	Placenta

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