Variant report

Variant	rs10097891
Chromosome Location	chr8:1726809-1726810
allele	A/C
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:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1726321..1728354-chr8:1771384..1774203,2	MCF-7	breast:
2	chr8:1715615..1723539-chr8:1723885..1728177,9	MCF-7	breast:
3	chr8:1725330..1728287-chr8:1728724..1731820,3	K562	blood:
4	chr8:1725864..1728236-chr8:1731701..1733830,2	MCF-7	breast:
5	chr8:1716816..1721615-chr8:1726505..1732038,6	K562	blood:
6	chr8:1717744..1722491-chr8:1723636..1726849,4	MCF-7	breast:
7	chr8:1711245..1713893-chr8:1726417..1729246,3	K562	blood:
8	chr8:1681316..1685438-chr8:1724958..1729595,5	K562	blood:
9	chr8:1710542..1713448-chr8:1725280..1729246,5	K562	blood:
10	chr8:1686924..1688783-chr8:1724884..1727054,2	MCF-7	breast:
11	chr8:1722780..1724453-chr8:1725815..1728009,2	K562	blood:
12	chr8:1726532..1728287-chr8:1729917..1731820,2	K562	blood:
13	chr8:1711365..1714898-chr8:1724612..1727757,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000182372	Chromatin interaction
ENSG00000253982	Chromatin interaction
ENSG00000104728	Chromatin interaction

Extended variants
information (count: 118 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10087654	0.87[ASN][1000 genomes]
rs10089222	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10100341	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.96[MEX][hapmap];0.98[MKK][hapmap];0.92[TSI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10102731	0.87[ASN][1000 genomes]
rs10105317	0.88[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10106153	0.89[ASN][1000 genomes]
rs10113471	0.83[ASN][1000 genomes]
rs10481354	0.88[CHB][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.85[ASN][1000 genomes]
rs11136421	0.81[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11136422	0.84[ASN][1000 genomes]
rs11136424	0.81[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.92[MEX][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1137514	0.82[AMR][1000 genomes]
rs11778824	0.94[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs12335115	0.89[ASN][1000 genomes]
rs12674711	0.86[ASN][1000 genomes]
rs13251071	0.84[ASN][1000 genomes]
rs13256424	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13261755	0.85[ASN][1000 genomes]
rs13540	0.86[ASN][1000 genomes]
rs2293977	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs28376731	0.81[ASN][1000 genomes]
rs2957085	0.81[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs3812477	0.94[CHB][hapmap];0.94[JPT][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4242538	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4242539	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs4370560	0.94[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs4372027	0.86[ASN][1000 genomes]
rs4595147	0.88[CHB][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];0.83[ASN][1000 genomes]
rs4639549	0.91[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs4875806	0.93[ASN][1000 genomes]
rs4875889	0.83[ASN][1000 genomes]
rs4875957	0.93[ASN][1000 genomes]
rs4875958	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.92[LWK][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];0.92[TSI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4876133	0.80[ASN][1000 genomes]
rs6558518	0.87[ASN][1000 genomes]
rs6558520	0.88[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6558521	0.88[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6558522	0.88[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6558523	0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6558524	0.89[ASN][1000 genomes]
rs6558525	0.88[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6558526	0.87[ASN][1000 genomes]
rs6558527	0.81[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6558528	0.88[ASN][1000 genomes]
rs6558531	0.86[ASN][1000 genomes]
rs6558532	0.86[ASN][1000 genomes]
rs6558533	0.94[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs6558534	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6558535	0.88[ASN][1000 genomes]
rs6558536	0.82[ASN][1000 genomes]
rs6558538	0.83[ASN][1000 genomes]
rs6981804	0.89[ASN][1000 genomes]
rs6982516	0.93[ASN][1000 genomes]
rs6984632	0.86[ASN][1000 genomes]
rs6986102	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6991773	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6991783	0.96[ASN][1000 genomes]
rs6993706	0.94[CHB][hapmap];0.94[CHD][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs7000162	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7001282	0.89[ASN][1000 genomes]
rs7005592	0.81[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7005699	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7008465	0.94[CHB][hapmap];0.91[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7010616	0.82[ASN][1000 genomes]
rs7013835	0.81[ASN][1000 genomes]
rs7013841	0.81[ASN][1000 genomes]
rs7014327	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.96[MEX][hapmap];0.92[TSI][hapmap];0.87[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7014823	0.96[ASN][1000 genomes]
rs7015858	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71499040	0.87[ASN][1000 genomes]
rs730377	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs730379	0.85[ASN][1000 genomes]
rs7341635	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7459507	0.86[ASN][1000 genomes]
rs7460230	0.85[ASN][1000 genomes]
rs7460287	0.93[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs7460365	0.88[ASN][1000 genomes]
rs7460866	0.81[ASN][1000 genomes]
rs7460972	0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs7461159	0.81[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.92[MEX][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7461259	0.85[ASN][1000 genomes]
rs7461600	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7463876	0.85[ASN][1000 genomes]
rs7463879	0.83[ASN][1000 genomes]
rs7465178	0.90[ASN][1000 genomes]
rs7818406	0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7822816	0.85[ASN][1000 genomes]
rs7827009	0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs7827285	0.94[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs7828950	0.85[ASN][1000 genomes]
rs7838456	0.86[ASN][1000 genomes]
rs7842425	0.88[CHB][hapmap];0.88[CHD][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.85[ASN][1000 genomes]
rs7844748	0.88[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7845723	0.87[CHB][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap]
rs7846610	0.88[CHB][hapmap];0.88[CHD][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.85[ASN][1000 genomes]
rs9022	0.92[ASN][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	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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	nsv609531	chr8:1717036-1965389	Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
22	nsv932825	chr8:1719042-1736355	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10097891	CLN8	cis	parietal	SCAN
rs10097891	CLN8	cis	lymphoblastoid	seeQTL
rs10097891	CTD-2336O2.1	cis	Nerve Tibial	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1713400-1727000	Weak transcription	NHDF-Ad	bronchial
2	chr8:1713400-1735800	Weak transcription	Fetal Brain Male	brain
3	chr8:1713600-1729600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr8:1714000-1728000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr8:1714000-1729800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr8:1714400-1729200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr8:1714800-1727000	Strong transcription	Fetal Intestine Small	intestine
8	chr8:1715400-1727800	Weak transcription	Small Intestine	intestine
9	chr8:1715400-1729200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr8:1716600-1727000	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr8:1717400-1728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:1717600-1731000	Weak transcription	Fetal Lung	lung
13	chr8:1717800-1727800	Weak transcription	Stomach Mucosa	stomach
14	chr8:1718000-1727800	Weak transcription	Fetal Kidney	kidney
15	chr8:1718000-1728000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr8:1718000-1732400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr8:1718000-1732800	Weak transcription	Fetal Heart	heart
18	chr8:1718000-1736000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:1718400-1733200	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr8:1719800-1729200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr8:1720800-1727200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr8:1721400-1727600	Weak transcription	Psoas Muscle	Psoas
23	chr8:1721400-1733800	Weak transcription	Hela-S3	cervix
24	chr8:1721600-1727000	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr8:1721600-1727800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr8:1721600-1732800	Weak transcription	Right Atrium	heart
27	chr8:1721600-1734200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:1721800-1727600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr8:1721800-1729400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr8:1721800-1734000	Weak transcription	Colon Smooth Muscle	Colon
31	chr8:1722000-1727600	Weak transcription	NHLF	lung
32	chr8:1722000-1730000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr8:1722000-1730200	Weak transcription	HUVEC	blood vessel
34	chr8:1722000-1730600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr8:1722000-1731000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr8:1722000-1734000	Weak transcription	Ovary	ovary
37	chr8:1722200-1734400	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr8:1722400-1727000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:1722400-1727200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:1722400-1727200	Weak transcription	NHEK	skin
41	chr8:1722400-1727200	Weak transcription	Osteobl	bone
42	chr8:1722400-1727600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr8:1722400-1727600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr8:1722800-1734200	Weak transcription	Colonic Mucosa	Colon
45	chr8:1723200-1731200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr8:1723800-1727000	Genic enhancers	Pancreas	Pancrea
47	chr8:1723800-1727200	Genic enhancers	Primary B cells from peripheral blood	blood
48	chr8:1724200-1727000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr8:1724400-1727000	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr8:1724600-1727000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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