Variant report

Variant	rs3098241
Chromosome Location	chr8:104425304-104425305
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr8:104423258-104429002	IMR90	lung:	n/a	n/a
2	MXI1	chr8:104425196-104428858	IMR90	lung:	n/a	chr8:104426636-104426645 chr8:104426634-104426643
3	POLR2A	chr8:104425272-104428004	K562	blood:	n/a	n/a
4	POLR2A	chr8:104424456-104425709	HepG2	liver:	n/a	n/a
5	MXI1	chr8:104425295-104429257	SK-N-SH	brain:	n/a	chr8:104426636-104426645 chr8:104426634-104426643

No.	Distal block	Cell Line	Cell type
1	chr8:104292150..104293871-chr8:104425235..104426887,2	MCF-7	breast:
2	chr8:104401208..104405161-chr8:104423386..104426686,3	K562	blood:
3	chr8:104424987..104428689-chr8:104510615..104514344,5	MCF-7	breast:

Variant related genes	Relation type
DCAF13	TF binding region
ENSG00000176406	Chromatin interaction
ENSG00000253477	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs1061195	0.93[ASN][1000 genomes]
rs11780843	0.81[ASN][1000 genomes]
rs12677876	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1370005	0.84[CEU][hapmap];0.95[CHB][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs1370006	0.98[ASN][1000 genomes]
rs1436595	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs1436597	0.87[ASN][1000 genomes]
rs1436598	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs1436599	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs16870396	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1865853	0.92[ASN][1000 genomes]
rs1865854	0.92[ASN][1000 genomes]
rs1865855	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2082971	0.93[ASN][1000 genomes]
rs2118057	0.87[CHB][hapmap];0.80[JPT][hapmap]
rs2241777	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs2241778	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2304501	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs2388720	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2575691	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs2575692	0.84[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs2575693	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs2687348	0.83[ASN][1000 genomes]
rs2687350	0.84[CEU][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs2687359	0.87[CHB][hapmap];0.86[CHD][hapmap];0.81[JPT][hapmap]
rs2687364	0.87[CHB][hapmap];0.85[JPT][hapmap]
rs2917549	0.81[ASN][1000 genomes]
rs2917551	0.85[ASN][1000 genomes]
rs2948446	0.87[CHB][hapmap];0.85[JPT][hapmap]
rs2948452	0.80[ASN][1000 genomes]
rs3098212	0.92[ASN][1000 genomes]
rs3098214	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs3098215	0.84[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs3098217	0.84[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3098218	0.91[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs3098219	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs3098220	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs3098221	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs3098222	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs3098223	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs3098224	0.84[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs3098225	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs3098227	0.84[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs3098232	0.82[MEX][hapmap]
rs3098233	0.84[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.88[ASN][1000 genomes]
rs3098236	0.98[ASN][1000 genomes]
rs3098237	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs3098240	0.90[ASN][1000 genomes]
rs3098242	0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3098243	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs3098244	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098245	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098248	0.89[ASN][1000 genomes]
rs3098249	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs3098250	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs3098254	0.82[MEX][hapmap]
rs3098255	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs3098256	0.88[ASN][1000 genomes]
rs3098257	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098258	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098259	0.84[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.93[ASN][1000 genomes]
rs3098260	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3133804	0.89[ASN][1000 genomes]
rs3133807	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3133809	0.88[ASN][1000 genomes]
rs3133810	0.82[MEX][hapmap]
rs3133811	0.95[ASN][1000 genomes]
rs3133813	0.84[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.98[ASN][1000 genomes]
rs3133814	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs3133815	0.99[ASN][1000 genomes]
rs3133816	0.99[ASN][1000 genomes]
rs3133817	0.84[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs3133819	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3134250	0.96[ASN][1000 genomes]
rs3134251	0.92[ASN][1000 genomes]
rs3134253	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs3134254	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3134255	0.97[ASN][1000 genomes]
rs3134258	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs3134261	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs3134262	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3134264	0.93[ASN][1000 genomes]
rs3134265	0.98[ASN][1000 genomes]
rs3134266	0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3134267	0.95[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs3134270	0.96[ASN][1000 genomes]
rs3134271	0.84[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs3134272	0.92[ASN][1000 genomes]
rs3134273	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs3134275	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3134277	0.84[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs3134278	0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs3134279	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3134280	0.88[ASN][1000 genomes]
rs3134281	0.92[ASN][1000 genomes]
rs3134282	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs3134285	0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3134286	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3134287	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3134289	0.95[ASN][1000 genomes]
rs3134290	0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3134291	0.95[ASN][1000 genomes]
rs3134292	0.84[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.99[ASN][1000 genomes]
rs3134293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3134295	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3134296	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3134297	0.84[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs719842	0.87[MEX][hapmap]
rs750606	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7816297	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs893044	0.92[ASN][1000 genomes]
rs975440	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1016395	chr8:104327541-104473005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1023048	chr8:104355188-104872701	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv539705	chr8:104355188-104872701	ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv1021345	chr8:104361854-104879684	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv1032085	chr8:104362187-104878345	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv1033477	chr8:104369940-104439632	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	nsv539706	chr8:104369940-104439632	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv1034183	chr8:104369940-104814008	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv539707	chr8:104369940-104814008	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv611832	chr8:104400808-104481735	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
14	esv2753239	chr8:104404824-104545824	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs3098241	DCAF13	cis	Muscle Skeletal	GTEx
rs3098241	ZFPM2	cis	cerebellum	SCAN
rs3098241	SLC25A32	cis	cerebellum	SCAN
rs3098241	SLC25A32	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104386000-104425600	Weak transcription	HSMMtube	muscle
2	chr8:104400000-104426000	Weak transcription	Stomach Mucosa	stomach
3	chr8:104400200-104425600	Weak transcription	Colonic Mucosa	Colon
4	chr8:104401600-104426600	Weak transcription	Esophagus	oesophagus
5	chr8:104404200-104425400	Weak transcription	Brain Angular Gyrus	brain
6	chr8:104404200-104426600	Weak transcription	Pancreas	Pancrea
7	chr8:104405800-104426600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:104405800-104426600	Weak transcription	Gastric	stomach
9	chr8:104410400-104425400	Weak transcription	Right Ventricle	heart
10	chr8:104410600-104425400	Weak transcription	Right Atrium	heart
11	chr8:104413200-104425600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr8:104413800-104425400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:104413800-104425400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr8:104413800-104425800	Weak transcription	Fetal Kidney	kidney
15	chr8:104416000-104425800	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr8:104417000-104426400	Weak transcription	Placenta	Placenta
17	chr8:104417400-104425400	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:104417400-104426400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr8:104418800-104426400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr8:104419000-104425400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr8:104419000-104426200	Weak transcription	Fetal Stomach	stomach
22	chr8:104419000-104426400	Weak transcription	Aorta	Aorta
23	chr8:104419000-104426600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:104419200-104425600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr8:104419600-104426400	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr8:104420000-104425600	Weak transcription	Brain Anterior Caudate	brain
27	chr8:104420400-104426200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr8:104420800-104426000	Enhancers	Liver	Liver
29	chr8:104421000-104426400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr8:104421600-104425400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr8:104422600-104425600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:104422800-104426600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:104422800-104426600	Weak transcription	Lung	lung
34	chr8:104422800-104426600	Weak transcription	Spleen	Spleen
35	chr8:104422800-104429600	Active TSS	GM12878-XiMat	blood
36	chr8:104423000-104425400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:104423400-104429400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:104423600-104425400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr8:104423600-104425800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr8:104423600-104426200	Enhancers	Primary B cells from peripheral blood	blood
41	chr8:104423600-104426400	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr8:104423600-104426400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr8:104423600-104426400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr8:104423800-104425400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:104423800-104425600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr8:104423800-104425800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:104423800-104426000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:104423800-104426200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:104423800-104426200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr8:104424000-104425600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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