Variant report

Variant	rs7743807
Chromosome Location	chr6:31854543-31854544
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:122)
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	chr6:31854294-31855555	HepG2	liver:	n/a	n/a
2	POLR2A	chr6:31854363-31854779	MCF-7	breast:	n/a	n/a
3	POLR2A	chr6:31854492-31854661	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31854520-31854570	ECC-1	luminal epithelium:	n/a
2	chr6:31854529-31854579	A549	lung:	n/a
3	chr6:31854529-31854579	HRCEpiC	kidney:	n/a
4	chr6:31854520-31854570	HEEpiC	esophagus:	n/a
5	chr6:31854520-31854570	K562	blood:	n/a
6	chr6:31854529-31854579	GM19239	blood:	n/a
7	chr6:31854520-31854570	SK-N-SH_RA	brain:	n/a
8	chr6:31854529-31854579	Jurkat	blood:	n/a
9	chr6:31854529-31854579	HCM	heart:	n/a
10	chr6:31854520-31854570	NB4	blood:	n/a
11	chr6:31854520-31854570	H1-hESC	embryonic stem cell:	embryo
12	chr6:31854520-31854570	GM12892	blood:	n/a
13	chr6:31854529-31854579	IMR90	lung:	fetal
14	chr6:31854529-31854579	ECC-1	luminal epithelium:	n/a
15	chr6:31854529-31854579	AG09319	gingival:	n/a
16	chr6:31854520-31854570	SK-N-SH	brain:	n/a
17	chr6:31854520-31854570	GM06990	blood:	n/a
18	chr6:31854520-31854570	AG09319	gingival:	n/a
19	chr6:31854529-31854579	NT2-D1	testis:	n/a
20	chr6:31854529-31854579	PFSK-1	brain:	n/a
21	chr6:31854520-31854570	Caco-2	colon:	n/a
22	chr6:31854520-31854570	IMR90	lung:	fetal
23	chr6:31854529-31854579	HCPEpiC	choroid plexus:	n/a
24	chr6:31854520-31854570	CMK	blood:	n/a
25	chr6:31854529-31854579	ovcar-3	ovarian:	n/a
26	chr6:31854529-31854579	NHBE	bronchial:	n/a
27	chr6:31854529-31854579	PrEC	prostate:	n/a
28	chr6:31854529-31854579	HRPEpiC	eye:	n/a
29	chr6:31854529-31854579	Hepatocyte	liver:	n/a
30	chr6:31854529-31854579	PANC-1	pancreas:	n/a
31	chr6:31854520-31854570	SAEC	small airway:	n/a
32	chr6:31854529-31854579	MCF10A-Er-Src	breast:	n/a
33	chr6:31854520-31854570	HRE	kidney:	n/a
34	chr6:31854529-31854579	ProgFib	skin:	n/a
35	chr6:31854520-31854570	ovcar-3	ovarian:	n/a
36	chr6:31854529-31854579	HCT-116	colon:	n/a
37	chr6:31854520-31854570	HepG2	liver:	n/a
38	chr6:31854520-31854570	AG04450	lung:	fetal
39	chr6:31854520-31854570	AG10803	skin:	n/a
40	chr6:31854520-31854570	RPTEC	kidney:	n/a
41	chr6:31854529-31854579	MCF-7	breast:	n/a
42	chr6:31854529-31854579	HEK293	kidney:	embryo
43	chr6:31854529-31854579	SK-N-MC	brain:	n/a
44	chr6:31854520-31854570	T-47D	breast:	n/a
45	chr6:31854520-31854570	HNPCEpiC	eye:	n/a
46	chr6:31854529-31854579	HCF	heart:	n/a
47	chr6:31854529-31854579	GM06990	blood:	n/a
48	chr6:31854529-31854579	H1-hESC	embryonic stem cell:	embryo
49	chr6:31854520-31854570	MCF10A-Er-Src	breast:	n/a
50	chr6:31854520-31854570	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:31843698..31845468-chr6:31852206..31854707,3	MCF-7	breast:
2	chr6:31841958..31846970-chr6:31854324..31857490,7	K562	blood:
3	chr6:31828758..31831666-chr6:31853611..31856072,2	MCF-7	breast:
4	chr6:31762216..31763831-chr6:31854405..31856951,2	MCF-7	breast:
5	chr6:31831274..31833961-chr6:31853684..31856241,2	K562	blood:
6	chr6:31831381..31833026-chr6:31853931..31855819,2	K562	blood:
7	chr6:31852573..31855279-chr6:31859068..31861656,3	MCF-7	breast:
8	chr6:31854355..31857404-chr6:31857986..31862400,4	K562	blood:
9	chr6:31632509..31634236-chr6:31853959..31856343,2	K562	blood:
10	chr6:31854115..31856826-chr6:31913867..31915528,2	MCF-7	breast:

No data

Variant related genes	Relation type
EHMT2	TF binding region
EHMT2	CpG island
ENSG00000204435	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204394	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs204894	0.80[EUR][1000 genomes]
rs2257331	0.90[AFR][1000 genomes]
rs2555456	0.86[EUR][1000 genomes]
rs2844451	0.88[AFR][1000 genomes]
rs41284523	0.81[EUR][1000 genomes]
rs41284527	0.97[EUR][1000 genomes]
rs416002	0.97[EUR][1000 genomes]
rs440160	0.93[EUR][1000 genomes]
rs544167	0.90[AFR][1000 genomes]
rs62395851	0.81[AFR][1000 genomes]
rs6907185	0.89[AFR][1000 genomes]
rs6939227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7383258	0.86[EUR][1000 genomes]
rs7755290	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
9	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
10	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
14	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
16	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
18	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
19	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
20	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
21	nsv884472	chr6:31813898-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
22	nsv508399	chr6:31829474-31902423	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
23	nsv884474	chr6:31836055-31870326	Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
24	nsv462875	chr6:31838441-31907147	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
25	nsv601960	chr6:31838441-31907147	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
26	nsv884475	chr6:31840625-31880320	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
27	nsv884476	chr6:31848000-31870326	Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
28	nsv884477	chr6:31850724-31870326	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
29	nsv884478	chr6:31850724-31874505	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
30	nsv884479	chr6:31850724-31878433	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
31	nsv884480	chr6:31851234-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
32	nsv884481	chr6:31851234-31878433	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
33	nsv884482	chr6:31851234-31880320	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
34	nsv966619	chr6:31852653-31870444	Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
35	nsv884483	chr6:31852692-31868075	Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	42 gene(s)	inside rSNPs	diseases
36	nsv884484	chr6:31854543-31879158	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	50 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31832000-31856000	Weak transcription	Right Atrium	heart
2	chr6:31833200-31864200	Weak transcription	Fetal Heart	heart
3	chr6:31847000-31857800	Strong transcription	Osteobl	bone
4	chr6:31847000-31860800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:31847000-31863200	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr6:31847000-31863600	Strong transcription	Fetal Brain Female	brain
7	chr6:31847000-31864000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:31847200-31857600	Strong transcription	Placenta Amnion	Placenta Amnion
9	chr6:31847200-31860600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:31847200-31861400	Strong transcription	Spleen	Spleen
11	chr6:31847200-31863800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:31847200-31864000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr6:31847200-31864200	Strong transcription	Fetal Stomach	stomach
14	chr6:31847200-31864200	Strong transcription	Thymus	Thymus
15	chr6:31847400-31856200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:31847400-31857400	Strong transcription	Primary B cells from peripheral blood	blood
17	chr6:31847400-31857600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:31847400-31857600	Strong transcription	Right Ventricle	heart
19	chr6:31847400-31858000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:31847400-31858000	Strong transcription	Lung	lung
21	chr6:31847400-31858200	Strong transcription	H9 Cell Line	embryonic stem cell
22	chr6:31847400-31858200	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr6:31847400-31858200	Strong transcription	Brain Inferior Temporal Lobe	brain
24	chr6:31847400-31860400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:31847400-31860800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:31847400-31861200	Strong transcription	Esophagus	oesophagus
27	chr6:31847400-31861600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr6:31847400-31861600	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr6:31847400-31861600	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr6:31847400-31861600	Strong transcription	Brain Anterior Caudate	brain
31	chr6:31847400-31861600	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr6:31847400-31862800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr6:31847400-31863200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:31847400-31863200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:31847400-31863400	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr6:31847400-31863600	Strong transcription	Brain Germinal Matrix	brain
37	chr6:31847400-31863800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:31847400-31863800	Strong transcription	Primary T cells from cord blood	blood
39	chr6:31847400-31863800	Strong transcription	Skeletal Muscle Male	skeletal muscle
40	chr6:31847400-31864000	Strong transcription	H1 Cell Line	embryonic stem cell
41	chr6:31847400-31864000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:31847400-31864000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr6:31847400-31864000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:31847400-31864000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr6:31847400-31864000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr6:31847400-31864000	Strong transcription	Adipose Nuclei	Adipose
47	chr6:31847400-31864000	Strong transcription	Fetal Thymus	thymus
48	chr6:31847400-31864200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr6:31847400-31864200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr6:31847400-31864200	Strong transcription	Cortex derived primary cultured neurospheres	brain

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