Variant report

Variant	rs4122189
Chromosome Location	chr6:31167927-31167928
allele	A/G
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	YY1	chr6:31167822-31168108	GM12878	blood:	n/a	n/a
2	POLR2A	chr6:31167424-31168342	GM12878	blood:	n/a	n/a
3	YY1	chr6:31167859-31168091	K562	blood:	n/a	n/a
4	CTCF	chr6:31167860-31168010	GM12872	blood:	n/a	n/a
5	POLR2A	chr6:31167484-31168041	GM12878	blood:	n/a	n/a
6	YY1	chr6:31167792-31168098	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:30583179..30585328-chr6:31166422..31169307,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCF19-1	chr6:31167732-31168707	XLOC_005244

Variant related genes	Relation type
HCG27	TF binding region
ENSG00000272501	TF binding region
ENSG00000204569	Chromatin interaction
ENSG00000222894	Chromatin interaction

Extended variants
information (count: 112 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1052989	0.92[ASN][1000 genomes]
rs1135811	0.89[EUR][1000 genomes]
rs11381232	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11507945	0.92[ASN][1000 genomes]
rs11961983	0.88[AFR][1000 genomes]
rs11967629	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs17197540	0.89[EUR][1000 genomes]
rs28360055	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28360056	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28360057	0.85[AFR][1000 genomes]
rs28360058	0.85[AFR][1000 genomes]
rs28360059	0.85[AFR][1000 genomes]
rs28360060	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28360061	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28360062	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28360063	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs28360064	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28360065	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28360066	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28360067	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs28397268	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28397269	0.81[AFR][1000 genomes]
rs28397270	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28397271	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28397273	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28397274	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28397276	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28397277	0.88[AFR][1000 genomes]
rs28397282	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28397284	0.88[AFR][1000 genomes]
rs28397285	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28397286	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs28749548	0.82[AFR][1000 genomes]
rs28749549	0.85[AFR][1000 genomes]
rs28749550	0.85[AFR][1000 genomes]
rs28749551	0.88[AFR][1000 genomes]
rs34467061	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4713441	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4713442	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6899874	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6899875	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6901685	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6907451	0.89[EUR][1000 genomes]
rs6913470	0.85[EUR][1000 genomes]
rs6913863	0.88[EUR][1000 genomes]
rs6921663	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6922077	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6922553	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6922756	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6922842	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6922994	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6927253	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6930438	0.89[EUR][1000 genomes]
rs6936474	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6936597	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6941912	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7453202	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7741829	0.90[ASN][1000 genomes]
rs7755702	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7772290	0.91[ASN][1000 genomes]
rs887464	0.90[ASN][1000 genomes]
rs915660	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9263869	0.87[ASN][1000 genomes]
rs9263875	0.86[ASN][1000 genomes]
rs9295957	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9295958	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9295960	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9357109	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9357113	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9357115	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9366769	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9368662	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9368663	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9378115	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9378227	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9380220	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9380221	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9380222	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380223	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9391712	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs9391815	0.85[ASN][1000 genomes]
rs9391818	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9391819	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9394042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9404983	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9405052	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9468882	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' 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	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
5	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
6	nsv1029442	chr6:31006647-31449207	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
7	nsv427750	chr6:31028290-31234581	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv428140	chr6:31028290-31462106	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	89 gene(s)	inside rSNPs	diseases
9	esv2758042	chr6:31028290-31497106	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
10	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
11	nsv1019637	chr6:31104401-31354706	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
12	nsv1029569	chr6:31104401-31412740	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
13	nsv538174	chr6:31104401-31412740	Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
14	nsv1034391	chr6:31131121-31279595	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
15	nsv1025909	chr6:31131121-31354706	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
16	nsv538175	chr6:31131121-31354706	Active TSS Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS 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	51 gene(s)	inside rSNPs	diseases
17	nsv1015890	chr6:31131121-31449207	Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
18	nsv538176	chr6:31131121-31449207	Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
19	esv32635	chr6:31141504-31250618	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
20	nsv1024887	chr6:31162849-31354706	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
21	nsv538177	chr6:31162849-31354706	Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
22	nsv1015903	chr6:31162849-31412740	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
23	nsv538178	chr6:31162849-31412740	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
24	nsv1031682	chr6:31162849-31449207	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
25	nsv538179	chr6:31162849-31449207	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers 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 miRNA	61 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs4122189	CCHCR1	Cis_1M	lymphoblastoid	RTeQTL
rs4122189	TCF19	Cis_1M	lymphoblastoid	RTeQTL
rs4122189	TCF19	cis	multi-tissue	Pritchard
rs4122189	CCHCR1	cis	multi-tissue	Pritchard
rs4122189	HLA-C	Cis_1M	lymphoblastoid	RTeQTL
rs4122189	LOC730399///LOC731974	Cis_chr	lymphoblastoid	RTeQTL
rs4122189	HLA-F	Cis_chr	lymphoblastoid	RTeQTL
rs4122189	TCF19	cis	lymphoblastoid	seeQTL
rs4122189	HCG27	cis	multi-tissue	Pritchard
rs4122189	HLA-B	cis	lymphoblastoid	seeQTL
rs4122189	HCG27	Cis_1M	lymphoblastoid	RTeQTL
rs4122189	CCHCR1	cis	lymphoblastoid	seeQTL
rs4122189	HLA-B	Cis_1M	lymphoblastoid	RTeQTL
rs4122189	DDR1	cis	lymphoblastoid	seeQTL
rs4122189	DDR1	Cis_1M	lymphoblastoid	RTeQTL
rs4122189	NKAPL	cis	parietal	SCAN

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31164400-31168400	Active TSS	Duodenum Smooth Muscle	Duodenum
2	chr6:31166200-31169800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:31166200-31169800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:31166200-31170000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:31166200-31170200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:31166200-31170400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr6:31166200-31170600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:31166200-31170600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr6:31166200-31170600	Weak transcription	NH-A	brain
10	chr6:31166200-31170800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr6:31166200-31171000	Weak transcription	HSMMtube	muscle
12	chr6:31166200-31171000	Weak transcription	Osteobl	bone
13	chr6:31166200-31171200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:31166200-31171200	Weak transcription	Fetal Lung	lung
15	chr6:31166200-31171600	Weak transcription	Brain Substantia Nigra	brain
16	chr6:31166200-31171600	Weak transcription	Ovary	ovary
17	chr6:31166200-31171800	Weak transcription	Aorta	Aorta
18	chr6:31166200-31171800	Weak transcription	Fetal Brain Male	brain
19	chr6:31166200-31172400	Weak transcription	Gastric	stomach
20	chr6:31166400-31168200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:31166400-31168400	Flanking Active TSS	Primary hematopoietic stem cells	blood
22	chr6:31166400-31168400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr6:31166400-31169800	Weak transcription	HMEC	breast
24	chr6:31166400-31170000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:31166400-31170000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr6:31166400-31170000	Weak transcription	Right Ventricle	heart
27	chr6:31166400-31170000	Weak transcription	HUVEC	blood vessel
28	chr6:31166400-31170800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:31166400-31170800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:31166600-31168200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr6:31166600-31169800	Weak transcription	Fetal Intestine Large	intestine
32	chr6:31166600-31170200	Weak transcription	Small Intestine	intestine
33	chr6:31166600-31170800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:31166600-31171200	Weak transcription	HSMM	muscle
35	chr6:31166800-31168000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr6:31166800-31168000	Enhancers	Pancreas	Pancrea
37	chr6:31166800-31168200	Enhancers	Primary B cells from peripheral blood	blood
38	chr6:31166800-31168800	Weak transcription	Fetal Intestine Small	intestine
39	chr6:31166800-31168800	Weak transcription	Fetal Muscle Leg	muscle
40	chr6:31166800-31169000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr6:31166800-31169000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr6:31166800-31169000	Weak transcription	Colonic Mucosa	Colon
43	chr6:31166800-31169800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:31166800-31169800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:31166800-31169800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr6:31166800-31169800	Weak transcription	Right Atrium	heart
47	chr6:31166800-31170000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr6:31166800-31170000	Weak transcription	NHLF	lung
49	chr6:31166800-31170200	Weak transcription	Psoas Muscle	Psoas
50	chr6:31166800-31170600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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