Variant report

Variant	rs2076030
Chromosome Location	chr6:26426856-26426857
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:26395411..26398038-chr6:26426386..26428479,2	K562	blood:
2	chr6:26424662..26427367-chr6:26444915..26446912,2	K562	blood:
3	chr6:26409830..26412787-chr6:26424238..26427076,2	K562	blood:

Variant related genes	Relation type
ENSG00000111801	Chromatin interaction

Extended variants
information (count: 147 )
Associated
traits (count: 33 )

rSNPs within LD-proxies of this variant (count:128)

rs_ID	r²[population]
rs10484443	0.89[CHB][hapmap]
rs12173854	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12174602	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12174623	0.88[EUR][1000 genomes]
rs12174631	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12174639	0.88[EUR][1000 genomes]
rs12176129	0.88[EUR][1000 genomes]
rs12176317	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs13191660	0.88[EUR][1000 genomes]
rs13195509	0.92[CEU][hapmap];0.87[LWK][hapmap]
rs13198716	1.00[YRI][hapmap]
rs13214027	0.84[CEU][hapmap];0.84[JPT][hapmap]
rs13216828	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs13220261	0.90[CEU][hapmap]
rs13220495	1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs13220522	0.81[AMR][1000 genomes]
rs16891725	1.00[CEU][hapmap];0.89[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap];0.82[MEX][hapmap];0.91[EUR][1000 genomes]
rs16901784	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap];0.81[EUR][1000 genomes]
rs1977	1.00[CEU][hapmap];0.92[JPT][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.90[EUR][1000 genomes]
rs1978	1.00[CEU][hapmap];0.92[JPT][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.90[EUR][1000 genomes]
rs1979	1.00[CEU][hapmap];0.91[JPT][hapmap];0.90[EUR][1000 genomes]
rs2072803	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2072806	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2073527	0.88[EUR][1000 genomes]
rs2073529	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs2073530	0.88[EUR][1000 genomes]
rs2073531	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs2093169	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs2235251	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2295593	0.88[EUR][1000 genomes]
rs2393593	1.00[YRI][hapmap]
rs2393667	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28362606	0.87[EUR][1000 genomes]
rs28551159	0.88[EUR][1000 genomes]
rs3047288	0.88[EUR][1000 genomes]
rs34107459	0.81[AMR][1000 genomes]
rs34273322	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34436535	0.88[EUR][1000 genomes]
rs34550936	0.88[EUR][1000 genomes]
rs34622023	0.88[EUR][1000 genomes]
rs34878490	0.88[EUR][1000 genomes]
rs35304979	0.88[EUR][1000 genomes]
rs35307327	0.88[EUR][1000 genomes]
rs35934643	0.88[EUR][1000 genomes]
rs35942482	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3734542	0.91[CEU][hapmap]
rs3734544	0.85[CEU][hapmap];0.89[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs3757138	0.88[EUR][1000 genomes]
rs3757150	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs3799378	0.83[CHD][hapmap];0.84[JPT][hapmap]
rs3799380	0.85[CEU][hapmap]
rs3799383	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap];0.88[EUR][1000 genomes]
rs3823158	0.92[CEU][hapmap]
rs41266839	0.81[AMR][1000 genomes]
rs4518487	0.84[CEU][hapmap]
rs55706012	0.81[AMR][1000 genomes]
rs58825580	0.81[EUR][1000 genomes]
rs6456728	0.85[CEU][hapmap]
rs66823108	0.90[EUR][1000 genomes]
rs66827971	0.81[EUR][1000 genomes]
rs67234939	0.88[EUR][1000 genomes]
rs67509210	0.88[EUR][1000 genomes]
rs68072215	0.90[EUR][1000 genomes]
rs68112369	0.81[EUR][1000 genomes]
rs6900118	0.83[CHD][hapmap]
rs6900665	0.85[EUR][1000 genomes]
rs6911765	0.89[CHB][hapmap];0.88[CHD][hapmap]
rs6920256	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap];0.83[EUR][1000 genomes]
rs71544290	0.88[EUR][1000 genomes]
rs71557332	0.86[EUR][1000 genomes]
rs71557334	0.88[EUR][1000 genomes]
rs71557335	0.88[EUR][1000 genomes]
rs72836482	0.88[EUR][1000 genomes]
rs72841536	0.90[EUR][1000 genomes]
rs7773938	0.85[CEU][hapmap];0.89[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs9348709	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9348712	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9348716	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9348718	0.89[CHB][hapmap];0.83[CHD][hapmap]
rs9348721	0.85[EUR][1000 genomes]
rs9357006	0.88[EUR][1000 genomes]
rs9358930	0.88[EUR][1000 genomes]
rs9358932	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9358934	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9358935	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9358937	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9358938	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9358939	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358944	0.85[CEU][hapmap];0.89[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs9358945	0.85[CEU][hapmap];0.89[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs9358946	0.85[CEU][hapmap];0.89[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs9366653	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9366654	0.89[EUR][1000 genomes]
rs9366655	0.92[CEU][hapmap];0.92[JPT][hapmap];0.90[EUR][1000 genomes]
rs9366656	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9366658	0.85[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs9379851	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9379852	0.88[EUR][1000 genomes]
rs9379853	0.88[EUR][1000 genomes]
rs9379854	0.88[EUR][1000 genomes]
rs9379855	1.00[CEU][hapmap];1.00[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9379856	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9379857	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9379858	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9379859	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9379863	0.88[EUR][1000 genomes]
rs9379864	1.00[CEU][hapmap];1.00[YRI][hapmap];0.88[EUR][1000 genomes]
rs9379871	0.88[EUR][1000 genomes]
rs9379873	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9379875	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9379882	0.88[EUR][1000 genomes]
rs9393703	0.88[EUR][1000 genomes]
rs9393704	0.88[EUR][1000 genomes]
rs9393705	1.00[CEU][hapmap];0.88[LWK][hapmap];0.88[EUR][1000 genomes]
rs9393706	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9393707	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9393708	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9393710	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9393711	0.88[EUR][1000 genomes]
rs9393712	0.88[EUR][1000 genomes]
rs9393713	1.00[CEU][hapmap];0.88[LWK][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9393714	0.92[CEU][hapmap];0.82[MKK][hapmap];0.88[EUR][1000 genomes]
rs9393715	0.87[EUR][1000 genomes]
rs9393718	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9393721	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs9393727	0.88[EUR][1000 genomes]
rs9393735	0.92[CEU][hapmap];0.84[JPT][hapmap]
rs9467772	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
4	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer 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 miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv482836	chr6:26352883-26520964	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription 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	49 gene(s)	inside rSNPs	diseases
6	nsv883492	chr6:26367689-26436592	Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv883493	chr6:26367689-26442786	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
8	nsv883494	chr6:26367833-26442786	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
9	nsv883495	chr6:26367833-26443853	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	esv3334611	chr6:26367893-26443308	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv482407	chr6:26369320-26550148	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
12	nsv883497	chr6:26369549-26442786	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv883498	chr6:26369549-26443853	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv883499	chr6:26377591-26454454	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
15	esv3427999	chr6:26378373-26453532	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
16	nsv462664	chr6:26379537-26451553	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
17	nsv601184	chr6:26379537-26451553	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription 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	27 gene(s)	inside rSNPs	diseases
18	esv2763996	chr6:26423901-26465384	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
19	nsv1017824	chr6:26425410-26465384	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers 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	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:33)

SNP	Gene	Cis/trans	Tissue	Source
rs2076030	BTN3A2	cis	cerebellum	SCAN
rs2076030	BTN3A2	cis	Adipose Subcutaneous	GTEx
rs2076030	BTN3A2	cis	Muscle Skeletal	GTEx
rs2076030	ZSCAN23	cis	cerebellum	SCAN
rs2076030	ZSCAN23	cis	parietal	SCAN
rs2076030	BTN3A2	cis	Artery Tibial	GTEx
rs2076030	BTN3A2	cis	Thyroid	GTEx
rs2076030	BTN3A2	Cis_1M	lymphoblastoid	RTeQTL
rs2076030	HIST1H2BD	cis	cerebellum	SCAN
rs2076030	BTN3A2	cis	lymphoblastoid	seeQTL
rs2076030	CMAH	cis	parietal	SCAN
rs2076030	BTN3A2	cis	Esophagus Muscularis	GTEx
rs2076030	BTN3A2	cis	lesional skin	skin_eQTL
rs2076030	BTN3A2	cis	Esophagus Mucosa	GTEx
rs2076030	BTN3A2	cis	lung	GTEx
rs2076030	HIST1H4L	cis	parietal	SCAN
rs2076030	BTN3A2	cis	multi-tissue	Pritchard
rs2076030	BTN3A2	cis	Skin Sun Exposed Lower leg	GTEx
rs2076030	BTN3A2	cis	lymphoblastoid	GTEx
rs2076030	ZKSCAN3	cis	parietal	SCAN
rs2076030	BTN3A2	cis	Heart Left Ventricle	GTEx
rs2076030	BTN3A1	Cis_1M	lymphoblastoid	RTeQTL
rs2076030	BTN3A2	cis	uninvolved skin	skin_eQTL
rs2076030	BTN3A2	cis	normal skin	skin_eQTL
rs2076030	ZNF192	cis	cerebellum	SCAN
rs2076030	BTN3A2///BTN3A3	Cis_1M	lymphoblastoid	RTeQTL
rs2076030	BTN3A2	cis	Whole Blood	GTEx
rs2076030	BTN3A3	cis	lymphoblastoid	seeQTL
rs2076030	BTN3A2	cis	Nerve Tibial	GTEx
rs2076030	LRRC16A	cis	parietal	SCAN
rs2076030	BTN3A2	cis	Stomach	GTEx
rs2076030	BTN3A2	cis	parietal	SCAN
rs2076030	BTN3A2	cis	Artery Aorta	GTEx

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26422200-26428400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:26422200-26439800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:26422400-26431000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:26422400-26432000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:26422400-26439400	Weak transcription	Primary T cells from cord blood	blood
6	chr6:26422400-26439400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:26422400-26439600	Weak transcription	Thymus	Thymus
8	chr6:26422600-26427000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr6:26422600-26427400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:26422600-26428200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:26422600-26430800	Weak transcription	A549	lung
12	chr6:26422600-26431000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr6:26422600-26431000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr6:26422600-26431000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr6:26422600-26431200	Weak transcription	Fetal Thymus	thymus
16	chr6:26422600-26431400	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr6:26422600-26432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:26422600-26432800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:26422600-26434200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr6:26422600-26434400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:26422600-26434600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr6:26422600-26439400	Weak transcription	HMEC	breast
23	chr6:26422600-26439600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:26422600-26439800	Weak transcription	Primary B cells from cord blood	blood
25	chr6:26422600-26440000	Weak transcription	Psoas Muscle	Psoas
26	chr6:26423000-26427000	Weak transcription	HUVEC	blood vessel
27	chr6:26423000-26427200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:26423000-26427200	Weak transcription	HSMMtube	muscle
29	chr6:26423000-26431000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:26423000-26431600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr6:26423000-26433200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:26423200-26427200	Weak transcription	Ovary	ovary
33	chr6:26423200-26427400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:26423200-26432600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr6:26423200-26432800	Weak transcription	GM12878-XiMat	blood
36	chr6:26423200-26440000	Weak transcription	Colonic Mucosa	Colon
37	chr6:26423400-26431000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr6:26423400-26431200	Weak transcription	Gastric	stomach
39	chr6:26423400-26431400	Weak transcription	Brain Substantia Nigra	brain
40	chr6:26423600-26427200	Weak transcription	NHDF-Ad	bronchial
41	chr6:26423600-26428800	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr6:26423600-26439400	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr6:26423600-26440400	Weak transcription	Right Ventricle	heart
44	chr6:26423800-26431000	Weak transcription	NHEK	skin
45	chr6:26423800-26431400	Weak transcription	Pancreas	Pancrea
46	chr6:26423800-26439600	Weak transcription	Colon Smooth Muscle	Colon
47	chr6:26423800-26439800	Weak transcription	Hela-S3	cervix
48	chr6:26424200-26427600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:26424800-26431400	Weak transcription	Right Atrium	heart
50	chr6:26424800-26431600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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