Variant report

Variant	rs34391493
Chromosome Location	chr6:26022648-26022649
allele	A/C
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	chr6:26020505-26022713	GM18505	blood:	n/a	n/a
2	ATF2	chr6:26020387-26022657	H1-hESC	embryonic stem cell:	n/a	n/a
3	TCF12	chr6:26020392-26022752	A549	lung:	n/a	n/a
4	GATA3	chr6:26020325-26022724	A549	lung:	n/a	chr6:26022570-26022578
5	POLR2A	chr6:26020494-26022751	U87	brain:	n/a	n/a
6	POLR2A	chr6:26020353-26022750	PFSK-1	brain:	n/a	n/a
7	RCOR1	chr6:26020513-26022667	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr6:26020495-26022765	HCT-116	colon:	n/a	n/a
9	POLR2A	chr6:26020302-26022826	SK-N-MC	brain:	n/a	n/a
10	IRF3	chr6:26022156-26022692	Hela-S3	cervix:	n/a	chr6:26022536-26022545
11	EP300	chr6:26021604-26022652	A549	lung:	n/a	chr6:26021820-26021836
12	NFYB	chr6:26022350-26022673	GM12878	blood:	n/a	chr6:26022536-26022546 chr6:26022534-26022547 chr6:26022534-26022549 chr6:26022534-26022548 chr6:26022536-26022546 chr6:26022534-26022549
13	CHD1	chr6:26020088-26022955	IMR90	lung:	n/a	chr6:26021724-26021734
14	POLR2A	chr6:26021609-26022655	HCT-116	colon:	n/a	n/a
15	MAZ	chr6:26020377-26022720	IMR90	lung:	n/a	n/a
16	POLR2A	chr6:26020432-26022860	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr6:26020261-26022922	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:26021656-26022722	Hela-S3	cervix:	n/a	n/a
19	CHD1	chr6:26020585-26022687	GM12878	blood:	n/a	chr6:26021724-26021734
20	ZBTB33	chr6:26020376-26022806	SK-N-SH	brain:	n/a	n/a
21	NFYA	chr6:26022088-26022666	Hela-S3	cervix:	n/a	chr6:26022536-26022546 chr6:26022534-26022547 chr6:26022534-26022549 chr6:26022534-26022548 chr6:26022536-26022546 chr6:26022534-26022549
22	POLR2A	chr6:26020416-26022708	HCT-116	colon:	n/a	n/a
23	POLR2A	chr6:26021379-26022749	ECC-1	luminal epithelium:	n/a	n/a
24	ZBTB33	chr6:26020496-26022714	A549	lung:	n/a	n/a
25	POLR2A	chr6:26021608-26022725	K562	blood:	n/a	n/a
26	POLR2A	chr6:26020426-26022668	GM12891	blood:	n/a	n/a
27	POLR2A	chr6:26020461-26022665	HL-60	blood:	n/a	n/a
28	POLR2A	chr6:26020429-26022746	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr6:26020386-26022783	GM12892	blood:	n/a	n/a
30	POLR2A	chr6:26020518-26022655	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr6:26020392-26022766	GM12892	blood:	n/a	n/a
32	IRF3	chr6:26022473-26022689	GM12878	blood:	n/a	chr6:26022536-26022545
33	POLR2A	chr6:26021719-26022655	U87	brain:	n/a	n/a
34	POLR2A	chr6:26020481-26022660	Hela-S3	cervix:	n/a	n/a
35	NFYA	chr6:26022411-26022666	K562	blood:	n/a	chr6:26022536-26022546 chr6:26022534-26022547 chr6:26022534-26022549 chr6:26022534-26022548 chr6:26022536-26022546 chr6:26022534-26022549
36	POLR2A	chr6:26020298-26023073	MCF-7	breast:	n/a	n/a
37	ZNF384	chr6:26022432-26022728	GM12878	blood:	n/a	n/a
38	POLR2A	chr6:26020351-26022880	PANC-1	pancreas:	n/a	n/a
39	RELA	chr6:26020520-26022784	GM18951	blood:	n/a	n/a
40	POLR2A	chr6:26020530-26022695	K562	blood:	n/a	n/a
41	POLR2A	chr6:26020325-26022664	H1-hESC	embryonic stem cell:	n/a	n/a
42	FOS	chr6:26022339-26022694	K562	blood:	n/a	chr6:26022538-26022547
43	POLR2A	chr6:26020235-26022819	H1-hESC	embryonic stem cell:	n/a	n/a
44	SP1	chr6:26020242-26022736	A549	lung:	n/a	chr6:26021704-26021718 chr6:26021819-26021833 chr6:26022535-26022556 chr6:26020582-26020603 chr6:26021825-26021839 chr6:26021745-26021759
45	ZBTB33	chr6:26020394-26022650	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr6:26020515-26022703	H1-hESC	embryonic stem cell:	n/a	n/a
47	NFYA	chr6:26022341-26022663	GM12878	blood:	n/a	chr6:26022536-26022546 chr6:26022534-26022547 chr6:26022534-26022549 chr6:26022534-26022548 chr6:26022536-26022546 chr6:26022534-26022549
48	TAF7	chr6:26020434-26022772	H1-hESC	embryonic stem cell:	n/a	n/a
49	SP1	chr6:26020254-26022763	HCT-116	colon:	n/a	chr6:26021704-26021718 chr6:26021819-26021833 chr6:26022535-26022556 chr6:26020582-26020603 chr6:26021825-26021839 chr6:26021745-26021759
50	IRF1	chr6:26022317-26022809	K562	blood:	n/a	chr6:26022769-26022781 chr6:26022769-26022781 chr6:26022770-26022784 chr6:26022536-26022545 chr6:26022769-26022786 chr6:26022768-26022782 chr6:26022770-26022780 chr6:26022770-26022781

No.	Distal block	Cell Line	Cell type
1	chr6:26020264..26023736-chr6:26216792..26220704,4	MCF-7	breast:
2	chr6:25785090..25786841-chr6:26022568..26024928,2	K562	blood:
3	chr6:26019943..26022943-chr6:27098200..27102148,7	MCF-7	breast:
4	chr6:26020614..26023729-chr6:26272152..26276212,4	MCF-7	breast:
5	chr14:75745174..75745829-chr6:26021851..26022783,2	Hela-S3	cervix:
6	chr6:26020721..26023023-chr6:27777113..27779197,2	MCF-7	breast:
7	chr6:26021111..26023259-chr6:27860792..27862368,2	K562	blood:
8	chr6:26017750..26036418-chr6:26116875..26130553,65	MCF-7	breast:
9	chr6:26020896..26022698-chr6:27805218..27807913,2	MCF-7	breast:
10	chr6:25711420..25713335-chr6:26022573..26024303,2	K562	blood:
11	chr6:26018945..26024445-chr6:27858774..27864727,7	MCF-7	breast:
12	chr6:26020252..26023371-chr6:27112256..27114607,3	MCF-7	breast:
13	chr6:26020260..26024010-chr6:27780504..27784636,5	MCF-7	breast:
14	chr6:26019620..26034082-chr6:26100355..26110400,33	MCF-7	breast:
15	chr5:14872363..14873864-chr6:26021710..26023410,2	MCF-7	breast:
16	chr6:24719372..24721476-chr6:26021686..26024000,3	K562	blood:
17	chr6:26020714..26025029-chr6:27113708..27118688,4	K562	blood:
18	chr6:17706222..17707873-chr6:26020674..26023550,2	MCF-7	breast:
19	chr6:26019525..26036768-chr6:26154463..26163826,38	MCF-7	breast:
20	chr6:25577909..25579750-chr6:26022470..26024866,2	K562	blood:
21	chr6:26022227..26024181-chr9:131872412..131874622,2	K562	blood:
22	chr6:26019660..26022685-chr6:27833901..27836758,3	MCF-7	breast:
23	chr11:62607107..62608993-chr6:26021546..26024523,3	MCF-7	breast:
24	chr6:26020982..26024830-chr6:26195555..26199073,5	MCF-7	breast:
25	chr6:26021190..26023372-chr6:27113779..27115327,2	MCF-7	breast:
26	chr14:60714826..60716505-chr6:26021297..26023355,2	MCF-7	breast:
27	chr6:25990980..25994781-chr6:26019644..26023390,9	MCF-7	breast:
28	chr6:24719119..24721965-chr6:26020764..26023234,2	MCF-7	breast:
29	chr6:26020523..26023508-chr6:26233779..26236758,2	MCF-7	breast:
30	chr6:26021018..26024759-chr6:27113066..27116254,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H3A-1	chr6:26022289-26022817	ncRnaDb_ncrna_FR202434_1

Variant related genes	Relation type
HIST1H1A	TF binding region
ENSG00000233224	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000119383	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000112308	Chromatin interaction
ENSG00000254718	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000216331	Chromatin interaction
ENSG00000187475	Chromatin interaction
ENSG00000272462	Chromatin interaction
ENSG00000124789	Chromatin interaction
ENSG00000184357	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000095321	Chromatin interaction
ENSG00000272057	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000272269	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000124575	Chromatin interaction
ENSG00000233822	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000168242	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000170345	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000184348	Chromatin interaction
ENSG00000218690	Chromatin interaction
ENSG00000100614	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000272065	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000197061	Chromatin interaction
ENSG00000180596	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10484433	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs10484435	0.80[AMR][1000 genomes]
rs13192365	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs13195692	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs13196552	0.89[AMR][1000 genomes]
rs13200888	0.85[AFR][1000 genomes]
rs13201821	0.89[AMR][1000 genomes]
rs13203673	0.80[AMR][1000 genomes]
rs13214280	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs13216785	0.81[AMR][1000 genomes]
rs13220395	0.80[AMR][1000 genomes]
rs16891235	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17587597	0.80[AMR][1000 genomes]
rs28360595	0.80[AMR][1000 genomes]
rs34791189	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs35116528	0.89[AMR][1000 genomes]
rs35249036	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35335639	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs35367169	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs35484309	0.81[AFR][1000 genomes]
rs35528636	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs36012762	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs3734528	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56195001	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs56294283	0.89[AMR][1000 genomes]
rs60512607	0.89[AMR][1000 genomes]
rs67296946	0.89[AMR][1000 genomes]
rs68149500	0.85[AFR][1000 genomes]
rs71557315	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs72834617	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs72834623	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 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	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	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
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv432857	chr6:25957109-26072445	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	451 gene(s)	inside rSNPs	diseases
8	nsv1015627	chr6:25973495-26100483	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
9	nsv538164	chr6:25973495-26100483	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
10	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
11	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
12	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
13	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
14	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
15	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
16	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs34391493	BTN3A2	Cis_1M	lymphoblastoid	RTeQTL
rs34391493	BTN3A2///BTN3A3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26019000-26023400	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr6:26019400-26022800	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:26019600-26022800	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr6:26019800-26022800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr6:26019800-26023000	Active TSS	Brain Germinal Matrix	brain
6	chr6:26019800-26023400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:26020000-26022800	Active TSS	H1 Cell Line	embryonic stem cell
8	chr6:26020000-26022800	Active TSS	Fetal Kidney	kidney
9	chr6:26020200-26022800	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr6:26020200-26022800	Active TSS	Fetal Brain Female	brain
11	chr6:26020200-26022800	Active TSS	Fetal Stomach	stomach
12	chr6:26020200-26022800	Active TSS	A549	lung
13	chr6:26020200-26023400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:26020400-26022800	Active TSS	Brain Inferior Temporal Lobe	brain
15	chr6:26020400-26024200	Active TSS	Thymus	Thymus
16	chr6:26020800-26022800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:26021400-26023000	Active TSS	K562	blood
18	chr6:26021800-26022800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr6:26021800-26022800	Flanking Active TSS	NH-A	brain
20	chr6:26021800-26023000	Flanking Active TSS	Fetal Thymus	thymus
21	chr6:26022000-26022800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr6:26022000-26022800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:26022000-26022800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
24	chr6:26022000-26022800	Flanking Active TSS	HUVEC	blood vessel
25	chr6:26022000-26023000	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr6:26022000-26023000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr6:26022000-26023000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:26022000-26023000	Flanking Active TSS	Hela-S3	cervix
29	chr6:26022200-26022800	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr6:26022200-26022800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr6:26022200-26022800	Active TSS	Brain Hippocampus Middle	brain
32	chr6:26022200-26022800	Flanking Active TSS	HepG2	liver
33	chr6:26022200-26023000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:26022200-26026600	Weak transcription	Spleen	Spleen
35	chr6:26022200-26026800	Weak transcription	Gastric	stomach
36	chr6:26022400-26022800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:26022400-26022800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:26022400-26022800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:26022400-26022800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr6:26022400-26022800	Active TSS	Fetal Muscle Leg	muscle
41	chr6:26022400-26022800	Active TSS	Osteobl	bone
42	chr6:26022400-26023000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr6:26022400-26023000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:26022400-26023400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:26022400-26025400	Weak transcription	Aorta	Aorta
46	chr6:26022400-26025400	Weak transcription	Left Ventricle	heart
47	chr6:26022400-26025600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:26022400-26025600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr6:26022400-26025600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:26022400-26025600	Weak transcription	Pancreas	Pancrea

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