Variant report

Variant	rs2773318
Chromosome Location	chr6:5258843-5258844
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	POLR2A	chr6:5257755-5258901	H1-hESC	embryonic stem cell:	n/a	n/a
2	KAP1	chr6:5258800-5259061	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:5230386..5232263-chr6:5256966..5259626,3	K562	blood:
2	chr6:5258576..5260130-chr6:5278247..5279774,2	K562	blood:
3	chr6:5230476..5232022-chr6:5258422..5260596,2	MCF-7	breast:

Variant related genes	Relation type
FARS2	TF binding region

Extended variants
information (count: 135 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs1055415	1.00[JPT][hapmap]
rs11752747	1.00[CEU][hapmap];0.95[GIH][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes]
rs12174086	0.84[ASN][1000 genomes]
rs12206736	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs13191012	0.94[ASN][1000 genomes]
rs1535041	1.00[JPT][hapmap]
rs1570085	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609808	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17139748	1.00[JPT][hapmap]
rs17139985	0.99[ASN][1000 genomes]
rs17140068	0.94[CEU][hapmap]
rs1884976	0.80[ASN][1000 genomes]
rs1970010	1.00[JPT][hapmap]
rs2145372	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2224391	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2224392	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2746220	1.00[JPT][hapmap]
rs2746221	1.00[JPT][hapmap]
rs2746222	1.00[JPT][hapmap]
rs2753214	0.80[ASN][1000 genomes]
rs2753222	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2753223	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753224	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753228	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753229	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753230	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753233	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753234	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753235	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2753236	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2753237	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753238	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2753239	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];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753240	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753243	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753244	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753245	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753246	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2753247	0.99[ASN][1000 genomes]
rs2753248	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2753249	0.99[ASN][1000 genomes]
rs2753255	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2773287	1.00[JPT][hapmap]
rs2773294	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2773296	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2773298	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2773299	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2773300	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2773302	0.97[ASN][1000 genomes]
rs2773304	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2773306	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2773307	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2773308	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2773309	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2773310	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773311	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773312	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773314	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773316	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773317	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773319	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773320	0.99[ASN][1000 genomes]
rs2773322	0.99[ASN][1000 genomes]
rs2773333	1.00[JPT][hapmap]
rs2773336	1.00[JPT][hapmap]
rs2773337	1.00[JPT][hapmap]
rs35048711	0.93[ASN][1000 genomes]
rs36055504	0.94[ASN][1000 genomes]
rs367803	0.94[JPT][hapmap]
rs391313	1.00[JPT][hapmap]
rs393391	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs393454	1.00[JPT][hapmap]
rs399283	1.00[JPT][hapmap]
rs409295	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs416803	1.00[JPT][hapmap]
rs419778	1.00[JPT][hapmap]
rs421720	0.94[JPT][hapmap]
rs4246073	1.00[JPT][hapmap]
rs429031	1.00[JPT][hapmap]
rs429490	1.00[JPT][hapmap]
rs434450	1.00[JPT][hapmap]
rs439356	1.00[JPT][hapmap]
rs445711	1.00[JPT][hapmap]
rs447604	1.00[JPT][hapmap]
rs4960074	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6909619	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6913120	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6925249	0.99[ASN][1000 genomes]
rs761360	1.00[JPT][hapmap]
rs761361	1.00[JPT][hapmap]
rs766339	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs766340	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7752203	1.00[ASN][1000 genomes]
rs7758400	0.88[ASN][1000 genomes]
rs928170	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9328289	0.88[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs9378420	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9378943	0.83[ASN][1000 genomes]
rs9392664	1.00[JPT][hapmap]
rs9392665	0.84[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9392666	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9405259	0.81[ASN][1000 genomes]
rs9405260	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9405807	0.82[CHD][hapmap];1.00[JPT][hapmap]
rs9405809	0.84[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs9405811	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9405813	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9504356	1.00[JPT][hapmap]
rs9504364	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9504365	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9504368	0.95[ASN][1000 genomes]
rs9504369	0.99[ASN][1000 genomes]
rs9504370	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs9504371	0.99[ASN][1000 genomes]
rs9784870	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
4	nsv1034681	chr6:5070351-5387176	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv538113	chr6:5070351-5387176	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1018152	chr6:5077025-5387176	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv600873	chr6:5089278-5400658	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1030254	chr6:5132261-5431585	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
9	nsv1034463	chr6:5137959-5345678	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
10	nsv1021646	chr6:5157795-5367254	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv538115	chr6:5157795-5367254	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv1029609	chr6:5187633-5397254	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	nsv1035080	chr6:5206533-5396019	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv538116	chr6:5206533-5396019	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv1016456	chr6:5216835-5315913	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	nsv538117	chr6:5216835-5315913	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
17	nsv1019428	chr6:5216835-5627839	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	nsv538118	chr6:5216835-5627839	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv522457	chr6:5245070-5260936	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv1028185	chr6:5247624-5340163	Active TSS Enhancers 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	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2773318	LYRM4	cis	parietal	SCAN
rs2773318	LYRM4	cis	lymphoblastoid	seeQTL
rs2773318	FARS2	cis	lymphoblastoid	seeQTL
rs2773318	MGC39372	cis	cerebellum	SCAN

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5208200-5259800	Weak transcription	Primary B cells from peripheral blood	blood
2	chr6:5215000-5259800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr6:5215400-5259800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:5215600-5259800	Weak transcription	NHDF-Ad	bronchial
5	chr6:5216400-5259600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:5216600-5259600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr6:5220800-5259600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr6:5227800-5259800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr6:5231000-5260200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr6:5231800-5259800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr6:5231800-5260000	Weak transcription	NHLF	lung
12	chr6:5231800-5260200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr6:5232000-5259800	Weak transcription	HUVEC	blood vessel
14	chr6:5232000-5260200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:5232400-5260000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr6:5233400-5259800	Weak transcription	Brain Angular Gyrus	brain
17	chr6:5233400-5259800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr6:5233400-5259800	Weak transcription	Brain Hippocampus Middle	brain
19	chr6:5235200-5259400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:5235200-5259800	Weak transcription	Adipose Nuclei	Adipose
21	chr6:5235600-5259800	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr6:5235800-5259800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr6:5236400-5259600	Weak transcription	Fetal Intestine Large	intestine
24	chr6:5236400-5260200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:5239000-5260200	Weak transcription	Colonic Mucosa	Colon
26	chr6:5239400-5259400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr6:5239800-5259800	Weak transcription	Colon Smooth Muscle	Colon
28	chr6:5240400-5260000	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr6:5240600-5259800	Weak transcription	Thymus	Thymus
30	chr6:5241000-5260400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr6:5241400-5260200	Weak transcription	Fetal Kidney	kidney
32	chr6:5241800-5259800	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr6:5243800-5259800	Weak transcription	Placenta	Placenta
34	chr6:5245200-5259600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr6:5245200-5259800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr6:5245200-5260000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr6:5246000-5259800	Weak transcription	Right Ventricle	heart
38	chr6:5246200-5259800	Weak transcription	Brain Anterior Caudate	brain
39	chr6:5247000-5259400	Weak transcription	Fetal Lung	lung
40	chr6:5247000-5260200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:5247200-5259800	Weak transcription	Esophagus	oesophagus
42	chr6:5247400-5259800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr6:5247400-5259800	Weak transcription	Fetal Thymus	thymus
44	chr6:5249000-5259600	Weak transcription	Spleen	Spleen
45	chr6:5249000-5259800	Weak transcription	Lung	lung
46	chr6:5249000-5260200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:5249200-5260200	Weak transcription	Gastric	stomach
48	chr6:5250000-5259800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr6:5250000-5259800	Weak transcription	A549	lung
50	chr6:5250200-5259400	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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