Variant report

Variant	rs2163625
Chromosome Location	chr11:8981537-8981538
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	RAD21	chr11:8980795-8981673	SK-N-SH	brain:	n/a	chr11:8981294-8981313 chr11:8981558-8981570
2	CTCF	chr11:8981500-8981650	HCFaa	heart:	n/a	n/a
3	RAD21	chr11:8981044-8981572	ECC-1	luminal epithelium:	n/a	chr11:8981294-8981313 chr11:8981558-8981570
4	CTCF	chr11:8981520-8981670	GM06990	blood:	n/a	n/a
5	SMC3	chr11:8980694-8981749	SK-N-SH	brain:	n/a	chr11:8981298-8981312
6	RAD21	chr11:8981016-8981607	IMR90	lung:	n/a	chr11:8981294-8981313 chr11:8981558-8981570
7	UBTF	chr11:8981356-8981545	K562	blood:	n/a	n/a
8	RAD21	chr11:8981031-8981581	H1-hESC	embryonic stem cell:	n/a	chr11:8981294-8981313 chr11:8981558-8981570
9	RAD21	chr11:8981080-8981632	HCT-116	colon:	n/a	chr11:8981294-8981313 chr11:8981558-8981570
10	RAD21	chr11:8980950-8981667	HCT-116	colon:	n/a	chr11:8981294-8981313 chr11:8981558-8981570
11	CTCF	chr11:8981169-8981544	MCF-7	breast:	n/a	chr11:8981296-8981314 chr11:8981291-8981312
12	CTCF	chr11:8981022-8981629	HCT-116	colon:	n/a	chr11:8981296-8981314 chr11:8981291-8981312
13	CTCF	chr11:8981003-8981545	K562	blood:	n/a	chr11:8981296-8981314 chr11:8981291-8981312
14	RAD21	chr11:8981013-8981538	HepG2	liver:	n/a	chr11:8981294-8981313
15	CTCF	chr11:8981067-8981679	K562	blood:	n/a	chr11:8981296-8981314 chr11:8981291-8981312
16	RAD21	chr11:8981008-8981561	MCF-7	breast:	n/a	chr11:8981294-8981313
17	CTCF	chr11:8981520-8981670	GM12872	blood:	n/a	n/a
18	RAD21	chr11:8980989-8981655	A549	lung:	n/a	chr11:8981294-8981313 chr11:8981558-8981570
19	IRF1	chr11:8980838-8981576	K562	blood:	n/a	chr11:8981030-8981047 chr11:8981029-8981042 chr11:8981030-8981044 chr11:8981027-8981041 chr11:8981029-8981043 chr11:8981032-8981043 chr11:8981031-8981041 chr11:8981028-8981045 chr11:8981029-8981042 chr11:8981031-8981042 chr11:8981029-8981042
20	GTF2F1	chr11:8981247-8981561	H1-hESC	embryonic stem cell:	n/a	chr11:8981472-8981483
21	RAD21	chr11:8981023-8981548	MCF-7	breast:	n/a	chr11:8981294-8981313
22	CTCF	chr11:8980814-8981716	A549	lung:	n/a	chr11:8981296-8981314 chr11:8981291-8981312
23	STAT3	chr11:8981140-8981673	MCF10A-Er-Src	breast:	n/a	n/a
24	CTCF	chr11:8981044-8981560	HCT-116	colon:	n/a	chr11:8981296-8981314 chr11:8981291-8981312
25	CTCF	chr11:8980949-8981789	SK-N-SH	brain:	n/a	chr11:8981296-8981314 chr11:8981291-8981312
26	RAD21	chr11:8981008-8981569	ECC-1	luminal epithelium:	n/a	chr11:8981294-8981313

No.	Distal block	Cell Line	Cell type
1	chr11:8706753..8709894-chr11:8978976..8982993,5	K562	blood:
2	chr11:8981281..8983336-chr11:9009757..9012558,2	K562	blood:
3	chr11:8981190..8983280-chr11:8983909..8986637,3	MCF-7	breast:
4	chr11:8973666..8975791-chr11:8980074..8981590,2	K562	blood:
5	chr11:8659357..8661041-chr11:8981138..8982951,2	K562	blood:
6	chr11:8980645..8982852-chr11:8983601..8986780,3	K562	blood:
7	chr11:8980645..8983033-chr11:8983601..8987670,5	K562	blood:
8	chr11:8710507..8713607-chr11:8978684..8982274,4	K562	blood:
9	chr11:8935646..8936651-chr11:8980737..8981722,3	MCF-7	breast:
10	chr11:8981088..8982840-chr11:9088115..9091017,2	K562	blood:
11	chr11:8979873..8982866-chr11:8983729..8987375,4	MCF-7	breast:
12	chr11:8961456..8964030-chr11:8978805..8982021,3	K562	blood:

Variant related genes	Relation type
TMEM9B-AS1	TF binding region
ENSG00000175356	Chromatin interaction
ENSG00000175348	Chromatin interaction
ENSG00000166441	Chromatin interaction
ENSG00000254860	Chromatin interaction
ENSG00000212607	Chromatin interaction

Extended variants
information (count: 95 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10219366	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1025438	0.85[CHB][hapmap];0.82[CHD][hapmap];0.86[JPT][hapmap]
rs10734639	1.00[CEU][hapmap];0.95[GIH][hapmap];0.90[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10743094	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10769974	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10769976	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10769977	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];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10840150	0.84[AMR][1000 genomes]
rs10840151	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.84[MKK][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10840153	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10840154	0.91[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10840155	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10840156	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11042128	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11042129	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11042131	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1136966	0.91[MEX][hapmap]
rs12794962	0.82[CHD][hapmap];0.80[GIH][hapmap];0.86[MEX][hapmap]
rs12798311	0.80[EUR][1000 genomes]
rs1347016	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1960180	0.83[MEX][hapmap]
rs2016844	0.91[CEU][hapmap];1.00[GIH][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs2043218	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2056903	0.91[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes]
rs2116510	0.83[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2116511	1.00[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2246878	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2247038	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2316523	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2316541	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2568029	0.86[MEX][hapmap]
rs2568034	0.91[CEU][hapmap]
rs2568042	0.91[CEU][hapmap];0.91[TSI][hapmap]
rs2568047	0.82[CHD][hapmap];0.82[GIH][hapmap];0.86[MEX][hapmap]
rs2568069	0.83[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568074	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2568075	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2568077	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2568079	0.91[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2568081	0.95[CEU][hapmap];0.84[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2568086	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568087	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568088	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2653556	0.87[CEU][hapmap];0.87[GIH][hapmap];0.86[MEX][hapmap]
rs2653565	0.91[CEU][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap]
rs2653590	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2653594	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2653597	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2653601	0.91[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2653604	0.83[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.83[LWK][hapmap];0.95[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2653611	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2742486	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2742487	1.00[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2742488	1.00[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2742489	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2742491	1.00[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2742493	0.82[ASW][hapmap];0.96[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.83[LWK][hapmap];0.95[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2742494	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2742495	0.91[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2742496	0.91[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2742497	0.91[CEU][hapmap];0.85[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2742502	0.82[MEX][hapmap]
rs2742504	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2742505	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2742512	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2742513	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2742514	1.00[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2742519	1.00[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2742521	0.91[CEU][hapmap]
rs3751063	0.91[CEU][hapmap];0.98[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3751065	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3751066	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3751068	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];0.95[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3763911	0.96[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3763912	0.96[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.84[MKK][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4370967	0.82[CHD][hapmap];0.80[GIH][hapmap];0.82[MEX][hapmap]
rs4909951	0.91[CEU][hapmap];1.00[GIH][hapmap];0.90[MEX][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4910068	0.82[MEX][hapmap]
rs4910181	0.80[AMR][1000 genomes]
rs7106152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7125458	0.86[MEX][hapmap]
rs72852790	0.82[ASN][1000 genomes]
rs72853712	0.82[ASN][1000 genomes]
rs7932377	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7936201	0.86[MEX][hapmap]
rs7942026	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7951226	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs909464	0.81[EUR][1000 genomes]
rs9300096	0.91[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.84[MKK][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs982273	0.87[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758256	chr11:8784813-9009573	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv2759803	chr11:8784813-9009573	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv435923	chr11:8839325-9000602	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv832062	chr11:8849295-9009472	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription 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 miRNA target site	31 gene(s)	inside rSNPs	diseases
5	esv3413845	chr11:8887279-9285127	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs2163625	C11orf17	cis	cerebellum	SCAN
rs2163625	TMEM9B	cis	parietal	SCAN
rs2163625	MRVI1	cis	cerebellum	SCAN
rs2163625	C11orf17	cis	multi-tissue	Pritchard
rs2163625	C11orf17	cis	lymphoblastoid	seeQTL
rs2163625	C11orf17	cis	Lymphoblastoid	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8944600-8985000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:8954400-8984400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:8963200-8985000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:8965800-8984800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:8966400-8984000	Weak transcription	Fetal Brain Male	brain
6	chr11:8968200-8985000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:8970600-8984400	Weak transcription	Right Ventricle	heart
8	chr11:8970600-8985000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr11:8970800-8984400	Weak transcription	A549	lung
10	chr11:8971200-8984400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr11:8972200-8982800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr11:8972800-8984200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr11:8973600-8985000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:8974800-8984000	Weak transcription	HepG2	liver
15	chr11:8974800-8984400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:8976200-8984000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr11:8977400-8984800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:8977600-8982800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr11:8977600-8984200	Weak transcription	Brain Germinal Matrix	brain
20	chr11:8977600-8985000	Weak transcription	Esophagus	oesophagus
21	chr11:8977600-8985000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr11:8977800-8982600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr11:8977800-8984000	Weak transcription	Dnd41	blood
24	chr11:8977800-8984200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr11:8977800-8984200	Weak transcription	Fetal Brain Female	brain
26	chr11:8977800-8984400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:8977800-8984400	Weak transcription	Fetal Thymus	thymus
28	chr11:8978000-8982800	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr11:8978000-8983000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:8978000-8983400	Weak transcription	Primary T cells from cord blood	blood
31	chr11:8978000-8983400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr11:8978000-8984200	Weak transcription	Thymus	Thymus
33	chr11:8978000-8984400	Weak transcription	Spleen	Spleen
34	chr11:8978000-8985000	Weak transcription	Gastric	stomach
35	chr11:8978000-8985000	Weak transcription	Lung	lung
36	chr11:8978200-8983000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr11:8978200-8984200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr11:8978600-8984000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr11:8978600-8984400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr11:8978800-8982800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr11:8978800-8983400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr11:8978800-8984000	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr11:8978800-8984600	Weak transcription	Placenta	Placenta
44	chr11:8979000-8984200	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr11:8979200-8984200	Weak transcription	Primary B cells from cord blood	blood
46	chr11:8979200-8984400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr11:8979400-8984200	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr11:8979400-8984400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr11:8980600-8981600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr11:8980600-8981600	Enhancers	Muscle Satellite Cultured Cells	--

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