Variant report

Variant	rs10896289
Chromosome Location	chr11:67811262-67811263
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	MYC	chr11:67810731-67811265	K562	blood:	n/a	chr11:67810822-67810831
2	TEAD4	chr11:67810843-67811379	K562	blood:	n/a	n/a
3	SPI1	chr11:67810562-67811476	HL-60	blood:	n/a	n/a
4	HDAC2	chr11:67811148-67811441	K562	blood:	n/a	n/a
5	MAZ	chr11:67810593-67811384	K562	blood:	n/a	chr11:67810822-67810831
6	USF1	chr11:67810843-67811347	K562	blood:	n/a	chr11:67810967-67810983
7	POLR2A	chr11:67810262-67811276	K562	blood:	n/a	n/a
8	POLR2A	chr11:67809974-67811428	HL-60	blood:	n/a	n/a
9	POLR2A	chr11:67810877-67811343	U87	brain:	n/a	n/a
10	NR2F2	chr11:67810804-67811325	K562	blood:	n/a	n/a
11	E2F6	chr11:67810750-67811264	K562	blood:	n/a	n/a
12	FOSL1	chr11:67810642-67811331	K562	blood:	n/a	chr11:67811119-67811130
13	RAD21	chr11:67811108-67811293	K562	blood:	n/a	chr11:67811159-67811172
14	SIN3AK20	chr11:67810438-67811502	MCF-7	breast:	n/a	n/a
15	UBTF	chr11:67810932-67811300	K562	blood:	n/a	n/a
16	MXI1	chr11:67810472-67811380	IMR90	lung:	n/a	n/a
17	CCNT2	chr11:67810155-67811308	K562	blood:	n/a	chr11:67810359-67810368
18	NR2F2	chr11:67810280-67811364	K562	blood:	n/a	n/a
19	UBTF	chr11:67810998-67811289	K562	blood:	n/a	n/a
20	MAX	chr11:67810834-67811268	K562	blood:	n/a	n/a
21	ZBTB7A	chr11:67810756-67811311	K562	blood:	n/a	n/a
22	BHLHE40	chr11:67810793-67811293	K562	blood:	n/a	chr11:67810967-67810983
23	ATF1	chr11:67811006-67811295	K562	blood:	n/a	n/a
24	FOSL1	chr11:67810903-67811327	K562	blood:	n/a	chr11:67811119-67811130
25	POLR2A	chr11:67810441-67811466	HL-60	blood:	n/a	n/a
26	MYC	chr11:67810586-67811293	K562	blood:	n/a	chr11:67810822-67810831
27	POLR2A	chr11:67809961-67811648	K562	blood:	n/a	n/a
28	MYC	chr11:67810478-67811279	K562	blood:	n/a	chr11:67810822-67810831
29	SIN3AK20	chr11:67810861-67811269	K562	blood:	n/a	n/a
30	TRIM28	chr11:67810874-67811325	K562	blood:	n/a	n/a
31	MAX	chr11:67810711-67811364	NB4	blood:	n/a	chr11:67810822-67810831
32	RCOR1	chr11:67810531-67811362	K562	blood:	n/a	n/a
33	MYC	chr11:67810607-67811347	K562	blood:	n/a	chr11:67810822-67810831
34	MAX	chr11:67810486-67811338	K562	blood:	n/a	chr11:67810822-67810831
35	EP300	chr11:67810896-67811291	K562	blood:	n/a	n/a
36	MAX	chr11:67810835-67811438	A549	lung:	n/a	n/a
37	MXI1	chr11:67810680-67811264	K562	blood:	n/a	n/a
38	ZC3H11A	chr11:67811158-67811271	K562	blood:	n/a	n/a
39	POLR2A	chr11:67810920-67811286	K562	blood:	n/a	n/a
40	ZBTB7A	chr11:67810620-67811291	K562	blood:	n/a	n/a
41	GATA3	chr11:67810769-67811364	MCF-7	breast:	n/a	chr11:67811015-67811022
42	ZNF263	chr11:67810880-67811403	K562	blood:	n/a	chr11:67811198-67811207
43	POLR2A	chr11:67810795-67811325	U87	brain:	n/a	n/a
44	MYC	chr11:67810802-67811365	NB4	blood:	n/a	chr11:67810822-67810831
45	MYC	chr11:67810846-67811301	MCF-7	breast:	n/a	n/a
46	ELF1	chr11:67810819-67811280	K562	blood:	n/a	n/a
47	JUN	chr11:67810958-67811304	K562	blood:	n/a	n/a
48	GATA2	chr11:67810892-67811287	K562	blood:	n/a	chr11:67811015-67811022
49	JUN	chr11:67810295-67811473	K562	blood:	n/a	n/a
50	JUN	chr11:67810895-67811348	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67808301..67812245-chr11:67979811..67982318,4	K562	blood:
2	chr11:67810552..67812245-chr11:67980611..67983549,2	MCF-7	breast:
3	chr11:67809131..67812171-chr11:67888117..67890461,4	MCF-7	breast:
4	chr11:67809744..67812462-chr11:67979811..67982598,3	K562	blood:

Variant related genes	Relation type
TCIRG1	TF binding region
ENSG00000110066	Chromatin interaction
ENSG00000110721	Chromatin interaction
ENSG00000255236	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1051806	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2075626	0.91[MEX][hapmap]
rs2511439	0.83[CHB][hapmap];0.82[GIH][hapmap];0.83[JPT][hapmap]
rs3763945	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs7127090	0.82[GIH][hapmap]
rs72926459	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72926470	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
3	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic 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	136 gene(s)	inside rSNPs	diseases
5	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
7	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
8	esv2758275	chr11:67524937-67859490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	87 gene(s)	inside rSNPs	diseases
9	nsv469856	chr11:67639037-67859490	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
10	nsv482760	chr11:67639037-67859490	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
11	nsv1047567	chr11:67747160-67819790	Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
12	nsv8836	chr11:67752879-67819799	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
13	nsv897836	chr11:67757350-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
14	nsv897837	chr11:67757350-67821036	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
15	nsv897838	chr11:67757350-67833543	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
16	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
17	nsv1050471	chr11:67764068-67821610	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
18	nsv468615	chr11:67765056-67816936	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
19	nsv555278	chr11:67765056-67816936	Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
20	nsv897841	chr11:67765056-67816936	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
21	nsv469964	chr11:67765056-67821036	Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
22	nsv897842	chr11:67765056-67821036	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
23	nsv897843	chr11:67765056-67833543	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
24	nsv1046054	chr11:67768796-67819790	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS 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	60 gene(s)	inside rSNPs	diseases
25	nsv897845	chr11:67774231-67821036	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
26	nsv555279	chr11:67789553-67816936	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
27	nsv897848	chr11:67789837-67816936	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
28	nsv897849	chr11:67789837-67821036	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
29	nsv555280	chr11:67793014-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
30	nsv897851	chr11:67793448-67821036	Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
31	nsv897852	chr11:67795066-67833543	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
32	nsv555281	chr11:67796691-67821036	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
33	nsv555282	chr11:67798567-67818325	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
34	nsv555283	chr11:67804074-67816936	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	10 gene(s)	inside rSNPs	diseases
35	nsv897853	chr11:67804074-67817876	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
36	nsv897854	chr11:67805476-67818325	Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
37	nsv897855	chr11:67805563-67842369	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
38	nsv555284	chr11:67806703-67817534	Active TSS Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	8 gene(s)	inside rSNPs	diseases
39	nsv897856	chr11:67806703-67821036	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs10896289	TPCN2	cis	cerebellum	SCAN
rs10896289	NDUFS8	cis	parietal	SCAN
rs10896289	SF1	cis	parietal	SCAN
rs10896289	SPDYC	cis	parietal	SCAN

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67806800-67819400	Weak transcription	Brain Germinal Matrix	brain
2	chr11:67807000-67817800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:67807800-67812400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr11:67807800-67819400	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr11:67807800-67820000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr11:67808000-67816600	Weak transcription	NHEK	skin
7	chr11:67808200-67812800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:67808200-67813000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:67808200-67820000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr11:67808200-67824600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:67808400-67811600	Weak transcription	Aorta	Aorta
12	chr11:67808400-67812800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:67808400-67815000	Weak transcription	Fetal Lung	lung
14	chr11:67808400-67817800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:67808400-67841000	Weak transcription	HMEC	breast
16	chr11:67808600-67811400	Enhancers	Placenta Amnion	Placenta Amnion
17	chr11:67808600-67812200	Genic enhancers	Fetal Stomach	stomach
18	chr11:67808600-67812400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr11:67808600-67812800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:67808600-67817600	Weak transcription	Brain Hippocampus Middle	brain
21	chr11:67808600-67818600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr11:67808600-67820600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr11:67808600-67823600	Weak transcription	Hela-S3	cervix
24	chr11:67808600-67828200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr11:67808600-67832200	Weak transcription	Right Atrium	heart
26	chr11:67808800-67811400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:67808800-67811400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:67808800-67811400	Weak transcription	Colon Smooth Muscle	Colon
29	chr11:67808800-67811400	Genic enhancers	A549	lung
30	chr11:67808800-67811800	Genic enhancers	Colonic Mucosa	Colon
31	chr11:67808800-67811800	Weak transcription	Osteobl	bone
32	chr11:67808800-67812200	Weak transcription	Small Intestine	intestine
33	chr11:67808800-67813600	Weak transcription	Rectal Smooth Muscle	rectum
34	chr11:67808800-67818000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr11:67808800-67818800	Strong transcription	Lung	lung
36	chr11:67808800-67842600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:67809000-67812600	Weak transcription	HepG2	liver
38	chr11:67809000-67821600	Strong transcription	NHLF	lung
39	chr11:67809000-67826600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr11:67809200-67821400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr11:67809200-67822600	Strong transcription	Liver	Liver
42	chr11:67809400-67816000	Weak transcription	HUVEC	blood vessel
43	chr11:67809400-67821000	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr11:67809400-67821000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr11:67809400-67821800	Strong transcription	Thymus	Thymus
46	chr11:67809400-67822000	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr11:67809400-67834800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr11:67809600-67815400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr11:67809600-67818400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr11:67809600-67818800	Strong transcription	Gastric	stomach

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