Variant report

Variant	rs12281209
Chromosome Location	chr11:67780320-67780321
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	chr11:67780124-67781369	U87	brain:	n/a	n/a
2	RCOR1	chr11:67779475-67781346	Hela-S3	cervix:	n/a	n/a
3	FOSL2	chr11:67778997-67782772	A549	lung:	n/a	chr11:67782281-67782291 chr11:67782280-67782292 chr11:67782282-67782291 chr11:67782281-67782291 chr11:67782281-67782291 chr11:67782281-67782291
4	ZBTB7A	chr11:67779550-67781030	ECC-1	luminal epithelium:	n/a	n/a
5	EP300	chr11:67779332-67782802	A549	lung:	n/a	n/a
6	MAX	chr11:67779513-67780320	Hela-S3	cervix:	n/a	chr11:67779790-67779800
7	SIN3AK20	chr11:67779917-67780508	A549	lung:	n/a	n/a
8	ZNF143	chr11:67780150-67781344	Hela-S3	cervix:	n/a	n/a
9	RCOR1	chr11:67779960-67782949	IMR90	lung:	n/a	n/a
10	PBX3	chr11:67779386-67781166	A549	lung:	n/a	n/a
11	POLR2A	chr11:67780182-67782571	ECC-1	luminal epithelium:	n/a	n/a
12	TFAP2A	chr11:67779542-67781061	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr11:67777218-67783087	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr11:67777291-67783079	U87	brain:	n/a	n/a
15	REST	chr11:67779759-67780379	A549	lung:	n/a	n/a
16	YY1	chr11:67779458-67781249	A549	lung:	n/a	n/a
17	SP1	chr11:67779196-67782876	A549	lung:	n/a	chr11:67782714-67782728 chr11:67782346-67782355 chr11:67782347-67782356 chr11:67782346-67782360
18	SP1	chr11:67776718-67782739	A549	lung:	n/a	chr11:67782714-67782728 chr11:67782346-67782355 chr11:67782347-67782356 chr11:67782346-67782360
19	POLR2A	chr11:67779131-67783150	Hela-S3	cervix:	n/a	n/a
20	SMARCB1	chr11:67779034-67783084	Hela-S3	cervix:	n/a	chr11:67782282-67782291
21	BCL3	chr11:67777390-67783349	A549	lung:	n/a	chr11:67782268-67782277
22	MXI1	chr11:67779868-67782202	IMR90	lung:	n/a	n/a
23	POLR2A	chr11:67778660-67783078	A549	lung:	n/a	n/a
24	POLR2A	chr11:67779006-67781056	A549	lung:	n/a	n/a
25	MAX	chr11:67777344-67783121	A549	lung:	n/a	chr11:67779790-67779800
26	CREB1	chr11:67779537-67780342	A549	lung:	n/a	n/a
27	REST	chr11:67776947-67782855	A549	lung:	n/a	chr11:67782466-67782475 chr11:67782075-67782089 chr11:67782425-67782438 chr11:67782093-67782106 chr11:67782268-67782277
28	NR3C1	chr11:67779381-67781273	A549	lung:	n/a	n/a
29	SIX5	chr11:67776699-67783266	A549	lung:	n/a	n/a
30	MAX	chr11:67779451-67782694	Hela-S3	cervix:	n/a	chr11:67779790-67779800
31	EP300	chr11:67779501-67782978	A549	lung:	n/a	n/a
32	POLR2A	chr11:67777643-67781175	A549	lung:	n/a	n/a
33	POLR2A	chr11:67777285-67783079	U87	brain:	n/a	n/a
34	POLR2A	chr11:67779242-67782855	Hela-S3	cervix:	n/a	n/a
35	MAX	chr11:67775570-67783343	A549	lung:	n/a	chr11:67776499-67776510 chr11:67776500-67776509 chr11:67776025-67776036 chr11:67779790-67779800 chr11:67776182-67776192 chr11:67776026-67776035 chr11:67776026-67776035
36	ETS1	chr11:67779315-67781080	A549	lung:	n/a	n/a
37	ELF1	chr11:67779319-67780401	A549	lung:	n/a	n/a
38	RFX5	chr11:67779651-67780354	Hela-S3	cervix:	n/a	n/a
39	FOSL2	chr11:67779804-67780388	A549	lung:	n/a	n/a
40	POLR2A	chr11:67779981-67781390	U87	brain:	n/a	n/a
41	TFAP2C	chr11:67779466-67781089	Hela-S3	cervix:	n/a	chr11:67780662-67780677
42	PBX3	chr11:67779434-67781410	A549	lung:	n/a	n/a
43	TCF12	chr11:67775698-67783378	A549	lung:	n/a	chr11:67782099-67782109 chr11:67782990-67783000 chr11:67782981-67782991 chr11:67782696-67782706 chr11:67776259-67776269
44	SMARCC1	chr11:67779846-67782707	Hela-S3	cervix:	n/a	chr11:67782282-67782291
45	JUND	chr11:67779467-67783009	A549	lung:	n/a	chr11:67782281-67782291 chr11:67782280-67782292 chr11:67782280-67782291 chr11:67782282-67782291 chr11:67782281-67782291 chr11:67782281-67782291 chr11:67782281-67782291
46	POLR2A	chr11:67779925-67781151	HepG2	liver:	n/a	n/a
47	TCF12	chr11:67779938-67782620	A549	lung:	n/a	chr11:67782099-67782109
48	FOXA2	chr11:67779614-67780387	A549	lung:	n/a	n/a
49	BCL3	chr11:67776809-67783348	A549	lung:	n/a	chr11:67782268-67782277
50	GATA3	chr11:67776826-67782913	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67780250..67781973-chr11:67889456..67890963,2	MCF-7	breast:
2	chr11:67778253..67781107-chr11:67810420..67812608,2	K562	blood:
3	chr11:67767693..67769603-chr11:67779964..67781851,2	K562	blood:
4	chr11:67779784..67784526-chr11:67980026..67983056,5	MCF-7	breast:
5	chr11:67778899..67781457-chr11:67928106..67930738,2	K562	blood:
6	chr11:67780000..67780893-chr20:23617975..23618833,2	Hela-S3	cervix:
7	chr11:67780316..67780831-chr18:11980531..11981129,2	Hela-S3	cervix:
8	chr11:67770338..67773597-chr11:67780108..67784129,5	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93B1-1	chr11:67776909-67782033	NONHSAT022487

Variant related genes	Relation type
ALDH3B1	TF binding region
ENSG00000110057	Chromatin interaction
ENSG00000255236	Chromatin interaction
ENSG00000101439	Chromatin interaction
ENSG00000141401	Chromatin interaction
ENSG00000110719	Chromatin interaction
ENSG00000110066	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11228121	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11501420	1.00[AMR][1000 genomes]
rs11501421	1.00[AMR][1000 genomes]
rs12279292	1.00[AMR][1000 genomes]
rs12286110	1.00[AFR][1000 genomes]
rs12290683	1.00[AMR][1000 genomes]
rs13377370	1.00[AMR][1000 genomes]
rs7114090	1.00[AMR][1000 genomes]
rs7128338	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 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	nsv428260	chr11:67524937-67797669	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
9	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
10	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
11	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
12	nsv1038960	chr11:67727827-67785555	Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	nsv897839	chr11:67765056-67793014	Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
21	nsv468613	chr11:67765056-67794643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
22	nsv555277	chr11:67765056-67794643	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
23	nsv468614	chr11:67765056-67799926	ZNF genes & repeats Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
24	nsv897840	chr11:67765056-67804605	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	nsv897844	chr11:67772729-67793014	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
33	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
34	nsv897846	chr11:67776465-67794643	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
35	nsv897847	chr11:67776465-67804605	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Weak transcription 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	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67771600-67797600	Weak transcription	Small Intestine	intestine
2	chr11:67772600-67792400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:67775000-67782400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr11:67777400-67780400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr11:67777400-67782600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
6	chr11:67777600-67781800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:67778000-67780400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:67778000-67781600	Weak transcription	HUVEC	blood vessel
9	chr11:67778200-67781600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:67778200-67782800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:67778400-67780800	Enhancers	Gastric	stomach
12	chr11:67778400-67781400	Weak transcription	Esophagus	oesophagus
13	chr11:67778400-67782000	Flanking Active TSS	Hela-S3	cervix
14	chr11:67778400-67782400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:67778400-67782400	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr11:67778400-67782600	Weak transcription	Thymus	Thymus
17	chr11:67778400-67782800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:67778400-67782800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr11:67778400-67782800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:67778400-67782800	Enhancers	Pancreas	Pancrea
21	chr11:67778400-67787400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:67778600-67780400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr11:67778600-67780400	Enhancers	Spleen	Spleen
24	chr11:67778600-67781200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:67778600-67781400	Enhancers	Fetal Muscle Trunk	muscle
26	chr11:67778600-67781600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr11:67778600-67782000	Enhancers	Brain Cingulate Gyrus	brain
28	chr11:67778600-67783000	Enhancers	Placenta	Placenta
29	chr11:67778600-67784000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:67778600-67784400	Weak transcription	Right Atrium	heart
31	chr11:67778600-67788000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr11:67778800-67781800	Enhancers	HMEC	breast
33	chr11:67778800-67782000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr11:67778800-67782400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:67778800-67782600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr11:67778800-67782800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr11:67778800-67782800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:67778800-67783000	Enhancers	Adipose Nuclei	Adipose
39	chr11:67778800-67784400	Weak transcription	Brain Angular Gyrus	brain
40	chr11:67779000-67780400	Enhancers	Brain Substantia Nigra	brain
41	chr11:67779000-67780400	Genic enhancers	NHLF	lung
42	chr11:67779000-67780600	Enhancers	NH-A	brain
43	chr11:67779000-67780800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr11:67779000-67781000	Enhancers	HSMMtube	muscle
45	chr11:67779000-67781200	Weak transcription	Brain Anterior Caudate	brain
46	chr11:67779000-67781400	Weak transcription	Colon Smooth Muscle	Colon
47	chr11:67779000-67781600	Weak transcription	Fetal Kidney	kidney
48	chr11:67779000-67782000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr11:67779000-67782600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:67779000-67782600	Enhancers	NHDF-Ad	bronchial

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