Variant report

Variant	rs60969594
Chromosome Location	chr11:67203442-67203443
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:67203411-67204869	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:67198736-67211579	HL-60	blood:	n/a	n/a
3	POLR2A	chr11:67198696-67204329	GM12878	blood:	n/a	n/a
4	POLR2A	chr11:67203149-67204122	HUVEC	blood vessel:	n/a	n/a
5	POLR2A	chr11:67200617-67205780	GM12878	blood:	n/a	n/a
6	POLR2A	chr11:67202528-67204581	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr11:67200521-67212166	K562	blood:	n/a	n/a
8	SMC3	chr11:67203436-67203505	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:67203284-67203585	HUVEC	blood vessel:	n/a	n/a
10	POLR2A	chr11:67199088-67207292	GM18505	blood:	n/a	n/a
11	POLR2A	chr11:67198721-67204334	GM12878	blood:	n/a	n/a
12	POLR2A	chr11:67203064-67203767	U87	brain:	n/a	n/a
13	POLR2A	chr11:67199177-67206380	GM19099	blood:	n/a	n/a
14	POLR2A	chr11:67198947-67207334	HL-60	blood:	n/a	n/a
15	POLR2A	chr11:67199446-67204664	GM12891	blood:	n/a	n/a
16	CTCF	chr11:67203300-67203450	GM12872	blood:	n/a	n/a
17	CTCF	chr11:67203392-67203498	GM12891	blood:	n/a	n/a
18	CTCF	chr11:67203380-67203530	GM12871	blood:	n/a	n/a
19	POLR2A	chr11:67201270-67204557	MCF-7	breast:	n/a	n/a
20	POLR2A	chr11:67201051-67204264	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:67201705-67209206	PFSK-1	brain:	n/a	n/a
22	PML	chr11:67200370-67206421	GM12878	blood:	n/a	n/a
23	HMGN3	chr11:67203314-67203759	K562	blood:	n/a	n/a
24	STAT5A	chr11:67200137-67206130	GM12878	blood:	n/a	chr11:67204620-67204631 chr11:67204709-67204716 chr11:67203878-67203890 chr11:67200355-67200367 chr11:67201441-67201453 chr11:67202211-67202219 chr11:67204675-67204687 chr11:67205486-67205498 chr11:67201551-67201563 chr11:67204583-67204591 chr11:67203902-67203913
25	FOXM1	chr11:67203291-67205608	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:67203429-67203643	HCT-116	colon:	n/a	n/a
27	POLR2A	chr11:67199010-67205520	GM12892	blood:	n/a	n/a
28	POLR2A	chr11:67202081-67203777	ECC-1	luminal epithelium:	n/a	n/a
29	POLR2A	chr11:67198625-67205482	GM12891	blood:	n/a	n/a
30	POLR2A	chr11:67202952-67204515	HUVEC	blood vessel:	n/a	n/a
31	PAX5	chr11:67203190-67203769	GM12892	blood:	n/a	n/a
32	POLR2A	chr11:67203238-67203563	A549	lung:	n/a	n/a
33	POLR2A	chr11:67199678-67205474	GM18526	blood:	n/a	n/a
34	BCLAF1	chr11:67203236-67204433	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:67201074-67209001	PFSK-1	brain:	n/a	n/a
36	POLR2A	chr11:67202451-67208499	SK-N-MC	brain:	n/a	n/a
37	POLR2A	chr11:67199974-67206444	GM12892	blood:	n/a	n/a
38	POLR2A	chr11:67203420-67204319	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr11:67198635-67206407	GM12891	blood:	n/a	n/a
40	NFATC1	chr11:67203210-67203670	GM12878	blood:	n/a	n/a
41	POLR2A	chr11:67202795-67204436	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr11:67200968-67205480	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:67200187-67206414	GM15510	blood:	n/a	n/a
44	MTA3	chr11:67198952-67207449	GM12878	blood:	n/a	n/a
45	POLR2A	chr11:67203221-67203444	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr11:67198622-67210790	GM12892	blood:	n/a	n/a
47	POLR2A	chr11:67203159-67203514	A549	lung:	n/a	n/a
48	POLR2A	chr11:67198810-67206466	GM12878	blood:	n/a	n/a
49	NFIC	chr11:67203119-67203546	GM12878	blood:	n/a	n/a
50	POLR2A	chr11:67199833-67207816	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67203434-67203484	PFSK-1	brain:	n/a
2	chr11:67203434-67203484	HCT-116	colon:	n/a
3	chr11:67203434-67203484	Jurkat	blood:	n/a
4	chr11:67203434-67203484	NH-A	brain:	n/a
5	chr11:67203434-67203484	GM19239	blood:	n/a
6	chr11:67203434-67203484	HCM	heart:	n/a
7	chr11:67203434-67203484	GM12878	blood:	n/a
8	chr11:67203434-67203484	CMK	blood:	n/a
9	chr11:67203434-67203484	SAEC	small airway:	n/a
10	chr11:67203434-67203484	Caco-2	colon:	n/a
11	chr11:67203434-67203484	U87	brain:	n/a
12	chr11:67203434-67203484	BJ	skin:	n/a
13	chr11:67203434-67203484	PANC-1	pancreas:	n/a
14	chr11:67203434-67203484	BE2_C	brain:	n/a
15	chr11:67203434-67203484	SK-N-SH_RA	brain:	n/a
16	chr11:67203434-67203484	SK-N-MC	brain:	n/a
17	chr11:67203434-67203484	GM12891	blood:	n/a
18	chr11:67203434-67203484	NHDF-neo	bronchial:	n/a
19	chr11:67203434-67203484	HepG2	liver:	n/a
20	chr11:67203434-67203484	K562	blood:	n/a
21	chr11:67203434-67203484	ProgFib	skin:	n/a
22	chr11:67203434-67203484	AG04450	lung:	fetal
23	chr11:67203434-67203484	HRPEpiC	eye:	n/a
24	chr11:67203434-67203484	GM06990	blood:	n/a
25	chr11:67203434-67203484	HCF	heart:	n/a
26	chr11:67203434-67203484	T-47D	breast:	n/a
27	chr11:67203434-67203484	AG09309	skin:	n/a
28	chr11:67203434-67203484	NHBE	bronchial:	n/a
29	chr11:67203434-67203484	MCF10A-Er-Src	breast:	n/a
30	chr11:67203434-67203484	SK-N-SH	brain:	n/a
31	chr11:67203434-67203484	GM12892	blood:	n/a
32	chr11:67203434-67203484	HAEpiC	amniotic membrane:	n/a
33	chr11:67203434-67203484	AoSMC	blood vessel:	n/a
34	chr11:67203434-67203484	RPTEC	kidney:	n/a
35	chr11:67203434-67203484	HL-60	blood:	n/a
36	chr11:67203434-67203484	ovcar-3	ovarian:	n/a
37	chr11:67203434-67203484	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:67203434-67203484	H1-hESC	embryonic stem cell:	embryo
39	chr11:67203434-67203484	HUVEC	blood vessel:	n/a
40	chr11:67203434-67203484	LNCaP	prostate:	n/a
41	chr11:67203434-67203484	HRCEpiC	kidney:	n/a
42	chr11:67203434-67203484	AG04449	skin:	fetal
43	chr11:67203434-67203484	NT2-D1	testis:	n/a
44	chr11:67203434-67203484	MCF-7	breast:	n/a
45	chr11:67203434-67203484	HNPCEpiC	eye:	n/a
46	chr11:67203434-67203484	NB4	blood:	n/a
47	chr11:67203434-67203484	A549	lung:	n/a
48	chr11:67203434-67203484	Hepatocyte	liver:	n/a
49	chr11:67203434-67203484	SKMC	muscle:	n/a
50	chr11:67203434-67203484	PrEC	prostate:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67201761..67204037-chr11:67264926..67266855,2	K562	blood:
2	chr11:67172860..67176369-chr11:67201428..67204494,3	K562	blood:
3	chr11:67201248..67204152-chr11:67232413..67236121,3	K562	blood:
4	chr11:67119575..67122290-chr11:67202664..67205561,2	K562	blood:
5	chr11:67201617..67208575-chr11:67270788..67277143,13	K562	blood:
6	chr11:67187544..67192614-chr11:67201349..67205044,6	K562	blood:
7	chr11:67158620..67160811-chr11:67201509..67205285,3	K562	blood:
8	chr11:67202465..67204507-chr11:67260404..67262451,2	K562	blood:
9	chr11:67202629..67203491-chr11:67273232..67273781,2	K562	blood:
10	chr11:67201204..67205243-chr11:67272634..67278205,5	MCF-7	breast:
11	chr11:67201373..67203481-chr11:67248801..67250929,2	MCF-7	breast:
12	chr11:67203143..67205164-chr11:67257463..67259295,2	K562	blood:
13	chr11:67201799..67203957-chr11:67229051..67231861,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255949	TF binding region
ENSG00000255949	CpG island
ENSG00000172663	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000270169	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000175482	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11227786	0.87[EUR][1000 genomes]
rs11227787	0.87[EUR][1000 genomes]
rs61889862	0.83[AMR][1000 genomes]
rs61889869	1.00[ASN][1000 genomes]
rs61889872	1.00[ASN][1000 genomes]
rs61891588	0.83[AMR][1000 genomes]
rs72934722	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers 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	271 gene(s)	inside rSNPs	diseases
2	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
3	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
4	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
5	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
6	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
8	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
9	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
10	nsv897805	chr11:67155210-67283891	ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
11	nsv897806	chr11:67155210-67294308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
12	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
13	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
14	nsv897809	chr11:67156875-67276235	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
15	nsv555254	chr11:67164495-67288594	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
16	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
17	nsv897811	chr11:67166984-67218909	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
18	nsv897813	chr11:67175692-67283891	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
19	nsv521723	chr11:67175692-67311258	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
20	esv1847460	chr11:67182600-67219337	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
21	nsv524096	chr11:67186000-67224988	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
22	nsv468604	chr11:67186000-67283891	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
23	nsv555256	chr11:67186000-67283891	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67196800-67210200	Weak transcription	Fetal Kidney	kidney
2	chr11:67197200-67203600	Strong transcription	Fetal Stomach	stomach
3	chr11:67197200-67203600	Weak transcription	Small Intestine	intestine
4	chr11:67197200-67203800	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr11:67197200-67203800	Weak transcription	NH-A	brain
6	chr11:67197200-67206200	Strong transcription	Brain Cingulate Gyrus	brain
7	chr11:67197200-67206800	Weak transcription	Hela-S3	cervix
8	chr11:67197200-67206800	Weak transcription	NHDF-Ad	bronchial
9	chr11:67197200-67207000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:67197200-67207000	Weak transcription	Right Atrium	heart
11	chr11:67197200-67209400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:67197200-67209800	Weak transcription	Fetal Heart	heart
13	chr11:67197200-67210000	Strong transcription	Fetal Brain Female	brain
14	chr11:67197200-67210000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr11:67197400-67206800	Strong transcription	Brain Hippocampus Middle	brain
16	chr11:67197400-67209400	Strong transcription	Fetal Intestine Large	intestine
17	chr11:67197600-67203600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:67197600-67203600	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr11:67197600-67204400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:67197600-67204800	Strong transcription	Fetal Intestine Small	intestine
21	chr11:67197600-67204800	Strong transcription	Right Ventricle	heart
22	chr11:67197600-67208200	Strong transcription	Brain Germinal Matrix	brain
23	chr11:67197600-67209400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:67198000-67205400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:67198200-67203600	Strong transcription	Brain Substantia Nigra	brain
26	chr11:67198200-67203600	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr11:67198200-67203600	Strong transcription	Left Ventricle	heart
28	chr11:67198200-67204000	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr11:67198200-67204400	Strong transcription	Brain Angular Gyrus	brain
30	chr11:67198200-67206800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr11:67198200-67207000	Strong transcription	Brain Anterior Caudate	brain
32	chr11:67198200-67207000	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr11:67198200-67209600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr11:67198200-67209600	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr11:67198200-67209800	Strong transcription	NHLF	lung
36	chr11:67198400-67204000	Strong transcription	Liver	Liver
37	chr11:67198400-67207800	Strong transcription	Lung	lung
38	chr11:67198800-67203600	Strong transcription	H1 Cell Line	embryonic stem cell
39	chr11:67198800-67203600	Strong transcription	Colon Smooth Muscle	Colon
40	chr11:67198800-67204000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:67198800-67207400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:67199200-67203800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr11:67199400-67204000	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr11:67199400-67207000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:67200000-67203600	Genic enhancers	Esophagus	oesophagus
46	chr11:67200000-67203800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr11:67200600-67204800	Genic enhancers	Placenta	Placenta
48	chr11:67200600-67205000	Weak transcription	Stomach Mucosa	stomach
49	chr11:67200600-67208800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:67200800-67203600	Genic enhancers	Spleen	Spleen

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