Variant report

Variant	rs58999825
Chromosome Location	chr11:67208426-67208427
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:43 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EBF1	chr11:67208159-67209055	GM12878	blood:	n/a	chr11:67208516-67208527
2	POLR2A	chr11:67198736-67211579	HL-60	blood:	n/a	n/a
3	POLR2A	chr11:67208252-67209047	GM12891	blood:	n/a	n/a
4	POLR2A	chr11:67208189-67210433	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:67207840-67208537	U87	brain:	n/a	n/a
6	POLR2A	chr11:67205666-67209002	K562	blood:	n/a	n/a
7	POLR2A	chr11:67200521-67212166	K562	blood:	n/a	n/a
8	POLR2A	chr11:67207966-67209003	K562	blood:	n/a	n/a
9	POLR2A	chr11:67207635-67209003	GM12878	blood:	n/a	n/a
10	POLR2A	chr11:67206644-67208974	HepG2	liver:	n/a	n/a
11	POLR2A	chr11:67207533-67209197	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr11:67208132-67211600	GM18505	blood:	n/a	n/a
13	POLR2A	chr11:67208080-67208452	HCT-116	colon:	n/a	n/a
14	POLR2A	chr11:67208403-67208510	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr11:67201705-67209206	PFSK-1	brain:	n/a	n/a
16	POLR2A	chr11:67208114-67209108	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr11:67204881-67211417	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr11:67208211-67209225	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:67208397-67208751	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr11:67201074-67209001	PFSK-1	brain:	n/a	n/a
21	MTA3	chr11:67207955-67209112	GM12878	blood:	n/a	n/a
22	POLR2A	chr11:67202451-67208499	SK-N-MC	brain:	n/a	n/a
23	POLR2A	chr11:67204657-67209717	ECC-1	luminal epithelium:	n/a	n/a
24	BCL3	chr11:67208021-67208502	A549	lung:	n/a	chr11:67208194-67208207
25	POLR2A	chr11:67198622-67210790	GM12892	blood:	n/a	n/a
26	POLR2A	chr11:67204834-67211350	MCF-7	breast:	n/a	n/a
27	POLR2A	chr11:67207397-67208953	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr11:67208172-67209104	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:67197957-67210886	GM12892	blood:	n/a	n/a
30	POLR2A	chr11:67207908-67208742	ProgFib	skin:	n/a	n/a
31	POLR2A	chr11:67198638-67208537	GM12892	blood:	n/a	n/a
32	POLR2A	chr11:67205603-67208501	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr11:67204755-67208474	U87	brain:	n/a	n/a
34	POLR2A	chr11:67208194-67209147	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr11:67208154-67211428	GM19099	blood:	n/a	n/a
36	POLR2A	chr11:67208268-67208530	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr11:67200689-67210558	K562	blood:	n/a	n/a
38	POLR2A	chr11:67198642-67211413	K562	blood:	n/a	n/a
39	POLR2A	chr11:67207504-67209035	GM12891	blood:	n/a	n/a
40	POLR2A	chr11:67207704-67213927	GM12878	blood:	n/a	n/a
41	POLR2A	chr11:67207840-67208515	U87	brain:	n/a	n/a
42	POLR2A	chr11:67197559-67209128	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:67208261-67209117	ECC-1	luminal epithelium:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67165362..67170814-chr11:67205782..67211749,9	K562	blood:
2	chr11:67206947..67211030-chr11:67273670..67277577,4	MCF-7	breast:
3	chr11:67201617..67208575-chr11:67270788..67277143,13	K562	blood:
4	chr11:67204954..67212426-chr11:67228820..67232211,6	K562	blood:
5	chr11:67207904..67210724-chr11:67272140..67274356,2	MCF-7	breast:
6	chr11:67207285..67211032-chr11:67270341..67273194,4	K562	blood:

No data

Variant related genes	Relation type
PTPRCAP	TF binding region
CORO1B	TF binding region
ENSG00000110697	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000270169	Chromatin interaction
ENSG00000167797	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10896175	1.00[EUR][1000 genomes]
rs11227796	1.00[EUR][1000 genomes]
rs11227804	1.00[EUR][1000 genomes]
rs12293606	1.00[EUR][1000 genomes]
rs1382089	1.00[EUR][1000 genomes]
rs1618605	1.00[EUR][1000 genomes]
rs1620333	1.00[EUR][1000 genomes]
rs1624189	1.00[EUR][1000 genomes]
rs1625032	1.00[EUR][1000 genomes]
rs1625892	1.00[EUR][1000 genomes]
rs1630068	1.00[EUR][1000 genomes]
rs1632616	1.00[EUR][1000 genomes]
rs1638558	1.00[EUR][1000 genomes]
rs1638559	1.00[EUR][1000 genomes]
rs1638560	1.00[EUR][1000 genomes]
rs1638561	1.00[EUR][1000 genomes]
rs1638562	1.00[EUR][1000 genomes]
rs1638563	1.00[EUR][1000 genomes]
rs1638570	1.00[EUR][1000 genomes]
rs1638572	1.00[EUR][1000 genomes]
rs1638575	1.00[EUR][1000 genomes]
rs1638576	1.00[EUR][1000 genomes]
rs1638577	1.00[EUR][1000 genomes]
rs1638581	1.00[EUR][1000 genomes]
rs1638584	1.00[EUR][1000 genomes]
rs1638587	1.00[EUR][1000 genomes]
rs1790729	1.00[EUR][1000 genomes]
rs1790730	1.00[EUR][1000 genomes]
rs1790734	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790736	1.00[EUR][1000 genomes]
rs1790741	1.00[EUR][1000 genomes]
rs1790743	1.00[EUR][1000 genomes]
rs1790744	1.00[EUR][1000 genomes]
rs1790745	1.00[EUR][1000 genomes]
rs1790749	1.00[EUR][1000 genomes]
rs1790750	1.00[EUR][1000 genomes]
rs1790754	1.00[EUR][1000 genomes]
rs1790756	1.00[EUR][1000 genomes]
rs1790763	1.00[EUR][1000 genomes]
rs1790764	1.00[EUR][1000 genomes]
rs1790765	1.00[EUR][1000 genomes]
rs1824712	1.00[EUR][1000 genomes]
rs2447590	1.00[EUR][1000 genomes]
rs2447591	1.00[EUR][1000 genomes]
rs2511058	1.00[EUR][1000 genomes]
rs2511059	1.00[EUR][1000 genomes]
rs2514013	1.00[EUR][1000 genomes]
rs2514014	1.00[EUR][1000 genomes]
rs2514015	1.00[EUR][1000 genomes]
rs2514064	1.00[EUR][1000 genomes]
rs2514262	1.00[EUR][1000 genomes]
rs2514263	1.00[EUR][1000 genomes]
rs3016861	1.00[EUR][1000 genomes]
rs35363135	1.00[EUR][1000 genomes]
rs56050553	1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56405884	1.00[EUR][1000 genomes]
rs57047868	1.00[EUR][1000 genomes]
rs57748654	1.00[EUR][1000 genomes]
rs57749415	1.00[EUR][1000 genomes]
rs57757103	1.00[EUR][1000 genomes]
rs57955602	1.00[EUR][1000 genomes]
rs596431	1.00[EUR][1000 genomes]
rs596944	1.00[EUR][1000 genomes]
rs601363	1.00[EUR][1000 genomes]
rs60136955	1.00[EUR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	1.00[EUR][1000 genomes]
rs604540	1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs60751057	1.00[EUR][1000 genomes]
rs611697	1.00[EUR][1000 genomes]
rs61282424	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61429992	1.00[EUR][1000 genomes]
rs61610719	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs618633	1.00[EUR][1000 genomes]
rs641081	1.00[EUR][1000 genomes]
rs7104627	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7121803	1.00[EUR][1000 genomes]
rs7124630	1.00[EUR][1000 genomes]
rs73490545	1.00[EUR][1000 genomes]
rs73490554	1.00[EUR][1000 genomes]
rs73501797	1.00[EUR][1000 genomes]
rs73501800	1.00[EUR][1000 genomes]
rs73506004	1.00[EUR][1000 genomes]
rs73506015	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506048	0.85[AFR][1000 genomes]
rs73506054	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73506056	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73506069	1.00[EUR][1000 genomes]
rs73506074	1.00[EUR][1000 genomes]
rs743679	1.00[EUR][1000 genomes]
rs7947114	1.00[EUR][1000 genomes]
rs8191436	1.00[EUR][1000 genomes]
rs8191446	1.00[EUR][1000 genomes]
rs8191449	1.00[EUR][1000 genomes]
rs949250	1.00[EUR][1000 genomes]
rs949251	1.00[EUR][1000 genomes]
rs949252	1.00[EUR][1000 genomes]
rs949253	1.00[EUR][1000 genomes]
rs949254	1.00[EUR][1000 genomes]
rs949255	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 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
24	nsv527056	chr11:67207426-67294308	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	115 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 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	chr11:67197200-67209400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:67197200-67209800	Weak transcription	Fetal Heart	heart
4	chr11:67197200-67210000	Strong transcription	Fetal Brain Female	brain
5	chr11:67197200-67210000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:67197400-67209400	Strong transcription	Fetal Intestine Large	intestine
7	chr11:67197600-67209400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:67198200-67209600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:67198200-67209600	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr11:67198200-67209800	Strong transcription	NHLF	lung
11	chr11:67200600-67208800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:67201000-67209800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:67201600-67210000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:67202200-67210200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr11:67202400-67209800	Weak transcription	HepG2	liver
16	chr11:67202400-67210200	Weak transcription	Psoas Muscle	Psoas
17	chr11:67203200-67210000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:67203200-67210400	Weak transcription	Ovary	ovary
19	chr11:67203800-67209800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr11:67203800-67210400	Weak transcription	Aorta	Aorta
21	chr11:67204800-67209400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:67204800-67209800	Genic enhancers	Right Ventricle	heart
23	chr11:67205000-67209800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr11:67205200-67208600	Strong transcription	Fetal Intestine Small	intestine
25	chr11:67205200-67208800	Strong transcription	Placenta Amnion	Placenta Amnion
26	chr11:67205200-67209800	Genic enhancers	Placenta	Placenta
27	chr11:67205400-67209400	Weak transcription	K562	blood
28	chr11:67205400-67209600	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr11:67205400-67209800	Weak transcription	NH-A	brain
30	chr11:67205600-67208800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:67205600-67209800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
32	chr11:67205600-67209800	Genic enhancers	Stomach Smooth Muscle	stomach
33	chr11:67205600-67210000	Weak transcription	Brain Angular Gyrus	brain
34	chr11:67205600-67210200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr11:67205600-67210400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:67205800-67209800	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr11:67205800-67211200	Enhancers	Primary B cells from cord blood	blood
38	chr11:67206000-67209800	Genic enhancers	Gastric	stomach
39	chr11:67206200-67209400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:67206200-67209400	Genic enhancers	Esophagus	oesophagus
41	chr11:67206200-67209800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr11:67206200-67209800	Strong transcription	Fetal Stomach	stomach
43	chr11:67206200-67210200	Genic enhancers	Fetal Muscle Trunk	muscle
44	chr11:67206200-67210200	Genic enhancers	Spleen	Spleen
45	chr11:67206400-67209800	Genic enhancers	Thymus	Thymus
46	chr11:67206600-67209600	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr11:67206600-67209800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:67206600-67209800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:67206600-67209800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
50	chr11:67206800-67209600	Strong transcription	H1 Cell Line	embryonic stem cell

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