Variant report

Variant	rs1638560
Chromosome Location	chr11:67220175-67220176
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	NFIC	chr11:67219482-67220465	ECC-1	luminal epithelium:	n/a	n/a
2	MAX	chr11:67219470-67220280	ECC-1	luminal epithelium:	n/a	n/a
3	POLR2A	chr11:67218683-67220346	GM12878	blood:	n/a	n/a
4	POLR2A	chr11:67219945-67220418	GM12878	blood:	n/a	n/a
5	TCF12	chr11:67219651-67220388	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr11:67217429-67220463	GM12892	blood:	n/a	n/a
7	POLR2A	chr11:67219918-67220458	GM12892	blood:	n/a	n/a
8	NFIC	chr11:67219441-67220474	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:67218019..67220766-chr11:67230531..67233882,3	K562	blood:
2	chr11:67167428..67170410-chr11:67219775..67221650,2	MCF-7	breast:

Variant related genes	Relation type
CABP4	TF binding region
ENSG00000172663	Chromatin interaction
ENSG00000172531	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs10896175	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227796	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227804	1.00[EUR][1000 genomes]
rs11821703	1.00[EUR][1000 genomes]
rs12293606	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1382089	1.00[EUR][1000 genomes]
rs1618605	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1620333	0.89[ASW][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.93[YRI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1624189	0.89[ASW][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625032	0.89[ASW][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625892	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1630068	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1632616	0.89[ASW][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.96[YRI][hapmap];0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638558	0.80[YRI][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638559	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638561	1.00[EUR][1000 genomes]
rs1638562	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638563	1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638570	1.00[EUR][1000 genomes]
rs1638572	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs1638575	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638576	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638577	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638581	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638584	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638585	0.93[YRI][hapmap];0.91[AMR][1000 genomes]
rs1638587	1.00[EUR][1000 genomes]
rs1790729	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs1790730	1.00[EUR][1000 genomes]
rs1790734	1.00[EUR][1000 genomes]
rs1790736	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790741	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790743	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790744	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790745	1.00[EUR][1000 genomes]
rs1790749	1.00[EUR][1000 genomes]
rs1790750	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs1790754	1.00[EUR][1000 genomes]
rs1790756	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790763	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790764	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790765	1.00[EUR][1000 genomes]
rs1824712	1.00[EUR][1000 genomes]
rs2054409	1.00[EUR][1000 genomes]
rs2447590	1.00[EUR][1000 genomes]
rs2447591	1.00[EUR][1000 genomes]
rs2447597	1.00[EUR][1000 genomes]
rs2511058	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2511059	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514013	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs2514014	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs2514015	1.00[EUR][1000 genomes]
rs2514024	1.00[EUR][1000 genomes]
rs2514045	1.00[EUR][1000 genomes]
rs2514064	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs2514262	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514263	1.00[EUR][1000 genomes]
rs2885171	1.00[EUR][1000 genomes]
rs3016861	1.00[EUR][1000 genomes]
rs35363135	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36052107	1.00[EUR][1000 genomes]
rs4148960	1.00[CEU][hapmap]
rs56050553	1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56405884	0.81[AMR][1000 genomes];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]
rs58999825	1.00[EUR][1000 genomes]
rs59500232	1.00[EUR][1000 genomes]
rs596431	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs596944	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs601363	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60136955	1.00[EUR][1000 genomes]
rs602220	0.81[AMR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs604540	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs60751057	1.00[EUR][1000 genomes]
rs611697	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61282424	1.00[EUR][1000 genomes]
rs61429992	1.00[EUR][1000 genomes]
rs61610719	1.00[EUR][1000 genomes]
rs618633	1.00[EUR][1000 genomes]
rs641081	1.00[MEX][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6591267	1.00[EUR][1000 genomes]
rs7104627	1.00[EUR][1000 genomes]
rs7121803	1.00[MEX][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7124630	0.89[ASW][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];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	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506015	1.00[EUR][1000 genomes]
rs73506054	1.00[EUR][1000 genomes]
rs73506056	1.00[EUR][1000 genomes]
rs73506069	1.00[EUR][1000 genomes]
rs73506074	1.00[EUR][1000 genomes]
rs743679	1.00[EUR][1000 genomes]
rs7934566	1.00[EUR][1000 genomes]
rs7941752	0.81[AMR][1000 genomes]
rs7947114	1.00[EUR][1000 genomes]
rs8191436	1.00[EUR][1000 genomes]
rs8191446	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs8191449	1.00[EUR][1000 genomes]
rs949250	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949251	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949252	0.94[ASW][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949253	0.80[YRI][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949254	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949255	0.81[AMR][1000 genomes];1.00[EUR][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	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
18	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
19	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
20	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
21	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
22	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
23	esv1813337	chr11:67217703-67235815	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1638560	RPS6KB2	cis	lymphoblastoid	seeQTL

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67211800-67231200	Weak transcription	Right Atrium	heart
2	chr11:67211800-67232000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:67212400-67226800	Enhancers	Primary B cells from peripheral blood	blood
4	chr11:67215400-67227200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:67215800-67230600	Weak transcription	Fetal Intestine Small	intestine
6	chr11:67217200-67231400	Weak transcription	Thymus	Thymus
7	chr11:67217800-67220400	Enhancers	Fetal Muscle Leg	muscle
8	chr11:67218000-67221400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:67218200-67220200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr11:67218200-67221600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:67218600-67221800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr11:67218600-67227000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr11:67219000-67220400	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr11:67219000-67231400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:67219200-67225800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr11:67219400-67220200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr11:67219600-67220200	Enhancers	Left Ventricle	heart
18	chr11:67219600-67220400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr11:67219600-67220400	Enhancers	Fetal Muscle Trunk	muscle
20	chr11:67219600-67220400	Enhancers	Pancreas	Pancrea
21	chr11:67219600-67220400	Enhancers	Right Ventricle	heart
22	chr11:67219600-67220400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr11:67219600-67220400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr11:67219600-67220600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr11:67219600-67220600	Enhancers	Stomach Smooth Muscle	stomach
26	chr11:67219800-67220200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
27	chr11:67219800-67220200	Flanking Active TSS	Gastric	stomach
28	chr11:67219800-67220200	Flanking Active TSS	Lung	lung
29	chr11:67219800-67220200	Active TSS	Psoas Muscle	Psoas
30	chr11:67219800-67220400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr11:67219800-67220400	Enhancers	HMEC	breast
32	chr11:67219800-67220400	Flanking Active TSS	HUVEC	blood vessel
33	chr11:67219800-67220600	Flanking Active TSS	HSMM	muscle
34	chr11:67219800-67221400	Weak transcription	Primary B cells from cord blood	blood
35	chr11:67219800-67226800	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr11:67220000-67220200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:67220000-67220200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr11:67220000-67220200	Enhancers	Brain Hippocampus Middle	brain
39	chr11:67220000-67220200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:67220000-67220200	Bivalent Enhancer	Fetal Stomach	stomach
41	chr11:67220000-67220200	Flanking Active TSS	Spleen	Spleen
42	chr11:67220000-67220400	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr11:67220000-67220400	Enhancers	Brain Angular Gyrus	brain
44	chr11:67220000-67220400	Enhancers	Brain Anterior Caudate	brain
45	chr11:67220000-67220400	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr11:67220000-67220400	Flanking Active TSS	Colonic Mucosa	Colon
47	chr11:67220000-67220400	Flanking Active TSS	Placenta	Placenta
48	chr11:67220000-67220400	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr11:67220000-67220400	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr11:67220000-67220400	Flanking Active TSS	Stomach Mucosa	stomach

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