Variant report

Variant	rs162390
Chromosome Location	chr21:44936826-44936827
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:44936376..44937297-chr21:45031478..45032290,2	MCF-7	breast:
2	chr21:44935245..44937496-chr21:45021049..45022786,2	MCF-7	breast:
3	chr21:44839515..44855046-chr21:44918803..44938582,70	MCF-7	breast:
4	chr21:44934187..44937130-chr21:45020979..45023437,3	MCF-7	breast:
5	chr21:44935059..44936997-chr21:45153609..45155904,2	MCF-7	breast:
6	chr21:44934887..44937881-chr21:45009259..45012818,3	MCF-7	breast:
7	chr21:44935610..44937483-chr21:44946827..44948859,2	MCF-7	breast:
8	chr21:44936672..44939278-chr21:45002074..45004794,2	MCF-7	breast:
9	chr21:44935246..44937447-chr21:45079035..45081469,3	MCF-7	breast:
10	chr21:44935745..44939889-chr21:44996444..44998643,4	MCF-7	breast:
11	chr1:153939416..153940023-chr21:44936682..44937393,2	Hela-S3	cervix:
12	chr21:44933239..44939119-chr21:45027942..45032046,11	MCF-7	breast:
13	chr21:44936778..44938519-chr21:44970859..44973730,2	MCF-7	breast:
14	chr21:44932097..44937071-chr21:45004878..45007611,5	MCF-7	breast:
15	chr21:44750832..44753167-chr21:44936068..44937734,2	MCF-7	breast:
16	chr21:44934396..44939488-chr21:45063795..45068503,7	MCF-7	breast:
17	chr21:44936168..44938346-chr5:25477509..25479943,2	MCF-7	breast:
18	chr21:44935247..44938888-chr21:45036868..45039173,3	MCF-7	breast:
19	chr21:44759707..44762996-chr21:44935896..44938308,3	MCF-7	breast:
20	chr21:44935626..44937329-chr21:45067508..45070010,2	MCF-7	breast:
21	chr21:44935195..44942837-chr21:45027341..45034401,13	MCF-7	breast:
22	chr21:44896300..44899568-chr21:44934496..44937957,5	MCF-7	breast:
23	chr21:44934950..44937426-chr21:44968683..44970792,2	MCF-7	breast:
24	chr21:44935152..44938727-chr21:45130277..45133903,3	MCF-7	breast:
25	chr21:44936296..44939345-chr21:45062332..45065604,3	MCF-7	breast:
26	chr21:44935404..44937954-chr8:127569330..127571915,2	MCF-7	breast:
27	chr21:44936721..44939320-chr21:45041699..45043482,2	MCF-7	breast:
28	chr21:44844533..44847872-chr21:44929082..44940063,13	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000168672	Chromatin interaction
ENSG00000185186	Chromatin interaction
ENSG00000254286	Chromatin interaction
ENSG00000160207	Chromatin interaction
ENSG00000160208	Chromatin interaction
ENSG00000142178	Chromatin interaction
ENSG00000143578	Chromatin interaction
ENSG00000214326	Chromatin interaction
ENSG00000237864	Chromatin interaction

Extended variants
information (count: 124 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs1003280	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs1073522	0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.88[ASN][1000 genomes]
rs1122873	0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.88[ASN][1000 genomes]
rs12165286	0.85[YRI][hapmap]
rs12626757	0.87[ASN][1000 genomes]
rs12627667	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs1378079	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs1378080	0.86[CHB][hapmap];0.81[JPT][hapmap];0.83[YRI][hapmap];0.88[ASN][1000 genomes]
rs141521	0.86[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]
rs1454648	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs1454650	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs1454651	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs1584917	0.93[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs1584918	0.93[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs1598206	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs162343	1.00[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs162344	0.86[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs162345	0.86[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs162366	0.86[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162367	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs162368	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162369	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs162371	0.86[CHB][hapmap];0.87[JPT][hapmap];0.88[YRI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162372	0.86[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs162373	0.89[ASN][1000 genomes]
rs162374	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs162375	0.86[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162376	0.86[CHB][hapmap];0.87[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162377	0.86[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs162378	0.86[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs162380	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs162381	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs162388	0.86[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162389	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162391	0.96[ASN][1000 genomes]
rs162393	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162394	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162395	0.94[ASN][1000 genomes]
rs162396	0.94[ASN][1000 genomes]
rs162398	1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs162399	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162400	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162402	0.90[ASN][1000 genomes]
rs162403	0.90[ASN][1000 genomes]
rs162404	0.88[ASN][1000 genomes]
rs167930	0.91[ASN][1000 genomes]
rs189094	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2246602	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs229357	0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.87[ASN][1000 genomes]
rs230640	1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs230642	1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs230643	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs230644	0.87[ASN][1000 genomes]
rs230645	1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs230646	1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs230647	0.94[ASN][1000 genomes]
rs2329442	0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs2838316	0.86[CHB][hapmap];0.80[JPT][hapmap];0.95[YRI][hapmap];0.87[ASN][1000 genomes]
rs2838317	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs2838319	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs2838320	0.95[YRI][hapmap]
rs2838321	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs2838322	0.87[ASN][1000 genomes]
rs2838323	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs2838324	0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.87[ASN][1000 genomes]
rs2838328	0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs2838329	0.88[ASN][1000 genomes]
rs2838330	0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs2838331	0.86[CHB][hapmap];0.81[JPT][hapmap];0.82[YRI][hapmap];0.88[ASN][1000 genomes]
rs2838336	0.86[CHB][hapmap]
rs2838337	0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap]
rs2838338	0.86[CHB][hapmap]
rs2838339	0.86[CHB][hapmap];0.95[YRI][hapmap]
rs2838341	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs2838343	0.86[CHB][hapmap]
rs28840140	0.88[ASN][1000 genomes]
rs3788062	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs463738	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4818833	0.82[ASN][1000 genomes]
rs4818843	0.87[ASN][1000 genomes]
rs4818850	0.85[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs4818856	0.88[ASN][1000 genomes]
rs4819219	0.91[YRI][hapmap]
rs4819264	0.86[ASN][1000 genomes]
rs4819270	0.92[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs4997353	0.81[ASN][1000 genomes]
rs6518301	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs6518302	0.86[CHB][hapmap];0.81[JPT][hapmap];0.95[YRI][hapmap];0.88[ASN][1000 genomes]
rs6518309	0.86[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs7276215	0.93[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.85[ASN][1000 genomes]
rs7276316	0.81[ASN][1000 genomes]
rs7276633	0.86[CHB][hapmap]
rs7277539	0.80[JPT][hapmap];0.82[YRI][hapmap]
rs7279958	0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs7279968	0.86[CHB][hapmap]
rs7282933	0.88[ASN][1000 genomes]
rs8133523	0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap]
rs86138	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs86139	0.86[CHB][hapmap];0.87[JPT][hapmap];0.88[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs91424	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs9306159	0.86[CHB][hapmap]
rs9976441	0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs9978811	0.85[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs9978934	0.91[YRI][hapmap]
rs9979935	0.91[YRI][hapmap]
rs9980185	0.81[JPT][hapmap]
rs9981291	0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs9981790	0.82[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs9983752	0.95[YRI][hapmap]
rs9983763	0.86[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs9984002	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057726	chr21:44711850-44957303	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
2	nsv544466	chr21:44711850-44957303	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv913868	chr21:44835508-44954522	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS 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	98 gene(s)	inside rSNPs	diseases
4	esv1839560	chr21:44864079-44973184	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
5	nsv913873	chr21:44879869-45142427	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
6	nsv587689	chr21:44884252-44986050	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
7	nsv1059264	chr21:44895863-44944515	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv1061539	chr21:44915533-45041824	Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
9	nsv1067171	chr21:44921187-45039471	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
10	nsv521700	chr21:44925334-45041790	Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
11	nsv470903	chr21:44925334-45061501	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
12	nsv459289	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
13	nsv587690	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44926800-44938200	Enhancers	Fetal Thymus	thymus
2	chr21:44928800-44941000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr21:44929200-44937800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr21:44929200-44938200	Enhancers	HSMM	muscle
5	chr21:44929200-44943400	Enhancers	Placenta Amnion	Placenta Amnion
6	chr21:44929600-44943400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr21:44929800-44938600	Enhancers	Esophagus	oesophagus
8	chr21:44929800-44938800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr21:44929800-44943600	Enhancers	HMEC	breast
10	chr21:44930200-44938400	Enhancers	Pancreas	Pancrea
11	chr21:44930200-44939000	Enhancers	Fetal Intestine Small	intestine
12	chr21:44930600-44939800	Enhancers	Fetal Intestine Large	intestine
13	chr21:44930800-44937800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr21:44932000-44937200	Weak transcription	Colon Smooth Muscle	Colon
15	chr21:44932600-44937800	Enhancers	Liver	Liver
16	chr21:44933400-44938200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr21:44934000-44938400	Enhancers	Adipose Nuclei	Adipose
18	chr21:44934000-44938400	Enhancers	Left Ventricle	heart
19	chr21:44934000-44938400	Enhancers	Lung	lung
20	chr21:44934200-44937800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr21:44934200-44937800	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr21:44934200-44938000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr21:44934200-44938000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr21:44934200-44938000	Enhancers	Duodenum Mucosa	Duodenum
25	chr21:44934400-44937600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr21:44934400-44938200	Enhancers	NH-A	brain
27	chr21:44934400-44938400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr21:44934400-44941200	Enhancers	HUVEC	blood vessel
29	chr21:44934600-44937200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr21:44934600-44937200	Enhancers	Thymus	Thymus
31	chr21:44934600-44937800	Enhancers	Primary hematopoietic stem cells	blood
32	chr21:44934600-44938000	Enhancers	Small Intestine	intestine
33	chr21:44934600-44938200	Enhancers	Right Atrium	heart
34	chr21:44934600-44938400	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr21:44934600-44940200	Enhancers	Placenta	Placenta
36	chr21:44934800-44937000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr21:44934800-44937200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr21:44934800-44937600	Weak transcription	Gastric	stomach
39	chr21:44935400-44938000	Enhancers	Fetal Stomach	stomach
40	chr21:44935400-44938400	Enhancers	Right Ventricle	heart
41	chr21:44935400-44943400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr21:44935600-44937000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr21:44935800-44937400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr21:44935800-44937400	Flanking Active TSS	HepG2	liver
45	chr21:44935800-44938000	Enhancers	Fetal Muscle Leg	muscle
46	chr21:44935800-44938200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr21:44935800-44938400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr21:44935800-44938400	Enhancers	Fetal Lung	lung
49	chr21:44936000-44937200	Enhancers	Spleen	Spleen
50	chr21:44936000-44937800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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