Variant report

Variant	rs162388
Chromosome Location	chr21:44936032-44936033
allele	A/G
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:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:44935245..44937496-chr21:45021049..45022786,2	MCF-7	breast:
2	chr21:44839515..44855046-chr21:44918803..44938582,70	MCF-7	breast:
3	chr21:44934187..44937130-chr21:45020979..45023437,3	MCF-7	breast:
4	chr21:44935059..44936997-chr21:45153609..45155904,2	MCF-7	breast:
5	chr21:44934887..44937881-chr21:45009259..45012818,3	MCF-7	breast:
6	chr21:44935610..44937483-chr21:44946827..44948859,2	MCF-7	breast:
7	chr21:44909088..44910939-chr21:44934470..44936766,2	MCF-7	breast:
8	chr21:44763296..44765156-chr21:44933587..44936210,2	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	chr21:44933239..44939119-chr21:45027942..45032046,11	MCF-7	breast:
12	chr21:44932097..44937071-chr21:45004878..45007611,5	MCF-7	breast:
13	chr21:44934396..44939488-chr21:45063795..45068503,7	MCF-7	breast:
14	chr21:44935247..44938888-chr21:45036868..45039173,3	MCF-7	breast:
15	chr21:44763228..44765264-chr21:44934553..44936247,2	MCF-7	breast:
16	chr21:44759707..44762996-chr21:44935896..44938308,3	MCF-7	breast:
17	chr21:44935626..44937329-chr21:45067508..45070010,2	MCF-7	breast:
18	chr21:44935195..44942837-chr21:45027341..45034401,13	MCF-7	breast:
19	chr21:44896300..44899568-chr21:44934496..44937957,5	MCF-7	breast:
20	chr21:44934950..44937426-chr21:44968683..44970792,2	MCF-7	breast:
21	chr21:44933741..44936265-chr21:45043174..45044886,2	MCF-7	breast:
22	chr21:44935152..44938727-chr21:45130277..45133903,3	MCF-7	breast:
23	chr21:44935404..44937954-chr8:127569330..127571915,2	MCF-7	breast:
24	chr21:44844533..44847872-chr21:44929082..44940063,13	MCF-7	breast:

No data

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

Extended variants
information (count: 137 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:124)

rs_ID	r²[population]
rs1003280	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs1073522	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs11089020	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs1122873	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs11701518	0.87[CHB][hapmap];0.90[YRI][hapmap]
rs12626757	0.90[ASN][1000 genomes]
rs12627667	0.82[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.84[YRI][hapmap]
rs1378079	0.81[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];0.91[ASN][1000 genomes]
rs1378080	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs141521	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.93[ASN][1000 genomes]
rs1454648	1.00[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs1454650	1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs1454651	1.00[CHB][hapmap];0.87[JPT][hapmap];0.81[YRI][hapmap];0.90[ASN][1000 genomes]
rs1584917	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs1584918	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs1598206	0.81[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs162343	0.89[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.97[YRI][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs162344	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162345	0.88[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs162366	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs162367	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs162368	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs162369	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs162371	0.93[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162372	1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs162373	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs162374	0.94[ASN][1000 genomes]
rs162375	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs162376	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs162377	1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs162378	1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[YRI][hapmap];0.93[ASN][1000 genomes]
rs162379	0.81[CEU][hapmap]
rs162380	0.86[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs162381	0.86[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs162389	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs162390	0.86[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162391	0.93[ASN][1000 genomes]
rs162393	0.91[ASN][1000 genomes]
rs162394	0.94[ASN][1000 genomes]
rs162395	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162396	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162398	0.89[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162399	0.83[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs162400	0.82[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs162402	0.93[ASN][1000 genomes]
rs162403	0.93[ASN][1000 genomes]
rs162404	0.91[ASN][1000 genomes]
rs167930	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1836856	0.87[CHB][hapmap];0.90[YRI][hapmap]
rs189094	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2246602	1.00[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs229357	1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs230640	0.86[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs230642	0.92[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs230643	0.91[ASN][1000 genomes]
rs230644	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs230645	0.89[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes]
rs230646	0.89[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs230647	0.91[ASN][1000 genomes]
rs2329442	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs2329443	0.80[ASN][1000 genomes]
rs2838316	1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs2838317	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[YRI][hapmap];0.90[ASN][1000 genomes]
rs2838318	0.85[CEU][hapmap]
rs2838319	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[YRI][hapmap];0.90[ASN][1000 genomes]
rs2838320	0.80[CEU][hapmap];0.86[CHB][hapmap]
rs2838321	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.84[YRI][hapmap];0.90[ASN][1000 genomes]
rs2838322	0.90[ASN][1000 genomes]
rs2838323	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs2838324	1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs2838325	0.81[CEU][hapmap];0.81[CHB][hapmap]
rs2838326	0.81[CEU][hapmap];0.81[CHB][hapmap]
rs2838328	0.82[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs2838329	0.91[ASN][1000 genomes]
rs2838330	0.82[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs2838331	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs2838336	0.81[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.84[YRI][hapmap]
rs2838337	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs2838338	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2838339	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2838340	0.81[CEU][hapmap];0.81[CHB][hapmap]
rs2838341	0.81[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.86[YRI][hapmap]
rs2838343	0.82[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.81[YRI][hapmap]
rs28840140	0.91[ASN][1000 genomes]
rs3788062	1.00[CHB][hapmap];0.87[JPT][hapmap];0.93[YRI][hapmap];0.90[ASN][1000 genomes]
rs389278	0.86[CHB][hapmap]
rs463738	0.91[ASN][1000 genomes]
rs4818833	0.84[ASN][1000 genomes]
rs4818843	0.90[ASN][1000 genomes]
rs4818850	0.82[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs4818856	0.91[ASN][1000 genomes]
rs4819212	0.87[CHB][hapmap]
rs4819219	0.87[CHB][hapmap]
rs4819264	0.89[ASN][1000 genomes]
rs4819270	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs4997353	0.84[ASN][1000 genomes]
rs6518301	0.82[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.87[YRI][hapmap];0.90[ASN][1000 genomes]
rs6518302	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs6518309	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs7275705	0.81[ASN][1000 genomes]
rs7276215	1.00[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs7276316	0.84[ASN][1000 genomes]
rs7276633	1.00[CHB][hapmap];0.82[JPT][hapmap];0.86[YRI][hapmap]
rs7277539	0.86[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs7279958	0.82[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.84[YRI][hapmap];0.91[ASN][1000 genomes]
rs7279959	0.86[CHB][hapmap]
rs7279968	0.82[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.84[YRI][hapmap]
rs7282933	0.91[ASN][1000 genomes]
rs7283362	0.87[CHB][hapmap];0.93[YRI][hapmap]
rs8131005	0.82[CEU][hapmap]
rs8131020	0.87[CHB][hapmap];0.93[YRI][hapmap]
rs8133523	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs86138	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs86139	0.93[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs91424	0.86[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs9306159	1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs9974710	0.80[ASN][1000 genomes]
rs9976441	0.82[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs9978811	0.83[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.89[YRI][hapmap];0.90[ASN][1000 genomes]
rs9980185	0.93[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs9981291	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs9981790	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs9983763	1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]
rs9984002	0.87[JPT][hapmap];0.81[ASN][1000 genomes]

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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs162388	HSF2BP	cis	Lymphoblastoid	GTEx
rs162388	HSF2BP	cis	multi-tissue	Pritchard

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44919800-44936800	Weak transcription	Fetal Brain Female	brain
2	chr21:44923400-44936600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr21:44923400-44936600	Weak transcription	Brain Germinal Matrix	brain
4	chr21:44926800-44938200	Enhancers	Fetal Thymus	thymus
5	chr21:44928800-44941000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr21:44929200-44937800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr21:44929200-44938200	Enhancers	HSMM	muscle
8	chr21:44929200-44943400	Enhancers	Placenta Amnion	Placenta Amnion
9	chr21:44929600-44943400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr21:44929800-44938600	Enhancers	Esophagus	oesophagus
11	chr21:44929800-44938800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr21:44929800-44943600	Enhancers	HMEC	breast
13	chr21:44930200-44938400	Enhancers	Pancreas	Pancrea
14	chr21:44930200-44939000	Enhancers	Fetal Intestine Small	intestine
15	chr21:44930600-44939800	Enhancers	Fetal Intestine Large	intestine
16	chr21:44930800-44937800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr21:44931400-44936400	Weak transcription	Fetal Kidney	kidney
18	chr21:44932000-44937200	Weak transcription	Colon Smooth Muscle	Colon
19	chr21:44932200-44936200	Weak transcription	Fetal Heart	heart
20	chr21:44932400-44936400	Enhancers	Stomach Mucosa	stomach
21	chr21:44932600-44937800	Enhancers	Liver	Liver
22	chr21:44932800-44936400	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr21:44933400-44938200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr21:44934000-44936400	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr21:44934000-44938400	Enhancers	Adipose Nuclei	Adipose
26	chr21:44934000-44938400	Enhancers	Left Ventricle	heart
27	chr21:44934000-44938400	Enhancers	Lung	lung
28	chr21:44934200-44936200	Enhancers	NHEK	skin
29	chr21:44934200-44936800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr21:44934200-44937800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr21:44934200-44937800	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr21:44934200-44938000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr21:44934200-44938000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr21:44934200-44938000	Enhancers	Duodenum Mucosa	Duodenum
35	chr21:44934400-44937600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr21:44934400-44938200	Enhancers	NH-A	brain
37	chr21:44934400-44938400	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr21:44934400-44941200	Enhancers	HUVEC	blood vessel
39	chr21:44934600-44937200	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr21:44934600-44937200	Enhancers	Thymus	Thymus
41	chr21:44934600-44937800	Enhancers	Primary hematopoietic stem cells	blood
42	chr21:44934600-44938000	Enhancers	Small Intestine	intestine
43	chr21:44934600-44938200	Enhancers	Right Atrium	heart
44	chr21:44934600-44938400	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr21:44934600-44940200	Enhancers	Placenta	Placenta
46	chr21:44934800-44937000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr21:44934800-44937200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr21:44934800-44937600	Weak transcription	Gastric	stomach
49	chr21:44935000-44936200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr21:44935200-44936200	Enhancers	Hela-S3	cervix

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