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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS129-00721
Organism
Homo sapiens
Tissue/cell
MCF10A
Coordinate
chr1:28921090-28922430
Target genes
Number: 29
Name
Ensembl ID
AL512288.1
ENSG00000240750
EYA3
ENSG00000158161
RP5
ENSG00000228589
PTAFR
ENSG00000169403
DNAJC8
ENSG00000126698
ATPIF1
ENSG00000130770
SESN2
ENSG00000130766
MED18
ENSG00000130772
PHACTR4
ENSG00000204138
RP1
ENSG00000229820
U6atac
ENSG00000221216
RCC1
ENSG00000180198
SNHG3
ENSG00000242125
SNORA73A
ENSG00000201808
SNORA73B
ENSG00000200087
PRDX3P2
ENSG00000231468
TRNAU1AP
ENSG00000180098
SNORA61
ENSG00000207311
SNORA44
ENSG00000207314
SNORA16A
ENSG00000207070
SNHG12
ENSG00000197989
RAB42
ENSG00000188060
TAF12
ENSG00000120656
RP11
ENSG00000229388
RNU11
ENSG00000209804
GMEB1
ENSG00000162419
YTHDF2
ENSG00000198492
EPB41
ENSG00000159023
RP4
ENSG00000225616
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
28921140
28921558
Enhancer Sequence
AAAAAAAAGA AAAGAAAAGA AAGGCCTGAG AGACCAGATG TGCAACTTCC TGTCCTTGAG 60
CCTCAGTGTC CCTATCTATC GATGGGGCTC ATAAAAGATC CCACCTTGAA GGGAGGTGGT 120
GACCACAAAT GAGACAGTGG ACAGGATGTG CTCACCCAGA GCCTGCCGCG CTGTGAATTG 180
AATGACAAAA GCTCTCATTC CCACTCCCTT TTTCTTGGCT GCGATGTGGC CACTCTGGCA 240
GCATTCCTGG GCTCAGACAC TGAGAAGCCA GCGTCAGGAA GCTGATGCAT GGGCAAAGGC 300
AGGTGCGGGG AATTCCAGGG GGAGCTTGGC TTGGAGGCTT CTTATGTCCT CAGGCTAAAA 360
TGATTCTGGG CATGGGATTA ATATGTGACG TCAAACCCAG GGTTGCTGGC CAATGCCCCC 420
CCGACCAGGC CCAGGGGCTG AAAAATGGAT GTTGGAGGCT GGGATGAACA TGAATGTGTA 480
GCAACTATGT TGGGCACACA GTGGCCACTG TGATGAGCCA CCAAGATCCC CCTTTCTGGC 540
TGGGGAACCC ATCAACCCTC TCCCCAGCTG CTGGAGTGCC ACTGGATGAT GGACTTCAGC 600
TTGCCCCACT CTCTGGGAAA GGCCCTCCCT TCAGGGCAGC TTGTATCCAA AGTTCATCTC 660
CTGGGGGGCC TTAAAGGACT CCCTCTTGCC CCAGCTCTGG ACAACTCTGA AAGTCAAAAC 720
CAACTTTATC AGTCTCTGTG GGCTTCATTG AGGACACTGT TGTGACATCA TAGCCAAGTT 780
ATCCCCTTGC CCAATCCTGC TTCCTTTTCT TCCCCAAACA GGTATCCATT TCAAGAATAT 840
CCCCTAATAA ACATCTGCAC ACTCATCTCC ATCTCAGAAT CTGCCTCCTG GTAACCTAAC 900
CTATGATGGG AACTGCTAGG CAGGGAATGT CCTGGGAGCA ATTAGGGAAG GCTTCATGGA 960
AGAGACACTG TTTATGTTAG GCCGAATCTC AGCAGGTGTA GGGCTTAGTG GGTATCATTG 1020
TGCTGTAGCA AAAAGCACAG CCACTTTGCT GGGTGCAGTG GCTCACGCCT GTAATCCCAG 1080
CACTTTCGGA GGCCTAGGCA GGCAGTTCAC TTGAGGTTGG GAGTTCGAGA CCAGTATGGC 1140
CAACACGGCG AAACCCTGTC TATACTAAAA ATACAAAAAT TAGCTGGGTG TGGTGGCTCA 1200
TGCCTGTAAT CCCAGCACTT AGGAGGCTGA AGCATGAGAA TTGCTTGAGC CCAGGAGGCA 1260
GAGGTTGCAG CGAGCCACGA TCCCGCCACT GCACTCCAGC CCTCTAACTT GGGTGGCAGA 1320
GCAACACTCC GTCTCATAAA 1340