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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS105-31240
Organism
Homo sapiens
Tissue/cell
IMR90
Coordinate
chr16:67866480-67867650
Target genes
Number: 20
Name
Ensembl ID
AC009095.4
ENSG00000237718
RLTPR
ENSG00000159753
ACD
ENSG00000102977
C16orf48
ENSG00000124074
C16orf86
ENSG00000159761
RANBP10
ENSG00000141084
TSNAXIP1
ENSG00000102904
THAP11
ENSG00000168286
NUTF2
ENSG00000102898
CENPT
ENSG00000102901
EDC4
ENSG00000038358
CTC
ENSG00000263126
NRN1L
ENSG00000188038
PSKH1
ENSG00000159792
CTRL
ENSG00000141086
PSMB10
ENSG00000205220
LCAT
ENSG00000213398
SLC12A4
ENSG00000124067
DUS2L
ENSG00000167264
DDX28
ENSG00000182810
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr16
67867011
67867153
chr16
67866717
67866788
Enhancer Sequence
ACGGTGAGGA GGGATAGAGA ATATAGAGAC ATGCCTTCAT CAGGGGTCTT GGTCTGGAGC 60
CGTTTTCCCT CAGGGCTAGG GACCCAGAAA CCACTTGCCC CTACCATCGC CCCTGTTCCC 120
AGCCCTATGT CACCAGCAGT GTGGACCGAA GAAGACCCCT GGGGTATGGG AATAGAGAGG 180
GCATATGAGT GAACCAACCA GGAGGGGCTG GGAAAGGCTT CACAGAGGTG ACTTCAGCAG 240
AATCACAAAG GATAAGTAGG GGTTAGCCAC ACAGAAAAGA GGGGCAATTG GAAAAGCATC 300
CACCCCAGAC ATGAAAGTAA CAATCCATGA TGGATACTAA AGTATTTTAA AATCTTTTAA 360
GAACTTGGGT ACCCCAGACA CCTTAGTCTC TCCAGTCCAG TCCCTCTCAG ATTCCAGAGC 420
CACATAAGTG TTCCCAGGGC GCAGCTCCTA CCTCATGGGT GTAAAACCTA TAATGAATGG 480
CTTCTCATTC CCTATAAAGA AACTCCACTG TCCCAGTCTG GCAGATGTCA ACGTATGCAT 540
CCTCTGCACC ATGAGCTCAC CACAGCCCTC ACCCACTGCC ACTCCCACTG ACTCAGGCCA 600
AATTCCCTGC TCCTTAGCAA AGCATCTTCC AGTTGCTGCC TCCCAACTTC TGCCCAGGCT 660
GTCCTCTAGC TCCTTTCCCA TTTCCCAGCT GGGAGCTACA AGGACAGTAA GACAATGAGC 720
AGGAACAGTG GGAACCCTCG GGACGCAGAA GTTCAGGGCA AATGCCTAGG CACACCCTGG 780
CTGGTCTGGG GAAAGCTGCC TAGAGAACAG AGCAGAAGGT GAGATTCTGA ACCCCTATCC 840
TCCATCTCCA GTGGCCGAGC CCCCAGAGAC CCGGGATCAG TCAGGCTCTG TGGTCCCGAG 900
GGCTGGCTGC CTGGAGCCCT GGGGGCAGGG GCACAAACAG CTGGCCCGGG CCCGGCTAGA 960
GCAATGGAAC CAGTTCTCAG AGTCCCAGGC CCTGCTCCTC TCTGAGACTC AGTTTTCCTC 1020
TTCGAACAGA GTCGACGCTG GGTTCCACCC AGACCCTGCT CCTCTCTGAG ACTCAGTTTT 1080
CCTCTTCGAA CAGAGTCGAC GCTGGGTTCC ACCCAGACCC CACTCCCCGG TCCCTCTAGT 1140
TGCTCAAGTA CTCGGGGAGC CCCCTCACAT 1170