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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS060-13278
Organism
Homo sapiens
Tissue/cell
GM12891
Coordinate
chr16:67866540-67867650
Target genes
Number: 23
Name
Ensembl ID
AC009095.4
ENSG00000237718
RLTPR
ENSG00000159753
C16orf86
ENSG00000159761
RANBP10
ENSG00000141084
TSNAXIP1
ENSG00000102904
THAP11
ENSG00000168286
NUTF2
ENSG00000102898
CENPT
ENSG00000102901
CTC
ENSG00000262141
EDC4
ENSG00000038358
AC040162.1
ENSG00000221526
NRN1L
ENSG00000188038
PSKH1
ENSG00000159792
CTRL
ENSG00000141086
PSMB10
ENSG00000205220
LCAT
ENSG00000213398
SLC12A4
ENSG00000124067
DUS2L
ENSG00000167264
DPEP2
ENSG00000167261
KARSP3
ENSG00000262962
DDX28
ENSG00000182810
AC130462.1
ENSG00000221789
NFATC3
ENSG00000072736
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
CGTTTTCCCT CAGGGCTAGG GACCCAGAAA CCACTTGCCC CTACCATCGC CCCTGTTCCC 60
AGCCCTATGT CACCAGCAGT GTGGACCGAA GAAGACCCCT GGGGTATGGG AATAGAGAGG 120
GCATATGAGT GAACCAACCA GGAGGGGCTG GGAAAGGCTT CACAGAGGTG ACTTCAGCAG 180
AATCACAAAG GATAAGTAGG GGTTAGCCAC ACAGAAAAGA GGGGCAATTG GAAAAGCATC 240
CACCCCAGAC ATGAAAGTAA CAATCCATGA TGGATACTAA AGTATTTTAA AATCTTTTAA 300
GAACTTGGGT ACCCCAGACA CCTTAGTCTC TCCAGTCCAG TCCCTCTCAG ATTCCAGAGC 360
CACATAAGTG TTCCCAGGGC GCAGCTCCTA CCTCATGGGT GTAAAACCTA TAATGAATGG 420
CTTCTCATTC CCTATAAAGA AACTCCACTG TCCCAGTCTG GCAGATGTCA ACGTATGCAT 480
CCTCTGCACC ATGAGCTCAC CACAGCCCTC ACCCACTGCC ACTCCCACTG ACTCAGGCCA 540
AATTCCCTGC TCCTTAGCAA AGCATCTTCC AGTTGCTGCC TCCCAACTTC TGCCCAGGCT 600
GTCCTCTAGC TCCTTTCCCA TTTCCCAGCT GGGAGCTACA AGGACAGTAA GACAATGAGC 660
AGGAACAGTG GGAACCCTCG GGACGCAGAA GTTCAGGGCA AATGCCTAGG CACACCCTGG 720
CTGGTCTGGG GAAAGCTGCC TAGAGAACAG AGCAGAAGGT GAGATTCTGA ACCCCTATCC 780
TCCATCTCCA GTGGCCGAGC CCCCAGAGAC CCGGGATCAG TCAGGCTCTG TGGTCCCGAG 840
GGCTGGCTGC CTGGAGCCCT GGGGGCAGGG GCACAAACAG CTGGCCCGGG CCCGGCTAGA 900
GCAATGGAAC CAGTTCTCAG AGTCCCAGGC CCTGCTCCTC TCTGAGACTC AGTTTTCCTC 960
TTCGAACAGA GTCGACGCTG GGTTCCACCC AGACCCTGCT CCTCTCTGAG ACTCAGTTTT 1020
CCTCTTCGAA CAGAGTCGAC GCTGGGTTCC ACCCAGACCC CACTCCCCGG TCCCTCTAGT 1080
TGCTCAAGTA CTCGGGGAGC CCCCTCACAT 1110