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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS108-15428
Organism
Homo sapiens
Tissue/cell
K562
Coordinate
chr16:67866470-67867650
Target genes
Number: 23
Name
Ensembl ID
AC009095.4
ENSG00000237718
RLTPR
ENSG00000159753
C16orf48
ENSG00000124074
C16orf86
ENSG00000159761
GFOD2
ENSG00000141098
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
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
GCCGAGAATT ACGGTGAGGA GGGATAGAGA ATATAGAGAC ATGCCTTCAT CAGGGGTCTT 60
GGTCTGGAGC CGTTTTCCCT CAGGGCTAGG GACCCAGAAA CCACTTGCCC CTACCATCGC 120
CCCTGTTCCC AGCCCTATGT CACCAGCAGT GTGGACCGAA GAAGACCCCT GGGGTATGGG 180
AATAGAGAGG GCATATGAGT GAACCAACCA GGAGGGGCTG GGAAAGGCTT CACAGAGGTG 240
ACTTCAGCAG AATCACAAAG GATAAGTAGG GGTTAGCCAC ACAGAAAAGA GGGGCAATTG 300
GAAAAGCATC CACCCCAGAC ATGAAAGTAA CAATCCATGA TGGATACTAA AGTATTTTAA 360
AATCTTTTAA GAACTTGGGT ACCCCAGACA CCTTAGTCTC TCCAGTCCAG TCCCTCTCAG 420
ATTCCAGAGC CACATAAGTG TTCCCAGGGC GCAGCTCCTA CCTCATGGGT GTAAAACCTA 480
TAATGAATGG CTTCTCATTC CCTATAAAGA AACTCCACTG TCCCAGTCTG GCAGATGTCA 540
ACGTATGCAT CCTCTGCACC ATGAGCTCAC CACAGCCCTC ACCCACTGCC ACTCCCACTG 600
ACTCAGGCCA AATTCCCTGC TCCTTAGCAA AGCATCTTCC AGTTGCTGCC TCCCAACTTC 660
TGCCCAGGCT GTCCTCTAGC TCCTTTCCCA TTTCCCAGCT GGGAGCTACA AGGACAGTAA 720
GACAATGAGC AGGAACAGTG GGAACCCTCG GGACGCAGAA GTTCAGGGCA AATGCCTAGG 780
CACACCCTGG CTGGTCTGGG GAAAGCTGCC TAGAGAACAG AGCAGAAGGT GAGATTCTGA 840
ACCCCTATCC TCCATCTCCA GTGGCCGAGC CCCCAGAGAC CCGGGATCAG TCAGGCTCTG 900
TGGTCCCGAG GGCTGGCTGC CTGGAGCCCT GGGGGCAGGG GCACAAACAG CTGGCCCGGG 960
CCCGGCTAGA GCAATGGAAC CAGTTCTCAG AGTCCCAGGC CCTGCTCCTC TCTGAGACTC 1020
AGTTTTCCTC TTCGAACAGA GTCGACGCTG GGTTCCACCC AGACCCTGCT CCTCTCTGAG 1080
ACTCAGTTTT CCTCTTCGAA CAGAGTCGAC GCTGGGTTCC ACCCAGACCC CACTCCCCGG 1140
TCCCTCTAGT TGCTCAAGTA CTCGGGGAGC CCCCTCACAT 1180