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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-18551
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr16:89760640-89761070
Target genes
Number: 28
Name
Ensembl ID
ACSF3
ENSG00000176715
RP11
ENSG00000259803
AC137932.5
ENSG00000260279
AC137932.6
ENSG00000261253
RP1
ENSG00000261574
ANKRD11
ENSG00000167522
SPG7
ENSG00000197912
RPL13
ENSG00000167526
CPNE7
ENSG00000178773
DPEP1
ENSG00000015413
C16orf55
ENSG00000167523
CHMP1A
ENSG00000131165
CDK10
ENSG00000185324
SPATA2L
ENSG00000158792
ZNF276
ENSG00000158805
C16orf7
ENSG00000075399
FANCA
ENSG00000187741
SPIRE2
ENSG00000204991
TCF25
ENSG00000141002
MC1R
ENSG00000258839
AC092143.2
ENSG00000256390
TUBB3
ENSG00000198211
DEF8
ENSG00000140995
CENPBD1
ENSG00000177946
AFG3L1P
ENSG00000223959
GAS8
ENSG00000141013
DBNDD1
ENSG00000003249
AC133919.6
ENSG00000222019
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr16
89760871
89761053
chr16
89760768
89760869
Enhancer Sequence
GTGAGGAGAT ACGGTTACCG CTCCTGGGGC CTCAGGAAGG GCTGGGACAG GAGCCGGGTC 60
ACCTGGTTCC TGAGCTCAGC CTCAGGGGAG GGGCAGGAGT GCAGTGGGGT CTTTGCCAGC 120
CTCCCACTCC CAGGGAGGTG GGCCTGAGCC TGGAAACCCA GGAGGAGGTG TGAGAACTTA 180
GCTTGCTGTT CTCAGGCTGG GAGCACAGAG GTCTGGAGGA GGCACGCCTG CCCCTGCACT 240
TGTCACCCCG GGAGGCCTGC GGGGCCCAGG AGGGGAGCCA GTGGTCCCTG CCTGTCCTTC 300
ACAGTGTCCC TGACCCAGCG TGCCTCACAC TGGCAGGGTC AGCAAAGGTC TGGCTGCAGT 360
CAGGTCCTCT GTTCCTCGCG CTGGCGGGGT CAGCAGACGT CTGGCCGCAG TGAGGTCCAC 420
TGTTCTCTGC 430