EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

EnhancerAtlas 2.0

Tag

Content

EnhancerAtlas ID

HS091-18550

Organism

Homo sapiens

Tissue/cell

HepG2

Coordinate

chr16:89759880-89760580

Target genes

Number: 28
Name	Ensembl ID

RP11	ENSG00000259803
AC137932.5	ENSG00000260279
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
C16orf3	ENSG00000221819
AC133919.6	ENSG00000222019
PRDM7	ENSG00000126856

HEDD

Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome	Start	End

chr16

89760345

89760477

Enhancer Sequence

TCCTTCTGAA GCATGGTGGC CCCTGGGGAC CAGGCCTGTC TGGTGGAGGT CTCCTTGGGG 60
ATGTCAGGCC GAAGCTGCAA CTGGCCTTGG GAATGTTAAG CTACAGGGTC TGTGCACACT 120
CAGAAACGTT GGGTCTAGGA CAGCCTCCAG GACACAGCAG GGCTGTGCCA CAAAATGGTG 180
AGAGACGGGC TCAGTGGCGT CAAGGGCCTG CCTAGATCAG ACACACCTCG CCTTGAGAGC 240
TGGAAACACC GTGGCCGTGA AACCATCTCT GGAGGGAAGG CTGCTTCACG GACTGAAGGA 300
CAGGCAGCTT GCATGCTTTC CCTGGTTCTT CCTCCTGGAT ACTTTTAACC AAACAGGGTC 360
ATGCTTAGCC AGGGCTGAAT ATCAGAGTTG GTCAGAATCA GGTCAGGACC CCAGTGTCGT 420
GTACTCCCCA TCTGAGAACG GGTTGGTAGT GGCTGGTGTG GCTGTGTGCC GAGGGTCCGT 480
GGTCCCTGCG ACTCTCAGGA CACCGCTGCA CGTGACAGCT CTCGCCCCCG GCAACCATTG 540
CTGTGTGTGC CACCTGGATC TGCAGGGCCT GGGGCAGAGG GTGGTCCGAG TTGGGACAGG 600
TTTCCAGGCC ACCACAGGCT CTCGGGGAGG CTGTGTCCTG TGGAGGCCTG GGCTGGGGGA 660
GAGGAGCCGG CTGTATTGAG GTGGGTGCTT CTGTGTGTAG 700