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

HS133-19899

Organism

Homo sapiens

Tissue/cell

melanoma

Coordinate

chr20:60922080-60923070

Target genes

Number: 22
Name	Ensembl ID

RP11	ENSG00000225106
TAF4	ENSG00000130699
LSM14B	ENSG00000149657
PSMA7	ENSG00000101182
SS18L1	ENSG00000184402
GTPBP5	ENSG00000101181
HRH3	ENSG00000101180
OSBPL2	ENSG00000130703
ADRM1	ENSG00000130706
LAMA5	ENSG00000130702
RPS21	ENSG00000171858
CABLES2	ENSG00000149679
SLCO4A1	ENSG00000101187
C20orf20	ENSG00000101189
OGFR	ENSG00000060491
COL9A3	ENSG00000092758
DPH3P1	ENSG00000233838
TCFL5	ENSG00000101190
DIDO1	ENSG00000101191
C20orf11	ENSG00000101193
SLC17A9	ENSG00000101194
NKAIN4	ENSG00000101198

TF binding sites/motifs

Number: 1

JASPAR ID

Coordinate

Motif Sequence

Strand

-Log10(p-value)

ZIC1

MA0696.1

chr20:60922201-60922215

GGCCCCCCGCTGCT

6.16

dbSUPER

Number of super-enhancer constituents: 2
ID	Coordinate	Tissue/cell

SE_61548	chr20:60911909-60958488	Toledo
SE_65356	chr20:60921947-60923207	Pancreatic_islets

HEDD

Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome	Start	End

chr20	60922495	60922535
chr20	60922274	60922332

GeneHancer

Number: 1
ID	Chromosome	Start	End

GH20I062346

chr20

60921948

60923207

Enhancer Sequence

CAGCCTGTGG GGTACACAGG AGGGGGGATC AGGCCCATCC TGGAGGCAGG TGGCAGGTGC 60
TCAGTCCCTT CCCTGAAGGG GCCTGTGATC CCCTCGATGG CTTGGCTTGC CACATGGACA 120
CGGCCCCCCG CTGCTGTTTC TCCAGCTGTC CGGCAGCAAG CGCTCGCCCA GACTCAGCGT 180
CCCCGAGCCT GTGGCTCTGA CGCAACTTCC CCAGGCTCAG GGAATGGACA CAAGGAAAGA 240
GGCGGTGGAG GACAGGGTCT CACAGGGCCT TTGTGGAGGC GGGACTGGGG AGCAGGTGTG 300
CACTGACCGG GTGGGGCCTA GGACAGGGCA CCTCAGGGGT CAGTAGAGTC CCCCTTGCCT 360
GCAGGTCAGG ATGGAGACCT GCGTTCTCCA AAACTGAGTT ATGCCCTTTC CACTTCGGCC 420
AGGACTCGAG CGTAAGCCCA AAACCTCCCT GAGCCAGAAG GGAAAGGGGT CCATTTGCAC 480
CCCCCAAGGC TCAGATTTCG CTTAGCAGGC AGGACTCCTA GGCATCCTGG TCACCTCCCT 540
AGGGCCAAGT GGCCAAGAAC TGCTTCCTTC TTCCAGCTGG GGTGGACACT AAGTCACAGG 600
GCTGGAATCT TGCCTTACGT CCCGTGGGCA GGGTGACAGC TGGAGAGAGA CAAGGCCTGA 660
GGTTGGAAGC ACCTACTGCT CAGTATTAGC CAGACCACAG CGGGAGTCCC TGCCCCAGAT 720
CAGGCTCTGC CGGAGGCTGC AGGGCCGTGC GTTCCCTGAG CAGGACCCCA GAAGTCAGTC 780
CAGTCCATGA GGATTAGACC CAGAGCCTCA AATGGTCCAG CTCTAGTCCT GTCCTCCACG 840
GGGCCCACCT CACAGGGCCT CGGGAATCAA TACTGCTTTC CCTCAGAATC CAGAAACATC 900
TGGGAGGGCC ATACCCTCAA TGAGAGGAAT TGGGAAATAA ACTGCCCGTC AGCACAGGTG 960
ATCAACAAAG AAGCTGCTCT GTCGTCACAC 990