EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-10749 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr16:512560-513320 
Target genes
Number: 45             
NameEnsembl ID
Z69890.1ENSG00000206168
Z97634.5ENSG00000236829
Z97634.3ENSG00000241145
LA16cENSG00000261691
JMJD8ENSG00000161999
FAM195AENSG00000172366
RPUSD1ENSG00000007376
STUB1ENSG00000103266
HAGHLENSG00000103253
NARFLENSG00000103245
C16orf13ENSG00000130731
RHBDL1ENSG00000103269
WFIKKN1ENSG00000127578
RAB40CENSG00000197562
NHLRC4ENSG00000257108
PIGQENSG00000007541
ITFG3ENSG00000167930
FAM173AENSG00000103254
METRNENSG00000103260
FBXL16ENSG00000127585
LUC7LENSG00000007392
CHTF18ENSG00000127586
CCDC78ENSG00000162004
WDR90ENSG00000161996
Z84812.3ENSG00000233614
Z84812.4ENSG00000260803
WDR24ENSG00000127580
WASIR2ENSG00000231439
NME4ENSG00000103202
WASH4PENSG00000234769
TMEM8AENSG00000129925
MRPL28ENSG00000086504
AXIN1ENSG00000103126
RGS11ENSG00000076344
RAB11FIP3ENSG00000090565
DECR2ENSG00000242612
AL022341.3ENSG00000228201
SNRNP25ENSG00000161981
RHBDF1ENSG00000007384
POLR3KENSG00000161980
MPGENSG00000103152
NPRL3ENSG00000103148
RHOT2ENSG00000140983
SOLHENSG00000103326
LMF1ENSG00000103227
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr16512930513020
chr16512688513189
Number: 1             
IDChromosomeStartEnd
GH16I000463chr16513201513350
Enhancer Sequence
TTCGCGTGCT CTCACTTGGC TTCTTTCCTC AGCACGATCC CTTCCCCAGC ACGATCCCTT 60
CCCCAGCACC ATCCCTTCCC CAGCACCATC CCTTCCGCAG CACCGTCCCT TCCCCGGCAC 120
CGTCCCTTCC CCAGTCCCCC GGCACCGTCC CTTCCCCAGT CCCTTCCCCA GCACCATCCC 180
TTCCCCAGCA CCGCACCATC CCTTCCCCAG CACCGTCCCT TCCCCAGCAC CATCCCTTCC 240
CCAGCACCGT CCCTTCCCCA GCACGATCCC TTCCCCAGCA CCATCCCTTC CCCAGCACCA 300
TCCCTTCCTC AGCACAATGT CTTCCCCAGC ACAATGTCTT CCCCAGCACC ATCCCTTTCC 360
CAGCACGATC CGTTGCGTGC TTGTGCCGTA TTTCGTTTCT TCATTCTCCT GGTGATGGGC 420
ACGTTTGTGT ACAACTCTTT GTGTGGATGC GTGTCTTCAA GTCCTTGGGG CCTGTATCTA 480
GGAGTGGGTC ATGTGCTGGG GTAAACTCGG TTCTTCACAG TGGCCGTGCC TTTTCACACT 540
CTCACCAGTC CCCATACTAT ACACTGTCCG TCTTACGTCA AGTTCTGAAG CTCTGAACAG 600
GCCATCTCAC TTCCTCATGT TTGGCCAGGC GGTGTAGGGG TGACGGTGGC GGGTCCTTTC 660
CCTCCTTCAT GCACGTGCAG GATAAGTAGA CCTTGGCTGG GGCCCTCAGA GTCAGCAGGT 720
GCAGTGAGGG AGACGGATGC CCTTGGACCT CGACCTCAGG 760