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

TagContent
EnhancerAtlas ID
HS048-13699 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr16:512840-513430 
Target genes
Number: 40             
NameEnsembl ID
HBA1ENSG00000206172
Z69890.1ENSG00000206168
Z97634.5ENSG00000236829
Z97634.3ENSG00000241145
RP1ENSG00000230428
AL049542.1ENSG00000256323
LA16cENSG00000261691
JMJD8ENSG00000161999
MSLNENSG00000102854
FAM195AENSG00000172366
RPUSD1ENSG00000007376
STUB1ENSG00000103266
HAGHLENSG00000103253
NARFLENSG00000103245
C16orf13ENSG00000130731
RHBDL1ENSG00000103269
WFIKKN1ENSG00000127578
RAB40CENSG00000197562
NHLRC4ENSG00000257108
PIGQENSG00000007541
ITFG3ENSG00000167930
METRNENSG00000103260
FBXL16ENSG00000127585
Z98881.1ENSG00000196674
CHTF18ENSG00000127586
WDR90ENSG00000161996
WDR24ENSG00000127580
NME4ENSG00000103202
TMEM8AENSG00000129925
MRPL28ENSG00000086504
AXIN1ENSG00000103126
MIR662ENSG00000207579
RGS11ENSG00000076344
RAB11FIP3ENSG00000090565
DECR2ENSG00000242612
AL022341.3ENSG00000228201
AL022341.1ENSG00000197727
RHOT2ENSG00000140983
SOLHENSG00000103326
C16orf11ENSG00000161992
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr16512930513020
Number: 1             
IDChromosomeStartEnd
GH16I000463chr16513201513350
Enhancer Sequence
CCATCCCTTC CCCAGCACCA TCCCTTCCTC AGCACAATGT CTTCCCCAGC ACAATGTCTT 60
CCCCAGCACC ATCCCTTTCC CAGCACGATC CGTTGCGTGC TTGTGCCGTA TTTCGTTTCT 120
TCATTCTCCT GGTGATGGGC ACGTTTGTGT ACAACTCTTT GTGTGGATGC GTGTCTTCAA 180
GTCCTTGGGG CCTGTATCTA GGAGTGGGTC ATGTGCTGGG GTAAACTCGG TTCTTCACAG 240
TGGCCGTGCC TTTTCACACT CTCACCAGTC CCCATACTAT ACACTGTCCG TCTTACGTCA 300
AGTTCTGAAG CTCTGAACAG GCCATCTCAC TTCCTCATGT TTGGCCAGGC GGTGTAGGGG 360
TGACGGTGGC GGGTCCTTTC CCTCCTTCAT GCACGTGCAG GATAAGTAGA CCTTGGCTGG 420
GGCCCTCAGA GTCAGCAGGT GCAGTGAGGG AGACGGATGC CCTTGGACCT CGACCTCAGG 480
TCTTGTCTGT CTCCTCCACA GAATTATTGC CTGACAGTGT CTCTAAGGGT TTTCTCAGAT 540
GCCAAGTCTT TAGATGGCTC TGGGGAAACG TGCTGTGTGT TGTTCCCCGG 590