EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-42431 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chrX:49049920-49050300 
Target genes
Number: 39             
NameEnsembl ID
RBM3ENSG00000102317
WDR13ENSG00000101940
WASENSG00000015285
SUV39H1ENSG00000101945
AC115617.2ENSG00000233585
U6ENSG00000207367
GATA1ENSG00000102145
HDAC6ENSG00000094631
PCSK1NENSG00000102109
PQBP1ENSG00000102103
TIMM17BENSG00000126768
SLC35A2ENSG00000102100
PIM2ENSG00000102096
AF207550.1ENSG00000184596
OTUD5ENSG00000068308
KCND1ENSG00000102057
GRIPAP1ENSG00000068400
TFE3ENSG00000068323
CCDC120ENSG00000147144
PRAF2ENSG00000243279
U4ENSG00000206936
WDR45ENSG00000196998
GPKOWENSG00000068394
MAGIXENSG00000017621
PLP2ENSG00000102007
PRICKLE3ENSG00000012211
SYPENSG00000237341
CACNA1FENSG00000102001
HSPB1P2ENSG00000230216
CCDC22ENSG00000101997
FOXP3ENSG00000049768
GAGE10ENSG00000215274
GAGE12JENSG00000224659
GAGE13ENSG00000237597
GAGE2EENSG00000205775
GAGE2DENSG00000240257
GAGE12IENSG00000241465
GAGE2CENSG00000236249
GAGE2BENSG00000231850
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chrX:49050137-49050157TGGCTGTGGGTGTTGGGGGG-7.35
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chrX4904994649049996
Enhancer Sequence
CTAAGGCAGG CAGGGGTGAG GAAGACAGCA CTGTGAGTGG ACTGCTTCAC GCTAGGCCCT 60
GGGGCCTCCT CGGATCACAG GTCCCCCAGA AGAGGCCTGT CTCTCCCCTG CCTTTTCAGC 120
TCTCAAGCCC ACAACACTTT CACCTGAAGG TGGCCCTCCC AGCTTGAGCT TGTGTGTGTA 180
CATGACACAG AGGATGTGGG AGTGTGATTG TGATATGTGG CTGTGGGTGT TGGGGGGAGG 240
GGAACTCTGG GATGATTTCC GAATCTGTGG AAAGTAATGT GTCTTTCTAC TTTTGTCTGC 300
ATGTGGGAAT TTTTGTCATT TTGTGTCTAG GCTGAGGGTA TGTGAGTACA GTGGTGTAGG 360
AATCAGTGTG TCTGTGTGGC 380