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

TagContent
EnhancerAtlas ID
HS051-07879 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr14:23070660-23071680 
Target genes
Number: 52             
NameEnsembl ID
TRAJ43ENSG00000211846
TRAJ42ENSG00000211847
TRAJ41ENSG00000211848
TRAJ40ENSG00000211849
TRAJ39ENSG00000211850
TRAJ38ENSG00000211851
TRAJ37ENSG00000211852
TRAJ36ENSG00000211853
TRAJ35ENSG00000211854
TRAJ34ENSG00000211855
TRAJ33ENSG00000211856
TRAJ32ENSG00000211857
TRAJ31ENSG00000211858
TRAJ30ENSG00000211859
TRAJ29ENSG00000211860
TRAJ28ENSG00000211861
TRAJ27ENSG00000211862
TRAJ26ENSG00000211863
TRAJ25ENSG00000211864
TRAJ24ENSG00000211865
TRAJ23ENSG00000211866
TRAJ22ENSG00000211867
TRAJ21ENSG00000211868
TRAJ20ENSG00000211869
TRAJ19ENSG00000211870
TRAJ18ENSG00000211871
TRAJ17ENSG00000211872
TRAJ16ENSG00000211873
TRAJ15ENSG00000211874
TRAJ14ENSG00000211875
TRAJ13ENSG00000211876
TRAJ12ENSG00000211877
TRAJ11ENSG00000211878
TRAJ10ENSG00000211879
TRAJ9ENSG00000211880
TRAJ8ENSG00000211881
TRAJ7ENSG00000211882
TRAJ6ENSG00000211883
TRAJ5ENSG00000211884
TRAJ4ENSG00000211885
TRAJ3ENSG00000211886
TRAJ2ENSG00000211887
TRAJ1ENSG00000211888
TRACENSG00000229164
AE000662.93ENSG00000259054
DAD1ENSG00000129562
ABHD4ENSG00000100439
AL160314.1ENSG00000228313
AL132780.1ENSG00000207765
PSMB5ENSG00000100804
C14orf119ENSG00000179933
ACIN1ENSG00000100813
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RUNX1MA0002.2chr14:23071129-23071140GTTTGTGGTTT+6.02
ZNF263MA0528.1chr14:23070954-23070975CTTCCTCCTTCCTTCTCCCCC-6.24
ZNF263MA0528.1chr14:23070970-23070991CCCCCATTTCTCTCTTCCTCC-6.57
ZNF263MA0528.1chr14:23070944-23070965ACATTCTCCCCTTCCTCCTTC-6.59
ZNF263MA0528.1chr14:23070951-23070972CCCCTTCCTCCTTCCTTCTCC-6.59
ZNF263MA0528.1chr14:23070948-23070969TCTCCCCTTCCTCCTTCCTTC-6.76
ZNF263MA0528.1chr14:23070978-23070999TCTCTCTTCCTCCCCTCCTCT-7.01
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_37574chr14:23070749-23072482HSMMtube
SE_46313chr14:23070813-23072848Osteoblasts
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr142307106323071142
chr142307129423071494
Number: 1             
IDChromosomeStartEnd
GH14I022601chr142307054423072704
Enhancer Sequence
GTAAGTAGAA TGGACAGCTT GTCCCACCTC CCTCATGGAG CCCAAGAAGG ATTCAGGATC 60
TTCCCAGAGC CTGCTACATT GAGCCCACTG ATTCCTAATT AACAGTGTGT ATGGGGTGGG 120
AGGAAAGGAT GTCAGTTGTG TGAGGGAAGA GGTGCATACA GACGGCACCA TATCTGATAA 180
TAGTGCTTCC TCACCATCTC CCTAGCCATG TGGATAGTTC CTGCCACTTC CTGCAACTTC 240
ACCTCAAACC CTATGCCAGT GCCGGCTAAC ACACACAAAC ACGTACATTC TCCCCTTCCT 300
CCTTCCTTCT CCCCCATTTC TCTCTTCCTC CCCTCCTCTC TTCTCACCAC ACAAGTACTT 360
CTTAGATTTA CCACCTGCAG ATCCTTGGCC AGCAATCTTG CATTCTCTGA TGTTACGATT 420
CCTGTGTTCT ACCTGGTTTT GGCCCCCCAC CTATCTGGTT ACCACAGTAG TTTGTGGTTT 480
GCAGACCAGC TGTCATCGGC ACTGTTACAT TGCAGCAGGG CATCCCACTA GCGGCAGCAG 540
CCACTCGCTC AAACAAGCCC CTTAAGCCAC TTCTTCCCAT ATTTCCCTTA TGATCTTCAC 600
CACACCCCTA CTGCCCCAGC CATAGCTACC CTTTCTCTTC TGGGCCCGAG TAAGTGCAGA 660
CAAACAGCAG CCAGAGCTCT CAGGCCTCTG TCCAGGATCC AGGCTGCTCC ACCCAGGCAG 720
CTCTTCCCGG GAGACTGCTG TCACACCAGC AGAACAAGCA CTGCCCCACC TCAGTCTCTC 780
ACCCGAGGCT CAGTCCACAC CCATCACTCC CTCCAACTGG CTGGACCACA GTTCTGTCCA 840
TCCATCAAGC CCCAAGCACA CACAGGTTCA AGAGCAATAG ATGCAAGAGC TCTGTGGGGT 900
TGGTGGTGTC ACTACCACCT GGGGCTAAAG GGAGCTGGGC ACGCTGTTTC AAGGGATAAG 960
ACGGTCCCGC TTATTATGTA CAGACTACAT GGTCTGTAAA TGTGATTGGA GTTGAATTCT 1020