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

TagContent
EnhancerAtlas ID
HS088-28287 
Organism
Homo sapiens 
Tissue/cell
HeLa-S3 
Coordinate
chr19:49361180-49362110 
Target genes
Number: 57             
NameEnsembl ID
LIG1ENSG00000105486
CARD8ENSG00000105483
ZNF114ENSG00000178150
CCDC114ENSG00000105479
CTCENSG00000248146
EMP3ENSG00000142227
TMEM143ENSG00000161558
SYNGR4ENSG00000105467
KDELR1ENSG00000105438
GRIN2DENSG00000105464
GRWD1ENSG00000105447
KCNJ14ENSG00000182324
CYTH2ENSG00000105443
LMTK3ENSG00000142235
SULT2B1ENSG00000088002
SPACA4ENSG00000177202
FAM83EENSG00000105523
SPHK2ENSG00000063176
RPL18ENSG00000063177
DBPENSG00000105516
AC008888.7ENSG00000232871
CA11ENSG00000063180
NTN5ENSG00000142233
FUT2ENSG00000176920
MAMSTRENSG00000176909
RASIP1ENSG00000105538
IZUMO1ENSG00000182264
FUT1ENSG00000174951
FGF21ENSG00000105550
BCAT2ENSG00000105552
HSD17B14ENSG00000087076
PLEKHA4ENSG00000105559
PPP1R15AENSG00000087074
TULP2ENSG00000104804
NUCB1ENSG00000104805
CTDENSG00000260366
DHDHENSG00000104808
BAXENSG00000087088
FTLENSG00000087086
GYS1ENSG00000104812
RUVBL2ENSG00000183207
LHBENSG00000104826
CGB5ENSG00000189052
CGB1ENSG00000213030
CGB7ENSG00000196337
NTF4ENSG00000167744
AC008687.1ENSG00000225950
SNRNP70ENSG00000104852
LIN7BENSG00000104863
HRCENSG00000130528
TRPM4ENSG00000130529
PIH1D1ENSG00000104872
RPL13AENSG00000142541
SNORD33ENSG00000199631
RPS11ENSG00000142534
SNORD35BENSG00000200530
MIR150ENSG00000207782
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:49361189-49361210AAAAAAAAAAAGAAACTGGCA-6.16
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_11592chr19:49361573-49363222CD20
SE_13446chr19:49361928-49364201CD34_Primary_RO01536
SE_18664chr19:49361795-49363520CD4p_CD25-_Il17-_PMAstim_Th
SE_19244chr19:49361851-49363223CD4p_CD25-_Il17p_PMAstim_Th17
SE_37651chr19:49360150-49361940HSMMtube
SE_59232chr19:49361792-49396070Ly3
SE_65554chr19:49361651-49363323Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr194936120649361349
chr194936135449361709
Number: 2             
IDChromosomeStartEnd
GH19I048856chr194936015149361940
GH19I048858chr194936196149364097
Enhancer Sequence
ATAATAATTA AAAAAAAAAA GAAACTGGCA TGTCTTAGTG ACAAATAGTA GAGTGGGCAT 60
GTCCATAATT GAAGTGCTTT AGGAGATATT TTGAGGTTCA GAACTGGGCC CTCTCAACTT 120
CCTCAACTAC CTGCTCTCCA GCTGTGTGCC ACTGTGGGGA CACAGAGGGT GATAATAAAT 180
GCACCAGCCT GGCAAAACAG CCCCACAAGA TGATGGAATT TGCTACTCTC ATTCTCAGAC 240
TTGCAGTCAG CTGTGGATAT TCTGAGCTAC CGTCCCATGA TGCTCAGACA AAACAGCAGG 300
CAACCAACTT GCAAGGTGAA CTGGGGACAC AAGGGAGATG CAAACCTCTC ACCGCACTGT 360
CTTGGCACAG AGTATCCAGG ACTACAATCC CCATGATGCT TAAAGAGCAA TGGCTGGGCC 420
AGGCGCGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCTGAGATG GGCAGATCAC 480
CTGTCAGCTG GTCAGGAGTT CGAGACCAGC TTGGTCAACA TGGTGAAACC TCATCTCTAC 540
CAAAAATATA AAAATCAGCC GGACGTGGTG GCAGGTGCCT GTAATCCTAG CTACTCGGGA 600
GGCTGAGGCA GGAGAATCGC TTGAACCCGG GAGACAGAGG TTGTAGTGAG CCGAGATCGT 660
GCCACTGCCC TCTAACCTTG GCGACAGAGC AAGACCTCAG TCTCAAAAAA AAAAAAAAAA 720
AGCAATGGCC GAAGACCAGC CTAGAAAGAC AGCCCAGACA CCTGAGAGGA GCTGGACACC 780
TGATAGGTTC AAGCTCTCTC TCACCTGAGC CCAGCTGAGA TCATTATGGA CTACAATACC 840
CATGACACCC AGGGAGCAAT GGCCTTGAGA ATACGGAAAG ACAGCCCTGA GGCCTGATGG 900
GAAACGTAGT CCCCTCCTTC TCACCTCTCT 930