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

TagContent
EnhancerAtlas ID
HS076-30220 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr19:49360880-49362110 
Target genes
Number: 78             
NameEnsembl ID
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
CGBENSG00000104827
CGB2ENSG00000104818
CGB5ENSG00000189052
CGB1ENSG00000213030
CGB7ENSG00000196337
NTF4ENSG00000167744
AC008687.1ENSG00000225950
KCNA7ENSG00000104848
SNRNP70ENSG00000104852
LIN7BENSG00000104863
C19orf73ENSG00000221916
PPFIA3ENSG00000177380
HRCENSG00000130528
TRPM4ENSG00000130529
AC011450.2ENSG00000235555
SLC6A16ENSG00000063127
CD37ENSG00000104894
AC011450.1ENSG00000197813
TEAD2ENSG00000074219
DKKL1ENSG00000104901
CCDC155ENSG00000161609
PTH2ENSG00000142538
SLC17A7ENSG00000104888
PIH1D1ENSG00000104872
ALDH16A1ENSG00000161618
RPL13AENSG00000142541
SNORD33ENSG00000199631
SNORD35AENSG00000200259
RPS11ENSG00000142534
FCGRTENSG00000104870
RCN3ENSG00000142552
NOSIPENSG00000142546
PRRG2ENSG00000126460
BCL2L12ENSG00000126453
C19orf76ENSG00000224420
CTBENSG00000243829
FUZENSG00000010361
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
TGTGCTCTCT GAAACATGTG CTGTGTCCAC TCAGGGTTAA ATGGATTAAG GGCAGTGCAA 60
GATGTGCTTT GTTAAACAGA TGCTTGAAGG CAGCATGCTC GTTAAGAGTC ATCACCACTC 120
CCTAATCTCA AGTACCCAGG GACACAAACA CTGCGGAAGG CCGCAGGGTC CTCTGCCTAG 180
GAAAACCAGA GACCTTTGTT CACTTGTTTA TCTGCTGACC TTCCCTCCAC TATTGTCCTA 240
TGACCCTGCC AAATCCCCCT CTGCGAGAAA CACCCAAGAA TGATCAATAA AAAAATAATA 300
ATAATAATTA AAAAAAAAAA GAAACTGGCA TGTCTTAGTG ACAAATAGTA GAGTGGGCAT 360
GTCCATAATT GAAGTGCTTT AGGAGATATT TTGAGGTTCA GAACTGGGCC CTCTCAACTT 420
CCTCAACTAC CTGCTCTCCA GCTGTGTGCC ACTGTGGGGA CACAGAGGGT GATAATAAAT 480
GCACCAGCCT GGCAAAACAG CCCCACAAGA TGATGGAATT TGCTACTCTC ATTCTCAGAC 540
TTGCAGTCAG CTGTGGATAT TCTGAGCTAC CGTCCCATGA TGCTCAGACA AAACAGCAGG 600
CAACCAACTT GCAAGGTGAA CTGGGGACAC AAGGGAGATG CAAACCTCTC ACCGCACTGT 660
CTTGGCACAG AGTATCCAGG ACTACAATCC CCATGATGCT TAAAGAGCAA TGGCTGGGCC 720
AGGCGCGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCTGAGATG GGCAGATCAC 780
CTGTCAGCTG GTCAGGAGTT CGAGACCAGC TTGGTCAACA TGGTGAAACC TCATCTCTAC 840
CAAAAATATA AAAATCAGCC GGACGTGGTG GCAGGTGCCT GTAATCCTAG CTACTCGGGA 900
GGCTGAGGCA GGAGAATCGC TTGAACCCGG GAGACAGAGG TTGTAGTGAG CCGAGATCGT 960
GCCACTGCCC TCTAACCTTG GCGACAGAGC AAGACCTCAG TCTCAAAAAA AAAAAAAAAA 1020
AGCAATGGCC GAAGACCAGC CTAGAAAGAC AGCCCAGACA CCTGAGAGGA GCTGGACACC 1080
TGATAGGTTC AAGCTCTCTC TCACCTGAGC CCAGCTGAGA TCATTATGGA CTACAATACC 1140
CATGACACCC AGGGAGCAAT GGCCTTGAGA ATACGGAAAG ACAGCCCTGA GGCCTGATGG 1200
GAAACGTAGT CCCCTCCTTC TCACCTCTCT 1230