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

TagContent
EnhancerAtlas ID
HS091-22672 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:861960-863090 
Target genes
Number: 50             
NameEnsembl ID
WDR18ENSG00000065268
HCN2ENSG00000099822
RNF126ENSG00000070423
FSTL3ENSG00000070404
PRSS57ENSG00000185198
PALMENSG00000099864
C19orf21ENSG00000099812
AC004449.6ENSG00000261204
AC112708.1ENSG00000213726
ARID3AENSG00000116017
KISS1RENSG00000116014
R3HDM4ENSG00000198858
MED16ENSG00000175221
PTBP1ENSG00000011304
LPPR3ENSG00000129951
CFDENSG00000197766
GZMMENSG00000197540
SHC2ENSG00000129946
ODF3L2ENSG00000181781
MADCAM1ENSG00000099866
TPGS1ENSG00000141933
CDC34ENSG00000099804
BSGENSG00000172270
GRIN3BENSG00000116032
C19orf6ENSG00000182087
CNN2ENSG00000064666
ABCA7ENSG00000064687
HMHA1ENSG00000180448
POLR2EENSG00000099817
GPX4ENSG00000167468
SBNO2ENSG00000064932
STK11ENSG00000118046
C19orf26ENSG00000099625
ATP5DENSG00000099624
MIDNENSG00000167470
CIRBPENSG00000099622
C19orf24ENSG00000228300
MUM1ENSG00000160953
EFNA2ENSG00000099617
AC005330.1ENSG00000240846
NDUFS7ENSG00000115286
AC005329.7ENSG00000248015
GAMTENSG00000130005
DAZAP1ENSG00000071626
RPS15ENSG00000115268
C19orf25ENSG00000119559
PCSK4ENSG00000115257
REEP6ENSG00000115255
ADAMTSL5ENSG00000185761
MEX3DENSG00000181588
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr19:862335-862347TGCAAGGGGGCG+6.02
KLF13MA0657.1chr19:862677-862695AAGGGAGGGGCGTGGCCT-6.2
KLF13MA0657.1chr19:862896-862914CCTAGAGGGGCGTGGCTT-7.15
KLF14MA0740.1chr19:862680-862694GGAGGGGCGTGGCC-6.25
KLF14MA0740.1chr19:862899-862913AGAGGGGCGTGGCT-6.25
KLF16MA0741.1chr19:862135-862146GGGGGCGGGGC-6.02
KLF16MA0741.1chr19:862290-862301GGGGGCGGGGC-6.02
KLF5MA0599.1chr19:862059-862069GGGGCGGGGC-6.02
KLF5MA0599.1chr19:862136-862146GGGGCGGGGC-6.02
KLF5MA0599.1chr19:862291-862301GGGGCGGGGC-6.02
KLF5MA0599.1chr19:862498-862508GGGGCGGGGC-6.02
KLF5MA0599.1chr19:862516-862526GGGGCGGGGC-6.02
SP1MA0079.4chr19:862115-862130CGTGGGCGGGGCCTG-6.12
SP1MA0079.4chr19:862681-862696GAGGGGCGTGGCCTG-6.62
SP1MA0079.4chr19:862900-862915GAGGGGCGTGGCTTG-6.82
SP2MA0516.2chr19:862495-862512GAAGGGGCGGGGCATGG-6.07
SP2MA0516.2chr19:862133-862150GAGGGGGCGGGGCATGT-6.84
SP3MA0746.2chr19:862681-862694GAGGGGCGTGGCC-6.18
SP4MA0685.1chr19:862287-862304ATAGGGGGCGGGGCTCG-6.01
SP4MA0685.1chr19:862132-862149TGAGGGGGCGGGGCATG-6.36
SP4MA0685.1chr19:862679-862696GGGAGGGGCGTGGCCTG-6.64
SP4MA0685.1chr19:862898-862915TAGAGGGGCGTGGCTTG-7
ZfxMA0146.2chr19:862167-862181GGGGGCGAGGCCTG+6.69
Number: 2             
IDChromosomeStartEnd
GH19I000861chr19861901862470
GH19I000862chr19862541864501
Enhancer Sequence
GCCTTCAGGC CTGGGAGGAG ACGCGGGGCC TGCAGGCCCC GGGAAGGGCC TGCAGAGGGA 60
GCGCGAAGCG GGGGGCAAGT AGGAACAGGG CCCAGGGAAG GGGCGGGGCG CGTAGGGGGC 120
GGGAACTGGA AGATGGGCGG AGCATGAGGG TGGCCCGTGG GCGGGGCCTG TATGAGGGGG 180
CGGGGCATGT GGGTAGGGTG GGGCCTTGGG GGCGAGGCCT GGAGAAGGTA CGGGGCCTCT 240
GGAGAGGGTG GGGCTGAAGA AGGGTCAGGG CGGGCAGAAA GGGCAGGAAC GGGTGGGATG 300
TGGAAGGACC TGTGGGTTAG GGTGGGAATA GGGGGCGGGG CTCGAGGAGG GGGCGGAGTC 360
CAGTAATAGC GGGACTGCAA GGGGGCGAGG CCAGGAAGAG GGTTGGGGCA TGAGGGGCAG 420
GGCATGGAGG AAGGGGCGGT ACCTGTGGGG AGGGTGGGGC TGGAGAAGGG TCAGGGCGGG 480
CAAAAGGGCA GGTGGCAGAG AAAGGGTGGG AGGTATAGGG GGCGGGCACG TGGAGGAAGG 540
GGCGGGGCAT GGGGACGGGG CGGGGCAGGT GGAAGGGGCG GGAACCTCTG AAGGGGCAGG 600
GCTGGTGCGG AGCGGGATCC CTGCTGTGGC AGGGAAGAGA AGGGGTCCTG AGCAGGGCAG 660
AGGTTTAAGA CCAGCCGAGG CTTGCATGGT AGCCGGGGCC AAGATTGGGT GGGGCTTAAG 720
GGAGGGGCGT GGCCTGAGGT GAGTGGGGAC TGAGCAGAGC AGGTGGCCAC TGAGACGCGT 780
TAGGGCAGAA GTGGGATCCA CGGCAAGTCA AAGCTTGGAA GAGCAGGAAT GAGGTGTGGG 840
ACCCCCATAC TGGAAAGGGC TTGGAGCGGG GTGGGGTCGG GGGAACACGT GGTGAGGTTG 900
AGGCCAGAGG GGGTGTGGCC AGGAGCTGGG GGCGGGCCTA GAGGGGCGTG GCTTGTGGTT 960
GTGGCCTAGG CGATAGGCGT GGCGCGGGGC TATTGACTAG TGAAGACCAA ATTAACACGG 1020
GAGGGATGAG CGAGCATTGT GGGGCGGGAG CGGCAGCCAG GTGAGGGGGT CTAACACGTG 1080
AGGCCGGGGT GGGCGCGGGC CGCCCCTCAC GGCCCCGTCC TGTTCCGGCA 1130