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

TagContent
EnhancerAtlas ID
HS133-14435 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr19:581590-582300 
Target genes
Number: 39             
NameEnsembl ID
WDR18ENSG00000065268
HCN2ENSG00000099822
FGF22ENSG00000070388
RNF126ENSG00000070423
FSTL3ENSG00000070404
PALMENSG00000099864
AC004449.6ENSG00000261204
ARID3AENSG00000116017
R3HDM4ENSG00000198858
MED16ENSG00000175221
PTBP1ENSG00000011304
LPPR3ENSG00000129951
CFDENSG00000197766
PPAP2CENSG00000141934
MIER2ENSG00000105556
C2CD4CENSG00000183186
SHC2ENSG00000129946
TPGS1ENSG00000141933
CDC34ENSG00000099804
BSGENSG00000172270
GRIN3BENSG00000116032
C19orf6ENSG00000182087
CNN2ENSG00000064666
ABCA7ENSG00000064687
HMHA1ENSG00000180448
POLR2EENSG00000099817
GPX4ENSG00000167468
SBNO2ENSG00000064932
STK11ENSG00000118046
C19orf26ENSG00000099625
ATP5DENSG00000099624
C19orf24ENSG00000228300
MUM1ENSG00000160953
AC005330.1ENSG00000240846
AC005329.7ENSG00000248015
DAZAP1ENSG00000071626
C19orf25ENSG00000119559
REEP6ENSG00000115255
MEX3DENSG00000181588
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZfxMA0146.2chr19:581999-582013CGGGGCGAGGCCTG+6.67
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr19581834581994
Enhancer Sequence
GGTGAGCCGT CTGCCCTCCT GCCCACATGC CCTGCTCTCG GGGTGGCCCA GGGCCACTCC 60
TGGTCCGTCC CTGCCAGCCC CACCGCTGAC CCAGAGCTTG GAACTGAGGA GCCCCAGGCA 120
GGGAGTTGAT GGGACCCCGA AAGAAAGTGT GGGATGGAGG GTCTAGCCCC GGGCAGCTGC 180
GGCTCAGTGG GCAGCGGGAC CCCGGGAGGA GGAGGCGGCA CCTCCGCCCC ACAGCCTCAC 240
CCGGCCCTTC CCTCCCGCTC ACTTGGCTGC AAGCCAGTGT CCTCCGTGGT GAGCCGGCCC 300
TTGCTGCTCT GCATGATCAG GCTCGGGAAC CTGAGGTCAG CCATGCTGTG CTCCGGCAGC 360
CCCTGCCTGC CTCCTCGCGG AGCCCTTCTG CCCCTTGGGC TGCGTGTGCC GGGGCGAGGC 420
CTGTGTGGGG CCTGTGATGG CAGCTCCTGG AAAACGCTGT GGGGCAGGGG TGAGGCCCAC 480
GAGGCCATGG GGACAGCTCA CCATGGGGAG CACACCTGCA GGTGGGGAGG GCTGCCTTTC 540
CCCACAGCAC TCAGAAGATG CACGTGGCCG GGGCTGATGA GCTGCCCCGA GCCACCCCTG 600
GGGGTCACTG AGGGCAGGGC TGGCAGCACA GATGCCCCTG CTCGGGGCCT GAGTGGGGCC 660
AGTGCTGACA GGCTGTCCTC TCGTCCTCTT TTTCATGGCG GCGGTCCTTC 710