EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-22695 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:1049440-1050910 
Target genes
Number: 44             
NameEnsembl ID
WDR18ENSG00000065268
RNF126ENSG00000070423
FSTL3ENSG00000070404
PALMENSG00000099864
C19orf21ENSG00000099812
AC004449.6ENSG00000261204
AC112708.1ENSG00000213726
ARID3AENSG00000116017
KISS1RENSG00000116014
R3HDM4ENSG00000198858
MED16ENSG00000175221
PTBP1ENSG00000011304
LPPR3ENSG00000129951
CFDENSG00000197766
CDC34ENSG00000099804
BSGENSG00000172270
GRIN3BENSG00000116032
C19orf6ENSG00000182087
CNN2ENSG00000064666
ABCA7ENSG00000064687
HMHA1ENSG00000180448
POLR2EENSG00000099817
GPX4ENSG00000167468
SBNO2ENSG00000064932
STK11ENSG00000118046
ATP5DENSG00000099624
MIDNENSG00000167470
CIRBPENSG00000099622
C19orf24ENSG00000228300
EFNA2ENSG00000099617
AC005330.1ENSG00000240846
NDUFS7ENSG00000115286
AC005329.7ENSG00000248015
GAMTENSG00000130005
DAZAP1ENSG00000071626
RPS15ENSG00000115268
C19orf25ENSG00000119559
PCSK4ENSG00000115257
REEP6ENSG00000115255
ADAMTSL5ENSG00000185761
MEX3DENSG00000181588
MBD3ENSG00000071655
U6ENSG00000252933
TCF3ENSG00000071564
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs115550680chr191050420hg19
rs12151021chr191050874hg19
TF binding sites/motifs
Number: 15             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2CMA0497.1chr19:1050844-1050859AAATTAAAAATAGAA+6.12
RREB1MA0073.1chr19:1049490-1049510CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049515-1049535CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049540-1049560CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049566-1049586CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049591-1049611CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049616-1049636CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049642-1049662CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049667-1049687CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049693-1049713CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049719-1049739CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049744-1049764CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049770-1049790CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049795-1049815CCCCCCACCACTCCCTCCCC+6.51
RREB1MA0073.1chr19:1049441-1049461CCCCCAACCACTCCCTCCCC+7.35
Number: 1             
IDChromosomeStartEnd
GH19I001050chr1910508361052336
Enhancer Sequence
GCCCCCAACC ACTCCCTCCC CGTGAGCCCC CCCACTCCCA CCCCGTGAGC CCCCCCACCA 60
CTCCCTCCCC GTGAGCCCCC CACCACTCCC TCCCCGTGAA CCCCCCACCA CTCCCTCCCC 120
GTGAGCCCCC CCACCACTCC CTCCCCGTGA GCCCCCCACC ACTCCCTCCC CGTGAACCCC 180
CCACCACTCC CTCCCCGTGA GCCCCCCCAC CACTCCCTCC CCGTGAACCC CCCACCACTC 240
CCTCCCCGTG AGCCCCCCCA CCACTCCCTC CCCGTGAGGC CCCCCACCAC TCCCTCCCCG 300
TGAACCCCCC ACCACTCCCT CCCCGTGAGC CCCCCCACCA CTCCCTCCCC GTGAACCCCC 360
CACCACTCCC TCCCCGTGAG CCCCCCCACC ACTCCCTCCC TGTGAGCCCC CCGACCGCTC 420
CCTCCCCGTG AGCCCCCCCA CCACTCCCTC CCTGTGAGCC CCCCCACCAC TCCCTCCCTG 480
TGAGTTCCCC CACCACTCCC TCCCTGTGAG TCCCCCACCA CTCCCTCCCT GTGAGCCGCC 540
CAAACCACTC CCTCCCTGTG AGCCCCCCAC CACTTCCTCC CTGTGAGCTC CCTGTGAGGC 600
CCCCGACCAG TCCCTCCCTG TGAGCAGTAA TGGCGCCACT GCACTCCAGC TTGGGCAACG 660
GAGTAAGACC CTGTCTCAAA ATAAATAGGG CGGGAGTGGT GGCTCACGCC TGTAATCCCA 720
GCACTTGGGC AAGCCGAGGT GGGAGGATTG CCTGAGGTCA GAGTTTGAGA CACAGCCTGG 780
CCAATATGGC AAAACCATCT CTACTAAAAA TACAAAAATT AGCCGGGTGT GATGGTGGCG 840
TGCACCTGTA ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA GAACTGCTTG AACCCTGGAG 900
GCGGAGGTTG CAGTGAGCCG AGACTGTGCC GTTGCACTCC AGCCTGGGCA ACAGAGTGAG 960
ACTCTGTCAC AAAAAAATAA AAATAAACAA ATAAATAAAA ATAAGGCTAT CACAGGGTTT 1020
TGGATGTAGC ATTTAATAGG TGCTCTGTGG CCAGGCGTGG TGGCTCAGGC CTGCAATCCC 1080
AGCACTTTGG GGGGCCGAGG CGGGTGGATC ACGAGGTCAG GAGATTGAGA TCATCCTGGC 1140
TAACATGGTG AAACAGTGAA ACCCCGTCTC TACTAAAAAT GCAAAAAAAT TAGCCGGACA 1200
TGGTGGCGGG CGCCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATGGCGTGAA 1260
CCCGGGAGGT GGAGCTTGCA GTGAGCCGAG ATCGTGCCGC TGCACTCCAG CCTGGGCAAC 1320
AGAGTGAAAC TCCGTCTCAA AAATAATAAT AATAATAATA ATAATAATAA TAATAATAAA 1380
TAATTAAAAA TTTTTTAAAA ACAGAAATTA AAAATAGAAG CTCTGTAACT GCCAGTGCAC 1440
TCTGTGAAGG GGGCTACTCT GAGACCCCTC 1470