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

TagContent
EnhancerAtlas ID
HS091-21534 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:79679550-79681980 
Target genes
Number: 56             
NameEnsembl ID
C17orf89ENSG00000224877
SLC38A10ENSG00000157637
LINC00482ENSG00000185168
TMEM105ENSG00000185332
RP11ENSG00000262877
BAHCC1ENSG00000171282
RP13ENSG00000229848
ACTG1ENSG00000184009
FSCN2ENSG00000186765
C17orf70ENSG00000185504
YENSG00000207021
TSPAN10ENSG00000182612
NPLOC4ENSG00000182446
PDE6GENSG00000185527
CCDC137ENSG00000185298
C17orf90ENSG00000204237
HGSENSG00000185359
ARL16ENSG00000214087
MRPL12ENSG00000262814
SLC25A10ENSG00000183048
GCGRENSG00000215644
AC174470.1ENSG00000215621
FAM195BENSG00000225663
PPP1R27ENSG00000182676
P4HBENSG00000185624
ARHGDIAENSG00000141522
ANAPC11ENSG00000141552
ALYREFENSG00000183684
NPBENSG00000183979
PCYT2ENSG00000185813
SIRT7ENSG00000187531
MAFGENSG00000197063
PYCR1ENSG00000183010
AC137723.5ENSG00000235296
MYADML2ENSG00000185105
NOTUMENSG00000185269
ASPSCR1ENSG00000169696
STRA13ENSG00000169689
LRRC45ENSG00000169683
RAC3ENSG00000169750
DCXRENSG00000169738
RFNGENSG00000169733
GPS1ENSG00000169727
DUS1LENSG00000169718
FASNENSG00000169710
CCDC57ENSG00000176155
SLC16A3ENSG00000141526
AC132872.1ENSG00000184551
CSNK1DENSG00000141551
CD7ENSG00000173762
SECTM1ENSG00000141574
TEX19ENSG00000182459
HEXDCENSG00000169660
C17orf101ENSG00000181396
C17orf62ENSG00000178927
NARFENSG00000141562
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr17:79680225-79680246TTTTACTTTTTTTTTTTTTTT+6.16
ZfxMA0146.2chr17:79679551-79679565GAGGCCGGGGCCCG-6.16
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_24622chr17:79678798-79681606Colon_Crypt_2
SE_24986chr17:79678720-79682705Colon_Crypt_3
SE_35549chr17:79677340-79681743HepG2
SE_41699chr17:79678768-79683021LNCaP
SE_68597chr17:79649851-79680224TC71
SE_68598chr17:79649851-79680224TC71
SE_68599chr17:79649851-79680224TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr177968080079681393
chr177967980079680508
chr177968139879681490
Enhancer Sequence
TGAGGCCGGG GCCCGGGACG CGGGGCGGAT GGGACCCTGG CGCCGCCGAG ACGCCTGCAA 60
AGGCAGCAGC CCGGCCCCAC GCACCCGGGG ATCGCCGCGC CCGGGGCTCC CTCCTGGAGA 120
GCGCGAGGAG GCCCCCGACG CCCGGATGGC CGATCCCGGG TGGCCCTCCA GTGGTGGCCG 180
CCGAGCTCGA GGCCTGCAGG GCGCAGCCGC GCTCCCCAGC TTCCCAGCCG GCTTCCCAGT 240
TCTCGGCAGG TGGCGATCCA GCCCCAGCTC TACACTTTAA TACCTGGTGA CCTTGGGGGA 300
GTCACTTGGC CTCTCTGAGC CACCCACCCC CATACATTCA AGAACGCTCC TTCCGCCTAG 360
TTAGAAGTTG TGGGGGGAGT TCTGTGAGGT GCACAGGTGT TGGCATCTAG AGACGTGCTG 420
GCTGTAGCAT ACCCAGGGTG TGGGCCAAGC CGCCCCCCAC CCAGGGGTGT TTAGCACACC 480
GCCGGACGTG TCCCTGGGCA AGTGGGGTGA CCCGATGCCC CGGCTTTGGG CTGCTTCCTT 540
CGGAGAGCTG CGTGGGCACT GGAAGCGATG TTAGGACCAG CACACCCCCA GGAGAGATGC 600
CAGGAGACCC TGCACGCGTG TGGTCCTGGC CCTATGAAAG CGGGCGTTTC TCAGCACGAG 660
AAGCAGCCAC CGTTTTTTTA CTTTTTTTTT TTTTTTAATG CTTATGGGGC AAAATAAGAC 720
AGAGCTCTCC TTGTTTCCCA GGGACAGCCA AGGGGCGTTG TTTTCTGACC GTGTCTTGCC 780
ACAGAGAACA AAGAAGAAAG GGCCTGAGGC TTTGCACAGT CTGCCCAGCA GGCCCTGCCC 840
TGTGAACCTG GCTGTGGTCA CTGGGCAGCC GCCTGTCTAG GGGACCTTTA TTTTAGCAGC 900
CTGTCCAGGG GACTTGTATT CCAGCAGCCT TTGAGGGGAC TGGCTTTACT AATGAGCAAC 960
AATGCTGGTC GCTGCGTGAA GGCCAGGTGA GCAGATGTGG GCGTCTTGGG GCACCTGAGA 1020
CCTCACTGGT CCTGGGAGAG GCCTTCAGAG CTCCCAGGCC ACAGGCAGCC ACGGCCAGTG 1080
AGATGCAGCC ACAGCGACAG GAAGGCGCTG GCATGGGCAG AAGAAGCGAG CCCCTCCTTG 1140
GCATCGGGCT CTTCCTTTCC TCCTGGGCGC CGCACAGGTG CCCCTCCCCC AGGGCCTCTC 1200
CCACGTTCAT CTGGGTGTTG AAGGCGGGAC CTGCGTGCTG CTGTCCCTTG TCCGGGGTCT 1260
GAGCCCCACT GCCCCTTGGC CCTCCCCAAC CAGGCGCTCT CTGGCTGCAG AACACCGCCT 1320
GGGGGAGGCG GGACTGCCCT CTGGCCTGGG AGGGCGGGAG GAGCCAGCTG CTGGCAGCAT 1380
ATGGCGCTGT GGTCAGGGTG TGCTCCTGAG GACTGCTCAC CAGGCCTCTC TGCCTGGCCG 1440
TCGGAAAGAT CTTTTAAAGC TTCTTGAGCA CTTTGTCCCA TGTCCCTACA GTCCCTACCG 1500
TCGCATCTGG CCGGGACGGG GGCTGCTACC TGTGTGGCCC AGTCCCTCTG TTCTGCTGGG 1560
CTCGCACAAT GGGAGGCCCC TCTCTGTCCC CACCCATCTT TGCCGACCCC TGGGCGTGCG 1620
TTACGGGGCC GCGCACGTGC AGGTCACACT GAGCGGCGGA AGGACTTCTT TGGGGTCAGT 1680
GCTGGGGGTG GGACCCAGGA GCTGGGATCC TGGGCCAGGT GCTGGCCTTC CTGTCTGGCC 1740
CTGGCCAATC CCCCTACTGC CGGGAGCTCT CAGCTGGCCA GGCGAGGAGG CAGAGGTCCT 1800
GTGAGTGGTG GAGGCCAACA GAATGGGAGG TTGTCGGGCT GACAGCCCCC GAGTGCCTGC 1860
CCACAGCTCC TAGGTGCTTT GCAGAGGAGG CCGCTATGCC CTGCCGCCAG CCACACCGTC 1920
CCCTTGTCTG CTGCTGAGCT CCTGCTGCCT TTCAAGGCCT TCTATGGCTA CCTCCTCAGT 1980
CTCCCATGGT CCTGCAGGCT CCCTCGCCGT TTCTGAGCGG CCATAAACGT TTGTCCCTCT 2040
TGAGACGTGG TGTGGTGGAT AAAAAGTAGG GCTCTGGGGT CTCCTCGCTG GGCCCAAATC 2100
CTGATGGCAC CAGCGGGTGC GTTACCTCTC CATGCCTCAG TTTCCTCATC TGCAGAAGGA 2160
GAATGGCGAG CCCCTGCGGC CAGTGCAGCC AATACTCAGG TGGTACGCGG GGCGCTCGCG 2220
GGGCTCGCGG ACACTCTCAG CTCCATGTCC ACTGGTGTGG TTGCTGTTGG AAAGCAGTGG 2280
TGTGAGCTGG TTCCAGGCAC GGGTGTGGAG TCCCCGGGCA GGGCCGTGGG AGGCCTTATC 2340
ACTGCCTCCT GCCTCAGTTT CCCCCTCTCT GGATGAACCT GGCACCGATC CCTCGGGGTC 2400
GCTGTGGGGT CTGAGAGCAC TCACTCCCGC 2430