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

TagContent
EnhancerAtlas ID
HS091-21580 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:79941540-79943380 
Target genes
Number: 54             
NameEnsembl ID
BAHCC1ENSG00000171282
ACTG1ENSG00000184009
FSCN2ENSG00000186765
C17orf70ENSG00000185504
YENSG00000207021
TSPAN10ENSG00000182612
NPLOC4ENSG00000182446
PDE6GENSG00000185527
CCDC137ENSG00000185298
C17orf90ENSG00000204237
HGSENSG00000185359
ARL16ENSG00000214087
RP13ENSG00000262049
MRPL12ENSG00000262814
SLC25A10ENSG00000183048
GCGRENSG00000215644
AC174470.1ENSG00000215621
FAM195BENSG00000225663
PPP1R27ENSG00000182676
RP11ENSG00000262831
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
UTS2RENSG00000181408
HEXDCENSG00000169660
C17orf101ENSG00000181396
C17orf62ENSG00000178927
NARFENSG00000141562
FOXK2ENSG00000141568
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr17:79942920-79942940CCCCCACACACACCCACGCA+6.07
RREB1MA0073.1chr17:79942655-79942675CACCCACACACACCCCCACA+6.17
RREB1MA0073.1chr17:79942647-79942667CCCACACACACCCACACACA+6.39
RREB1MA0073.1chr17:79942761-79942781CCCACACACACCCACACACA+6.39
RREB1MA0073.1chr17:79943102-79943122CCCGCACACACCCACACACA+6.39
RREB1MA0073.1chr17:79942657-79942677CCCACACACACCCCCACACA+6.6
RREB1MA0073.1chr17:79942759-79942779CCCCCACACACACCCACACA+7.19
RREB1MA0073.1chr17:79942667-79942687CCCCCACACACCCACATACC+7.39
ZfxMA0146.2chr17:79941970-79941984CCCGCCTCGGCCTC+6.01
ZfxMA0146.2chr17:79942213-79942227GAGGCCGAGGCGGG-6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177994270179942868
Number: 1             
IDChromosomeStartEnd
GH17I081984chr177994270179942868
Enhancer Sequence
CATGGTGGGT CGTGCTCTGG GGGAGGCTGA CTGTGTGGGG CACAGGATCG TTCAGCTGGC 60
CAGGGACGGG GGACGGGACA GTGGGGGGTG CTGGGGAAGG AGGGACATGA GTCTTAGCAC 120
CAGTTCTGCC TTCCCTGGGT TGGGCCCAAA CAGCTTCCTG TTTTTTGATA ACTGGCAACT 180
GAAAATGAGC ATCTCATGTT TTTTTTTTTT TGAGCTGGAG TCTCGCTCTG TCGCCCAGGC 240
TGGAGCTCAG TGGCGCAGTC TCGGCTCACT TCAAGCTCCG CCTCCCGGGT TCACACCATT 300
CTGCCTCAGC CTCCCGAGTA GCTAGGACTA CAGGTGCCCG CCACCACACC CGGCTAATTT 360
TTGTATTTTA GTAGAGGCAG GGTTTCACCA TGTTGGCCTG CTGGTCTGGA ACTGCTGACC 420
TCATGATCTA CCCGCCTCGG CCTCCCAAAG TCCTCCCAAA GGATTGCAGG CGTGAGCCTC 480
TGCGCCCCGC CCACGTCATT CTTCATGTGG AAGTTTTTCT TTCTTTCTGG GGTCAGTTGT 540
GCCTTCCCTG GCTCAGGGTG TCAGCAGCAT TCACCCACCA GCCTGACCAC CTGCTCATAG 600
AATTGCCCAG AATGTTAGAG CCGAAAGCGC TGCATGGATG CCGCAAGGGC AGCCTGTAAT 660
CCCAGCACTT TAGGAGGCCG AGGCGGGCAG ATCACCTGAG GTCAGGAGTT TGGGACCAGC 720
CGGCCAACAT AATGAAACCC CGTCTCTACT AAAAATACAA AAATTAGCCG TGGGTGGTGG 780
CGGATGCCTG TAGTCCCAGC TACTCAGCAG GCTGAGGCAG GAGAATGGCG TGAACCCGGG 840
AGGCGGAGCT TGCAGTGAGC CGAGATTGTG CTGCCACTGC ACTCCAGCCT GGGCGACAGA 900
GTGAGACTTT GTCTCAAAAA AAAAAAAAAG AGCAGCAAAC ATTTACCATC TCATGTGGCT 960
TCTGAGGGTC AGGAATCTGG GAGCAGCTTA GCTCAGTGTC TGTCCTGAGG CTGCAGTCAG 1020
GTTCGGTGGA GCTGCAATCT TTTGAAGCCC CCACTGGGAC ACGAGGACTG TCTCCAACAC 1080
AGTTCACTCC TGTGGCGCCT GCATGTACCC ACACACACCC ACACACACCC CCACACACCC 1140
ACATACCCGC ACACCCGTAC ACACCCCCAC ACACCCCTGC ACACACCCCA CACACACCTG 1200
CACACCCCCG CACACACACC CCCCACACAC ACCCACACAC ACCCCTACAG CAACGTGCAC 1260
ACACCCCCAC ACCCGCACAC ACCCGCACAC ACCCCACACA CCTGCACACA CCCACACACC 1320
TGCGTGCACA CCCCCCCACA CACCTGCACA CACCGCCCAC ACCAACATGC ACACACCTCC 1380
CCCCCACACA CACCCACGCA CACACCTGTA CACACACACC TACACATCTG CGCACATACC 1440
CGCACACACC TGCATGTAAA CATGCACACA CACGCACATC TGCACGCACA TGCGCACACC 1500
TGCACACACC CACACACCAA CATGCACACA TCCACACACA TACCTGCACA CAACTGCACA 1560
CCCCCGCACA CACCCACACA CACATATGCA CACACGCACG CACACCTGCA CATACCTGCA 1620
CACTCACATG CACACACGCA TGCTGGTGCA GCCCTGCCGG GGAGCCTCCA AGGCCCTCAC 1680
TCCAGAGTGA ATAGGAGGGT AGCCTTCTCC GTGGGGGTCA GCCTCTCCCT GGAGGCCAGG 1740
GCGGGGCAGT CACCCTCTCT GTGTCTGGAG AATCAGTCTG GGATTTAGAA GGAATAGTTG 1800
CTTTTCTTCC TAAGGAAGTT TCTCATGTCT TATACCCTCC 1840