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

TagContent
EnhancerAtlas ID
HS091-21533 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:79671750-79673930 
Target genes
Number: 57             
NameEnsembl ID
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
UTS2RENSG00000181408
HEXDCENSG00000169660
C17orf101ENSG00000181396
C17orf62ENSG00000178927
NARFENSG00000141562
RAB40BENSG00000141542
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73354145chr1779673423hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr17:79672210-79672222AAACAAACAAAC-6.32
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_24986chr17:79669183-79672059Colon_Crypt_3
SE_35549chr17:79668087-79672052HepG2
SE_41699chr17:79671082-79672020LNCaP
SE_41699chr17:79672476-79673244LNCaP
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: 2             
ChromosomeStartEnd
chr177967272479672819
chr177967257479672688
Number: 1             
IDChromosomeStartEnd
GH17I081705chr177967247779673244
Enhancer Sequence
GTCCTGGGCA GAATGAGGCA TTTCTGGGGT GCCCAGTTCG CCTGTGGCCT CATGTGCCGT 60
GGTCCCGTAT CTCAGGTTCT GCAGCTACCG TCATTGTCTG CAGCCTGCAC ACCTGTGCGG 120
CATCCTGCAG CCTCCTGGGA CCTACTCCCT GCCACGGATG TGCACGACTT TGCATGTGGA 180
GACCATGTTT CTAATGGAGG GAAACAGACA CTAAGCTGAG AGAGGAAAAA GAGGCTGGGC 240
GTGGTGGCTC ACGCCTGTAA TCCCAGCGCT TCGGGAGGCC GAGACGGGTG GATCACTTGA 300
GGTCAGGAGT TCGAGGCCAG CCTGGCCAAC ATGGTAAAAC CCCGTCTCTA CTAAAAATAC 360
AAAAAAAAAA AAATTAGCTG GGCCTGGTGG CACATGCCTG TAATCCCAGC TACTCGGGAG 420
GCTGAGGCAG GAGAATAGCT TGAACCCGGG AGACTGTCTC AAACAAACAA ACAAAATAAA 480
TAAATAAAAA TAAAAATAAA TAAATAAATA AAAATACAAA AATTAGCCGG CGTGGTGGCA 540
GGTGCCTGTA ATCCCAGCTA CTTGGGAGGC TGAGGCAAGA GAATTGCTTG AACCAGGGAG 600
GCGGAGGTTG CAGTGAGCCA AGATCATACT ACTGCCTTCC AACTTGGCAA CAGAGCAAGA 660
CCCTGTCTCA AAAAAAAAAA AAAAAAAAAA AGAGGAAAAA GAAAGGAAGA AATTATACCA 720
AATAGAACAT TGTAAGCATT GTGGGGAAAA GGAGGGAAGA GGCTCAAGGT GGGAGGGAGA 780
GTTCCAAGTT CAAGGTGGGC TTCAAAGAGG AGGCAGACAT TGTAGAAGAG AGCACGGCCT 840
TCCTGGCGGA GGACGGGGAG GCACCAAGGT CACCAGGCAA GAGGGTGTCT GACAATTCAG 900
GGAGCAGCAG CGAGGTACAG GCTGGCGCAG GCGAAGGGGT GTAACAAGCA GCTCCGTCCT 960
TGGGTCTTTG CAAGGAAACC AGTGAACTTG AAGCCGCCAG TTGCGTTTGG TCATCGGGTT 1020
GCGTGAACCT CTCCACCGGA GCCCTCCCCT CAGCCCCTTT CCCCCACTGG GGAACCAGGT 1080
TGTGTACTGT AGAGTGTCCC ATGTTCCAGA TGCGTGGGGT GCCCATGGGG CAGCATCACT 1140
CATGCCTGAG AACTGGAAGG TAGTTTAAAG GCTGATTAGA TTCAGGCCGA GCGTTTGGGT 1200
AAGAATAGCT GGGATTACTG TAGAGCCTGT TGTGTAAACT GGATTGCTTT TGAGGAGGGA 1260
GAAGATGTTA TTAATAGCCT TCCCAGGCCG TGGGGACACG CAGCCCCCTG CCCTCGGGTG 1320
GTGCTGGGTC TCCATGCGCC ACGTCAGAAG CGCAGCGTGC CCGTCAGTCC CATGGCGGGT 1380
TGTCATTTTC TCGGCACACG TGCACTGCAG TGTGGCTGAG AAAGGAATGG CGCTGCTTTT 1440
ATCTACAAAG CACTTTTGGT GTCGTTCTTT CCTGTCTCAT AAGTTACGCT TTCTAAGCGA 1500
GAGGGGAGTA GAGTATTGAG GGAAGGACTG TGAAGCATGT TTTTATTTAT TTATGAAACC 1560
GAGTCTCACT CTGTCACCCA GGCTGGAGTG CAATGGCGCG ATCTCAGCCC CCGCCTCCCG 1620
GGTTCAAGCA ATTCTCATGC CGCAGCCTCC CGAGTAGCTG GGATTACAGG CGCGCACCAC 1680
TAGAGACAGG GTTTCACCAT ATTGGTCAGG CTGGTTTCAA ACTTGACCTC AAGTGATCCA 1740
CCCGCCTTGG CCTCCCAAAG CGCTAGGATG ACAGGCGTGA GCCACCGGAG CCACCACTCC 1800
CGTCCGAGGC ATGTTACAAA GAGTTATTGG GCAGACCTGC CTCTGACTAG CATGAGAGAA 1860
AAAGCACCAG CTGGACTCGC GAGGCCAAGG CAGGAGAATC GCTTGAACCC AGGAGGTGGA 1920
GGTTGCAGTG AGCTGAGGTC GCACCACTGC ACTCCAGCCT GGATGACAGA GTGAGACTCC 1980
GTCTCAAAAA AAAGAGAAAA GAAAAGAAAA AGCACCAGCT GGTTAAGGAT TGATGAGTTG 2040
GGAGACGTGA CTTCCAACTC CAGGCTTCGC TGGGGCCTCC GCTGCACCTC CCTTTGGGGC 2100
TTTAGACTGG GGTGGCCCAG CAGTGGAGGC GTTAGCTCCC CCCAGCCCTT TGTCACCTGG 2160
CTCCCCTTCT TTCCTGCTCC 2180