EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-48803 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr9:132944300-132947530 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10819610chr9132946615hg19
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:132946044-132946062TTTTCCTTCCTTCCTTTT-6.4
EWSR1-FLI1MA0149.1chr9:132945986-132946004TCTCCCTTCCTTCCTTCT-6.82
EWSR1-FLI1MA0149.1chr9:132946068-132946086CCTTCCCTCCTTCTTTTC-6.84
EWSR1-FLI1MA0149.1chr9:132946013-132946031TCTTCCTTCCTTCTTTCT-6.96
EWSR1-FLI1MA0149.1chr9:132945952-132945970TCTTTCTTCCTTCCTTTC-7.18
EWSR1-FLI1MA0149.1chr9:132945956-132945974TCTTCCTTCCTTTCTTTC-7.55
EWSR1-FLI1MA0149.1chr9:132945990-132946008CCTTCCTTCCTTCTTTCT-7.85
IRF1MA0050.2chr9:132946085-132946106CTTTTCTTTCTTTTTTTTTTT+6.41
IRF1MA0050.2chr9:132946032-132946053TTTCTCTTTCTCTTTTCCTTC+6.58
IRF1MA0050.2chr9:132946888-132946909CTTTTCTTTCTTTTTTTCTTT+6.5
IRF1MA0050.2chr9:132946020-132946041TCCTTCTTTCTCTTTCTCTTT+7.31
IRF1MA0050.2chr9:132946026-132946047TTTCTCTTTCTCTTTCTCTTT+7.95
RORAMA0071.1chr9:132947139-132947149TGACCTTGAT-6.02
ZNF263MA0528.1chr9:132946005-132946026TCTCTCTCTCTTCCTTCCTTC-6.21
ZNF263MA0528.1chr9:132946036-132946057TCTTTCTCTTTTCCTTCCTTC-6.37
ZNF263MA0528.1chr9:132945982-132946003TCTCTCTCCCTTCCTTCCTTC-6.59
ZNF263MA0528.1chr9:132946001-132946022TCTTTCTCTCTCTCTTCCTTC-6.75
ZNF263MA0528.1chr9:132946060-132946081TTCTTTTCCCTTCCCTCCTTC-7.15
ZfxMA0146.2chr9:132946332-132946346CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_01355chr9:132944380-132946017Adrenal_Gland
SE_02208chr9:132942695-132946160Aorta
SE_02208chr9:132946282-132946975Aorta
SE_02208chr9:132947022-132950543Aorta
SE_08194chr9:132944351-132946184Brain_Inferior_Temporal_Lobe
SE_08194chr9:132946885-132950699Brain_Inferior_Temporal_Lobe
SE_26746chr9:132942345-132945978Esophagus
SE_26746chr9:132946241-132952005Esophagus
SE_33552chr9:132945142-132946124H2171
SE_33552chr9:132947093-132950919H2171
SE_47051chr9:132945005-132945936Ovary
SE_54529chr9:132942297-132965766Stomach_Smooth_Muscle
SE_68936chr9:132944534-132946002H9
SE_68936chr9:132947052-132950555H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9132944663132945968
Number: 2             
IDChromosomeStartEnd
GH09I130182chr9132944618132946924
GH09I130184chr9132947137132950640
Enhancer Sequence
GCCACTCCCC AAGGCAGTAG GGGAGTATTG TGGTTGGGGG GAGATGACAG CAATGACGAC 60
CACCGTTTAC CCAGTGGGCA CTCGGGACCA GGAGTGCTGA GTGCTGCCCT CTCCCCAAAG 120
CCCTGGGAGT AGGGACCCTT ATACCCATTT TACAGATGAG GAAAGGGAGG CCCAGGCAAG 180
TTCAGGGACA CGCCCAAGTC CCCCCAGCCA GCCAATCGAT GGCCAGTCGG GGTTCAGGCT 240
TAGATCTTTA TGTTGCCAGA GCCACGCCCT TCCCACCCGG CGCCTGCCTC CCACCGTCTC 300
TGTGAGCCTC AAAACCTTGG AGTTCCCTGC CAAGGGGAGG GAGCGCCCAG TCCCTGGGAG 360
CATCCAAGCC GCTGCTGGAG CATCAGACAC TGGCCAGGCA TCCCGGACTC CTGGGCTGGG 420
TGTGAGGTTG GTGGCAGATA GGATCCTTCC CGCTGGTTCC AGAGGTTCTG CCTCCTGCAG 480
GAGATTTGGG GCAGCCTCCG CCTTGCCTTC CTCCAGGAAG GAGGCAGAGT TGAGGCCTTG 540
TGGAAAGGCG GCAGGAGGAG AGGCGCTGAT AGGAGTGTGT GGCGCAGCTG TGCCCTGGCC 600
TCAACGGCTT CCTCAGCCTC CACCCACCCC AGTGGAGGCT CAGCAGGTGC TGACCGTGTG 660
TGGGCGCTGG GCTGATCTCA ATGGTCATCC TCCCGCCCTG GGAACTTAGG AGCAACGTAC 720
CGCCATCTTA CGGTGCTGGC ACCACCCCTG CTCCTGGGAA GCCTTGTCAC GGACAAGGTG 780
GTGAGGACTG AGTGCCCCTG GCCATCCTGC CCTGCCCTGT GCCTGGCTCA GCCCAGGTGC 840
CTTCGGAGGT ATCTGTCCGA CAGAGAAAGA GACCAAGTCC TCACAGGTGC AGTGTGGGTT 900
TTGGGGGCAT GGTGGCCAAG GGGACCCCCG TGACTTTTAG CTCCTTGAGG TCTGGGCCAC 960
ATCTTGTGGT CTTTGGTGTC TGTGGGGTGT GTGGCCCGGG GTGTCCTCGC CTCTGCAGAA 1020
GGCTGGGATC TTTCCGAAGA GTTTTTCCCT GCAGTGCTGT GGTTTGCTCT CCCTGGTGAC 1080
CAGGACAGGA CCTGCCTGTG CTCCTGACCT ACAGTCTGTC GGGGAAGGGG GACAGCCAGG 1140
GAGTTGAGAG TTGGGTCCTG GTTCCAGCCT GGCTTGCTGT GGCCTCTGGC TGCCCCTCTC 1200
AGGGCCGCAG TCTCTCCATC TGTTCCACTC TCTGTGAGAT GCGATGTCAC CATTTCTCAG 1260
CTCCGGGTGC CCTGACCATG CGGCTGGGGG GGGGAGCTCC TTGCCCAGGA GGGGTGCAGG 1320
GCAGTTGCTG GCTTTGGCAC TTCTGAGCCA CCGAGGGGGC CCCAGGAAGC TGGTGAGGCA 1380
TCCAGGCCAC TGTGCTCTGG ATTCCCTGGC AGGGGAGCAG GGGGAGGGCA GGAGGAATGT 1440
GGCTTTGAGG AATGTTTAAC CCAAGGCAGA AATAGCACTC TGCCTTTTTA TTTCAGGCTT 1500
GAGTTTTCAG CAGGGAAGTG GGTTCAGTGT GCCTTTCTCT CTCTCCAGCT GTGGGGCCAT 1560
GGCCACCTCG GCTCCCCCAC AGCCCTAGCC TTTGGGGATG GAAAGTGGCC TCTTTATCTC 1620
TCTTTCTTTC TTTCTTTTTC TTTCCTTCTC TCTCTTTCTT CCTTCCTTTC TTTCTTTTTT 1680
TCTCTCTCTC CCTTCCTTCC TTCTTTCTCT CTCTCTTCCT TCCTTCTTTC TCTTTCTCTT 1740
TCTCTTTTCC TTCCTTCCTT TTCTTTTCCC TTCCCTCCTT CTTTTCTTTT CTTTCTTTTT 1800
TTTTTTGAGA CAGAGTCTCG CTCTGTCGCC CAGGCTGGAG TGCAGTGGCA TGATCTCGGC 1860
CCACTGCAAG CTCTGCCTCC CGGGTTCACG CCATTCTCTG GCCTCAGCCT CCCGAGTAGC 1920
TGGGACCACA GGCGCCCGCC ACCATACCCT GCTAATTTTT TGTGTTTTTT AGCAGAGATG 1980
GGGTTTCACT ATGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCATTATC CACCCGCCTC 2040
GGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCCACCGC GCCCGGCGTC TTTTCTTTTC 2100
TTTCTTCTGC TATGGGAAAC AGAAAGAGCC CTAGACTTGG AACCAAACAG AGCTGGGTTC 2160
AAATCCTTTG CTCTCCACTT CTAGCCCTGT GACCACTTCC TTCTCTGAAT CTCTGCAGAA 2220
CTGGGAGAGG GATGCTGAGC CAAGATGGCT TTTCTGGTGG TCTGGTGTCC GGGGCTCCTC 2280
TCAGGGACCC ACAGGCCTGG ATTCAAATCC CAAGGCCTCT ACTGGTTAGT TCTGGGACCT 2340
TGGTCTGGCC TTTCCCACCG AGCCCTCAGA CTTCATCTGT GAAATGGGCA GATGCCTCCC 2400
AGGATTGTGG ATGGCATTCA TGCGAAAACA TTGGTGACAG GGCCTGGCAC GGCTTATCCC 2460
AGGCTTTTAA TCCCTCCTGA TGCATCCCCG CGCCTTCACC TATAAAACAG GAAGACAATG 2520
CCTCTTGCAG ACTTTTTGCT AGGTTGGATG AGGGAGCCAT GCAGCGTGCT AGGGCAGCCC 2580
AGAGGCACCT TTTCTTTCTT TTTTTCTTTT TCTTTTTTTG TTTTGAGACA GAGTCTCGCT 2640
CTGTCACCCA GGCTGGAGTG AAATGGTGCA ATCTCGGCTC ACTGCAACGT CTGCCTCCCA 2700
GGTTCAAGCG ATTCTCTTGC CTCAGCCTCC CAAGTAGCTG GGATTACAGG CGTGCACCAC 2760
CACGCCTGGC TAATTTTTTT TTTTTGTATT TTAGTAGAGA CAGGTTTTCG CCATGTTGGC 2820
CAGGGTGGTC TTGATTTCCT GACCTTGATC CGCCTGTCTC AGCCTCCCAA AGTGCTGGGA 2880
TTCCGTGAGC TGAGATTGCG CCACTGCAGT CCAGCCTGGG CGACAGAATA AGACTCCGAG 2940
ACTCCGTCTC AAAAAAAAAA AAAGGGGCTG GGGTTACAGG TGTAAGCCAC CGCGCCCGGC 3000
CATCCCAGAG GCAGGCACCT ATTCATCGGA CCCAGCCCTC TGCTTCCTCC CACTGGCCAT 3060
GGATGGGACC CATCCTCGTC CACACTCGCA TCAAAGCCCA GCGGCTACTT CCAGGGGGGA 3120
TGTCCTTGGG CCCGGCCTCC TCCTCAGTCC TGGTGGTGAC GACATGTTTC ATAGTCCCCC 3180
TTGATTCAGC TGGGAGCTGT GAGGACCGAC TGCATCTTAT TGCATGACTG 3230