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

TagContent
EnhancerAtlas ID
HS091-11269 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr12:124852780-124856560 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFICMA0161.2chr12:124853805-124853816TCTGCCAAGAA-6.02
SRFMA0083.3chr12:124855929-124855945TGACCTTATTTGGAAA-6.01
TFAP2CMA0524.2chr12:124855566-124855578AGCCCCAGGGCA+6.11
ZBTB18MA0698.1chr12:124855136-124855149CATCCAGATGTGA+6.07
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00866chr12:124852302-124857914Adrenal_Gland
SE_02192chr12:124852573-124855748Aorta
SE_02420chr12:124853362-124855303Astrocytes
SE_03150chr12:124852582-124854142Brain_Angular_Gyrus
SE_03150chr12:124854154-124855845Brain_Angular_Gyrus
SE_03868chr12:124852326-124856486Brain_Anterior_Caudate
SE_04770chr12:124852265-124856998Brain_Cingulate_Gyrus
SE_05769chr12:124851534-124858012Brain_Hippocampus_Middle
SE_06714chr12:124852249-124856790Brain_Hippocampus_Middle_150
SE_07720chr12:124852393-124856669Brain_Inferior_Temporal_Lobe
SE_23639chr12:124852547-124855286Colon_Crypt_1
SE_24091chr12:124853655-124854883Colon_Crypt_2
SE_25142chr12:124853624-124855051Colon_Crypt_3
SE_26654chr12:124852402-124856810Esophagus
SE_28184chr12:124853346-124855413Fetal_Intestine
SE_29418chr12:124853184-124855403Fetal_Intestine_Large
SE_29559chr12:124852384-124855597Fetal_Muscle
SE_31405chr12:124852239-124857127Gastric
SE_38211chr12:124852268-124855751HUVEC
SE_40749chr12:124851606-124856969Left_Ventricle
SE_41561chr12:124852351-124857884LNCaP
SE_42183chr12:124852349-124856857Lung
SE_44453chr12:124852334-124855577NHDF-Ad
SE_45099chr12:124853338-124855555NHLF
SE_46642chr12:124852508-124855752Ovary
SE_46642chr12:124855953-124856916Ovary
SE_47406chr12:124852344-124856831Panc1
SE_47472chr12:124853387-124855312Pancreas
SE_48155chr12:124851582-124857802Psoas_Muscle
SE_48612chr12:124852376-124856560Right_Atrium
SE_49559chr12:124852544-124855378Right_Ventricle
SE_50109chr12:124852450-124856867Sigmoid_Colon
SE_51247chr12:124852084-124856783Skeletal_Muscle
SE_52804chr12:124852392-124856729Small_Intestine
SE_54428chr12:124852458-124853210Spleen
SE_54428chr12:124853228-124855766Spleen
SE_54615chr12:124852448-124855767Stomach_Smooth_Muscle
SE_65244chr12:124852447-124857871Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12124853600124854800
Number: 1             
IDChromosomeStartEnd
GH12I124367chr12124851691124856859
Enhancer Sequence
TCACTGTCAT TTTCCTTCCC ACTCATGAAG GCCGGTTGGG GGGCAGGGCA CGAGAGGGGG 60
AATAAGGGCC TGGGGACATT CATCGGAACA TGCTGGGCCT GCAACAGTAC ATCCCCTCTC 120
CACCCAGCCC TTGCCTCAGT TTCCCCATGG TCATCAAGCT GGGACAATCC TTGCCACCAT 180
CCTAGGGCTA GGAGGGAGAG GGAGGGCTGG TTTGTGAACA GGCATCCCTT GCCTCTCCAA 240
GGCCCCAAGA TAAAACCCTG ACCCGTCACT TCCACCCGTG GGGCCTGCCC ACCTCTCTGA 300
CCTCTCCGCC CTCTCTGCCC TGGGCTGCTC ACTCCACTCT ACACCCTGCT ATAGGCCTCT 360
CTGCTGTCCA CTGGACATAC GCTCATGCGG CCACAGGGCC TTTGCACTGG TGGTTCCCAG 420
GGGGTCTGGC TTTCCCTCAC ACTAAGGCTC TCATTGCCCT CCAATGTCAC CTCCCCAGAG 480
GCCCTCCCTG CCTGACCAGC CCACTCTCCC CTGCTCCCCA TGCCCCATCT GCCCATCACC 540
CACTCATCCC GTAAACAATG GTTTCCTTCT CCATGCCCTC ACTAGAATGT AAGTGCCTGG 600
AGTCAGGGCC TTGTCTGTGC AGTTTCCAGC GCCCCCGGCG CCTGGCGCAT GCTGGTGCCA 660
TCAGTCACTT GCAGAATAAA GTAACAAAGG TGAAATTGCT GTTATGATCT TCCAAAATGC 720
CAGAGGGACA GCTGAAGGAG CTGCACTCCA GCCCCCTCTT GGGGTGACCT CTAGGGGGTG 780
TCCCAAAGCA GATCCAAAGG AGGGCAGCTA ATCTCTGAGC GCCCACTGTG GCCCGTCATT 840
AACTGAGTTA TTCTTGCAAT AAGCCATCCA CGCCCACCTT ACAGATGAGA AAACTGAGGC 900
TTGGGGGAGG GGACTCCCAA GGCCAGGCCC TGCCAAAAAA GCACCCAGGC ACCTTCTCTG 960
AAGAGTAAGA GAGGGGAAGG CAGGCAGGCT CGGGGTTTTG CAATTGAAGC CACTATCTCT 1020
GGTCGTCTGC CAAGAAAACA CCCAGGCAGA GCCACCTCGA AGAAAGTGCC AGCGGGCCGA 1080
AGGAGAATGT GATTTTCTCT CTCCCAAAGT CACCGGGGCG GGGGGCCAGA TGAGAGTCAT 1140
CTTGCGTCCA TCCAGGAACA CAGAGCTCCC CCACTGGGGC TGCCAGGCAG GAGGGATGAT 1200
ACTGGGCGGG CAGCCAGGAG CAGGGGTCGC CTGGGGGGCC CGCCCGTCCC ACCAGCCCTT 1260
CCCGGGAGGC CCTGGCTGCC AGGGCCTACT CTGACGCATC TCGTCCGCGT CCTCCAGCGT 1320
CCGCCCGGCC CTGCGCAGTC GTGGCCGGCA GAGGGAGGGG TGGCGGGCTG CCGGCCAGGA 1380
CGAGGTCAGC AGGCTGGCCA GAGTCCAGCC TCGTTCACTG AGAGGGCAAA GCAGGCCCCA 1440
AGGGCGGGGG CCTGGGCCTA GTCGCACAGG GCGGGACAAA CCAGGTGTCC TGACTCCCAG 1500
CCGAGGACTC CTGCACCCGG GGGCTGTGTG CTGGACACTG GGCAAGGGGT GGACGTACGC 1560
CAGGCCCAGC TCGGGGAGGG AGGACACGGC CCTGGGCGGG GCTGCAGGGG AGAGGACGGG 1620
AGGCTGCAAG TGCCCTGCGG GGCCTCAGGC CTAGCCTGAG TGTTCTGGGG ACGGACAGGA 1680
TGCAAGCTGA TCCCCCGGCT CCCCAGTCCG GGGCCAGCCA CATGGACCCA AAATACAGAC 1740
TCTGGGAGGC AGCTTATCAA TGGGGCTGCC CCATGACCTC AGCGGTCCCC CGGCGAAGGC 1800
AGAAACATGT GTTTCTATGA CTCTGTCCCC ACAGCCAGCA GGAGCGGGGC GGGGAGCCGT 1860
CTGCCCTGAC CCCGCTATCC AGGCACAATG GCCCTGGCTG CCTGCCTCCA GGGCAGACCC 1920
AGCCACACCA TGAACACTGT TTTCCAAGCT GGGACTGTCG GGCAAGAAGC TCAGGGATTT 1980
GGTGCCCTCA GAAACCCGCA GGCCAGGCCT TTGCTCATCA CAGGGTCAGG GTCAGGCCGT 2040
CCACTTCTCA CACGCATGGG CGCGGTTCCT GTTGGCAGTG GTTCCTGGGG ACCCTGAGAT 2100
TTTGTTTTGT GGAACCTATA GAGATCCGGG TGAACCTCAG TTCCTAGGGA ATGTCCTAGG 2160
ACTTCCCCCT TTAACATGGC CCAGGGTGAA CCCCAGGGCA GAGACAAGGG CCCCGCATGA 2220
CCCTGCGGGT CTGATTTTCC TCCCTCGCTT GCTCTGCCCA GGACCATTCC AAGGGACTTG 2280
GGAGGGGAGA AAACAGACCA CACTGTAGTT GAAATAAAAT GGCCTGCCTG CCCCACCAGA 2340
AAACAATTCC TCCAGCCATC CAGATGTGAG CAGGACGCAG TCTCCGCGGG TCTGCCCTCT 2400
GCCAACCGAG ATTGGCCCTA ACTTGGGTAG CCATCTTTGG TTCTGGGCTG GAGGCCTTGA 2460
GGCCCAAAGC ATCTGTGCTG AAAATGGGTA AAAGGTGGCA TTCTCAGGGA TGTGGGGTCA 2520
CCCAGGCCAG GAGCAAAGAC AGAGGCCAGA AAGGAAAGAA CACACCTCAG AGACATCAAC 2580
ACCCAAACAG GACGACACTG GGGTCCTCCA GGCCACCCCA GCTGGAGAGG AATTTGCAAG 2640
GGGAACCTCT GCACCTGTGA TCCAAGGTGA TCACCTGTGA TCCTGAGCCC TGGACCCTTG 2700
GCTGATGGGA GATGAGCCAC CAAAAACATG TTGAACCTGT GGCTTTTCCC CAACCCCACG 2760
GCCACCACGC TCGCATCTCC ATCACCAGCC CCAGGGCACT TGCAGCTGCC TCCTGACTGT 2820
GCCTCTCACT CCCAGCAAAT CCCCCACATG GTTTCATGGG TAAATCACAT CTGGCTCTCT 2880
TGGGAGAGGC TCGTAAAGGC CTTCTCACTG CCCTGAGAAC AAAATGCAGC CCCCACCTGC 2940
CAGGGCGTGA CTCAGTGCCC CCACCCCCGT GAGAGCTGCC CCCCGTCCTG CCAGGCTGCC 3000
CCCTCCCTGA GCCACCCTTT GGCACCTGAA TCCACCAAGC TCATTCCCAC CTCGGGCCTT 3060
CGCACTTGCT GTTCCCACCA CGCTGAGGGT AGAACTGTGT CCCCCCAGAG AAGGTACATT 3120
CAAGTCCTAA CCCAGGGTCT CTGTGAATGT GACCTTATTT GGAAATAGAC TGTTTGCTGA 3180
TATAATCAAG TTAAGATGAA GCTGCACTAG ATTAGGACAG CTGCCCATCC AATGCCTGGT 3240
GTCCTCAGAA GAAGAAAGTG TGGACACAGA GATGCACAGG GCGAAGGTCA TGTGACAGCA 3300
GAGCCAAAGA CGGAGTGGCA TGCCAGCAAT CACGACCGCC AGCAGCGGCC AGGAGCTGGA 3360
AGAGGCGGGA TGGATCTGCC CAGAGGCTCG GAGGCTGCGT CTCGGCCTGC ATGGTGCCCC 3420
CAGGCTCCTG GCCTCCAGGA CTGTATTTGT TAAAAGCCAC CTGGCTCGAA CTACCTTGTG 3480
AGGGCGGCCC TAGGAAGCGA GCAGGCTGCC TGGCACACTC TCTCCCTAGC GCTGCCCAGG 3540
GCTGCCTCCT CTGTCCGGGT CTCAGCTTGG ATGTCACCTC CTGGGGAGGT CCTCCCGGCC 3600
ACACCTCCGC CCCTTCCTGG CCTGCATCTC TCATTCCTGG ACTCTACTCC AAGTCTGCCT 3660
CCCTAACCAC ACCTCGGGCT CCCCCAAAGC AGGCAGAGCC AGACTGGGTG CGGCTGTCTA 3720
AGTAGGTAGT CGCTGCTCAG TGTCTGCAGA CAAAAGCCAA GGTTAGGGCT GCCTGGCGCC 3780