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

TagContent
EnhancerAtlas ID
HS139-14092 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr12:124853210-124855760 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFICMA0161.2chr12:124853805-124853816TCTGCCAAGAA-6.02
TFAP2CMA0524.2chr12:124855566-124855578AGCCCCAGGGCA+6.11
ZBTB18MA0698.1chr12:124855136-124855149CATCCAGATGTGA+6.07
Number of super-enhancer constituents: 36             
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_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_54428chr12:124853228-124855766Spleen
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
TTTCCCTCAC ACTAAGGCTC TCATTGCCCT CCAATGTCAC CTCCCCAGAG GCCCTCCCTG 60
CCTGACCAGC CCACTCTCCC CTGCTCCCCA TGCCCCATCT GCCCATCACC CACTCATCCC 120
GTAAACAATG GTTTCCTTCT CCATGCCCTC ACTAGAATGT AAGTGCCTGG AGTCAGGGCC 180
TTGTCTGTGC AGTTTCCAGC GCCCCCGGCG CCTGGCGCAT GCTGGTGCCA TCAGTCACTT 240
GCAGAATAAA GTAACAAAGG TGAAATTGCT GTTATGATCT TCCAAAATGC CAGAGGGACA 300
GCTGAAGGAG CTGCACTCCA GCCCCCTCTT GGGGTGACCT CTAGGGGGTG TCCCAAAGCA 360
GATCCAAAGG AGGGCAGCTA ATCTCTGAGC GCCCACTGTG GCCCGTCATT AACTGAGTTA 420
TTCTTGCAAT AAGCCATCCA CGCCCACCTT ACAGATGAGA AAACTGAGGC TTGGGGGAGG 480
GGACTCCCAA GGCCAGGCCC TGCCAAAAAA GCACCCAGGC ACCTTCTCTG AAGAGTAAGA 540
GAGGGGAAGG CAGGCAGGCT CGGGGTTTTG CAATTGAAGC CACTATCTCT GGTCGTCTGC 600
CAAGAAAACA CCCAGGCAGA GCCACCTCGA AGAAAGTGCC AGCGGGCCGA AGGAGAATGT 660
GATTTTCTCT CTCCCAAAGT CACCGGGGCG GGGGGCCAGA TGAGAGTCAT CTTGCGTCCA 720
TCCAGGAACA CAGAGCTCCC CCACTGGGGC TGCCAGGCAG GAGGGATGAT ACTGGGCGGG 780
CAGCCAGGAG CAGGGGTCGC CTGGGGGGCC CGCCCGTCCC ACCAGCCCTT CCCGGGAGGC 840
CCTGGCTGCC AGGGCCTACT CTGACGCATC TCGTCCGCGT CCTCCAGCGT CCGCCCGGCC 900
CTGCGCAGTC GTGGCCGGCA GAGGGAGGGG TGGCGGGCTG CCGGCCAGGA CGAGGTCAGC 960
AGGCTGGCCA GAGTCCAGCC TCGTTCACTG AGAGGGCAAA GCAGGCCCCA AGGGCGGGGG 1020
CCTGGGCCTA GTCGCACAGG GCGGGACAAA CCAGGTGTCC TGACTCCCAG CCGAGGACTC 1080
CTGCACCCGG GGGCTGTGTG CTGGACACTG GGCAAGGGGT GGACGTACGC CAGGCCCAGC 1140
TCGGGGAGGG AGGACACGGC CCTGGGCGGG GCTGCAGGGG AGAGGACGGG AGGCTGCAAG 1200
TGCCCTGCGG GGCCTCAGGC CTAGCCTGAG TGTTCTGGGG ACGGACAGGA TGCAAGCTGA 1260
TCCCCCGGCT CCCCAGTCCG GGGCCAGCCA CATGGACCCA AAATACAGAC TCTGGGAGGC 1320
AGCTTATCAA TGGGGCTGCC CCATGACCTC AGCGGTCCCC CGGCGAAGGC AGAAACATGT 1380
GTTTCTATGA CTCTGTCCCC ACAGCCAGCA GGAGCGGGGC GGGGAGCCGT CTGCCCTGAC 1440
CCCGCTATCC AGGCACAATG GCCCTGGCTG CCTGCCTCCA GGGCAGACCC AGCCACACCA 1500
TGAACACTGT TTTCCAAGCT GGGACTGTCG GGCAAGAAGC TCAGGGATTT GGTGCCCTCA 1560
GAAACCCGCA GGCCAGGCCT TTGCTCATCA CAGGGTCAGG GTCAGGCCGT CCACTTCTCA 1620
CACGCATGGG CGCGGTTCCT GTTGGCAGTG GTTCCTGGGG ACCCTGAGAT TTTGTTTTGT 1680
GGAACCTATA GAGATCCGGG TGAACCTCAG TTCCTAGGGA ATGTCCTAGG ACTTCCCCCT 1740
TTAACATGGC CCAGGGTGAA CCCCAGGGCA GAGACAAGGG CCCCGCATGA CCCTGCGGGT 1800
CTGATTTTCC TCCCTCGCTT GCTCTGCCCA GGACCATTCC AAGGGACTTG GGAGGGGAGA 1860
AAACAGACCA CACTGTAGTT GAAATAAAAT GGCCTGCCTG CCCCACCAGA AAACAATTCC 1920
TCCAGCCATC CAGATGTGAG CAGGACGCAG TCTCCGCGGG TCTGCCCTCT GCCAACCGAG 1980
ATTGGCCCTA ACTTGGGTAG CCATCTTTGG TTCTGGGCTG GAGGCCTTGA GGCCCAAAGC 2040
ATCTGTGCTG AAAATGGGTA AAAGGTGGCA TTCTCAGGGA TGTGGGGTCA CCCAGGCCAG 2100
GAGCAAAGAC AGAGGCCAGA AAGGAAAGAA CACACCTCAG AGACATCAAC ACCCAAACAG 2160
GACGACACTG GGGTCCTCCA GGCCACCCCA GCTGGAGAGG AATTTGCAAG GGGAACCTCT 2220
GCACCTGTGA TCCAAGGTGA TCACCTGTGA TCCTGAGCCC TGGACCCTTG GCTGATGGGA 2280
GATGAGCCAC CAAAAACATG TTGAACCTGT GGCTTTTCCC CAACCCCACG GCCACCACGC 2340
TCGCATCTCC ATCACCAGCC CCAGGGCACT TGCAGCTGCC TCCTGACTGT GCCTCTCACT 2400
CCCAGCAAAT CCCCCACATG GTTTCATGGG TAAATCACAT CTGGCTCTCT TGGGAGAGGC 2460
TCGTAAAGGC CTTCTCACTG CCCTGAGAAC AAAATGCAGC CCCCACCTGC CAGGGCGTGA 2520
CTCAGTGCCC CCACCCCCGT GAGAGCTGCC 2550