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

TagContent
EnhancerAtlas ID
HS045-17134 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr12:124853290-124855650 
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
CTGCTCCCCA TGCCCCATCT GCCCATCACC CACTCATCCC GTAAACAATG GTTTCCTTCT 60
CCATGCCCTC ACTAGAATGT AAGTGCCTGG AGTCAGGGCC TTGTCTGTGC AGTTTCCAGC 120
GCCCCCGGCG CCTGGCGCAT GCTGGTGCCA TCAGTCACTT GCAGAATAAA GTAACAAAGG 180
TGAAATTGCT GTTATGATCT TCCAAAATGC CAGAGGGACA GCTGAAGGAG CTGCACTCCA 240
GCCCCCTCTT GGGGTGACCT CTAGGGGGTG TCCCAAAGCA GATCCAAAGG AGGGCAGCTA 300
ATCTCTGAGC GCCCACTGTG GCCCGTCATT AACTGAGTTA TTCTTGCAAT AAGCCATCCA 360
CGCCCACCTT ACAGATGAGA AAACTGAGGC TTGGGGGAGG GGACTCCCAA GGCCAGGCCC 420
TGCCAAAAAA GCACCCAGGC ACCTTCTCTG AAGAGTAAGA GAGGGGAAGG CAGGCAGGCT 480
CGGGGTTTTG CAATTGAAGC CACTATCTCT GGTCGTCTGC CAAGAAAACA CCCAGGCAGA 540
GCCACCTCGA AGAAAGTGCC AGCGGGCCGA AGGAGAATGT GATTTTCTCT CTCCCAAAGT 600
CACCGGGGCG GGGGGCCAGA TGAGAGTCAT CTTGCGTCCA TCCAGGAACA CAGAGCTCCC 660
CCACTGGGGC TGCCAGGCAG GAGGGATGAT ACTGGGCGGG CAGCCAGGAG CAGGGGTCGC 720
CTGGGGGGCC CGCCCGTCCC ACCAGCCCTT CCCGGGAGGC CCTGGCTGCC AGGGCCTACT 780
CTGACGCATC TCGTCCGCGT CCTCCAGCGT CCGCCCGGCC CTGCGCAGTC GTGGCCGGCA 840
GAGGGAGGGG TGGCGGGCTG CCGGCCAGGA CGAGGTCAGC AGGCTGGCCA GAGTCCAGCC 900
TCGTTCACTG AGAGGGCAAA GCAGGCCCCA AGGGCGGGGG CCTGGGCCTA GTCGCACAGG 960
GCGGGACAAA CCAGGTGTCC TGACTCCCAG CCGAGGACTC CTGCACCCGG GGGCTGTGTG 1020
CTGGACACTG GGCAAGGGGT GGACGTACGC CAGGCCCAGC TCGGGGAGGG AGGACACGGC 1080
CCTGGGCGGG GCTGCAGGGG AGAGGACGGG AGGCTGCAAG TGCCCTGCGG GGCCTCAGGC 1140
CTAGCCTGAG TGTTCTGGGG ACGGACAGGA TGCAAGCTGA TCCCCCGGCT CCCCAGTCCG 1200
GGGCCAGCCA CATGGACCCA AAATACAGAC TCTGGGAGGC AGCTTATCAA TGGGGCTGCC 1260
CCATGACCTC AGCGGTCCCC CGGCGAAGGC AGAAACATGT GTTTCTATGA CTCTGTCCCC 1320
ACAGCCAGCA GGAGCGGGGC GGGGAGCCGT CTGCCCTGAC CCCGCTATCC AGGCACAATG 1380
GCCCTGGCTG CCTGCCTCCA GGGCAGACCC AGCCACACCA TGAACACTGT TTTCCAAGCT 1440
GGGACTGTCG GGCAAGAAGC TCAGGGATTT GGTGCCCTCA GAAACCCGCA GGCCAGGCCT 1500
TTGCTCATCA CAGGGTCAGG GTCAGGCCGT CCACTTCTCA CACGCATGGG CGCGGTTCCT 1560
GTTGGCAGTG GTTCCTGGGG ACCCTGAGAT TTTGTTTTGT GGAACCTATA GAGATCCGGG 1620
TGAACCTCAG TTCCTAGGGA ATGTCCTAGG ACTTCCCCCT TTAACATGGC CCAGGGTGAA 1680
CCCCAGGGCA GAGACAAGGG CCCCGCATGA CCCTGCGGGT CTGATTTTCC TCCCTCGCTT 1740
GCTCTGCCCA GGACCATTCC AAGGGACTTG GGAGGGGAGA AAACAGACCA CACTGTAGTT 1800
GAAATAAAAT GGCCTGCCTG CCCCACCAGA AAACAATTCC TCCAGCCATC CAGATGTGAG 1860
CAGGACGCAG TCTCCGCGGG TCTGCCCTCT GCCAACCGAG ATTGGCCCTA ACTTGGGTAG 1920
CCATCTTTGG TTCTGGGCTG GAGGCCTTGA GGCCCAAAGC ATCTGTGCTG AAAATGGGTA 1980
AAAGGTGGCA TTCTCAGGGA TGTGGGGTCA CCCAGGCCAG GAGCAAAGAC AGAGGCCAGA 2040
AAGGAAAGAA CACACCTCAG AGACATCAAC ACCCAAACAG GACGACACTG GGGTCCTCCA 2100
GGCCACCCCA GCTGGAGAGG AATTTGCAAG GGGAACCTCT GCACCTGTGA TCCAAGGTGA 2160
TCACCTGTGA TCCTGAGCCC TGGACCCTTG GCTGATGGGA GATGAGCCAC CAAAAACATG 2220
TTGAACCTGT GGCTTTTCCC CAACCCCACG GCCACCACGC TCGCATCTCC ATCACCAGCC 2280
CCAGGGCACT TGCAGCTGCC TCCTGACTGT GCCTCTCACT CCCAGCAAAT CCCCCACATG 2340
GTTTCATGGG TAAATCACAT 2360