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

TagContent
EnhancerAtlas ID
HS098-14918 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr12:124853480-124855740 
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
GTTATGATCT TCCAAAATGC CAGAGGGACA GCTGAAGGAG CTGCACTCCA GCCCCCTCTT 60
GGGGTGACCT CTAGGGGGTG TCCCAAAGCA GATCCAAAGG AGGGCAGCTA ATCTCTGAGC 120
GCCCACTGTG GCCCGTCATT AACTGAGTTA TTCTTGCAAT AAGCCATCCA CGCCCACCTT 180
ACAGATGAGA AAACTGAGGC TTGGGGGAGG GGACTCCCAA GGCCAGGCCC TGCCAAAAAA 240
GCACCCAGGC ACCTTCTCTG AAGAGTAAGA GAGGGGAAGG CAGGCAGGCT CGGGGTTTTG 300
CAATTGAAGC CACTATCTCT GGTCGTCTGC CAAGAAAACA CCCAGGCAGA GCCACCTCGA 360
AGAAAGTGCC AGCGGGCCGA AGGAGAATGT GATTTTCTCT CTCCCAAAGT CACCGGGGCG 420
GGGGGCCAGA TGAGAGTCAT CTTGCGTCCA TCCAGGAACA CAGAGCTCCC CCACTGGGGC 480
TGCCAGGCAG GAGGGATGAT ACTGGGCGGG CAGCCAGGAG CAGGGGTCGC CTGGGGGGCC 540
CGCCCGTCCC ACCAGCCCTT CCCGGGAGGC CCTGGCTGCC AGGGCCTACT CTGACGCATC 600
TCGTCCGCGT CCTCCAGCGT CCGCCCGGCC CTGCGCAGTC GTGGCCGGCA GAGGGAGGGG 660
TGGCGGGCTG CCGGCCAGGA CGAGGTCAGC AGGCTGGCCA GAGTCCAGCC TCGTTCACTG 720
AGAGGGCAAA GCAGGCCCCA AGGGCGGGGG CCTGGGCCTA GTCGCACAGG GCGGGACAAA 780
CCAGGTGTCC TGACTCCCAG CCGAGGACTC CTGCACCCGG GGGCTGTGTG CTGGACACTG 840
GGCAAGGGGT GGACGTACGC CAGGCCCAGC TCGGGGAGGG AGGACACGGC CCTGGGCGGG 900
GCTGCAGGGG AGAGGACGGG AGGCTGCAAG TGCCCTGCGG GGCCTCAGGC CTAGCCTGAG 960
TGTTCTGGGG ACGGACAGGA TGCAAGCTGA TCCCCCGGCT CCCCAGTCCG GGGCCAGCCA 1020
CATGGACCCA AAATACAGAC TCTGGGAGGC AGCTTATCAA TGGGGCTGCC CCATGACCTC 1080
AGCGGTCCCC CGGCGAAGGC AGAAACATGT GTTTCTATGA CTCTGTCCCC ACAGCCAGCA 1140
GGAGCGGGGC GGGGAGCCGT CTGCCCTGAC CCCGCTATCC AGGCACAATG GCCCTGGCTG 1200
CCTGCCTCCA GGGCAGACCC AGCCACACCA TGAACACTGT TTTCCAAGCT GGGACTGTCG 1260
GGCAAGAAGC TCAGGGATTT GGTGCCCTCA GAAACCCGCA GGCCAGGCCT TTGCTCATCA 1320
CAGGGTCAGG GTCAGGCCGT CCACTTCTCA CACGCATGGG CGCGGTTCCT GTTGGCAGTG 1380
GTTCCTGGGG ACCCTGAGAT TTTGTTTTGT GGAACCTATA GAGATCCGGG TGAACCTCAG 1440
TTCCTAGGGA ATGTCCTAGG ACTTCCCCCT TTAACATGGC CCAGGGTGAA CCCCAGGGCA 1500
GAGACAAGGG CCCCGCATGA CCCTGCGGGT CTGATTTTCC TCCCTCGCTT GCTCTGCCCA 1560
GGACCATTCC AAGGGACTTG GGAGGGGAGA AAACAGACCA CACTGTAGTT GAAATAAAAT 1620
GGCCTGCCTG CCCCACCAGA AAACAATTCC TCCAGCCATC CAGATGTGAG CAGGACGCAG 1680
TCTCCGCGGG TCTGCCCTCT GCCAACCGAG ATTGGCCCTA ACTTGGGTAG CCATCTTTGG 1740
TTCTGGGCTG GAGGCCTTGA GGCCCAAAGC ATCTGTGCTG AAAATGGGTA AAAGGTGGCA 1800
TTCTCAGGGA TGTGGGGTCA CCCAGGCCAG GAGCAAAGAC AGAGGCCAGA AAGGAAAGAA 1860
CACACCTCAG AGACATCAAC ACCCAAACAG GACGACACTG GGGTCCTCCA GGCCACCCCA 1920
GCTGGAGAGG AATTTGCAAG GGGAACCTCT GCACCTGTGA TCCAAGGTGA TCACCTGTGA 1980
TCCTGAGCCC TGGACCCTTG GCTGATGGGA GATGAGCCAC CAAAAACATG TTGAACCTGT 2040
GGCTTTTCCC CAACCCCACG GCCACCACGC TCGCATCTCC ATCACCAGCC CCAGGGCACT 2100
TGCAGCTGCC TCCTGACTGT GCCTCTCACT CCCAGCAAAT CCCCCACATG GTTTCATGGG 2160
TAAATCACAT CTGGCTCTCT TGGGAGAGGC TCGTAAAGGC CTTCTCACTG CCCTGAGAAC 2220
AAAATGCAGC CCCCACCTGC CAGGGCGTGA CTCAGTGCCC 2260