EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS111-01300 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr12:124853320-124855580 
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
CACTCATCCC GTAAACAATG GTTTCCTTCT CCATGCCCTC ACTAGAATGT AAGTGCCTGG 60
AGTCAGGGCC TTGTCTGTGC AGTTTCCAGC GCCCCCGGCG CCTGGCGCAT GCTGGTGCCA 120
TCAGTCACTT GCAGAATAAA GTAACAAAGG TGAAATTGCT GTTATGATCT TCCAAAATGC 180
CAGAGGGACA GCTGAAGGAG CTGCACTCCA GCCCCCTCTT GGGGTGACCT CTAGGGGGTG 240
TCCCAAAGCA GATCCAAAGG AGGGCAGCTA ATCTCTGAGC GCCCACTGTG GCCCGTCATT 300
AACTGAGTTA TTCTTGCAAT AAGCCATCCA CGCCCACCTT ACAGATGAGA AAACTGAGGC 360
TTGGGGGAGG GGACTCCCAA GGCCAGGCCC TGCCAAAAAA GCACCCAGGC ACCTTCTCTG 420
AAGAGTAAGA GAGGGGAAGG CAGGCAGGCT CGGGGTTTTG CAATTGAAGC CACTATCTCT 480
GGTCGTCTGC CAAGAAAACA CCCAGGCAGA GCCACCTCGA AGAAAGTGCC AGCGGGCCGA 540
AGGAGAATGT GATTTTCTCT CTCCCAAAGT CACCGGGGCG GGGGGCCAGA TGAGAGTCAT 600
CTTGCGTCCA TCCAGGAACA CAGAGCTCCC CCACTGGGGC TGCCAGGCAG GAGGGATGAT 660
ACTGGGCGGG CAGCCAGGAG CAGGGGTCGC CTGGGGGGCC CGCCCGTCCC ACCAGCCCTT 720
CCCGGGAGGC CCTGGCTGCC AGGGCCTACT CTGACGCATC TCGTCCGCGT CCTCCAGCGT 780
CCGCCCGGCC CTGCGCAGTC GTGGCCGGCA GAGGGAGGGG TGGCGGGCTG CCGGCCAGGA 840
CGAGGTCAGC AGGCTGGCCA GAGTCCAGCC TCGTTCACTG AGAGGGCAAA GCAGGCCCCA 900
AGGGCGGGGG CCTGGGCCTA GTCGCACAGG GCGGGACAAA CCAGGTGTCC TGACTCCCAG 960
CCGAGGACTC CTGCACCCGG GGGCTGTGTG CTGGACACTG GGCAAGGGGT GGACGTACGC 1020
CAGGCCCAGC TCGGGGAGGG AGGACACGGC CCTGGGCGGG GCTGCAGGGG AGAGGACGGG 1080
AGGCTGCAAG TGCCCTGCGG GGCCTCAGGC CTAGCCTGAG TGTTCTGGGG ACGGACAGGA 1140
TGCAAGCTGA TCCCCCGGCT CCCCAGTCCG GGGCCAGCCA CATGGACCCA AAATACAGAC 1200
TCTGGGAGGC AGCTTATCAA TGGGGCTGCC CCATGACCTC AGCGGTCCCC CGGCGAAGGC 1260
AGAAACATGT GTTTCTATGA CTCTGTCCCC ACAGCCAGCA GGAGCGGGGC GGGGAGCCGT 1320
CTGCCCTGAC CCCGCTATCC AGGCACAATG GCCCTGGCTG CCTGCCTCCA GGGCAGACCC 1380
AGCCACACCA TGAACACTGT TTTCCAAGCT GGGACTGTCG GGCAAGAAGC TCAGGGATTT 1440
GGTGCCCTCA GAAACCCGCA GGCCAGGCCT TTGCTCATCA CAGGGTCAGG GTCAGGCCGT 1500
CCACTTCTCA CACGCATGGG CGCGGTTCCT GTTGGCAGTG GTTCCTGGGG ACCCTGAGAT 1560
TTTGTTTTGT GGAACCTATA GAGATCCGGG TGAACCTCAG TTCCTAGGGA ATGTCCTAGG 1620
ACTTCCCCCT TTAACATGGC CCAGGGTGAA CCCCAGGGCA GAGACAAGGG CCCCGCATGA 1680
CCCTGCGGGT CTGATTTTCC TCCCTCGCTT GCTCTGCCCA GGACCATTCC AAGGGACTTG 1740
GGAGGGGAGA AAACAGACCA CACTGTAGTT GAAATAAAAT GGCCTGCCTG CCCCACCAGA 1800
AAACAATTCC TCCAGCCATC CAGATGTGAG CAGGACGCAG TCTCCGCGGG TCTGCCCTCT 1860
GCCAACCGAG ATTGGCCCTA ACTTGGGTAG CCATCTTTGG TTCTGGGCTG GAGGCCTTGA 1920
GGCCCAAAGC ATCTGTGCTG AAAATGGGTA AAAGGTGGCA TTCTCAGGGA TGTGGGGTCA 1980
CCCAGGCCAG GAGCAAAGAC AGAGGCCAGA AAGGAAAGAA CACACCTCAG AGACATCAAC 2040
ACCCAAACAG GACGACACTG GGGTCCTCCA GGCCACCCCA GCTGGAGAGG AATTTGCAAG 2100
GGGAACCTCT GCACCTGTGA TCCAAGGTGA TCACCTGTGA TCCTGAGCCC TGGACCCTTG 2160
GCTGATGGGA GATGAGCCAC CAAAAACATG TTGAACCTGT GGCTTTTCCC CAACCCCACG 2220
GCCACCACGC TCGCATCTCC ATCACCAGCC CCAGGGCACT 2260