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

TagContent
EnhancerAtlas ID
HS051-06773 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr12:113669590-113672500 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr12:113670104-113670116TGCCCCCTGGCA-6.62
ZIC1MA0696.1chr12:113670675-113670689CACAGCAGGTGGCC-6.33
ZIC4MA0751.1chr12:113670674-113670689GCACAGCAGGTGGCC-6.16
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00883chr12:113664391-113671759Adrenal_Gland
SE_01635chr12:113668074-113671857Aorta
SE_01635chr12:113671879-113672586Aorta
SE_03074chr12:113670515-113671448Bladder
SE_03506chr12:113670303-113671468Brain_Angular_Gyrus
SE_04226chr12:113668219-113671573Brain_Anterior_Caudate
SE_04226chr12:113671763-113672686Brain_Anterior_Caudate
SE_05290chr12:113668185-113671971Brain_Cingulate_Gyrus
SE_06123chr12:113668589-113673221Brain_Hippocampus_Middle
SE_07164chr12:113668204-113672804Brain_Hippocampus_Middle_150
SE_08283chr12:113668652-113671919Brain_Inferior_Temporal_Lobe
SE_09132chr12:113670809-113671120Brain_Mid_Frontal_Lobe
SE_09783chr12:113664182-113681103CD14
SE_26345chr12:113670026-113671154Duodenum_Smooth_Muscle
SE_26677chr12:113664465-113671657Esophagus
SE_27860chr12:113666514-113670777Fetal_Intestine
SE_28798chr12:113666400-113670853Fetal_Intestine_Large
SE_29890chr12:113669050-113671988Fetal_Muscle
SE_37095chr12:113664640-113672337HSMMtube
SE_40725chr12:113664070-113673220Left_Ventricle
SE_41860chr12:113670871-113671741LNCaP
SE_41860chr12:113671823-113672557LNCaP
SE_42290chr12:113664247-113673161Lung
SE_44290chr12:113669973-113671773NHDF-Ad
SE_47597chr12:113669662-113670175Pancreas
SE_48084chr12:113663861-113673266Psoas_Muscle
SE_48792chr12:113667499-113671975Right_Atrium
SE_49644chr12:113668928-113671654Right_Ventricle
SE_50157chr12:113669359-113671777Sigmoid_Colon
SE_51183chr12:113663840-113675194Skeletal_Muscle
SE_53751chr12:113670201-113671818Spleen
SE_60802chr12:113634217-113672070DHL6
SE_61851chr12:113631410-113672028Toledo
SE_64197chr12:113669556-113671579HSMM
SE_65505chr12:113667937-113672747Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12113670616113671636
Number: 1             
IDChromosomeStartEnd
GH12I113226chr12113664004113672117
Enhancer Sequence
TTGATAAAGG AGGCAGGTAT GAGCAGAGGT ATTTAAAGCC TGGAAACTAG GAATAACCTT 60
GAAAACAGTC AGCGGGGCCA CTGTTAGAGC AGTGTAGAGA CAGACCACAG TCCACACCGC 120
GTGACAGGCG GTGGTCTCAC CCACCACATT CAGGGAATCA GGACGAGTCT GAATGTAGTG 180
GGCAGTCCAA GGAATTTCCC AGGGTAACTC TGGTCACACT CAGCTCTGCC TTCTCCCTGC 240
CTTTAAAGCC AGCTGCTGCC TAAGATGGGC TGGACCATGT GCCTTTTCTG AGTGAAGGAA 300
GGATTGGGCT CGCGGGGGCT GGCTGAGGTC TGAGCAGGAT GCTCCGTCTC TGCTTTGGTG 360
CCGGGTTGTT TATGGTTTTC AGGTGACAGG TCCTGCAGCT AAGGCCCAAG GTCACAGCGC 420
AGAGAGCTGA CCTCTCCCTC CTTCACGCCG ATGCCTGGCA CATCATCTGG AGTTCCCTAG 480
GACACAGTGC AGCCTCAGCA ATGTGGAGGA TCCCTGCCCC CTGGCAGGGG CCCCCATGTG 540
GCACCCTGGT CCCCTTTTCA GGGTCTTCAT GCAGCCAGGG CGAGTTGGCA CCAGGCTCAG 600
TCAAGGTGGG CCAGAGCTGT TGGCCGCAGG GCCGCCGTAG CCAGGAGGAG TTGGGAGAGA 660
TCCTCGCCGG CTGGCACCAG AGAAGAATAC ACCCCGAGGT GTGCGCTCCA TCACTGATGT 720
CTGTGCCGTG GCTCTGCCTC TGACCAGATG GCCCCAGCAT ACTTGCCAAA GAGTGAAGAA 780
GCCCAAGGGG CTTGCACAGC TTTTGTCACT TGTGATACCA TGGTGAGTGG AGTGGTTGAG 840
CTGAGTATAG TGCTTAGCTG CTCTAAGCCT CAGCCTGCTC ATCTGTAGAA TGTGACCATG 900
ATGGCATCTA CCAGTAGAGT CGTCATGGGG GATTGAGTGA GAGCATGTGT GTGATCACAT 960
GGTCAGTGCT CAGCCGGTCA TAGGCATTAT TATCATGGCA GAAACTGGGC TTCCTTGGAA 1020
TATCCTCCAT GAGCAGAGGT CCTGAACCCA GGCCACGATT CAGATCCTTC TTGCCTCACT 1080
CCTGGCACAG CAGGTGGCCC CTGCCAAGCT GGGACGCCTC CGTGTAGCAG CTGGAGACCA 1140
AGCAGCAATT AGATTTTCAC AGGCTCCCAC CGAGCTTGGG CATTTGGCTC CGCTGGAGTC 1200
ATTCCCCTGG CTTTTTCAGG GCCTCACCAA GGCAGAGCGT CGGGTGTCAC CAGACCAGCA 1260
GTGGTGCCAA TTAAAATGAG TAAGCATCCA GCATGCTGGG CGAGAGCCTT GCAGCCGAGC 1320
CTTGGAGCTT TCACTTCCTC AGCCCTCCAC ATCTTCATGG GGGGGATCCT GTCTGTTGCC 1380
TCAGGCCCCC TGCCATGAGA TGCCATCTCT TCCCGTCCCC CTTTCCCGCA CACAAGACGC 1440
TGCCGCTCTA AATGGCAGTC GTGGCAGCTG GGTGCAGGCT GAAGCACCTG CCACTCTCCT 1500
CCCCACTCGC CTGGGGGAGG GCTGAGTTCA CGTTTCCTCT GAGAGCGCTT CATGAGCCAG 1560
AACCGTGAAC TTCTCAGCTT CCCCATCGGG GAGGCAATAT GGGAGGGCTT GGATGGCTCA 1620
CAGCAGCGTG CCGCTGGGGG CATCAGGTTG CAGTGCCCTC TGCGGGGAGG TTTCAAATGA 1680
CAGCAAGGTA GCCCAGGAAC AAACCTGGAG TGACGTCAAT CTTGAGACAG CCCCCACGCC 1740
GCCTTCCTGC TCCAGGAGCC CTGGGTGGCT CTCCATTCTT GCCCTTGGCT AGAGTGAATC 1800
CTCTGGTTCG GACATCCTCT GACTGTCACC CTTCTCCCCG CAGTCAGGTA TGCCTGGGGA 1860
GAGGATGTGC CTGGGTCAGG GTATGTGCAG TCATAATCAT GGCCTGTGGG TGTTGAGCCC 1920
TCGCCGTGTG TCAGGCGGTA TCCAAAGCAC TTTTGTGCTG CTATCATTTG GTCCTCCCTC 1980
CCAGCAGATT TGGGGGGCCG TTACTTTCAA TATCATCTCA AAGAAGAGGA AACGGAGGCT 2040
CTCAGAGGTT GAAACTTATC CAAGGTCACA AAGACACTTT GACTTCCTTT GAACCCATGT 2100
CTAGTGACTC CAGAACCAGT CTCTTACCTA GTATGCCCCC CTCCGTGAGG TAGAGCTCTG 2160
TGGAAGAGGT AGCATTTTAG GCTGAATTTC TTTGTTTCCC AAAAGGAAGT TGGTTTCTAT 2220
CTTTATCCTT TTTTTAAATT AAACTTTTAT TTCCTCCAAG GCAATTATTC TAAATGGAGT 2280
TCCATACCTA GAGCTCCCTT TCATATTGTA AAAATAGCAC AACTGATGGC GTTTCATGGT 2340
GAAGCTGTGT TGGATCATCC CAGAGAAGCT CCGAGACAGG GCAAGTGAAC ACCAGACCAC 2400
AAAGGACAGC TACAGTGTCA CCATCTGTGG AAACTAGGCT TTTCCCCCAT GCACGCCTTT 2460
TCCTGATTCT TCCTCTGCAT AGAGACATTT GGCTACTTTT TCCATCATGG TGGTTAGAAC 2520
AAGAAAATTT GGGCGGAAAA TGGGAGTTCT CAGGAGCCAA GATTTGGGCC TGGGAAAGGA 2580
AGGATGAAGA GGAGCAGTTT GGAGCGGGGC ATGAGGTTAG ACTCTCAAGG CCAGGTGGGC 2640
TTGCTGAGGG CAGTGATCCT CTGAGGTTGT TGACTCCCAG TGGCAGGTGA CCCCTTATCA 2700
GGACTTGCCT GGTAGAAGTC CCTGGACTGA GCCAGATAAC TAAATTGGGA CCATTGGTGC 2760
TTGTGTTGCC TTTTGTACCG GGTACCCTTT ACGCCTTGTT TGCTTTTTGT TGGAGATATT 2820
TATCTCCTTG TAAAAAGTGC AGTTCTTTCC CTACCCCAGT CATGAGGCTC TGGCTCAGAG 2880
GAGGTACAAG ATTGTAGCAA AAAATTTGAG 2910