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

TagContent
EnhancerAtlas ID
HS037-09464 
Organism
Homo sapiens 
Tissue/cell
ESC 
Coordinate
chr12:113668370-113670650 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr12:113670104-113670116TGCCCCCTGGCA-6.62
Nr2f6MA0677.1chr12:113669422-113669436TGACCTTTAACCCT-7.01
RxraMA0512.2chr12:113669422-113669436TGACCTTTAACCCT-7.04
SRFMA0083.3chr12:113669481-113669497TCTCCTTATATGGGCA+6.15
SRFMA0083.3chr12:113669481-113669497TCTCCTTATATGGGCA-7.06
Sox3MA0514.1chr12:113668939-113668949CCTTTGTTTT+6.02
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00883chr12:113664391-113671759Adrenal_Gland
SE_01635chr12:113668074-113671857Aorta
SE_03506chr12:113670303-113671468Brain_Angular_Gyrus
SE_04226chr12:113668219-113671573Brain_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_09783chr12:113664182-113681103CD14
SE_26345chr12:113668747-113669722Duodenum_Smooth_Muscle
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_42290chr12:113664247-113673161Lung
SE_44290chr12:113669973-113671773NHDF-Ad
SE_47597chr12:113669662-113670175Pancreas
SE_48084chr12:113663861-113673266Psoas_Muscle
SE_48792chr12:113667499-113671975Right_Atrium
SE_49644chr12:113668214-113668917Right_Ventricle
SE_49644chr12:113668928-113671654Right_Ventricle
SE_50157chr12:113669359-113671777Sigmoid_Colon
SE_51183chr12:113663840-113675194Skeletal_Muscle
SE_52527chr12:113668194-113669763Small_Intestine
SE_53751chr12:113665943-113668697Spleen
SE_53751chr12:113668950-113669826Spleen
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
chr12113669097113670107
Number: 1             
IDChromosomeStartEnd
GH12I113226chr12113664004113672117
Enhancer Sequence
CCTATTGGAT TAGAGCTCAT CCATATGACC TTGTTTTATC TTAGTCACCT TTAAAGGCCC 60
TTTCTCCAAA CACAGTCACA TTCTTTCACC ATGTTGGCCA GGCTGATCTC AAATTCCTGA 120
CCTCGAGTGA TCTATCCGCC TTGGCCTCCT GAAGCGCTGG GATTACAGGC ATGAGCCACC 180
ATGCCTGGCC CATCCATTTG TCTTTGTATC ACATAGCTCA GTGCCCACAA TATGCAGGTA 240
CTCAACAAAT AGTGGTCAGA ATCAACGTAC TTGGATTTCT GGGGCCTCGC AGCCCATGGG 300
AGTGGCAGTG TAAGGGCCCG AGTTAGAGGT GGGCAGCCTC CCTCCTGCCG CCTCTCCTCA 360
CCATTGCTTT GAGTCCCATT GCTCTCAGCA CAGCTGAGTG TCCTGGTGGC TGCCATCACT 420
GACCTTTGTC TTTGGTTGCT GTAAACCTTT GAAGTACTAA GGAGTTGGCA GAATGCAGAT 480
GCAGGCCATC CGCGGAGTTG GCAACGACAT GAGCATGGGC TACTGGGAAC GAAGCAAGCT 540
TTCTAAGGCT GAGTCACCAT CAAGCCTGGC CTTTGTTTTG GCCCAGCAGC CGCTGAGGCC 600
TTCTCAGCAC TGTACCTCCA CGCTCCATGT CTGGTTGGGC ACCCCTAACA AAACACCATG 660
GACTGGTGGC TTAAATGACA GAAATCTAAT TTCTCACAGG TCTGGAGGCT GGAAGTCCAA 720
GACCAAGGTG TCAGCAGGTT TGGTTTCTTG CGAAGCCTCT TTCCTTGGCT CGCAAATGGT 780
TATCTTCTTG CTGTGTCCCC ACATGATTGT CCCTGAGTCT GTGTGTCTGT CCTCTTCAGA 840
TAAGGACACC AGTCCTATTG GATTAGGGCT CATCCATATG ACCTTGTTTT ACCTTAATCA 900
CCTTTAAAGG CCCTTTCTCC AAAGACAGTC ACATTCTGAG CTACTGGGGG TTAGGACTTC 960
AGCCTATGAA TTTGAGGGGG ACACAGTTCA GGCCATCACA CTCCTACCCA TTCTTCAGAG 1020
GCAGGGACTG AGGAATCTGG CTGTGCTGCC TGTGACCTTT AACCCTATGT GAGGGCCTTA 1080
TCCCTGCAGG AAACTGGAGG GTTTGGGTTT TTCTCCTTAT ATGGGCAATT GTGGATTTAA 1140
TCCAAGACTC AGACATCTTT GGGCTCTAAG TGCGGCTGCT GCAGTGCTAA TGAATGACTC 1200
ACAGGCAGCA TGGTGTCAGG TTGATAAAGG AGGCAGGTAT GAGCAGAGGT ATTTAAAGCC 1260
TGGAAACTAG GAATAACCTT GAAAACAGTC AGCGGGGCCA CTGTTAGAGC AGTGTAGAGA 1320
CAGACCACAG TCCACACCGC GTGACAGGCG GTGGTCTCAC CCACCACATT CAGGGAATCA 1380
GGACGAGTCT GAATGTAGTG GGCAGTCCAA GGAATTTCCC AGGGTAACTC TGGTCACACT 1440
CAGCTCTGCC TTCTCCCTGC CTTTAAAGCC AGCTGCTGCC TAAGATGGGC TGGACCATGT 1500
GCCTTTTCTG AGTGAAGGAA GGATTGGGCT CGCGGGGGCT GGCTGAGGTC TGAGCAGGAT 1560
GCTCCGTCTC TGCTTTGGTG CCGGGTTGTT TATGGTTTTC AGGTGACAGG TCCTGCAGCT 1620
AAGGCCCAAG GTCACAGCGC AGAGAGCTGA CCTCTCCCTC CTTCACGCCG ATGCCTGGCA 1680
CATCATCTGG AGTTCCCTAG GACACAGTGC AGCCTCAGCA ATGTGGAGGA TCCCTGCCCC 1740
CTGGCAGGGG CCCCCATGTG GCACCCTGGT CCCCTTTTCA GGGTCTTCAT GCAGCCAGGG 1800
CGAGTTGGCA CCAGGCTCAG TCAAGGTGGG CCAGAGCTGT TGGCCGCAGG GCCGCCGTAG 1860
CCAGGAGGAG TTGGGAGAGA TCCTCGCCGG CTGGCACCAG AGAAGAATAC ACCCCGAGGT 1920
GTGCGCTCCA TCACTGATGT CTGTGCCGTG GCTCTGCCTC TGACCAGATG GCCCCAGCAT 1980
ACTTGCCAAA GAGTGAAGAA GCCCAAGGGG CTTGCACAGC TTTTGTCACT TGTGATACCA 2040
TGGTGAGTGG AGTGGTTGAG CTGAGTATAG TGCTTAGCTG CTCTAAGCCT CAGCCTGCTC 2100
ATCTGTAGAA TGTGACCATG ATGGCATCTA CCAGTAGAGT CGTCATGGGG GATTGAGTGA 2160
GAGCATGTGT GTGATCACAT GGTCAGTGCT CAGCCGGTCA TAGGCATTAT TATCATGGCA 2220
GAAACTGGGC TTCCTTGGAA TATCCTCCAT GAGCAGAGGT CCTGAACCCA GGCCACGATT 2280