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

TagContent
EnhancerAtlas ID
HS023-06337 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr12:113669740-113672330 
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
CAGGGAATCA GGACGAGTCT GAATGTAGTG GGCAGTCCAA GGAATTTCCC AGGGTAACTC 60
TGGTCACACT CAGCTCTGCC TTCTCCCTGC CTTTAAAGCC AGCTGCTGCC TAAGATGGGC 120
TGGACCATGT GCCTTTTCTG AGTGAAGGAA GGATTGGGCT CGCGGGGGCT GGCTGAGGTC 180
TGAGCAGGAT GCTCCGTCTC TGCTTTGGTG CCGGGTTGTT TATGGTTTTC AGGTGACAGG 240
TCCTGCAGCT AAGGCCCAAG GTCACAGCGC AGAGAGCTGA CCTCTCCCTC CTTCACGCCG 300
ATGCCTGGCA CATCATCTGG AGTTCCCTAG GACACAGTGC AGCCTCAGCA ATGTGGAGGA 360
TCCCTGCCCC CTGGCAGGGG CCCCCATGTG GCACCCTGGT CCCCTTTTCA GGGTCTTCAT 420
GCAGCCAGGG CGAGTTGGCA CCAGGCTCAG TCAAGGTGGG CCAGAGCTGT TGGCCGCAGG 480
GCCGCCGTAG CCAGGAGGAG TTGGGAGAGA TCCTCGCCGG CTGGCACCAG AGAAGAATAC 540
ACCCCGAGGT GTGCGCTCCA TCACTGATGT CTGTGCCGTG GCTCTGCCTC TGACCAGATG 600
GCCCCAGCAT ACTTGCCAAA GAGTGAAGAA GCCCAAGGGG CTTGCACAGC TTTTGTCACT 660
TGTGATACCA TGGTGAGTGG AGTGGTTGAG CTGAGTATAG TGCTTAGCTG CTCTAAGCCT 720
CAGCCTGCTC ATCTGTAGAA TGTGACCATG ATGGCATCTA CCAGTAGAGT CGTCATGGGG 780
GATTGAGTGA GAGCATGTGT GTGATCACAT GGTCAGTGCT CAGCCGGTCA TAGGCATTAT 840
TATCATGGCA GAAACTGGGC TTCCTTGGAA TATCCTCCAT GAGCAGAGGT CCTGAACCCA 900
GGCCACGATT CAGATCCTTC TTGCCTCACT CCTGGCACAG CAGGTGGCCC CTGCCAAGCT 960
GGGACGCCTC CGTGTAGCAG CTGGAGACCA AGCAGCAATT AGATTTTCAC AGGCTCCCAC 1020
CGAGCTTGGG CATTTGGCTC CGCTGGAGTC ATTCCCCTGG CTTTTTCAGG GCCTCACCAA 1080
GGCAGAGCGT CGGGTGTCAC CAGACCAGCA GTGGTGCCAA TTAAAATGAG TAAGCATCCA 1140
GCATGCTGGG CGAGAGCCTT GCAGCCGAGC CTTGGAGCTT TCACTTCCTC AGCCCTCCAC 1200
ATCTTCATGG GGGGGATCCT GTCTGTTGCC TCAGGCCCCC TGCCATGAGA TGCCATCTCT 1260
TCCCGTCCCC CTTTCCCGCA CACAAGACGC TGCCGCTCTA AATGGCAGTC GTGGCAGCTG 1320
GGTGCAGGCT GAAGCACCTG CCACTCTCCT CCCCACTCGC CTGGGGGAGG GCTGAGTTCA 1380
CGTTTCCTCT GAGAGCGCTT CATGAGCCAG AACCGTGAAC TTCTCAGCTT CCCCATCGGG 1440
GAGGCAATAT GGGAGGGCTT GGATGGCTCA CAGCAGCGTG CCGCTGGGGG CATCAGGTTG 1500
CAGTGCCCTC TGCGGGGAGG TTTCAAATGA CAGCAAGGTA GCCCAGGAAC AAACCTGGAG 1560
TGACGTCAAT CTTGAGACAG CCCCCACGCC GCCTTCCTGC TCCAGGAGCC CTGGGTGGCT 1620
CTCCATTCTT GCCCTTGGCT AGAGTGAATC CTCTGGTTCG GACATCCTCT GACTGTCACC 1680
CTTCTCCCCG CAGTCAGGTA TGCCTGGGGA GAGGATGTGC CTGGGTCAGG GTATGTGCAG 1740
TCATAATCAT GGCCTGTGGG TGTTGAGCCC TCGCCGTGTG TCAGGCGGTA TCCAAAGCAC 1800
TTTTGTGCTG CTATCATTTG GTCCTCCCTC CCAGCAGATT TGGGGGGCCG TTACTTTCAA 1860
TATCATCTCA AAGAAGAGGA AACGGAGGCT CTCAGAGGTT GAAACTTATC CAAGGTCACA 1920
AAGACACTTT GACTTCCTTT GAACCCATGT CTAGTGACTC CAGAACCAGT CTCTTACCTA 1980
GTATGCCCCC CTCCGTGAGG TAGAGCTCTG TGGAAGAGGT AGCATTTTAG GCTGAATTTC 2040
TTTGTTTCCC AAAAGGAAGT TGGTTTCTAT CTTTATCCTT TTTTTAAATT AAACTTTTAT 2100
TTCCTCCAAG GCAATTATTC TAAATGGAGT TCCATACCTA GAGCTCCCTT TCATATTGTA 2160
AAAATAGCAC AACTGATGGC GTTTCATGGT GAAGCTGTGT TGGATCATCC CAGAGAAGCT 2220
CCGAGACAGG GCAAGTGAAC ACCAGACCAC AAAGGACAGC TACAGTGTCA CCATCTGTGG 2280
AAACTAGGCT TTTCCCCCAT GCACGCCTTT TCCTGATTCT TCCTCTGCAT AGAGACATTT 2340
GGCTACTTTT TCCATCATGG TGGTTAGAAC AAGAAAATTT GGGCGGAAAA TGGGAGTTCT 2400
CAGGAGCCAA GATTTGGGCC TGGGAAAGGA AGGATGAAGA GGAGCAGTTT GGAGCGGGGC 2460
ATGAGGTTAG ACTCTCAAGG CCAGGTGGGC TTGCTGAGGG CAGTGATCCT CTGAGGTTGT 2520
TGACTCCCAG TGGCAGGTGA CCCCTTATCA GGACTTGCCT GGTAGAAGTC CCTGGACTGA 2580
GCCAGATAAC 2590