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

TagContent
EnhancerAtlas ID
HS020-11496 
Organism
Homo sapiens 
Tissue/cell
CD34+ 
Coordinate
chr12:113669700-113672570 
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
TCCACACCGC GTGACAGGCG GTGGTCTCAC CCACCACATT CAGGGAATCA GGACGAGTCT 60
GAATGTAGTG GGCAGTCCAA GGAATTTCCC AGGGTAACTC TGGTCACACT CAGCTCTGCC 120
TTCTCCCTGC CTTTAAAGCC AGCTGCTGCC TAAGATGGGC TGGACCATGT GCCTTTTCTG 180
AGTGAAGGAA GGATTGGGCT CGCGGGGGCT GGCTGAGGTC TGAGCAGGAT GCTCCGTCTC 240
TGCTTTGGTG CCGGGTTGTT TATGGTTTTC AGGTGACAGG TCCTGCAGCT AAGGCCCAAG 300
GTCACAGCGC AGAGAGCTGA CCTCTCCCTC CTTCACGCCG ATGCCTGGCA CATCATCTGG 360
AGTTCCCTAG GACACAGTGC AGCCTCAGCA ATGTGGAGGA TCCCTGCCCC CTGGCAGGGG 420
CCCCCATGTG GCACCCTGGT CCCCTTTTCA GGGTCTTCAT GCAGCCAGGG CGAGTTGGCA 480
CCAGGCTCAG TCAAGGTGGG CCAGAGCTGT TGGCCGCAGG GCCGCCGTAG CCAGGAGGAG 540
TTGGGAGAGA TCCTCGCCGG CTGGCACCAG AGAAGAATAC ACCCCGAGGT GTGCGCTCCA 600
TCACTGATGT CTGTGCCGTG GCTCTGCCTC TGACCAGATG GCCCCAGCAT ACTTGCCAAA 660
GAGTGAAGAA GCCCAAGGGG CTTGCACAGC TTTTGTCACT TGTGATACCA TGGTGAGTGG 720
AGTGGTTGAG CTGAGTATAG TGCTTAGCTG CTCTAAGCCT CAGCCTGCTC ATCTGTAGAA 780
TGTGACCATG ATGGCATCTA CCAGTAGAGT CGTCATGGGG GATTGAGTGA GAGCATGTGT 840
GTGATCACAT GGTCAGTGCT CAGCCGGTCA TAGGCATTAT TATCATGGCA GAAACTGGGC 900
TTCCTTGGAA TATCCTCCAT GAGCAGAGGT CCTGAACCCA GGCCACGATT CAGATCCTTC 960
TTGCCTCACT CCTGGCACAG CAGGTGGCCC CTGCCAAGCT GGGACGCCTC CGTGTAGCAG 1020
CTGGAGACCA AGCAGCAATT AGATTTTCAC AGGCTCCCAC CGAGCTTGGG CATTTGGCTC 1080
CGCTGGAGTC ATTCCCCTGG CTTTTTCAGG GCCTCACCAA GGCAGAGCGT CGGGTGTCAC 1140
CAGACCAGCA GTGGTGCCAA TTAAAATGAG TAAGCATCCA GCATGCTGGG CGAGAGCCTT 1200
GCAGCCGAGC CTTGGAGCTT TCACTTCCTC AGCCCTCCAC ATCTTCATGG GGGGGATCCT 1260
GTCTGTTGCC TCAGGCCCCC TGCCATGAGA TGCCATCTCT TCCCGTCCCC CTTTCCCGCA 1320
CACAAGACGC TGCCGCTCTA AATGGCAGTC GTGGCAGCTG GGTGCAGGCT GAAGCACCTG 1380
CCACTCTCCT CCCCACTCGC CTGGGGGAGG GCTGAGTTCA CGTTTCCTCT GAGAGCGCTT 1440
CATGAGCCAG AACCGTGAAC TTCTCAGCTT CCCCATCGGG GAGGCAATAT GGGAGGGCTT 1500
GGATGGCTCA CAGCAGCGTG CCGCTGGGGG CATCAGGTTG CAGTGCCCTC TGCGGGGAGG 1560
TTTCAAATGA CAGCAAGGTA GCCCAGGAAC AAACCTGGAG TGACGTCAAT CTTGAGACAG 1620
CCCCCACGCC GCCTTCCTGC TCCAGGAGCC CTGGGTGGCT CTCCATTCTT GCCCTTGGCT 1680
AGAGTGAATC CTCTGGTTCG GACATCCTCT GACTGTCACC CTTCTCCCCG CAGTCAGGTA 1740
TGCCTGGGGA GAGGATGTGC CTGGGTCAGG GTATGTGCAG TCATAATCAT GGCCTGTGGG 1800
TGTTGAGCCC TCGCCGTGTG TCAGGCGGTA TCCAAAGCAC TTTTGTGCTG CTATCATTTG 1860
GTCCTCCCTC CCAGCAGATT TGGGGGGCCG TTACTTTCAA TATCATCTCA AAGAAGAGGA 1920
AACGGAGGCT CTCAGAGGTT GAAACTTATC CAAGGTCACA AAGACACTTT GACTTCCTTT 1980
GAACCCATGT CTAGTGACTC CAGAACCAGT CTCTTACCTA GTATGCCCCC CTCCGTGAGG 2040
TAGAGCTCTG TGGAAGAGGT AGCATTTTAG GCTGAATTTC TTTGTTTCCC AAAAGGAAGT 2100
TGGTTTCTAT CTTTATCCTT TTTTTAAATT AAACTTTTAT TTCCTCCAAG GCAATTATTC 2160
TAAATGGAGT TCCATACCTA GAGCTCCCTT TCATATTGTA AAAATAGCAC AACTGATGGC 2220
GTTTCATGGT GAAGCTGTGT TGGATCATCC CAGAGAAGCT CCGAGACAGG GCAAGTGAAC 2280
ACCAGACCAC AAAGGACAGC TACAGTGTCA CCATCTGTGG AAACTAGGCT TTTCCCCCAT 2340
GCACGCCTTT TCCTGATTCT TCCTCTGCAT AGAGACATTT GGCTACTTTT TCCATCATGG 2400
TGGTTAGAAC AAGAAAATTT GGGCGGAAAA TGGGAGTTCT CAGGAGCCAA GATTTGGGCC 2460
TGGGAAAGGA AGGATGAAGA GGAGCAGTTT GGAGCGGGGC ATGAGGTTAG ACTCTCAAGG 2520
CCAGGTGGGC TTGCTGAGGG CAGTGATCCT CTGAGGTTGT TGACTCCCAG TGGCAGGTGA 2580
CCCCTTATCA GGACTTGCCT GGTAGAAGTC CCTGGACTGA GCCAGATAAC TAAATTGGGA 2640
CCATTGGTGC TTGTGTTGCC TTTTGTACCG GGTACCCTTT ACGCCTTGTT TGCTTTTTGT 2700
TGGAGATATT TATCTCCTTG TAAAAAGTGC AGTTCTTTCC CTACCCCAGT CATGAGGCTC 2760
TGGCTCAGAG GAGGTACAAG ATTGTAGCAA AAAATTTGAG AGCTGGGCCA CCCTGGGGCC 2820
TGCCGGACCA GGGGCATACT GGGGCCAGTG TGCACTCTCT GAAGGGACAA 2870