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

TagContent
EnhancerAtlas ID
HS105-10311 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr10:73531560-73533110 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr10:73532980-73533000GGGCGGTGGGTGGAGTGGGG-6.45
ZNF263MA0528.1chr10:73531839-73531860CACCTCCCATTCTCCTCCTCC-6.1
ZNF263MA0528.1chr10:73531842-73531863CTCCCATTCTCCTCCTCCCTC-6.95
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_02126chr10:73529220-73534492Aorta
SE_02934chr10:73528955-73533818Bladder
SE_04467chr10:73529333-73535298Brain_Anterior_Caudate
SE_06313chr10:73529027-73537202Brain_Hippocampus_Middle
SE_09212chr10:73519913-73539677CD14
SE_10507chr10:73526194-73535094CD19_Primary
SE_11555chr10:73525717-73536174CD20
SE_11867chr10:73525696-73533295CD3
SE_13733chr10:73528072-73533652CD34_Primary_RO01536
SE_14459chr10:73526218-73535033CD4_Memory_Primary_7pool
SE_15435chr10:73530503-73534050CD4_Memory_Primary_8pool
SE_15862chr10:73530190-73534176CD4_Naive_Primary_7pool
SE_16389chr10:73528051-73534117CD4_Naive_Primary_8pool
SE_16982chr10:73528073-73533985CD4p_CD225int_CD127p_Tmem
SE_17364chr10:73520062-73535154CD4p_CD25-_CD45RAp_Naive
SE_17829chr10:73522939-73535186CD4p_CD25-_CD45ROp_Memory
SE_18298chr10:73519827-73535875CD4p_CD25-_Il17-_PMAstim_Th
SE_19115chr10:73520065-73535185CD4p_CD25-_Il17p_PMAstim_Th17
SE_20080chr10:73525819-73535313CD56
SE_20879chr10:73527995-73534359CD8_Memory_7pool
SE_21529chr10:73528231-73534294CD8_Naive_7pool
SE_21976chr10:73527911-73534794CD8_Naive_8pool
SE_22329chr10:73522842-73535294CD8_primiary
SE_23531chr10:73528126-73534311Colon_Crypt_1
SE_24957chr10:73531333-73534227Colon_Crypt_3
SE_25673chr10:73528060-73534177DND41
SE_26143chr10:73524367-73534193Duodenum_Smooth_Muscle
SE_26620chr10:73529081-73534644Esophagus
SE_29438chr10:73531233-73534038Fetal_Intestine_Large
SE_31624chr10:73529147-73534199Gastric
SE_37028chr10:73521981-73535534HSMMtube
SE_40874chr10:73524079-73535781Left_Ventricle
SE_42187chr10:73520149-73536258Lung
SE_44709chr10:73522832-73534109NHDF-Ad
SE_49200chr10:73529144-73534161Right_Atrium
SE_50063chr10:73522901-73536984Sigmoid_Colon
SE_52370chr10:73523085-73535246Small_Intestine
SE_53294chr10:73524204-73537013Spleen
SE_59774chr10:73453131-73536958Ly4
SE_62254chr10:73471895-73536454Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr107353180073532400
chr107353183173532355
Enhancer Sequence
TCTGCTACTG GGTGCTCTGC AAGCTGGGTC CCTGTGCCCT GGATCTCTAG AAATGTTTCT 60
CAAATTGGGG CTGCTGAACA GAGGGCAGCC CAGCCAAGTG AGGGCAGGAA GTGGGCAAGA 120
AAGCAGGAAG GGTCTCACAG GGCCACCAGG GAGGGCAGTG CAGGGCAGGT GGCCCATGAC 180
AGGTGGGATG CTGGCTTGCC TGCCTGCCAC CATCCTCTGT TCCTTCTGGA AGCCATGCCC 240
TGCCATGAGC CATGGCCTTG GTGCTGAGAC TGTCCATTCC ACCTCCCATT CTCCTCCTCC 300
CTCTGACTGT CACCTTGAGA AGCATCCACC CTGGGGCTTA GGGCAGCTGT GTCTGTGACA 360
TGTGGAGCCC TCCTCCTCCT CAGAGGCCCA GGCCAGCCTC CAAGTGCTGA GATAGCCAGC 420
TGCCTGTGGG CACCCAGGTT GCTAAGGTAT CTTCCAGGTT CAGCCTCCTC CTCTCCCTCT 480
TATCCTATCA CCCTCTCCTT CTATTCCATC CTGCCCACTG GGTCCCTGTG CCAAGCCCTC 540
CACCTCCCTC CTGCCTCCCT CCGAGTCCCT GCATGACTCA TACTTTCCCT GGGCCCTCCC 600
TATAAAGTTT GGTTCCACAG GCTCTTTGAA GAGATCCAGC CTCTTCAGCT CTGGGCAGGC 660
AAGAACTAGG CAACCAGGCC ATGGGTACCA GGGCCTCTGC CCCCAGCCCG GGAGCCCCTG 720
TGTTGGGGCC AGGATACTAT CTGAACATGC TGACAGTCTG GACTTTGGAA GGGGAAAATG 780
GTGCTTCCCT GTGTGGGCTT CTGTGTTTGA GCTGAGGAAA CTGAGGCCAG AGAGATGCCG 840
TAATTTATCC AGGGACCCAG AAGGGGCTCA TAGCTGAGCT GAAGAGTGTC CCACATCCTC 900
CCCAGTACTC CACACTGGTC CCTGAGTGGC AGCCTTGCTA GGATGGCAGG AATCAGCTGA 960
CCACTTATTC CTGGGCCATC AGACCCTTAG AATAGGGACC AGGTGGGCAG TGCTGCCTCT 1020
GTGTCTGAAA GTGGACCCAC CGTGACCAGT GCCCAGTGCC CACCAAGGCT CAGCCAGGGG 1080
TTTCACCAGG GCATGGGGCA CTGGCTGAGC ATACCACGCC CTCTGTGTCC TCTGCAACAC 1140
TAGAGCCCTG AGACTAGAGG GGCAGAAAGA TGCCAGCTGT CAAAAGCCAG TGATATCCAC 1200
CAGAACACAC TGACCGCCCC CACCCTGTGC CTCTCCTTCT TTGCAGAAGC TACCTGTGCC 1260
CTGGGTTCTC TGGGCAGGGA AGGGCTGGAC AGGCAGCCCT CAGGGGACAG CCCTGCCTGC 1320
CACTTGGGCA GCTGTCAGAG CATGCAGATG TGCCCGATGC CTAGCTGGGG CACTTGGCAC 1380
AGTTGCCACT GCACCCTGCC TAGGGGTCCC AGCAGCCTCT GGGCGGTGGG TGGAGTGGGG 1440
TGCACGGTCA CACAGGCTGA GAGGGCCCCC AGGACGCCCC CATCCCACAG TTCCCACTCC 1500
AGTCTGCTGT CTTCTCCCAG CTTTTTCCCA GCGCCCCGCC TCCCCCGACC 1550