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

TagContent
EnhancerAtlas ID
HS105-20487 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr12:111875160-111876870 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr12:111875984-111875995GGGCGGGAAGG+6.62
Foxd3MA0041.1chr12:111876775-111876787GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr12:111876779-111876791GTTTGTTTGTTT+6.32
ZNF263MA0528.1chr12:111875163-111875184CCTTCTCTTTCCTCCTCCCCT-6.68
ZNF263MA0528.1chr12:111875160-111875181CTCCCTTCTCTTTCCTCCTCC-7.91
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00313chr12:111864961-111876909Adipose_Nuclei
SE_01105chr12:111875129-111875715Adrenal_Gland
SE_03792chr12:111876078-111876589Brain_Angular_Gyrus
SE_06099chr12:111871624-111877058Brain_Hippocampus_Middle
SE_08462chr12:111871579-111877036Brain_Inferior_Temporal_Lobe
SE_09337chr12:111861899-111889874CD14
SE_11164chr12:111861758-111877253CD20
SE_11924chr12:111863179-111876859CD3
SE_13643chr12:111874368-111877168CD34_Primary_RO01536
SE_14612chr12:111865393-111876978CD4_Memory_Primary_7pool
SE_16453chr12:111871162-111876524CD4_Naive_Primary_8pool
SE_17009chr12:111875524-111876100CD4p_CD225int_CD127p_Tmem
SE_17538chr12:111862008-111876816CD4p_CD25-_CD45RAp_Naive
SE_17816chr12:111861604-111877277CD4p_CD25-_CD45ROp_Memory
SE_18496chr12:111861894-111877196CD4p_CD25-_Il17-_PMAstim_Th
SE_19231chr12:111871009-111876974CD4p_CD25-_Il17p_PMAstim_Th17
SE_20028chr12:111865094-111877131CD56
SE_21344chr12:111875707-111876761CD8_Memory_7pool
SE_22364chr12:111862617-111877141CD8_primiary
SE_32074chr12:111875365-111876717Gastric
SE_38040chr12:111862345-111877177HUVEC
SE_40041chr12:111874575-111876898K562
SE_40792chr12:111871734-111876987Left_Ventricle
SE_42263chr12:111871824-111877003Lung
SE_46057chr12:111874138-111877122Osteoblasts
SE_48851chr12:111875330-111876644Right_Atrium
SE_50268chr12:111867336-111876981Sigmoid_Colon
SE_52677chr12:111871145-111876910Small_Intestine
SE_53326chr12:111861897-111876991Spleen
SE_62745chr12:111834432-111886877Tonsil
SE_67523chr12:111874559-111876883u87
SE_68830chr12:111872359-111875415H9
SE_68830chr12:111875460-111876867H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12111875686111876044
Enhancer Sequence
CTCCCTTCTC TTTCCTCCTC CCCTGTGGGG AAAGGGCACC TGAGGCAGCA GGGTGCAGAC 60
CAAGGGGGGA TCTGGCCCAT AATGAACAGG GTGGTGGGGG TCTAGGAGCC GCTGCCCTGT 120
GGACTGGGCC CACTGGGCAT TCAGGGCAGC AGGCAGGCTC ACTTGCAGAA GTCCAAGGAG 180
TGGGTTCCAT TATCATCCCC ATTTTACAGG TGAGGAAACT GAAGCACAGC AGGCCAAAGT 240
AATTTGCTCA GGGCCCTGCA TTTGAAGGGT CTGTGAAGGA GGGGCCAGGC TTGGGGTCCT 300
GGTGGGGGGC ATAGCAGAGA AGCGCCCTGT GGCCTGTAGT TCCCACACTG ATTCAGTCGC 360
TGGAACTGGC TCATTGCCTT CAGTTTGCCC CCCAAGGAGC TTGGGAAAAG GGGGCTGAGA 420
TCACCCATCA CACCCCATAC CTCCCTCTGC TTCCCAGGCA CTTGAGAGCT TGGGGGTCCC 480
AGGTACCTAC CCAAGTGCTC ATCCATCCAT CCACCCGGCA AACCCTCCAA GTACCTCCTC 540
TGGGCCTGCC CCAGGGCTGG GCCTCAGCTG GCAGCAAGGT TTGGTGCCCA CCCCAACCCC 600
AAGAGGAACT CTCCCAGTCA GATGGTGGAG GCAGTTGCGT CATCAGGAAA CCATGGCCGG 660
TTCGATAAGC TCAGTGCTGA GGGAGAGGCA CAGGAATTGC ACTAATCATG ACTCAGTGGT 720
CAGAGAAGGC TCCCTGGAGG AGAGGAGGTT TTCTCTGCTG GGACATGCAG TTTGGGTCAG 780
GCAGGGCATC ACAAATGCAG GGGCTGGGTG GCAGGGGAAG GTGTGGGCGG GAAGGCGGCT 840
GGAGGGAGAC CAGGTGTTGG GGGTGCTGGG GCTGGGGGTG GGCAGATGAG GATTGGAGCC 900
CTGGCTCAAC TTCGCTATTC CCCATGGCTG GGGCACTGTG TGATTTTGCC TCCCAGAGTC 960
TGTAGCATGG GGGCTCCTGA TGGTGCCCTT GCGGGGAGGT CAGGGGGCTG ACACACCTGA 1020
GCCTGCCTTT CAGCCTGCCC TCTTCCCTGG CCAGCTGGAG GGGCCTTGGG AGGCCCACCC 1080
CAGCCCTGAG AGCACTGGCT TGTAGCATCC CTATCACTCA TGGTCTTCAC TGGGGTGGGG 1140
GATGGCAGTA GGGGCAATCA TCCCCTATGC CCCCCGTTAC CCAGCACAAA GGATGCTTAG 1200
CCAGCAAAAG GCTTATGATG AATGTTGAGC ACCCACCACC TAGCAGGCAC TGGCTCGCGG 1260
CCAAGGACAC CACGTGAGCA AAGCCAAGTC ACGGCAGAGA CCTGCATCAA GGAATGCGCA 1320
AGACCAGCTC ATAGGACAAC AGGCAGGGAA GGAAGTGAAG GGGCTTTGCG GCTCAGGATT 1380
TAGATACTGT GGTCAGGGAG GGCCTCCCTG AGGAGATGAC ACTTTGAAAA GCAGTCGTAT 1440
TTGTGAAGCT GTGGGGGGAG CTGCCTCTCT GAGGGCACAG GCCCCGAGTG CACCTGGCAC 1500
ACTGAAGAAG AGTGGAGGCC AGTGTGGCTG GATCAGAGCG AGGGAGGGAG GCCCAAGAGG 1560
CTGAGGAGGT AACAAGGGTC TCTCAGATGA GGACCACAGG GGAGTTTTTG TTTTTGTTTG 1620
TTTGTTTGTT TGAGACAGTC TTGCTCTGTT GCCCAGGCTG CAGTGCAGTG CAGTGGCGCA 1680
ATCTTGGCTT ACTGCAGCCT CTGCCTCCCG 1710