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

TagContent
EnhancerAtlas ID
HS095-07836 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr12:111874680-111877280 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr12:111875984-111875995GGGCGGGAAGG+6.62
Foxd3MA0041.1chr12:111876775-111876787GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr12:111876779-111876791GTTTGTTTGTTT+6.32
IRF9MA0653.1chr12:111876977-111876992AGTTTCGCTTTTGTT-6.52
ZNF263MA0528.1chr12:111875163-111875184CCTTCTCTTTCCTCCTCCCCT-6.68
ZNF263MA0528.1chr12:111875160-111875181CTCCCTTCTCTTTCCTCCTCC-7.91
Number of super-enhancer constituents: 34             
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_17009chr12:111871252-111875326CD4p_CD225int_CD127p_Tmem
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
GCATCTCTGG CTAATCACTT CCCCCGCCCC CCTCCCGCCA CACACATACA CGGGAAAAGC 60
AGGCTGGTGT GTGTCCTGTT GCCCACACCA CACTCAGTCA CTCAGTGTGA GCTGGGGTGC 120
CACCTGCCTG GAGGGGGGAT CTGACTCTGA ACAGGGATTC TGTATTTGGG GGTGTCACAC 180
TCACCATGTC TGTCTCTGCC TCTACCATCT GACTGGGAGA ATTCCTCTCA GGGTTGGGGT 240
GGGCACCAAG CCTTGCTCCC AGTAGGGGCC CAGCCCTGGG TTGGGCCCAG AGGAGGTGCT 300
TGGAGGGTTT ACTGGGTGAC GGATGGATGA GCACTTGGGT AGGGGCCTGG GACCCCCAAA 360
GCCCTCAGAT GTCTGGGAAA TAGGGGGATG TTCTGGCTGG GGAGGTTTCT GTTTCTGGCA 420
TTGGGGGGCT CTTGCCAGGA AAGGGCTTTT CTGGCAGCCA TGTGGCTTTT CTGGAAGCTT 480
CTCCCTTCTC TTTCCTCCTC CCCTGTGGGG AAAGGGCACC TGAGGCAGCA GGGTGCAGAC 540
CAAGGGGGGA TCTGGCCCAT AATGAACAGG GTGGTGGGGG TCTAGGAGCC GCTGCCCTGT 600
GGACTGGGCC CACTGGGCAT TCAGGGCAGC AGGCAGGCTC ACTTGCAGAA GTCCAAGGAG 660
TGGGTTCCAT TATCATCCCC ATTTTACAGG TGAGGAAACT GAAGCACAGC AGGCCAAAGT 720
AATTTGCTCA GGGCCCTGCA TTTGAAGGGT CTGTGAAGGA GGGGCCAGGC TTGGGGTCCT 780
GGTGGGGGGC ATAGCAGAGA AGCGCCCTGT GGCCTGTAGT TCCCACACTG ATTCAGTCGC 840
TGGAACTGGC TCATTGCCTT CAGTTTGCCC CCCAAGGAGC TTGGGAAAAG GGGGCTGAGA 900
TCACCCATCA CACCCCATAC CTCCCTCTGC TTCCCAGGCA CTTGAGAGCT TGGGGGTCCC 960
AGGTACCTAC CCAAGTGCTC ATCCATCCAT CCACCCGGCA AACCCTCCAA GTACCTCCTC 1020
TGGGCCTGCC CCAGGGCTGG GCCTCAGCTG GCAGCAAGGT TTGGTGCCCA CCCCAACCCC 1080
AAGAGGAACT CTCCCAGTCA GATGGTGGAG GCAGTTGCGT CATCAGGAAA CCATGGCCGG 1140
TTCGATAAGC TCAGTGCTGA GGGAGAGGCA CAGGAATTGC ACTAATCATG ACTCAGTGGT 1200
CAGAGAAGGC TCCCTGGAGG AGAGGAGGTT TTCTCTGCTG GGACATGCAG TTTGGGTCAG 1260
GCAGGGCATC ACAAATGCAG GGGCTGGGTG GCAGGGGAAG GTGTGGGCGG GAAGGCGGCT 1320
GGAGGGAGAC CAGGTGTTGG GGGTGCTGGG GCTGGGGGTG GGCAGATGAG GATTGGAGCC 1380
CTGGCTCAAC TTCGCTATTC CCCATGGCTG GGGCACTGTG TGATTTTGCC TCCCAGAGTC 1440
TGTAGCATGG GGGCTCCTGA TGGTGCCCTT GCGGGGAGGT CAGGGGGCTG ACACACCTGA 1500
GCCTGCCTTT CAGCCTGCCC TCTTCCCTGG CCAGCTGGAG GGGCCTTGGG AGGCCCACCC 1560
CAGCCCTGAG AGCACTGGCT TGTAGCATCC CTATCACTCA TGGTCTTCAC TGGGGTGGGG 1620
GATGGCAGTA GGGGCAATCA TCCCCTATGC CCCCCGTTAC CCAGCACAAA GGATGCTTAG 1680
CCAGCAAAAG GCTTATGATG AATGTTGAGC ACCCACCACC TAGCAGGCAC TGGCTCGCGG 1740
CCAAGGACAC CACGTGAGCA AAGCCAAGTC ACGGCAGAGA CCTGCATCAA GGAATGCGCA 1800
AGACCAGCTC ATAGGACAAC AGGCAGGGAA GGAAGTGAAG GGGCTTTGCG GCTCAGGATT 1860
TAGATACTGT GGTCAGGGAG GGCCTCCCTG AGGAGATGAC ACTTTGAAAA GCAGTCGTAT 1920
TTGTGAAGCT GTGGGGGGAG CTGCCTCTCT GAGGGCACAG GCCCCGAGTG CACCTGGCAC 1980
ACTGAAGAAG AGTGGAGGCC AGTGTGGCTG GATCAGAGCG AGGGAGGGAG GCCCAAGAGG 2040
CTGAGGAGGT AACAAGGGTC TCTCAGATGA GGACCACAGG GGAGTTTTTG TTTTTGTTTG 2100
TTTGTTTGTT TGAGACAGTC TTGCTCTGTT GCCCAGGCTG CAGTGCAGTG CAGTGGCGCA 2160
ATCTTGGCTT ACTGCAGCCT CTGCCTCCCG GGTTCAAGTG ATTCTCCTGC GTCAGCCTCC 2220
CAAGTAGCTG GGACTACAGG TACCTGCCAC CATGCCCGAC TAATTTTTGT ATTTTTGTAT 2280
TTTTTTGTGT GAGATGGAGT TTCGCTTTTG TTGCCCAGGC TGGAGTGCAG TGGCACGATC 2340
TTGGCTCACC ACAACCTCTG CCTCCTGGGT TCAAGCGATT CTCCTGCCTC AGCCTCCCGA 2400
GCAGCTGGGA TTATAGGCAT GTGTCATCAC ACCTGGCTAA TTTTGTATTT TTAGTAGAGA 2460
CAGAGTTTCT CCATGTTGGT CAGGCTGGTC TCTAACTCCT GACCTCAGGT GATCTGCCTT 2520
GCCTCGGCCT CCCAACGTGC TGGGATTACA GGTGTGAGCC ACCGCACCTG GCCTAATTTT 2580
TGTATTTTTA ATAGAGACAG 2600