EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS136-00203 
Organism
Homo sapiens 
Tissue/cell
Monocyte 
Coordinate
chr1:21643320-21644880 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr1:21644137-21644148CCACACCCTCC+6.32
Klf1MA0493.1chr1:21644135-21644146AGCCACACCCT+6.02
MITFMA0620.2chr1:21644318-21644336ACAGGTCATGTGACTTCT+6.53
MITFMA0620.2chr1:21644318-21644336ACAGGTCATGTGACTTCT-6.53
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00105chr1:21640019-21654616Adipose_Nuclei
SE_00854chr1:21642962-21648227Adrenal_Gland
SE_01643chr1:21642185-21648218Aorta
SE_02944chr1:21642987-21644019Bladder
SE_02944chr1:21644056-21645524Bladder
SE_03598chr1:21643482-21644096Brain_Angular_Gyrus
SE_03598chr1:21644394-21645277Brain_Angular_Gyrus
SE_04518chr1:21643279-21645748Brain_Anterior_Caudate
SE_05710chr1:21643177-21645586Brain_Cingulate_Gyrus
SE_05944chr1:21639044-21646536Brain_Hippocampus_Middle
SE_08398chr1:21643228-21645720Brain_Inferior_Temporal_Lobe
SE_26127chr1:21642960-21646679Duodenum_Smooth_Muscle
SE_26770chr1:21642974-21647847Esophagus
SE_28486chr1:21644573-21646764Fetal_Intestine
SE_29337chr1:21644662-21646709Fetal_Intestine_Large
SE_31433chr1:21643029-21648183Gastric
SE_39164chr1:21643088-21645576IMR90
SE_42174chr1:21642958-21646742Lung
SE_44380chr1:21642937-21647054NHDF-Ad
SE_45045chr1:21643168-21646698NHLF
SE_46660chr1:21643459-21645622Ovary
SE_47592chr1:21643574-21645731Pancreas
SE_48583chr1:21642944-21648219Right_Atrium
SE_50108chr1:21643010-21645670Sigmoid_Colon
SE_52633chr1:21642919-21645734Small_Intestine
SE_53334chr1:21642938-21645903Spleen
SE_54639chr1:21639148-21648300Stomach_Smooth_Muscle
SE_56171chr1:21642916-21645508u87
SE_65263chr1:21643359-21649820Pancreatic_islets
SE_67931chr1:21642916-21645508u87
SE_68932chr1:21643728-21645709H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12164383121644195
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
GGAGCCTCCA ATCAATTATT GAAAGTTCAA AAACAGTGAG CAACATCATA CCTATGTATC 60
ATTTAGGGAG GCAGAATCAG GCTGCGCTTG GTGGCTCACA CCTGTAATCC CAGCACTTTG 120
GGAGGCCGAG GTGGGCGGAT CACCTGAGGT CAGGAGTAAC AGTATCAAGA CAGTCACTGA 180
AGAGTCTCTC CCAGTCTCTT CCCCTGGGAG AGAGAGTGGT AAGAAACGGA CTGGGGGTGT 240
GGGGGTATGG GGGATTCAAC TGCATTTGGG ATGTTTTATT CCTTAAGCTG AACACTTACA 300
TACCAGTGTT TGGTTTTACT GAGCCTGATG CTTTTAATAT GTCTGAGATA TTTTGCTACC 360
CACCAGAATA GGTCAGACAG ACTTGGGCTT CGAGCCAGCC CTGTGCTTTG CTGCCATGCG 420
ATCCTAGTCT TCTCTGTGAA GTGGGAATCC TATCGCCCAC TGTTAGCTCC CGGGACTCTT 480
CTGAGAATTA AACAAGGTCG TGTCTGCAAA GGGCCTGGCA TCCGGTGGCT GCCATTGTTC 540
CTGCTGCTGT TGGGAGGGTC TCCCAAAATG AACAGACAGA GGGGAAGGCC AGCTCGCAGG 600
CCTCAGATGG GGAAAAGGGT TTGCTTGTCA CAAGGCCAGT CCAGCCCGCG GCGACGCTGA 660
GCTGGTGACG CATCTGCAGC TCTGGGGATT GAGCAATCTT GGTCCCCTGA CCGGGATGGA 720
GTCATGGGCC CAGGCTGGCT GGAGCCCCTC TACTGCTCCC CACCCGCTTC TCAGACTTTG 780
TGTTCCTGGC CTTCTTGGGA CCCCTCCAGG CTGGCAGCCA CACCCTCCCC TCTGTGAGCT 840
AGGCAGGAAA GCCCGGTTCC ATTCCTGCCC AGTTCTCTTC GGCCTCTCCT GAGCCCCTGC 900
TCCCCAACTC AAGGTGGGGT CCTAACCACC TTGCATCCAA ACAGATCCTC TGGAGACGCA 960
CGAGTGGGTC AGGGCAGTCA AGAGCTGTGC AGGCTCAGAC AGGTCATGTG ACTTCTGTAG 1020
GTCCCTGGCT TTAGCAGGTG TGGCCGAAGG TGTGGGGTGC CAGTGTCTGT CTCCTGGTTC 1080
AAATCCAGGC TCGGGGTGTG ACCCCAATGT TCTTGAACTT AAATCAGAGC CACCGCGATC 1140
TCTTTCTCGA AGTGGGGACA AAACACATGC AAAGCAGGGC CTGCCCCTCC AAGGTGCACC 1200
TTGAAGGTAT CAGACGGCAT GGACGAGGTC CCCTCGCTGG CTGCTGTGAC GGTTAAACGA 1260
TTCTTCCCAG CTCTGCACAA CTCAAGTGAT AGCTGTTGGA CTCGGAGATG AACAAGAGTG 1320
AGGGAAACGG TGGGGGAGAG CAGTGGGCAA GACCTGGCGT GGCAAGTGGG GAGCAGGAGG 1380
CCCTCGTGTG GACTCGCAGA GACCCAAACC CAATGAAACA AGTACCCTGC TGGCGCATGT 1440
GCAGGAACTG ATCAGCGTTC CTGAGGGCCC AAGGACATTT CCAGGGCACA GCTTGGGGAG 1500
GGCAGCAGAG TGGGAGCAGC TGTGAAATTG GGTTTCAGGT CATGACGCAG TTGGGGAACT 1560