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

TagContent
EnhancerAtlas ID
HS026-00498 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr1:21644470-21646120 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs201385905chr121645339hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr1:21644930-21644945AGGTCAGCCTGGCCT+7.13
SREBF1MA0595.1chr1:21645053-21645063GTGGGGTGAT-6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00105chr1:21640019-21654616Adipose_Nuclei
SE_00854chr1:21642962-21648227Adrenal_Gland
SE_01643chr1:21642185-21648218Aorta
SE_02944chr1:21644056-21645524Bladder
SE_02944chr1:21645843-21646528Bladder
SE_03598chr1:21644394-21645277Brain_Angular_Gyrus
SE_04518chr1:21643279-21645748Brain_Anterior_Caudate
SE_04518chr1:21645844-21646711Brain_Anterior_Caudate
SE_05710chr1:21643177-21645586Brain_Cingulate_Gyrus
SE_05944chr1:21639044-21646536Brain_Hippocampus_Middle
SE_08398chr1:21643228-21645720Brain_Inferior_Temporal_Lobe
SE_08982chr1:21644985-21645172Brain_Mid_Frontal_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_46660chr1:21645855-21646940Ovary
SE_47592chr1:21643574-21645731Pancreas
SE_47592chr1:21645786-21646790Pancreas
SE_48583chr1:21642944-21648219Right_Atrium
SE_50108chr1:21643010-21645670Sigmoid_Colon
SE_50108chr1:21645842-21646761Sigmoid_Colon
SE_52633chr1:21642919-21645734Small_Intestine
SE_52633chr1:21645749-21646973Small_Intestine
SE_53334chr1:21642938-21645903Spleen
SE_54639chr1:21639148-21648300Stomach_Smooth_Muscle
SE_56171chr1:21642916-21645508u87
SE_56171chr1:21645755-21646598u87
SE_65263chr1:21643359-21649820Pancreatic_islets
SE_67931chr1:21642916-21645508u87
SE_67931chr1:21645755-21646598u87
SE_68932chr1:21643728-21645709H9
SE_68932chr1:21645866-21648182H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12164572921645787
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
AGTGGGGACA AAACACATGC AAAGCAGGGC CTGCCCCTCC AAGGTGCACC TTGAAGGTAT 60
CAGACGGCAT GGACGAGGTC CCCTCGCTGG CTGCTGTGAC GGTTAAACGA TTCTTCCCAG 120
CTCTGCACAA CTCAAGTGAT AGCTGTTGGA CTCGGAGATG AACAAGAGTG AGGGAAACGG 180
TGGGGGAGAG CAGTGGGCAA GACCTGGCGT GGCAAGTGGG GAGCAGGAGG CCCTCGTGTG 240
GACTCGCAGA GACCCAAACC CAATGAAACA AGTACCCTGC TGGCGCATGT GCAGGAACTG 300
ATCAGCGTTC CTGAGGGCCC AAGGACATTT CCAGGGCACA GCTTGGGGAG GGCAGCAGAG 360
TGGGAGCAGC TGTGAAATTG GGTTTCAGGT CATGACGCAG TTGGGGAACT TATTTCCTTC 420
ATCCCTGCCC TTTCCTGACC CTGTCCCACT CCCTTAACAA AGGTCAGCCT GGCCTAGGGG 480
TGTCCTCCCT GGAGACCTCC CCTCCCTTGT GCCTCAGCCT CTCACTGTCT TTGGGGCAGA 540
CATTTCTCCG CTCTGGGCTT CAGTTTCTCT ATCTGTAAAA TGGGTGGGGT GATATTTCAG 600
GCCTTAGCAA CTTCTAAAAT CCCATTTTTT GAAGATTTAG AACCAGTGAG CCTTCCTGAG 660
GCCCACTTCA CAAGCCTATC CAAGCAGAGG TGGCAAAATC CTCCTCCCTG GGTGAGAGGC 720
AGGCGACACC CCTGAGTTGG TCACACCAGC CTTCCAAGGA GCTAACCCGA CCTGACAGTC 780
ACTTCAGCCT GGCCAGGCCC CCAGGCAGTG TGCCAAAAAG CGGACGGGGG AGGGGATTTG 840
CAGCAAGAGC TACAGCTCCC CAGAGGCCGC ACTTCTGTCG GGGGAGACGC TGAGCGAGGG 900
TCAGAAGAAA GTCAGCATGG GAAATGTGAC GTCAGCAGAG GCAGATGCGA AGGAATACTA 960
TCCGAAAATG CTTCCGTAAA CTCACCCTCC CAGGAAGCCA AATTCTGTGG GTTTTCAGTG 1020
GAGCTGGGTC TGTACAATCT CCCGGGCTCC GTTTTCTCAT CAGCTAAGTC AAAATAATAA 1080
AGTGAGGCCA GGCACGGTGG CTCAAGCTCG TAATCCAAGC ACTTTGGGAA GCCAAGGTGG 1140
GTGGATTGCC TGAGCTTAGG AGTTCGAGAC CAGCTTGGGC AACATGGTGA AACCCCGTCT 1200
CCACTAAAAT ACAAAAAAGT AGCCAGGCGT GGTGGTGTGC GTCTATAATC CCAGCTACTT 1260
GGGAGGCTGA GGTGGGACAA TCGCTTGAAC CCGGGAAGTG GAGGTTGCAG TGAGCCGAGA 1320
TCGCATCACT GCTTTCCAGC CTGGGAGACA GAGCGAGACT CCGTCTCAAA ATAATAATAA 1380
TCATAATCAT AATCATAATC ATAATCATAA AGTGGACTAC GCAGGGCTTT TCTAGAGACA 1440
TGATAAGACC TCGTGTCTAA ATGGCCTGGT ACATACTAGG GCCTCCATAA ATGCCGGCTC 1500
CATGCTGCCC CCACCTCTGT CCACCAGGGC ACCCCCGGCA CCAAGGGCCA GACTCCCTCT 1560
GCTGCCCCCA ATCTGCTTCT CAGACTTTCT GCTCCTGGCC TTCCTGGGAG CCCTCCAAGC 1620
CAGCAGCTGT GCCCTCCCCT CTGTGAACTG 1650