EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS099-18498 
Organism
Homo sapiens 
Tissue/cell
HSMMtube 
Coordinate
chr5:139057640-139059250 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3822742chr5139059017hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PLAG1MA0163.1chr5:139058399-139058413CCCCCTTGAGCCTC-6.35
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00187chr5:139052580-139059377Adipose_Nuclei
SE_03140chr5:139056739-139059366Brain_Angular_Gyrus
SE_03865chr5:139055996-139061963Brain_Anterior_Caudate
SE_04768chr5:139026027-139072090Brain_Cingulate_Gyrus
SE_05771chr5:139026065-139074431Brain_Hippocampus_Middle
SE_06683chr5:139027027-139071104Brain_Hippocampus_Middle_150
SE_07722chr5:139028082-139075240Brain_Inferior_Temporal_Lobe
SE_08785chr5:139056815-139058122Brain_Mid_Frontal_Lobe
SE_08785chr5:139058412-139058594Brain_Mid_Frontal_Lobe
SE_08785chr5:139058627-139059015Brain_Mid_Frontal_Lobe
SE_11063chr5:139026860-139059578CD20
SE_13414chr5:139056780-139058400CD34_Primary_RO01536
SE_13414chr5:139058435-139059304CD34_Primary_RO01536
SE_20188chr5:139056880-139059135CD56
SE_25255chr5:139058189-139058964Colon_Crypt_3
SE_26778chr5:139056356-139058039Esophagus
SE_27739chr5:139056202-139058212Fetal_Intestine
SE_28684chr5:139056665-139058254Fetal_Intestine_Large
SE_29581chr5:139056057-139058505Fetal_Muscle
SE_30930chr5:139056057-139058331Fetal_Thymus
SE_31417chr5:139056046-139059186Gastric
SE_33677chr5:139055902-139059162H2171
SE_34346chr5:139057922-139059244HCT-116
SE_36941chr5:139027373-139059446HSMMtube
SE_40649chr5:139056032-139059400Left_Ventricle
SE_41599chr5:139057494-139058017LNCaP
SE_42197chr5:139056073-139059249Lung
SE_45813chr5:139056829-139059282Osteoblasts
SE_47229chr5:139058326-139059295Panc1
SE_47460chr5:139056780-139058230Pancreas
SE_47460chr5:139058237-139058680Pancreas
SE_48055chr5:139055919-139062629Psoas_Muscle
SE_48579chr5:139055935-139059336Right_Atrium
SE_49460chr5:139056809-139057877Right_Ventricle
SE_51090chr5:139055934-139059157Skeletal_Muscle
SE_53351chr5:139057715-139058567Spleen
SE_55730chr5:139057497-139059261u87
SE_58504chr5:139012442-139092243Ly1
SE_63555chr5:139056584-139057808HSMM
SE_65250chr5:139036623-139059169Pancreatic_islets
SE_67548chr5:139057497-139059261u87
SE_68692chr5:139057230-139059117H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5139058350139058600
Number: 1             
IDChromosomeStartEnd
GH05I139676chr5139056126139059178
Enhancer Sequence
CCCCATCTCT GCAGCCCACA AGACACCTGC CTTCTGCCTT CTCCCCTCAC CCAGTATCTG 60
GGCTGCCGGG GTTGTCGTCC AGGGCAGGGC AGATGAGCTT AGTTGGGCAG GAGCTGGATG 120
AGCTGACTTG ACGGTTTTTG TCCCTGATCT CACTGACCCT GGTCCCCAAC AACTAGCCAG 180
GGTCACTGAT TCCTGAAAGG GTCACCAGTC TCTGAGGAGA GGGGCTGAAA AGACCATCCT 240
GGTCTTGGCC GTTATGAGGT GGGAGGGAAC ACAGCTATCC TTGGACACAC ATGGTCTTCT 300
TGCTTCAGCT CTGACCTCTG ATGCCCCCCA ACCCAGCCTG GATTCCCTGC CAGGGCCCCC 360
CGGCTCTGTC CTGGTGGAAT CTGCCATCTT GCCCAGCTCT TCCTCCTCAC CCATTTCCCT 420
CTGCTAGGAA GGAGCCCTAG GTGGTCTGGT GCCCACTGGG GAGGGACAGG GAGTATCTGA 480
CTGTTGATGG CGGCTACTCG CCTCACCCTA GAGACAGAGC TTTTCCTTTC CCCACACCCG 540
GTCCTCTTTG GCCACTCCTT AGTCCTGGGG AAGCCCCCCC TCCCCCCCGC TTGGGGCCTC 600
AGTTTCCCCC TCTGTAAATG CAGAGGGTTG GACTAGATGC TCTCTTGGGA CAGGCTTGAG 660
TCCTGTGACT AGGGGGGTTT TGGGGTTGCC TGGGGACAAA GATCCAGTGT GTGCTGCCCT 720
CAAGCCCAGG GCGTGATGGG GCCCGCCAGA TGTGCGCCTC CCCCTTGAGC CTCCAGCTGC 780
TCTGGGGCTG GGCCCTGTCC TCCCACCCCT CTCTTGGGGC ATGCTAGGCC ACAGCAGGCA 840
GACAGGGAAG CAAGGCTGGA GAGCCGGGAC TGATGAGGAA ACCGCCGCCT TGCTCCATCT 900
GGCCCAGTCC CTTCAGCTGA GGAGGCAGCT CAGACGCCTT AGCCTTGAAA CCTGAGTAGA 960
GCAGGCCCTG CCCCGGGATG GGCTGCCTTG GAAATATGGA GGTGGCCAGA GGACAGGCTC 1020
CTGCTGGGCT CCATTCCCTT GAGGGTCACG CCTACTCCTC AGTGCCAGCC TGCCCCAGCC 1080
AGAGGTCCCT CCTGGCAACA GCCCACCCCG GCTCTCTGGG TTCTCACTGA GACCTCCACC 1140
CAGGCCCTAC TCTGCAGGCC TTGTGAGGCC TCTGCCCACC ACCGCCCCCA ATCTGGGAGC 1200
CAGGCCAGAG CACCACAGTG AGGCCTGAGT AGAGACAAGA ATGAGGTCTG AGACGATAAT 1260
GATTGTGGTT CGGGGGTTGA GAAGGAAGCG TGTGCCAGGG TGTGCACAAG CATGTCCTCT 1320
CACTGTGGCA GGGGACGGCT GGTCCTCTGG CCCTGTGCTG CTCGCCCTGT AGCAGGCGGG 1380
GAGAAGATCC CTGAAATAAG GGTTCTGCAC TCATTGGCAA ACTGGGTTAC ACAAAGGCAA 1440
CCAGGTTCCT TTGCCTGCAG GACATGTCAG AGCCTTGAAA TAACTGATGT GTATTAGTAA 1500
TCCCCAGATG AGGATCCAGG GGCAGCCTTC CAGACTTAAT GATCTGTACC ATCAAGCACT 1560
CTTCTCCTCA GATGGAGAAG GAAGATTAGG ATGTGGAGGT GGTTTTTTTC 1610