EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-27956 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr5:139056520-139058160 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RARA(var.2)MA0730.1chr5:139057466-139057483TGACTTCTAATTGACCT-6.09
ZNF263MA0528.1chr5:139057518-139057539GGAGGAGGGAGGGGGTGAGCA+7.24
Number of super-enhancer constituents: 38             
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_11063chr5:139026860-139059578CD20
SE_13414chr5:139056780-139058400CD34_Primary_RO01536
SE_20188chr5:139056880-139059135CD56
SE_26221chr5:139056720-139057563Duodenum_Smooth_Muscle
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_47460chr5:139056780-139058230Pancreas
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_54845chr5:139055998-139057753Stomach_Smooth_Muscle
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: 2             
ChromosomeStartEnd
chr5139056887139057262
chr5139057354139058068
Number: 1             
IDChromosomeStartEnd
GH05I139676chr5139056126139059178
Enhancer Sequence
GCCCCCGCAT GCCCCTCTGC CCCCCAGCTT TCCATGACTC GTCCCCCCTC AGCCCCCCGT 60
GCTCTGTCCC CGCCCGTCAG CCCCTGGTCC CAGCTCCCGG CTGGCCGGCT CCTGCATGGA 120
CAAAGGGGTC CTTTGTGGGC TGACCGCGGC TGGCGGGGCG GCGGGGCGCT GGCTCCGCAT 180
TGCTGATGAA ACGGAGCCCT TTGTTGTCCC TCCTCAGGCG CAGTATTTCT TTTTGGGGGC 240
TGGATGTGTT CCTGGCAGGG CCGATGATGG ATGCGCCCGC CGCCGCCCGC CTGCCCGCCA 300
GCTTTCCCTC CCGCTCATTC CCGCTCCGCT TCAACGCAGC CCTGACTCCT CCCCTGCTGC 360
CTGGGCACTG CCAGGCCCTT CCTGGCCTGG AAGGGGATGG CTGTGTGCCC TAGAGTAGAA 420
GACTGGGACC TGGGAGAACG TCCCCTCTAT GTCCTCCTCT TCCATGAGTA GGGCAAATGG 480
GGCTTTTGGT CAGGGGTCCA CTGGGACCAG GACATCAGTT TTTCCTAAGG TCTGAAGGAG 540
AAGATGAGCC AGGTATCAGG GCCGATTTGG AACAAGCTTG AGGACCAGAT GTTCATGTCT 600
GTCTACTCTG GATTTGAAAA CAGAGTTGTC CCTGTGAGCC AGTCCCTCCG TGTACCCACC 660
TCCCTTCAAC TTCTGTGGCT GAAAAACCAT AGTGTTCTGC CTGCAGCACC TGTTTGGTGA 720
CATATCACAT CCTCTGGTCC CAAGCTCAGT ATGTCCCAGG ACCTCAGAGG CTGGGGGTGG 780
GTGGGCCCTG AAGAAGGATA GAATAGTGGA AGATCAGAGA AATTCCAAGA GAGGAACAGA 840
ACATGAGGTT TGGTCCCCAC CAGGAGAGAC TCAGGACGGA GACAAAAGCC GAGACACTCA 900
GCCAGAGCGC CAGCCCTGAG CGCAGGCCGG CTGTGTTGGA AGGAGCTGAC TTCTAATTGA 960
CCTGCCCGCC CCGCACGCAG AGCCAGATCC TGGAGCTGGG AGGAGGGAGG GGGTGAGCAG 1020
AGCAGGAACA GCGTTAATGC AGCTATCGAT TTCTGCCACC AGCCAGCAGG CCGCAGAGGC 1080
GGGGGACGCA CACAGGGGCT GGGGCGCAGC CTGCTCCCCT CCCCATCTCT GCAGCCCACA 1140
AGACACCTGC CTTCTGCCTT CTCCCCTCAC CCAGTATCTG GGCTGCCGGG GTTGTCGTCC 1200
AGGGCAGGGC AGATGAGCTT AGTTGGGCAG GAGCTGGATG AGCTGACTTG ACGGTTTTTG 1260
TCCCTGATCT CACTGACCCT GGTCCCCAAC AACTAGCCAG GGTCACTGAT TCCTGAAAGG 1320
GTCACCAGTC TCTGAGGAGA GGGGCTGAAA AGACCATCCT GGTCTTGGCC GTTATGAGGT 1380
GGGAGGGAAC ACAGCTATCC TTGGACACAC ATGGTCTTCT TGCTTCAGCT CTGACCTCTG 1440
ATGCCCCCCA ACCCAGCCTG GATTCCCTGC CAGGGCCCCC CGGCTCTGTC CTGGTGGAAT 1500
CTGCCATCTT GCCCAGCTCT TCCTCCTCAC CCATTTCCCT CTGCTAGGAA GGAGCCCTAG 1560
GTGGTCTGGT GCCCACTGGG GAGGGACAGG GAGTATCTGA CTGTTGATGG CGGCTACTCG 1620
CCTCACCCTA GAGACAGAGC 1640