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

TagContent
EnhancerAtlas ID
HS116-09203 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr12:124905150-124906440 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73225423chr12124905924hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr12:124905652-124905665AGCAGCTGCCCCC+6.03
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00866chr12:124905085-124909436Adrenal_Gland
SE_03101chr12:124905073-124905924Bladder
SE_03101chr12:124905965-124907305Bladder
SE_03150chr12:124905101-124907194Brain_Angular_Gyrus
SE_03868chr12:124905079-124908818Brain_Anterior_Caudate
SE_04770chr12:124905025-124909610Brain_Cingulate_Gyrus
SE_05769chr12:124902481-124909803Brain_Hippocampus_Middle
SE_06714chr12:124904922-124908677Brain_Hippocampus_Middle_150
SE_07720chr12:124903978-124909561Brain_Inferior_Temporal_Lobe
SE_08801chr12:124905704-124905897Brain_Mid_Frontal_Lobe
SE_08801chr12:124906196-124906748Brain_Mid_Frontal_Lobe
SE_23639chr12:124906156-124908775Colon_Crypt_1
SE_24091chr12:124906175-124908734Colon_Crypt_2
SE_25142chr12:124906081-124908719Colon_Crypt_3
SE_26654chr12:124903711-124909443Esophagus
SE_28184chr12:124905521-124908931Fetal_Intestine
SE_29418chr12:124905224-124908876Fetal_Intestine_Large
SE_29559chr12:124904796-124908878Fetal_Muscle
SE_31405chr12:124904869-124909654Gastric
SE_33696chr12:124902492-124909084H2171
SE_37608chr12:124902402-124909198HSMMtube
SE_40749chr12:124904671-124909558Left_Ventricle
SE_41561chr12:124904106-124905370LNCaP
SE_41561chr12:124905417-124908737LNCaP
SE_42183chr12:124904107-124909623Lung
SE_44425chr12:124906015-124908843NHDF-Ad
SE_46642chr12:124905655-124906019Ovary
SE_46642chr12:124906021-124907274Ovary
SE_47472chr12:124906028-124908773Pancreas
SE_48155chr12:124905355-124908934Psoas_Muscle
SE_48612chr12:124904654-124909524Right_Atrium
SE_50109chr12:124902748-124909560Sigmoid_Colon
SE_51247chr12:124905085-124909176Skeletal_Muscle
SE_53001chr12:124902814-124908894Small_Intestine
SE_54615chr12:124904991-124909657Stomach_Smooth_Muscle
SE_65244chr12:124902509-124909711Pancreatic_islets
SE_67111chr12:124902492-124909084H2171
SE_68754chr12:124906053-124909578H9
Number: 1             
IDChromosomeStartEnd
GH12I124418chr12124903356124909545
Enhancer Sequence
CTCTGCCTTG GTCTTTTCCA TGTAGATTGG GTCTGAAAGC CGGAGCAACC AGCCCTCCAT 60
GAACCCCGGC CAAATGGGAC GAGTAAAAGG GGCAGCCTCA GAAAGTGATG CCACGATGCC 120
CCCACTTGCG GGCATGGAGC CCAGCTTGCC AATGCCCACA GCCGTTCCCC TTACAATGTA 180
AAATGTTTCT GCAATGCTCT GGCCAGTGCC AAGCCAGGAC CCCACCTCCA ATGGGCATTC 240
TGTGAGGCCT CTGAGCTGGG CCTCAAATCT CACTGCCCTC AACAGAAAGC CCCCAGCTGG 300
CAGCCTCCTG CCAAGTACGA CCGCCAGGGG GGCTCCCAGG CGGCCCCAGG CTAAACCCAG 360
CCCACAAACA TGGCAATCGA GAAAGACGTT TTATAATCAG ATGCCAATAT TTGCAATTCA 420
GGGGATGTGG GTGCCCGACT TCTCCTTTAA CAATTCAAGA GAGCTCCTTC CTGCGCTCAG 480
CAATGGCAGC CCGGCTCCGG ACAGCAGCTG CCCCCGCAGA CGGGCACAGA CTGGCTGGTC 540
CACCTGGCTC CCAGCCAGAC GTCAGCCTCA CTCACTGTCA AGACCTGACT GTCCCCGCCG 600
GCCTCTCCGT TGGCAGCTCC TGCTCCAGAC CCCTCTGGAA GCTCTACTGA AGCCTTGTCC 660
TGGGCTGCCT CTCAGCCAAA GAACATCATG AAGTTTACTC CCCAGCACAA AGACTTCTAA 720
TCCCCTCATC CTGAAGGAGG ACTGCTCGAT GGCCAGTTTC TGAAATGCTT CCATCCTGGG 780
GAGCCCTAAC CTAGAGTCCG CCGTGCCGTC CACTCCCTGA GGGAGACGTC GTCACTCAGA 840
AGATGGGCTA TTTATAGGGC TTGTTTCTCC ACACTGGTTT TTCAGGCATG GAGAGATTTT 900
TCCCCACTCT GCTCGGTCTC TCTCCTTCTA CGGTTATCAG CTCATGAGGG GCAGGCGCTG 960
GGAACAGCTG TCCTTTAAAA TAAGTGCCTC ATCCTCCTGG CCTCCCTCCT ACAACCAGGA 1020
AGCCCGAGCA GGGTGTCCAC CAAGCTGGGG TGGGCAGGTC CCCATCTCTG AGAAACGTGA 1080
TTCAGGGGAA TGCTGCTTAA GACACACGGA CGGCAGCCTT TCTCCTCTGA CCCCAAGATG 1140
CTGGGGGAAG GCCCAGGGGC CACGTCCAAC ATGCAGCCTC ATCCAGCCAC CTTCTCCCAC 1200
CTGCAGCCTC TCCAGGCACA GTCCAACCAG CCTTGTGGGT GCAAAACAAC GGCTTTACCA 1260
TTCTCTGGGG ACACTTTGTG TCTACCGGCC 1290