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

TagContent
EnhancerAtlas ID
HS050-40731 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr2:240160860-240162820 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2CMA0497.1chr2:240162287-240162302ATCTATTTTTGGAAA-6.76
PRDM1MA0508.2chr2:240162671-240162681TCACTTTCAC+6.02
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_01381chr2:240160030-240163177Adrenal_Gland
SE_03478chr2:240160216-240163213Brain_Angular_Gyrus
SE_03965chr2:240160099-240163777Brain_Anterior_Caudate
SE_04828chr2:240159900-240163875Brain_Cingulate_Gyrus
SE_05792chr2:240159564-240163806Brain_Hippocampus_Middle
SE_07096chr2:240160454-240163615Brain_Hippocampus_Middle_150
SE_07753chr2:240159994-240164006Brain_Inferior_Temporal_Lobe
SE_09036chr2:240160961-240161317Brain_Mid_Frontal_Lobe
SE_09036chr2:240161436-240162244Brain_Mid_Frontal_Lobe
SE_09036chr2:240162475-240162717Brain_Mid_Frontal_Lobe
SE_09164chr2:240153575-240168187CD14
SE_26643chr2:240160518-240163205Esophagus
SE_29598chr2:240161205-240162754Fetal_Muscle
SE_37020chr2:240160876-240163198HSMMtube
SE_39363chr2:240158867-240161455Jurkat
SE_39363chr2:240161736-240162984Jurkat
SE_40663chr2:240159956-240163825Left_Ventricle
SE_42224chr2:240160338-240163299Lung
SE_48049chr2:240159976-240163799Psoas_Muscle
SE_48824chr2:240160026-240163294Right_Atrium
SE_49711chr2:240161348-240162150Right_Ventricle
SE_49711chr2:240162267-240163113Right_Ventricle
SE_50196chr2:240160976-240163147Sigmoid_Colon
SE_51102chr2:240159755-240163674Skeletal_Muscle
SE_52573chr2:240161078-240162241Small_Intestine
SE_53377chr2:240161323-240163361Spleen
SE_54492chr2:240159978-240162949Stomach_Smooth_Muscle
SE_65310chr2:240159947-240163132Pancreatic_islets
SE_66243chr2:240158867-240161455Jurkat
SE_66243chr2:240161736-240162984Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2240161951240162602
Number: 1             
IDChromosomeStartEnd
GH02I239238chr2240159917240163496
Enhancer Sequence
CAAGGCTGCC CCCATTTCAG ACACAAGTCC TGGGCCTCCT GGACTTCTAA AGATCGGCTA 60
TAAATCAGGA GTTCCCACAA GCCCCTCTCA GGTTCTGTAA TTTGCTAGAA GGGCTCACAA 120
AACTCAGAAA AACACTTTAC CATGTTGATG GGTTTATTGT AAAAGATGCA AATAAACAGT 180
AACATGAAGG CAGGGTCTGG AGGGGTCCTG AGTGCAGGAG CCTCTGTGTC AGTACCACTG 240
GGGTCAGCAG GTGCGGCTGA ACATGCTGCT CCTCTCGTCT CTGCGTCCTG GTGACTGGCC 300
CCATCCCGAG GCTATCCAGG GGTCCTGCCC TAAGTCACTT CATTAGCATA AACTCAGAAG 360
CACATAAGAA GCTCCTCCTT AGGAATAACG AAAGGCTCGC TGGACACTCA GGAAGCTCCT 420
GGGATCCTAA GAGCTCCCTG CCAGGAACGA GGACAAAGAC CAGATAAGGC TTATTCTTCC 480
ACCACACAGA GATGCTGCTT GTTCTCGTTG TGTGCCACTG GGCCTGGCTA GTCTCATAAC 540
AACCTGTACA TTCAAACCCC CAACACTGCC ATGTTCACAT CTTTGTAGAA TGACATGGAA 600
ATGCTCGAAG GGAAAGCTGT TCTGAGGCGG CACTGGGTTA ATAGGAAGTG CCTGCCTCTC 660
GCGGAACAGG GCAGCCATGT GGAACTATCA GAAAACAGCA GGAGTGTCTC AAGCACAGGC 720
GGCCTTGGAG GCGGCGGCAC AGACATGGGT CTCAGTGCCG GACGCTAACC CCACATGTGG 780
AGGCCCCGTG AGCCCCAGCC AGCTGGAAGC ACGGCCACAG TCTCTTTAAG ACAAGATCCC 840
GGCCTGAGCC GTCCTTGGTC GTCCACCTGG ACAGCATGAC AGATGCCGCA TCCCTCATTA 900
TGAAAGGCTG GGGCTCAGGG CAGCAGCCAT GATCGAGAAG CCAAACACTA AAGGCGTTTT 960
GCCAGAGGTG GCTGGTGGAA CACAATCCTG GGGGTAAAGC AGTGGCGGTG AGTGCACTTT 1020
GCAGGCGCAG GGGCCACCAG GCCTGGGAAA GACAGCTTTG GAACGGACCT AAACAAAGCG 1080
TGGCCAGTGG GGCAAAGAAC GTCTGTCACC AGGGTGAAAT AGACAAGCTG CGGTACACAG 1140
CCAGCTGGAA CGCATGACGG CATCCGTGAA TGTGCACAGA ATAGATTCTT AACGCTGTGT 1200
TTTTTCAGAT ATCATATTCC AGAGTGAGTT AAAATGAAAT TAGTGATGAG AGGTGGAATT 1260
TCCATATTTA TCTGCCTCTG GGCTGAAATT TCTCAGGCTG AGGAGAAAGC GGTGCTAAGA 1320
ACCCAGCGTT TACAAGCAGG AAAATAATGA AGATGGGAAG CAAAGTACCA CTTCCTCATC 1380
ACACGCCTGC TGCAAGCAGG TTCCCCCTTA TCTGTCTCCG CTTGAGAATC TATTTTTGGA 1440
AACCCTGCTG GACAGGGACG ATCGTACTGA GTGTCCTCAA ACAGCATTTA ATCAGCGCTG 1500
GGGCTGCAGA CCAGATGCAC ACTGAGAGGG AGGCCGAGGA GCACGGGTAC CTCGTGTCCT 1560
CACCAGCACA TGATGTGCCC CAGTGTGCTC AATGCACCCA CAGTCAACTG CAGTGACCAC 1620
ATCACTCTTG CCAGGAGTCC CTTTCGCGCC GACAGGACCC AGCCTGAACT GAGCATTGTT 1680
TGAGACTCGG AGTCCGCCCA TGGGAGGAAC AGGACTAAGA CAGACAGTGC TTTTGCTTTT 1740
CAGAATCCAC CTTGCATCAG ACGGGTAGGT ATGTCTAACC AGAAACCCGG CCTTCTGGAG 1800
CCAAAGGAAC CTCACTTTCA CCCGGAGGGC CCAGGCCCCC CACTTCACAC TTGGGGAAAT 1860
GGCCTCAAGG GCTGTGCAGT TTCCTAGGAT CACGGAGTGA GCACCAGCCG GAATCCAGTT 1920
CTGTCTCAAT TAAACCAGCG GCTTGTCTGA AGCTGGACCT 1960