EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-05466 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:204434550-204436630 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12092943chr1204434927hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:204435756-204435777GAAGAAAAAGAGAAAGAGAGA-6.4
JUN(var.2)MA0489.1chr1:204434965-204434979AGGAGATGACTCAG+6.75
MSCMA0665.1chr1:204435404-204435414AACAGCTGTT+6.02
MSCMA0665.1chr1:204435404-204435414AACAGCTGTT-6.02
MYF6MA0667.1chr1:204435404-204435414AACAGCTGTT+6.02
MYF6MA0667.1chr1:204435404-204435414AACAGCTGTT-6.02
ZNF263MA0528.1chr1:204435752-204435773AGAGGAAGAAAAAGAGAAAGA+6.22
ZNF263MA0528.1chr1:204436518-204436539GGAGAAGCGGAGGAAGGAAGA+6.28
ZNF263MA0528.1chr1:204435269-204435290GGAGAAGGAAGTGAGGGGGAG+6.42
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00064chr1:204429083-204439520Adipose_Nuclei
SE_01898chr1:204432147-204436806Aorta
SE_03188chr1:204432859-204436777Brain_Angular_Gyrus
SE_03975chr1:204432055-204439410Brain_Anterior_Caudate
SE_04850chr1:204428109-204440381Brain_Cingulate_Gyrus
SE_05834chr1:204428180-204440061Brain_Hippocampus_Middle
SE_06778chr1:204428166-204440350Brain_Hippocampus_Middle_150
SE_07775chr1:204428249-204440457Brain_Inferior_Temporal_Lobe
SE_09120chr1:204434706-204435487Brain_Mid_Frontal_Lobe
SE_09120chr1:204435944-204436706Brain_Mid_Frontal_Lobe
SE_10255chr1:204434252-204436503CD19_Primary
SE_10905chr1:204414650-204438582CD20
SE_25125chr1:204435258-204436196Colon_Crypt_3
SE_26688chr1:204434390-204435646Esophagus
SE_30246chr1:204429678-204437104Fetal_Muscle
SE_31610chr1:204434210-204436656Gastric
SE_37407chr1:204433844-204437287HSMMtube
SE_40776chr1:204428531-204437031Left_Ventricle
SE_42225chr1:204428390-204439096Lung
SE_48201chr1:204434134-204437036Psoas_Muscle
SE_48746chr1:204432136-204436808Right_Atrium
SE_49909chr1:204432030-204436617RPMI-8402
SE_50149chr1:204434299-204436802Sigmoid_Colon
SE_51536chr1:204432640-204437206Skeletal_Muscle
SE_52421chr1:204434243-204436716Small_Intestine
SE_58430chr1:204415099-204506026Ly1
SE_59794chr1:204415680-204491493Ly4
SE_61475chr1:204430067-204500813Toledo
SE_62377chr1:204415291-204492168Tonsil
SE_65868chr1:204434264-204436879Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1204434679204436514
chr1204434923204435081
Number: 1             
IDChromosomeStartEnd
GH01I204460chr1204429650204437135
Enhancer Sequence
AGTCACTCGA CATCCAATGA AAGGGGCACA AGAACATATG GGACATCCGG GAATACATGT 60
ATCTGCTGTC CTAGGAGACC AGGAGCCAAG TTGAAGAAGG AGGCGAAGCT CTGGCTGAGA 120
TGGACAAGAG TGTGGCCAAA GCCACTTCAG GAGGGGACAG TCTGATAAGC GTGAGGCAGC 180
CAGTAAGGCA ATCCAGTGCT GTTGGGCCTC TCCTGCAACA CGGGCTTTCC GGGGGATTCT 240
CCCAGAGGCG TGACAGGGAG CAGAGCAGAC AGCTGTTTTT CCCAGCCCCT CTACTGAGGC 300
TAGAGCAGGT GGGCGGCCCA AATGGTGCCC AGGGAAGCTT GGCCCTGGTC TAAAGCCTCA 360
ATATCCACAA GCCCCATGGA CCCAAAGCAG AGAGAGACCC AGAACCCTTA GATAGAGGAG 420
ATGACTCAGA CACATGTGCC TTCTGGGTAA ATGCTATTTG AGGAAGAAAG CGTCAAAGCA 480
GTGGTCTGGG CAGGGGAGGA CCTGGTAGAA GCTTGGCTCC TCTGGCTTCC GAGTCAGCCG 540
GCTCTGAACG GCCGGAATGT CAGGGAGCCT GCCTTGGCCC CACTTCCTCT CTCAAAATAC 600
GTGTGTGGTG GTAGGATTCT CAGACAAGGT CCCAAACGGT CTCCCATCCC AGAGCTGCTT 660
TCAGTCACCC AGGAGGGTTC CTAAAGAAGC CCCTAGCAAG GCCTGTAGCC CAGCCCTAGG 720
GAGAAGGAAG TGAGGGGGAG GGAGAGCTGG TGCATGACAG GTTTCTGCCT GAGGGGTCTG 780
CTCAGGGCAG CCTGGGAGGC CACACCAGGG ACGAGGCTTC AGCTCAGATG GAGATAAGGC 840
CGGCATGTGG TTCCAACAGC TGTTTCTGGC GGGAGTCTAG CTCCGGCCTG TGCACATAGC 900
AACGCCTCAC ATCTCTCACC CAACCTCTTG GCTACTCTCA AGTCCTCTCT GCCTCTTGGG 960
GCAGATGACA GCAACTGAGC TCCTCATTTG AATATCCAGA CTGTTTCCTC TGGTTGACCC 1020
TCTCTTGTTA GGCTTGCTCC CCTGGGTGTG CATGGGCGGC GGGGGGTGGG GGTGCACAGA 1080
GGGGAGGGCA GCAGTGGGGA CAGTTGGCAT GTGAGGCCCT GGCTCTGCCA AGTTCGTGCC 1140
TGTGTCCCAG TCAAAACAAT AGCACCACTG TCAGCAATTA ACCCACAAGA GAAAGGAGAG 1200
AGAGAGGAAG AAAAAGAGAA AGAGAGAGAG ACAGTGGGGG GAGGGAAGAG AAGGCAAGAG 1260
AGGGAGAGAA CAGAGTGGTC ACTGAAGGCC ACTCTCATGT CCTTTCTGTA CCACTCACTG 1320
GCACCATAAG AAAACAAAAG CCACTTACGT TTGCCCAGCT GGCAGGCCCT GGTGGCATCA 1380
CCCGATGCTG GCTGGGGGAG TCTGCCGGGC AGAGGCTGGC AGCAGGGGTA TCAGGCTGGC 1440
ATTTGGAGCC AGCCAGTTCC AGAGCTGGCT CCGCTGGCCT GGGATAAGGA GGTTCCCTCT 1500
GGCTGGAAGC CCGACGAAAG CGGGGCGGTG GTATAGGCCG AGGGCCCAAG GGGTCCCCCC 1560
TCCCAGCAGG CTGAGCCCCT GCAACAAGCT GAGCCGGGGA GGACCAAGGC CGCATTTCCC 1620
CACTCAGAAC TGGCAAGAGC TTTTTGCTTT GTGTCCGCTT CTTCAAGGAG ATTCTGGGCT 1680
GAGCTCTGTC TCAGAACTCT GATGACATGC AGGGGATGGG GAAGGGTGAG GGAGTAGGGG 1740
AGGCAGGAGA GAGAAGGAGT GACAGAGGTG ACCACCTACC AGGGTGCCCT GACTCAGTGA 1800
GCAGGCCCAG CTGGGTGTGA GGAACTCAGA GCTGGGAACA GGAATCTCCC AGTCCCTATA 1860
AATAGCGGGA ACAGCCCCAC CTCTCAGAGC AGGGCCTTTA AAAATCCCTG AGCTCTAGGG 1920
ATGTGGCTTA TCCCAGGAGC TGATTCTGCT TTTGGGGGGA CTCTCTTAGG AGAAGCGGAG 1980
GAAGGAAGAA CTGTGTAGCT CTTCAGAGTT GGGAAGGTTC CCAAAGGCTA GACACAAGGT 2040
GGGAAAACCC CAGTGCCCCT TAAACAATGG CTAAGGAGGA 2080