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

TagContent
EnhancerAtlas ID
HS099-01853 
Organism
Homo sapiens 
Tissue/cell
HSMMtube 
Coordinate
chr1:204434450-204436690 
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
TAAGAGAAGA GCAGACGACT CAGTGCCTTT TTCCTCGTGG TGTCCCCTCC CTATGAGGTA 60
CTCCAGACCT AAACTCAAAC TCTAGATGAA AAGACTTTCT AGTCACTCGA CATCCAATGA 120
AAGGGGCACA AGAACATATG GGACATCCGG GAATACATGT ATCTGCTGTC CTAGGAGACC 180
AGGAGCCAAG TTGAAGAAGG AGGCGAAGCT CTGGCTGAGA TGGACAAGAG TGTGGCCAAA 240
GCCACTTCAG GAGGGGACAG TCTGATAAGC GTGAGGCAGC CAGTAAGGCA ATCCAGTGCT 300
GTTGGGCCTC TCCTGCAACA CGGGCTTTCC GGGGGATTCT CCCAGAGGCG TGACAGGGAG 360
CAGAGCAGAC AGCTGTTTTT CCCAGCCCCT CTACTGAGGC TAGAGCAGGT GGGCGGCCCA 420
AATGGTGCCC AGGGAAGCTT GGCCCTGGTC TAAAGCCTCA ATATCCACAA GCCCCATGGA 480
CCCAAAGCAG AGAGAGACCC AGAACCCTTA GATAGAGGAG ATGACTCAGA CACATGTGCC 540
TTCTGGGTAA ATGCTATTTG AGGAAGAAAG CGTCAAAGCA GTGGTCTGGG CAGGGGAGGA 600
CCTGGTAGAA GCTTGGCTCC TCTGGCTTCC GAGTCAGCCG GCTCTGAACG GCCGGAATGT 660
CAGGGAGCCT GCCTTGGCCC CACTTCCTCT CTCAAAATAC GTGTGTGGTG GTAGGATTCT 720
CAGACAAGGT CCCAAACGGT CTCCCATCCC AGAGCTGCTT TCAGTCACCC AGGAGGGTTC 780
CTAAAGAAGC CCCTAGCAAG GCCTGTAGCC CAGCCCTAGG GAGAAGGAAG TGAGGGGGAG 840
GGAGAGCTGG TGCATGACAG GTTTCTGCCT GAGGGGTCTG CTCAGGGCAG CCTGGGAGGC 900
CACACCAGGG ACGAGGCTTC AGCTCAGATG GAGATAAGGC CGGCATGTGG TTCCAACAGC 960
TGTTTCTGGC GGGAGTCTAG CTCCGGCCTG TGCACATAGC AACGCCTCAC ATCTCTCACC 1020
CAACCTCTTG GCTACTCTCA AGTCCTCTCT GCCTCTTGGG GCAGATGACA GCAACTGAGC 1080
TCCTCATTTG AATATCCAGA CTGTTTCCTC TGGTTGACCC TCTCTTGTTA GGCTTGCTCC 1140
CCTGGGTGTG CATGGGCGGC GGGGGGTGGG GGTGCACAGA GGGGAGGGCA GCAGTGGGGA 1200
CAGTTGGCAT GTGAGGCCCT GGCTCTGCCA AGTTCGTGCC TGTGTCCCAG TCAAAACAAT 1260
AGCACCACTG TCAGCAATTA ACCCACAAGA GAAAGGAGAG AGAGAGGAAG AAAAAGAGAA 1320
AGAGAGAGAG ACAGTGGGGG GAGGGAAGAG AAGGCAAGAG AGGGAGAGAA CAGAGTGGTC 1380
ACTGAAGGCC ACTCTCATGT CCTTTCTGTA CCACTCACTG GCACCATAAG AAAACAAAAG 1440
CCACTTACGT TTGCCCAGCT GGCAGGCCCT GGTGGCATCA CCCGATGCTG GCTGGGGGAG 1500
TCTGCCGGGC AGAGGCTGGC AGCAGGGGTA TCAGGCTGGC ATTTGGAGCC AGCCAGTTCC 1560
AGAGCTGGCT CCGCTGGCCT GGGATAAGGA GGTTCCCTCT GGCTGGAAGC CCGACGAAAG 1620
CGGGGCGGTG GTATAGGCCG AGGGCCCAAG GGGTCCCCCC TCCCAGCAGG CTGAGCCCCT 1680
GCAACAAGCT GAGCCGGGGA GGACCAAGGC CGCATTTCCC CACTCAGAAC TGGCAAGAGC 1740
TTTTTGCTTT GTGTCCGCTT CTTCAAGGAG ATTCTGGGCT GAGCTCTGTC TCAGAACTCT 1800
GATGACATGC AGGGGATGGG GAAGGGTGAG GGAGTAGGGG AGGCAGGAGA GAGAAGGAGT 1860
GACAGAGGTG ACCACCTACC AGGGTGCCCT GACTCAGTGA GCAGGCCCAG CTGGGTGTGA 1920
GGAACTCAGA GCTGGGAACA GGAATCTCCC AGTCCCTATA AATAGCGGGA ACAGCCCCAC 1980
CTCTCAGAGC AGGGCCTTTA AAAATCCCTG AGCTCTAGGG ATGTGGCTTA TCCCAGGAGC 2040
TGATTCTGCT TTTGGGGGGA CTCTCTTAGG AGAAGCGGAG GAAGGAAGAA CTGTGTAGCT 2100
CTTCAGAGTT GGGAAGGTTC CCAAAGGCTA GACACAAGGT GGGAAAACCC CAGTGCCCCT 2160
TAAACAATGG CTAAGGAGGA AACCAGGACA GAATGAAGTA GAATGCTAAG CTGTCACAGA 2220
AGGCATCAGC AGCCAGGGGC 2240