EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS007-01255 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr1:204434650-204436400 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12092943chr1204434927hg19
TF binding sites/motifs
Number: 8             
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
ZNF263MA0528.1chr1:204435269-204435290GGAGAAGGAAGTGAGGGGGAG+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: 1             
ChromosomeStartEnd
chr1204434923204435081
Number: 1             
IDChromosomeStartEnd
GH01I204460chr1204429650204437135
Enhancer Sequence
AGGCGAAGCT CTGGCTGAGA TGGACAAGAG TGTGGCCAAA GCCACTTCAG GAGGGGACAG 60
TCTGATAAGC GTGAGGCAGC CAGTAAGGCA ATCCAGTGCT GTTGGGCCTC TCCTGCAACA 120
CGGGCTTTCC GGGGGATTCT CCCAGAGGCG TGACAGGGAG CAGAGCAGAC AGCTGTTTTT 180
CCCAGCCCCT CTACTGAGGC TAGAGCAGGT GGGCGGCCCA AATGGTGCCC AGGGAAGCTT 240
GGCCCTGGTC TAAAGCCTCA ATATCCACAA GCCCCATGGA CCCAAAGCAG AGAGAGACCC 300
AGAACCCTTA GATAGAGGAG ATGACTCAGA CACATGTGCC TTCTGGGTAA ATGCTATTTG 360
AGGAAGAAAG CGTCAAAGCA GTGGTCTGGG CAGGGGAGGA CCTGGTAGAA GCTTGGCTCC 420
TCTGGCTTCC GAGTCAGCCG GCTCTGAACG GCCGGAATGT CAGGGAGCCT GCCTTGGCCC 480
CACTTCCTCT CTCAAAATAC GTGTGTGGTG GTAGGATTCT CAGACAAGGT CCCAAACGGT 540
CTCCCATCCC AGAGCTGCTT TCAGTCACCC AGGAGGGTTC CTAAAGAAGC CCCTAGCAAG 600
GCCTGTAGCC CAGCCCTAGG GAGAAGGAAG TGAGGGGGAG GGAGAGCTGG TGCATGACAG 660
GTTTCTGCCT GAGGGGTCTG CTCAGGGCAG CCTGGGAGGC CACACCAGGG ACGAGGCTTC 720
AGCTCAGATG GAGATAAGGC CGGCATGTGG TTCCAACAGC TGTTTCTGGC GGGAGTCTAG 780
CTCCGGCCTG TGCACATAGC AACGCCTCAC ATCTCTCACC CAACCTCTTG GCTACTCTCA 840
AGTCCTCTCT GCCTCTTGGG GCAGATGACA GCAACTGAGC TCCTCATTTG AATATCCAGA 900
CTGTTTCCTC TGGTTGACCC TCTCTTGTTA GGCTTGCTCC CCTGGGTGTG CATGGGCGGC 960
GGGGGGTGGG GGTGCACAGA GGGGAGGGCA GCAGTGGGGA CAGTTGGCAT GTGAGGCCCT 1020
GGCTCTGCCA AGTTCGTGCC TGTGTCCCAG TCAAAACAAT AGCACCACTG TCAGCAATTA 1080
ACCCACAAGA GAAAGGAGAG AGAGAGGAAG AAAAAGAGAA AGAGAGAGAG ACAGTGGGGG 1140
GAGGGAAGAG AAGGCAAGAG AGGGAGAGAA CAGAGTGGTC ACTGAAGGCC ACTCTCATGT 1200
CCTTTCTGTA CCACTCACTG GCACCATAAG AAAACAAAAG CCACTTACGT TTGCCCAGCT 1260
GGCAGGCCCT GGTGGCATCA CCCGATGCTG GCTGGGGGAG TCTGCCGGGC AGAGGCTGGC 1320
AGCAGGGGTA TCAGGCTGGC ATTTGGAGCC AGCCAGTTCC AGAGCTGGCT CCGCTGGCCT 1380
GGGATAAGGA GGTTCCCTCT GGCTGGAAGC CCGACGAAAG CGGGGCGGTG GTATAGGCCG 1440
AGGGCCCAAG GGGTCCCCCC TCCCAGCAGG CTGAGCCCCT GCAACAAGCT GAGCCGGGGA 1500
GGACCAAGGC CGCATTTCCC CACTCAGAAC TGGCAAGAGC TTTTTGCTTT GTGTCCGCTT 1560
CTTCAAGGAG ATTCTGGGCT GAGCTCTGTC TCAGAACTCT GATGACATGC AGGGGATGGG 1620
GAAGGGTGAG GGAGTAGGGG AGGCAGGAGA GAGAAGGAGT GACAGAGGTG ACCACCTACC 1680
AGGGTGCCCT GACTCAGTGA GCAGGCCCAG CTGGGTGTGA GGAACTCAGA GCTGGGAACA 1740
GGAATCTCCC 1750