EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-04678 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr1:204434740-204436190 
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
ATCCAGTGCT GTTGGGCCTC TCCTGCAACA CGGGCTTTCC GGGGGATTCT CCCAGAGGCG 60
TGACAGGGAG CAGAGCAGAC AGCTGTTTTT CCCAGCCCCT CTACTGAGGC TAGAGCAGGT 120
GGGCGGCCCA AATGGTGCCC AGGGAAGCTT GGCCCTGGTC TAAAGCCTCA ATATCCACAA 180
GCCCCATGGA CCCAAAGCAG AGAGAGACCC AGAACCCTTA GATAGAGGAG ATGACTCAGA 240
CACATGTGCC TTCTGGGTAA ATGCTATTTG AGGAAGAAAG CGTCAAAGCA GTGGTCTGGG 300
CAGGGGAGGA CCTGGTAGAA GCTTGGCTCC TCTGGCTTCC GAGTCAGCCG GCTCTGAACG 360
GCCGGAATGT CAGGGAGCCT GCCTTGGCCC CACTTCCTCT CTCAAAATAC GTGTGTGGTG 420
GTAGGATTCT CAGACAAGGT CCCAAACGGT CTCCCATCCC AGAGCTGCTT TCAGTCACCC 480
AGGAGGGTTC CTAAAGAAGC CCCTAGCAAG GCCTGTAGCC CAGCCCTAGG GAGAAGGAAG 540
TGAGGGGGAG GGAGAGCTGG TGCATGACAG GTTTCTGCCT GAGGGGTCTG CTCAGGGCAG 600
CCTGGGAGGC CACACCAGGG ACGAGGCTTC AGCTCAGATG GAGATAAGGC CGGCATGTGG 660
TTCCAACAGC TGTTTCTGGC GGGAGTCTAG CTCCGGCCTG TGCACATAGC AACGCCTCAC 720
ATCTCTCACC CAACCTCTTG GCTACTCTCA AGTCCTCTCT GCCTCTTGGG GCAGATGACA 780
GCAACTGAGC TCCTCATTTG AATATCCAGA CTGTTTCCTC TGGTTGACCC TCTCTTGTTA 840
GGCTTGCTCC CCTGGGTGTG CATGGGCGGC GGGGGGTGGG GGTGCACAGA GGGGAGGGCA 900
GCAGTGGGGA CAGTTGGCAT GTGAGGCCCT GGCTCTGCCA AGTTCGTGCC TGTGTCCCAG 960
TCAAAACAAT AGCACCACTG TCAGCAATTA ACCCACAAGA GAAAGGAGAG AGAGAGGAAG 1020
AAAAAGAGAA AGAGAGAGAG ACAGTGGGGG GAGGGAAGAG AAGGCAAGAG AGGGAGAGAA 1080
CAGAGTGGTC ACTGAAGGCC ACTCTCATGT CCTTTCTGTA CCACTCACTG GCACCATAAG 1140
AAAACAAAAG CCACTTACGT TTGCCCAGCT GGCAGGCCCT GGTGGCATCA CCCGATGCTG 1200
GCTGGGGGAG TCTGCCGGGC AGAGGCTGGC AGCAGGGGTA TCAGGCTGGC ATTTGGAGCC 1260
AGCCAGTTCC AGAGCTGGCT CCGCTGGCCT GGGATAAGGA GGTTCCCTCT GGCTGGAAGC 1320
CCGACGAAAG CGGGGCGGTG GTATAGGCCG AGGGCCCAAG GGGTCCCCCC TCCCAGCAGG 1380
CTGAGCCCCT GCAACAAGCT GAGCCGGGGA GGACCAAGGC CGCATTTCCC CACTCAGAAC 1440
TGGCAAGAGC 1450