EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS178-03607 
Organism
Homo sapiens 
Tissue/cell
Skeletal_muscle 
Coordinate
chr10:104419920-104421920 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:104420893-104420911CCTCCCCTCCTGCCTTCC-6.52
INSM1MA0155.1chr10:104420285-104420297TGCCTGGGGGCA+6.04
Myod1MA0499.1chr10:104420724-104420737AGCAGCTGTCACC+6.41
Myod1MA0499.1chr10:104421196-104421209GGGAACAGCTGCA-6.98
SNAI2MA0745.2chr10:104420213-104420223TGCACCTGTT-6.02
ZNF263MA0528.1chr10:104420892-104420913CCCTCCCCTCCTGCCTTCCCC-6.13
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00959chr10:104420854-104421516Adrenal_Gland
SE_03928chr10:104419982-104421719Brain_Anterior_Caudate
SE_04957chr10:104419949-104421554Brain_Cingulate_Gyrus
SE_05850chr10:104419953-104422142Brain_Hippocampus_Middle
SE_06794chr10:104420308-104421508Brain_Hippocampus_Middle_150
SE_07900chr10:104419649-104421175Brain_Inferior_Temporal_Lobe
SE_12288chr10:104420050-104421428CD3
SE_14923chr10:104420080-104421867CD4_Memory_Primary_7pool
SE_17681chr10:104419681-104421932CD4p_CD25-_CD45RAp_Naive
SE_18133chr10:104419610-104422076CD4p_CD25-_CD45ROp_Memory
SE_19041chr10:104419944-104422038CD4p_CD25-_Il17-_PMAstim_Th
SE_19414chr10:104420035-104422247CD4p_CD25-_Il17p_PMAstim_Th17
SE_20458chr10:104419970-104421992CD56
SE_21775chr10:104419870-104420884CD8_Naive_7pool
SE_22797chr10:104419903-104422097CD8_primiary
SE_23338chr10:104419990-104421715Colon_Crypt_1
SE_23909chr10:104420007-104421824Colon_Crypt_2
SE_24984chr10:104420046-104421676Colon_Crypt_3
SE_26660chr10:104420250-104421905Esophagus
SE_29601chr10:104419904-104422066Fetal_Muscle
SE_31097chr10:104419904-104421866Fetal_Thymus
SE_31421chr10:104415469-104421974Gastric
SE_36963chr10:104419171-104422446HSMMtube
SE_41790chr10:104420028-104420406LNCaP
SE_42120chr10:104415488-104421991Lung
SE_44897chr10:104420217-104421082NHLF
SE_50092chr10:104419821-104422066Sigmoid_Colon
SE_52411chr10:104419864-104422065Small_Intestine
SE_53301chr10:104419901-104422036Spleen
SE_55138chr10:104419946-104421398Thymus
SE_62334chr10:104369841-104439105Tonsil
SE_65286chr10:104419766-104421916Pancreatic_islets
SE_66695chr10:104421157-104421796Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10104420025104421916
chr10104420109104421849
Number: 1             
IDChromosomeStartEnd
GH10I102659chr10104419656104421945
Enhancer Sequence
TTGATTGAGG CTGGGAGGTG GAGGTTGCAG TGAGCTGAGA TCTTGCCACT GCACTCCAAC 60
CTGGGCAACA GAGCAAGATC CTGTCTCAAA GAAAAAAAAG AAAAATAAAG ACTTTGGGGC 120
TGGCCAGACC AAACCATAGC CTTGGTCTTG CTAACTGCCT CCGCCTTCCT GCCCTGAGGG 180
AGTAGAGGAT GACTCGGGTG GGGTGGTGGA CCCTTGCTTC ATTGTTCCCC TCCCCAGTGT 240
GGCAGGGAGC CAGGAGCAGT ATGACAACAG CTGGCCTACC CCTTCCCTCC CCGTGCACCT 300
GTTTGGGGCT AAAGGGAGTG GGGAAATGAC TGGAGCACAG TGCCCCTCCA GCCCAGGGTG 360
CAGGATGCCT GGGGGCAGGT GCCGGTGGAC AGTCACTTCA CTCCACTCAA ATCTGCTTCT 420
GTCTCACTGT CCCTTTCTCC AGTTCTCAGG AGCCCTGAGA CATCCCCCGT GCCAAGAGTT 480
GGGAGCCAAG ATAAAAAGCT GCCTAATTTC TTTCCCACTT GGCCTAGTTT TGTTTTGGCT 540
GAGGGGAGAG GCCCTTTCCC CAGGTGCGTC AATCCACTGA GATGTGGAGG GGACATTCTG 600
GTGGGAATGG GATGGGCTTG AGCCCCTCCA TGTCCCAGCT TTGAAGCCCA CTCCAGACAA 660
TGACACGCTC AGGCACACAT CTATAGGTGA AGCAGCAGCT GCCCAGAGTT GGCTTGGGGG 720
GGGTTCCCTA GGCAGCCAGG GAAGCAGGGA GACGCTAACC CACCCAGCTG TCCCCAGCCA 780
CCCAGCTGTC CCTGGCTTTG TAGGAGCAGC TGTCACCCAG CTCCCAAAAG GGTCGGGGCA 840
GAGGAGGCCC AGAAAGAGCT GGGGCTGCCC CAGGGAACAG GCTTATTCAG AAGTCATCGG 900
AGGGGCCTTC TCTGCCCTGA ACTGGTGGCC CCTTGGAGGG CTGGCTGCAG CCACAGGTGC 960
CCCAGTGCCC AGCCCTCCCC TCCTGCCTTC CCCCAAAGGC CATCACGCCT CCCCTTTCCG 1020
GGAAGGGTTG GGGATCTGAC CACGTCTCCC TACCCCACAG ACTGGGGCCG ACAGCTCCTG 1080
TGGCCCAGAT GTGCTGAGCC CGCAGCGAGG CCACCGCGAG GGAGTGGGTG GGGGTGGTTT 1140
CCTCTGCTGC CTGCCGGCCC CAGCTCTTTC ATGTTGCCGC CCTCCCCATC CCAGCCCGGA 1200
GCCAAGCAGC TGGGCCGCTC CTGCCCCCTC CCTCGGCCTC GCTCCCAGCT GTCTTTGGGG 1260
TGGGGCAGGG CAGCTGGGGA ACAGCTGCAA GGCAGGAGCC TGGGGGGTGA TGGGTGCCCC 1320
CTGCAACTGC CGGAAACGGT CTTTGGGCCA AGAAGGGAGT CTGAAGGGTG GGGGTGGAGA 1380
GGGCGAGGCC TAGGGGATGA TCGGCTCCAC CCCTTCTCCC AGCGCATCTG GCCAGGAGAC 1440
CCCAGCTCAA AGCCCCCTCC AGCTTCAAAG GGCACCCTGG GGTGGGAGGC AGGAGACGAG 1500
GGTGGATGCC CTGACCCACT GAGTCCGCAC CCCAGGGCCC CTCTCTCCAA GCTGTGACCT 1560
CACCTCAGGG TTCTTAACAG GCCTTGCTAA CACTCTCCCA CTCAGATCCT GTCATTGTCA 1620
CCATGGCCTT CCTAAGACAC CCTCATCTTC TCCCATCCGA GGGTGGGGGA GAACCAATTC 1680
GATTCGCAAC TTCAGGACCC AGGACCCATC TAGCCGCCTG GGGGATTCCC TACCCCACCT 1740
CTGCAGCCTG TAAATTCTGG GGGAGGAGGC CCTGGAGGGA GGATCAGAGG CATGTCCTTC 1800
CCCAACCTCC CACTCTGGCC TACTAAGAAA TGGGAGCAGG GCTGACCCTA TGAAAGTGTG 1860
GGAGGTGAAG GAGCTGGAGT CGTGATTCCT GGGTATCCCC AGACAGACAT CACCACACTA 1920
CAGCCCCTCT TCTAAGGTGA TCCCAGCACT TTGGGAGGCT GAAGCAGGAG GATCCCTTGA 1980
TGAGACCAGC ATGGGCAGTA 2000