EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-04591 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr10:104419740-104421980 
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
GTTGGCTCAT GCCTGGAATC CCAGCAGTTT GAAGGTGGAT GGATCACTTG AGTTCAGGAG 60
TTCAAAACCA GCCTGGGCCA CATGGTGAAA CCCCATCTCT ACTAAAACGA AAAATTAGCC 120
AGGCGTGGTG CCACGGGCCT GTGGTCCTAG CTACTCTGGA GGCTGAAGTG GGAGGATTGC 180
TTGATTGAGG CTGGGAGGTG GAGGTTGCAG TGAGCTGAGA TCTTGCCACT GCACTCCAAC 240
CTGGGCAACA GAGCAAGATC CTGTCTCAAA GAAAAAAAAG AAAAATAAAG ACTTTGGGGC 300
TGGCCAGACC AAACCATAGC CTTGGTCTTG CTAACTGCCT CCGCCTTCCT GCCCTGAGGG 360
AGTAGAGGAT GACTCGGGTG GGGTGGTGGA CCCTTGCTTC ATTGTTCCCC TCCCCAGTGT 420
GGCAGGGAGC CAGGAGCAGT ATGACAACAG CTGGCCTACC CCTTCCCTCC CCGTGCACCT 480
GTTTGGGGCT AAAGGGAGTG GGGAAATGAC TGGAGCACAG TGCCCCTCCA GCCCAGGGTG 540
CAGGATGCCT GGGGGCAGGT GCCGGTGGAC AGTCACTTCA CTCCACTCAA ATCTGCTTCT 600
GTCTCACTGT CCCTTTCTCC AGTTCTCAGG AGCCCTGAGA CATCCCCCGT GCCAAGAGTT 660
GGGAGCCAAG ATAAAAAGCT GCCTAATTTC TTTCCCACTT GGCCTAGTTT TGTTTTGGCT 720
GAGGGGAGAG GCCCTTTCCC CAGGTGCGTC AATCCACTGA GATGTGGAGG GGACATTCTG 780
GTGGGAATGG GATGGGCTTG AGCCCCTCCA TGTCCCAGCT TTGAAGCCCA CTCCAGACAA 840
TGACACGCTC AGGCACACAT CTATAGGTGA AGCAGCAGCT GCCCAGAGTT GGCTTGGGGG 900
GGGTTCCCTA GGCAGCCAGG GAAGCAGGGA GACGCTAACC CACCCAGCTG TCCCCAGCCA 960
CCCAGCTGTC CCTGGCTTTG TAGGAGCAGC TGTCACCCAG CTCCCAAAAG GGTCGGGGCA 1020
GAGGAGGCCC AGAAAGAGCT GGGGCTGCCC CAGGGAACAG GCTTATTCAG AAGTCATCGG 1080
AGGGGCCTTC TCTGCCCTGA ACTGGTGGCC CCTTGGAGGG CTGGCTGCAG CCACAGGTGC 1140
CCCAGTGCCC AGCCCTCCCC TCCTGCCTTC CCCCAAAGGC CATCACGCCT CCCCTTTCCG 1200
GGAAGGGTTG GGGATCTGAC CACGTCTCCC TACCCCACAG ACTGGGGCCG ACAGCTCCTG 1260
TGGCCCAGAT GTGCTGAGCC CGCAGCGAGG CCACCGCGAG GGAGTGGGTG GGGGTGGTTT 1320
CCTCTGCTGC CTGCCGGCCC CAGCTCTTTC ATGTTGCCGC CCTCCCCATC CCAGCCCGGA 1380
GCCAAGCAGC TGGGCCGCTC CTGCCCCCTC CCTCGGCCTC GCTCCCAGCT GTCTTTGGGG 1440
TGGGGCAGGG CAGCTGGGGA ACAGCTGCAA GGCAGGAGCC TGGGGGGTGA TGGGTGCCCC 1500
CTGCAACTGC CGGAAACGGT CTTTGGGCCA AGAAGGGAGT CTGAAGGGTG GGGGTGGAGA 1560
GGGCGAGGCC TAGGGGATGA TCGGCTCCAC CCCTTCTCCC AGCGCATCTG GCCAGGAGAC 1620
CCCAGCTCAA AGCCCCCTCC AGCTTCAAAG GGCACCCTGG GGTGGGAGGC AGGAGACGAG 1680
GGTGGATGCC CTGACCCACT GAGTCCGCAC CCCAGGGCCC CTCTCTCCAA GCTGTGACCT 1740
CACCTCAGGG TTCTTAACAG GCCTTGCTAA CACTCTCCCA CTCAGATCCT GTCATTGTCA 1800
CCATGGCCTT CCTAAGACAC CCTCATCTTC TCCCATCCGA GGGTGGGGGA GAACCAATTC 1860
GATTCGCAAC TTCAGGACCC AGGACCCATC TAGCCGCCTG GGGGATTCCC TACCCCACCT 1920
CTGCAGCCTG TAAATTCTGG GGGAGGAGGC CCTGGAGGGA GGATCAGAGG CATGTCCTTC 1980
CCCAACCTCC CACTCTGGCC TACTAAGAAA TGGGAGCAGG GCTGACCCTA TGAAAGTGTG 2040
GGAGGTGAAG GAGCTGGAGT CGTGATTCCT GGGTATCCCC AGACAGACAT CACCACACTA 2100
CAGCCCCTCT TCTAAGGTGA TCCCAGCACT TTGGGAGGCT GAAGCAGGAG GATCCCTTGA 2160
TGAGACCAGC ATGGGCAGTA TAAGGAGATC CTGTCTCTAT AAAAAATTAA AATATTAGGC 2220
TGGGCGCGGT GGCTCATGCC 2240