EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-03767 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr10:104419650-104422100 
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
AAAAAAAAAA AAAAGTCCCA TGCCAGTGGT CCAAGCCTCA CTGACCCCTA GCCACCCCTC 60
CCCTCAGAAA AATAAAGGCT TGCCGAGCAC GTTGGCTCAT GCCTGGAATC CCAGCAGTTT 120
GAAGGTGGAT GGATCACTTG AGTTCAGGAG TTCAAAACCA GCCTGGGCCA CATGGTGAAA 180
CCCCATCTCT ACTAAAACGA AAAATTAGCC AGGCGTGGTG CCACGGGCCT GTGGTCCTAG 240
CTACTCTGGA GGCTGAAGTG GGAGGATTGC TTGATTGAGG CTGGGAGGTG GAGGTTGCAG 300
TGAGCTGAGA TCTTGCCACT GCACTCCAAC CTGGGCAACA GAGCAAGATC CTGTCTCAAA 360
GAAAAAAAAG AAAAATAAAG ACTTTGGGGC TGGCCAGACC AAACCATAGC CTTGGTCTTG 420
CTAACTGCCT CCGCCTTCCT GCCCTGAGGG AGTAGAGGAT GACTCGGGTG GGGTGGTGGA 480
CCCTTGCTTC ATTGTTCCCC TCCCCAGTGT GGCAGGGAGC CAGGAGCAGT ATGACAACAG 540
CTGGCCTACC CCTTCCCTCC CCGTGCACCT GTTTGGGGCT AAAGGGAGTG GGGAAATGAC 600
TGGAGCACAG TGCCCCTCCA GCCCAGGGTG CAGGATGCCT GGGGGCAGGT GCCGGTGGAC 660
AGTCACTTCA CTCCACTCAA ATCTGCTTCT GTCTCACTGT CCCTTTCTCC AGTTCTCAGG 720
AGCCCTGAGA CATCCCCCGT GCCAAGAGTT GGGAGCCAAG ATAAAAAGCT GCCTAATTTC 780
TTTCCCACTT GGCCTAGTTT TGTTTTGGCT GAGGGGAGAG GCCCTTTCCC CAGGTGCGTC 840
AATCCACTGA GATGTGGAGG GGACATTCTG GTGGGAATGG GATGGGCTTG AGCCCCTCCA 900
TGTCCCAGCT TTGAAGCCCA CTCCAGACAA TGACACGCTC AGGCACACAT CTATAGGTGA 960
AGCAGCAGCT GCCCAGAGTT GGCTTGGGGG GGGTTCCCTA GGCAGCCAGG GAAGCAGGGA 1020
GACGCTAACC CACCCAGCTG TCCCCAGCCA CCCAGCTGTC CCTGGCTTTG TAGGAGCAGC 1080
TGTCACCCAG CTCCCAAAAG GGTCGGGGCA GAGGAGGCCC AGAAAGAGCT GGGGCTGCCC 1140
CAGGGAACAG GCTTATTCAG AAGTCATCGG AGGGGCCTTC TCTGCCCTGA ACTGGTGGCC 1200
CCTTGGAGGG CTGGCTGCAG CCACAGGTGC CCCAGTGCCC AGCCCTCCCC TCCTGCCTTC 1260
CCCCAAAGGC CATCACGCCT CCCCTTTCCG GGAAGGGTTG GGGATCTGAC CACGTCTCCC 1320
TACCCCACAG ACTGGGGCCG ACAGCTCCTG TGGCCCAGAT GTGCTGAGCC CGCAGCGAGG 1380
CCACCGCGAG GGAGTGGGTG GGGGTGGTTT CCTCTGCTGC CTGCCGGCCC CAGCTCTTTC 1440
ATGTTGCCGC CCTCCCCATC CCAGCCCGGA GCCAAGCAGC TGGGCCGCTC CTGCCCCCTC 1500
CCTCGGCCTC GCTCCCAGCT GTCTTTGGGG TGGGGCAGGG CAGCTGGGGA ACAGCTGCAA 1560
GGCAGGAGCC TGGGGGGTGA TGGGTGCCCC CTGCAACTGC CGGAAACGGT CTTTGGGCCA 1620
AGAAGGGAGT CTGAAGGGTG GGGGTGGAGA GGGCGAGGCC TAGGGGATGA TCGGCTCCAC 1680
CCCTTCTCCC AGCGCATCTG GCCAGGAGAC CCCAGCTCAA AGCCCCCTCC AGCTTCAAAG 1740
GGCACCCTGG GGTGGGAGGC AGGAGACGAG GGTGGATGCC CTGACCCACT GAGTCCGCAC 1800
CCCAGGGCCC CTCTCTCCAA GCTGTGACCT CACCTCAGGG TTCTTAACAG GCCTTGCTAA 1860
CACTCTCCCA CTCAGATCCT GTCATTGTCA CCATGGCCTT CCTAAGACAC CCTCATCTTC 1920
TCCCATCCGA GGGTGGGGGA GAACCAATTC GATTCGCAAC TTCAGGACCC AGGACCCATC 1980
TAGCCGCCTG GGGGATTCCC TACCCCACCT CTGCAGCCTG TAAATTCTGG GGGAGGAGGC 2040
CCTGGAGGGA GGATCAGAGG CATGTCCTTC CCCAACCTCC CACTCTGGCC TACTAAGAAA 2100
TGGGAGCAGG GCTGACCCTA TGAAAGTGTG GGAGGTGAAG GAGCTGGAGT CGTGATTCCT 2160
GGGTATCCCC AGACAGACAT CACCACACTA CAGCCCCTCT TCTAAGGTGA TCCCAGCACT 2220
TTGGGAGGCT GAAGCAGGAG GATCCCTTGA TGAGACCAGC ATGGGCAGTA TAAGGAGATC 2280
CTGTCTCTAT AAAAAATTAA AATATTAGGC TGGGCGCGGT GGCTCATGCC TGTAATCCCA 2340
ACACTTTGGG AGGCCAAGGC AAGCAGATCA CTTGAGGTCA GGAGTTCGAG ACCAGCCTGG 2400
CCAACATGGT GAAAGCCCAA CTCTACTAAA AATAAAAAAA ATTATCTGGG 2450