EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-18100 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr21:45557180-45558990 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr21:45557324-45557334GGCACGTGCC+6.02
HES2MA0616.2chr21:45557324-45557334GGCACGTGCC-6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00694chr21:45556304-45562174Adipose_Nuclei
SE_03663chr21:45557613-45558345Brain_Angular_Gyrus
SE_03880chr21:45556870-45558575Brain_Anterior_Caudate
SE_04775chr21:45556224-45561784Brain_Cingulate_Gyrus
SE_05779chr21:45550964-45561867Brain_Hippocampus_Middle
SE_06690chr21:45556941-45561734Brain_Hippocampus_Middle_150
SE_07737chr21:45556140-45558445Brain_Inferior_Temporal_Lobe
SE_09453chr21:45556638-45561889CD14
SE_10160chr21:45556978-45567753CD19_Primary
SE_10883chr21:45549670-45568864CD20
SE_12057chr21:45557327-45561939CD3
SE_14927chr21:45557173-45566664CD4_Memory_Primary_7pool
SE_16681chr21:45557708-45558699CD4_Naive_Primary_8pool
SE_16681chr21:45558784-45561608CD4_Naive_Primary_8pool
SE_17033chr21:45557478-45566541CD4p_CD225int_CD127p_Tmem
SE_17488chr21:45556658-45567697CD4p_CD25-_CD45RAp_Naive
SE_17928chr21:45556798-45567404CD4p_CD25-_CD45ROp_Memory
SE_18688chr21:45556913-45567005CD4p_CD25-_Il17-_PMAstim_Th
SE_19210chr21:45556311-45566981CD4p_CD25-_Il17p_PMAstim_Th17
SE_20083chr21:45557255-45567673CD56
SE_22987chr21:45557144-45566653CD8_primiary
SE_24239chr21:45558102-45558823Colon_Crypt_2
SE_30176chr21:45557726-45558616Fetal_Muscle
SE_31647chr21:45556787-45561933Gastric
SE_37564chr21:45556510-45561714HSMMtube
SE_40890chr21:45556355-45562047Left_Ventricle
SE_42286chr21:45556722-45566264Lung
SE_48538chr21:45556048-45561610Psoas_Muscle
SE_50113chr21:45556829-45561735Sigmoid_Colon
SE_51445chr21:45557107-45561723Skeletal_Muscle
SE_52463chr21:45556734-45561663Small_Intestine
SE_53405chr21:45552282-45566904Spleen
SE_55261chr21:45558125-45558765Thymus
SE_58720chr21:45552566-45596359Ly1
SE_59125chr21:45557380-45640832Ly3
SE_60477chr21:45556693-45597600DHL6
SE_61237chr21:45557180-45641526HBL1
SE_61527chr21:45545883-45641600Toledo
SE_62281chr21:45556124-45641130Tonsil
SE_65639chr21:45554700-45561714Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr214555794245558217
chr214555823645558599
chr214555759645558554
Number: 2             
IDChromosomeStartEnd
GH21I044137chr214555689245567922
GH21I005115chr214555753345566332
Enhancer Sequence
GCGTATTTGA GCTCCAAGGT CTTCCGCTTT CCATGTGGAG CAGATGGGAA GGGGGTGCAC 60
CTGTCTGCTG TCCAATGTGG TCAGTGGAGC GGCGATGGGA GGGGGTGGTG ATAGGAGCAG 120
TCTCTGGGTT TAGGGTCTGG GCAGGGCACG TGCCTGCCCT CTGACTTGGG AGCTGTTCTT 180
AGGGTTGGGT CTTAGGTAGC GTTGTAGCGA GCCATGCTTT TGTTTCTGCT TCTCTGCTGC 240
CTCTTCTCTC AGCATTCCTG GTACCCAGCA GCTTGTCAGA GTGGGTTTGG GGCTCCCTCT 300
TATCTCATCA CTGTGCTGTA GGTCTCGTCA CGTTGAAATC AGTCTCTGAG TATTTACTCC 360
TTGCAAGTGC CAGTTTTTTT TCTCTCTCTC TCTCTTTTTT TTTTTTTTTT TCTGTAGAGA 420
TGAGGTCTTG GTCTGTTGCC CAGGCAGGGA TGCAGTGGCA CGATCCTAGT TCACTGCAGC 480
CATGATCTCC TGGGCTCAAG CCATCCTCCA GCCTCATCCT CCTGAGTAGC CGAGACTATA 540
GGCGCATGTC ACCATGCCCA TGGTTTTGTT TTTTTTTTTT TTTGGCCATG TATGTAGCCC 600
AAATTGGTCT GGAACTTCTG GGCTCGAGTA ACCCTCCTGC CTCCCAAAGT GCTGGGATTC 660
CAGGCCTGAG CCACCGCGCC TGGCCCCAAT TCTCTTATGG AACCTTGCAG GATCAGAAAT 720
GGGTTTCCTT CTTGGTAGTT TGGGCGGCGG TCCTGACAGG AAGAAGGGAG GCCGCCTTGG 780
CGTGGCTGTT TTGGTAGCTG GACCGTGAAT CATGGAGGCC TGGCTGGCTC CCACACGGTG 840
GCGTCCTTGA GTTCCAGATC CTCTTTCTGT TCTCTGTGTC TCCTCTCTCT CTTTGCACAT 900
TCATGGAGGT TCTCTGGGCA CCGCCCCCAT GGCCCTGCCT GAGAGGTGGA GGTGGTGCCA 960
GGCTGACCCT CCAGGGACAG CTCTGCCACC TGCAGGAGCA CTGGCCACAG TGCATCGGAG 1020
CGTGCAGGTG GCTTCTGTGC CATGGTGTGG GTGGCAGCCC CAGCACGGCC GGCCCCGGTC 1080
GGCAGCTCCT GTTTCAAGGG CAGGTTGGAG GCTGGCTGGC CGCTTGCCCC ACCCTGGGCA 1140
GCCTGCACCC AGAGTCGAGG GGTAGGCAGT CTCCATCCGA AGAATGCGCC CCTCCTTATC 1200
CCGAAACCTC AGAGGCCTCC TTCCTCAGAT GCCAGCTGTT TTCTCAGTGC CCTTGGCCGT 1260
GCCCTCACCC CTCTCTCACC GGAAGCCCCA CCCCAGCCTG TCGTCCCCGG TCTCCTGAAA 1320
GCCAGCAAGC CTCGTCGGTG CCGCCCACAC CCCTGACCTC ACGCAGCCCC ACGTCAGGCT 1380
CGATCTTTTG TCCAGTTGTC CCTGCGTCGC TGCCGTCTCC ACGAGGCTCT GACCACTGAC 1440
ACCGTGTGTG GCGGGGCGCA GGGGCAGCTG GAGGGTGTGC TGGGGGCTCC GTGCCCTGGC 1500
ATGGCTCCTC CACATTTTGC CAACCCAGAG GCACAGGCGT GAGGTGTGTG GTGGTTCTCA 1560
GGGTCAGTGG GTCTTGGCCT TGGCTTTCAA GGTGTTGATG GGCCCTGGGA CTGATGTGCC 1620
CGTGTGTCTG AGCCCACGTC CCCTGGGCGA AGCTCCCATT TTCACTGACC TGTCCAGAGC 1680
GTTCTGGGTG AGCCTGCCCT GCGTGTCCAT GGTGCGGCGC GCTCTAATGA GCTGCAGCCG 1740
TGGCCACTCT GCACCCTCTG AGACAGTCAC CCATGGGGAC GGCGAACACC CACTGCCTCC 1800
AGAAGATTCC 1810