EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-32556 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr9:132178050-132180240 
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:132179707-132179725CATTCCCTCCTTCCCTTC-6.04
EWSR1-FLI1MA0149.1chr9:132179580-132179598GCTTGCTTCCTTTCATCC-6.21
EWSR1-FLI1MA0149.1chr9:132179716-132179734CTTCCCTTCCTCCTTTCC-6.25
EWSR1-FLI1MA0149.1chr9:132179711-132179729CCCTCCTTCCCTTCCTCC-6.33
EWSR1-FLI1MA0149.1chr9:132179732-132179750CCTTCTCTCCTTCCTTCT-6.46
EWSR1-FLI1MA0149.1chr9:132179611-132179629CCATCCATCCATCCTTCC-6.59
EWSR1-FLI1MA0149.1chr9:132179720-132179738CCTTCCTCCTTTCCTTCT-6.67
EWSR1-FLI1MA0149.1chr9:132179728-132179746CTTTCCTTCTCTCCTTCC-7.5
FOSL1MA0477.1chr9:132179648-132179659AGTGACTCATC+6.02
HSF1MA0486.2chr9:132178448-132178461TTCTGGAATCTTC+6.2
JUNDMA0491.1chr9:132179648-132179659AGTGACTCATC+6.32
LBX2MA0699.1chr9:132179184-132179194GCCAATTAGC+6.02
Spz1MA0111.1chr9:132179240-132179251GCTGTAACCCT-6.14
ZNF263MA0528.1chr9:132179443-132179464GGGGGGGGGGGAGGGGGAGGG+6.12
ZNF263MA0528.1chr9:132179724-132179745CCTCCTTTCCTTCTCTCCTTC-6.27
ZNF263MA0528.1chr9:132179708-132179729ATTCCCTCCTTCCCTTCCTCC-6.34
ZNF263MA0528.1chr9:132178360-132178381TTCCCCTGCCCTTCCTGCTCA-6.38
ZNF263MA0528.1chr9:132179728-132179749CTTTCCTTCTCTCCTTCCTTC-7.06
ZNF263MA0528.1chr9:132179711-132179732CCCTCCTTCCCTTCCTCCTTT-8.47
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_08391chr9:132173476-132178923Brain_Inferior_Temporal_Lobe
SE_24377chr9:132178283-132179067Colon_Crypt_2
SE_25152chr9:132178084-132179205Colon_Crypt_3
SE_27812chr9:132173435-132179502Fetal_Intestine
SE_28837chr9:132172879-132179559Fetal_Intestine_Large
SE_30314chr9:132173755-132179457Fetal_Muscle
SE_32244chr9:132178126-132179249Gastric
SE_33461chr9:132173837-132181369H2171
SE_34497chr9:132174503-132180346HCT-116
SE_34852chr9:132173683-132178728HeLa
SE_43266chr9:132173694-132179421Lung
SE_54312chr9:132178067-132180059Spleen
SE_55039chr9:132173443-132178714Stomach_Smooth_Muscle
SE_61500chr9:132144538-132260190Toledo
SE_65248chr9:132173595-132179713Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9132178219132179344
Number: 1             
IDChromosomeStartEnd
GH09I129409chr9132172217132179878
Enhancer Sequence
GAGGCAAGTC CCTGAGCTGC TTTGAGCCTC AGTCTTCCCA TCTGGCAAAT GGGGATAATA 60
ATCACAACCA CCATTGATTG TGAACTTACT CAGTGCCAGG TACTCCACCG AGGTCTGTAC 120
ATTTCCTTAT CTAATTCTGC CCTCAAAACA ACCAAGTGAG GTAAAGACCA CGATGATCCC 180
ACTTTCACAG ATGAAGGGGC AGAGCCTCAG AGAGGTGAAG TCACTTGCTG GGGACACAGC 240
TGGAAGATGG TGCAGTCGCT GTCACACACC CCTGAGAGCG AGTGTCCAGC TGCTGCTCCT 300
GTCTCTGTTG TTCCCCTGCC CTTCCTGCTC ACCCCCTGTA CTTTTCGGTG GCTCCGGCCA 360
CAGCCCTCCC TTTGTATTTG AACCCTTGGA TCCAGCCATT CTGGAATCTT CTGAGTCTGG 420
TGCAGATCCA GCCCCCTCAG TGGGAGACAT CCTCAGGGGT AGATGGTGGC TTGAAGAAAG 480
CCAGGTGGGC CCCACATGGT CCCCACAGTC AACCCGGCGG CTCACAGCTG ATCGGCCATC 540
CACCGTGTCT CCCCCTGCCA TTTACACCGA AGGGTTGGGG TTCCTAACAC ACCCGGGTGG 600
ACGCGTGGCC TCCAGATGGT GCAGTTAATC CCGCTGGAAG CCGTAAATCA GCGAGATTGT 660
CCCAGCTTCC CCTCCCCTCC TCCGTGCTGT CACCTCCAGA AGCTGGTGGG AGAAGCACCC 720
CTCCAGCCCC GCCCTCCCGC CCCGGCCTTT GTTCCTGCTC AGTAGCCGGC AGGACGTGGC 780
CCAGTCACGG TCTCCACGGC CCACGTTTGA ATCTCAGCCC TGTCACTGCC TGGCACGGTG 840
GCTTTGGCCA AGCACTTCAT CTCCTGTTAT CCTCAGTTTC CTCATCCATG AAATAGGGTG 900
GGTCACAGCA CCTGCCTGGT CCTAAAGATG GGGGCTGCTG TGTGTGAGCG CTCCACCCTG 960
GACCTGGCTC CCGGGGGGTC CTCGGATATG CTGCTGGTTA TAACAAGTTC TTACTCTGGG 1020
CTAGGTGTTG TAATGCTTTA GCTCAGTGAA TCCTCAAACA AGCACATTAT GACCCTTTTA 1080
TAGGTGGGGA AGCTCCCACT CCGAGAAGGG AAGTAAGTTG CCCAAGGCCA CACAGCCAAT 1140
TAGCAGAACT GGGATTAAAT CAGGCAGGCC TGTGCAGCTC TAAAGACCTC GCTGTAACCC 1200
TAGGTTCCTG GCCCTCCCTA CTGAGGCCCT CTGAGGCTCT CTACCAAACC AGCATCTGCA 1260
GTGACAGCAT CGTTAGCCCT GCCTGGAGCC GTTGGGTTAA TAGGTCCTTA ATAAAGCCAG 1320
CAGAGGCGTC TGCAGCTTCG CAGGGCAGGG GCCGAGGGGC CAGGTGCAGC AGATGTGTCC 1380
TAATGAAAAT ATCGGGGGGG GGGGAGGGGG AGGGGACCAT GGGGTGAGCC GCCTGCTCAC 1440
GTCTCCAGCT TCCTGACCTC TGTGGCTGAG TCACTGGAGG CCTCCAGGTG CAGGGGACAA 1500
TCAATTCCAT CACTCATTCC ATCTATGCTG GCTTGCTTCC TTTCATCCAT TCACCCATCA 1560
TCCATCCATC CATCCTTCCA TTCCATCCAT CCTCTCCCAG TGACTCATCC TCCCTCCCTG 1620
GCTTCCATGC ATCCATCCAT CCATGAATCC ACTCACCCAT TCCCTCCTTC CCTTCCTCCT 1680
TTCCTTCTCT CCTTCCTTCT GCCCATCTGT CCACCCAGTG TTTACTGAGC ACCCGTCTTG 1740
AGCCAAGCCT TATGTGACGT GCCCAGGTTC CTCCCTCTGA GGGACTCACA TTCTCAAAAG 1800
GATGCAAAAC AACTAAGCCC AAGTGCACAG GGCACTAGGA GAGGAGAGGG CGTCTCGGGG 1860
GCTCTGACAC TGGGCTCTGC ACACCTTCCT CAGCCAAGCT CGCCAGGTGA CCTTGGGCAG 1920
ATCACACTCC CTGGAGGCCA CTCTCTTCTA CCTGTTCAAA AAAGGGTGTC CTCGTCCATT 1980
CGGCTGCTAT GACCTTAGAC TGGGTTATTT ATAAACAAGT TTATAGTTCA CATTTCTGGA 2040
GGTTGAGAAG TCCAAGATCA AGGTGCCTGC AGATTTGGTG TCTGATGAGG GCCCTTTCCT 2100
CACAGATGGT GCCTTATAGC CTTGTCCTCA CATGGTGGAA GGGGCGAGCA GGCTCCCCAG 2160
GCCTCTTGCC TAAAAGCATA GATACCATTC 2190