EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-15582 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr2:85152290-85154160 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr2:85153002-85153021GGGTGCCTTCTGGTGGCCA-7.09
CTCFMA0139.1chr2:85153109-85153128GGGCCACCAGGGGGCGCCA+8.48
EWSR1-FLI1MA0149.1chr2:85152316-85152334TGTTGCTTCATTCCTTCC-6.13
EWSR1-FLI1MA0149.1chr2:85152320-85152338GCTTCATTCCTTCCTTGC-6.79
Foxd3MA0041.1chr2:85153523-85153535GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr2:85153527-85153539GTTTGTTTGTTT+6.32
KLF14MA0740.1chr2:85153318-85153332GGAGGGGCGTGGCA-6.06
SP3MA0746.2chr2:85153319-85153332GAGGGGCGTGGCA-6.08
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_10467chr2:85152411-85153224CD19_Primary
SE_10467chr2:85153647-85154542CD19_Primary
SE_14858chr2:85152185-85154666CD4_Memory_Primary_7pool
SE_15828chr2:85152431-85154332CD4_Naive_Primary_7pool
SE_17329chr2:85150774-85154544CD4p_CD25-_CD45RAp_Naive
SE_18307chr2:85150779-85154763CD4p_CD25-_Il17-_PMAstim_Th
SE_19290chr2:85152241-85154577CD4p_CD25-_Il17p_PMAstim_Th17
SE_22056chr2:85152158-85154691CD8_Naive_8pool
SE_24195chr2:85153080-85153423Colon_Crypt_2
SE_24195chr2:85153770-85154270Colon_Crypt_2
SE_25084chr2:85152974-85153457Colon_Crypt_3
SE_25084chr2:85153774-85154325Colon_Crypt_3
SE_27502chr2:85152280-85153403Esophagus
SE_27502chr2:85153883-85154364Esophagus
SE_32545chr2:85152205-85153149GM12878
SE_32545chr2:85153223-85155068GM12878
SE_34685chr2:85152236-85155103HeLa
SE_35873chr2:85151006-85155048HMEC
SE_43289chr2:85152136-85153652Lung
SE_45342chr2:85153616-85154158NHLF
SE_47378chr2:85152158-85155396Panc1
SE_50337chr2:85152152-85154468Sigmoid_Colon
SE_52528chr2:85152250-85153473Small_Intestine
SE_52528chr2:85153680-85154430Small_Intestine
SE_54030chr2:85152520-85153581Spleen
SE_54030chr2:85153652-85154458Spleen
SE_55909chr2:85152237-85153558u87
SE_55909chr2:85153733-85154923u87
SE_57573chr2:85153731-85154373VACO_503
SE_58212chr2:85152446-85152965VACO_9m
SE_58212chr2:85153042-85153511VACO_9m
SE_58212chr2:85153624-85154273VACO_9m
SE_59563chr2:85151112-85174538Ly3
SE_65145chr2:85151065-85153445NHEK
SE_65145chr2:85153665-85154405NHEK
SE_67823chr2:85152237-85153558u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr28515304685153400
Number: 1             
IDChromosomeStartEnd
GH02I084923chr28515092685154924
Enhancer Sequence
TCTCGTTTTC AATAAATTTT TGCTTTTGTT GCTTCATTCC TTCCTTGCTT TGTTTGTGCA 60
TTTTGTCCAA TCCTTTGTTC AAACTGCCAA GAACCTGGAC ACCCTCCACC CATAACATAA 120
CCAGATTGCT GCCTTTGAGC CTCTTCTTTT TTAGAAATTC TAAAGGCGCT ACTGAGAATA 180
TGATGCATGT CCCTTCAGCC ACTAGCTGTT CCCATCTCTT CTGGGAGATG TTCAGCGCTG 240
GGTCCTCTCC ACCTGCCCAC AGGTTTAGGG AGCCGAGGGA GCCTTCCAGA GCCTCTAAGT 300
CACCTCTCTA GGAGGCTGTC TGCCTGGCCC ACACACAGGC AGGCCCCATT CTTGGCCTCC 360
CCAAGCCAAG AGGGCACAGA CTGATGATCC AGGGCAGGTC TAGGCAAGTG GGGCATGCAG 420
GGATGTTGTA TTAAAGCTTA AGCATCATGA GAGGATCTGA TGACTCAGGG AGCAATTTCT 480
TGAGCCCATA TTGTCCACCT GGGAAGAAAT TGTGGCTGAG GAGTATTCAG GAGCAGCTAT 540
GGGGGAGAGA GGGGCAGAAA TACACCTCAA GGTAGGCCTC TACTGGGTTC AGGAGGTCCC 600
GGGGCTAGGC AGAGAAAGGC AAGCTTGAGA CCCAACAGCG CCACCCACCA TGCATAAATC 660
GGTTCCCTAG TCATCAATTC GCTTATGAAT ACGGAGGCCC CGGAAAGGTG AAGGGTGCCT 720
TCTGGTGGCC AGCTGTGGAG GTGGCCTCGG AGAAGGGTGA CCCGAGTGAC AAGTTGCAGT 780
GAGCGCTGGC TGCGTGCCCA GCCGCGTTGC ACAACTCCCG GGCCACCAGG GGGCGCCATT 840
CTCACACATT CCAGAGCAAA CGGTGCTCCT TGGAGTTGAG CGGCGCGACG GTCCTGCAGC 900
AGCTAGCCTG GGATGTACCC ACAGCTCACC GGGGAGTCCG GGCCACACGT CAGCTGGATC 960
TTGAATGAGA TGAAGACGGG GAGAAAGGGC CTTCCGGACA AAGGGCTTAC GCCCTGGATA 1020
AAGGGCGTGG AGGGGCGTGG CACGTTCAGT CTGGACACAG CATAAAGTGC ATTGGAGAGA 1080
GGCGGGAGAC AGGATGGAAA GGAGGGTGGG AAGAGCTATG AAGCTCCCCA GGGCCTTGCT 1140
AACGCGTTTG GACTTTATCC CGCGCCAGAC TTTTTAAAGG TGGTAAGTAG TTTACAGATG 1200
TGCGTTTTGA GGCCAGCACA TTTTGTTGTT GTCGTTTGTT TGTTTGTTTT TCTTTGAGAC 1260
GGGGTCTCAC TCCCAGGCTG GAGTGCAATA ACGTGATCTC AGCTCACTGC AACCTCCGCC 1320
TCCCAGGTTC AAGCGATTCC CCTGCCTCAA CCTGTCGAAT AGCTGGGGCT ACAGGCGCCC 1380
ACCACCACGC CTGGCTAATT TTTGTATTTT TAGTGGAGAC GGGGTTTCAC CACGTTGGCC 1440
AGGCTGGTCT CGAACTCCTG ACTTCAGGTG ATCCTCCCGC CAAGGCCTCC CAAAATCCTG 1500
GGATTACGGC CATCGTGCCG GGCCAGCAGC ACAGCGTCTT AAGCAATTTT GGATATGAAT 1560
ACCTTCGAGA CGAGCTTGCG CTCCCACAGA CCCCACCACT CCTACAGTCT GTAATTACCC 1620
CCAGCTGCAC CCATATGCGT AGCTTCCCTG GTCCAGAGGG ACGTGCGTGT GTGACCCTGC 1680
AGGATAGTGG GGTGGCCCTG CATGGCATGG CTGCCAGTGC TAAGAGGGGT GTGCCGCCAG 1740
CCTCTGATCC CTCTCACCGG CGGGCCCCCC ATCATCATCA CTATATGATG ACCTGAGGCG 1800
TCCAGGCTCC CGAGGAAAGC CTGCCGCCCT GGTTCCTACA AGGGACGCCT AAACACAGAG 1860
TCCTAAACAC 1870