EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS012-25841 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr8:145038930-145041350 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11787365chr8145041333hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr8:145040223-145040235TGCCCCCTGGCA-6.62
KLF4MA0039.3chr8:145039873-145039884CCACACCCTCC+6.32
RREB1MA0073.1chr8:145039159-145039179CCCCCACCCCCCCGCCCACC+6.13
RREB1MA0073.1chr8:145039149-145039169CCCCAACCAACCCCCACCCC+7.4
RREB1MA0073.1chr8:145039148-145039168CCCCCAACCAACCCCCACCC+9.78
RUNX1MA0002.2chr8:145041231-145041242AAACCACAGAC-6.62
ZNF263MA0528.1chr8:145040343-145040364CCTCACGCCCCTTCCTCCTTC-6.42
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_02906chr8:145040086-145040764Bladder
SE_09260chr8:145034556-145040156CD14
SE_12121chr8:145039150-145040900CD3
SE_14847chr8:145039197-145041588CD4_Memory_Primary_7pool
SE_16928chr8:145039798-145041337CD4p_CD225int_CD127p_Tmem
SE_17383chr8:145034326-145054098CD4p_CD25-_CD45RAp_Naive
SE_17884chr8:145039216-145041514CD4p_CD25-_CD45ROp_Memory
SE_18961chr8:145039229-145042264CD4p_CD25-_Il17-_PMAstim_Th
SE_19196chr8:145039718-145041365CD4p_CD25-_Il17p_PMAstim_Th17
SE_23034chr8:145039553-145040644CD8_primiary
SE_23735chr8:145039917-145040401Colon_Crypt_2
SE_31395chr8:145039839-145041000Gastric
SE_37176chr8:145039935-145042270HSMMtube
SE_44278chr8:145040057-145041129NHDF-Ad
SE_46680chr8:145039958-145041197Ovary
SE_50057chr8:145039713-145041288Sigmoid_Colon
SE_52367chr8:145039878-145041226Small_Intestine
SE_55146chr8:145040283-145041253Thymus
SE_61753chr8:145002108-145053930Toledo
SE_62528chr8:145001740-145054046Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr8145040615145041072
chr8145040786145041230
Number: 1             
IDChromosomeStartEnd
GH08I143964chr8145038538145042092
Enhancer Sequence
TCTTAGGCCT ATCCTGTGCC TGCTCTGTTA GCTTCCCAGG TAGCCACTCG TTTAGCAAGA 60
AAGAAGAGAA AGAGATGCAC TTTCAAAAGG TCAAAAGACA CATTCATTTG AAAAACAGAG 120
CAGAATAAAA ATCATAAAAG CCACAACCAG AGACCTTTAC TGCAGCTACC TCCTTCTGCT 180
CCTGCAGACC CACACTTCCA GCCCTGACCA GCCCCACTCC CCCAACCAAC CCCCACCCCC 240
CCGCCCACCC TGGTGTGCCC CTGTGGATGG CCTTCCCCAC CCTCACCGTC CCACTTGGCC 300
CCAGCCCACC TGACACACCA GCCTGCCCAA GAGCACCCAG ACTCACACCA GCCACCCTGA 360
TGCCGTCCTG GGGCCTTCCT TTCCTGCAGC ACTGGCCCTG GGTCTGCCGC TACTCCTGGA 420
GCCACACAGG GACACAAAGT GATCCCCATC CCATTCCTGG TCCTGGGTCT CCTCTGCCTC 480
CAGGAAGAAG CAGCAACAGT CCTGCCAAGA GCTGACCACC AGCTGGGAGG ACTCTTCTGC 540
AGCTAACCAG GACCCAAATC CTGGAGAGCA GGCCCCACAG GCTGATGTCC CAAGTCCTAC 600
AGGATCCTGT CTTCCCAGCT GGCACCCTCC TTCCACCGTC TGAACGCGTG TTCCCAACTC 660
CCCTTCCACT GGGCCTACAG ATGACCCGGC CCATGCCCCA TTTTGGGTCC CTGACCTCAT 720
GACCCACGGC CCCTGCTCTC CCAGCCCCGC ATCTCCCTAC CCACTGTGGG TCTGTGGGCA 780
TCACCCATGA CCCCAGCGGT GGGAGATCTG GGCACCTGGT CCCACTAGCA TCGCCCTTCC 840
CAGCCTCCTC CAGTCCCTTC TTGAGGTACC TGGCCCCTGG CCCCTCTGCT GCCAGCTCCT 900
CTTGGGCCTC ACTGGGGAAA CTGAGGCCAC AGGGCACCAC TGCCCACACC CTCCCAACAG 960
CCCAACCCTG GGAAAATCTC CAGGGCCCTC AGTGGTGAGC AGCAGTCTGG ACTGGCCACT 1020
GATGATGTGT GGCTGGGTAA ATGTGAGCGA CCACTCAGTA CTCACCCTGG GCCAGGTGAT 1080
GCCCATGCCC CCTGTGACCA TGCAGGTCCC TCAGGCCAAG GCCCAGGGAA CTCCTTCCCC 1140
AGGGAACTCG GGCCAGCATC CAGCTGAGGC TGTGACCTGC TGCGGCCTAG CCTCCATGTC 1200
ACCGCTCTGT CCTGGAGAGG GTTCTCCCTC CCTGCCACCC TGCTGGACCC ACCATAGCCT 1260
GGCACCAGCA GGGCCTCCTG AGCACTTCCC ACATGCCCCC TGGCACCTCC AATCCGACGA 1320
CACCCCAAGC AGTCCCGCTG AGGTCCCAAC ACCCCTCATC ACCTGGTCCC AGCACCATCC 1380
AGGCCTCACC CTGCTCCCAA CGTGGCCCTG CTTCCTCACG CCCCTTCCTC CTTCGCAGAC 1440
CCAACAGGCC CCCATGGCTG CACAGCTGCC CACTGCTCTG CTTCCCGGCT GCCTCTTCTC 1500
ATAGGCACCT AAGCTCTGGA GGACCCCAGG CTCAGAGCTC TGGCCCGAGG CCTGCCCTAG 1560
TGATGGCCTC CCAGCCTGGC CTCCCCACCT CAGCCCAGCA TTTCCTGCAC CTCAGTGTCT 1620
GCACACGCAT ACCTATCTCA CAGGCATCTC TGATTTTATG CACCCAAGGC TAAGCGCTGG 1680
CTCTTCCGCC CTCTCTGCCG CAGGCACATC CTCTCCACCC CAGGCTGCTC TCTACCTCCA 1740
CAGCCACCAC GGGGGACTCC TCAGCCGCTC CTTGGGAGGC ACCAGGCCAG GATCTTGCAG 1800
GGGTCCAGCC AGCTCCAAGT CCACCTATCC CTCCCACCCA ACGCTTGTTT CAAGCCACAC 1860
CTGCCACAGG ACAGGGCGGG GCTCGGCTGG GGGGGTACAA AAGTGAAGCA ACACATAGTC 1920
CCCGCGTCAG GAAGCTGGAT TCTGCCACAG GACAGGGCAG GGCTCGGCTC GGGGGCACAG 1980
AAGTGAAGCA ATACACAGCC CCTGCGTCAG GAAGCCGGAT TGGTGGAAGG GGAGATGTTT 2040
ACAATCATCC CTGTAACCCA CAAGCCCACG GCCAGACCCT ATGAGCGTGA CACCAAGCAT 2100
GACATCGAGC CTCCTTGAAC ATCTCGACCT CAGCCCCAAG CAAATTCCAC AAAGATTAAC 2160
GACAGAGATG TTTAAAAAAA TGCAGCAGTG CTGGAAGCAA CTCTCAGCAG ATGTTTTTCT 2220
AAAAGAAGGC CATTTTAAGC ATAGCATAAA ATCCAGAAAT CATAAAAGAC TGGTGAGTGT 2280
TAAAAATTGA TATGGCTAAA GAAACCACAG ACAGAATTAG GCCAGGCGCG GTGGCTCACG 2340
CCTGTAATCC CAGCACTTTG GGAGGCCGAG GTGGGCAGAT CACGAGGTCA GGAGATCGAG 2400
ACTGTCCTGG CTAACACGGT 2420