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

TagContent
EnhancerAtlas ID
HS193-28900 
Organism
Homo sapiens 
Tissue/cell
U87 
Coordinate
chr5:150455080-150456920 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3792783chr5150455732hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SP2MA0516.2chr5:150456429-150456446CAAAGCCCCACCCACAT+6.07
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_01392chr5:150455183-150456483Adrenal_Gland
SE_02605chr5:150454842-150456793Astrocytes
SE_09226chr5:150454881-150456345CD14
SE_15204chr5:150455351-150456738CD4_Memory_Primary_7pool
SE_17941chr5:150455174-150468518CD4p_CD25-_CD45ROp_Memory
SE_18317chr5:150453499-150468432CD4p_CD25-_Il17-_PMAstim_Th
SE_19111chr5:150454771-150468362CD4p_CD25-_Il17p_PMAstim_Th17
SE_23141chr5:150454841-150456487Colon_Crypt_1
SE_23836chr5:150455200-150456402Colon_Crypt_2
SE_25002chr5:150455220-150456142Colon_Crypt_3
SE_27123chr5:150453721-150456784Esophagus
SE_28253chr5:150455196-150456191Fetal_Intestine
SE_31853chr5:150454852-150456622Gastric
SE_32472chr5:150455256-150456379GM12878
SE_35096chr5:150455032-150456331HeLa
SE_36009chr5:150453747-150457034HMEC
SE_37013chr5:150454502-150457000HSMMtube
SE_40909chr5:150454783-150457437Left_Ventricle
SE_42116chr5:150454765-150456478Lung
SE_47695chr5:150455440-150456016Pancreas
SE_48796chr5:150455153-150456074Right_Atrium
SE_50074chr5:150454947-150456817Sigmoid_Colon
SE_51316chr5:150455114-150456779Skeletal_Muscle
SE_51803chr5:150454642-150456818Skeletal_Muscle_Myoblast
SE_52353chr5:150454959-150456784Small_Intestine
SE_53309chr5:150455146-150456609Spleen
SE_56023chr5:150454657-150457156u87
SE_58791chr5:150431451-150475486Ly1
SE_59083chr5:150437761-150478457Ly3
SE_60748chr5:150431201-150478526DHL6
SE_61344chr5:150438255-150475360HBL1
SE_62297chr5:150437930-150538770Tonsil
SE_63588chr5:150454628-150456818HSMM
SE_64498chr5:150454519-150456918NHEK
SE_67545chr5:150454657-150457156u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5150455274150456118
chr5150455260150455927
Enhancer Sequence
CTACTGTTGC CATCTTTATG TCCATGAGGA CCTGATATTT AGCTCCACTT ATAAGTGAGA 60
AAATGCAGCA TTTGGTTTTC TGTTCCTGTG TTAATGTGCT TAGGACAATA TTTTCTAAAA 120
GTCTATGTTG CCAGTTTCCT GAGGACCAGA TCACGCAGGA GTTGCACCTG CAGAGACAGA 180
AGTGGGCTGG AGAGGGACCA GGGCTCCTAA GTCTGCTGCT GAAGCTGACT ATAGCGAAGG 240
CAAAGGACAA GTGGCCTGAA GGCCAACAGA GAGCCTGGCC AATGCTCTGC CCAGTGGGTG 300
GAGACTGAGC CAAAGGCCCT TGACTCATAG GGCAGTCCCA TACCTGCCCT GGCCTCTCAG 360
CATGACTCCT TGGTGACACA ACTCCCACAG CACCCACACA CCTACACCCA CCTACCCCAC 420
ACACACACCC CTGCCTGGGC TGCCCGGTTT GTCCACTGTG TAGGTGCTCA AGGACGCAGA 480
GCTCCTGCCT CTCAAGGAAC AGCCTCAGGG TGAGGTCCCT GGGAGAGAAG AGTTCAGCTC 540
TGCCCAGAGC AGCCCTCAGA CAAACAGCCA GCTGCTGCTC ACCAGTCATC CATTCCAATC 600
TGAAGAGTGA CTGTCCTGGG CCAGTCATGG GAAAATCATC AAGAACTTCC CACAATGGTC 660
ATGGTGGCCG CCAAGGTCTT TCTCTGGGGG TTGGGAGCTG TGCTCCCCCA CAAAACAAGG 720
GGACCCAGCT GCCCTGTGCC TTCCTGTGGC AACTCTCTGG AGGATGCCTG GATACCCTCC 780
CTACAGACGG CCAGGGATAG GAGGGGCAGG CACTGCAGGC ATGTGGGGGC ATAGCAGCAA 840
GAATCTAGGA GGGCAGGCAC AGCAAGGCCT GGCCCAGAGG GAAACCAGGA GCTGCCAGAG 900
CCAAAGAGAG GGTGACCCAA TCATTGGTTG TTATAGAGTT TTTAAGACTT GGAAGAGAAT 960
GCCCTGAGAT GCCAGAGAGT GAAACATTTT CATTCTAAAG CTGGGAAACC AAAGTCGGCA 1020
AAGGCGAACA GACGTGCCCA CAGCCACATG GGACAGCAGT GGCACAGAAG AAATGCACAC 1080
CTCGTCCTCT GGTGGCCACT GTGCACTCTC TTACCACACC ATGCTACTGC TCAACCTCTC 1140
CCCCTCCCTC ACAGTGGTCA GGTAAGCAAT GAGGGAAAAT GATGGAGGTG AGAAAGGAAG 1200
AACCCGGGCT GATGTGGGCC CACAAAAGAA AGAAGTCTGG AATAACACTG GAAGGGGCTG 1260
CCTACGAGGT GGAAAGCGCC CTGATCCCAG GGGTCGGGGT CACGCAGAGG GGCACTGGGG 1320
CTGTTGAGGG AATGCAAGCC AGGTGTCTTC AAAGCCCCAC CCACATCTGA GTTTCCGCCA 1380
CTCCAAACAG GGACAGATGT TTGAGACAAA GCAAAGGACA ACTCATCCAG AGGGGACACA 1440
GCATGGACCA CAAGTGGCAG AGGGTTGAAG GCAAGTGTCT TAGTCTGCTT TCTGCAACTA 1500
TTCTGTTGAA TATCACAGAC TGGGTAATTT ATAAAGAACA AGTTTATTTG GCTCATGGTT 1560
CTGGATGATG AGAAATCCAA GTGCATGACA CCACCATCTG ACAAGGGTCA TGCCAAGGTG 1620
GAAGACAGAA GGAGAAAATG AGTGATTGAA ATAGAGAGTG TATTAGCCAA ACTGGCCCCT 1680
TTTATAACTA ACCTCCCGTC CCCCTACCCC GTGATAGTGA CATTAATCTA TTTATGAGGG 1740
CAGAGCTGAC AATCCATTCA TGAAGCAGAG GGATTACGTT TCCAAGATAT GAACTTTTGG 1800
GGGACACATT CAAACCTTAG CAGCAAGTTA TCCAGAGCAC 1840