EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-27158 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr5:150454850-150456660 
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: 3             
ChromosomeStartEnd
chr5150455274150456118
chr5150455023150455538
chr5150455260150455927
Enhancer Sequence
TCGGTATCTG AGAGACTCCT TCAATTTTTC TTTTTTCTTT TTACTGTATT GTTTGCTTTT 60
TTTCTGCTTC AACTTTTATT TTAGATTCGG GGGGTACATG TGCAGGTTTG CTACCTGGGT 120
ATACTGCGTG ATTTGGGTAG GGGTGATCCC ATCACCTGGG TACTGAGCAT AGTTCCCAAC 180
AGTTTTTCAA CTCTGCCTCC CTCCCTCCCC ACTCTAGCAG TCCCCAGTGT CTACTGTTGC 240
CATCTTTATG TCCATGAGGA CCTGATATTT AGCTCCACTT ATAAGTGAGA AAATGCAGCA 300
TTTGGTTTTC TGTTCCTGTG TTAATGTGCT TAGGACAATA TTTTCTAAAA GTCTATGTTG 360
CCAGTTTCCT GAGGACCAGA TCACGCAGGA GTTGCACCTG CAGAGACAGA AGTGGGCTGG 420
AGAGGGACCA GGGCTCCTAA GTCTGCTGCT GAAGCTGACT ATAGCGAAGG CAAAGGACAA 480
GTGGCCTGAA GGCCAACAGA GAGCCTGGCC AATGCTCTGC CCAGTGGGTG GAGACTGAGC 540
CAAAGGCCCT TGACTCATAG GGCAGTCCCA TACCTGCCCT GGCCTCTCAG CATGACTCCT 600
TGGTGACACA ACTCCCACAG CACCCACACA CCTACACCCA CCTACCCCAC ACACACACCC 660
CTGCCTGGGC TGCCCGGTTT GTCCACTGTG TAGGTGCTCA AGGACGCAGA GCTCCTGCCT 720
CTCAAGGAAC AGCCTCAGGG TGAGGTCCCT GGGAGAGAAG AGTTCAGCTC TGCCCAGAGC 780
AGCCCTCAGA CAAACAGCCA GCTGCTGCTC ACCAGTCATC CATTCCAATC TGAAGAGTGA 840
CTGTCCTGGG CCAGTCATGG GAAAATCATC AAGAACTTCC CACAATGGTC ATGGTGGCCG 900
CCAAGGTCTT TCTCTGGGGG TTGGGAGCTG TGCTCCCCCA CAAAACAAGG GGACCCAGCT 960
GCCCTGTGCC TTCCTGTGGC AACTCTCTGG AGGATGCCTG GATACCCTCC CTACAGACGG 1020
CCAGGGATAG GAGGGGCAGG CACTGCAGGC ATGTGGGGGC ATAGCAGCAA GAATCTAGGA 1080
GGGCAGGCAC AGCAAGGCCT GGCCCAGAGG GAAACCAGGA GCTGCCAGAG CCAAAGAGAG 1140
GGTGACCCAA TCATTGGTTG TTATAGAGTT TTTAAGACTT GGAAGAGAAT GCCCTGAGAT 1200
GCCAGAGAGT GAAACATTTT CATTCTAAAG CTGGGAAACC AAAGTCGGCA AAGGCGAACA 1260
GACGTGCCCA CAGCCACATG GGACAGCAGT GGCACAGAAG AAATGCACAC CTCGTCCTCT 1320
GGTGGCCACT GTGCACTCTC TTACCACACC ATGCTACTGC TCAACCTCTC CCCCTCCCTC 1380
ACAGTGGTCA GGTAAGCAAT GAGGGAAAAT GATGGAGGTG AGAAAGGAAG AACCCGGGCT 1440
GATGTGGGCC CACAAAAGAA AGAAGTCTGG AATAACACTG GAAGGGGCTG CCTACGAGGT 1500
GGAAAGCGCC CTGATCCCAG GGGTCGGGGT CACGCAGAGG GGCACTGGGG CTGTTGAGGG 1560
AATGCAAGCC AGGTGTCTTC AAAGCCCCAC CCACATCTGA GTTTCCGCCA CTCCAAACAG 1620
GGACAGATGT TTGAGACAAA GCAAAGGACA ACTCATCCAG AGGGGACACA GCATGGACCA 1680
CAAGTGGCAG AGGGTTGAAG GCAAGTGTCT TAGTCTGCTT TCTGCAACTA TTCTGTTGAA 1740
TATCACAGAC TGGGTAATTT ATAAAGAACA AGTTTATTTG GCTCATGGTT CTGGATGATG 1800
AGAAATCCAA 1810