EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-28337 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr5:150454890-150456600 
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
TTACTGTATT GTTTGCTTTT TTTCTGCTTC AACTTTTATT TTAGATTCGG GGGGTACATG 60
TGCAGGTTTG CTACCTGGGT ATACTGCGTG ATTTGGGTAG GGGTGATCCC ATCACCTGGG 120
TACTGAGCAT AGTTCCCAAC AGTTTTTCAA CTCTGCCTCC CTCCCTCCCC ACTCTAGCAG 180
TCCCCAGTGT CTACTGTTGC CATCTTTATG TCCATGAGGA CCTGATATTT AGCTCCACTT 240
ATAAGTGAGA AAATGCAGCA TTTGGTTTTC TGTTCCTGTG TTAATGTGCT TAGGACAATA 300
TTTTCTAAAA GTCTATGTTG CCAGTTTCCT GAGGACCAGA TCACGCAGGA GTTGCACCTG 360
CAGAGACAGA AGTGGGCTGG AGAGGGACCA GGGCTCCTAA GTCTGCTGCT GAAGCTGACT 420
ATAGCGAAGG CAAAGGACAA GTGGCCTGAA GGCCAACAGA GAGCCTGGCC AATGCTCTGC 480
CCAGTGGGTG GAGACTGAGC CAAAGGCCCT TGACTCATAG GGCAGTCCCA TACCTGCCCT 540
GGCCTCTCAG CATGACTCCT TGGTGACACA ACTCCCACAG CACCCACACA CCTACACCCA 600
CCTACCCCAC ACACACACCC CTGCCTGGGC TGCCCGGTTT GTCCACTGTG TAGGTGCTCA 660
AGGACGCAGA GCTCCTGCCT CTCAAGGAAC AGCCTCAGGG TGAGGTCCCT GGGAGAGAAG 720
AGTTCAGCTC TGCCCAGAGC AGCCCTCAGA CAAACAGCCA GCTGCTGCTC ACCAGTCATC 780
CATTCCAATC TGAAGAGTGA CTGTCCTGGG CCAGTCATGG GAAAATCATC AAGAACTTCC 840
CACAATGGTC ATGGTGGCCG CCAAGGTCTT TCTCTGGGGG TTGGGAGCTG TGCTCCCCCA 900
CAAAACAAGG GGACCCAGCT GCCCTGTGCC TTCCTGTGGC AACTCTCTGG AGGATGCCTG 960
GATACCCTCC CTACAGACGG CCAGGGATAG GAGGGGCAGG CACTGCAGGC ATGTGGGGGC 1020
ATAGCAGCAA GAATCTAGGA GGGCAGGCAC AGCAAGGCCT GGCCCAGAGG GAAACCAGGA 1080
GCTGCCAGAG CCAAAGAGAG GGTGACCCAA TCATTGGTTG TTATAGAGTT TTTAAGACTT 1140
GGAAGAGAAT GCCCTGAGAT GCCAGAGAGT GAAACATTTT CATTCTAAAG CTGGGAAACC 1200
AAAGTCGGCA AAGGCGAACA GACGTGCCCA CAGCCACATG GGACAGCAGT GGCACAGAAG 1260
AAATGCACAC CTCGTCCTCT GGTGGCCACT GTGCACTCTC TTACCACACC ATGCTACTGC 1320
TCAACCTCTC CCCCTCCCTC ACAGTGGTCA GGTAAGCAAT GAGGGAAAAT GATGGAGGTG 1380
AGAAAGGAAG AACCCGGGCT GATGTGGGCC CACAAAAGAA AGAAGTCTGG AATAACACTG 1440
GAAGGGGCTG CCTACGAGGT GGAAAGCGCC CTGATCCCAG GGGTCGGGGT CACGCAGAGG 1500
GGCACTGGGG CTGTTGAGGG AATGCAAGCC AGGTGTCTTC AAAGCCCCAC CCACATCTGA 1560
GTTTCCGCCA CTCCAAACAG GGACAGATGT TTGAGACAAA GCAAAGGACA ACTCATCCAG 1620
AGGGGACACA GCATGGACCA CAAGTGGCAG AGGGTTGAAG GCAAGTGTCT TAGTCTGCTT 1680
TCTGCAACTA TTCTGTTGAA TATCACAGAC 1710