EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS138-34130 
Organism
Homo sapiens 
Tissue/cell
MSC_BM 
Coordinate
chr5:150454740-150456560 
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
CAGAACACTT GTTTCTTGTT GGTGGCTGAT GAAGGAGAAA TTTCAACTGA TTGGAAATGT 60
GTTATTTCTT AAACCAGATG AGTGAGCATG TAGGTGCCTG CGTGTTACCC TCGGTATCTG 120
AGAGACTCCT TCAATTTTTC TTTTTTCTTT TTACTGTATT GTTTGCTTTT TTTCTGCTTC 180
AACTTTTATT TTAGATTCGG GGGGTACATG TGCAGGTTTG CTACCTGGGT ATACTGCGTG 240
ATTTGGGTAG GGGTGATCCC ATCACCTGGG TACTGAGCAT AGTTCCCAAC AGTTTTTCAA 300
CTCTGCCTCC CTCCCTCCCC ACTCTAGCAG TCCCCAGTGT CTACTGTTGC CATCTTTATG 360
TCCATGAGGA CCTGATATTT AGCTCCACTT ATAAGTGAGA AAATGCAGCA TTTGGTTTTC 420
TGTTCCTGTG TTAATGTGCT TAGGACAATA TTTTCTAAAA GTCTATGTTG CCAGTTTCCT 480
GAGGACCAGA TCACGCAGGA GTTGCACCTG CAGAGACAGA AGTGGGCTGG AGAGGGACCA 540
GGGCTCCTAA GTCTGCTGCT GAAGCTGACT ATAGCGAAGG CAAAGGACAA GTGGCCTGAA 600
GGCCAACAGA GAGCCTGGCC AATGCTCTGC CCAGTGGGTG GAGACTGAGC CAAAGGCCCT 660
TGACTCATAG GGCAGTCCCA TACCTGCCCT GGCCTCTCAG CATGACTCCT TGGTGACACA 720
ACTCCCACAG CACCCACACA CCTACACCCA CCTACCCCAC ACACACACCC CTGCCTGGGC 780
TGCCCGGTTT GTCCACTGTG TAGGTGCTCA AGGACGCAGA GCTCCTGCCT CTCAAGGAAC 840
AGCCTCAGGG TGAGGTCCCT GGGAGAGAAG AGTTCAGCTC TGCCCAGAGC AGCCCTCAGA 900
CAAACAGCCA GCTGCTGCTC ACCAGTCATC CATTCCAATC TGAAGAGTGA CTGTCCTGGG 960
CCAGTCATGG GAAAATCATC AAGAACTTCC CACAATGGTC ATGGTGGCCG CCAAGGTCTT 1020
TCTCTGGGGG TTGGGAGCTG TGCTCCCCCA CAAAACAAGG GGACCCAGCT GCCCTGTGCC 1080
TTCCTGTGGC AACTCTCTGG AGGATGCCTG GATACCCTCC CTACAGACGG CCAGGGATAG 1140
GAGGGGCAGG CACTGCAGGC ATGTGGGGGC ATAGCAGCAA GAATCTAGGA GGGCAGGCAC 1200
AGCAAGGCCT GGCCCAGAGG GAAACCAGGA GCTGCCAGAG CCAAAGAGAG GGTGACCCAA 1260
TCATTGGTTG TTATAGAGTT TTTAAGACTT GGAAGAGAAT GCCCTGAGAT GCCAGAGAGT 1320
GAAACATTTT CATTCTAAAG CTGGGAAACC AAAGTCGGCA AAGGCGAACA GACGTGCCCA 1380
CAGCCACATG GGACAGCAGT GGCACAGAAG AAATGCACAC CTCGTCCTCT GGTGGCCACT 1440
GTGCACTCTC TTACCACACC ATGCTACTGC TCAACCTCTC CCCCTCCCTC ACAGTGGTCA 1500
GGTAAGCAAT GAGGGAAAAT GATGGAGGTG AGAAAGGAAG AACCCGGGCT GATGTGGGCC 1560
CACAAAAGAA AGAAGTCTGG AATAACACTG GAAGGGGCTG CCTACGAGGT GGAAAGCGCC 1620
CTGATCCCAG GGGTCGGGGT CACGCAGAGG GGCACTGGGG CTGTTGAGGG AATGCAAGCC 1680
AGGTGTCTTC AAAGCCCCAC CCACATCTGA GTTTCCGCCA CTCCAAACAG GGACAGATGT 1740
TTGAGACAAA GCAAAGGACA ACTCATCCAG AGGGGACACA GCATGGACCA CAAGTGGCAG 1800
AGGGTTGAAG GCAAGTGTCT 1820