EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS158-46653 
Organism
Homo sapiens 
Tissue/cell
Pancreas 
Coordinate
chr5:150455170-150456860 
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
TTAATGTGCT TAGGACAATA TTTTCTAAAA GTCTATGTTG CCAGTTTCCT GAGGACCAGA 60
TCACGCAGGA GTTGCACCTG CAGAGACAGA AGTGGGCTGG AGAGGGACCA GGGCTCCTAA 120
GTCTGCTGCT GAAGCTGACT ATAGCGAAGG CAAAGGACAA GTGGCCTGAA GGCCAACAGA 180
GAGCCTGGCC AATGCTCTGC CCAGTGGGTG GAGACTGAGC CAAAGGCCCT TGACTCATAG 240
GGCAGTCCCA TACCTGCCCT GGCCTCTCAG CATGACTCCT TGGTGACACA ACTCCCACAG 300
CACCCACACA CCTACACCCA CCTACCCCAC ACACACACCC CTGCCTGGGC TGCCCGGTTT 360
GTCCACTGTG TAGGTGCTCA AGGACGCAGA GCTCCTGCCT CTCAAGGAAC AGCCTCAGGG 420
TGAGGTCCCT GGGAGAGAAG AGTTCAGCTC TGCCCAGAGC AGCCCTCAGA CAAACAGCCA 480
GCTGCTGCTC ACCAGTCATC CATTCCAATC TGAAGAGTGA CTGTCCTGGG CCAGTCATGG 540
GAAAATCATC AAGAACTTCC CACAATGGTC ATGGTGGCCG CCAAGGTCTT TCTCTGGGGG 600
TTGGGAGCTG TGCTCCCCCA CAAAACAAGG GGACCCAGCT GCCCTGTGCC TTCCTGTGGC 660
AACTCTCTGG AGGATGCCTG GATACCCTCC CTACAGACGG CCAGGGATAG GAGGGGCAGG 720
CACTGCAGGC ATGTGGGGGC ATAGCAGCAA GAATCTAGGA GGGCAGGCAC AGCAAGGCCT 780
GGCCCAGAGG GAAACCAGGA GCTGCCAGAG CCAAAGAGAG GGTGACCCAA TCATTGGTTG 840
TTATAGAGTT TTTAAGACTT GGAAGAGAAT GCCCTGAGAT GCCAGAGAGT GAAACATTTT 900
CATTCTAAAG CTGGGAAACC AAAGTCGGCA AAGGCGAACA GACGTGCCCA CAGCCACATG 960
GGACAGCAGT GGCACAGAAG AAATGCACAC CTCGTCCTCT GGTGGCCACT GTGCACTCTC 1020
TTACCACACC ATGCTACTGC TCAACCTCTC CCCCTCCCTC ACAGTGGTCA GGTAAGCAAT 1080
GAGGGAAAAT GATGGAGGTG AGAAAGGAAG AACCCGGGCT GATGTGGGCC CACAAAAGAA 1140
AGAAGTCTGG AATAACACTG GAAGGGGCTG CCTACGAGGT GGAAAGCGCC CTGATCCCAG 1200
GGGTCGGGGT CACGCAGAGG GGCACTGGGG CTGTTGAGGG AATGCAAGCC AGGTGTCTTC 1260
AAAGCCCCAC CCACATCTGA GTTTCCGCCA CTCCAAACAG GGACAGATGT TTGAGACAAA 1320
GCAAAGGACA ACTCATCCAG AGGGGACACA GCATGGACCA CAAGTGGCAG AGGGTTGAAG 1380
GCAAGTGTCT TAGTCTGCTT TCTGCAACTA TTCTGTTGAA TATCACAGAC TGGGTAATTT 1440
ATAAAGAACA AGTTTATTTG GCTCATGGTT CTGGATGATG AGAAATCCAA GTGCATGACA 1500
CCACCATCTG ACAAGGGTCA TGCCAAGGTG GAAGACAGAA GGAGAAAATG AGTGATTGAA 1560
ATAGAGAGTG TATTAGCCAA ACTGGCCCCT TTTATAACTA ACCTCCCGTC CCCCTACCCC 1620
GTGATAGTGA CATTAATCTA TTTATGAGGG CAGAGCTGAC AATCCATTCA TGAAGCAGAG 1680
GGATTACGTT 1690