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

TagContent
EnhancerAtlas ID
HS180-50443 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr9:135994440-135996350 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs59449333chr9135995304hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF740MA0753.2chr9:135995814-135995827ACCCCCCCCCCAC+6.32
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_00682chr9:135992529-135999630Adipose_Nuclei
SE_00941chr9:135987489-135999300Adrenal_Gland
SE_03180chr9:135991932-135996409Brain_Angular_Gyrus
SE_03904chr9:135987523-136000869Brain_Anterior_Caudate
SE_04821chr9:135987134-136024535Brain_Cingulate_Gyrus
SE_05796chr9:135975584-136025980Brain_Hippocampus_Middle
SE_06709chr9:135987770-135999285Brain_Hippocampus_Middle_150
SE_07782chr9:135987299-136019128Brain_Inferior_Temporal_Lobe
SE_08796chr9:135994706-135995671Brain_Mid_Frontal_Lobe
SE_08796chr9:135995838-135996326Brain_Mid_Frontal_Lobe
SE_11572chr9:135995475-135998687CD20
SE_14394chr9:135994483-136011929CD4_Memory_Primary_7pool
SE_16859chr9:135995865-135998028CD4p_CD225int_CD127p_Tmem
SE_17482chr9:135995498-135999468CD4p_CD25-_CD45RAp_Naive
SE_17768chr9:135995422-136025692CD4p_CD25-_CD45ROp_Memory
SE_18626chr9:135995731-135998323CD4p_CD25-_Il17-_PMAstim_Th
SE_19123chr9:135995631-135998216CD4p_CD25-_Il17p_PMAstim_Th17
SE_19979chr9:135995661-135996602CD56
SE_20743chr9:135995422-136000873CD8_Memory_7pool
SE_23083chr9:135994779-135996675Colon_Crypt_1
SE_23731chr9:135994789-135995227Colon_Crypt_2
SE_23731chr9:135995289-135996712Colon_Crypt_2
SE_24697chr9:135994813-135998026Colon_Crypt_3
SE_26484chr9:135994314-135996614Duodenum_Smooth_Muscle
SE_26644chr9:135987567-135999307Esophagus
SE_29849chr9:135993682-135996573Fetal_Muscle
SE_31496chr9:135992120-135999153Gastric
SE_33626chr9:135992796-135997831H2171
SE_34626chr9:135994676-136005394HeLa
SE_40917chr9:135987525-135999450Left_Ventricle
SE_41634chr9:135987722-135996589LNCaP
SE_42210chr9:135987263-136000526Lung
SE_47570chr9:135994870-135995348Pancreas
SE_47570chr9:135995842-135996609Pancreas
SE_48127chr9:135986843-135999277Psoas_Muscle
SE_48745chr9:135992130-135996703Right_Atrium
SE_49539chr9:135994784-135995649Right_Ventricle
SE_49539chr9:135995837-135996604Right_Ventricle
SE_50127chr9:135987674-136000960Sigmoid_Colon
SE_51366chr9:135987756-135999305Skeletal_Muscle
SE_52380chr9:135987803-136000487Small_Intestine
SE_53581chr9:135992724-135999186Spleen
SE_62626chr9:135987373-136020779Tonsil
SE_65763chr9:135986901-135996538Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9135994562135994927
chr9135995063135995322
Enhancer Sequence
GGGTCATTGG TGGCTTGGCT TAGAATCGGG AAGATAAGCG GAAGCCCAGA TGTGAGGAGA 60
TCTGGCAGCC CAGAGGGAAG CACCGGGTGG AAGCTAGGTA GGGAAACAGG GATGCGGGGG 120
AAGGCAGAAA CTGTCTGGTG GTTTCCAGAG AGGACAGGGA CCAAGTGCGC AGCGTCAGCT 180
CTGGCAGGCC ACATAGACAC CAGGAAACCA GCCCCAGGAC GGGGGGTGTT GGCAGGAGGG 240
ACAGGGACTT CCCCGCCCCC TCCCTTGGGC CCTTGGTAAA TGGTCATTGT GTTCAGTTTC 300
CGGCAGTGGC CTCCTCTCCT GCCAGGATCC TGGTTTTCCT GACCCAGCCA GAAGCTTCCC 360
CTTTGATTTC TAAATAGCAG TCGAGGTCTG GATCTCAGTG CTGAGGCTGG GCAAGGAGCG 420
CCAGGGCCAG AGAGAGGGAA GACAAGACCC CCAGGCAGGG GTGGGGCTCA GCTCTGCCTC 480
TCCCTCAGTT CCTCAGGGAC GGAGAGAGGG AACCTGCACG GCCACTGTGA GCGCTCCGCC 540
GGACCCTCCC AGCACACAAA GCCCGAGCTG CTGCCAGAGG TAATGAAAGC CAGATGAGCG 600
CTGGGCTGGT GTCAGCCTCC CACCCCCACC CTCCCAGGGG TCCCTCTCCA GCCGCCAATG 660
AGGACCAGAG CCCTGGATAG ATGAGGGTTG AGGGAACACG TCTGGTCCGG CCATCTGCCA 720
AGCTCAGGAG GAAAGGGTCT CTCAGGCGTG TGGTGTTCCC CCACCAAGAG CTCTGCCCAA 780
CACTGGGCGG AGAAACAAGT CGCATCCAGG CCCTGTCTAG GTACCGGGAC ACCAAGAGGC 840
ACGAGACTCA GGCTAACAAT CGCCAGCAAT CACAACGCGC CACAGTCTAA AGCCATGAAG 900
CGACTGGAGA CGCAGCAAGG CAACACGATG CCGCACGGGG ACTCAGGAGG TTCACTGTGA 960
AGGCTGCAGC CCAGCCAAAG CTCTGATGGG CCCTGAGCCC CCGATCCAGG AATGGCCTCT 1020
GTGCAGGCCC TGTGCCCAGG CAGAGCAGGG CGAGGGGGGC ATCTCTGGAT TCCACTCCCT 1080
CTGCTGTGTA GTCAGCAGCA GTCAGGTGGG AGGCAGATGG CACCACCCAG AGACCCAGGG 1140
CACACGAGAA ACAAGCCCCC GCCCTCACCT AGTCACCCTC CCCTCCATCC ATCACAGGTA 1200
CACCACTCCC TTCTCTGAAT CCTACCCAGT CCTTACCGAT TCAGGGTGTT GGCACTCTTT 1260
CCAGTTAAGC AGAAACAAGT CTTGCCCGCC CTGGGCCTGG GCCACCCTCC TCCCCTCACC 1320
ACCAGGACAT CTGGTCCCAC GTGTTGGAGG CCTGCTGCTC CACCCCATCC CCCGACCCCC 1380
CCCCCACCCC GCTCTGAGCA GCCCCGATGT CCCTGGTCAC CAGATCCACA TCTGCCCCAA 1440
GTAGGGTCTG TCTGGAAGGC CCCTATGGTC TCATCACCTC TGAGGATTCT AGGATTTGGC 1500
CTTCCCGACC ACTTGTTCCA CACCTGCATC GTAAAGGCTA ACGACGCGCT GCGGGCCCTG 1560
GGTGGGAACT GAGTGAAATA AGGCACAGGC CACCGATGTA AACAGGGACA GTGCCGCAGA 1620
AAAAGGTCCA CCTGGGCTGC AGCGGCCTTG GTGACAGCAG GCCCTGGAAC GGTATTGAGG 1680
GGCGCAAAAC CCCAGCCGTG GTCCCTACTG TTGGACGGGG CGCGGCGGCA GCCCCCACTG 1740
CCCACCCTGC TGGCTGATTT CTGCAGAAGG CCCCGACCCC CACCTATGGA GGAGAGAGGA 1800
GGGAGGCGGC CCGCTGGGAT CGCCCGGCCC CGTCCGGGGC TCGCCCCGAC CTGCCCAGCT 1860
CTGCCGCGGG TGGGGAGGCT CCGACGCACC CCCCGCCCGA CCGCCCCAGC 1910