EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS177-24294 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr9:135989220-135990550 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAXMA0058.3chr9:135990128-135990138ACCACGTGCT+6.02
TFAP4MA0691.1chr9:135990042-135990052AACAGCTGAT+6.02
Number of super-enhancer constituents: 47             
IDCoordinateTissue/cell
SE_00682chr9:135987462-135992405Adipose_Nuclei
SE_00941chr9:135987489-135999300Adrenal_Gland
SE_03180chr9:135988963-135991884Brain_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_08796chr9:135989685-135989991Brain_Mid_Frontal_Lobe
SE_08796chr9:135990001-135990359Brain_Mid_Frontal_Lobe
SE_08796chr9:135990412-135990821Brain_Mid_Frontal_Lobe
SE_10762chr9:135989711-135990508CD19_Primary
SE_11572chr9:135986926-135992196CD20
SE_13449chr9:135987436-135991013CD34_Primary_RO01536
SE_14179chr9:135988107-135989509CD34_Primary_RO01549
SE_14394chr9:135988918-135992104CD4_Memory_Primary_7pool
SE_17482chr9:135988605-135989418CD4p_CD25-_CD45RAp_Naive
SE_17768chr9:135987018-135992483CD4p_CD25-_CD45ROp_Memory
SE_18626chr9:135987510-135992595CD4p_CD25-_Il17-_PMAstim_Th
SE_19123chr9:135986881-135992627CD4p_CD25-_Il17p_PMAstim_Th17
SE_19979chr9:135987366-135991267CD56
SE_20743chr9:135989076-135990032CD8_Memory_7pool
SE_20743chr9:135990385-135991926CD8_Memory_7pool
SE_22298chr9:135987350-135992210CD8_primiary
SE_23083chr9:135989068-135993969Colon_Crypt_1
SE_23731chr9:135989045-135989394Colon_Crypt_2
SE_23731chr9:135989543-135989832Colon_Crypt_2
SE_23731chr9:135989904-135990340Colon_Crypt_2
SE_24697chr9:135989110-135993380Colon_Crypt_3
SE_26644chr9:135987567-135999307Esophagus
SE_29849chr9:135987727-135991184Fetal_Muscle
SE_31496chr9:135987762-135992067Gastric
SE_33626chr9:135988184-135992123H2171
SE_34626chr9:135987861-135991429HeLa
SE_40917chr9:135987525-135999450Left_Ventricle
SE_41634chr9:135987722-135996589LNCaP
SE_42210chr9:135987263-136000526Lung
SE_47570chr9:135989098-135990050Pancreas
SE_48127chr9:135986843-135999277Psoas_Muscle
SE_48745chr9:135987771-135991876Right_Atrium
SE_49539chr9:135988256-135991378Right_Ventricle
SE_50127chr9:135987674-136000960Sigmoid_Colon
SE_51366chr9:135987756-135999305Skeletal_Muscle
SE_52380chr9:135987803-136000487Small_Intestine
SE_53581chr9:135987715-135991865Spleen
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
chr9135989434135989663
chr9135989897135990476
Enhancer Sequence
CAGTATCCTG AGTGTCCAAG TCACCGGCAG TGGCTCTGAG ATCTCGTGCA GGACAAGCCC 60
GCCACAGGGG ACTAAACATT AACCCTGGGG GAGCCCAGCA CAGCACCCAG GTCCTGGCTG 120
AGCACCATCA GTGCCTGCTG GACAGAGGTG TCCCCAGGCA GGCCAATCCC CAGGAGGGGC 180
TGAAGCCAGG TGGCCTCGGC TGTCCCTGAG CAGGTCTAGA GAGCGGCTCC TCCGTGAGCT 240
GGCAGGCCAG CAGCTGGCCC AGCCCTGCTT GGTGTCATGT GATCCCTGCA CCCTTCCCCC 300
ACCCCCGGGG GGCCCTCTTC TGCCAGCCGG GTGGTGGGGA AGGATGCAGG CCCAACACTG 360
AGAGCCATGC ATGCTTGGGG TAAGGGAGTT GCCACCCTGT CACACAGTCG GGGAGACGCT 420
CTAGCCCGCG TGGAGCTGGC CTGTCTTCTC TGGTCGCTTC CCGTCACAGC AGCAGCAGGC 480
ATGGAACCAG ACCATAGAGC TACGTGGAGT ACAGGGGCTG TTTAAACCAT CTGCTCAGAT 540
GGTGGAGGTG CAGGCTCCAG AGAGAGCTGC CCTGGGGTCT GGGAACAAAG TGGCAGAGTA 600
AGGCCTCTAT CCCTTGCCCC CTCACAGGAC AGAGAAAGAA AGCAGCCAAC AGCCCTGGCA 660
GCTGCCCCAG AACCCTCTGC AGCAAGAAAG GCAGGGTTCC AGCACCCACA GGCCACCCTA 720
GGTCACTCTG TTAGCAGACA GCCCATCTGG GCAGCGCCTG GGCCCCAGGG CACTCTGGCC 780
GGGCTGGGAG CTCAGAGCGG GAGGAGCAGG AACGGCCTAG TGAACAGCTG ATGCAGAGAA 840
AACGCTTTCC CCTGAGGGCA GGTGCCCAGG CAGCCGCTAT GAGCTGACTG CTAGGAGGAG 900
AAAAGAACAC CACGTGCTTG GCTGTGTCCT CAAGGGACAC TCCTGTCCCA CCCCTAGCAG 960
GCATGCTGAT GTCCCTGGGC TCTGGGACCC AGTCGGCAGC TGTGCCTGTA AACACACTGT 1020
CTGGCCTTCT AACATTTGGG TCAGTGCAGT GAGGGTGGCA TGGGGTCCCC GGTGAGCAGG 1080
GGCCCCCACA CCCCAATGTC TCCAGGGACA CAGCCCAGAG CCCTGAAGAT GAGGATGGGA 1140
AACAGGGCCT GGTGGTGTCT GGTGAGTGTG TCACCTGATC AGCCTTCTCA GAGTGACAGG 1200
CCAGCAGGAT GCCGTGTCCC TGGCTGACAG AAGGAGGAAG CCACAGGCCA AACCCAGACT 1260
CCCTCTGGGT AGAATAGTGA GGGTCTTGAG GAACCCTACG GGGCCTGCCC CAGCCCTGCC 1320
ATCTCCCCGC 1330