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

TagContent
EnhancerAtlas ID
HS010-00030 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr1:19802710-19804300 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PBX1MA0070.1chr1:19802911-19802923CAATCAATCAAA+6.18
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00361chr1:19802985-19804456Adipose_Nuclei
SE_01199chr1:19802720-19804257Adrenal_Gland
SE_04046chr1:19802014-19804336Brain_Anterior_Caudate
SE_05833chr1:19801521-19805226Brain_Hippocampus_Middle
SE_07251chr1:19802953-19805485Brain_Hippocampus_Middle_150
SE_08066chr1:19802672-19804379Brain_Inferior_Temporal_Lobe
SE_09593chr1:19800551-19814880CD14
SE_10714chr1:19802454-19805661CD19_Primary
SE_12250chr1:19802072-19805474CD3
SE_13780chr1:19802862-19805602CD34_Primary_RO01536
SE_14589chr1:19801689-19805595CD4_Memory_Primary_7pool
SE_15716chr1:19802613-19805170CD4_Memory_Primary_8pool
SE_16772chr1:19802038-19805402CD4_Naive_Primary_8pool
SE_17553chr1:19800597-19813835CD4p_CD25-_CD45RAp_Naive
SE_18042chr1:19800983-19815154CD4p_CD25-_CD45ROp_Memory
SE_18410chr1:19800356-19813842CD4p_CD25-_Il17-_PMAstim_Th
SE_19269chr1:19801969-19806261CD4p_CD25-_Il17p_PMAstim_Th17
SE_21264chr1:19801983-19805636CD8_Memory_7pool
SE_21829chr1:19802483-19805231CD8_Naive_7pool
SE_22220chr1:19801825-19805679CD8_Naive_8pool
SE_22607chr1:19800179-19812105CD8_primiary
SE_23237chr1:19803317-19804067Colon_Crypt_1
SE_23924chr1:19802639-19802941Colon_Crypt_2
SE_23924chr1:19803562-19803976Colon_Crypt_2
SE_25786chr1:19801757-19805583Duodenum_Smooth_Muscle
SE_26537chr1:19802505-19805527Esophagus
SE_29645chr1:19803362-19805147Fetal_Muscle
SE_31447chr1:19802308-19805352Gastric
SE_41031chr1:19802601-19804170Left_Ventricle
SE_42185chr1:19801749-19805404Lung
SE_45720chr1:19802951-19804259Osteoblasts
SE_47234chr1:19802920-19805189Panc1
SE_48688chr1:19802526-19805197Right_Atrium
SE_50058chr1:19801658-19813904Sigmoid_Colon
SE_51211chr1:19802610-19805560Skeletal_Muscle
SE_52345chr1:19801632-19806547Small_Intestine
SE_53453chr1:19801782-19805512Spleen
SE_54550chr1:19802486-19805119Stomach_Smooth_Muscle
SE_62519chr1:19761354-19815005Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11980333619803680
chr11980391319804113
Number: 1             
IDChromosomeStartEnd
GH01I019474chr11980113619806349
Enhancer Sequence
TAGATAGATA GGCAGGCAGG CAGGCACTGT GGCACATGCC TGTTATCCCA GCTGGCAGGC 60
ACTGTGGCAC ATGCCTGTTA TCCCAGCTGC ATGAGAGGCT GAAGGGGGAG GACTGCTTGA 120
GCCGAGGAGG CTGAGGCTAC AGTGAGCCAA GATGGAACCA TGCACTCCAG CCTGGGCAAC 180
AGAATGAGAC CCTGTCTCAA TCAATCAATC AAACAGGCCA ATTTTGTCTT TCCTCTCAGA 240
ATCCCTGCAT CTTACACTGT ATATGGTGAC CAGGGCTGGG ATGGGGCTTC ATAGGAAAAA 300
GCCAAAGGAT CCTGCAAGGC TTTGTCACCC AATAGTCCCC ATGGAGGGCT GTCGCAATGA 360
TTAAGATGTG CTGCTGCCAC TCACGTCACA GGCAGGAAGA GCCAGGGACA CTGACACTAC 420
TGCACAAAGA ACCGTCCTGT CCAGTAGGCC AAGCCACACA GTGGCCGACG CTAGGCTAAG 480
ACTATCTCGC CCTTTCAGCT GAGTGGCTAT CTTTTGGAAA ACAGATTGCA GTTCACAAAG 540
TTCCATCTCC TTGCATTTCA ACAAGTGGAA CCAAAAAAAC CTCCTAAACA AAACCCAGAC 600
CTCTTCAGCC ACTGTGGCTA GACGTACAGG GGAACCTCTC GGCCCCAGTT TCCTCATCTA 660
TAAAATAAAC ATCCCCATGG GCTGGTGCCA GAGAGGCAGG AGAGGGGAAT TCCATCAGCA 720
TGCGCTGAGT GCGGTGGACC TGGACCTCCA TGGCAACTGC CATTAACTAG CTGGGGGCCC 780
TTCAGCAAGT TACTACACCT CTCTGAGCTC CGGTTTCCTT ATCTGCAAAA TGAGGAAACA 840
GACCTCACAG GGTTGGTGTT GAGAGAATTA CAGACAATGA CTGTGGGCAT CCGGTAAATA 900
CTGGCAGAAG GAAGGGGCCA CTCTGTGAGT GAACACTCAA TACCAGCCTA CAGACTGAAG 960
GTATCCTTCA TTTCATGGCA TCCCCTGATG CCTGTGCCAT GAGTGCACTC CTCAAGACCA 1020
AGAATGGACT CTGCTTAACC ACACCCCAGC CCATCCTCTC TGCCTGAACA AGGTCTCAAA 1080
TCTCAGGACA ACCAGGGGTC CACACCACCC TGTGCCCAAA AGAGATTTCA GGATAGAAGG 1140
TGTCTGGAGG GTATACACTG AGGACATGAC AACAGCTCAC ATTGGAAATT CTCAGCAGAG 1200
GAACTAACAG CCAAGCCTGG CCGCTGCTCT TTTGGAGTCT GAGTTCCTCA GTGTCTCAAG 1260
ACTTTTCACA CCAGAAGGAT GTGGTGGATT AAGGCTCCTC CTTCCAGTTT CTGAGCACAA 1320
AACTGCAACG CAGGGAGCCC ACTCATGTGA AACCAACGAC AGCCCATCAG GGTCAAAGCC 1380
TCACGACGGA GAAGCCTTCA GCAGCAACAC TCTACCTGCC AATCACTGCT GCAACTGAGA 1440
AGGGAAAAGG GCACCGGTAC CACCGGAAAA TGCCACTGGC TCAATTCTAA TTGGAAGCTC 1500
CAGCAGATAG GGTGCAATGC AAAAGCATCT TTTCATAACT TTTTTTGAAA GAAAGATGGG 1560
GTCTTACTAT GTTGCCCAGG TTGGCCTTGA 1590