EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS056-10653 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr22:50358950-50361760 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr22:50360814-50360825TCTTATCTCCC+6.62
STAT3MA0144.2chr22:50361435-50361446CTTCTGGGAAG+6.14
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00426chr22:50354389-50365028Adipose_Nuclei
SE_01044chr22:50353163-50364855Adrenal_Gland
SE_03028chr22:50360221-50362060Bladder
SE_10057chr22:50358614-50362150CD14
SE_11301chr22:50352524-50359995CD20
SE_23129chr22:50351668-50361534Colon_Crypt_1
SE_23738chr22:50359167-50359464Colon_Crypt_2
SE_23738chr22:50359832-50360227Colon_Crypt_2
SE_23738chr22:50360755-50361322Colon_Crypt_2
SE_24687chr22:50358274-50361811Colon_Crypt_3
SE_26808chr22:50352758-50362649Esophagus
SE_29459chr22:50359471-50361120Fetal_Intestine_Large
SE_31381chr22:50340030-50364844Gastric
SE_34375chr22:50357707-50359409HCT-116
SE_34375chr22:50359481-50361777HCT-116
SE_35554chr22:50359231-50361852HepG2
SE_41142chr22:50352558-50364901Left_Ventricle
SE_42159chr22:50339996-50364887Lung
SE_47471chr22:50359873-50362146Pancreas
SE_48365chr22:50351987-50364883Psoas_Muscle
SE_49074chr22:50351981-50364875Right_Atrium
SE_49617chr22:50360257-50361838Right_Ventricle
SE_50117chr22:50351572-50362866Sigmoid_Colon
SE_52469chr22:50352428-50362961Small_Intestine
SE_53398chr22:50352718-50362711Spleen
SE_56937chr22:50357703-50359707VACO_400
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50354738-50364978Pancreatic_islets
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
SE_69071chr22:50358133-50359569H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr225036020050361351
Enhancer Sequence
AGGTGCCGGG AAGGACAAGC CACCGGTTCC CATAGACCTG GCCCAACCAG CGTGCCCTGA 60
GTCCAGTCTG GTCCAGTGAG GCTTTTCCCA TTACCCCACC CCCCACTGCC AAAATGGGAC 120
CCTCGGGCAG CAGCCATTGC GGCCCACCTG CTCCTGGGCC AACTGCCATG GGCATTCCCC 180
AGCCCCCAGC CATGGGCATC CCCAGCCCCG GCTTCAGCCA GGCAAAGGCC CTCCACGCAG 240
ATTGCTTTTG GGAAACTGAA GGCCAGAGAG GCAGGAACCT TGGGCAGATG TCAGAATAGG 300
ACTCTGGTCC TTCCCACTGC TGTGCCCCAC ACACTGCTGC TGAGGGCTGG CTGGGGACCC 360
CTCTAAGGTG GCCTACAGGG TGGGGACATC TGCCAGGGCC CTGGGAATGG GTGCAGGGCG 420
CTGGGCTGAG GCTCCCAGCG AGATAGCTCT GGCCTTCTAG CACAGGGGAT GGCGCGCTTG 480
GGGGCGCCTC TGGACATAGC CCTCCACCCC CTGACTCAGG AGGAGACAGG GCCCAGCCAG 540
CCTCGGGTCC TTCCTCAGGC TCTCGGCCAC AGGTCATCTG CCTGACTGAG CACCACGGCC 600
CAGGGGCGGC AGGAGCTGGT GGAGGATTCC TGTGGGCCTT TTCTGGCTCC TGGGGCGGCC 660
CATAGTGAGC TTTCAGAGAC ATCTCTGAGG GCACCATCCT GGTCCAGAGA CAAGCAGAGC 720
TCCAGAGCCC AAGCGCCAGG AATCTGCTCC CCTGCCGGCC CCACCCCACC TCTGCTGCTT 780
TGGCTCTGCT GGGCCACTTG ACTTTGGGTG CTGGACGAAG GGGAAGGATT CAGGGCCTCC 840
CCAACCCTTC CCTGGCCCCC TCCAGCCCCC CAGCTGTCTG GGCTCCTGCA CACCCTTCCC 900
CTAGACACTC CCTGGGGCTC TGGCAGGATC CAAGTGACCG TAGGCCTGGT TCCTCCCCGC 960
CAGTCCCCAC CCTAGACCTG CGGTCTGGCC TCTCCCTGGG GGTCGAAGCC CAGCAGAATC 1020
CACTGTGTTC CTGCAGGGCC TCTGTGGGCT CCTAGGTGGG TCCTTCCCTA TGGACTGGGC 1080
CCCTCCCACC CTGCCTAGGA GCCTCCAGGG CTGCAGTACC CCTTGGCCAC TCGGGTTGAG 1140
GGATGATGTG TATCCCCAGC CATGCTCACC CCTGCAGGGT GTACACCAGG TGACTGGTCT 1200
GGACCTGCTG CCTGCAGGAT CTGGGGCCAG AGTCCAGGTC AGAACCAGCC CACCGCCCTG 1260
AGCCTCTCTC AGGGGAAGAT GGGGTACCCA AGCACATCCA CCCCAGGGCA CCCTCCTCCT 1320
AGCTTGCAGA CCTGGGCCTG CTTGGCCGCT TATGACTTCG GGTGGGCGCC TGGCCTCTGA 1380
GGCTGTTTCC CCCACCTGGG TCATTCAGAG CTGGGTCCAG GTGACCCATC CCCAAGGGAG 1440
GCCCCTTGCT TGTTCATGGG GGAGCAAACC CTCACCCCAC CCATCCTGGT CGACATCTGG 1500
GGCACGGCAC CCTGGGAGAG GCTTTCCTGC AGGGCCCTGG CCAGGAGGAG GGCAGTGGCC 1560
AGGCTGGAGG GGCAGGCCCT GCCCCCACCC TGCCTTGTCA GGCCTTACTG CCGGGAACCC 1620
GGGGGCCAGA GGCTGTTCAG TTGTGAAACG AAAGCTCAGG GTTTCGCCAG GGCTGCCCGG 1680
GAAGCGGTGG GCCTGGAAGC CATGTGCCAG AGGATCTAGC ACCGCCATGA GAGGCCTCTG 1740
TCTGCAGAAA GGGGAAGGAC TCATTGAGAA ATTCCGGGCT GGGAATCTAT CTTGGGCCCT 1800
GTACTCTCTC AGCCCCGGCA GGGGTCAGGG GCAGGGGTCA GGGATGGACA GAGACCCAGC 1860
AAGCTCTTAT CTCCCCTGTG CTCTGTGGGC AGACTGGCTG ACACCCTTCC CTAACGCCTG 1920
CCTGGGGCCC TAGGCCCAGC CGCACCTGGA CGCTGCCCAC GCAGATCCCC CAGCGGCCCC 1980
CGTCCAGCCT TGGTGTCCTG ACTGCTTCCT TTGGAGGAGC CTGGGTGCCT CAGACCCGGT 2040
GTGGGCTTAG CTCCCCCTTC TGTCTCCCTT GCTCTCCCCG ACTCCCCGGG GCCCGGTGTG 2100
ATGCTGGTGT CATATCACAC CGCGAGCTCA GCCTGAGGGT CCAATGGGTG TGTGGGTGTG 2160
TGGTCAGCCC TCAGCCGCTG CCTGTCCAGG CTGCCACCGC CCATCCAGGG AGCTGCTCGG 2220
CCTCTGCCCA CAGAACAGCC CCGCAGCTGC ACAGGTGGCT TCCTACAGTT TCCTTTCGTG 2280
CTGTTTCCGC GACAGCTCAG GGGCTCCCGG GCCAGTTGGG TGCCCGGCAC GGGGTGGTGT 2340
TCGCAGGGGC TGCCAGGGAT CACTTCCCTT TGCCGCGCAG CTTTGGCACC ACAGCCATGC 2400
TAAGGTTTCG TTTCTGGAGC TGCTTTGGAA GAAAGAAACT GAACAGCGCC CTGATGGCTA 2460
CAGAAGGTCT GTGTCCCAGT CTCTCCTTCT GGGAAGCTGG GCTGGCCTTG GGCCCAGAGG 2520
CGGTCGAGCA GCCTGGCAAG AAGAACGGAC CTCGGAGCGG AACCTTGCCC CCTGTGTGGG 2580
TGCCGGGCAG GCTGTGGGGC ACGACCAGCC TTGGCCCCTC CCCCGACCTG TTTACTGACC 2640
AGGCCACCCT CAGGGGCATA GCTGTGGACA AACCAATCAG TTCCAAGGCT GCCGAGTGAG 2700
CCAGGACGGC ATCTGTGTGG CCCAGCCTGC ACTGACAGCT GGAACGACGC ACTCACCACA 2760
GTACGCAGCG GTCACATGAC ACTGAGGACC ACAGCCTGTT CAGGACTCCC 2810