EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-18922 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr22:50323170-50325950 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr22:50323343-50323362CGGCCAGCAGGTGGCGCTG+8.7
HSF1MA0486.2chr22:50323696-50323709GAAGCTTCTAGAA-6.28
NR3C1MA0113.3chr22:50324561-50324578TGGAACATACTGTTCCA+6.24
NR3C1MA0113.3chr22:50324561-50324578TGGAACATACTGTTCCA-6.35
NR3C2MA0727.1chr22:50324561-50324578TGGAACATACTGTTCCA+6.32
NR3C2MA0727.1chr22:50324561-50324578TGGAACATACTGTTCCA-6.46
RREB1MA0073.1chr22:50323470-50323490TGGAAGGGGGAGGTTGGGGT-6.01
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_10057chr22:50324323-50325785CD14
SE_10530chr22:50323350-50326033CD19_Primary
SE_11301chr22:50322859-50332155CD20
SE_17545chr22:50323050-50325513CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50322972-50325308CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50324731-50325180Colon_Crypt_1
SE_23738chr22:50323444-50323987Colon_Crypt_2
SE_23738chr22:50324768-50325170Colon_Crypt_2
SE_24687chr22:50322337-50324432Colon_Crypt_3
SE_26808chr22:50323935-50325201Esophagus
SE_31381chr22:50323229-50325862Gastric
SE_34375chr22:50323439-50325507HCT-116
SE_35007chr22:50324408-50325745HeLa
SE_42159chr22:50323334-50325969Lung
SE_47471chr22:50324650-50325152Pancreas
SE_50117chr22:50323350-50325929Sigmoid_Colon
SE_52469chr22:50324192-50325679Small_Intestine
SE_53398chr22:50323416-50325883Spleen
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50323311-50325453Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr225032415650325119
chr225032345450323800
chr225032380850323900
chr225032402650325791
Number: 1             
IDChromosomeStartEnd
GH22I049927chr225032160450325768
Enhancer Sequence
TCTGATCCGC CCCTCCCCAC GCGGCGCCGC CCGCGCCCCG CCCGCTCCCG CCGGACACAG 60
CGGACCCTGC CTCGGATCGC GACCCCTGCC CGGGCCCAGC AGGTGGACCG CGAGGCCGCG 120
CGAGGTACCG CCCCTCGGAG CCGCCCGGCC TGGGTCGGGG ACCGGGACGC GCGCGGCCAG 180
CAGGTGGCGC TGTGGGACCG CCCTGCTCGG CCCGGCTCCC GGGACTCGGC CGGCCCCTGC 240
CCGCTGCACC TGCCCCGTCA CACCTCGGCG CTGCCGGGGC GTCTTTCTAA AAGGGGAACT 300
TGGAAGGGGG AGGTTGGGGT GAACTGTGGA CCTCCGCTGT CCTTCTGGGC CCAGGCAGAG 360
ACCCTGCCAT AGCCCTGGGG GAGTCCCACC CTCTGGGAGC CAGGACTGGG GTCTGCAGGG 420
CCGAGAGGGC CTCCACTTTG GTTCCCAGAC CCCGGCATCT TGCTTTGGCA CATACGCAGG 480
TCCTGGAGAT GGCTTCCATC CCCACAGGGC ACTCCTTGTC AGGCTAGAAG CTTCTAGAAG 540
TGCCCCCTGG TCAAGCCCAC CCCTGGCTTT GCTGTAAACG CGTCCCTTGG TCGAATGCAA 600
CAGACAGTGG GCGGGATCCG CAGGATGAGA CGTTCTGTGA GCCAGCGGTT CTCAACAGGC 660
AGCTGTTGTG TCCTCCAGGG GACAGGGGAC CGCCTCTGGA GGTGCTGTGG GTTGTCACGA 720
CCTGGTGAGG AGTGCTTCTG CCAGGGCACA GGACACCCTG CCACAGAGGA TGGCCCCCAC 780
CAGAGGACAA GCCAGCTCCC GCTGCCACCA AGGCAGACAG ATGCTCACAG CAGTCCCTGG 840
ACAGGGGCCT GGACCTCAGC CAAGGCATGT TAGACAGGGA GGCGGCCATG GTGTGAACGT 900
GGGTCTGCTC TGGGAACACG AATCATGGGG TGGGGTCCGC GCAGGCCGGG ACCACCTATG 960
CGTGCTGCGT CCTGCTGTCC TGGATGTACC ACATCCCCCT GAAGATGACC GTTGCCTGCT 1020
CAACCTCATG ACAGGGCCGG TCTAATAGCC AGTGCCAGCG GGCAAGGCAG AGACACAGCC 1080
ATGGGGCATC CCATGGCCAG GCTGTGCATC TCCACAGGGG CCCAGAACCA CAGCAGGAGT 1140
CCTCGACGCA GGCACACACT GAGGATGGCA TGGGCCTCCT CTGCACTGTG TTTGGGGAGG 1200
GTCTTCCACA GGCACTTGAC CTTAACCCCT CCTTTACCAC CCGTGCCTTT GGTCTGCAGA 1260
GTCAGATCGT AAGTAGCAGC CGGGACACCG GAGTTGGGCT TGGACGGCGG TGGAGCTGGT 1320
CCTGCTCTGT GCCTGTTCAG AGCTGTCCTT TTGTGTCCCC CAGTATTGGG TTGGAACAGA 1380
GTCCCCAAAT GTGGAACATA CTGTTCCAGC TCCCAGAAGC CTTCCAGGTG CCGTGTGTCC 1440
TGGCGGGGGC TGCAAGAGGC AGCCACTTAT CTGTCCTCTG CTTTGGAGGG GATTTTCTCG 1500
CTCAGGAGGG CCCAGTGTGC TCACCATGTC TTGGTCATCT GGTCTCATTA GCACAGCACC 1560
ATCGATAGAG GGGGCCAGTG TGACATCCTG GGGACATTCA TTCAGCTGGT GCCAGTCTCT 1620
GGATTATTGT GAGAGAGGGC AGGAACGTTA CCATAGCCCT GGGGAGGAAC TGAGTGTTTC 1680
CTGTTTTGAG TTCCAAGGCA GTGTGACTGA TCTTCCTGCC AGACAGGAGA TGGAGAAGAA 1740
TGCACACCCA GCAGTGGCCT CACTGCACAC CTGGGGCTGG GGAGCCTTCT CTAGCAAAGG 1800
CGCCACATCT AGCTGGGTTG TTTTTGCAAC AGTCCACTCT CCTCCAGGAC CCACCCACCT 1860
GCCTTTTGCA GTGGTCAGAT TGGTGGAATA AAAGGAGATC CTTGGCCGGG CATGGTGGCT 1920
CACGCCACTG TATTCCTAGC ACTTTGGGAG GCCAAGGTAG GTGGATCACC TGAGGTCAGG 1980
AGTTCCAGAC CAGGAACATG GCAAAACCCC ATCTCTACTA AAAATACAAA AATTAGCCAG 2040
GCACGGCGGC AGGCACCTGT AATCCCATCA ACTCAGGAGG CTGAGGCAAG AGAACCACTG 2100
GGACTCGAGA GGCGGAGGCT GCAGTGAGCC GAGATCGCTC TGCTGCACTC CAGTCTGGGT 2160
GACAGAGCGA GACTCCGTCT CAAAAAAAAA AAAAAAAGGA GATCCTTGCA TTCTTTTAGA 2220
TCTTTAGATG TGTCCCTAGT TTCCCCCAGT TTTGATTTAC TATTTTGGGT GGGGATGGTC 2280
ACAGATTTGC ACTGGACTTA CCCATTATGA TGGCCAAGGA AATGGTGTCT ACCATCAAGA 2340
ATGTCAGCTC CATCCGTCCT GTGACTGGGG AAATGACCCA CTGGATGAAT GTGCAGACTC 2400
GAGGCTGGTG GATCAGACCT GGCCCGAATT CCACTGCTTC CCTGGCTCCT GTCAGCCCCT 2460
CGCTCTAACG GGAGCCATGA GGATGCTTCA GGCCTTCAGA TGCCAGCATC ACTCAAACCC 2520
TGTGTCCAGC ACTTCTGAAG ATGTGTGCGT ATTTCCGTTG CACTGTGTCT GGTTACCGAG 2580
GTCGGCGGCC ACAGGCCGTC TGGTGGTGGT GGCGGGCGGG GGCGGGGGCA GGGGGCCAGA 2640
ATCATCATGG TGTGGATTTG CCTTGGCGTT GCACATCTTC CTCTTAGGGA CTCAGCCTTC 2700
ACTTTAGTGA GATTTCTCTG GGTCAGAAAC CCACTCAGGT CTAGAAACTG GGCAGCGTCA 2760
TGACTTTTTA TTTATTTATT 2780