EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-23189 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr22:50323160-50325640 
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
chr225032316950324139
Number: 1             
IDChromosomeStartEnd
GH22I049927chr225032160450325768
Enhancer Sequence
CTGGGGGGGC TCTGATCCGC CCCTCCCCAC GCGGCGCCGC CCGCGCCCCG CCCGCTCCCG 60
CCGGACACAG CGGACCCTGC CTCGGATCGC GACCCCTGCC CGGGCCCAGC AGGTGGACCG 120
CGAGGCCGCG CGAGGTACCG CCCCTCGGAG CCGCCCGGCC TGGGTCGGGG ACCGGGACGC 180
GCGCGGCCAG CAGGTGGCGC TGTGGGACCG CCCTGCTCGG CCCGGCTCCC GGGACTCGGC 240
CGGCCCCTGC CCGCTGCACC TGCCCCGTCA CACCTCGGCG CTGCCGGGGC GTCTTTCTAA 300
AAGGGGAACT TGGAAGGGGG AGGTTGGGGT GAACTGTGGA CCTCCGCTGT CCTTCTGGGC 360
CCAGGCAGAG ACCCTGCCAT AGCCCTGGGG GAGTCCCACC CTCTGGGAGC CAGGACTGGG 420
GTCTGCAGGG CCGAGAGGGC CTCCACTTTG GTTCCCAGAC CCCGGCATCT TGCTTTGGCA 480
CATACGCAGG TCCTGGAGAT GGCTTCCATC CCCACAGGGC ACTCCTTGTC AGGCTAGAAG 540
CTTCTAGAAG TGCCCCCTGG TCAAGCCCAC CCCTGGCTTT GCTGTAAACG CGTCCCTTGG 600
TCGAATGCAA CAGACAGTGG GCGGGATCCG CAGGATGAGA CGTTCTGTGA GCCAGCGGTT 660
CTCAACAGGC AGCTGTTGTG TCCTCCAGGG GACAGGGGAC CGCCTCTGGA GGTGCTGTGG 720
GTTGTCACGA CCTGGTGAGG AGTGCTTCTG CCAGGGCACA GGACACCCTG CCACAGAGGA 780
TGGCCCCCAC CAGAGGACAA GCCAGCTCCC GCTGCCACCA AGGCAGACAG ATGCTCACAG 840
CAGTCCCTGG ACAGGGGCCT GGACCTCAGC CAAGGCATGT TAGACAGGGA GGCGGCCATG 900
GTGTGAACGT GGGTCTGCTC TGGGAACACG AATCATGGGG TGGGGTCCGC GCAGGCCGGG 960
ACCACCTATG CGTGCTGCGT CCTGCTGTCC TGGATGTACC ACATCCCCCT GAAGATGACC 1020
GTTGCCTGCT CAACCTCATG ACAGGGCCGG TCTAATAGCC AGTGCCAGCG GGCAAGGCAG 1080
AGACACAGCC ATGGGGCATC CCATGGCCAG GCTGTGCATC TCCACAGGGG CCCAGAACCA 1140
CAGCAGGAGT CCTCGACGCA GGCACACACT GAGGATGGCA TGGGCCTCCT CTGCACTGTG 1200
TTTGGGGAGG GTCTTCCACA GGCACTTGAC CTTAACCCCT CCTTTACCAC CCGTGCCTTT 1260
GGTCTGCAGA GTCAGATCGT AAGTAGCAGC CGGGACACCG GAGTTGGGCT TGGACGGCGG 1320
TGGAGCTGGT CCTGCTCTGT GCCTGTTCAG AGCTGTCCTT TTGTGTCCCC CAGTATTGGG 1380
TTGGAACAGA GTCCCCAAAT GTGGAACATA CTGTTCCAGC TCCCAGAAGC CTTCCAGGTG 1440
CCGTGTGTCC TGGCGGGGGC TGCAAGAGGC AGCCACTTAT CTGTCCTCTG CTTTGGAGGG 1500
GATTTTCTCG CTCAGGAGGG CCCAGTGTGC TCACCATGTC TTGGTCATCT GGTCTCATTA 1560
GCACAGCACC ATCGATAGAG GGGGCCAGTG TGACATCCTG GGGACATTCA TTCAGCTGGT 1620
GCCAGTCTCT GGATTATTGT GAGAGAGGGC AGGAACGTTA CCATAGCCCT GGGGAGGAAC 1680
TGAGTGTTTC CTGTTTTGAG TTCCAAGGCA GTGTGACTGA TCTTCCTGCC AGACAGGAGA 1740
TGGAGAAGAA TGCACACCCA GCAGTGGCCT CACTGCACAC CTGGGGCTGG GGAGCCTTCT 1800
CTAGCAAAGG CGCCACATCT AGCTGGGTTG TTTTTGCAAC AGTCCACTCT CCTCCAGGAC 1860
CCACCCACCT GCCTTTTGCA GTGGTCAGAT TGGTGGAATA AAAGGAGATC CTTGGCCGGG 1920
CATGGTGGCT CACGCCACTG TATTCCTAGC ACTTTGGGAG GCCAAGGTAG GTGGATCACC 1980
TGAGGTCAGG AGTTCCAGAC CAGGAACATG GCAAAACCCC ATCTCTACTA AAAATACAAA 2040
AATTAGCCAG GCACGGCGGC AGGCACCTGT AATCCCATCA ACTCAGGAGG CTGAGGCAAG 2100
AGAACCACTG GGACTCGAGA GGCGGAGGCT GCAGTGAGCC GAGATCGCTC TGCTGCACTC 2160
CAGTCTGGGT GACAGAGCGA GACTCCGTCT CAAAAAAAAA AAAAAAAGGA GATCCTTGCA 2220
TTCTTTTAGA TCTTTAGATG TGTCCCTAGT TTCCCCCAGT TTTGATTTAC TATTTTGGGT 2280
GGGGATGGTC ACAGATTTGC ACTGGACTTA CCCATTATGA TGGCCAAGGA AATGGTGTCT 2340
ACCATCAAGA ATGTCAGCTC CATCCGTCCT GTGACTGGGG AAATGACCCA CTGGATGAAT 2400
GTGCAGACTC GAGGCTGGTG GATCAGACCT GGCCCGAATT CCACTGCTTC CCTGGCTCCT 2460
GTCAGCCCCT CGCTCTAACG 2480