EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-14071 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr22:50362250-50364920 
Target genes
Number: 9             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HEY2MA0649.1chr22:50364388-50364398GGCACGTGTC-6.02
Npas2MA0626.1chr22:50364388-50364398GGCACGTGTC+6.02
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00426chr22:50354389-50365028Adipose_Nuclei
SE_01044chr22:50353163-50364855Adrenal_Gland
SE_10057chr22:50363395-50364983CD14
SE_17909chr22:50362716-50365069CD4p_CD25-_CD45ROp_Memory
SE_19477chr22:50362118-50364919CD4p_CD25-_Il17p_PMAstim_Th17
SE_23129chr22:50363042-50364827Colon_Crypt_1
SE_23738chr22:50363659-50364809Colon_Crypt_2
SE_24687chr22:50361864-50363457Colon_Crypt_3
SE_24687chr22:50363517-50364841Colon_Crypt_3
SE_26808chr22:50352758-50362649Esophagus
SE_26808chr22:50363561-50364843Esophagus
SE_29459chr22:50363708-50364757Fetal_Intestine_Large
SE_31381chr22:50340030-50364844Gastric
SE_34375chr22:50362078-50364952HCT-116
SE_35007chr22:50363379-50364948HeLa
SE_35554chr22:50363866-50364772HepG2
SE_41142chr22:50352558-50364901Left_Ventricle
SE_41617chr22:50363670-50364696LNCaP
SE_42159chr22:50339996-50364887Lung
SE_48365chr22:50351987-50364883Psoas_Muscle
SE_49074chr22:50351981-50364875Right_Atrium
SE_50117chr22:50351572-50362866Sigmoid_Colon
SE_50117chr22:50362880-50364872Sigmoid_Colon
SE_52469chr22:50352428-50362961Small_Intestine
SE_52469chr22:50363083-50364861Small_Intestine
SE_53398chr22:50352718-50362711Spleen
SE_53398chr22:50363456-50364874Spleen
SE_56937chr22:50362431-50363537VACO_400
SE_56937chr22:50363556-50364515VACO_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
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr225036400050364777
chr225036288950363014
Number: 1             
IDChromosomeStartEnd
GH22I049968chr225036264050364777
Enhancer Sequence
CTCCACAGAG CCTCCAGGCC CTGAGCAGTG GGACAGCCGG GGGCAGCTGG AGGCACCTGC 60
AGGCACCAGG TCCAGACCCA TCCTCCTGGC CAGGTCCCTG CAGAATCTCC CAGGGGTGCC 120
GTGCCCCAGA TGCCAGCCAG CATGGGTGGA GTGGGTGTTC GCTCCCCCAT GAACAAGCAA 180
GGGGTCTCTC TTGGGGATGG GTCACCTGGA CCCAGCTCTG AATGATCCAG GTGGGGGAAA 240
CTGAAGCCCA GAGGCCAGGC GCCCACCCAA AGTCATAAGG GGCCAAGCAG GCTCAGGTCT 300
GTAAGCCAAG AGGAGGCTAG CCTGGGGTGG GTGTGCTTCT GGGAGCCCCA TCTTCCCCTG 360
GAAGGCCAGG GCGTGGCTGG CTGTGAGCTC TCCCCTAATC CTGCCACCTG CCCTCCTGCA 420
GGGCCCTGGG CTGCACTCTG CTGCTCCACT GACACAGGTG GGGGCCAGCT GAGGAGCCGA 480
TGGCCCTCCA GGCCCAGCAC ATGATGCAGC CCCATGCCAC TCTCCTGGCC TGAAGCCCTG 540
TGGCCACTGT GCTGAGGCTG GCTCTGTGGG CTTCCTCCGG ACTCTGGGGC TTGGCCTGTG 600
CAGGGCAGGT GCTCGGATGT CCCGGAGGAG CTCCTGGGCA GCGTCCGTTG GGCCCCTCAC 660
CAGAACTGCT GTGATCAGTG ACCCCCACCC CACTGGCCAC TCCAGCAGGT GGCGGGGGGC 720
ATGGAGAAGG GAAGCACTGG TGCCCCAGTC CTCAGGCCAG ACCCAGCCCA AAGGTGGTCT 780
GAGCATTCCC TGAGGCCGCT GAGTGTCCTG CCAGGGTCCG GGCTGTGCGA CCGCCCTGGA 840
CTGCACCTGG GAAGACGTTC CCATCAGGCG GCTGGGCCTG CTCTGGTTTG CAGGTGCCCT 900
GGGTCCTGGG GCCCAGTGAC TGGCTCCACC CCTTGGGCCA GGCCAGGCAG AGCTGTTTGC 960
CTGCAACCAG GGACCAGGGG TCCTGGGCCA CTGGACGCTG CCAAGGCTAC AGTGTGCCAG 1020
GAAAGCATGA GGACCTTTTC TGGGCCTCTA TGTCTAGAAA GGACATGAGA TATGGGCCCT 1080
CATATCCCAT GGGGGAGCGG GTCAGTGTAG AGAGGACCAG GGACCTGGAA ATGCCAGGAT 1140
TGAGTCTCAG GCCACATGTA CAACCTGCTG GCCAGGTCCC CACAGAGGCA GCCCTATCCC 1200
ACGGAGCATC CCAGAGGGGC CACCCCAAGA CTCCCAACCC TCCACTTGCC CCTGTCTGGT 1260
TTTCTGCTTA CCAAATCCTC CCACTTTTCA CTCAGGAGGG AACCAGACGT TCCTGAGCCT 1320
GGGGGCTCAC CCCTGCCTGA GAGGCATGAC CAAGACCTAT GTGGGCGGGA TCATTCCAGA 1380
TGTAGCAGAA ACATGGTGAG GGCTCTTTGG GGCCACTATC ACCATCAGCC TTTGCACAGG 1440
TGGGCTCCCC AGTGGGGCCT GGGAGACAGC ACAGGCAGCT CTGCAGAGAT CTGGGGAGAG 1500
GGGCTTGGCA GTGGGGCAGC AGGTGCAAAG GCCCTGAGGC AGGCGGAGGG GCCAGGACCA 1560
CAGTCCCATC CAGCACTCGC CCTGGGCCCT GCCTCCTGGT CTACTCCATG CCCAGGGTCC 1620
CCCTCAACAG TCTGTTCCGT GTGGGATGAG CTGAGGGGAG GAAGCAGGGG TCTCAGAAGC 1680
ACAAGGGCCC TGAGCAGAGC CCTGGGGACT GTCTCCTGCT GTGAGACAGG ACTGGGCAGG 1740
GGCTGGCAGG CATGTGTCTG GGTGGCCCAT GCCAGCCGTG GAGCAGGCCA GGGGCTGCTC 1800
TGATGCCCAC AGGACTGCCC ATTTGCCAGC ACAGGACCTG GCCCTGGAGG GTCCTGGAGT 1860
CCCAGCTCTA CCCTGAAGCA GCCACCTCAG TCCTCCCTCT AGAAAGGACC AGCAGGGTCT 1920
ACCGGGCCAC CCAGGAATGC AGGCAACTCT TATGATGTGT AGGCACCTGT GTGTCCACAT 1980
CTGTACACGT AGAAAAGTGT CGGTGGGTGT GTAAATCTAT ACATGTTCCA AGTGTGTGTG 2040
TCTGGGTTTT TGTGCATGTG CATGTGTGTG TGTGCATGTG AATCTCTGTG TGTGCAGGTG 2100
TGATTTCCTG TGTGCACGTC TATGTGTATA TGCATGTGGG CACGTGTCTG CCATGTATGT 2160
GTGTGCTCCA ATGTGTGTGA TCCTGTGTGT GCACACGTGT GTGTGCATGC ACGCGTCTGC 2220
ACCTGGGCAG GACCTGGCCT AGGAAGAGCC TGGAGCCAAG ACTAGCAGTT CTCCCCTCCC 2280
CCGCCCCCAA ATGACGTGGC CGCTGCCACC GCGTGACTCA CCCTCCCTTC ACTCAAAGGG 2340
CACAGCAGCA CGTGGGGGCG CCTCCTGTGA CTCAGCACCT CCCGGAGGCG GTGAAGGGGG 2400
ACGCTGGTGA CAGGGGAGGA GTCTGGAGCT GAGAGGCGAA CGGAGAGCAC AGTGGAGCAC 2460
ACGGGCCCTG CCCACCCGCC TGTCCTGTCC AAGGATGCTG GGGCCCCGAC CAGCCGGTCA 2520
CAGGCGCNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 2580
NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 2640
NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 2670