EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS087-14230 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr22:50329480-50331660 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr22:50329661-50329672GGAGGGTGTGG-6.32
MEF2BMA0660.1chr22:50330962-50330974GCTATTAATAGC+6.14
MEF2BMA0660.1chr22:50330962-50330974GCTATTAATAGC-6.14
MEF2BMA0660.1chr22:50330992-50331004GCTATAAATAGT+6.18
Nr5a2MA0505.1chr22:50329861-50329876GTTGGCCTTGACCTT-6.62
ZEB1MA0103.3chr22:50331448-50331459CCCACCTGCCC+6.14
ZNF263MA0528.1chr22:50329580-50329601GGAGCAGGGACGGAGGGGAGG+6.39
ZNF263MA0528.1chr22:50329615-50329636GGAGCAGGGACGGAGGGGAGG+6.39
ZNF263MA0528.1chr22:50329577-50329598GGAGGAGCAGGGACGGAGGGG+6.56
ZNF263MA0528.1chr22:50329612-50329633GGAGGAGCAGGGACGGAGGGG+6.56
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_03028chr22:50330257-50330910Bladder
SE_10057chr22:50329482-50331113CD14
SE_10530chr22:50329417-50331525CD19_Primary
SE_11301chr22:50322859-50332155CD20
SE_12420chr22:50329511-50330959CD3
SE_17545chr22:50326591-50331700CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50326643-50331570CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50329041-50330887Colon_Crypt_1
SE_23738chr22:50326901-50330921Colon_Crypt_2
SE_23738chr22:50330990-50331681Colon_Crypt_2
SE_24687chr22:50326851-50332818Colon_Crypt_3
SE_26808chr22:50326694-50332325Esophagus
SE_28169chr22:50329511-50330607Fetal_Intestine
SE_29459chr22:50329662-50330703Fetal_Intestine_Large
SE_31381chr22:50326539-50332985Gastric
SE_34375chr22:50329499-50331658HCT-116
SE_35007chr22:50329748-50331112HeLa
SE_42159chr22:50329569-50333037Lung
SE_47471chr22:50329736-50330581Pancreas
SE_47471chr22:50330625-50330862Pancreas
SE_47471chr22:50331041-50331735Pancreas
SE_49712chr22:50329828-50332142Right_Ventricle
SE_50117chr22:50329562-50332768Sigmoid_Colon
SE_52469chr22:50329581-50332615Small_Intestine
SE_53398chr22:50326561-50333542Spleen
SE_56937chr22:50327618-50330661VACO_400
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50329632-50332479Pancreatic_islets
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
SE_69071chr22:50329560-50330581H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr225033000050330846
chr225033072550331030
Enhancer Sequence
GGGCGGAGGG GAGCCTGGGG GTCTGGGAGA AGGAGGGGTG CGGGGTGTGG GGCCTGGGGT 60
GAGCAGGGGT GGGGGCGGAG GGGAGGGTGG GGGTCCGGGA GGAGCAGGGA CGGAGGGGAG 120
GGTGGGGGTC CGGGAGGAGC AGGGACGGAG GGGAGGGTGG AGGTCCGGGA GGAGCAGGGG 180
TGGAGGGTGT GGGGCCTGGG CTGAGCATGG GAGGGGACCT GCAGCCCGTG CCCAGCCCCA 240
TAGGGACCCG CCCGCGCTCC TCCCCCGCCG CCCCGGCCCC GCGCTCCTCG TCGCTGGGAA 300
CCCCCTGCGG GAGCAATGAC GATGAGCAGG ACGATGGCTG TGAGGGCCCG GCCCGAGCTC 360
TGGGGCGTGG GCCGGAGCGC GGTTGGCCTT GACCTTCTTG GAAAGCCCTT GGCGGCAGGT 420
GACTCCGCTT AGTCACGGCC CCGGGGGCGG GGGCTCCCCG AAGGAAAGGA GCCCCCGCGG 480
GAGCAGGCGC AGAATGAGAT GCACGAGCGC CACCGCCGCC GCCGCACACC CCCCGCCCCC 540
CCGGGGTGGA AGCCAGAACC TGCGTCCCCA GCTCCCCCAG GCCCGCCCAC AGGGCGCCTG 600
GCTGGGCCTC CGAGCTTTCC TGTTTTCTCT GCAGCCTGGC TGGGCTTAGG GAGAGGTGGG 660
GGGTGCGCCT CTTGATGCTG GGGACGCGTG TGGCACAGGG AGCCGGGTGC AGCCAAGGCT 720
TGGAGGGGTG CCCCCCGCCC CACCCAGGTC ACACTTCACC CTTCGTGGGG TCGGGATCTG 780
GTCTTTTTAC AAGCTAGGCG CCCTCCCCCC TTTTTTTTTT TTTTTTTTTC TCAAAAATGA 840
TCACAGGGAA TGAGCCTCAG CCAGGACAGC GGGCTATGAG GCTGCCTGTT GCCCCCACCA 900
GCCTGAATTC TGGCAGGGCC CTTCTCCTCC ACCCACAGCC CTCCATCCAC ACCCCTCCAG 960
TGGCTCCAAG GCCCATCTGA CTTGGCCTCA GTTCACCTGT TTACTTCAGG GACACCTGGT 1020
TATACTGCCA GAGGCAGGTT GGGGGGCCTG CAGGGCCGGC CTCTCTCAAA TCCACTTCTG 1080
GCTCTGCGGT CCCCACAGCA CTTCCTTACC CCTTCCCCAT GCTGGAATCT GAGAACCAGA 1140
TATGGGGGTC CTGGTCTCAG CATCCCTTTC CATCCGGGGT GCCCTGCTGC TGCCAGCTCA 1200
CGTGCCCACC ATCCCATCCT CCTCAGGGTC AGTGTGGCTG CAGAACGGCC TCCGGGGAGA 1260
GCAGGGTGGG GGCTGTAGCC TGGTGCACCC CCAGCCTGCT GTCCCAGGTG AATGCAGACC 1320
CCTGGCTCAG CTGCTGACCA GATAACAGTG GCCCTTGTGC CGAAGCCTGG GTGGGGGCTG 1380
GGGTACCAGC CCCGGGTGTC TCCGGGCACA GAATGGCACC CACCCCCACC CCACCCGCAG 1440
GCAGCGGCCA GCAGGAGACA TTGTCCGTCC CCCTCAACCC TGGCTATTAA TAGCTCCTCT 1500
GGGCTAGGAG CGGCTATAAA TAGTCCCAGC CCCTCACACA GGCCCATTCA GGCACCCGCT 1560
GCCTGGGTGT GCACAGCAGC CACACTTGCG CTCACTCAGA GCTGTGCACG CGGGAACCGT 1620
GCCACTTCTG CCCCTCCACG CCATCTGCAC TGCACAGATC CAGGCTGTCC CTGCAGCCCT 1680
CACTGGGTCT CCTGTGGCAG GGGAGGGCCC TGAACCCTCT GGAGGCTTTT CCCTTGCCCC 1740
CTCCCGCCAC GCCCAGGGTC CCCTTGGGGC TTCTAGCTAC TCTAGGGTCT TGCTCTGGGG 1800
CTTCTGGAAG TCAGATGCAT TCACCCAAAG CCAGCCTGGG GCGGGGGGAG GTCCACCTGG 1860
AGGGAGGCCC AGCCCCTGCA GAGACCTAAG CCTGGCCTCT GCCCCAAGCA CTGCTGCCTC 1920
GGGCCATGAG GCTCACAGGG TCTCCTTAGC CCAAGGCTGG TCCAGCCTCC CACCTGCCCT 1980
GTGGGGCAGA CGTCACTGAA TTCCCACTCC TTGCCCTGGA GGCCTCATTG CCGTCAACTA 2040
GGCTATGGCC CCCACTGTGA CTCCCACTCC CAGGGTGACA GAATGGGCAC CTGGTCCAGG 2100
AAAGCCTGCT CTGTGGACCC CCTACCCGTC CACACTGTCC ACGCCCCATG GCTAGTGGTG 2160
ACAGGAGACA GGATGGGGGG 2180