EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS002-06558 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr22:50329640-50332560 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr22:50332208-50332223GGGTCACTGTGTCCT+6.14
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
Number of super-enhancer constituents: 33             
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_47471chr22:50331041-50331735Pancreas
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: 4             
ChromosomeStartEnd
chr225033000050330846
chr225033072550331030
chr225033157150331948
chr225033224250332511
Enhancer Sequence
AGGTCCGGGA GGAGCAGGGG TGGAGGGTGT GGGGCCTGGG CTGAGCATGG GAGGGGACCT 60
GCAGCCCGTG CCCAGCCCCA TAGGGACCCG CCCGCGCTCC TCCCCCGCCG CCCCGGCCCC 120
GCGCTCCTCG TCGCTGGGAA CCCCCTGCGG GAGCAATGAC GATGAGCAGG ACGATGGCTG 180
TGAGGGCCCG GCCCGAGCTC TGGGGCGTGG GCCGGAGCGC GGTTGGCCTT GACCTTCTTG 240
GAAAGCCCTT GGCGGCAGGT GACTCCGCTT AGTCACGGCC CCGGGGGCGG GGGCTCCCCG 300
AAGGAAAGGA GCCCCCGCGG GAGCAGGCGC AGAATGAGAT GCACGAGCGC CACCGCCGCC 360
GCCGCACACC CCCCGCCCCC CCGGGGTGGA AGCCAGAACC TGCGTCCCCA GCTCCCCCAG 420
GCCCGCCCAC AGGGCGCCTG GCTGGGCCTC CGAGCTTTCC TGTTTTCTCT GCAGCCTGGC 480
TGGGCTTAGG GAGAGGTGGG GGGTGCGCCT CTTGATGCTG GGGACGCGTG TGGCACAGGG 540
AGCCGGGTGC AGCCAAGGCT TGGAGGGGTG CCCCCCGCCC CACCCAGGTC ACACTTCACC 600
CTTCGTGGGG TCGGGATCTG GTCTTTTTAC AAGCTAGGCG CCCTCCCCCC TTTTTTTTTT 660
TTTTTTTTTC TCAAAAATGA TCACAGGGAA TGAGCCTCAG CCAGGACAGC GGGCTATGAG 720
GCTGCCTGTT GCCCCCACCA GCCTGAATTC TGGCAGGGCC CTTCTCCTCC ACCCACAGCC 780
CTCCATCCAC ACCCCTCCAG TGGCTCCAAG GCCCATCTGA CTTGGCCTCA GTTCACCTGT 840
TTACTTCAGG GACACCTGGT TATACTGCCA GAGGCAGGTT GGGGGGCCTG CAGGGCCGGC 900
CTCTCTCAAA TCCACTTCTG GCTCTGCGGT CCCCACAGCA CTTCCTTACC CCTTCCCCAT 960
GCTGGAATCT GAGAACCAGA TATGGGGGTC CTGGTCTCAG CATCCCTTTC CATCCGGGGT 1020
GCCCTGCTGC TGCCAGCTCA CGTGCCCACC ATCCCATCCT CCTCAGGGTC AGTGTGGCTG 1080
CAGAACGGCC TCCGGGGAGA GCAGGGTGGG GGCTGTAGCC TGGTGCACCC CCAGCCTGCT 1140
GTCCCAGGTG AATGCAGACC CCTGGCTCAG CTGCTGACCA GATAACAGTG GCCCTTGTGC 1200
CGAAGCCTGG GTGGGGGCTG GGGTACCAGC CCCGGGTGTC TCCGGGCACA GAATGGCACC 1260
CACCCCCACC CCACCCGCAG GCAGCGGCCA GCAGGAGACA TTGTCCGTCC CCCTCAACCC 1320
TGGCTATTAA TAGCTCCTCT GGGCTAGGAG CGGCTATAAA TAGTCCCAGC CCCTCACACA 1380
GGCCCATTCA GGCACCCGCT GCCTGGGTGT GCACAGCAGC CACACTTGCG CTCACTCAGA 1440
GCTGTGCACG CGGGAACCGT GCCACTTCTG CCCCTCCACG CCATCTGCAC TGCACAGATC 1500
CAGGCTGTCC CTGCAGCCCT CACTGGGTCT CCTGTGGCAG GGGAGGGCCC TGAACCCTCT 1560
GGAGGCTTTT CCCTTGCCCC CTCCCGCCAC GCCCAGGGTC CCCTTGGGGC TTCTAGCTAC 1620
TCTAGGGTCT TGCTCTGGGG CTTCTGGAAG TCAGATGCAT TCACCCAAAG CCAGCCTGGG 1680
GCGGGGGGAG GTCCACCTGG AGGGAGGCCC AGCCCCTGCA GAGACCTAAG CCTGGCCTCT 1740
GCCCCAAGCA CTGCTGCCTC GGGCCATGAG GCTCACAGGG TCTCCTTAGC CCAAGGCTGG 1800
TCCAGCCTCC CACCTGCCCT GTGGGGCAGA CGTCACTGAA TTCCCACTCC TTGCCCTGGA 1860
GGCCTCATTG CCGTCAACTA GGCTATGGCC CCCACTGTGA CTCCCACTCC CAGGGTGACA 1920
GAATGGGCAC CTGGTCCAGG AAAGCCTGCT CTGTGGACCC CCTACCCGTC CACACTGTCC 1980
ACGCCCCATG GCTAGTGGTG ACAGGAGACA GGATGGGGGG CATGGGGGCT GCTGTTATTG 2040
TGTCCAGAGG AGAAAAGGAA AACAATCCTG TTTACGGAAA AGGAATGTCC GTCCACTGCC 2100
GCCAGCCAGT GGCCTTCCTG GGGGGACAGA GGCCCTTTGT TGGGAAAACA GGAAGCGAGG 2160
ATTTCCAGGA TCTGCCAGGC CGCCCGCCGG CCACCCGCCC CACTTCCGCC AATTCTCGGC 2220
AGCCTGCGCT GGCCACCAGC TGCCCGTCGG TCCATCCACG TTTCTGTCTA TCCGTCTGAC 2280
CGTGGGGCCC AGGCGTACAG CCTTAGCACA TCCTGCTCTA TGTGGTGCCT CAGTCACACA 2340
GGGACAAACA CCCACAGGGT CCTCGCAGGG CCTGGGAGGG CTGCCTGGGA GCTGAGACCC 2400
AAGGAGTGAG GACCCGTGCC CCACATAGGG AAGGGCAGTG CCAGACATGG AGAAGGCGGA 2460
TGGGGCAGGG GCCACGGGCC AGGAACCGGG GAGGCGGGAA CAGCCAAAGG GAAGCTGTGC 2520
CAGACTCTCC CCTCCCCACC CAAGAGCCAG GGATGGTTTT GGGGTTAGGG GTCACTGTGT 2580
CCTTACTACC CAAACCCACT TACAGTCCAT GGCCCACGCG ATGCTCGCCT GTCACTGACC 2640
CGGGACAGCA TGGGCTCACT CGTGCATGAA CACCAGACGT GTGTACACTC AGCGGACACT 2700
CACCTGTGCA CACACAGCAC ACACGTGCAC ACACCACGGA CACTCTGACC TGTGCACACA 2760
CAGCACACAC GTGCACACTC AGCGGACACT CACCTGTGCA CACACAGCAC ACACGTGCAC 2820
ACACCAGCAC CCCCCAGCAC GGATGCAGGC ACCGTCATGA GCACGGAGAC CACCCCAGGA 2880
CACCAGCAGC TGCACCCCCC GGCGGGGCTG CACTGGCCGA 2920