EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-06194 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr11:65068680-65070540 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs655433chr1165069275hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr11:65069728-65069743GTGCTGAGTCAGCAG-7.55
MAFFMA0495.3chr11:65069728-65069743GTGCTGAGTCAGCAG+7.61
MAFGMA0659.1chr11:65069725-65069746TTCGTGCTGAGTCAGCAGGCC+6.31
MAFGMA0659.1chr11:65069725-65069746TTCGTGCTGAGTCAGCAGGCC-6.39
MAFKMA0496.2chr11:65069726-65069745TCGTGCTGAGTCAGCAGGC-6.04
MAFKMA0496.2chr11:65069726-65069745TCGTGCTGAGTCAGCAGGC+6.36
Myod1MA0499.1chr11:65069555-65069568AGGGACAGCTGCT-7.52
MyogMA0500.1chr11:65069558-65069569GACAGCTGCTG+6.14
RESTMA0138.2chr11:65069095-65069116ATCCGCACCATGGAGAGGACT+6.59
Tcf12MA0521.1chr11:65069558-65069569GACAGCTGCTG+6.02
ZNF263MA0528.1chr11:65069176-65069197GGGGCAGGGGAGGGAAGAGGG+7.06
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_00332chr11:65063191-65070540Adipose_Nuclei
SE_03505chr11:65068922-65069370Brain_Angular_Gyrus
SE_03505chr11:65069377-65070108Brain_Angular_Gyrus
SE_04140chr11:65068501-65070288Brain_Anterior_Caudate
SE_06057chr11:65068011-65070679Brain_Hippocampus_Middle
SE_07047chr11:65068386-65070521Brain_Hippocampus_Middle_150
SE_27474chr11:65069029-65070158Esophagus
SE_28272chr11:65068900-65070402Fetal_Intestine
SE_29490chr11:65068821-65070419Fetal_Intestine_Large
SE_29716chr11:65067995-65070685Fetal_Muscle
SE_34967chr11:65069370-65070426HeLa
SE_36992chr11:65057722-65070777HSMMtube
SE_42714chr11:65068484-65070270Lung
SE_44186chr11:65068329-65070376NHDF-Ad
SE_44803chr11:65069503-65070138NHLF
SE_46915chr11:65069009-65069441Ovary
SE_46915chr11:65069455-65070073Ovary
SE_50465chr11:65068319-65070347Sigmoid_Colon
SE_51908chr11:65068413-65070520Skeletal_Muscle_Myoblast
SE_53043chr11:65068791-65070200Small_Intestine
SE_53693chr11:65068747-65070343Spleen
SE_54859chr11:65068703-65070413Stomach_Smooth_Muscle
SE_63700chr11:65068312-65070534HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116506900365069988
chr116506892465069931
Number: 1             
IDChromosomeStartEnd
GH11I065288chr116505600765070529
Enhancer Sequence
GGAAGGGAGG CAGTGATGGG CCCGGAATGG TGCTTCAGAG CCAGATTGTG AAGTCTTGCT 60
AAGGCATTTG GACCTGATTC TTTCTGCCCC AGAGAATCTT GGAAGGGTTT GCCTCCCACC 120
CCCTGTGCCT CACCCTGACC ACCCAACAAG GACCAACTTA AGAGGAGTCC CAGGTGCAGC 180
CTCAGTACCT GGTAGCATGT AGCAAAGGGG TGGTTTGAGG GGAGAGGGGC TCAGGGGAGG 240
GGCCTGGGTC TGTTGGGGCA GGTCGGGAGG AAGAGGGGCA CCAAGTGGGC CATTGGAATA 300
CTGGAAGCAG CACTCCAGTG AGACATGGGC GTTGGAGGGG TAGATGTGGG AGTCACTGCA 360
GTCAAAAGCC ACAGAACTGG GTGCTGGGAG GGTGGCCGAG AGATGGATGG GCAACATCCG 420
CACCATGGAG AGGACTCTGG CCAGCACTTG CACTTAGCAT CACTGATCAA CAAGGCAAAA 480
GGGTGGGACT GGCCTGGGGG CAGGGGAGGG AAGAGGGATG GCAACAGAGA GGTGCTGGGA 540
TTTCTGGCTA AAGAGACCAG AAGACACCCA TGGTTGTTCA TGGCAAGACT CCCAGCTGCA 600
TTCAGGCATT TGGGACCTTC TGTCACCGTC ATTGGTCATT CTGGGTCTTC AGTCCCCAAG 660
CGACCATGCC TACTGCTGCT TTCGTGGGTC AGCCCTGGAA ATGCCCAGGG GCCTAGGGGC 720
TGGCCTGCCC TCAGACCCAG CTGGACTGCC GCTGGCTCTG AATTCCTCCA TCCTGCCCCG 780
CCTCTTCCCG GGGCTCTAGG CTCCTCCCCA CCCAGAGCCT GCCTGACAGC TGAGGCCCTG 840
CAGCTGCCCA GGCAAAGGGG CCCCTGGGAG GTCTCAGGGA CAGCTGCTGC CCATAACCTT 900
GCTGACCCTG GCCCCTGCAC ACTGCTCCCT GAGATCCCAG GCTTCTGCCC AGCAGCCAGC 960
AGGACCCTAC CAAGCCCCAT CTTCTCTGCT CACTCCCATC GCTCCCAGAT CTTCCCAGGG 1020
GCTGAAGCAT TTTGGGCTGA GCATTTTCGT GCTGAGTCAG CAGGCCCCAC CCAAAGAGTG 1080
AGAAAAGCTG CTGGGTAGAG GCACCCCTAG CCCCGCTCCT GCTTCAGAGG AAGTGCCTTT 1140
CAGGGGTGGA TGAGGGGTAC ACCTGCCTCC GTCAGGCAGG CTTGGCCCTG TTCAACAGGG 1200
TGGGGACCCT GCCCTCCCAC CACCTGCCTC CTACCACAGA ACAGGGCACA AGGGTGGCAC 1260
AAGGGGAAAA AGGAGAAGGC ACCATCACTC CTGATTCCCA GCGAATAGGG GGAAAAGGCA 1320
TACTCACTCC TGATTCCTGG CAGCTTCTTC CCTTGAAGGT CCACTTTCCT CCTGAGGACT 1380
CGAGGCCCCT TCAAATTGCC CCTTAGAATG TTTCTAGTAA TAGTAGTTGC CTCTGGGGAC 1440
GGGTGTCCAA GGGCTAGGGG TCAGGAGTAG GAGGGCTCAG AGAACGATTT GTCATGTCCA 1500
CACTCAACCT GTTTGAATTT TTTTTTTTAT TTTTTTGGAG ACAGAGTCTC ACTCTGTCGC 1560
CCAGTCTAAG TGCTGTGGTG CCATCACAGC TCGCTGCAGC CTCAACCTCC CAGGCTCAAG 1620
TGATCCTCTT GCATCCGCCT CCTGAGTAGC TGGGACCACA GGTGTGCGCC ACCACACCCA 1680
GCTAATTTTT GAGTTTTTGA TAGAGACAGT TTCGCCACGT TGCCCAGGCC AGTTCAAGCA 1740
ATCCTCCTGC CTGAGCCTCC CAAATTGTTG GGACTACAGG CATGAACCAC CACACCCAGC 1800
TGTGTTTGAA ATTTTTTACC ATGTGTCTGG ATTACTTTAA AAGAAGGTGG GGGCCAGGCG 1860