EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS099-06638 
Organism
Homo sapiens 
Tissue/cell
HSMMtube 
Coordinate
chr13:114863600-114865930 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1574170chr13114863842hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr13:114864105-114864123TGAGGGGAGGCAGGAAGG+6.15
KLF5MA0599.1chr13:114865676-114865686GCCCCGCCCC+6.02
PLAG1MA0163.1chr13:114865369-114865383CCCCCGTAGCCCCC-6.49
RREB1MA0073.1chr13:114865129-114865149CCCCCCCACAGCCCCCCACA+6.21
RREB1MA0073.1chr13:114865199-114865219CCCCCCCACAGCCCCCCACA+6.21
RREB1MA0073.1chr13:114865223-114865243CCCCCCCACAGCCCCCCACA+6.21
RREB1MA0073.1chr13:114865247-114865267CCCCCCCACAGCCCCCCACA+6.21
RREB1MA0073.1chr13:114865271-114865291CCCCCCCACAGCCCCCCACA+6.21
RREB1MA0073.1chr13:114865320-114865340CCCCCCCACAGCCCCCCACA+6.21
RREB1MA0073.1chr13:114865344-114865364CCCCCCCACAGCCCCCCACA+6.21
ZNF263MA0528.1chr13:114864102-114864123GGATGAGGGGAGGCAGGAAGG+6.71
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_06573chr13:114861612-114865200Brain_Hippocampus_Middle
SE_06573chr13:114865383-114868882Brain_Hippocampus_Middle
SE_17352chr13:114863586-114864687CD4p_CD25-_CD45RAp_Naive
SE_17352chr13:114865417-114866379CD4p_CD25-_CD45RAp_Naive
SE_22425chr13:114863578-114864479CD8_primiary
SE_29941chr13:114863329-114865176Fetal_Muscle
SE_29941chr13:114865273-114868127Fetal_Muscle
SE_31056chr13:114865437-114867252Fetal_Thymus
SE_32435chr13:114863749-114864461Gastric
SE_32435chr13:114864580-114865084Gastric
SE_32435chr13:114865431-114866341Gastric
SE_37803chr13:114863307-114865150HSMMtube
SE_37803chr13:114865369-114868556HSMMtube
SE_43224chr13:114863283-114864542Lung
SE_44821chr13:114864377-114865077NHLF
SE_46527chr13:114863569-114865107Osteoblasts
SE_47322chr13:114862543-114864750Panc1
SE_47322chr13:114865354-114868998Panc1
SE_48488chr13:114865431-114868042Psoas_Muscle
SE_50252chr13:114863090-114864529Sigmoid_Colon
SE_50252chr13:114865396-114867356Sigmoid_Colon
SE_53247chr13:114863633-114864512Small_Intestine
SE_53247chr13:114865498-114866423Small_Intestine
SE_56179chr13:114863714-114865020u87
SE_67713chr13:114863714-114865020u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13114863668114864189
Number: 1             
IDChromosomeStartEnd
GH13I114096chr13114862428114868829
Enhancer Sequence
TCTGGGGGCT GCAGGGGAGC ACGGCACCTG GCTAAAGACA CAGCACACAG GGCTACAGCG 60
GGCAGCCTGT GGTCAACAGC TCATCAGCGA CGAGCCAGGC CCAGCCAAGA CAGCAGGAAA 120
AAAAATCAAA CGGGAGGCCA TGCCCTCTAC CCTGGGGGCA GAGCTGAGAG GACAGAGAAC 180
AGGCGGACAA GGCAACAGGG ACCCAGGTGC GGGTCAGCAG GCGCTAAGGA TCCCAGGGTC 240
TGCGTGCCCA GCCAGGCCTC ACACCAGCGA CATCCAGGGG TCTGCACCAG AGCCATGGGG 300
GAACAGAGAC ACGAACAGGT GAAAGTTCAG CAGGGCTGCA GGCGCCCAGG CCAGCCCTGA 360
GGCAGAGACG TGAACAGGCG AAAGTGCAGC AGGGCTGCAG CCCTGAGACC TGGTGGGCTG 420
GGGTCAGGAC GTTAAGGGTG TGTGTGTGTG GAATGGGGCT GGCCGGCCCC CTCCCAACAA 480
GATGTAGGAA ACCCCATGGC CGGGATGAGG GGAGGCAGGA AGGGCAAGGG GCATGGAGGC 540
CGGCTGAGAG TCCAGAGGAG AGACCAGCCC AGACCCAGGG AAGAAGGAAC CCCGTGGGAT 600
GTCCCAGACA GCAAGGAGAG AGGCAGTGGA AGGCACAAGG GCGGGAGAAA GACCTCAGAA 660
GGGATTTAAA GAATGAAGAA ATAAAAGCTC TGAAATTTAT TTTAACAGAG CTTTGGGCTA 720
CACTCTAACC TTTGCTTCAG CAGCACAAGA AAAAGAGGCT GCACAGAGTG GCCCCGCAGG 780
CCAGAAGGCA GCAACGCCCA CTGATGCCGG ACCACAGCAG TCGGGGCCCG GCCACCCGAG 840
CCCCCCAGAC CACAGCAGTC GGGGCCCGGC CACCCGAGCC CCCCAGACCA CAGCAGTCGG 900
GGCCCGGCCA CCCGAGCCCC CCAGACCACA GCAGTCGGGG CCCGGCCACC CGAGCCCCCC 960
AGACCACAGC AGTCGGGGCC CGGCCACCCG AGCCCCCCAG ACCACAGCAG TCGGGGCCCG 1020
GCCACCCGAG CCCCCCAGAC CACAGCAGTC GGGGCCCGGC CACCCGAGCC CCCCAGACCA 1080
CCCCTCCTTT TCTCAAGGTC AGAACAGCAG TGAAGGTCAG AGCCAGAAGC ACAGCAGACG 1140
CTCCCAAGCC ACAGGCAGCT GCTGAGGCCT GAGCCGGGGA CGAAGCTCCT CCCTGCATGG 1200
GGACACGCGG GGCTGCAGCC ACTCCCAGGC CTCCATCACA CAGGGACGGT ACAGAAATAG 1260
CGTGTCTTGT GGGTGGGTGC TGGGTCGGGG AGGGAGGGCG ACTGCCTCTC CCTTTCCAGG 1320
CACATTTGGA TTCCCCGGGG TGTCCGGGAA TGACTCAGGC CTCTGGTCAG CGCTTCTCAG 1380
ACCTGTGTTC ACACAGCGCG TCTCCCTCCT TTCCCTCCCT GCCTGGGACC TAAGTACGGC 1440
TCTGTTTAAA ACTGGCCCAA ATGCAGGGTC AGCGCCTGAG ATGCAGCCCC CACAGCAGCC 1500
CCCCCACAGC CCCCCCACAG CCCCCCCAGC CCCCCCACAG CCCCCCACAG CAGCCCCCCC 1560
ACAGCCCCCA CAGCAGCCCC CCCACAGCCC CCACAGCAGC CCCCCCACAG CCCCCCACAG 1620
CAGCCCCCCC ACAGCCCCCC ACAGCAGCCC CCCCACAGCC CCCCACAGCA GCCCCCCCAC 1680
AGCCCCCCAC AGCAGCCCCC CCACAGCCCC CCCACAGCAG CCCCCCCACA GCCCCCCACA 1740
GCAGCCCCCC CACAGCCCCC CACAGCAGCC CCCCGTAGCC CCCACCCCAC AGCCCCCCCA 1800
CAGCCCCCCT GCAGCCCCCC ACAGCCCCCA CATGCTCCAC TCGATGCTCA CACGCACAGT 1860
TTTATCTCCT TAACTCTAAT GCTGTTTAAA AACTATTGTC CTAATCAAGC AAGAAAAACT 1920
GCAGGTTTGC AAAGCGTCTG CTCTGGAAGA GCGGCAGGCC AGGGTGGAGA GACCACACTG 1980
CCACACCTGA ACACAGCAAG GCTTTCCAAA CTCTGCGCAA TAGGAAGACG CCGAATGGTA 2040
AATGGAGGAG CTCGCAGGAG ACGCAGCTCT GACTCTGCCC CGCCCCGGCC CGCGGTGCTG 2100
AGGGCGCGCC GATGTGGATG CCTCTGTGCC AGCACCAGCG GCTGCCCCTC GGCCCCGACC 2160
CTCCCCACTG CGTCCTGGGG CACCCTCAGA GCTTCGGCCA TGGGGTGCAC AGCACCCTCC 2220
AAGCATTCTG AAAGGAGATT TTAGACTCTT GTGCGCAACA CCCAGGAGCC GCCCGCCTGC 2280
AAAGCACTTG GTCAGCGTGG CCTGGAAAGG GGAGGAAGGT CCTGGAGGCA 2330