EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS134-01135 
Organism
Homo sapiens 
Tissue/cell
Mesendoderm 
Coordinate
chr1:44014070-44016890 
Target genes
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs2842188chr144014280hg19
rs2819336chr144015809hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr1:44016018-44016028GCCCCGCCCC+6.02
KLF5MA0599.1chr1:44015762-44015772GGGGCGGGGC-6.02
SP1MA0079.4chr1:44015760-44015775GAGGGGCGGGGCCTG-6.22
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00616chr1:44009256-44025211Adipose_Nuclei
SE_03403chr1:44013988-44014536Brain_Angular_Gyrus
SE_04240chr1:44003988-44015177Brain_Anterior_Caudate
SE_05040chr1:44001099-44015486Brain_Cingulate_Gyrus
SE_05040chr1:44015834-44021066Brain_Cingulate_Gyrus
SE_05962chr1:44000439-44020958Brain_Hippocampus_Middle
SE_07193chr1:44003475-44015024Brain_Hippocampus_Middle_150
SE_07193chr1:44016119-44020709Brain_Hippocampus_Middle_150
SE_08033chr1:44003431-44015175Brain_Inferior_Temporal_Lobe
SE_08033chr1:44015878-44020741Brain_Inferior_Temporal_Lobe
SE_23218chr1:44005985-44017477Colon_Crypt_1
SE_23829chr1:44013362-44015343Colon_Crypt_2
SE_23829chr1:44015459-44017409Colon_Crypt_2
SE_24870chr1:44012836-44017627Colon_Crypt_3
SE_26649chr1:44010798-44020559Esophagus
SE_27645chr1:43995619-44017587Fetal_Intestine
SE_28595chr1:44005404-44017604Fetal_Intestine_Large
SE_31538chr1:44004919-44019003Gastric
SE_41575chr1:44001646-44015303LNCaP
SE_41575chr1:44015364-44020400LNCaP
SE_47657chr1:44013015-44015395Pancreas
SE_47657chr1:44015425-44018793Pancreas
SE_50363chr1:44005822-44020588Sigmoid_Colon
SE_52524chr1:44004832-44019377Small_Intestine
SE_56987chr1:44014752-44017377VACO_400
SE_65452chr1:44004903-44018198Pancreatic_islets
SE_69138chr1:44014239-44017340H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr14401573144016125
chr14401666044016751
chr14401453644014607
Number: 1             
IDChromosomeStartEnd
GH01I043539chr14400545944020850
Enhancer Sequence
CCCTCCTCCC CAGAGCCTGT GGAGCACACA GGGTCTGTTG TCTGTCGTCA TGCTCTCCCC 60
CTCGTTCTAT GGGTGGCCTG TCTAGACTCT GCTCCCTGTG GGACTTCCCG CAGATTCCGT 120
TGCTTTCTCT CTCTGGGCCT GTTTTCCTAT TGCACAATGG GGATAATCAC TCCTACCTGG 180
AAAGGTTAAC TGAGGTCACA TGGATGAGGT GCCTGGAACC TAGTATGTAT TCCCCTTATC 240
TGAGGCCATG ACCTGGGGCT CTTGCTCTGT CCCTGGGAAC CAGGCTTGTC TCTGAGTGGG 300
CTCCAGGGGG GTACCAGGAA CAGTCACAGG AGCTCACTGA GTCCCAGCTT AAGCTGCTCA 360
GACCCAGGGA TATCTGTCTC TCCAGAAGCT CCCTGCCCTG CCTTCGCCGG CCCTCATGGC 420
CCTGCCTCCG TGTGTACATG TGTATGTGTA TTCCATGGGA AAGGCACAAA ATAGCAGTCA 480
GTCTCTCCAT AGAAGAGCCT TGATGGTGGC CCAGTTTGAC TCTCCCTGGG GCTGGACCCC 540
TACAGCCTCC CTGGGAGGTG GTTGCAGCCC CCTTCCTCCA GCCAGTTCCA CTTACTCCTT 600
TCTTAGGCCA CTTCCTCCCA CCCTGCATGG GCTTGGTGGC TCGAGAATGT TGCCGTCCAT 660
ACCCCGGGAG CTGTGCTGAA AGGGCTGTGC GGCCCCCGAC CACTGTGTGT GTCAGGGAGG 720
GGGCACGCTC TCGTGGGGTG TCAGGCCAGG TGGCAGTGGG TAACTGGCAG AAAGGCCCTC 780
CTGGTGTGCT CTGGTGGCAC CCTGTTGACC CAGTCTCAGA AGTTGTGTTC CGACCCTCAC 840
TGAACACCAG CTGTGGGTCA GGCACGGGGC AGAGTAGTTC AAGTAGCTTG GTTTGCTGCC 900
TGCCTGGGGA CCTGACACTG TGGGATCTGG TCAGTGCTGG GATGGGAAGC TCTGGGCACC 960
TCAGGCCATG GGACACAGAG CAGGCTCCTA CAGCAGCTTG GCTGGGTGGG ACATGAGAGA 1020
GGGGCTGGGC TGGGCACACT CAAAGGCAGG GAGGAGTCTG AGGGCCTGGC CTGTCAGGGT 1080
GGCCTAGGTG GTGGGTCCAA GCTGTGTGCT CTGCACAGTG CTAGGCCTGT ACTATAGTAG 1140
GTGCTCAAAA AATACTTGTT GAAAGAGTAA AGAAGCCGGG TGTGGTGGCT CATACCCGTA 1200
ATCCCAACAC TTTGGGAGGC CAAGGCAGGT GGATCGCCAG AGCTCAGGAG TTTGAGACCA 1260
GCCTGGCAAT GTGGTGAAAC CCTGTCTTTA CCAAAAATAC AAAAAATTAG CCAGGCATGG 1320
TGGTGTGCAC CTGTGGTCCC AGCTACTCGG GAGGCTGAGG TGGGAGGATT GCTTGAGCCT 1380
AGGAGGTGGA GGCGGAGGTT ACAGTGAGCT GAGATTGTGC CACTTGTACT CCAACCTGGG 1440
TGACAAAGTG AGACCCCCCT CTCAAAAAAA AAAAAGACTA AAGAAAAGTG AGCCTGAGAG 1500
CTTAGGAGGA GCACATTTCA GAGGGGAACG GAGAGAGGAA CATCAGGCCC GTTGGTAGCT 1560
GAGGAGAGGT GCGGTTAGAT CTGTGCTCCC CAAAGATCCT CTGCTGAACA TAAGGGGCAA 1620
CGCCTTGTCT CCTGTGCTGT GTCCTGCGGG TGGAGGTGGA TTGGAGGGAA GCGGAGGGCG 1680
AGGCCTGGTT GAGGGGCGGG GCCTGCCTGT CTGGTCCCCC GGGCTGCCTT GGGCCAGCTT 1740
GGCCTAGTCT GTTGGGTGGG CGGGCAGGGT GCAGGCTCCT CTCCAGCCTC CAAGGGAGGG 1800
GAGTTGTTCT GCCTCCTCGA TAGCCCCAGG CCTTGGGCAC AGCCCAGCCT CCCACGGCTC 1860
TTGGGCCCTC CTCCTTCCAG GCCGCCGGTG ACCCACACCT GGCTCTCCTC CCCGGCGTCT 1920
CCTCTCCGCT TCTTTGTTTG GAGCGGAGGC CCCGCCCCAC CCCGCCCCCA GGCGCACTCG 1980
CCCGGCCATT CCGGTTCAGC CGGTTCCAGC CCCCAGTTTC TGCCGCTGCA GGTCCCGGCA 2040
GGAGCTGGAG GGGCACTTTC TCCCTGGGTT TCTCTTCCCT GGTGCAGCAG GGGCCGCGGT 2100
CCTCATCCTC CTGGTTCCTC AGTTCGGTCC TTCTTTCATT CTCCACCCCT GGGTGCCAGG 2160
AACTGGGTCA GACACTGGGA CAGGAATCCA GACAGGCATG CTATCTGCCC TGCCCAGGGT 2220
TATGTTCTAG GAGGGGAAGC AGCCATTAAT CAAACACCAA AAATGTGGAA AAGTAATAAT 2280
CTCACACGTG TGCATAATAA ACTGTGAGTG AAAGTTATAA GCTCGGCAGG TAGGTAATAA 2340
GCTAGGAGCA GTGCTGTGGG AGGCAAGGGA GTTACCCGGG AGTTTCAAAC TAGGAACTGA 2400
GCTCATAGGT TGGGGGCAGG GGGACTGGAG AAGGCAGTGA TACTTAAATG GAGAGCAGAA 2460
GGATGAATGG AAGTTAGAGT GTATGGCGGA GGTTGGCAGA AGCAGCAGCT TATGCAAAGG 2520
CCCTGTGGCT GCAGGGAACA TGACGTTGCT CTTTAGAGGA GCCAAAGCTG GGGCTCTGGG 2580
GAGAGCAGCT GGGTCAGACC CCGCGGCTTT GTCTGCCATA ACAGGTGTTT GGAGAGTGAT 2640
TCGGCAGGTC TTTGGAGGGT TTTGATAGGG CGGGGTGTCG GGGGAGGCTG TCAGCTCACT 2700
CTGGACACTG AGTAGAGAAC AGACGGGAGG CGTGGGGCAG GCCTGGAGGC AGGGGCTTCC 2760
GCGTGTTAGG CCAGTGGAGT GCCAGTCAAG GGAAGGTGGT ATCTGGACTA GGGTGTGGCA 2820