EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS024-04394 
Organism
Homo sapiens 
Tissue/cell
Cerebellum 
Coordinate
chr13:114895560-114897900 
Target genes
Number: 2             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ETV6MA0645.1chr13:114896549-114896559AGCGGAAGTG+6.02
SPIBMA0081.2chr13:114896547-114896559AAAGCGGAAGTG+6.92
ZfxMA0146.2chr13:114897398-114897412CGCGCCGGGGCCTC+6.05
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_02428chr13:114893350-114898369Astrocytes
SE_06573chr13:114894702-114898081Brain_Hippocampus_Middle
SE_11986chr13:114892548-114897666CD3
SE_14520chr13:114891694-114898663CD4_Memory_Primary_7pool
SE_15438chr13:114893646-114898611CD4_Memory_Primary_8pool
SE_15834chr13:114893425-114898460CD4_Naive_Primary_7pool
SE_16408chr13:114893489-114898461CD4_Naive_Primary_8pool
SE_17059chr13:114892497-114898204CD4p_CD225int_CD127p_Tmem
SE_17352chr13:114883523-114898593CD4p_CD25-_CD45RAp_Naive
SE_17971chr13:114889785-114898652CD4p_CD25-_CD45ROp_Memory
SE_18337chr13:114885848-114898460CD4p_CD25-_Il17-_PMAstim_Th
SE_19216chr13:114891633-114898595CD4p_CD25-_Il17p_PMAstim_Th17
SE_20430chr13:114891575-114897903CD56
SE_21254chr13:114892707-114898117CD8_Memory_7pool
SE_21556chr13:114892919-114898512CD8_Naive_7pool
SE_21920chr13:114891246-114898628CD8_Naive_8pool
SE_22425chr13:114891567-114897746CD8_primiary
SE_24261chr13:114895985-114896524Colon_Crypt_2
SE_24261chr13:114896906-114898561Colon_Crypt_2
SE_29941chr13:114892597-114897857Fetal_Muscle
SE_31056chr13:114893340-114897840Fetal_Thymus
SE_32435chr13:114895173-114898574Gastric
SE_37803chr13:114893162-114898288HSMMtube
SE_38174chr13:114892445-114898535HUVEC
SE_38982chr13:114893337-114898060IMR90
SE_43224chr13:114892484-114898583Lung
SE_44466chr13:114892717-114898071NHDF-Ad
SE_44821chr13:114892380-114898265NHLF
SE_46527chr13:114892491-114898096Osteoblasts
SE_47322chr13:114891521-114898036Panc1
SE_47981chr13:114895854-114896593Pancreas
SE_47981chr13:114896984-114897365Pancreas
SE_48488chr13:114892642-114898596Psoas_Muscle
SE_50252chr13:114893364-114898585Sigmoid_Colon
SE_52117chr13:114893615-114897928Skeletal_Muscle_Myoblast
SE_53247chr13:114893444-114898197Small_Intestine
SE_54100chr13:114892688-114898662Spleen
SE_56179chr13:114891820-114898609u87
SE_62671chr13:114874284-114928516Tonsil
SE_63914chr13:114893642-114897933HSMM
SE_66755chr13:114893665-114895984Jurkat
SE_67713chr13:114891820-114898609u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13114895800114897600
Enhancer Sequence
CCCCGGGGTA TCAGGCCAGC AGCACAGTTA CATGAGACTA ACCCCAAACC AGCGCACCCA 60
CAGGTCACCC TCAGGGTCTC CAGCCCAGAC TGCATCTCTG CTCAAATGCA GGAGGTGCCC 120
TGTCTCCCCA GCTACTTGGG GCACAGATAC CCCTCAGGCA GCCAGCCCTG CAGGTGACCT 180
CTGGAGGGGA GAGGAAACGG GGACTTCTTG CTGGAGCCAC ATCCAGAGAG TCGGGCAGCT 240
GGCATTTGGG CCTCTCTACC CGTCCTCACT GCTGCTGCCC CTGGGAGGGT CAAAGGTTCA 300
GATGATATCC AGGCCCCACG TGGGATTAGC AGCCTAAGCC TCAGCTGAGC CAGGGTTTCA 360
CTGGCTTGTT TAAAGTGGAG CACAGAGCCT GACCAAGTTG TGGCATCTCC AAACCTCCTT 420
CTCTCCGAGG GATCCTCCAG GGTGCCTGAC CCCCACGCCT GTCGGAAGTG GGGCCGAGTG 480
CCCGCAGGCC GGTGAAGCTG CCTTCTGGGA GACTCAGGGT CTGAGTATCT GGTCTGAGAC 540
TCTGGTCTTC CCTCGCCCTC CTGTTCTACT TCCCATGCCT TCTGTAAAGT CCTGCCGTGG 600
CCTGAAGTGT AGCCCTTCCT GGAGTACACA GCGAGCATGC TGTGCCGGCT GTGGGCCCCC 660
CACCCCCGAG CCGCAAAGCC CCAGGCCGCC TCTGCCTGCT GCCTGGAGAC CTGGCACTGC 720
CCCACAGGGG CACCCACCTC CAGCCCTCCT GCCCCCGTGA CTGAGGAAGC CCAGTGCTTC 780
TCACACTCCT CAGACTCGCT GGCTGAGCCA AGCAGCCTTG GCTGAAGGAA AGAGCAGCAA 840
ACTGACCCCC ACGGGCCGCG ACCTTTCCCC ACCCAGGCAA GGCGACCTCA GGCACTTCAG 900
GGAGCGCCAG CTCTGGCTTT CTTGTATGAA AGTGACAGCG GATTTAAACC ACATTAACAA 960
AAGAAATCCC TCCTCTCTGG ACTACTCAAA GCGGAAGTGC TGCCACATCC TAGCTGCAGC 1020
GCTTCTGGGC CAAATATCAA GACAGTGTCT CAGCGATGAT CCGCAAACCA AAATAAAGCC 1080
GACAGGAAAC AGCCCGCTGG TTTAGGGGAG CTGGAATGCC TCCGGCAGCA TCAAATGTCA 1140
TCAACAACTG ACACTCAGCC CGTTCCCGGA GGCCTCTTCA CACGGGAAGA GGCCGGCTGC 1200
GAAGTGCGGC TCAGTGGGGG AGAAGGACCG TGGGGACCGC GACACTGCAG GCCCTGGAAG 1260
CCTCTCCAGC CTGAACCGCG CTGTGGTCCA GCACACTCAT GGCATGAATA TGGAACAGTC 1320
ACTCCAGGAA ACGGTCTTGC TCTGGGGGAG GGGGAGGACT TCCACATCAC TCTCCCAAGA 1380
TAAAACAACC AGGGAAAAGC AGATCCCTCC AGATAAACCA GAAGTCCAGA CACAGCCTCC 1440
TCTCCGGAAA CGCCTCCGGG AGCCCACTTC AGAAGCTGCT GAAGCCCAGA GAAAAACCGC 1500
AGCCTCGCAG GCCCTGGTCG CCACCAGCTC GCCCGCCACT TCTCAGTGGA AAGGGACGTG 1560
GTGCCGATGG GTCCGGGGTC TCCCCGCCCC GCGGGAGCCC TCAGCCAGAA CGCCCCACCA 1620
GCACACACGC ACACATGCAC ACACACAAAC GCGCGCACAC ACACGCGCCC ACACACAAAT 1680
ACACACGCGC GCACACATGC ATCCACACAC AAATACGCAC CCACACATGC ACCCACAAAC 1740
GCACGCGCAC ACACACCGCC CACACATGGA CACACAAACA CAAGCACACA CAAACACGCG 1800
CGCACGCAGG CACAGACGCG CGCGCACAGC AGCAGCAGCG CGCCGGGGCC TCACGCCCCT 1860
GGGGAGAAGC GTGAAGGAGC CTCCACATTC CCCGGAAAGG AAGTTTCTGG GCGCAGCGGA 1920
GAAAGGGAGA TGCCGAGACC CCGACGTCAG TGGATTTGAC ACCTGAAGTG CAGGCGCCCA 1980
GACAGCCTCA GGCGCGCGCA CTCCTGCAAA CACGCGGGGC ACACGCTCGG GCGCACACGC 2040
GGACAGACGT CCCTCGGCGC AGGGACCCCA CCTCCTCCGC CGCTACCAGG GACCGGGGCC 2100
GCTCCGGGCG CAGAGGAGGC GCAGGGAGCC GCGTTACCCC GGAGCCGACT CGACCCAGCC 2160
CGAGGCCCGG GGAGGCGGGG AGGTGGGGAG GGGCCGCGGA GCCGGACCAG CCGTTCTCCG 2220
GGGAGCGCGC CGCGCCTGGA GGGCGTCTCC GCCGGGGTCC CCAGCAAGGA TCTGCGGAGG 2280
GGAGGCGGGC GCGGGAGAGG ACAGGGTCGG GCCGGGGGGT CGGACGCGTG GCTGCCGGCG 2340