EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS095-08739 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr13:114895650-114897900 
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
TGCATCTCTG CTCAAATGCA GGAGGTGCCC TGTCTCCCCA GCTACTTGGG GCACAGATAC 60
CCCTCAGGCA GCCAGCCCTG CAGGTGACCT CTGGAGGGGA GAGGAAACGG GGACTTCTTG 120
CTGGAGCCAC ATCCAGAGAG TCGGGCAGCT GGCATTTGGG CCTCTCTACC CGTCCTCACT 180
GCTGCTGCCC CTGGGAGGGT CAAAGGTTCA GATGATATCC AGGCCCCACG TGGGATTAGC 240
AGCCTAAGCC TCAGCTGAGC CAGGGTTTCA CTGGCTTGTT TAAAGTGGAG CACAGAGCCT 300
GACCAAGTTG TGGCATCTCC AAACCTCCTT CTCTCCGAGG GATCCTCCAG GGTGCCTGAC 360
CCCCACGCCT GTCGGAAGTG GGGCCGAGTG CCCGCAGGCC GGTGAAGCTG CCTTCTGGGA 420
GACTCAGGGT CTGAGTATCT GGTCTGAGAC TCTGGTCTTC CCTCGCCCTC CTGTTCTACT 480
TCCCATGCCT TCTGTAAAGT CCTGCCGTGG CCTGAAGTGT AGCCCTTCCT GGAGTACACA 540
GCGAGCATGC TGTGCCGGCT GTGGGCCCCC CACCCCCGAG CCGCAAAGCC CCAGGCCGCC 600
TCTGCCTGCT GCCTGGAGAC CTGGCACTGC CCCACAGGGG CACCCACCTC CAGCCCTCCT 660
GCCCCCGTGA CTGAGGAAGC CCAGTGCTTC TCACACTCCT CAGACTCGCT GGCTGAGCCA 720
AGCAGCCTTG GCTGAAGGAA AGAGCAGCAA ACTGACCCCC ACGGGCCGCG ACCTTTCCCC 780
ACCCAGGCAA GGCGACCTCA GGCACTTCAG GGAGCGCCAG CTCTGGCTTT CTTGTATGAA 840
AGTGACAGCG GATTTAAACC ACATTAACAA AAGAAATCCC TCCTCTCTGG ACTACTCAAA 900
GCGGAAGTGC TGCCACATCC TAGCTGCAGC GCTTCTGGGC CAAATATCAA GACAGTGTCT 960
CAGCGATGAT CCGCAAACCA AAATAAAGCC GACAGGAAAC AGCCCGCTGG TTTAGGGGAG 1020
CTGGAATGCC TCCGGCAGCA TCAAATGTCA TCAACAACTG ACACTCAGCC CGTTCCCGGA 1080
GGCCTCTTCA CACGGGAAGA GGCCGGCTGC GAAGTGCGGC TCAGTGGGGG AGAAGGACCG 1140
TGGGGACCGC GACACTGCAG GCCCTGGAAG CCTCTCCAGC CTGAACCGCG CTGTGGTCCA 1200
GCACACTCAT GGCATGAATA TGGAACAGTC ACTCCAGGAA ACGGTCTTGC TCTGGGGGAG 1260
GGGGAGGACT TCCACATCAC TCTCCCAAGA TAAAACAACC AGGGAAAAGC AGATCCCTCC 1320
AGATAAACCA GAAGTCCAGA CACAGCCTCC TCTCCGGAAA CGCCTCCGGG AGCCCACTTC 1380
AGAAGCTGCT GAAGCCCAGA GAAAAACCGC AGCCTCGCAG GCCCTGGTCG CCACCAGCTC 1440
GCCCGCCACT TCTCAGTGGA AAGGGACGTG GTGCCGATGG GTCCGGGGTC TCCCCGCCCC 1500
GCGGGAGCCC TCAGCCAGAA CGCCCCACCA GCACACACGC ACACATGCAC ACACACAAAC 1560
GCGCGCACAC ACACGCGCCC ACACACAAAT ACACACGCGC GCACACATGC ATCCACACAC 1620
AAATACGCAC CCACACATGC ACCCACAAAC GCACGCGCAC ACACACCGCC CACACATGGA 1680
CACACAAACA CAAGCACACA CAAACACGCG CGCACGCAGG CACAGACGCG CGCGCACAGC 1740
AGCAGCAGCG CGCCGGGGCC TCACGCCCCT GGGGAGAAGC GTGAAGGAGC CTCCACATTC 1800
CCCGGAAAGG AAGTTTCTGG GCGCAGCGGA GAAAGGGAGA TGCCGAGACC CCGACGTCAG 1860
TGGATTTGAC ACCTGAAGTG CAGGCGCCCA GACAGCCTCA GGCGCGCGCA CTCCTGCAAA 1920
CACGCGGGGC ACACGCTCGG GCGCACACGC GGACAGACGT CCCTCGGCGC AGGGACCCCA 1980
CCTCCTCCGC CGCTACCAGG GACCGGGGCC GCTCCGGGCG CAGAGGAGGC GCAGGGAGCC 2040
GCGTTACCCC GGAGCCGACT CGACCCAGCC CGAGGCCCGG GGAGGCGGGG AGGTGGGGAG 2100
GGGCCGCGGA GCCGGACCAG CCGTTCTCCG GGGAGCGCGC CGCGCCTGGA GGGCGTCTCC 2160
GCCGGGGTCC CCAGCAAGGA TCTGCGGAGG GGAGGCGGGC GCGGGAGAGG ACAGGGTCGG 2220
GCCGGGGGGT CGGACGCGTG GCTGCCGGCG 2250