EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-10280 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr13:114895540-114897910 
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
AGATGGGCTT TCTGCTGGAG CCCCGGGGTA TCAGGCCAGC AGCACAGTTA CATGAGACTA 60
ACCCCAAACC AGCGCACCCA CAGGTCACCC TCAGGGTCTC CAGCCCAGAC TGCATCTCTG 120
CTCAAATGCA GGAGGTGCCC TGTCTCCCCA GCTACTTGGG GCACAGATAC CCCTCAGGCA 180
GCCAGCCCTG CAGGTGACCT CTGGAGGGGA GAGGAAACGG GGACTTCTTG CTGGAGCCAC 240
ATCCAGAGAG TCGGGCAGCT GGCATTTGGG CCTCTCTACC CGTCCTCACT GCTGCTGCCC 300
CTGGGAGGGT CAAAGGTTCA GATGATATCC AGGCCCCACG TGGGATTAGC AGCCTAAGCC 360
TCAGCTGAGC CAGGGTTTCA CTGGCTTGTT TAAAGTGGAG CACAGAGCCT GACCAAGTTG 420
TGGCATCTCC AAACCTCCTT CTCTCCGAGG GATCCTCCAG GGTGCCTGAC CCCCACGCCT 480
GTCGGAAGTG GGGCCGAGTG CCCGCAGGCC GGTGAAGCTG CCTTCTGGGA GACTCAGGGT 540
CTGAGTATCT GGTCTGAGAC TCTGGTCTTC CCTCGCCCTC CTGTTCTACT TCCCATGCCT 600
TCTGTAAAGT CCTGCCGTGG CCTGAAGTGT AGCCCTTCCT GGAGTACACA GCGAGCATGC 660
TGTGCCGGCT GTGGGCCCCC CACCCCCGAG CCGCAAAGCC CCAGGCCGCC TCTGCCTGCT 720
GCCTGGAGAC CTGGCACTGC CCCACAGGGG CACCCACCTC CAGCCCTCCT GCCCCCGTGA 780
CTGAGGAAGC CCAGTGCTTC TCACACTCCT CAGACTCGCT GGCTGAGCCA AGCAGCCTTG 840
GCTGAAGGAA AGAGCAGCAA ACTGACCCCC ACGGGCCGCG ACCTTTCCCC ACCCAGGCAA 900
GGCGACCTCA GGCACTTCAG GGAGCGCCAG CTCTGGCTTT CTTGTATGAA AGTGACAGCG 960
GATTTAAACC ACATTAACAA AAGAAATCCC TCCTCTCTGG ACTACTCAAA GCGGAAGTGC 1020
TGCCACATCC TAGCTGCAGC GCTTCTGGGC CAAATATCAA GACAGTGTCT CAGCGATGAT 1080
CCGCAAACCA AAATAAAGCC GACAGGAAAC AGCCCGCTGG TTTAGGGGAG CTGGAATGCC 1140
TCCGGCAGCA TCAAATGTCA TCAACAACTG ACACTCAGCC CGTTCCCGGA GGCCTCTTCA 1200
CACGGGAAGA GGCCGGCTGC GAAGTGCGGC TCAGTGGGGG AGAAGGACCG TGGGGACCGC 1260
GACACTGCAG GCCCTGGAAG CCTCTCCAGC CTGAACCGCG CTGTGGTCCA GCACACTCAT 1320
GGCATGAATA TGGAACAGTC ACTCCAGGAA ACGGTCTTGC TCTGGGGGAG GGGGAGGACT 1380
TCCACATCAC TCTCCCAAGA TAAAACAACC AGGGAAAAGC AGATCCCTCC AGATAAACCA 1440
GAAGTCCAGA CACAGCCTCC TCTCCGGAAA CGCCTCCGGG AGCCCACTTC AGAAGCTGCT 1500
GAAGCCCAGA GAAAAACCGC AGCCTCGCAG GCCCTGGTCG CCACCAGCTC GCCCGCCACT 1560
TCTCAGTGGA AAGGGACGTG GTGCCGATGG GTCCGGGGTC TCCCCGCCCC GCGGGAGCCC 1620
TCAGCCAGAA CGCCCCACCA GCACACACGC ACACATGCAC ACACACAAAC GCGCGCACAC 1680
ACACGCGCCC ACACACAAAT ACACACGCGC GCACACATGC ATCCACACAC AAATACGCAC 1740
CCACACATGC ACCCACAAAC GCACGCGCAC ACACACCGCC CACACATGGA CACACAAACA 1800
CAAGCACACA CAAACACGCG CGCACGCAGG CACAGACGCG CGCGCACAGC AGCAGCAGCG 1860
CGCCGGGGCC TCACGCCCCT GGGGAGAAGC GTGAAGGAGC CTCCACATTC CCCGGAAAGG 1920
AAGTTTCTGG GCGCAGCGGA GAAAGGGAGA TGCCGAGACC CCGACGTCAG TGGATTTGAC 1980
ACCTGAAGTG CAGGCGCCCA GACAGCCTCA GGCGCGCGCA CTCCTGCAAA CACGCGGGGC 2040
ACACGCTCGG GCGCACACGC GGACAGACGT CCCTCGGCGC AGGGACCCCA CCTCCTCCGC 2100
CGCTACCAGG GACCGGGGCC GCTCCGGGCG CAGAGGAGGC GCAGGGAGCC GCGTTACCCC 2160
GGAGCCGACT CGACCCAGCC CGAGGCCCGG GGAGGCGGGG AGGTGGGGAG GGGCCGCGGA 2220
GCCGGACCAG CCGTTCTCCG GGGAGCGCGC CGCGCCTGGA GGGCGTCTCC GCCGGGGTCC 2280
CCAGCAAGGA TCTGCGGAGG GGAGGCGGGC GCGGGAGAGG ACAGGGTCGG GCCGGGGGGT 2340
CGGACGCGTG GCTGCCGGCG GACACTCACC 2370