EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-11282 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr14:100029100-100032020 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr14:100029513-100029524AAGCAATAAAA+6.32
HSF1MA0486.2chr14:100029457-100029470GAAGATTCTGGAA-6.16
KLF14MA0740.1chr14:100029757-100029771AGCCACGCCCCCCT+6.95
KLF16MA0741.1chr14:100029758-100029769GCCACGCCCCC+6.62
SP1MA0079.4chr14:100029755-100029770CAAGCCACGCCCCCC+7.85
SP2MA0516.2chr14:100029754-100029771CCAAGCCACGCCCCCCT+6.23
SP3MA0746.2chr14:100029757-100029770AGCCACGCCCCCC+6.74
SP4MA0685.1chr14:100029755-100029772CAAGCCACGCCCCCCTC+7.98
SP8MA0747.1chr14:100029758-100029770GCCACGCCCCCC+6.44
ZNF263MA0528.1chr14:100031729-100031750AGGGAAGGAGGAGGAGGAAAG+6.48
Znf423MA0116.1chr14:100030927-100030942GCCCCCCAGGGGGGC-6.32
Znf423MA0116.1chr14:100030927-100030942GCCCCCCAGGGGGGC+7.52
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_00922chr14:100028972-100033417Adrenal_Gland
SE_06477chr14:100025942-100030276Brain_Hippocampus_Middle
SE_24879chr14:100029502-100030232Colon_Crypt_3
SE_26586chr14:100025792-100033964Esophagus
SE_27780chr14:100028359-100034032Fetal_Intestine
SE_28740chr14:100028345-100039820Fetal_Intestine_Large
SE_31455chr14:100026673-100033598Gastric
SE_40985chr14:100029359-100033851Left_Ventricle
SE_41558chr14:100026296-100033958LNCaP
SE_42529chr14:100026803-100033842Lung
SE_47508chr14:100029389-100030308Pancreas
SE_47508chr14:100030502-100032086Pancreas
SE_49276chr14:100029421-100031983Right_Atrium
SE_50321chr14:100030308-100032001Sigmoid_Colon
SE_52517chr14:100028367-100031583Small_Intestine
SE_54552chr14:100023051-100046861Stomach_Smooth_Muscle
SE_61471chr14:100013991-100069569Toledo
SE_65289chr14:100029330-100043813Pancreatic_islets
SE_68735chr14:100026872-100030616H9
SE_68735chr14:100030817-100031791H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr14100030417100030542
chr14100030597100031707
Number: 1             
IDChromosomeStartEnd
GH14I099560chr14100026360100044326
Enhancer Sequence
TGTACAAATG TATGCACATG CCCACATGTA CACACAAAGG CACGCTCCCA GAAACATCCA 60
CACACAAGTG CATATTCACA CACTCACCCT CATATGCACA CACACACCCA TATGCACACA 120
CACACACAGG TATGTGCACA CTCACACACT CACTCTGTCT CTCCAGGGTC TTGACACTGC 180
GGAAAGAGTA TTGAGCTGGG GAACAGTCCA GGGGTCATTT ATTTTAATTA TTAAAACAGC 240
AGCCACTTAC TCTCGAGCCG TCTATAATGC CACTTAATTA CCTAGTACAT AAAACGGCCT 300
TTGCATCTTA GCAGAGTAAT AAATCAGCTC AGAACCAGAG TTTAAAGCAT CCAAGCTGAA 360
GATTCTGGAA GGGTAGAGGG GGATCCTTTG CCCCCTCCAC TCCCCAACCC AAGAAGCAAT 420
AAAACAGATG CCTCAGCCAT GGCAGGGACT GGGTGCACTG GGAGGCCAGG CATCCTCCCT 480
CCTGCTTCTC CGTCCACTCC TCGGGCCTGG GCCCCTGCCC TGCCGCGTTC CATCCTTTGT 540
ATGGTCAACA ATAGCCCCGC CAGATGGCGC GGTGCAGGGA GCAGCCTCTG CAAGGCAATC 600
GCTCATGCTG TCAGGACCCA GCAGGGCTGT GGGCAGGAGA CCTGGGAAAC TGGCCCAAGC 660
CACGCCCCCC TCACCCTGCC CTGGCCACCT TCTGCTCCTG AGCCCACAGG CACAGGCAGC 720
TTCGAGCACA ACTGGGCCAT CTGGGAATAA CTCGGGCAGG TACATCCCCC AAAGGGGGAG 780
CCGGCAGAAG CACCAGATAA TAAGGTGGTC ACTCTGCATC TGCAAGATAT AGGGAGGAAA 840
TGGGAGGGTG AGAGAGCAGG CAGGGAGATG TCAGGCACCA TGCTTCCCAC GAGGCGGGCA 900
GAAGGCAGCG GCATGGCGCT CACCAGCCGG CAGACATAAA TCACCCACTC CCGTGGGCCG 960
TGCTGGCCTC CATGTGCCAG CATCCCTTGT GCCTCTCTGT GGGCAAGGGG ACATGCAAAA 1020
TGGCATAGGC AGGAAGGAAT AAATTCACTG TGCCATTCCT GGGCACGAGC CAGATGGGCT 1080
AGCAGAGTCT GCCCTCTGAG CACGGCCTCC AGGGTATGTG GGGCAGGGGG TGGGCACAGG 1140
TCCTTGGCAA TGGAACCCTG GGCTGTTCCC AAACTTGGCC ATTTCAAGCA TCGCTTCAAG 1200
TAAGCAGCCT GGGCACGGAC CATCTGCAAG TGTATAAGCA GCCCGTTTTC CTGCAGGAAA 1260
AATTTCCAGC CTACATGTAC ACAGGTGGTG GGATTGCTGG TTGAAGGGGA CTTGCCTTTG 1320
CAATTGTCTA GAAATGACCA GATTACGCTC CATAGAGGCT GGACCTCACT CCCATTAGCC 1380
ATGGAAGAGA GCACTGTCTC TCCACAGAAG TTTCTTGTTT TGTTGTTTGT TCTGCGCAGT 1440
GAAGGGGACA GACAGGTGGA GACCTCTTCG CACCCACTGC TGCGTCCTTG CTGCTCTCTG 1500
GTCCTGATAA CCAAGAAGCA CCAGGGTCTT GCACTCTCCT CCTTGCACCC TCCCCAGACC 1560
CACAAGATGG AAGAGGGTGG AGAAGCCAGC AGCAGCAGGG CCCAGCTGAC CCCAGGACAT 1620
GCCCCATATG CCTGTGCCCA CCTTGCAGCA TGTTAGGGTT TTGGTCAGCA GGAGCACGTC 1680
CGCACTTTTC TGAAGCCTCC TCCTCCATGG AGCCTTCCTG ATTTCCCTAT TGAGTTGCAC 1740
GACACCGTTT ATCTGTCCTG GGCGCCAGCA CCTCTAGTTC TTTTTTATTC TATCTCATCT 1800
TGTAATGTCT CTACCACCTG ACTCTGAGCC CCCCAGGGGG GCAGGCCCCA GCTGGCTGGT 1860
GTGTGCATCC CCGAGGGCCT GTCATGCAGT CCCAGTGGCA GGAAGTATCT GGCTGGGGCA 1920
ATCAGGAGGC TGAGACAGTA CTGGCTGCTG GTTCGTCCAG GCCCATCTCA CAACAGCAGG 1980
AACAACATCC AGCCTTTTAA GGCCCCTTGG CAACCGTCCA AATTAAATTT TCCTTACAGA 2040
AGGCTAGGAA CCCAGCCAAC CTGAGCCTTC TGGACAGACT GAGTTCAGCT TAGAGGGACA 2100
CTGGACACGG GTGGGGAGGG CGTGGGGACA AGTGCAGAGA AAACACTCAC TGGAGAACGT 2160
GCACTCGTCC ATGGAAGCTC CAGAAGGTGC GGGATCTGCG TGGCGGCAGC TGCCACAGGG 2220
GGCAACCAAC CGCCTTCCAA GGAGAGGGGA CGCAGACCCT CTCCCGGCAG CCCGCGGCCT 2280
CTGATCATGC AGCCAGGCGG CTGCACTTGG CTTTTAGTCA TGGGCCGGTG AGCTCACTGT 2340
CCCCCAACTG GTTTTCCACC AAGAGCTGCT GAAACTAAAG CATGGCCACT TGGGGATGAT 2400
GGGACTTGGC CCTGTTCTTG GGCTCGCTGG AGCCCATCCC CCTGCATTAA TTCCAGCTGC 2460
CCCTCTCACC TTCCACAGCT CGTCGTGTGC ACAATCCCCT CCTCCTCCAC CACCCCTGCG 2520
GGGCTCAGCT CTGAGCAGGC TCTCTCACGC CATGGAGGTC TGACCCCCAG TGCAGAGGGA 2580
TGCCTGGGTT GGCACCCCCT GGCATGCAAT GCCTGGCACA ATGTGGAGAA GGGAAGGAGG 2640
AGGAGGAAAG CCTTCAATCC CTCCCATAAA AGGGAGACAA CCTAGAACCC TCTACAAGAG 2700
ATCATCTAAA ACCTTAGTAG CACTGGCCTG GACAAATTCA AGTTCTAGAA TAACTGGAAG 2760
CCTAAAAATT AGGTTGGTCA CATGCTCCAG GTGCATGAAC CCAGGGGCAG AGTGTGTCTC 2820
TGTGATTCAT GCAGCCAGGA GGGAGGCTGG GAGCGGGGGC AGGCTGCATG GGCAGCCGGG 2880
AAGAGCTGCC TCCTCTCTCC CTGGTGCAGG TGGATACAGA 2920