EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS143-01036 
Organism
Homo sapiens 
Tissue/cell
NGP 
Coordinate
chr14:100039060-100041950 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CENPBMA0637.1chr14:100039543-100039558CCCGCCTAGAGCGAA+6.27
KLF4MA0039.3chr14:100040254-100040265CCACACCCTCC+6.32
SCRT1MA0743.1chr14:100039174-100039189GTGCAACAGGTGCTC+6.69
SCRT2MA0744.1chr14:100039174-100039187GTGCAACAGGTGC+6.98
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00922chr14:100035637-100043899Adrenal_Gland
SE_06477chr14:100038631-100041912Brain_Hippocampus_Middle
SE_23140chr14:100036955-100039552Colon_Crypt_1
SE_23140chr14:100040149-100047008Colon_Crypt_1
SE_23807chr14:100039076-100039579Colon_Crypt_2
SE_23807chr14:100040162-100043519Colon_Crypt_2
SE_24879chr14:100039033-100039685Colon_Crypt_3
SE_24879chr14:100039766-100043514Colon_Crypt_3
SE_26586chr14:100036268-100048060Esophagus
SE_27780chr14:100036471-100039970Fetal_Intestine
SE_27780chr14:100039991-100043446Fetal_Intestine
SE_28740chr14:100028345-100039820Fetal_Intestine_Large
SE_28740chr14:100039953-100043495Fetal_Intestine_Large
SE_31455chr14:100036155-100044158Gastric
SE_40985chr14:100034161-100047061Left_Ventricle
SE_41558chr14:100034157-100047015LNCaP
SE_42529chr14:100036484-100047048Lung
SE_47508chr14:100038066-100043477Pancreas
SE_49276chr14:100037919-100046958Right_Atrium
SE_50321chr14:100037583-100043539Sigmoid_Colon
SE_52517chr14:100037952-100043555Small_Intestine
SE_54552chr14:100023051-100046861Stomach_Smooth_Muscle
SE_57311chr14:100039853-100043812VACO_400
SE_61471chr14:100013991-100069569Toledo
SE_65289chr14:100029330-100043813Pancreatic_islets
SE_68735chr14:100039105-100043753H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14100040610100041006
Number: 1             
IDChromosomeStartEnd
GH14I099560chr14100026360100044326
Enhancer Sequence
ATATGAAACT GTCCCATCCA TGGATTTGTT TGCCAGTTTA TCCATCTTCC AAAGGAGACT 60
TCTGTCTGTC TTGCTTCATG GAAGTATCCC AGGAGCATGG AAACGGGGCC TGGTGTGCAA 120
CAGGTGCTCA GTAAACGGCT AAGGAAGGAA TGTCTGCCCA AGTCCCAGGC AGGGTGGGAG 180
GCACGGACCT GAGGCAGCGC CTTCTCTTAG CTCTGAGCCC TGCCTTCGCC TCCTACAAGA 240
TAGGATGGCA GCAGCCTCAG AGCAGAAGGC ACCCTGGTGA CCGCAGGAGA CGCCACACAT 300
AAAGGCAGAG AACAGAGCCT GGTGCTAAAA ATGAGAGGGG ACAAGTGAAG CCTAAGCTGT 360
TTCCGGGGCG CTCAGACCAG GCAGGGACTC AGGCGTGCAG CTGCCTGGGC ACCGCTTCAT 420
TTCCCCCGGT GCCTCGGAGT CCCCGCGGGA CCTGCTGCTC AGCGGTCCAG CGTCACTCAG 480
CCTCCCGCCT AGAGCGAACA GGACCTCCAG GTGCTCCCTG CAGGGGATTG AGCCATGGGT 540
GGCCAGGACT CTAGCAGGAA CCCTCAGGGA GCCGGCTCTG CCTGGTGCAT GGGTCGAGGT 600
GCTCATCAGT TTCAGAAGCT GCTCCCAGGC CCCCATTTTC CCAATCCCCT TAGAAGAGTT 660
TTGTTCTGAG CTCCACTGAA GGTCATTTAG TCTTAAATGG AAGCAGGGAA CCCTCAGCTG 720
TCACCCACGT GAAGGAAAAC CAGCTGAGGC CATGCCTTTG AGGTCCGGCG CTCCTCCCCC 780
ACCCTGGGCC TCAGTCTCCC CATGGAGGTG CTGGCTATCC AGAGCCCTGC TGATGGCAGG 840
CAGTCACCAG TGAGGCAGAC CCGGCCTGGA CGTTCTGGCT CAAAGGACAG GGTGCAGCCA 900
GATGCCAACA CTTCCCTCCA GGGCAGGGGC CTGCAGCTGC AGAGCTTGGC TCTAAATAAC 960
GCCAACCTCC TTGCTCTGCA CAGCCCTGGG GTGGCCCTGC AGTCCCCATG ACACAGGGCA 1020
GAGGTGCTGC CTTTGGGTGG GACGGCAGCC CTCCAGGAGA TGCACCCCTC ACAACCCACC 1080
CAATCCCTCT GCCCCTGCCC TGCAGAAGCC TGGTTAGAGC CCATAGCCTC ACTCTTCTGG 1140
GCCGCCGAGC ACTCCAGGGC CTCTATGCAA GTGAGGGGCA TGCGCTGGGG CCTCCCACAC 1200
CCTCCCTAGG TGCAATTCTC CTTGTCTCAT CAACTCGTCT CATCCTGGGA TGCGAAGGGT 1260
GGTCAGGGAC AGCCGTGTTC ATGAGCTGCC ATTTGGAACT GGCATTTGGA TCTTGATGGA 1320
ATGTCCTAAT TGACAGGAGG GCTCAGTGCA CATGCCAGGG ACGCGCAGGA GTTAAATTCT 1380
GAGACAGGAG TGCTGCTCTG TCCTGCTTCT GCTGTGCCTG CCCAGCCTCC AGAACAAGAC 1440
CATGTGCTGC AAGCTGCCAC CCAGCTGTGC TCTCTGACCC GCCACCTGCC CTCAGCACCA 1500
GCAACACTAG CAAGACCTCA GCCTCCCACC AGGGAAGCTC AACAAAGAAG TGAACATTGC 1560
TCCAGGGATT TTTTTTTGTC TGGCAGAAGC AGTTAGATCT GATCTCAGCT GGAATCCTTC 1620
CTGGATTGGA AGACACTGAG CCACTCTCCG TGCTATATCC CGGCCACAGC TCACTCTCCC 1680
CCAAACAGGT CCTGTCACAC CCCATACGCT CCCCTCACCC TCCCACATGC TCCCCTCACC 1740
CCATCCCCAC TCACTCCTCA CAGGCCGAGG CACAGGGAAC CCTGCCAAGT TCAATCCAGA 1800
CCTTGGGCAG GGAGGCAATA AAGCTAAGGG AGGTGGGGAA CTCCCGGCCT GTGAGGAGGG 1860
GAGGCAGGGT GGCCTGCGAG GAATTTAGGG AATGCAGGGA GATAAGGGGA GAGCGGAGAG 1920
GAGAGGCAGT GGTGCTGACA GCATTAGCCT GCTGGGAAGG AGCTTCATGA GCACCATCTG 1980
ATTTACTTGG TCCTTGTGTC CGCCCGAGGG GCACCAGCCG GGTCAGGTGG CCTGACCACT 2040
CACAGCTATG ACCCAGGCAC ATTACTGAAC CTGCTTCCAC ATCTGCAAAA GAGACTGGTG 2100
GATGGCCTGC AGGGGATTCT AGGAGGTTAA GGAGGTCAGG GGCCAGATCC CCACCCAGGG 2160
ACAGGCTGTA GAAGCCATTC TGTGGGACGC TGGCCATCCC ATGGGTCACC CCCAGGGTTG 2220
CACCCACAGA CCCTGAGAAG CCAGTGACTG GTCAAGGTCA CAGGGCAAAT GCCTTCAAGG 2280
AGGGGCAGAA AGACTTCCTG GAGGGTCGAG ACTGCAGCCA GAGGGTGGCC TTTTGGATGG 2340
CATCTGGAAC GGGGCTTGGT CCCAGCCTCC ACGGGGATGG TCAGGGTGCT CTTCCTTCCT 2400
GCTGGCTGGC CCTGCCCCCA GGATCCAGCC CTGTTCCACC TGAGTTCCCG TACACAGGAG 2460
TCTTCGTGGG GTGAGGCCGC GTCCTGGCCC TCAGCCAGCG CAGGGCATTA GGATGCTTAG 2520
TGTGCATTAG TGACTGCGCC AGGGGAGTGC CAAGGCCCTC AGGAACCTGG GAGAGGCCCC 2580
ATGACTCATG AGCGTGGCTC CTGGGTCCCC CTGCCGCCAG GGCCTCAGCC GCCTACTGTC 2640
TACCATCCAG AGCTCAGCTG GCACCAGCGC CCAGCAATCA CTCAGCGACC CTCACCCCCT 2700
TCTGTTGGTA ACACACCTCG AAGGGTTGCC AGAAAGACCT GCTGAGAAAG GGAGAAAACT 2760
CTCTCAAGAG CTCAAAGCAC CACAAAAATG CAAGCTGCCA ACACCAAAGG AAATCACCCA 2820
CAAACATATG TGACCACTAA CTTTCTTCCC CTTAAATGGA CAACAGGGTG GCAGCCCTGT 2880
ATGTCCCACC 2890