EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS044-04293 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr14:69013710-69016210 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:69014046-69014064TCTGCCTTCCTTCCGGCC-6.01
EWSR1-FLI1MA0149.1chr14:69014042-69014060TCATTCTGCCTTCCTTCC-6.29
EWSR1-FLI1MA0149.1chr14:69014050-69014068CCTTCCTTCCGGCCATCC-6.52
FOSL1MA0477.1chr14:69014411-69014422CATGAGTCACC-6.62
Gata4MA0482.1chr14:69015867-69015878TCTTATCTCCT+6.14
JUNDMA0491.1chr14:69014411-69014422CATGAGTCACC-6.02
RELMA0101.1chr14:69014693-69014703GGAAATCCCC-6.02
ZNF263MA0528.1chr14:69014789-69014810GGAGGCAGAGGAGGAAGGAGA+6.49
ZNF263MA0528.1chr14:69014786-69014807GAGGGAGGCAGAGGAGGAAGG+7.37
ZNF263MA0528.1chr14:69015968-69015989GGGGGAGGGATGGGGGGAGAA+7.45
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00280chr14:69013195-69016338Adipose_Nuclei
SE_02138chr14:69010722-69016204Aorta
SE_02855chr14:69013201-69016119Astrocytes
SE_26121chr14:69009907-69022951Duodenum_Smooth_Muscle
SE_27035chr14:69010181-69016211Esophagus
SE_29630chr14:69013272-69016194Fetal_Muscle
SE_31476chr14:69012827-69016141Gastric
SE_33922chr14:69013159-69016144HCC1954
SE_34393chr14:69012531-69017225HCT-116
SE_34776chr14:69012407-69017481HeLa
SE_35882chr14:69008956-69017800HMEC
SE_36916chr14:69009078-69023396HSMMtube
SE_39270chr14:69012828-69016205IMR90
SE_40886chr14:69010251-69016249Left_Ventricle
SE_42158chr14:69012628-69016232Lung
SE_44258chr14:69009133-69016264NHDF-Ad
SE_45174chr14:69013192-69016207NHLF
SE_46405chr14:69008922-69016288Osteoblasts
SE_46762chr14:69013377-69016115Ovary
SE_48463chr14:69010224-69016220Psoas_Muscle
SE_48603chr14:69012522-69016119Right_Atrium
SE_50095chr14:69010708-69016245Sigmoid_Colon
SE_51137chr14:69009336-69023150Skeletal_Muscle
SE_51695chr14:69012785-69016165Skeletal_Muscle_Myoblast
SE_53910chr14:69012463-69016206Spleen
SE_54588chr14:69010107-69019497Stomach_Smooth_Muscle
SE_56133chr14:69007080-69016268u87
SE_63481chr14:69012785-69016179HSMM
SE_64342chr14:69010181-69016262NHEK
SE_67879chr14:69007080-69016268u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr146901430469014714
chr146901497269015327
Number: 1             
IDChromosomeStartEnd
GH14I068542chr146900936669022847
Enhancer Sequence
TGAATGGTCT GCCTATTTCA TGATGTTCTC AGCTTGGAAA CATTTTTTTT GTGCAACTCC 60
AACTCAAGCA CCAGCAAATC CAGCCTCTCC TCACCTCCTA TTACAAATGG CTGTCATGGA 120
CTAGACCGGT GCCTAACAAA CAGCCCACAC TTCGGGATCT GAGTTCAGGT TCCGGCACGA 180
TTAGTGCAGG TGGCTTCTGG CTCTAAATCT CTCAGAGGAG ACATCTTCTT CTGGGGGCTG 240
ATTCACACGT GAGTGCTGAT CATGACCTTG TGTCGGGATT AACCTCCTTT CTCAGCATCT 300
CCTGCTACAT TCCATCTGTT TCTAAAGACA CCTCATTCTG CCTTCCTTCC GGCCATCCAC 360
TGTTACCTTT CACTTCCTGT CGGCACGTAC AGGCCAGGGA CTTTACTCAA GTCACTGAAC 420
ATTTTGGGGA AATGAAATGA AAACATAAAG AGAAGGCCAG TCCACAAAAC AGCTCAAAAT 480
GGAGATGCTC TGGCTGAAGG AAGGAGTGTT GGGGTCCAGG AGCCCCGCTC ACTCCTCAGC 540
ACCCGGGAGC ATCACGGAAT CTAAGGTGAA CCTCCGGGGC AGGAGACACA GCACTGGCCT 600
TAGAGTCCAC AAGCCCGGGT TCCTTGGCCC TGTCTCTTTC CCTCTCTCTG TTGTCTGTAG 660
CTCCCTCCTA GCTCTGAAAC TCCAAGTACA AGTGAGCAGG TCATGAGTCA CCAAGCCTCT 720
TTTCCTGGGC GTTTTTCCTT CCGGGGAGAG AACAGCCAGG CTTGGACAAA AAGTGTTGGG 780
ACACCCTGAA GCAGAACACA CTCCCTGTCA TTCCTGGCCT CACTCTCCTC CAGAACGAAA 840
GCACCCAGAC CTGCAGGCCT TTTTTAGGAA TGAAGTCACT GGTCTGTGTA GGTTGACAGA 900
GTGTCCTTGG AAAAGGCTGC TTGGGAAGGA AACTCACAAG GCATGGGTAT CCCCACTGGA 960
AGAATCCAGA GCAAAACCCT TCTGGAAATC CCCCACCCCA CATATACACA AGGAAACTCC 1020
ATGGAAGGCA TCCTGTCTTG GAGGCCTCAG TGGGTTCCTC CTGGAGAGTT TAAGGGGAGG 1080
GAGGCAGAGG AGGAAGGAGA GAAACCTAAA GTCAGCAGGA TATTCTCATG TTCTCTCTCT 1140
GTTAATTGCC TCCTCTCTTT TTCTAAGAAG GCTGAGATAC CGAGGCTTCC TCACCCACCA 1200
CCCCTTCCTC TACCTCCCCT TAGTGCTGGG TGAGTTCATC CATCAGGACC CCTGCCTGGG 1260
ACTGTCCTCA CTCTCCCGCT GTGGCTCACT TGCCCCCAGG GCCCATCCCA GCCCAGCCCA 1320
GCCCTGCCCA GCCCAGCCTG CTGCATGCTT CTACCCCGGC TCCCACTCAG GCTCGTGCGT 1380
CACTGCTATT CATCTTGTTT AGTGCTTGGC TTGGCTGCAG ATGCTGTAAA TATGGTAATT 1440
TTAGACTCCC TGATTGGAAA GGATTGCAGA GCGGGTTGTG GGGGAGGACG GCAGTTTGAT 1500
TTACTCCGCA GGAGCTGGTT CCGAGATGGC TCTCCACCCT CTGTGCACGC CTCTTCTCCA 1560
AGCTGTGCCC CATCAGGCCC TACTCTTAGT GTTGAGTCCT GACTTCTTGG GGTCTTGGGA 1620
GAAATGAGAG GGACAGAGTG GATGTCTGTG CGTTCTGGGC CTGAAGAATT GCTGGTTAGC 1680
ACAGAGCATC ACATGCAAGG AGGCCGGAAG TGTAGTCAGT GATGCGCAGG GTGGGCGTCC 1740
TGACACTGCT AAGACAATGC CCAAGGCTGA TGACCCAGGA TTATCCCCCC ACCCAGGGCA 1800
CACTGGGGAT GAAGTGGGGG CTGCCCGAGG CCTCTGACCC CTTCTGAGCT CTCTCCCTTT 1860
TCTGTTCTCC TTTCTTTCCT GACCTCCCTC CATGGGGGGC CATCAGTCCC CAGGGCCTTC 1920
TGCCAGGCAC TCACAGGGTT GTCAGCAAAT CCCTCCTCCC ACCCCTTTGT TGAATAAAGA 1980
CCTAATTTGC ATTTGATTAC AGGACCCCTG AGTGGGTAGG GGTGTATTCA GATCCCCAGG 2040
GAGTGACTGT GAGGCTGGCA TTTCAGGCCC TGGGAGTCAG AGTGGGAGCT GAGGGTTTTG 2100
AGCCCCAGGA GTAGGTCAGG TTCTTCAAAA GCCACCAGAT AGTCTCCCAG CTGTCTGTCT 2160
TATCTCCTCA GGACAACCCT AACTCCAAGG CTGGTGACTG AGTCAGACTT GGAACATCCC 2220
CGTTTTTGAG CCACAGTCTA TAGTCACAGA ATGTTCCAGG GGGAGGGATG GGGGGAGAAA 2280
AGGAGGGCAC AACTCACATT TCTTTGAGCC CCAAACTTCA TTTGACCAGT GAGGAGTGGC 2340
TTGCACCAAA TCATTGGTGC AGCTAACCAC AAGAATGTTA GCTCTTATCT AGTGCTTCAT 2400
CCATGCCCTG GACACATTTT TTTTTTTTTT TTTTTTTTTT GAGACGGAGT TTCGCTCTGT 2460
CGCCCAGGCT GGAGTGCAGT GGCGCGATCT CGACTCACTG 2500