EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS048-11638 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr14:69013610-69016140 
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
ATTCTGGGCA AGTGAGAAGA GCAGAAACAC CTCTGTGCAG TTTATCAGGA CTTTCTCCTT 60
CTAGCACACC CTGAGGGTGA GGCCAGAATT AGTCATGTGC TGAATGGTCT GCCTATTTCA 120
TGATGTTCTC AGCTTGGAAA CATTTTTTTT GTGCAACTCC AACTCAAGCA CCAGCAAATC 180
CAGCCTCTCC TCACCTCCTA TTACAAATGG CTGTCATGGA CTAGACCGGT GCCTAACAAA 240
CAGCCCACAC TTCGGGATCT GAGTTCAGGT TCCGGCACGA TTAGTGCAGG TGGCTTCTGG 300
CTCTAAATCT CTCAGAGGAG ACATCTTCTT CTGGGGGCTG ATTCACACGT GAGTGCTGAT 360
CATGACCTTG TGTCGGGATT AACCTCCTTT CTCAGCATCT CCTGCTACAT TCCATCTGTT 420
TCTAAAGACA CCTCATTCTG CCTTCCTTCC GGCCATCCAC TGTTACCTTT CACTTCCTGT 480
CGGCACGTAC AGGCCAGGGA CTTTACTCAA GTCACTGAAC ATTTTGGGGA AATGAAATGA 540
AAACATAAAG AGAAGGCCAG TCCACAAAAC AGCTCAAAAT GGAGATGCTC TGGCTGAAGG 600
AAGGAGTGTT GGGGTCCAGG AGCCCCGCTC ACTCCTCAGC ACCCGGGAGC ATCACGGAAT 660
CTAAGGTGAA CCTCCGGGGC AGGAGACACA GCACTGGCCT TAGAGTCCAC AAGCCCGGGT 720
TCCTTGGCCC TGTCTCTTTC CCTCTCTCTG TTGTCTGTAG CTCCCTCCTA GCTCTGAAAC 780
TCCAAGTACA AGTGAGCAGG TCATGAGTCA CCAAGCCTCT TTTCCTGGGC GTTTTTCCTT 840
CCGGGGAGAG AACAGCCAGG CTTGGACAAA AAGTGTTGGG ACACCCTGAA GCAGAACACA 900
CTCCCTGTCA TTCCTGGCCT CACTCTCCTC CAGAACGAAA GCACCCAGAC CTGCAGGCCT 960
TTTTTAGGAA TGAAGTCACT GGTCTGTGTA GGTTGACAGA GTGTCCTTGG AAAAGGCTGC 1020
TTGGGAAGGA AACTCACAAG GCATGGGTAT CCCCACTGGA AGAATCCAGA GCAAAACCCT 1080
TCTGGAAATC CCCCACCCCA CATATACACA AGGAAACTCC ATGGAAGGCA TCCTGTCTTG 1140
GAGGCCTCAG TGGGTTCCTC CTGGAGAGTT TAAGGGGAGG GAGGCAGAGG AGGAAGGAGA 1200
GAAACCTAAA GTCAGCAGGA TATTCTCATG TTCTCTCTCT GTTAATTGCC TCCTCTCTTT 1260
TTCTAAGAAG GCTGAGATAC CGAGGCTTCC TCACCCACCA CCCCTTCCTC TACCTCCCCT 1320
TAGTGCTGGG TGAGTTCATC CATCAGGACC CCTGCCTGGG ACTGTCCTCA CTCTCCCGCT 1380
GTGGCTCACT TGCCCCCAGG GCCCATCCCA GCCCAGCCCA GCCCTGCCCA GCCCAGCCTG 1440
CTGCATGCTT CTACCCCGGC TCCCACTCAG GCTCGTGCGT CACTGCTATT CATCTTGTTT 1500
AGTGCTTGGC TTGGCTGCAG ATGCTGTAAA TATGGTAATT TTAGACTCCC TGATTGGAAA 1560
GGATTGCAGA GCGGGTTGTG GGGGAGGACG GCAGTTTGAT TTACTCCGCA GGAGCTGGTT 1620
CCGAGATGGC TCTCCACCCT CTGTGCACGC CTCTTCTCCA AGCTGTGCCC CATCAGGCCC 1680
TACTCTTAGT GTTGAGTCCT GACTTCTTGG GGTCTTGGGA GAAATGAGAG GGACAGAGTG 1740
GATGTCTGTG CGTTCTGGGC CTGAAGAATT GCTGGTTAGC ACAGAGCATC ACATGCAAGG 1800
AGGCCGGAAG TGTAGTCAGT GATGCGCAGG GTGGGCGTCC TGACACTGCT AAGACAATGC 1860
CCAAGGCTGA TGACCCAGGA TTATCCCCCC ACCCAGGGCA CACTGGGGAT GAAGTGGGGG 1920
CTGCCCGAGG CCTCTGACCC CTTCTGAGCT CTCTCCCTTT TCTGTTCTCC TTTCTTTCCT 1980
GACCTCCCTC CATGGGGGGC CATCAGTCCC CAGGGCCTTC TGCCAGGCAC TCACAGGGTT 2040
GTCAGCAAAT CCCTCCTCCC ACCCCTTTGT TGAATAAAGA CCTAATTTGC ATTTGATTAC 2100
AGGACCCCTG AGTGGGTAGG GGTGTATTCA GATCCCCAGG GAGTGACTGT GAGGCTGGCA 2160
TTTCAGGCCC TGGGAGTCAG AGTGGGAGCT GAGGGTTTTG AGCCCCAGGA GTAGGTCAGG 2220
TTCTTCAAAA GCCACCAGAT AGTCTCCCAG CTGTCTGTCT TATCTCCTCA GGACAACCCT 2280
AACTCCAAGG CTGGTGACTG AGTCAGACTT GGAACATCCC CGTTTTTGAG CCACAGTCTA 2340
TAGTCACAGA ATGTTCCAGG GGGAGGGATG GGGGGAGAAA AGGAGGGCAC AACTCACATT 2400
TCTTTGAGCC CCAAACTTCA TTTGACCAGT GAGGAGTGGC TTGCACCAAA TCATTGGTGC 2460
AGCTAACCAC AAGAATGTTA GCTCTTATCT AGTGCTTCAT CCATGCCCTG GACACATTTT 2520
TTTTTTTTTT 2530