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

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EnhancerAtlas ID
HS047-02895 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr1:204416710-204418310 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NKX2-3MA0672.1chr1:204417337-204417347TTCAAGTGGT-6.02
Six3MA0631.1chr1:204417428-204417445GACAGGGTATCACCATG+6.11
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00064chr1:204415801-204417319Adipose_Nuclei
SE_00064chr1:204417530-204422553Adipose_Nuclei
SE_03975chr1:204415223-204416998Brain_Anterior_Caudate
SE_04850chr1:204414465-204417204Brain_Cingulate_Gyrus
SE_04850chr1:204417565-204418666Brain_Cingulate_Gyrus
SE_05834chr1:204414554-204422838Brain_Hippocampus_Middle
SE_06778chr1:204414634-204417237Brain_Hippocampus_Middle_150
SE_07775chr1:204414572-204417332Brain_Inferior_Temporal_Lobe
SE_07775chr1:204417757-204421412Brain_Inferior_Temporal_Lobe
SE_10255chr1:204417782-204418559CD19_Primary
SE_10905chr1:204414650-204438582CD20
SE_25125chr1:204416348-204417318Colon_Crypt_3
SE_25125chr1:204417816-204422942Colon_Crypt_3
SE_26688chr1:204416875-204421560Esophagus
SE_28866chr1:204417158-204423024Fetal_Intestine_Large
SE_30246chr1:204415638-204416972Fetal_Muscle
SE_31610chr1:204415095-204416911Gastric
SE_31610chr1:204417780-204422694Gastric
SE_34711chr1:204415846-204421729HeLa
SE_40776chr1:204415081-204417377Left_Ventricle
SE_40776chr1:204417564-204421617Left_Ventricle
SE_42225chr1:204414898-204417247Lung
SE_42225chr1:204417746-204421550Lung
SE_48201chr1:204414946-204421702Psoas_Muscle
SE_48746chr1:204414986-204417248Right_Atrium
SE_48746chr1:204417807-204421419Right_Atrium
SE_50149chr1:204415315-204422829Sigmoid_Colon
SE_51536chr1:204415200-204417241Skeletal_Muscle
SE_51536chr1:204417745-204423045Skeletal_Muscle
SE_52421chr1:204416678-204422949Small_Intestine
SE_58430chr1:204415099-204506026Ly1
SE_59794chr1:204415680-204491493Ly4
SE_62377chr1:204415291-204492168Tonsil
SE_65868chr1:204415035-204417231Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1204417545204418214
Number: 1             
IDChromosomeStartEnd
GH01I204445chr1204415101204423341
Enhancer Sequence
GGGATGAGAT CAGGGATGTG AGGAGAGAAA ACAGGCAGCG TGTGTGGACT CCCAGCTTCT 60
TTCTCTCACC CCAGCATTCC GGCCTTGTCC CTCCCTCACT TTCCCTCAGG TTCTTTGTAA 120
AATAGCCCTG TTAGACTTGG TGATCTCTAA AGTCCTTTCC AGCTATAACT CTCAGCAAAA 180
AATGAGAGGG AAACAAAAAG AGAAAAAGAA TGGACATGTG AGGAAGAGGT TCGGTGGAGA 240
TGCACCTTGG TGAGGGGTGA GGGGACAAGC CCCAGCCAGA ACTCTGAACA GAGGTGTCAC 300
CCAGCTGAAA CACGGGGTGC ATCCAGGCTG AGTCCGGGGT GACTTCCATG GGGTGCCAGA 360
GGACACTGCT GCCAGAGGGG AGGCAAGACC ACACACTGGG AGAAGGCCCT GGGACACTCG 420
GTCCCTACTC TATGCCACCA GATGTTCATC CTACTAAAGT ATCAGAGCTG AGTGAGCCAA 480
GTCTCCAAAG GAGGTCTACT TTCTTTCATT CAAAAAACTT ATTTATTTAT TCATTTATTT 540
ATTTATTTTG AGACAGAGTC TTGCTCTGTC ACCCAGGCTG GAGTGCAGGG GTGTGATCTC 600
GGCTCAGTGC AACCTCTGCC TCCCCGGTTC AAGTGGTTCT CATGCCTCAG CTTCCTGAGT 660
ACCTGGGATT TACAGGCACC CGCCACCACA CCCAGCTAAT TTTTGTATTT CTAGTAGAGA 720
CAGGGTATCA CCATGTTGGC CACTCCTGAC CTCAAGTGAT CCCCCTGCCT CAGCCTCCCA 780
AAGTGCTGGG ATTGCAGGCA TGAGCCACCA CACCCAGCCT CATTCAACAA ATATCTATTG 840
AATCCTAACA TGTGCCAGGC ATTTTCTAGA GTCTGGGCAT AAAGCAGCAA ATAAGACAGA 900
CAAAAATTAG CCGGGCGTGG TGGTGTGCGC CTGTAGTCTC ATCTACTCGG GAGGCTGAAG 960
TGGGAGGATG ATTTGTGCCT GGGAGGCAGA GGTTGCAGTG AGCCAAGATT GTGCCATTGC 1020
ATTCCAGCCT GGGTGACAGA GATCCTGTCT CAAAAAAAAA AAAAAAAAAA CCTGCCTCAG 1080
GGAGCTTTCA TTCTATGTCA ACATTCATAC TCCATACCAA AGTATCTCAT AACCACAAGA 1140
AGGGGAAGCT GGGAACTGAG AAGTGCACCT TGGGCGTGAC CAGCTCCTCC TCTTCTCCCT 1200
GGAGAATAGG TCCATCCTGC CAAAGCACTG AGTCACTGGC AGGGGCAAAG GTGTCCCCTC 1260
AGGCCCCAAG AGGACCCAGG TCAGGTTTGA TCAGACTTAG ACGTATGAAG ATTCAATACA 1320
AGGGACTCAG AAGCTGAGCC CTGAATGCAG AGGGTCTCAG ACCCCATCTT CAGGCTCCAC 1380
GAAATCAATT TAACCTCCAG GAGATGGGAG ATGGATACCC CAGAGCTCAC CTCACAATCC 1440
ACATCTAACC ATATTCCCTC AGTTGCTTCA GTCACATCAT CCTCCCATGC TTGAAGTTCT 1500
AGCACTCTCT CCTGCTGTCC CAGCCCAAAT CTCCAGGAGA AAAATGTAGA GTTGACTGGA 1560
ATGGTCTTGC TGGTGACTGG GAGGGAAGGG CTAAAGCCTC 1600