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

TagContent
EnhancerAtlas ID
HS129-03537 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr1:223920480-223922450 
Target genes
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr1:223922394-223922411TGGCACACCATGTACCA-6.01
Gata4MA0482.1chr1:223920574-223920585TCTTATCTCCC+6.62
Nr5a2MA0505.1chr1:223921780-223921795GACCTCAAGGCCAGC+6.22
USF2MA0526.2chr1:223921349-223921365CCAGGTCACGTGAGTC+6.03
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00224chr1:223917623-223923297Adipose_Nuclei
SE_01908chr1:223920427-223922082Aorta
SE_02306chr1:223920308-223921944Astrocytes
SE_04026chr1:223920429-223923012Brain_Anterior_Caudate
SE_05036chr1:223920530-223922321Brain_Cingulate_Gyrus
SE_05972chr1:223920132-223922577Brain_Hippocampus_Middle
SE_07159chr1:223920244-223923166Brain_Hippocampus_Middle_150
SE_07996chr1:223920284-223922259Brain_Inferior_Temporal_Lobe
SE_09681chr1:223920277-223921825CD14
SE_19702chr1:223921073-223922029CD4p_CD25-_Il17p_PMAstim_Th17
SE_23408chr1:223920555-223922971Colon_Crypt_1
SE_24051chr1:223920713-223921438Colon_Crypt_2
SE_24051chr1:223921499-223922031Colon_Crypt_2
SE_24051chr1:223922112-223922463Colon_Crypt_2
SE_25230chr1:223920636-223922879Colon_Crypt_3
SE_26209chr1:223920732-223921934Duodenum_Smooth_Muscle
SE_26925chr1:223921184-223922005Esophagus
SE_31491chr1:223920239-223923646Gastric
SE_33950chr1:223920559-223921591HCC1954
SE_38254chr1:223917692-223922239HUVEC
SE_41495chr1:223920316-223922995Left_Ventricle
SE_42269chr1:223920225-223923100Lung
SE_45872chr1:223920277-223921720Osteoblasts
SE_49408chr1:223920327-223922010Right_Atrium
SE_50365chr1:223920440-223922961Sigmoid_Colon
SE_53249chr1:223920551-223922027Small_Intestine
SE_65644chr1:223920306-223922506Pancreatic_islets
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1223921475223921876
chr1223922041223922091
chr1223922066223922385
Number: 1             
IDChromosomeStartEnd
GH01I223730chr1223917704223922480
Enhancer Sequence
CTTCTACAGG TGGGGACGTT AGCATTATAA TGACATGGTA AAGTTCTGAA GGTAACAAGG 60
GGTTGCCTGT TCCAGTTTCT GCCAGTTTTG GGGGTCTTAT CTCCCTCTGG TATCTGGGCA 120
GAGGTCAAGA AGCTCTGGCA CCATCAGGGG CCAGCTTGTT TCTTTAAGCA GCTGTGCCTA 180
CAAATAAAGG GACTAAAGAA AACAATAAGA AAACCCAGTT ATTTCCTGGG GGTTGCTCTG 240
GTATCCAGCG TGTTTTACTT CACCAAGCGC AATTCTTCCC AGTGCAGGCA CTGGGTGTAA 300
CTGTGACAGC CAGCACCAAC CTGCCCACAC ACCTCCTGTC CTGCAGGACT GTCAGCAGCC 360
TCTGCACTAT AGTGTGACAG AGCCACAGGT AGCTCAGGTG TGCCTCAGCC CAGCCTCTCC 420
TGCACTCCCC CTCCCCTGGC TCCCCAACTC TGCCTCACTT CTGTTTGTGA AGGAAAGACA 480
GCAGTAGCGG AAGGGAAAGA AGGAGAAAAT GCAGAGCAAA TATTATGCTT TCCTCTTGGA 540
AAACCTCCAG GAGCTGCAAA TATTAGTAAT CCAGCTGCAT CCCACCCCCC AGGATGGGCT 600
GGGCCTGTCA CACAGCCAAC CTTCAGGATG CAGACACCCA GGCTGGGGAG CACAGCTCTG 660
GAAATTTACT GACATGGCCC TGAATGAATT TATCTTTTCA GTAGAAGGCC CTGGAGTTTA 720
AAGGAGTCAT TCATAAGGTC TGTCTGGGAG TGCCTTGTCC TCAGAGGAGG GTCTGGGTGG 780
GTTGGAGTGG AAGGAAGGGC TGGCTACCTG GTGTGCTCTC CGTGGGTCCC CAAGAAAGGC 840
AGCCCTGCTG GGGGCAGTGA AGCCCTTATC CAGGTCACGT GAGTCTTGGA AGGGGAAGGC 900
TGCTGTGCTT AACGATTCAA AAACACAAAT CAAACCTCCT TTCCCAAACA AATTAGAAGG 960
TGTGGAGGAA GCTTGAATTC AGAGAGGATT TCCCAGAGAC CCATAGGCAA AAGTGGCTTA 1020
ACTGAGCCCA GTGGGTGTCC CAGAATGGGC CAGAGAGAAT GACACTAAAA AGTCTTTGAA 1080
CAAATGAGCA AATGAATACA GGAATGCTCA TCTGCCATAG GCACAAACGT GGTAAACGTT 1140
CCCTGAGAGA ACTGACAGCC CAGGGGTGCA GGGAGAGAAA CGGTCCCAAC TGCAGACTGG 1200
GTCCCAACTG CAGACTCGGT CCCAACTGCA GACTCAGGAG GAGGGAGGCT GTTAAGGGGC 1260
CGTCTTTCCT TCTGTTATGT GAGGAGAAAA GCAGGGAAGG GACCTCAAGG CCAGCCTCTC 1320
CCAGGAGCTG CTGTTCTCAG CCCCGGGATC CAGCGCTACA GGGAAGTGCA GGGGAGGCTC 1380
CACAGTCCCG GCTGGAGACC CGGTCAGGCC TGGGTGGCCA CTCTTCTTTG TAGTGGCCAC 1440
CCTCGTGTCA CCAGCAAATG CTTTTGTATC TACACCCTTC TCAGTGCTCC CCCTCTTTTA 1500
AAAAATGTAC TTTCTTTTTT TAAAAAGAGT TGGGTCTTGC CTTGTCACCT ATGCTGGAGT 1560
GCAGTGTTGC TGTCACAGCT CACTGCAAAC TCCACCTCCT GGGCTCAACC CATCCTCCCA 1620
CCTCAGCCTC CCAGGTAGCT GGGACCACAG GCACACACCA GGACACCTCG CCCAGTGCTC 1680
ACTATTTACC TTTATTTCTT CCTTATTCGG ACACCCCTTG CTTCCAAAGA AGAGTTTCGG 1740
AAGGCTCAAG ACGGTGAGAC AGACACCTTA TGCACTGCTT CACTCTCCCC CGCAGCTCCC 1800
CTCCCTCCTC ACTGACCCCC GGCCACAACC CTCTCTCCTT GCCCCTCACC AGCCGGCACC 1860
CTTGGCAACC CTGGCACCCT TTCGAGGACA AGACTGCCAA ATGTGGCCAA GGTCTGGCAC 1920
ACCATGTACC AATCGAAACT CCACTTCCCT TGAGTTTCAG TTTCCACGCC 1970