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

TagContent
EnhancerAtlas ID
HS052-08679 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr12:52418870-52420020 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr12:52419607-52419626TTACCAGCAGAGGGCACCA+7.85
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01015chr12:52418988-52420568Adrenal_Gland
SE_01838chr12:52418905-52419813Aorta
SE_03795chr12:52419121-52419814Brain_Angular_Gyrus
SE_04021chr12:52417333-52420328Brain_Anterior_Caudate
SE_05176chr12:52418685-52420454Brain_Cingulate_Gyrus
SE_05966chr12:52416302-52421515Brain_Hippocampus_Middle
SE_07218chr12:52418556-52420183Brain_Hippocampus_Middle_150
SE_07944chr12:52416412-52420722Brain_Inferior_Temporal_Lobe
SE_08806chr12:52419304-52419566Brain_Mid_Frontal_Lobe
SE_08806chr12:52419661-52419815Brain_Mid_Frontal_Lobe
SE_19846chr12:52416375-52420362CD4p_CD25-_Il17p_PMAstim_Th17
SE_23310chr12:52417342-52420086Colon_Crypt_1
SE_23835chr12:52419074-52420096Colon_Crypt_2
SE_24905chr12:52418355-52420465Colon_Crypt_3
SE_26342chr12:52418035-52421120Duodenum_Smooth_Muscle
SE_27026chr12:52418650-52420166Esophagus
SE_30252chr12:52418982-52421234Fetal_Muscle
SE_34732chr12:52418799-52421674HeLa
SE_38567chr12:52415886-52420142HUVEC
SE_40781chr12:52418902-52421724Left_Ventricle
SE_44280chr12:52419085-52420211NHDF-Ad
SE_45503chr12:52419049-52419922NHLF
SE_46044chr12:52418960-52419980Osteoblasts
SE_47765chr12:52419277-52419701Pancreas
SE_48081chr12:52418617-52421907Psoas_Muscle
SE_48629chr12:52418463-52421761Right_Atrium
SE_49724chr12:52419076-52420106Right_Ventricle
SE_50349chr12:52416625-52420920Sigmoid_Colon
SE_51135chr12:52418530-52421933Skeletal_Muscle
SE_52700chr12:52416626-52420911Small_Intestine
SE_53734chr12:52418788-52420608Spleen
SE_54908chr12:52418581-52420576Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr125241904352419671
chr125241930152419935
Enhancer Sequence
AGTCTCTCTG TCGCCCAGGC TGGAGTGCAA TGGCACAACC CCGGCTCACT GCACCCTCCG 60
TCCCCCGGGT TCAAGTGATT CTCCTGCCTC AGTCTCCCGA GTAGCTGGGA TTCCAGGCGG 120
CCGCCACCAC GCCCGGCTAA TTTGTCATAT TTTTAGTAGA GATGGGGTTT CGCCATGTTG 180
GCCAGGCTGG TCTCGAACTC CTGACCTCAG GTGATCCACC TGCCTCGGCC TCCCAAACTG 240
CTGGGATTAC AGGGGTGAGC CACCGCCCCA GGCCTCTTTC GGCACTGCCC TCAACCACAT 300
GGGCCTCACT GTTCTTCCGG CGTACCCAGA CTTTCCCCAT CTCAGCGCCT TCCCACCGGT 360
CCTGTGTTTC CATGGCCTTT CCCCGGGTAG GGGCCTTTCT TTTCCTAGCT TCGCTCAGTT 420
CCCTGCTACA TTGTCGCCTC CTCGCAGAAG CCGTCTCTGG CCGTTCCGTA TCGCTAGCGC 480
CCTCTATCAT TCGCTAGCAG CTCACCCGGC TCTGTTTTTC TTCATTGCAC TTCTCGTTAT 540
GTGCCGTTCT CTTATAAATG TTTTTGTCTT TATCCCTCCC ATAGAAGACA CCTCCATGAA 600
AGGCCAGGGC TTTCCGAGGT TCTTTTCCTC TGTGGTTCCT AGAAGAGGGC CTGGCACATA 660
GCCGGCCTTG GCTAGCTTTT TGCGTAAATG TGAAGGGATC CACCTTCCTC CCTTATAAGA 720
GGTAGCAGTA CCTCCTGTTA CCAGCAGAGG GCACCACCGT ACAGCACTTG GGGGCCGCAG 780
GGGATCCTGC TGGGATGGGA GGTATTTAAA AAGCCCACAG GCCTCTCCTC CCATAATGTG 840
GGCGCTCCCA CAGCTGGGAC CGGAAGCAGG AGGGCCCCCT GCGCTAATCT GCCCTGGCAG 900
CAGCGAGCTG GCACGCCCTG GGTGCATCAT CCGGTGTGCT CTGGTGCCCA AGGTCGGAAT 960
ACCCTCACTG GTGGCTTGGA CACACCCCTG AGCAGCTGAT GCTTCTGGAC AGATCACACC 1020
CTGTCCCGGG CTCTCAAAAT GAGGGCAATG ACATGAGCTG CACTGCTCGC TCACGCGTTT 1080
GCTGTGAGGT TGGGACAGGA GTGCATGGGA AATGTTTTAT GAATGTAAAC ATGGGACAAA 1140
TATAATTTAT 1150