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

TagContent
EnhancerAtlas ID
HS045-70862 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr9:123683810-123685100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1014530chr9123685092hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxo1MA0480.1chr9:123684458-123684469TGTAAACAAGA-6.02
RELAMA0107.1chr9:123684071-123684081GGAAATTCCC-6.02
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01292chr9:123683981-123684525Adrenal_Gland
SE_01664chr9:123680685-123684564Aorta
SE_01664chr9:123684681-123686588Aorta
SE_05342chr9:123674762-123684591Brain_Cingulate_Gyrus
SE_06145chr9:123680720-123684735Brain_Hippocampus_Middle
SE_11823chr9:123681415-123697392CD3
SE_15020chr9:123680779-123692584CD4_Memory_Primary_7pool
SE_15500chr9:123681522-123692469CD4_Memory_Primary_8pool
SE_16326chr9:123681322-123692243CD4_Naive_Primary_8pool
SE_16854chr9:123681565-123685232CD4p_CD225int_CD127p_Tmem
SE_17311chr9:123680688-123701002CD4p_CD25-_CD45RAp_Naive
SE_17766chr9:123674711-123700821CD4p_CD25-_CD45ROp_Memory
SE_18313chr9:123675977-123700962CD4p_CD25-_Il17-_PMAstim_Th
SE_19108chr9:123680709-123699940CD4p_CD25-_Il17p_PMAstim_Th17
SE_20050chr9:123683797-123696495CD56
SE_20905chr9:123681287-123692470CD8_Memory_7pool
SE_21626chr9:123681499-123684867CD8_Naive_7pool
SE_21944chr9:123681434-123685136CD8_Naive_8pool
SE_22312chr9:123679588-123700473CD8_primiary
SE_26718chr9:123683748-123686514Esophagus
SE_32579chr9:123681342-123699293GM12878
SE_43058chr9:123683701-123684556Lung
SE_49159chr9:123680700-123684577Right_Atrium
SE_50248chr9:123683668-123684658Sigmoid_Colon
SE_52520chr9:123680686-123684572Small_Intestine
SE_58895chr9:123680733-123708417Ly3
SE_61111chr9:123630545-123707493HBL1
SE_62230chr9:123630172-123700621Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9123684222123684378
chr9123684918123685057
Number: 1             
IDChromosomeStartEnd
GH09I120921chr9123683879123684278
Enhancer Sequence
GGCCTTTTGC AAGTGAGGCA TAGTGGCTCA CAGAGTTGAG GGTCTGCTTG TGTCTCACAG 60
CCGATCCACC AAGAGCCAAA CAGTGAGGCT CAGGGAGTTA CTCCACGGAG CAGCATATCA 120
TATTAACTCT TACCACGTTG CAGAGTGTAA AGTTCCAAGA ACATGCATTT GGTCCTTACT 180
CTTACTCTCT GAGGGCCTGC CGATGGAGAG GTTGCTGAGA AGCAGATGGG AGAGTGCTCA 240
AAACCAGCTC TGGGTGGGAC AGGAAATTCC CCTGAACTCT CTGAATGAGA GGGACCAGCT 300
CAGAGAAAGG AGAAGGAGGT GTGGACACTC GCCTGCCTCT GGTCCAGCGG TAGGGGGATA 360
GCTGCCCTGC CAGCACTGCT ATCACGGTCT GGACATCACA GATCCTGGAA AGGCCTTGCA 420
GAGCTGACTT AATATCCTCA TTTTACAGAT ACAGAAACAG GGCCTGGGAA TTGCTGCTAG 480
CCAAGCAGAG AATTATGCAG AACCACCCCT GGACATCAGG CTCCTGATCC CTGGGCCACA 540
GTTTGCTGCA AGAAGAGGGC TTTGGCTGAA AGGAGCCAGG CACTTCCCAG TGGAGGTAGA 600
GAGGGCGGCT GAGCAACGAG ACTCCTCTGC AGGTCTCAGG GCCCCGTGTG TAAACAAGAG 660
GATTTGATTT TGAGCAGTGA CTCCTGCCTG TTTGGATTCG TGGACCAATA CGAGTGTGTT 720
TTTTTTTAAA TTGAGAGATT AACAAAGAGA TTGTCATCTT TTTAATTTTA CTTAGCAAAG 780
GCTTTGCCAA AAACTATCAT CTACGATTAC ATCCTTTCAT TTATATAAAG ACATGCATAG 840
GACAGACGCA ATCTCAGAGT AAAAGTTTGG TTTTATAAAT GGAAAGAATT TAGTTTACAT 900
AAACTGATTT ATAGAATTGC CTTATTTTTA TCATTTTGTC ATGAGCTGGT GGGAATGGAT 960
CAGTTCTGGA TAGCATGTGG GAACCTCTGA GCAGGACATG TAACCTATGA GGGTCCTTCC 1020
AGCTTGGGAG GGCCAGGGTT CTAAATTGTA GCTCCTGAAA ATGTCTCTCT GGCCTATCAC 1080
ACTTCCAAAT GTGTCTCTTA TTCCTAGAAG CACCGTTTGA CAGAGCTCAG GACGTGAGCT 1140
GATAATGGTC TCTCCCCACC TAAAGGCAAA CAGAGGCAGA CAGAACCATC TAGATGAGGA 1200
GTTTGCTAAC CTTTTTTATG TAAAGGGGTG GATAGTAAAT ATTTTGGGCT ATGAAGTCTT 1260
TGTTGCAAGT ACTCAATTTT ATATAATTTT 1290