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

TagContent
EnhancerAtlas ID
HS177-05805 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr12:111847130-111848190 
Target genes
Number: 6             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3803170chr12111847740hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr12:111847769-111847781TGTCAGGGGTCG+6.32
SPDEFMA0686.1chr12:111847840-111847851ACCCGGATGTG+6.32
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00313chr12:111840072-111852138Adipose_Nuclei
SE_01105chr12:111846175-111849016Adrenal_Gland
SE_06099chr12:111840410-111853163Brain_Hippocampus_Middle
SE_09337chr12:111840182-111853434CD14
SE_11164chr12:111840062-111852388CD20
SE_13643chr12:111846114-111850454CD34_Primary_RO01536
SE_14612chr12:111840371-111851485CD4_Memory_Primary_7pool
SE_17538chr12:111840572-111851864CD4p_CD25-_CD45RAp_Naive
SE_17816chr12:111840454-111851319CD4p_CD25-_CD45ROp_Memory
SE_18496chr12:111840343-111850646CD4p_CD25-_Il17-_PMAstim_Th
SE_19231chr12:111840599-111851056CD4p_CD25-_Il17p_PMAstim_Th17
SE_20028chr12:111840668-111851190CD56
SE_22364chr12:111841872-111850729CD8_primiary
SE_32074chr12:111846839-111848988Gastric
SE_38040chr12:111840331-111852503HUVEC
SE_40041chr12:111841629-111851323K562
SE_40792chr12:111840630-111853567Left_Ventricle
SE_42263chr12:111840633-111853413Lung
SE_46057chr12:111843649-111853600Osteoblasts
SE_47422chr12:111840368-111852366Panc1
SE_48851chr12:111845998-111852289Right_Atrium
SE_50268chr12:111841664-111852291Sigmoid_Colon
SE_52677chr12:111841692-111851154Small_Intestine
SE_53326chr12:111840640-111853266Spleen
SE_56066chr12:111843581-111853355u87
SE_62745chr12:111834432-111886877Tonsil
SE_67523chr12:111843581-111853355u87
SE_68830chr12:111846249-111848972H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12111847615111848064
chr12111847309111847501
Enhancer Sequence
TGCAATTGGC ACTCAATAAG TGCAAGCCAT TGCTGTTCAT GCCCAATAGG GGCTGGCACT 60
TAATTGCCAG GTTTCCTGGG AAAACGGTCC CCAAGGGCCC GCGGGCGTTC AGCATCTTTG 120
ACGAGGCAGG GCAGGAAGCC GCTGCCGTCT GGCAGACCGG AGACGCCTGC CTCGGCGAGT 180
CCAGAGGTGC AGTGCTAGCT GCTCATTCCC TGCAAGGCCC CATTCCTCAC TACCCACCCT 240
TCCCAAGGAA ACTGAGGCGG GCAGGCTGCC CAGGGGAAGT GACTCAGCCG GGGTCACTTG 300
CTGAGTCAGG CCTTATTGGA CCCAGGAGTC CTGCACCCCA CCTCCCCAGC TTCCCGGGGC 360
TTGAGATCCC TTGGAGACTG AGCAGGTCCT GAGGCCTGGC AGCAGGACCA GGCCACCACT 420
GGACATCTGC TCAATGGGGC CCTGCTGCCG GGGTGACAAG CATCCCTCTA CCAGGGCTCC 480
AGGGTTCTGC TGGCCACCAC TAGCCATCCT TCCTCCCAGC AGGGGCAGAG GACACTTCCC 540
CAGGGGAACA GGTCCTCCTG GTGCCCCCCC ACTCCCCGCC CCAGCCGGAA ACCCGGCAGC 600
TGAGCAGTTA GATAGAAGAT TTTTCCTCCC ACGCCACCCT GTCAGGGGTC GGCCAGCAGG 660
GCCGGGCCAC AGGCTTCCTT GTGAGCCAGG CCTGGAGCCC CTGGGGGCCC ACCCGGATGT 720
GGCTACCCCC CGGCTGGCCA GTGGGGAGCC GGCTGCTGCC CAGGACATGT GTCCCCAGGG 780
AGGCCTGGGA GGAAGGAAGT CTATGCCCTC CTCACAGGGG CTGACTCACA GGCGCCCAAT 840
GGGGGGCCCC AGCTGGGAGA CTGGGAATGT GATCAATCAG GGAGGTGGAC ACACAAGGGG 900
ACCTCTGACA TGGGATCTGC CCTTTCAGAG CTCACACACT GGTGTCATCT CAAGGAGGAG 960
AGGCCCAGAG AGGGCAGTGT ATGCTGCGAG AGGCGAGGTA ATTGAGGGCT TACGCATGTC 1020
CCTCCTGATG TCCCCAAGTA GCACGTGGGG AGGAGGTTCA 1060