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

TagContent
EnhancerAtlas ID
HS073-03438 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr12:111846830-111849000 
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
GGGGCCAAAT CTGGGCTCTG CCAGCTTCCA GGTGTGAGGT CCTAGGCAGG TTACCTGGCT 60
TCTCTGATCT GGACCTCGCC TGCCCGATGG AAGCCAAGAG TTCCAGCCTC CCCAGGGTTG 120
GGTGTGTGAA GTACAGTGTC AGGACTGGAA CTGTGTTGGC TGTACTTGCT CTGGCTGTGT 180
GATCTTGGGC TGGTCCCTTA GCCTCTCTGA GCCACAGGTC TTTTTGTCTA TGAAATAGGG 240
GGGTTGCCAA CTCCCTGTTA GGGTGGTTTT GAGAAAAGGA GGCATGCACA GTGCCCGGCA 300
TGCAATTGGC ACTCAATAAG TGCAAGCCAT TGCTGTTCAT GCCCAATAGG GGCTGGCACT 360
TAATTGCCAG GTTTCCTGGG AAAACGGTCC CCAAGGGCCC GCGGGCGTTC AGCATCTTTG 420
ACGAGGCAGG GCAGGAAGCC GCTGCCGTCT GGCAGACCGG AGACGCCTGC CTCGGCGAGT 480
CCAGAGGTGC AGTGCTAGCT GCTCATTCCC TGCAAGGCCC CATTCCTCAC TACCCACCCT 540
TCCCAAGGAA ACTGAGGCGG GCAGGCTGCC CAGGGGAAGT GACTCAGCCG GGGTCACTTG 600
CTGAGTCAGG CCTTATTGGA CCCAGGAGTC CTGCACCCCA CCTCCCCAGC TTCCCGGGGC 660
TTGAGATCCC TTGGAGACTG AGCAGGTCCT GAGGCCTGGC AGCAGGACCA GGCCACCACT 720
GGACATCTGC TCAATGGGGC CCTGCTGCCG GGGTGACAAG CATCCCTCTA CCAGGGCTCC 780
AGGGTTCTGC TGGCCACCAC TAGCCATCCT TCCTCCCAGC AGGGGCAGAG GACACTTCCC 840
CAGGGGAACA GGTCCTCCTG GTGCCCCCCC ACTCCCCGCC CCAGCCGGAA ACCCGGCAGC 900
TGAGCAGTTA GATAGAAGAT TTTTCCTCCC ACGCCACCCT GTCAGGGGTC GGCCAGCAGG 960
GCCGGGCCAC AGGCTTCCTT GTGAGCCAGG CCTGGAGCCC CTGGGGGCCC ACCCGGATGT 1020
GGCTACCCCC CGGCTGGCCA GTGGGGAGCC GGCTGCTGCC CAGGACATGT GTCCCCAGGG 1080
AGGCCTGGGA GGAAGGAAGT CTATGCCCTC CTCACAGGGG CTGACTCACA GGCGCCCAAT 1140
GGGGGGCCCC AGCTGGGAGA CTGGGAATGT GATCAATCAG GGAGGTGGAC ACACAAGGGG 1200
ACCTCTGACA TGGGATCTGC CCTTTCAGAG CTCACACACT GGTGTCATCT CAAGGAGGAG 1260
AGGCCCAGAG AGGGCAGTGT ATGCTGCGAG AGGCGAGGTA ATTGAGGGCT TACGCATGTC 1320
CCTCCTGATG TCCCCAAGTA GCACGTGGGG AGGAGGTTCA CCCACAGGCT GCCCTCCTAG 1380
GGTCTCCCCT GTCTGCCCTC AACCCAGAGG CAGTGAAAGG AAGAAGCCAC GGCCTTGGGA 1440
TGGGGGGCGT GCGGGATTCT GATGGTGCTG CCTCTCCGCA GGGAGATGGT TCTTGGCTTT 1500
CCCTACCTCC TGAAACCTAG CTGGGGCGGT GGCTGGGATG TCAGGCTGGC GGTGTGGGCA 1560
GAGGAAGCCA GAGGACATTT CCTGTTCTGG CAGACTGTGC TGGCCTGATA AATGTCCCCG 1620
GGGCACAAGG TGACCCCAGC AAGGGTGCAT CAGTGTCCAG CCAGCTGCCC CGTGGCCTGG 1680
GGTAGAACCC ACCTCTCTGC CTCCCCAGGG ACCCTGCCTT CGCCCCCTGC TTCCCGTGGG 1740
CATCTCTGCG TCTGGCAACT TGAATGCTGT GAAAGGGCAG CAGGCCGCCT GCCAGGCAGT 1800
GTGTGTCAGA ATCCCACAAC TCTCTGGGCC TCCTTAGGCC ACAGGGTCTG GACTCTATGA 1860
ACAGTTGGTG CTAGGCATGG GGAAGATAGA AATGTTCCTT GTGGCCTAGA TTCAACCAGG 1920
AGGCCTCCCT GGAGGAAGTG TCCCCTCTGA AGGTGTGAGA CTTCCTGCCT ATATCTGTGA 1980
GCTGGGGCAG GGGAGAGTGG AGGCTCTGGA CTGGCCCAAT TTAACTTCAT TTACCACACT 2040
TTAAGAAATC TTCCCCAGGC TGGGAGCAGT GGTTCACACT TGTAATCCCA GCACTTTGGA 2100
AGGTCAAGGT GGGAGGATCA CTTGAGCCCA GGAGTTTGAA ACCAGCCTGG GCAGCATAGT 2160
GAGACCCTGT 2170