EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-07392 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr10:73487280-73488630 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESRRBMA0141.3chr10:73487833-73487844TCAAGGTCATT+6.32
EsrraMA0592.2chr10:73487832-73487843GTCAAGGTCAT+6.32
EsrrgMA0643.1chr10:73487833-73487843TCAAGGTCAT+6.02
GSCMA0648.1chr10:73488272-73488282GCTAATCCCC+6.02
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_02934chr10:73486910-73488715Bladder
SE_09212chr10:73484129-73491054CD14
SE_10507chr10:73485978-73488661CD19_Primary
SE_11555chr10:73485897-73488778CD20
SE_11867chr10:73484726-73488748CD3
SE_13733chr10:73486358-73488127CD34_Primary_RO01536
SE_14459chr10:73483306-73489682CD4_Memory_Primary_7pool
SE_15435chr10:73484590-73488708CD4_Memory_Primary_8pool
SE_15862chr10:73484394-73488163CD4_Naive_Primary_7pool
SE_16389chr10:73485724-73488585CD4_Naive_Primary_8pool
SE_16982chr10:73485320-73488266CD4p_CD225int_CD127p_Tmem
SE_17364chr10:73484300-73489706CD4p_CD25-_CD45RAp_Naive
SE_17829chr10:73483903-73489104CD4p_CD25-_CD45ROp_Memory
SE_18298chr10:73483783-73519050CD4p_CD25-_Il17-_PMAstim_Th
SE_19115chr10:73482362-73488665CD4p_CD25-_Il17p_PMAstim_Th17
SE_20080chr10:73484903-73489563CD56
SE_20879chr10:73485106-73489566CD8_Memory_7pool
SE_21529chr10:73485576-73488462CD8_Naive_7pool
SE_21976chr10:73485746-73488508CD8_Naive_8pool
SE_22329chr10:73484190-73489579CD8_primiary
SE_23810chr10:73485999-73488671Colon_Crypt_2
SE_24957chr10:73485955-73488646Colon_Crypt_3
SE_25673chr10:73485894-73488487DND41
SE_26620chr10:73485943-73489591Esophagus
SE_31197chr10:73485996-73489322Fetal_Thymus
SE_31624chr10:73485741-73488772Gastric
SE_37028chr10:73486037-73492185HSMMtube
SE_39632chr10:73485959-73488525Jurkat
SE_42187chr10:73485498-73489526Lung
SE_46906chr10:73486840-73488598Ovary
SE_49982chr10:73486066-73488620RPMI-8402
SE_50063chr10:73485183-73489646Sigmoid_Colon
SE_52370chr10:73485196-73489499Small_Intestine
SE_53294chr10:73485446-73490497Spleen
SE_55134chr10:73485756-73488660Thymus
SE_59774chr10:73453131-73536958Ly4
SE_62254chr10:73471895-73536454Tonsil
SE_66842chr10:73485959-73488525Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr107348762573488016
Number: 1             
IDChromosomeStartEnd
GH10I071725chr107348495873489596
Enhancer Sequence
GGAGAGACGG CTTGCAGGAA CCATCCACAT CCTCCAGTTC CTGCCTCAGA GACCGGGGAC 60
AGCCCCAGTG AGGGGCCGGG GAGTACAGAG TGAGACAGTC CCCTTAGAGA CTGGGTGTCT 120
CAGGGTGTTC ACGACACATA CACACACACA CACGCACATA TGCCCACGCA CACCTCCTCT 180
CCCTGTCCTC CTAACCACTA GCACCCCATT TTGCAGATGA GGAAACTGAG GCAAAGCACT 240
GCACTGGCAC AGCACTGGAC AGGCACAGCA CTGGACAGAA AGCAGGTCTG GTTCTCCAGG 300
AAGCCCAGTT GCTCCCACTT GCTCAGCAAG AACCTGACAG ACCTCTGCTT CCTGTACATC 360
TGTGCCTCTC AGGTTTGCAA ACCATCTTGC CTCCTCCTGT CTCTGCTGCT AAAAACAGGC 420
TGAAACCGAC CAGAGGCTGG TGGCATGTAG CCAGACTCAT GGAGGACAGG CCACACCCCA 480
GCTCCCTGCC ACCTCTCTCA TCTTGTCATT GTACTGTCAG CCTGGCCCTG TTTTTTCCCC 540
ACAACCCTTG GAGTCAAGGT CATTTGGACA AGCAGATTGA GGAAGGGTAA GGCGCACAGT 600
TTTGCAAGAG GAGTGGTTAG TTTCTGTTTA CCGAAAAAGA GTTCCTGAAA TTCATCCATG 660
CAAACTCCCC CCCGCACCCA CCCTACCCAG GATCTTCCCC AGCCAAGTTC TGGGTGAAGC 720
CAAATTTAGG TTCCAGCCTG TGAACAGCTG TGCTCTGGAG TGGACATGTT AGTTTGCATA 780
GTGGGTTCTG GGTGTCTGGA CATGAAAATT CTAATGACAC AGCAGAGCTT TGGGAACCCT 840
AGAAGCAGCG ATGCAGAGAA ACTTTTACAC CCATATGCCT CTCTGCCCCC AGCCCTGCCA 900
CCCTCCCCAC CCCAGAGTCC TCCACTGGTC AGGCTGCTGT TTTCGGCTTC TACCAGCCAG 960
AAGCTCTGTC ACTTCTCTCC AGCTGATTCC CAGCTAATCC CCAAAGAGAA AGCAGGGCTG 1020
ATCCCAGAGG CAGTGACCAG ATGCCAGACA CACACGCCTC TGCTGCACAT GCAGAGGCCC 1080
CTCCCTTAGT GCTGGTCACC ACATGCAAAG TCTGTATGGG GCATCACAGC CCCTTCCCCA 1140
TTTGCTTCCC TCTCTACTTT GCTGGCAAGT TCCTACCGGC CCCAGCTCTG TTTGGCTGGG 1200
AAGAGGGTGC CTCTCCTGTT CTGGGGCCAG CTCACCCCAG CATAGAGCAA AGAGCTAAAA 1260
GCTAAAAACT CCTGGGCTCC AGCAATCCTC CCGCCTCAGC CTCCCTAGTA GCTGGGATTA 1320
CAGATGCATG TCACCACCCC CGGCTAATTT 1350