EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS085-00344 
Organism
Homo sapiens 
Tissue/cell
Heart 
Coordinate
chr10:73486960-73488550 
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
ATTAGCCGAC TTGTTCAGGG TCACACAGCG GTAAGGGTGG AGCCAGGCTT CATGCCTTGG 60
CAGCCAGCTT GAGCCTGTCC CCTTAACCAC TACACTCCAC TGCCTCACAT AAGCCTCTTC 120
AAAGCCCAGT CAGAAACCAC TGCCTCATCC CCACAGGGTA ATTTTAAGGT GAGAATTTGA 180
GGGCTGGCCC CTGGGGCAGG TGCTTGGTGG CACTGTAGTA CACAGCCTCC ACACCCATGA 240
GACCCGGGAG AGCTGGGGGC CTTCCTGAAG GCAATGTGGG GACTCTGGCT TTCCGCTGGA 300
CTCATTTTCC CAGCAGCAGG GGAGAGACGG CTTGCAGGAA CCATCCACAT CCTCCAGTTC 360
CTGCCTCAGA GACCGGGGAC AGCCCCAGTG AGGGGCCGGG GAGTACAGAG TGAGACAGTC 420
CCCTTAGAGA CTGGGTGTCT CAGGGTGTTC ACGACACATA CACACACACA CACGCACATA 480
TGCCCACGCA CACCTCCTCT CCCTGTCCTC CTAACCACTA GCACCCCATT TTGCAGATGA 540
GGAAACTGAG GCAAAGCACT GCACTGGCAC AGCACTGGAC AGGCACAGCA CTGGACAGAA 600
AGCAGGTCTG GTTCTCCAGG AAGCCCAGTT GCTCCCACTT GCTCAGCAAG AACCTGACAG 660
ACCTCTGCTT CCTGTACATC TGTGCCTCTC AGGTTTGCAA ACCATCTTGC CTCCTCCTGT 720
CTCTGCTGCT AAAAACAGGC TGAAACCGAC CAGAGGCTGG TGGCATGTAG CCAGACTCAT 780
GGAGGACAGG CCACACCCCA GCTCCCTGCC ACCTCTCTCA TCTTGTCATT GTACTGTCAG 840
CCTGGCCCTG TTTTTTCCCC ACAACCCTTG GAGTCAAGGT CATTTGGACA AGCAGATTGA 900
GGAAGGGTAA GGCGCACAGT TTTGCAAGAG GAGTGGTTAG TTTCTGTTTA CCGAAAAAGA 960
GTTCCTGAAA TTCATCCATG CAAACTCCCC CCCGCACCCA CCCTACCCAG GATCTTCCCC 1020
AGCCAAGTTC TGGGTGAAGC CAAATTTAGG TTCCAGCCTG TGAACAGCTG TGCTCTGGAG 1080
TGGACATGTT AGTTTGCATA GTGGGTTCTG GGTGTCTGGA CATGAAAATT CTAATGACAC 1140
AGCAGAGCTT TGGGAACCCT AGAAGCAGCG ATGCAGAGAA ACTTTTACAC CCATATGCCT 1200
CTCTGCCCCC AGCCCTGCCA CCCTCCCCAC CCCAGAGTCC TCCACTGGTC AGGCTGCTGT 1260
TTTCGGCTTC TACCAGCCAG AAGCTCTGTC ACTTCTCTCC AGCTGATTCC CAGCTAATCC 1320
CCAAAGAGAA AGCAGGGCTG ATCCCAGAGG CAGTGACCAG ATGCCAGACA CACACGCCTC 1380
TGCTGCACAT GCAGAGGCCC CTCCCTTAGT GCTGGTCACC ACATGCAAAG TCTGTATGGG 1440
GCATCACAGC CCCTTCCCCA TTTGCTTCCC TCTCTACTTT GCTGGCAAGT TCCTACCGGC 1500
CCCAGCTCTG TTTGGCTGGG AAGAGGGTGC CTCTCCTGTT CTGGGGCCAG CTCACCCCAG 1560
CATAGAGCAA AGAGCTAAAA GCTAAAAACT 1590