EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-05771 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr10:73528520-73529730 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10999992chr1073528898hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr10:73529251-73529262TAAGTAAATAT+6.14
SPIBMA0081.2chr10:73529404-73529416AAAGGGGAAGTG+6.07
Number of super-enhancer constituents: 53             
IDCoordinateTissue/cell
SE_02126chr10:73528123-73528920Aorta
SE_02126chr10:73529220-73534492Aorta
SE_02934chr10:73528117-73528935Bladder
SE_02934chr10:73528955-73533818Bladder
SE_04467chr10:73529333-73535298Brain_Anterior_Caudate
SE_06313chr10:73529027-73537202Brain_Hippocampus_Middle
SE_09212chr10:73519913-73539677CD14
SE_10507chr10:73526194-73535094CD19_Primary
SE_11555chr10:73525717-73536174CD20
SE_11867chr10:73525696-73533295CD3
SE_13733chr10:73528072-73533652CD34_Primary_RO01536
SE_14459chr10:73526218-73535033CD4_Memory_Primary_7pool
SE_15435chr10:73527858-73529997CD4_Memory_Primary_8pool
SE_15862chr10:73528269-73530045CD4_Naive_Primary_7pool
SE_16389chr10:73528051-73534117CD4_Naive_Primary_8pool
SE_16982chr10:73528073-73533985CD4p_CD225int_CD127p_Tmem
SE_17364chr10:73520062-73535154CD4p_CD25-_CD45RAp_Naive
SE_17829chr10:73522939-73535186CD4p_CD25-_CD45ROp_Memory
SE_18298chr10:73519827-73535875CD4p_CD25-_Il17-_PMAstim_Th
SE_19115chr10:73520065-73535185CD4p_CD25-_Il17p_PMAstim_Th17
SE_20080chr10:73525819-73535313CD56
SE_20879chr10:73527995-73534359CD8_Memory_7pool
SE_21529chr10:73528231-73534294CD8_Naive_7pool
SE_21976chr10:73527911-73534794CD8_Naive_8pool
SE_22329chr10:73522842-73535294CD8_primiary
SE_23531chr10:73528126-73534311Colon_Crypt_1
SE_23810chr10:73528169-73528907Colon_Crypt_2
SE_23810chr10:73529148-73530087Colon_Crypt_2
SE_24957chr10:73528132-73529848Colon_Crypt_3
SE_25673chr10:73528060-73534177DND41
SE_26143chr10:73524367-73534193Duodenum_Smooth_Muscle
SE_26620chr10:73524294-73528963Esophagus
SE_26620chr10:73529081-73534644Esophagus
SE_28398chr10:73525468-73531080Fetal_Intestine
SE_29438chr10:73525430-73530510Fetal_Intestine_Large
SE_31197chr10:73528252-73531379Fetal_Thymus
SE_31624chr10:73524419-73528897Gastric
SE_31624chr10:73529147-73534199Gastric
SE_37028chr10:73521981-73535534HSMMtube
SE_40874chr10:73524079-73535781Left_Ventricle
SE_42187chr10:73520149-73536258Lung
SE_44709chr10:73522832-73534109NHDF-Ad
SE_49200chr10:73524322-73528938Right_Atrium
SE_49200chr10:73529144-73534161Right_Atrium
SE_49982chr10:73528141-73529932RPMI-8402
SE_50063chr10:73522901-73536984Sigmoid_Colon
SE_52331chr10:73525159-73531553Skeletal_Muscle_Myoblast
SE_52370chr10:73523085-73535246Small_Intestine
SE_53294chr10:73524204-73537013Spleen
SE_55134chr10:73529228-73530172Thymus
SE_59774chr10:73453131-73536958Ly4
SE_62254chr10:73471895-73536454Tonsil
SE_64128chr10:73524230-73531553HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr107352906473529499
Enhancer Sequence
GCCACTGTGC TCGGCCTCAT TCTAAACACT TTTACATAGA TTAGTTTATG TAATCCTTCC 60
ACCCTATGAG GTAGGTACTA GTATCATCTC CATTTTACAG ATGAGAAAAC GGAAGCACAG 120
AGAGATTAGT ATCTTGCCCA CAGCCTCACA ACTAATAAGT GATGGTGTCA GGATCTGAAC 180
CCAGGTAGTC AGCCTCTGGA GGTCTGGTGC CATCTGACTA CTCTCTAGAG AATAGAGGTA 240
GCTGGGGACT GACTGGAGGC CCCACCTCCT TCTTGAAGAC GGACAAATGT CATGACCAAT 300
GAAAGCCCAG CTTGCCTGGC CACGTCTACC ACATAGTTTT ACTTTTGGTT TTACATTAAA 360
TAACATTGAA TCATATATAG AAGAGGTTAT TCCCTTTACA ATTATTTCAG TCCTGATTAC 420
ATCAAAGAGA AAGTCTCAGT TTGATGCTAA TATGTCTCTA AAACATTTGC TAATCTCCTT 480
TTCTTTTTAA ATTTTATTTT ATTTTAATTT TTTGCAAGGG AAAGCAGCAG TTTTCAGACT 540
CCGAGCCTTC CCAGGCTAAA GTTTCCAACT AGAATTCAAT ACCCTTATAT GGTTTTCCTG 600
TTACGTTCTT TTATGGTTTT GTTCTATTTA TGACAAGTGA TACTGGCTTT CCACTAATGA 660
CAGCGATAAA AAGTTTCCTT TTAAAGATCT ACATACTCAA ATAAAAGAAT GAGTAGATTT 720
AAAGAAAAAA ATAAGTAAAT ATTATGAAAG GCAGACACTG CAGAGATCAC AAAGGTGATA 780
AGCAAATGAC TGAAGCTAGG GAAACACCAT CATGGAATTA ACCTTCAGAG GAGGGTGGTC 840
AGCCTCACTG AGACCACGTC ACCCAACCTG TCCATTGCAC AGACAAAGGG GAAGTGTGTG 900
TTTGTGTTCC CATGATGAGT GAACAGCAGA GGCAGGGTTT GACCCCAGGT CCCCATGGGA 960
AATAAGATCC TACGCAGAAA GGCTAAAGGA ATGGGCTTGC TTGGCTTGGT AAGTAGCAGA 1020
GCAACCTCAT TATTGGATTA CTGATGAGAA AGATGGTGGC CACTGTCTTT GTCTTTGGTG 1080
ATGGCCAGCC AAAGTGAATG GACCGAATGT AAAAAGATCA GATGTAAGAA AGATCCACCA 1140
AGATAAGCAA ACCCAGGGCC AGGCTTGCCT TCAAGTTGCA ATGTCCCCAT CTCCTGACAA 1200
CTTTAAGAAG 1210