EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS002-01466 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr10:73526420-73528080 
Target genes
Number: 3             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1867982chr1073527047hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TBX21MA0690.1chr10:73526543-73526553TTCACACCTT-6.02
TBX2MA0688.1chr10:73526542-73526553ATTCACACCTT-6.02
TFAP2CMA0524.2chr10:73527470-73527482TGCCCTGGGGCT-6.11
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_02126chr10:73524367-73528032Aorta
SE_02934chr10:73526148-73527997Bladder
SE_04467chr10:73524244-73527791Brain_Anterior_Caudate
SE_06313chr10:73522866-73528610Brain_Hippocampus_Middle
SE_09212chr10:73519913-73539677CD14
SE_10507chr10:73526194-73535094CD19_Primary
SE_11555chr10:73525717-73536174CD20
SE_11867chr10:73525696-73533295CD3
SE_13733chr10:73526586-73527822CD34_Primary_RO01536
SE_14459chr10:73526218-73535033CD4_Memory_Primary_7pool
SE_15435chr10:73527858-73529997CD4_Memory_Primary_8pool
SE_15862chr10:73526784-73527682CD4_Naive_Primary_7pool
SE_16389chr10:73526488-73527484CD4_Naive_Primary_8pool
SE_16982chr10:73526639-73528052CD4p_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_20879chr10:73526279-73527855CD8_Memory_7pool
SE_21529chr10:73526336-73527747CD8_Naive_7pool
SE_21976chr10:73527911-73534794CD8_Naive_8pool
SE_22329chr10:73522842-73535294CD8_primiary
SE_23531chr10:73524507-73528093Colon_Crypt_1
SE_23810chr10:73524399-73527973Colon_Crypt_2
SE_24957chr10:73524359-73528104Colon_Crypt_3
SE_26143chr10:73524367-73534193Duodenum_Smooth_Muscle
SE_26620chr10:73524294-73528963Esophagus
SE_28398chr10:73525468-73531080Fetal_Intestine
SE_29438chr10:73525430-73530510Fetal_Intestine_Large
SE_31197chr10:73526977-73527651Fetal_Thymus
SE_31624chr10:73524419-73528897Gastric
SE_37028chr10:73521981-73535534HSMMtube
SE_40874chr10:73524079-73535781Left_Ventricle
SE_42187chr10:73520149-73536258Lung
SE_44709chr10:73522832-73534109NHDF-Ad
SE_49200chr10:73524322-73528938Right_Atrium
SE_50063chr10:73522901-73536984Sigmoid_Colon
SE_52331chr10:73525159-73531553Skeletal_Muscle_Myoblast
SE_52370chr10:73523085-73535246Small_Intestine
SE_53294chr10:73524204-73537013Spleen
SE_55134chr10:73526604-73527141Thymus
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: 2             
ChromosomeStartEnd
chr107352643773526878
chr107352689673527242
Enhancer Sequence
GTCACATTTA GTTCTCATAA CACCCCCAAC ATGGGTGGTA TCATCCCTAT TTTAAAGATG 60
AGGAAACAGA CTCAGAGAAG TGACTTGCCC AAGGCCACAC AGTGCTGTGT GACTGAGCTG 120
AGATTCACAC CTTGGACAGG CCAGCACTGC AGACAGGAAG AGCCACCCAC CTCTCCAGAA 180
CCCTCCAGTG GGCAGGCGGG GCTGATGCCT CATCCTTCAG CTATTTAGAA AAAATGAACT 240
GACCGTGCAT TGACCTCCAC GCCCTCCGTG CAACATTCCT GCTCTGCCTC AGACCCAAGC 300
TGAAAACATC ATTCTTTCAT TCCACAAATA TTTACCAAGG TCCTAACATG GGCCAGGCCC 360
AGGCAGGGAG GCTGTGGGGA TGCAGAGTTC CATCAGGGGC ATCTGCTCAG AACTTGGGCC 420
TGGACCTGTG CCTGAGATTT CTAGCTGTGG CACCCTCAGA TGTTTCTGTC CCAGTACAAG 480
GGAAAGGAGC TCTTGTTGGC ATCTTCTCAG AATGCCAGTT TTTGTGACCT TCACCTCTCT 540
CCACCCAGCA GGCCCCGGGT GACCCCTGTG AGTGTGCACG GGATGGGTGT GTGTGGGTGT 600
GGACAGGCCT GTGTATTTTT CATGACAGGG CGTGAGCTTA GCCCACAGTC GCCAAGGCAA 660
CGCCCTAGCC TTTGGAGGTG GGACCCAAGC TTGGTTAGTC GGGCCTAGGA AGCCCCACCC 720
AAACAGCTGA ACTCTGACCA GCTGCTAGAG GTTGTCAAGT AAACAGTTAT TAATTGCCTG 780
CTGTGGCTGG CCCTGCACTA GATGCAAAAG GTCCCGTCCT TGGTCTCACA GGACATCCCA 840
AAGAGAATGG GACCTGGTTC CAGCTCCCCG CCAGGCCCCA TCCCCCAGGA TGGTCCACAG 900
GCTGGGGCTG GGGCTGTAGG AAAAGACTAT GTTCTGTCTT TATCAAGATG CAGAGGGAAA 960
CAGAGGCATG GATCAATCAG GACTGGGGCT GCCAAGGCTA AGAAAGGAAG CGTCACAAGG 1020
CATAGGCTCA GGGCCTGAAG CCAGCAAGTC TGCCCTGGGG CTTTCTGGCC AGTGAGGACA 1080
AAGGGCATCT CAGATGTGTT TATTGATACC TGCCCCCGCA GGAAGTGTCC ATTCACATCA 1140
GACCAAGGGG GCTGGGAAGG GGAAGCCAGG CTCTATTGAA GGAAGCGGCA CTTCCAGCAC 1200
CTTGGGAAAG CCTCCGTGCA TCCGGGGCTG GAGCTGGAGG CTAGCATGCC TCCCCAGGGA 1260
GGGCCTAGGC AGCTGGCCAG AGGTCCCGGC CCGTGGATGC TTCTGTGGAT GAACCCCTCC 1320
CAGACTCCCC AGGCCCTTTT GGAGGAGGAC TGTGTGCAGC TCAGGCTCCC GGCTCCAGCC 1380
AGCCACCCTC ACGCTTCTAT GCTGTGAAGA CGTCCTCAGG GTCCAGCTCA AGTCTTTTTG 1440
CCCCCTACTA CTCTGTGCCA GGCATCATTC TAAGTGCTTG TTTGTTTGGT TGGCTTTGTT 1500
GCTGTTGTTG TTGTTGTTGT TGTTTGAGAT GGAGTCTCGC TCTGTTGCCC AGGCTGGAGT 1560
TCAGTGGTGC AATCTCAGCT CACTGCAACC TCCGCCTCCC AGGTTGAAGC AACTCTCCTG 1620
CCTCAGCCTC CCGAGTAGCT GGGACTACAG GCACCCGCCA 1660