EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-14455 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr17:17727130-17728870 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GabpaMA0062.2chr17:17727622-17727633GTCACTTCCGG-6.14
Stat4MA0518.1chr17:17727626-17727640CTTCCGGGAAACTG+6.15
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00344chr17:17720528-17729084Adipose_Nuclei
SE_00881chr17:17727083-17731669Adrenal_Gland
SE_02989chr17:17727076-17728929Bladder
SE_03206chr17:17727157-17728124Brain_Angular_Gyrus
SE_03206chr17:17728290-17728719Brain_Angular_Gyrus
SE_06389chr17:17714600-17732045Brain_Hippocampus_Middle
SE_12214chr17:17727074-17728410CD3
SE_12688chr17:17727507-17728266CD34_adult
SE_14781chr17:17723184-17730304CD4_Memory_Primary_7pool
SE_17733chr17:17725350-17731822CD4p_CD25-_CD45RAp_Naive
SE_20996chr17:17727041-17729030CD8_Memory_7pool
SE_22841chr17:17727091-17730952CD8_primiary
SE_23173chr17:17727060-17728976Colon_Crypt_1
SE_23799chr17:17727010-17728952Colon_Crypt_2
SE_24725chr17:17724801-17730019Colon_Crypt_3
SE_26625chr17:17720649-17731613Esophagus
SE_27885chr17:17727076-17730457Fetal_Intestine
SE_28899chr17:17727037-17730445Fetal_Intestine_Large
SE_31441chr17:17724607-17731734Gastric
SE_33480chr17:17727125-17729049H2171
SE_34007chr17:17727154-17731941HCC1954
SE_34262chr17:17727051-17732342HCT-116
SE_34795chr17:17727093-17730805HeLa
SE_36316chr17:17727079-17730243HMEC
SE_39928chr17:17727115-17730848K562
SE_42125chr17:17727048-17730383Lung
SE_44649chr17:17727128-17728161NHDF-Ad
SE_46728chr17:17727084-17728925Ovary
SE_48150chr17:17721465-17732285Psoas_Muscle
SE_50203chr17:17720773-17732067Sigmoid_Colon
SE_51164chr17:17723081-17731665Skeletal_Muscle
SE_52449chr17:17727010-17730923Small_Intestine
SE_53726chr17:17726515-17728817Spleen
SE_54926chr17:17727086-17730019Stomach_Smooth_Muscle
SE_57042chr17:17727063-17728944VACO_400
SE_57388chr17:17727145-17727919VACO_503
SE_60863chr17:17723038-17753684DHL6
SE_61850chr17:17725940-17761172Toledo
SE_62888chr17:17723024-17755643Tonsil
SE_63332chr17:17727040-17744985NCI-H82
SE_64851chr17:17727109-17728904NHEK
SE_65718chr17:17713037-17732290Pancreatic_islets
SE_68738chr17:17727198-17728994H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr171772760017728600
chr171772860017728732
Enhancer Sequence
CCCCACCTCC CCACGGCGGC GGGGGCTCGA GTTTCACCCC GCGGCGCTGA ATGGGGTTGG 60
GGTTACTAGC GGACGTCCGC CTTTAACCCG CTCGGTGCCA GCGTCTGCCG GGGTTACTGG 120
CGGTCACTGG CCCTCAGCTC CCGCCCCCTT CGTTAAAGGG TCAAAGCAGA GAAGTCCTGG 180
CCCAACACAC CAGAACTCTG TGTTCGAAAT CACTGGTTCG CTGGCACCCT GAGCGAGCCT 240
TAACCGCTCC AACCCTCCGT TTACTCCTCC AGAAAACAGG ACAGTCATTA TCTCCCTGGC 300
GTCGAATGGT AGAAGGGAGA TAATATGGGT GCAGCACTTA GTACGCAAGA AGCGTTTAAT 360
TAAGGCCAAG GGCTGCCGAG TGGCAGCTGC GGTGGGTGCA GGGACCTCCC CCTTCTAGGG 420
CAGCCCCAGG AAGGGGCCAC CCCTCACCAC AGCGGGGCTG ATGGTCTGGG ATGAGGCCAC 480
TCCTGAAAAC AGGTCACTTC CGGGAAACTG AGGCCTGGAA ATAAGGGTTT CCTGACTGCC 540
AGCACCGATG TCCCTCTGCC AGATGGGTGA AGTCTGCCCC TCCCCCTCAA GGCCTCACAA 600
CCCAGCAGTC ACCAAGTGAG TCCCGACCCA CTATTCATTG TAGGGCCCTG GGAAGCCAGG 660
AAGGGCTGCA GTCCCTAGGA CAGAAGATGG GTAAGGAAGG GGTGACAGGC TCTAGGGTTC 720
TTTTGAGGAG GTGCCTGGGC CTGTCTTCCC TCTTTTGTCA AAGGTAAAAG TTACACACAC 780
ACACACACAC AAAGTGATCA GAGCCTGGCC AGTTGATTTT GCAGCCAAGT AGACCACCAG 840
CAAAGCCTGC CTCTGCCCCA AACTGCAGGC CAGCGCCTCT GCCTGGTCCA CACCCCAGTT 900
GGCTGCAACC TGAGAGGGTG CCTGAACCCT GGGCAGACCC AGCGACTCAG CAGTCCATTG 960
GGGGCTGGGG TCCCTGCGGC CTCAACCTTG CTCTCTATTC AGGACCCTAA GCAAGAAAAC 1020
CCAGCCATGT CTCTCTCGCA ACCTGTCCTC GCCACCGCCG TCCAGCCCAG GCCCTTATTT 1080
CCCAGCTTTG GGAGGTTCAA GGACAACAGA CGGCCTCTCT AGCATGGCCC AACCCTCCCC 1140
TCAGCCCGCG GGTGTTCCCT CACCCCCAAA ACAAAACACA GCATTGCTCT TGGCAAAGGC 1200
TCTGACATGA GTGACTTAAG ACAGGGAAGC GTCCTTGACC CAAAAGCACA CTGAGAGCTG 1260
AACTCCAGGC ATGAGTTCCC CATGGCCTCC CAGCCTGGTT CTTTCATTAC TTTGCTCCCC 1320
AGTTTCTGAG CCTAGAATGT GGTGAGACCA ACAAGCAGAT ACTAGCCTGA GACAGCAGGG 1380
CCAGGGCCAC TGTGAACAGT CAAGCCTGTC CCCTCCCCTT ACCCATCTTG GCTTTACCAC 1440
ATATTCCTGC CTCTTATTGT GTCTTTATTT GTCTCATCTT CCTGCTCTAA CCCCCTCCCA 1500
TCCCACTGAG GAAGCGCGAT GGGAGAGGGC GGTTGCTCTC TGAGCCCCAG GGGCAGCAGA 1560
GTCATTAAAG ACTCTGATGG GGGTGGGGCG GGGGGGGCCT TCCAAGAGGA GGGGGTGTGA 1620
CCTGGGAACA GAGGGCTGGC CCTTGGGCAG AGGGCACAGA CTAAGCTAAG ATGCCCCGAG 1680
GAAGGGGGAA GGGCCTGGGT GCCACTGGCC ATGGCCAGCC TCTGAAACTC AAGGCCTGGC 1740