EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS093-29772 
Organism
Homo sapiens 
Tissue/cell
HL-60 
Coordinate
chr8:37754250-37756580 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs71515732chr837755638hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr8:37755954-37755969GAGGTCAATAGTTCA+7.41
RARAMA0729.1chr8:37755954-37755972GAGGTCAATAGTTCAAGA+6.96
RREB1MA0073.1chr8:37755426-37755446CCCCCAACCTCCACCCACCC+7.06
ZNF263MA0528.1chr8:37755420-37755441TCCCCTCCCCCAACCTCCACC-6.03
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_09599chr8:37753801-37755988CD14
SE_09599chr8:37756136-37763918CD14
SE_10497chr8:37754508-37755972CD19_Primary
SE_11173chr8:37752662-37758580CD20
SE_14010chr8:37752809-37758979CD34_Primary_RO01536
SE_14790chr8:37752502-37759379CD4_Memory_Primary_7pool
SE_20173chr8:37754040-37756041CD56
SE_21238chr8:37752701-37755994CD8_Memory_7pool
SE_21238chr8:37756156-37759111CD8_Memory_7pool
SE_23170chr8:37754183-37755979Colon_Crypt_1
SE_23170chr8:37756191-37757141Colon_Crypt_1
SE_23891chr8:37755064-37755804Colon_Crypt_2
SE_23891chr8:37756219-37757128Colon_Crypt_2
SE_24768chr8:37754344-37756052Colon_Crypt_3
SE_24768chr8:37756186-37758997Colon_Crypt_3
SE_26135chr8:37753635-37755885Duodenum_Smooth_Muscle
SE_26135chr8:37756209-37757133Duodenum_Smooth_Muscle
SE_27862chr8:37753712-37756122Fetal_Intestine
SE_27862chr8:37756160-37759334Fetal_Intestine
SE_28713chr8:37752720-37759515Fetal_Intestine_Large
SE_32119chr8:37754137-37756045Gastric
SE_32119chr8:37756150-37759016Gastric
SE_42881chr8:37754105-37756027Lung
SE_42881chr8:37756188-37758975Lung
SE_47899chr8:37754317-37754684Pancreas
SE_47899chr8:37755006-37755802Pancreas
SE_47899chr8:37756248-37757108Pancreas
SE_50695chr8:37754061-37756012Sigmoid_Colon
SE_50695chr8:37756196-37759039Sigmoid_Colon
SE_52841chr8:37754114-37756070Small_Intestine
SE_52841chr8:37756190-37757145Small_Intestine
SE_58531chr8:37727988-37756036Ly1
SE_61393chr8:37737268-37774158HBL1
SE_62701chr8:37728353-37762703Tonsil
SE_65617chr8:37754378-37758993Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr83775500037755600
Enhancer Sequence
AATCCAGGAA CCCAGAAACA TCTTACAAAC ATCAATTAAG TCTGGCAACA TGCTCTATTT 60
ACAAATAGAG AAACTTGGGT GTTTAGGGAC AGAGAAGCCC AACAATGAGT CAGGGCTGCT 120
GTGGGCACTG GACCCAGGAC TCTGGAATCT CCATCTCTGG CAGGGAGATG TGATCTACCT 180
CTCAAGGGGA TAAAATGTCC ACATAAGAAA CAGGTGGCAG AGAAGGAAGT GAATACACAC 240
ATGTTGGGAT GGCGCAAGAC AACGGATGGC CAACAGCACC CATTTGAAGC TGAAGGGAAG 300
CCAACCCACC ACCCCCAGTG TCATTTAATC AGATGGAAGA TCAGCATTGC TGCAGCCCCT 360
CCTTAGCAAA AACACTGCTC ACCTTATGGC TTGTAAATTG ATGCTGTGAG ATACCCCATC 420
CATCCTCACA TCAAGGCTAG TTTTATCTGA TGTGAGTTCA GAAATGCCTA TTCATCTCTG 480
GCCAGGTAAG TTTGCATCAT CAAATATTCC ATTTGCAAGC CTACATGCTG AAATGGAACC 540
CACCCCACAG TAAAGGGAGC CTCCAGAGGA CAAACCCTCT GGCTTTTCCT GTCTCCCACA 600
GAAGGGAAAG TTAAAAGGCT ATGTATATCT AAAACACACA AAGCAAATCA GTGTGATTCC 660
TAGACTATAG GCTTTCGGTG CTAACTGACT GGCCTGTGTA TTTAAGATCT AACAAAGTAA 720
CCAGCTAAGC TAATCGAGGC TAGCTTTGGC ATACTAGATG AACATAATCG AACGTTCCTT 780
TGGGTGAAGC ACTGCCCTTT CCGAACACCT GTGAAACAAA TAATTCGGTA ATATCATGGA 840
GTGAATGGTT TTTGCCCAGT TTTTACTGCA GAAGTGAAAT AACCTGACAC AATCTTTGGG 900
AGCTACAGGC GAGCAGACAT CCACCAGGAT TAGGACCAGA GAGAAGAACT CTACCAACTC 960
CAAAAGGAAA CAATGCCCAG TTCTGCTCCG TCAAGGGCCC ACCCGGGCTC CTTCCAACCT 1020
GGAGAAATCT TTACTAACAT GGGGCCCAGG GCACACACCA CACTGTTGTA ACATTCTTTC 1080
TGTAGGGGCA AATTCTCTTC ACCAACCCCC TAGGCAAGTA TGAGGTAGGG GAAGGGGTTA 1140
GCAAGTCATG TGACAGCCGG CAAACGCCAT TCCCCTCCCC CAACCTCCAC CCACCCCGCA 1200
TTGTAAAGGC GTTGCGCCCG GGGTTAGCCT TTAGGGTGGG GGTGTCAGCT GGTTTCATGC 1260
CTCCTGTTCC TCTGCCCTGC GCCCTGGCCC AGTCATTCTC GGCTCGAAGT GTTCTTCTAT 1320
TCAGTGAAAT ACCCAGGAGG CCTTCCACCC AAGCGAAGGC GAGTATCAGA CACGGGCTAC 1380
CACCCTAGTA AGAAGAAGGC ACCTGCCCAC GTATAGTTGG AATTCATCTA AAATTCACTT 1440
AGTGCTTACT GTGTGCCAGA CGCTGAGGGG CGTCCTGCAG ATTCAAAAGC GCCCCAGGCC 1500
CGGCGCGGTG GCTCACGCCT GTAATCCCAA TACTTTGGGA GGCCGAGGTG GGCGGATCAC 1560
CTGAAGTCAG AAATTCGAGA CCAGCCTGGC CAACACGGTG AAACCCCGTC TCTACTAAAA 1620
ATACAAAAAT TAGCCGGGCG GGCCGGGCGC GGTGGCTCAC GCGTGTAATC CCAGCACTTT 1680
GGGAGGCCGA GGTGGGTGGA TCACGAGGTC AATAGTTCAA GACCATCCTG GCCAATCTGA 1740
TGAAACCCCG TCTCTACTAA AAATACAAAA ATTAGCCGGG CGTGGTGGCG CACGCCTGTA 1800
GTCCCAGCTA CTCGGGAGGC TCAGGCAGGA GAATCGCTTG AACCCAGGAG GCGGAGGTTG 1860
CAGTGAGCCG AGATCGTGCC ACTGCACTGC AGCCTGGCGA CAGAGTGAGA CTCAGTCTCA 1920
AAAAAAAAAA AAAAAAAATT AGCCGGGCGT GGTGGTGCGC GCCTGTAATC CCAGCTACTC 1980
GGGAGGCTGA GGCAGGAGAA TCACGTGAAC CTGCGAGGCG AAGTTTGCAG TGAGCTGAGA 2040
TCGTGCCATT GCCATTGCAC TCCAGCCCGG GCGACAGAGA CTCTGTCTAA AAAAAAAAAA 2100
AAAAAAAGCG CCCCAGATAC GGCCCCTTCT TCCAAGAAGA CCCAAAGCTG GCAGAGCTGG 2160
GCGGGACAGC CGCAGAAGGG GAAGCCAGGT GAGAACACCA GCACCGGCCG AGGGCTCCGT 2220
CCCGAAAGGC CTTCCCCGCT GCTGCCCGGC TTACTCTCGA AGGGTCCAGC GCCCAGACCG 2280
CCCTGCCGGA GGGGTCCGCG CCCCCAGGCC GGGCCCTCCC CTCCCCGCCC 2330