EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-24164 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr8:37753600-37756580 
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: 36             
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_65617chr8:37753039-37754357Pancreatic_islets
SE_65617chr8:37754378-37758993Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr83775420037754600
chr83775500037755600
chr83775396837754000
Enhancer Sequence
GTGGATCACC TGAGGTCAGG AGTTCGAGAC CAGCCTGACC AACATGGTGA AACCCCATCT 60
CTACTAAAAA TACAAAAATT AGCCGGACAT GGTGGCGGGT GCCTGTAATC CCAGCTACTC 120
GGGAAGCTGA GGCAGGAGAA TTGCTAGAAC CCAGGAGGCA GAGGTTTCAG TGAGCCGAGA 180
TCACGCCATT GCACTCCAGC CTGGGGGACA GAGTGAGACG CCATCTCAAA AAAAAAAAAA 240
ATTCCACCTT TCAATGCATA TCTTATTCTT TAAATCTCAG CTATCTTGGG CACCAGGGCA 300
TCAGACAGCA CCCTTGGCAC CTTGGAAAGT CCCAGAAAGT TGTAGATGGA AAGTGGAAAT 360
TTCATCTACC CATAGAGATG CAAAGAAGCC TTCCTTTGCA GTTATTTTAA GAAAGAAAAA 420
AAAATCAACT AAGCACCATT TTCCTGGAAG TCAATACTGT GACTAGGTGG TAATCGGTTC 480
ACATAATAGG TGGGAGTTAT TGTATAGGTT TAGGGTTACA TTGGATAAAA TAAGAAAAAT 540
GAAGATGCAG AGACTGAACT CTTCCTGAAA AAAAGAGAGC TCAAGGTTTC AATCTCTCAC 600
AAAGCAGTTG CCAACCTTTT CAATCACTTC TTGGATACAT TGGCCCCATT AATCCAGGAA 660
CCCAGAAACA TCTTACAAAC ATCAATTAAG TCTGGCAACA TGCTCTATTT ACAAATAGAG 720
AAACTTGGGT GTTTAGGGAC AGAGAAGCCC AACAATGAGT CAGGGCTGCT GTGGGCACTG 780
GACCCAGGAC TCTGGAATCT CCATCTCTGG CAGGGAGATG TGATCTACCT CTCAAGGGGA 840
TAAAATGTCC ACATAAGAAA CAGGTGGCAG AGAAGGAAGT GAATACACAC ATGTTGGGAT 900
GGCGCAAGAC AACGGATGGC CAACAGCACC CATTTGAAGC TGAAGGGAAG CCAACCCACC 960
ACCCCCAGTG TCATTTAATC AGATGGAAGA TCAGCATTGC TGCAGCCCCT CCTTAGCAAA 1020
AACACTGCTC ACCTTATGGC TTGTAAATTG ATGCTGTGAG ATACCCCATC CATCCTCACA 1080
TCAAGGCTAG TTTTATCTGA TGTGAGTTCA GAAATGCCTA TTCATCTCTG GCCAGGTAAG 1140
TTTGCATCAT CAAATATTCC ATTTGCAAGC CTACATGCTG AAATGGAACC CACCCCACAG 1200
TAAAGGGAGC CTCCAGAGGA CAAACCCTCT GGCTTTTCCT GTCTCCCACA GAAGGGAAAG 1260
TTAAAAGGCT ATGTATATCT AAAACACACA AAGCAAATCA GTGTGATTCC TAGACTATAG 1320
GCTTTCGGTG CTAACTGACT GGCCTGTGTA TTTAAGATCT AACAAAGTAA CCAGCTAAGC 1380
TAATCGAGGC TAGCTTTGGC ATACTAGATG AACATAATCG AACGTTCCTT TGGGTGAAGC 1440
ACTGCCCTTT CCGAACACCT GTGAAACAAA TAATTCGGTA ATATCATGGA GTGAATGGTT 1500
TTTGCCCAGT TTTTACTGCA GAAGTGAAAT AACCTGACAC AATCTTTGGG AGCTACAGGC 1560
GAGCAGACAT CCACCAGGAT TAGGACCAGA GAGAAGAACT CTACCAACTC CAAAAGGAAA 1620
CAATGCCCAG TTCTGCTCCG TCAAGGGCCC ACCCGGGCTC CTTCCAACCT GGAGAAATCT 1680
TTACTAACAT GGGGCCCAGG GCACACACCA CACTGTTGTA ACATTCTTTC TGTAGGGGCA 1740
AATTCTCTTC ACCAACCCCC TAGGCAAGTA TGAGGTAGGG GAAGGGGTTA GCAAGTCATG 1800
TGACAGCCGG CAAACGCCAT TCCCCTCCCC CAACCTCCAC CCACCCCGCA TTGTAAAGGC 1860
GTTGCGCCCG GGGTTAGCCT TTAGGGTGGG GGTGTCAGCT GGTTTCATGC CTCCTGTTCC 1920
TCTGCCCTGC GCCCTGGCCC AGTCATTCTC GGCTCGAAGT GTTCTTCTAT TCAGTGAAAT 1980
ACCCAGGAGG CCTTCCACCC AAGCGAAGGC GAGTATCAGA CACGGGCTAC CACCCTAGTA 2040
AGAAGAAGGC ACCTGCCCAC GTATAGTTGG AATTCATCTA AAATTCACTT AGTGCTTACT 2100
GTGTGCCAGA CGCTGAGGGG CGTCCTGCAG ATTCAAAAGC GCCCCAGGCC CGGCGCGGTG 2160
GCTCACGCCT GTAATCCCAA TACTTTGGGA GGCCGAGGTG GGCGGATCAC CTGAAGTCAG 2220
AAATTCGAGA CCAGCCTGGC CAACACGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT 2280
TAGCCGGGCG GGCCGGGCGC GGTGGCTCAC GCGTGTAATC CCAGCACTTT GGGAGGCCGA 2340
GGTGGGTGGA TCACGAGGTC AATAGTTCAA GACCATCCTG GCCAATCTGA TGAAACCCCG 2400
TCTCTACTAA AAATACAAAA ATTAGCCGGG CGTGGTGGCG CACGCCTGTA GTCCCAGCTA 2460
CTCGGGAGGC TCAGGCAGGA GAATCGCTTG AACCCAGGAG GCGGAGGTTG CAGTGAGCCG 2520
AGATCGTGCC ACTGCACTGC AGCCTGGCGA CAGAGTGAGA CTCAGTCTCA AAAAAAAAAA 2580
AAAAAAAATT AGCCGGGCGT GGTGGTGCGC GCCTGTAATC CCAGCTACTC GGGAGGCTGA 2640
GGCAGGAGAA TCACGTGAAC CTGCGAGGCG AAGTTTGCAG TGAGCTGAGA TCGTGCCATT 2700
GCCATTGCAC TCCAGCCCGG GCGACAGAGA CTCTGTCTAA AAAAAAAAAA AAAAAAAGCG 2760
CCCCAGATAC GGCCCCTTCT TCCAAGAAGA CCCAAAGCTG GCAGAGCTGG GCGGGACAGC 2820
CGCAGAAGGG GAAGCCAGGT GAGAACACCA GCACCGGCCG AGGGCTCCGT CCCGAAAGGC 2880
CTTCCCCGCT GCTGCCCGGC TTACTCTCGA AGGGTCCAGC GCCCAGACCG CCCTGCCGGA 2940
GGGGTCCGCG CCCCCAGGCC GGGCCCTCCC CTCCCCGCCC 2980