EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-15962 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr15:31648800-31650630 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Sox6MA0515.1chr15:31648824-31648834CCATTGTTTT+6.02
Number of super-enhancer constituents: 51             
IDCoordinateTissue/cell
SE_03886chr15:31648565-31655882Brain_Anterior_Caudate
SE_04794chr15:31625728-31662350Brain_Cingulate_Gyrus
SE_05780chr15:31615643-31660953Brain_Hippocampus_Middle
SE_06977chr15:31649426-31650446Brain_Hippocampus_Middle_150
SE_07743chr15:31648589-31661204Brain_Inferior_Temporal_Lobe
SE_09581chr15:31639901-31655889CD14
SE_10240chr15:31648675-31655369CD19_Primary
SE_10960chr15:31626557-31662684CD20
SE_11880chr15:31648421-31655860CD3
SE_14523chr15:31648547-31655602CD4_Memory_Primary_7pool
SE_15793chr15:31648906-31650337CD4_Memory_Primary_8pool
SE_15822chr15:31643985-31650779CD4_Naive_Primary_7pool
SE_16411chr15:31648902-31651105CD4_Naive_Primary_8pool
SE_16933chr15:31648740-31650727CD4p_CD225int_CD127p_Tmem
SE_17341chr15:31615669-31661138CD4p_CD25-_CD45RAp_Naive
SE_17846chr15:31627800-31662260CD4p_CD25-_CD45ROp_Memory
SE_18423chr15:31625736-31660967CD4p_CD25-_Il17-_PMAstim_Th
SE_19192chr15:31648594-31655523CD4p_CD25-_Il17p_PMAstim_Th17
SE_20027chr15:31632742-31662471CD56
SE_20872chr15:31648560-31650314CD8_Memory_7pool
SE_21471chr15:31644105-31655331CD8_Naive_7pool
SE_21943chr15:31636903-31660938CD8_Naive_8pool
SE_22346chr15:31627768-31662564CD8_primiary
SE_23077chr15:31649340-31650687Colon_Crypt_1
SE_23726chr15:31648893-31649198Colon_Crypt_2
SE_23726chr15:31649397-31650120Colon_Crypt_2
SE_23726chr15:31650154-31650533Colon_Crypt_2
SE_24682chr15:31649337-31650098Colon_Crypt_3
SE_24682chr15:31650152-31654718Colon_Crypt_3
SE_26685chr15:31648750-31650094Esophagus
SE_30907chr15:31629910-31655826Fetal_Thymus
SE_31418chr15:31648839-31650527Gastric
SE_32685chr15:31648668-31650081GM12878
SE_39693chr15:31648786-31655712Jurkat
SE_40604chr15:31626796-31650659Left_Ventricle
SE_42098chr15:31633786-31650756Lung
SE_43752chr15:31648679-31651041MM1S
SE_47479chr15:31649515-31650494Pancreas
SE_48562chr15:31648591-31650732Right_Atrium
SE_50055chr15:31633725-31655819Sigmoid_Colon
SE_52342chr15:31648650-31655588Small_Intestine
SE_53298chr15:31648645-31650724Spleen
SE_55094chr15:31648698-31650790Thymus
SE_58529chr15:31616151-31660715Ly1
SE_59212chr15:31615375-31658617Ly3
SE_60275chr15:31642507-31659231Ly4
SE_61508chr15:31616115-31660220Toledo
SE_62250chr15:31615508-31660953Tonsil
SE_65426chr15:31647618-31650173Pancreatic_islets
SE_66562chr15:31648786-31655712Jurkat
SE_67212chr15:31648679-31651041MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr153164979031650058
Number: 1             
IDChromosomeStartEnd
GH15I031337chr153162942931662397
Enhancer Sequence
TAATTCACTT AGGAGAATGG GAGGCCATTG TTTTAAGGCT TATATGTCTG GAAATGTCTT 60
GATCCTGGTC TGAGGTTGAT TCACGTTTCT CTGGGTTGAA TCATAGGTGG GAATGGTTTA 120
CTCGTGCGGT TTGGAGCTCT GATGTTGCTG TGGAGAAGAC TGAAGCTTTT CTGATTCTGG 180
CTGTGTGCAC CTCCCGGTCT CTTTGCCTCT CAGGGCCTTT TGGGCTTGTG CCTTTACCAG 240
GGCTTGGAGG TGTGCACGTG TGTGGAGGTG CTTGGCCAAG CTCTGTCCTC TGCAGCGGGC 300
CCGTCGGGTG GCATCTGGAA AACATTCTTG CCACTTTCTT CACGATCACC TCACCTCCTG 360
TGTTCTCAGG GCTGCCTGCA GTTCCTTTTA TTTGGAGCTG TTGGTCTGAT CCTTACATTT 420
TCATATTTTT TCCCTCTTAC CCATCCATTT GTATTTTTGC TCTGTTTTCT GTGAAATTCT 480
CTCAGTGTTC TCTCCCAACC CTGCTATTGG GATTTTTATT TCTGCCACAT TTTTCCTTCT 540
GTATCTTTAC TTTCAGACTC AGGTTTCTAA GCCTTTGCTT TCAAACTCAG GTTTCTAAGC 600
TTCCCTTTTA AAGGCACATG CGGTTCTTGT TTCCGCCAGG CCGTCTATGC GGTGAGGATG 660
TTAGTGACAG CTCTGGAAGT CTTCTCGTTG CGTGGCCTCT GCTCCCTCCA CATCACCTGT 720
CTCTGCTCCT TGGTCTGGGT CTCTTGCCCA CCCACGTCAG GCTCTTCTGC ATTGTCTGCT 780
GATCCTTGAT GTCTGGTGAC ACGGCCCAGA GAGCCTCGAG CTGCGTGGGG GCTTCTGGGT 840
GCCCATCAGG CTCAGCGACG GTGGCCTCCT GTGGGTGGTC TACTGGGCCA TCTCCTTCCG 900
GGTTTTCCCC CAAGAGGAGT GTTCTGCTCC TGCCTGGGGG AGGGAGGGTG GTCCTGCTGC 960
ACACTGGGAG AGAAGCTGGG AGGCAGCACT CTGTGAGTGG GCTGTTCCCC ACACCCCTGT 1020
TCTGGAGGCT GCCCTACTCT GAGCTGGGTC TGGAGTCGTC AGTCCAGAGC TCCCTCCTGT 1080
GTAGACCCTC CCAGAAAGTC AGCCTCTGGT TCCTGGCAGG TGCAGGAAGG GCAAGCAGCC 1140
ATCTGTAAGG TGAGGAAAGA CCTTGTGTCC ACAGCTGCTT TATCTGATGT TCAGGTGCCC 1200
CCCACCAACT GCACCCCCAC CCCCGCCAGA GACTCCCGAG CCTTTGTGGG GAAACGTGGA 1260
TTGCTTCCTT GCCTTCTCTG CTGTCTTTCT AATTTCTTGC TTCCAGATTA TTTTTGTTAC 1320
TCTCTTTCCC TTTTGCTTTG TCTGTTAAAA TCCACTTTCT TTCATTGTAG TGGGATCTGG 1380
GGCTGGAAGG GTGGTGGGTG CCTGTGCCTG ACCTGCCAGC TTTATCCAGA GTTCCTGTTA 1440
GGCCTTTGGT CCAGTGCAGG AGGCGTGGGG AGAGATGAGG GTAAGGTAAG CACTAGGTAG 1500
GGGGCGGCTG AGAGTTGTCC AGCTGTTGGG CAGCCAGCAT CTCCTTTGTT CTTGCCCAAC 1560
AATGTTATCC AGGAGTTTGC CAGAGATACA TCCAGCAATA TCCTGGAAGC AACTGAAGGC 1620
AGCTCACAAG AAGACAGTTG TGCAGTGGAA GGAGGGGGTC CAAACCTAAG GTTGGCAGGT 1680
TGACTATAGT ACAGTTGCGA TTGTCTGCAT TCTTACAGTT TCTGTCAAAA CATCGTTTTC 1740
CCAAGTGGCT GGTCAGCTCC CCTGTGGTTA ACATGCTTGC AGCAATGGAT GAGAGCTCCA 1800
GTTGCTCCAC CAGCATTTAG TATTGTCAGT 1830