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

TagContent
EnhancerAtlas ID
HS108-04301 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr1:226830210-226832460 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PRDM1MA0508.2chr1:226830224-226830234TCACTTTCAC+6.02
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_03159chr1:226831402-226831814Brain_Angular_Gyrus
SE_03869chr1:226830187-226835847Brain_Anterior_Caudate
SE_04801chr1:226830320-226836156Brain_Cingulate_Gyrus
SE_05781chr1:226818536-226856817Brain_Hippocampus_Middle
SE_06710chr1:226826915-226833278Brain_Hippocampus_Middle_150
SE_07746chr1:226830174-226831921Brain_Inferior_Temporal_Lobe
SE_09326chr1:226829843-226833738CD14
SE_10211chr1:226830474-226832905CD19_Primary
SE_10887chr1:226827072-226836052CD20
SE_11833chr1:226830248-226831171CD3
SE_11833chr1:226831806-226832799CD3
SE_13607chr1:226829934-226831475CD34_Primary_RO01536
SE_14432chr1:226829962-226831640CD4_Memory_Primary_7pool
SE_14432chr1:226831716-226834997CD4_Memory_Primary_7pool
SE_15808chr1:226830084-226831495CD4_Naive_Primary_7pool
SE_15808chr1:226831790-226833460CD4_Naive_Primary_7pool
SE_16856chr1:226830580-226831435CD4p_CD225int_CD127p_Tmem
SE_17296chr1:226828059-226836385CD4p_CD25-_CD45RAp_Naive
SE_17765chr1:226829280-226836457CD4p_CD25-_CD45ROp_Memory
SE_18263chr1:226827876-226835812CD4p_CD25-_Il17-_PMAstim_Th
SE_19160chr1:226829937-226833625CD4p_CD25-_Il17p_PMAstim_Th17
SE_20012chr1:226830445-226832939CD56
SE_21910chr1:226830152-226833980CD8_Naive_8pool
SE_22315chr1:226829855-226834688CD8_primiary
SE_26570chr1:226829167-226831464Esophagus
SE_26570chr1:226831703-226832339Esophagus
SE_42228chr1:226830522-226834327Lung
SE_50140chr1:226830537-226833707Sigmoid_Colon
SE_53341chr1:226830464-226832821Spleen
SE_54498chr1:226830150-226831438Stomach_Smooth_Muscle
SE_55112chr1:226830612-226831373Thymus
SE_55112chr1:226831379-226832149Thymus
SE_58303chr1:226819953-226937809Ly1
SE_59629chr1:226819233-226928465Ly4
SE_60416chr1:226819368-226929640DHL6
SE_61009chr1:226812849-226900772HBL1
SE_62233chr1:226813614-226929647Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1226830783226832074
Number: 1             
IDChromosomeStartEnd
GH01I226642chr1226829947226833784
Enhancer Sequence
GAATCGGACT GCCTTCACTT TCACTCCAAG CCCATCGGCT GGCCTCACAA AGCCCAAGGA 60
GCTCCTCCTC GGGAGACCCC CACAGGAACC AGCAGAAGAA GGAAGACGGA GGCAGGGCAG 120
CAGGGGGTGT CGGGGGTGGC TGGTCCTGAT CCTGCTGCTA CGGTGGAGCT AAGAGAGGGG 180
ACTGGGGGCA GGGTCTACTC AGGGCCCCAC TAGATCCCCT TGGCTGCCTC GGCCCTTCCA 240
TAAAGCGAGG GCTTCCAAAG CCAGAACCTG TCCTGGTGGG AGAAGTGGTC TGTCCTCAAG 300
TCCCCATCTC TGCTGCTCTC AGGCAGCCTG AAGGCTGAGC CTGCCCATAA GTGTCTCTGG 360
CTCTTTCCAA AGAGGTGAAA TCTTCTGGAG CACAAAGTTC AGGTCAGAAA GTGGCCTTGG 420
AAGGGGTCCC AGTGTGGATG GAGAAGGCCG TATTGTGGGG GAAAGGCAGG GGGCTCCCTC 480
AGCCTCTGCT CATCCCAGAG ACATGCCTGG TGCACCCCAC CCCATCGACA CCAGGCCTCC 540
TCATAGGTGA GCCCCCAGTC CAAAAAGCCT GAGAAAATGC TTCCAACTCA ACTGCCTCAC 600
GGCCCTGGCC TCCACACGAG CAGCTCCAGC TGAACTGGCG GGGACCACCT AGACACTGGG 660
GAAGGTAACA GGGGCAGGGA CAGCAGAGCA CTTGAGCAGC CGGGGGCTGA ATCGCTGGCC 720
CTGAGCTGCC GGGACACGCC ACCTCCCCCA GCACACAGCT CTGCGCTTCT ACCTTCTCCA 780
GAGCAGAGGT GGGGTGAGTC ATCCCACCCC CGCTCCTCTG CTCTCCTTTT AGAGCCCCAG 840
TCTCCCTACA CAACAGGCTC AGAGGCTGCC CACAGCCCTT GAGGAGGCAG AAATCAGCAG 900
TGTCAGTTGC AGGATGGGGA AGTTTTCTCC CCTTTGCCCT GTGTGGGCGG GAGCTGCCCA 960
CAGAGGCCCC GCCCGCCTGC CCTCCACCTG GCCCTCCACT CTTCCTGCAT CTGTCTCCCA 1020
GGCCTTGTTC CAACACTGCC CACCAACTTC TCCAAGTTGC TGGTTTGGGA CCCAGAACAG 1080
ACTAAACAAA AACTACAGCC TCTTAAAAAT GACAGGCTTT AGAAACCACT GTATTAATTG 1140
AAATTTGCAC GGAAAGAAAA GGGAAGAAAA AAACAAATCC TTTGGGTGTG AACTTAGGCC 1200
TGGCTGGTTA GGACCTTCCA GGAGGTGATG AGGGCTGGAG GGGGAAGTCA GTAGCTTTGG 1260
GTTGGGCCCT TGCATGCACA CACAACCATG TGCGCACATA CACACACATG TGCTCATGCA 1320
CACACATGCA CATAAACGCG GACTCCTGTG CACCACTGCA CACACACAGG TGCACCCATG 1380
CAGGACACGC ACAGAGCACA CCCCTCACAT GCAGAGCCAG GTCAGTGGTG ACGGGGGCAT 1440
TGAGGCAGGG GCTGCGTGTG CATCCATGTG TGTACTGTGT AGAAAAGGGG CAGCCAGGCT 1500
GTGGGAGGGA CTCCTGAGGG CGCTGTAGGG GACCGCATGG TGGGTGGCTG CACTTCTGCA 1560
AAGAGCTCTC AGCACCCCCT TAAACAGGAA GCAGACCTCA ATGTGAAATC CCTTTTCACA 1620
TGGCCTTTCT CCAAAAAGGG CCCCCGTGGC TCAAAGCGGG CAGTCACTCA CTGCCCAGGA 1680
GAGGAAAGAG GCTGGGGGGA GATGTCCACA GGGGGTGCCA GCTGGATGGT GGGGCGGGAT 1740
GCCCACAGGA AGGTGAGGCT CAGCCCCTCC CCACACTCCC CTGCCTGCCC GAGACAAAGT 1800
CGAAGCTCCA AGCCATGCAG GGAAGCAGAG ACCTGCTCGC CCACTCACAG GACGCTGGGG 1860
GAGGAGGGGA CTCAAGATCA GGTGGAGGAA GTGCTCCTTT GAGACAGGCC AGCCCAGGGA 1920
GCCAACAGGT GGCAGGCGAA AGCCACCCAG AGCTCCTAGG TGCTAGGGGC GGGCTCTCAC 1980
CTGCACTCCC CAGGCCCCTG GTCCCAATGT CAGGAAGACA GTGTTGACTC TCCAGGACAA 2040
GTCACAAATC TCAGAGCATG CCCCAGAGCC ACTGAGCACA TGTCGGCGGG AGCCAGAGTC 2100
CCAAGAAGCC CCGACGTGCA GACGCCACCA GCAACTGCAT CACATTCTCC TTAGTGCCAC 2160
CCTTCTGCCC CCGCCATGCC CAGCATTGTT TGGTGACCGG CCCTTCCCTT TCTCTGTGAC 2220
ATGTCTCAAA CTCTCTTGCC CTGGGACTCA 2250