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

TagContent
EnhancerAtlas ID
HS108-16505 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr17:27465850-27468900 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXP2MA0593.1chr17:27468112-27468123TTTGTTTACAT-6.14
ZNF263MA0528.1chr17:27466890-27466911CAAGGAGGAAGAGAGGAAAGA+6.06
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_03450chr17:27466746-27467344Brain_Angular_Gyrus
SE_03450chr17:27467458-27468851Brain_Angular_Gyrus
SE_03910chr17:27464585-27469139Brain_Anterior_Caudate
SE_04884chr17:27464587-27469899Brain_Cingulate_Gyrus
SE_05843chr17:27464629-27469649Brain_Hippocampus_Middle
SE_07476chr17:27464967-27469290Brain_Hippocampus_Middle_150
SE_07806chr17:27464698-27469377Brain_Inferior_Temporal_Lobe
SE_09987chr17:27464458-27470145CD14
SE_13853chr17:27463262-27469083CD34_Primary_RO01536
SE_19008chr17:27462501-27469905CD4p_CD25-_Il17-_PMAstim_Th
SE_19489chr17:27463266-27469062CD4p_CD25-_Il17p_PMAstim_Th17
SE_28031chr17:27466483-27469023Fetal_Intestine
SE_28952chr17:27466677-27469078Fetal_Intestine_Large
SE_30293chr17:27464913-27469119Fetal_Muscle
SE_32448chr17:27465607-27468850Gastric
SE_34898chr17:27464930-27468684HeLa
SE_37582chr17:27464663-27469415HSMMtube
SE_40250chr17:27466651-27467422K562
SE_40250chr17:27467475-27468766K562
SE_41080chr17:27463489-27469104Left_Ventricle
SE_42354chr17:27464813-27469093Lung
SE_48211chr17:27464869-27469058Psoas_Muscle
SE_49086chr17:27464930-27469026Right_Atrium
SE_50708chr17:27464953-27469080Sigmoid_Colon
SE_51291chr17:27464666-27469119Skeletal_Muscle
SE_52472chr17:27465030-27469067Small_Intestine
SE_53778chr17:27465158-27469087Spleen
SE_65361chr17:27464894-27468217Pancreatic_islets
SE_66834chr17:27464629-27468481Jurkat
SE_66834chr17:27468487-27468972Jurkat
SE_68762chr17:27466740-27469015H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr172746700027468828
Enhancer Sequence
TCCATTTCCC CTGGTTCACC TGCACTGTTG TCCTTCTACA TCAGCTGCCA GAAGAGCAGC 60
TTGGGAGGAA AGCAGGGGTT CCCAATGATG ACCCGCCCCT CCACCCACCA ACCTGAATAT 120
GCTTTACGTG GAACTGCTTG AGAGGAAGGG AAGCTCTCTA AGGAATGAAC TGAAGGCCAT 180
GCTGCCAGAC AGCGGGGGAG GGGGAGATGA GCTTGGCAGG GACAACCTGG CCCTTGCAGT 240
CCAGCCTCCA GCCAGAGCCC TCCCCAGCCC CAGGGCGGAA CAGAAAGCAG CCGGGCACCC 300
GCCTCACTGC AGGCCAGCCC AGAGGAAGCA GGTGCACTGG AATGGCTTCC TGCCGCAACT 360
GCAGTTGCAG AAGGGTCTTG GTTTCCTCCT CCAACGACTG AACCTGCTGG AGGCCCCCCT 420
TCCCTGGGGA TGCTCACTGC CCCTCTGGAG GGCACTTTGC TGTCTGCTTG GATATCACTG 480
TGCATGGCCC TAAATCTGTG ACCTGGTGCT AGTGGCCCGG GGGTGGCTGG GGGAGAGTAC 540
CCTAGACCAG GAAGCGCCCA TCTCTCAGGG TGAGGAGCTC TCTCTGACCT CTCCCCCACC 600
CCCGGGCATA CTGCCCACAC AACTCAGCCC TGGTGCCAGT TTGGGGGCTG AGGCAGGGCA 660
GTCCTGAGCA CAGAGAGATA CAAGTACTCA CGGGTACATC TCAGGCTCCT GATGCACCTC 720
CGCACCAGGC CAGCCCACGT ACTCTGCCAA CTGCTGACAC AACTGAAAAC CTTACCCTTG 780
GTGGCTGGGA GGGGTAGAGT CAGGGGAACG GGAAGGACTG GGAGCAGCTA TGTCTCTCCT 840
CACTTTCTTT TTTAAGGAAC TTACTTATCT GGAGTAATCT CTACTAAAAA AGAGACTTAG 900
GGCCAGTCAG AGCATCCCCA ACACGCCATC TGTGCCCCTT GCAAGTGTCC TATGCACAGA 960
AATGGAGGTG GCCATGCTAA GACTACTCTT GGGGACAGCG AGAAGGGTGC TCCCTGACAA 1020
CTCCAAGGAC CATCCCCTCT CAAGGAGGAA GAGAGGAAAG AGCTATACCA GCAACAAAGC 1080
AGAGACAAGA CTACCGAGGA CCTTGGGTGC TGTGGGGCTG GGGCTTTGGA AGAAAACAGT 1140
GTTCTAAGGA ATGAAGGCCA AAAAAGCACT AATGGTTGGT GGGGAAGGCG TGTCACAGCC 1200
TTGGGGGTGG ATGCAACCCC AGGAAACTGA GGTTCAGAAG ACAGTGCCCC TCCAAAACTC 1260
CTGAAGTCAT GAGTCAGGCC CAGGATGCCC TGCTCCTAGC CACGGAGGGG TTTTGAGGCT 1320
TCCGGGGCTG AGTAACTCCC TTCTTACCAA GAAGCTCGGA GAGGAGCCCC AAGGCTGCCC 1380
CACCCCTCTC CCCACCTACT TCAGCCACAT CTGGGGAAAT CACAAAAAGG TCCCTCCTTT 1440
CCTAAATGAG GAAATAGCAT GAGGAGCCTG GGACATTTCC GGGGTGGGGG GTCAGAGGGA 1500
CACTCACCCG CATGGCCTGG CCTGGAGCAG CCCAGAGCAA GGAGACTCCG CTCTGATGCT 1560
GCTCTGGCTC CGTTAGCAGC TCAAAATAGC ACAGGCTGTG GCCCCGCCCA GTTCCCGCCC 1620
TCTCCCCGGC CCCTCCCGTC CCGAGCTGCC CAGCCCTAGT TGGAGCCAGC AGCCCGGAGG 1680
ACTTCGGGTA TCAGGTATGC CAGGAGGGAG AGGGTGATAC AGCAGTGTGT GTGGAAGGGA 1740
AGGAGAAGGC TCTTAGGGTA AAGCCATTGG GGTGGGGGGC AGGCAGTGTT AGGGGGTTAG 1800
GGCAAGGACA GGGAGGGTGA GACTTGCCTA TGGACACACA CCCCAGCTCC GGGACAGCTG 1860
GGCTGATATG GCTCCTAAAA ATAGCAGAGG AATTTGAGAC CTGCAGCCCC CGGCCCCACA 1920
GGCCAAGCTT GAGACAAGCA CATGCGCACT CATGTGCATG TACACGTATA CACACACACA 1980
CACACACACC AGCATGCACG AACATTCAAT CAACACAGTG TTCTTGAGAA CACCCAAATC 2040
ATAGGCCTAC CCTAGCCATC TAATTACTGC GGCAGAGGCC AAGACAGCCA CTAACGTCAC 2100
ATCCAAGACA GCACACGGGG CCCACTGCAC ACTGTGCCCA AACAGCAGCC GCAAAGCAGT 2160
CCTGTAAGGT CTGGCAGGAG CAGAGACCCA CACGGGCAGG CCCACTTACT GCCCCACTGC 2220
CATCAGCACA CAGGGGACAT GCAGAGAATC AATTACACTC TCTTTGTTTA CATCCCTCTC 2280
CCCTCCACAG ACGCCAGGGA CTGCACAGGC AGAGAGGAGG GTGGGGTGGG CCTCAGCCCT 2340
GCAGACAGAG GAAGTCATGG GTGTCTAGCC AATGAGTGAT GGCTGCCTGT GAAAAGCCAG 2400
TGTTTCTTGT GAAGAGAAAT CCTGGCCTGG CTCTCCAGTT AGCACCATGG GATGCCTAGA 2460
CCAGGACTAG GGACCCGCTG AGACGCTGAA ATGGGAGCTG GAGAACAGAA TGTCAAGGGG 2520
CCAAAAGACA GGGAGAGCAA GTCTCAGAAG CCGTCAGCTC TGCAGAAAAA AGGAAACAGT 2580
CATTGCCTCC CTCTTCCTCT TTAGGAAAAA AAAAAAATGG GGTGGGGGTG GTGCTAGGAA 2640
GCCCTGATAC AGAACCGCCT CCTAACCAGT CTGGCATACA CCCCATGCTT CTTGCCCCTG 2700
GCCAGCTCTA AGGGCCATTG GTTCTATACA TTGTCTGACT TTCTCCATGA AAAGATTGGT 2760
AAGCACTGCC AGAGAGGATG GAAACCCAGC CCTGCCTCCT ACCTGCCATG CGCTGTCCAA 2820
GTCTCACTGT CATATAGTCA CATACACAGA CTCTTAGGAC ACGGCGCTTG TGTCCTGCTC 2880
TCTAGGGAGT GGGATGTCCC CCCAGGGGAA GCATCTGGCC CTTCTGAAGC ACGTGCAGTG 2940
TCACAGGTCT TCACATCTTC AGTGGCTACT TAGAACAATG GTGCCAGCCT CAGCTGCTCA 3000
CTGAAATCCA CTGGGGAACT TGAAAAAAAT ACTGATGCCT GGAGCCCACC 3050