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

TagContent
EnhancerAtlas ID
HS104-25083 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr17:27466080-27468890 
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
CCCTTGCAGT CCAGCCTCCA GCCAGAGCCC TCCCCAGCCC CAGGGCGGAA CAGAAAGCAG 60
CCGGGCACCC GCCTCACTGC AGGCCAGCCC AGAGGAAGCA GGTGCACTGG AATGGCTTCC 120
TGCCGCAACT GCAGTTGCAG AAGGGTCTTG GTTTCCTCCT CCAACGACTG AACCTGCTGG 180
AGGCCCCCCT TCCCTGGGGA TGCTCACTGC CCCTCTGGAG GGCACTTTGC TGTCTGCTTG 240
GATATCACTG TGCATGGCCC TAAATCTGTG ACCTGGTGCT AGTGGCCCGG GGGTGGCTGG 300
GGGAGAGTAC CCTAGACCAG GAAGCGCCCA TCTCTCAGGG TGAGGAGCTC TCTCTGACCT 360
CTCCCCCACC CCCGGGCATA CTGCCCACAC AACTCAGCCC TGGTGCCAGT TTGGGGGCTG 420
AGGCAGGGCA GTCCTGAGCA CAGAGAGATA CAAGTACTCA CGGGTACATC TCAGGCTCCT 480
GATGCACCTC CGCACCAGGC CAGCCCACGT ACTCTGCCAA CTGCTGACAC AACTGAAAAC 540
CTTACCCTTG GTGGCTGGGA GGGGTAGAGT CAGGGGAACG GGAAGGACTG GGAGCAGCTA 600
TGTCTCTCCT CACTTTCTTT TTTAAGGAAC TTACTTATCT GGAGTAATCT CTACTAAAAA 660
AGAGACTTAG GGCCAGTCAG AGCATCCCCA ACACGCCATC TGTGCCCCTT GCAAGTGTCC 720
TATGCACAGA AATGGAGGTG GCCATGCTAA GACTACTCTT GGGGACAGCG AGAAGGGTGC 780
TCCCTGACAA CTCCAAGGAC CATCCCCTCT CAAGGAGGAA GAGAGGAAAG AGCTATACCA 840
GCAACAAAGC AGAGACAAGA CTACCGAGGA CCTTGGGTGC TGTGGGGCTG GGGCTTTGGA 900
AGAAAACAGT GTTCTAAGGA ATGAAGGCCA AAAAAGCACT AATGGTTGGT GGGGAAGGCG 960
TGTCACAGCC TTGGGGGTGG ATGCAACCCC AGGAAACTGA GGTTCAGAAG ACAGTGCCCC 1020
TCCAAAACTC CTGAAGTCAT GAGTCAGGCC CAGGATGCCC TGCTCCTAGC CACGGAGGGG 1080
TTTTGAGGCT TCCGGGGCTG AGTAACTCCC TTCTTACCAA GAAGCTCGGA GAGGAGCCCC 1140
AAGGCTGCCC CACCCCTCTC CCCACCTACT TCAGCCACAT CTGGGGAAAT CACAAAAAGG 1200
TCCCTCCTTT CCTAAATGAG GAAATAGCAT GAGGAGCCTG GGACATTTCC GGGGTGGGGG 1260
GTCAGAGGGA CACTCACCCG CATGGCCTGG CCTGGAGCAG CCCAGAGCAA GGAGACTCCG 1320
CTCTGATGCT GCTCTGGCTC CGTTAGCAGC TCAAAATAGC ACAGGCTGTG GCCCCGCCCA 1380
GTTCCCGCCC TCTCCCCGGC CCCTCCCGTC CCGAGCTGCC CAGCCCTAGT TGGAGCCAGC 1440
AGCCCGGAGG ACTTCGGGTA TCAGGTATGC CAGGAGGGAG AGGGTGATAC AGCAGTGTGT 1500
GTGGAAGGGA AGGAGAAGGC TCTTAGGGTA AAGCCATTGG GGTGGGGGGC AGGCAGTGTT 1560
AGGGGGTTAG GGCAAGGACA GGGAGGGTGA GACTTGCCTA TGGACACACA CCCCAGCTCC 1620
GGGACAGCTG GGCTGATATG GCTCCTAAAA ATAGCAGAGG AATTTGAGAC CTGCAGCCCC 1680
CGGCCCCACA GGCCAAGCTT GAGACAAGCA CATGCGCACT CATGTGCATG TACACGTATA 1740
CACACACACA CACACACACC AGCATGCACG AACATTCAAT CAACACAGTG TTCTTGAGAA 1800
CACCCAAATC ATAGGCCTAC CCTAGCCATC TAATTACTGC GGCAGAGGCC AAGACAGCCA 1860
CTAACGTCAC ATCCAAGACA GCACACGGGG CCCACTGCAC ACTGTGCCCA AACAGCAGCC 1920
GCAAAGCAGT CCTGTAAGGT CTGGCAGGAG CAGAGACCCA CACGGGCAGG CCCACTTACT 1980
GCCCCACTGC CATCAGCACA CAGGGGACAT GCAGAGAATC AATTACACTC TCTTTGTTTA 2040
CATCCCTCTC CCCTCCACAG ACGCCAGGGA CTGCACAGGC AGAGAGGAGG GTGGGGTGGG 2100
CCTCAGCCCT GCAGACAGAG GAAGTCATGG GTGTCTAGCC AATGAGTGAT GGCTGCCTGT 2160
GAAAAGCCAG TGTTTCTTGT GAAGAGAAAT CCTGGCCTGG CTCTCCAGTT AGCACCATGG 2220
GATGCCTAGA CCAGGACTAG GGACCCGCTG AGACGCTGAA ATGGGAGCTG GAGAACAGAA 2280
TGTCAAGGGG CCAAAAGACA GGGAGAGCAA GTCTCAGAAG CCGTCAGCTC TGCAGAAAAA 2340
AGGAAACAGT CATTGCCTCC CTCTTCCTCT TTAGGAAAAA AAAAAAATGG GGTGGGGGTG 2400
GTGCTAGGAA GCCCTGATAC AGAACCGCCT CCTAACCAGT CTGGCATACA CCCCATGCTT 2460
CTTGCCCCTG GCCAGCTCTA AGGGCCATTG GTTCTATACA TTGTCTGACT TTCTCCATGA 2520
AAAGATTGGT AAGCACTGCC AGAGAGGATG GAAACCCAGC CCTGCCTCCT ACCTGCCATG 2580
CGCTGTCCAA GTCTCACTGT CATATAGTCA CATACACAGA CTCTTAGGAC ACGGCGCTTG 2640
TGTCCTGCTC TCTAGGGAGT GGGATGTCCC CCCAGGGGAA GCATCTGGCC CTTCTGAAGC 2700
ACGTGCAGTG TCACAGGTCT TCACATCTTC AGTGGCTACT TAGAACAATG GTGCCAGCCT 2760
CAGCTGCTCA CTGAAATCCA CTGGGGAACT TGAAAAAAAT ACTGATGCCT 2810