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

TagContent
EnhancerAtlas ID
HS147-08781 
Organism
Homo sapiens 
Tissue/cell
NHEK 
Coordinate
chr11:57055410-57057260 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs112715224chr1157055896hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:57055423-57055441CTTTCCCTCCCTCCTCCC-6.31
Sox3MA0514.1chr11:57056853-57056863AAAACAAAGG-6.02
ZNF263MA0528.1chr11:57055422-57055443CCTTTCCCTCCCTCCTCCCTT-6.48
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_00258chr11:57056418-57057897Adipose_Nuclei
SE_24251chr11:57056300-57057148Colon_Crypt_2
SE_31504chr11:57056317-57057210Gastric
SE_36201chr11:57055048-57057554HMEC
SE_37251chr11:57055647-57058685HSMMtube
SE_42553chr11:57056348-57057135Lung
SE_46610chr11:57055311-57058687Osteoblasts
SE_55925chr11:57054906-57059175u87
SE_64652chr11:57055395-57057432NHEK
SE_65615chr11:57056488-57057142Pancreatic_islets
SE_67692chr11:57054906-57059175u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr115705612957057101
Number: 1             
IDChromosomeStartEnd
GH11I057287chr115705543857058281
Enhancer Sequence
CTGCCTGGGG TGCCTTTCCC TCCCTCCTCC CTTGACCCTC TGAAAAACAC CACCTTCCAG 60
TCCTTCCCCG CCAATTGCTC CATGACATGT CTCTTCAAGC CCTGAGTCAG TGAACCGTGC 120
TACATGGTCT TGCATTGTAC ACTTGTAACC ATTATCATCC CTATGACACC ATATTTTAGT 180
TTATCTTCTT GACAGACCTT GACCCTGGAG ACACAGGCTA TTCCTTACTC ATCTCCGCAT 240
CCCCAGCCTG AATAACAAAT GGTGTGATAA AATGTCTGCT GGATTGAACT GAACTGGAGA 300
ATTTGCTGAG TGCTTCAGCA TGCCCTGGCA GGGTCTCTGC CCCTCAGAAC CCACACTTCC 360
CCTTCACTGT ATCCACCTTG CACCCTGCAC AAATGCCAAA AAGGCTTTAA GGTCAAAAGA 420
ATTAGCACTG TCTTAGAAAT TGTATAGAGG TGGTCCAGAT GGTCCCCAAC TTACAGTGGT 480
TCAGCGTACA ATTTTCTGAC TTTAAGATGG TGTAAAAGCA ATACACATTC ATTAGAAACC 540
ATTCTTCAAA TTTTGAATTT TGATCTTTGC CCAGGCTAGC AATAAGTGGA AATATGCTCT 600
CCTGTGATGC TGGGCAGCAG GAATGAGCTG CAGCTCCCAC TGAGCCACAC TATCACGAGA 660
GCAAACAACT GGTACTCGAC AGTATACTGT GTTGCCAGAT GATTTTGCCC AACTGTAGGC 720
TAATGCCAGT GTCTGAGCAT GTTTAAAGTA GGCTAGGCTA AGCTATGATG TTCAGTAAGT 780
TAGGTGTAGT AAATGCATTT TCAACTTACA ATGGATTTAT TGGGCACTAA CCCCACATCA 840
TAAGTCAAGA AGCAACTGTA TTATAAAACT AAGACTGGGG GAGGGCAATG TTTAACCTGG 900
AGACATGGAT TACTCATGAT AACAATGTAG GATGCCAGGG ACTGAACATA ACAAACTCAA 960
GGGGAGGGGA GGTCCCTTCT CAGCTATCCA GCACCCCAAA GCTTGAATCA ATAGCTCCTT 1020
CCCACGCTGG GTGAAATCAG CCCTGAGCTG TCTGTGAATC AGAGGAAGTG TTTGTGTGTG 1080
TGTGTGTGTG TGTTGGAGAG GGTCCGGGGG AAGGATGTAT ATGTGCATCC TGAGGTGGAA 1140
AAATCCCTAA ACTCACTTGT GTGGTGAAGC AGGGCTGGAG GCTTCTAGAG CCCTAGGGAG 1200
GGCGCAGCCT TTGACTTTCG GACAGACCTG GTTAGAAGCC TCACTGCTTT GCTGCCAGCT 1260
GATAAAGGAG CCAGATGAAA GGGCCCAGCA TAGCTCCTGG CCTTTGGAGC ATGCCCTTTA 1320
TCCATAGAAT GCTACTCTTC TCCTGATGTC CATCTTCCCC TAGCGCTGAG CCCAAAGCAC 1380
AGAAGGCATC CTGTTTGGAG CCAGGCTGGC TGGGGTTAAC AAGAGAAAGG CAGCTGTTTC 1440
CCGAAAACAA AGGGCTGGGT CAATAAATCT GCCGCAGCAG CCGTGGATCA GTGAGGGCAA 1500
AGGCTCCCGC GGGGAGCAGC CAGCCAGTTT CTCTGAAACG TCTAGAACAG AGCCATCCAG 1560
GAAAGCAAGG CTGAGGCTTG AAAGGCCCTT AGGTAGGCCT GTCCTGGGGT CAATATCCTC 1620
AGAGCACAGG GTCCCTCTCC TCACCCCCAG CACCTTCCAG GATCAGACTC AGAGTCTCAC 1680
AGAATCACAG AGCTGGAAAG GACCCCAAGC ATTCTCCAAT GCAGTTTTTT ATCTGGGGAA 1740
CATGTTAAGA ATTCATCCAT CTATGAACTT GGATAGGTCA GGGGGAAAAG GTTCACTAAT 1800
CTATAACTGA AGTTTAGCAT TTATTTCTAT CATGAACCTA AGCAACAAAC 1850