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

TagContent
EnhancerAtlas ID
HS108-02062 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr1:68165370-68167140 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3962382chr168165693hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PAX5MA0014.3chr1:68165452-68165464ATGGTCACGCTC-6.37
ZNF263MA0528.1chr1:68166534-68166555GGGGGAAGGGGCAGAAGAGGA+6.09
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_02387chr1:68166569-68167337Astrocytes
SE_27725chr1:68165776-68167750Fetal_Intestine
SE_29142chr1:68165684-68167885Fetal_Intestine_Large
SE_38054chr1:68165922-68167557HUVEC
SE_40089chr1:68165860-68167362K562
SE_41280chr1:68165990-68167378Left_Ventricle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr16816630068167119
Number: 1             
IDChromosomeStartEnd
GH01I067700chr16816573068167787
Enhancer Sequence
AAAGTAATTA GGGTAACAGA GGGCTCATCT GAAGGCAAAA GTTATTTGCT ACTCACAGTG 60
GTAAAGGGGT ACAGTAGCAA ATATGGTCAC GCTCTGAAAA CAAGCACAAG GCCCTAGCCA 120
TGCCAGGCTG TGCAAAGACA GCTAGAACTG ACGGTGGGAC CAGGCTCCAC AAAGATGGTC 180
AGAGGTTTTT TTTTTTTTTT TTTTTTTTTT TGAGACGGAG TCTCACTCTG TCGCCCAGGC 240
TGGAGTGCAG TGGCGCGATC TCGGCTCACT GCAAGCTCCG CCTCCCGGGT TCATGCCATT 300
CTCCTGCCTC AGCCTCCCGA GTAACTGGGA CTACAGGCGC GCCCGCCACC AGGCTGGCTA 360
ATTTTTTGTA TTTTTAGTAG AGATGGGGTT TCACCGTGTT AGCCAGGATG GTCTTGATCT 420
CCTGACCTCG TGATCCGCCC GTCTTGGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC 480
ACCGCGCCCG GCCATGGTCA GAGTTTTAAG CCAACAGATT ATAATCCTGG CATAGGGAAT 540
GAGGGACAAA TACTCAAAAG ACGGTCGCCT AGCCCCAAAC AAGGATTATA GAGCCCCAAA 600
TAAAAAGGTT TAGAGGGAAT ATCCATGTGT TTATGTGTAA CTGACCCTCG TGCCAGGGAA 660
AAACTGATCA TGGCACATAT CCAGAAGAGG TGGAAAGCCC CATGACATGC ATCTCCACAC 720
TGAGTTCCAA TCACTACCCG CAGGCCTGGG TTTCTTGTCC ATGTTAAGGC TAAGTATACA 780
TCTCATCTGC CTCTTCCAGC TTCATTACCT TCCCTTCCCC CATCTTTTAA AAACTCACCC 840
CTACCCAATC CCATCCATCA TCCCCAACTC TCCTCCACTG AGAGTTACAA GAACTTTGTA 900
ATTTGGTCAG AAGCAGTAAA AAGTGCTTGT TAGTTGTTGC CTCTTTTTCA AAACCGATGT 960
ATCTAAATCC TTCAGTCTTT TACTAGAAAG GGCCCAGGGA CTGTCTTTTG CCCCTACCTT 1020
TTGTAAGTGT GGAGTGCTGG CTCTCAGAAG CAGGGGCCAT CTCTGCAGCG TGTCCGGTTC 1080
ATAGCCTGGG GCTTGTTGGC TGCCTCCCGC CCTTGTTCTT TGATGATTTT GCCCTCCCCT 1140
CATCTCTGTG GGAATCCCAG CCCTGGGGGA AGGGGCAGAA GAGGAGGCAG GGCACCTTCA 1200
GCAAACACAT AGTGAATATG AGTCACCACC ATCTAATGAC CTTTCCATTT GTTATCAGTT 1260
TCCACTACCT CAGCTAGTCT CAGGATGGGA AACAGCCCTC CACAGGTCAG AGTCATTACG 1320
TCACTCCTCA GCAGCCTCTC TAGCTCCCCT GTTGGTTTCA GGATAGGCAA GCAGGATAGG 1380
AGGGCGGGAT CGGGGGTCTT CTGCACACTG GCTTCCAGTC CTCTTTTCTC CTCCTCTCAT 1440
CTCCTCCCAG GACCTCATTC CAACGCATAC TGTTCTTCTC TCACTCAGCC CAAACATCAC 1500
CACCCTTGGA AGCCTTTTTA GAGGTCTTTG TTGATGTGGA GCTAGTCCCT CTTTCCTCTG 1560
GGCTCTCACA GCACTCTGTG TTCACCTGAG TTATAGCACT TGCCACATGA TACTACGATG 1620
ATTAGTTTAC ATATCTGTCA TTCCCATCCT CCTTGCTCAG ACTGTGACAT GGGCTGGTGT 1680
AAGTCTTATT CATTTGGGTG TCATGGGAGC CTGACTCTCA GCAGCTTGCT CTCAGGAGGT 1740
GCTCAGAAAA TGTTAACTGA GTGAAGGAAG 1770