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

TagContent
EnhancerAtlas ID
HS108-07028 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr11:13359520-13361240 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs2896635chr1113359745hg19
rs1037169chr1113361005hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESRRBMA0141.3chr11:13359628-13359639AATGACCTTGA-6.32
EsrraMA0592.2chr11:13359629-13359640ATGACCTTGAG-6.02
EsrrgMA0643.1chr11:13359629-13359639ATGACCTTGA-6.02
IRF1MA0050.2chr11:13359703-13359724AAAATGAAACTGAAATCACTG-6.12
JUNMA0488.1chr11:13359903-13359916ATTACATCATCTT-6.82
JUND(var.2)MA0492.1chr11:13359902-13359917GATTACATCATCTTC-6.41
NFE2L1MA0089.2chr11:13360170-13360185TTTGCTGAGTCACTG-6.81
Nfe2l2MA0150.2chr11:13360172-13360187TGCTGAGTCACTGAA-6.02
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_19448chr11:13359051-13362690CD4p_CD25-_Il17p_PMAstim_Th17
SE_36817chr11:13353194-13361966HMEC
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr111335985613360227
Number: 1             
IDChromosomeStartEnd
GH11I013337chr111335909113361942
Enhancer Sequence
GAAACAACAC TGACTAGCAT GAAAAAAAAG CCTGGTGTGT GGTTTCTGCC AATAGTTTTT 60
GTGTTGTTAT TTTTGTTGTG ATTCCTGCAC TGAGTATTTT CTCAGAAAAA TGACCTTGAG 120
CTGTACGACT CATGCCTGTT CAGACCCACA GACACATGAT ACTCACTATA TCCAAAGCTC 180
AGAAAAATGA AACTGAAATC ACTGAAGTTT GTGGGTTTTT TTTTTAAATT CTTCTTGCCA 240
GAAGGAGACA AATGAAGGAA AAAAAACAAG CCGATTTCAT TTTCATTAAG AGGAATTTGT 300
AGAGTTATTT CTGGGGTCAG GCAGGATACA TTCAGACGAA CATTTTAGAT CTAGGGCTGG 360
GAAGATCCCG AGACTCGTTA TAGATTACAT CATCTTCCTC CAAGTGCACT TGCCAGGCAA 420
ATGGACAAGT GCATTTTAGA AAGGTTTTCA GTTGTTCACG TTTAAACAGA AAGGATCACC 480
TGGCTAACTT TTAGTTAACC CATTGAACAG ATGTGCCATT CCCCCAGCCC ATTGGTTATT 540
CATGTCCTTG TTACTGGTTT TTGATATCCT TGCCCCGTAG GTGGGAGGAG GGATGGGTAT 600
GAGCCTGCCC TGCCCTCTTT CTCCTACTTG GGACAGAGCT GTTGCTTTTA TTTGCTGAGT 660
CACTGAAGCA ATAGAGCATG TGCAGAGTCC CAGCCTGGAG GTGGGCATAT CTGGGTTCCA 720
GTCCCTGCTC TAGCCCTTCT CAGCTGTGTG ATCTTGGACA AGTTGCCATA CCTCTCTGAG 780
CCTCAGTGTC ATCTTCTATG TGATGTCGAT GCCTCCCCCA AAAGGTCGTT ACGAGGACCA 840
AAGGAGACAC GTCAGGGCAG GAACCATCCT AGGCACGTGT TTGATGCTCA GTAAACGGGA 900
CGTGGTCAGT GTTCAGAGTT GTGGGGGTGG CAGGTGACTG CTCTGTTTCA CCTCCACTCA 960
CAGCAACAGG GCCTGTGGTG TCACCTAGAC ATCTCATAGG CATCCCACAC TGAACATGTC 1020
CCAAACCAGC AGCTCCTCCC TGGATGGGTG GATGGTGTAC AGGGACCTCT TCCTCCAGCT 1080
GTCACATGGG GCATGTACCT GGCAAGTGGC TTTGCAGCCC TAGCTGCCCC CTTGGCTGGG 1140
GGCCTTTGTG CAGTTCATGG ACTGGGAGTC ACCCCCATGT CTAGACCGTC AGGAAACCCA 1200
TTGGCTTTTC CTTTAGAGCA TACCAAGAAT CAACTTCTCA GAACATAGCA AGAGTTGACT 1260
TTTTGTCACC CTGCCGTGGC CACTCAGACT GACTCCTCTT ACACCTCACA TCCCATTGAT 1320
CAGCACAGCC CCTGGAAATA TGTCTAGAAT CCAGCTGCTT CTCATCACCC CCACACCTAA 1380
TACAGAGGGC TGAGTCATAG CATCTCTTCC CCGGACTGTT GTAGCCGTCT CCTAACTCAG 1440
CTTCCTGCCC TGCTTTTACA CACACACACA CACACACACA CACATGGTAT CTTCTCACCA 1500
CTGCAGCCAG ACTTAAAACC TAAGAGGGAT CATGTCACTC CCCATTTTAC TCAGAGTCAA 1560
GGCCAAGATC CTTACTGGGG TCTGCAGGCC CCCACACCTG GCCCTCTGAC TGCACCCCTA 1620
CCTTCCTTAG CTGTCTCCTC TCCCTAGCAT GCCCCAGGTC GCTGGTCCCC TAGCACTGGG 1680
CAGCTCCCTG CGGCCCTGTT CACTAGCTGT CCTCTGCCTG 1720