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

TagContent
EnhancerAtlas ID
HS187-04163 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr11:13359810-13361530 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs1037169chr1113361005hg19
rs6486122chr1113361524hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
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: 2             
ChromosomeStartEnd
chr111335985613360227
chr111336042413361428
Number: 1             
IDChromosomeStartEnd
GH11I013337chr111335909113361942
Enhancer Sequence
AGGAATTTGT AGAGTTATTT CTGGGGTCAG GCAGGATACA TTCAGACGAA CATTTTAGAT 60
CTAGGGCTGG GAAGATCCCG AGACTCGTTA TAGATTACAT CATCTTCCTC CAAGTGCACT 120
TGCCAGGCAA ATGGACAAGT GCATTTTAGA AAGGTTTTCA GTTGTTCACG TTTAAACAGA 180
AAGGATCACC TGGCTAACTT TTAGTTAACC CATTGAACAG ATGTGCCATT CCCCCAGCCC 240
ATTGGTTATT CATGTCCTTG TTACTGGTTT TTGATATCCT TGCCCCGTAG GTGGGAGGAG 300
GGATGGGTAT GAGCCTGCCC TGCCCTCTTT CTCCTACTTG GGACAGAGCT GTTGCTTTTA 360
TTTGCTGAGT CACTGAAGCA ATAGAGCATG TGCAGAGTCC CAGCCTGGAG GTGGGCATAT 420
CTGGGTTCCA GTCCCTGCTC TAGCCCTTCT CAGCTGTGTG ATCTTGGACA AGTTGCCATA 480
CCTCTCTGAG CCTCAGTGTC ATCTTCTATG TGATGTCGAT GCCTCCCCCA AAAGGTCGTT 540
ACGAGGACCA AAGGAGACAC GTCAGGGCAG GAACCATCCT AGGCACGTGT TTGATGCTCA 600
GTAAACGGGA CGTGGTCAGT GTTCAGAGTT GTGGGGGTGG CAGGTGACTG CTCTGTTTCA 660
CCTCCACTCA CAGCAACAGG GCCTGTGGTG TCACCTAGAC ATCTCATAGG CATCCCACAC 720
TGAACATGTC CCAAACCAGC AGCTCCTCCC TGGATGGGTG GATGGTGTAC AGGGACCTCT 780
TCCTCCAGCT GTCACATGGG GCATGTACCT GGCAAGTGGC TTTGCAGCCC TAGCTGCCCC 840
CTTGGCTGGG GGCCTTTGTG CAGTTCATGG ACTGGGAGTC ACCCCCATGT CTAGACCGTC 900
AGGAAACCCA TTGGCTTTTC CTTTAGAGCA TACCAAGAAT CAACTTCTCA GAACATAGCA 960
AGAGTTGACT TTTTGTCACC CTGCCGTGGC CACTCAGACT GACTCCTCTT ACACCTCACA 1020
TCCCATTGAT CAGCACAGCC CCTGGAAATA TGTCTAGAAT CCAGCTGCTT CTCATCACCC 1080
CCACACCTAA TACAGAGGGC TGAGTCATAG CATCTCTTCC CCGGACTGTT GTAGCCGTCT 1140
CCTAACTCAG CTTCCTGCCC TGCTTTTACA CACACACACA CACACACACA CACATGGTAT 1200
CTTCTCACCA CTGCAGCCAG ACTTAAAACC TAAGAGGGAT CATGTCACTC CCCATTTTAC 1260
TCAGAGTCAA GGCCAAGATC CTTACTGGGG TCTGCAGGCC CCCACACCTG GCCCTCTGAC 1320
TGCACCCCTA CCTTCCTTAG CTGTCTCCTC TCCCTAGCAT GCCCCAGGTC GCTGGTCCCC 1380
TAGCACTGGG CAGCTCCCTG CGGCCCTGTT CACTAGCTGT CCTCTGCCTG GAACACATCT 1440
GTCACCTCTC ACCTCCTCCT GTCCAGCCTC CTTGGGGCCT TTCTAACTGC CTCCCTCCTG 1500
TGGTCTGCCT CCTCCCCATC TCTGACTTTC CTCCCGAGCA CTTACTGCCA TCCAGCACCC 1560
GACATAACTT ACTTGTTTCG TTTGCTTGCC TTCCTCACCA GGAGGTGTGC CAGATGAGGA 1620
CAAGGATTTT TATATCCCTA CCCCCATCTG CAGCACTGCC ATGGAGAACA GTGCCTGGCA 1680
CTTGGATGCC CTCAGTAAAT ATTTGTTGAG AGACTAATAA 1720