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

TagContent
EnhancerAtlas ID
HS077-00986 
Organism
Homo sapiens 
Tissue/cell
H128 
Coordinate
chr1:203965340-203967100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs78448052chr1203965400hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:203966232-203966250CCTTCCCTCCCCCCTCCC-6.02
EWSR1-FLI1MA0149.1chr1:203966228-203966246TCTTCCTTCCCTCCCCCC-6.32
TBPMA0108.2chr1:203966558-203966573CTATAAAAAGCCCTG+6.42
ZNF263MA0528.1chr1:203965794-203965815GGAGAAGGAGAAGCAGGATGG+6.09
ZNF263MA0528.1chr1:203966646-203966667CATTCCACCCCTTCCTCCTTT-6.17
ZNF263MA0528.1chr1:203966228-203966249TCTTCCTTCCCTCCCCCCTCC-6.32
ZNF263MA0528.1chr1:203966224-203966245CTTCTCTTCCTTCCCTCCCCC-6.38
ZNF263MA0528.1chr1:203966231-203966252TCCTTCCCTCCCCCCTCCCCT-7.1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1203966600203966906
chr1203965600203966600
Number: 1             
IDChromosomeStartEnd
GH01I203996chr1203965194203966596
Enhancer Sequence
AGCCAAAAGC GCTGCTGGAT GGGGAGGGTG CAGGCGGGGC TTTTCTTGCA CCATCCTGGC 60
GCCTGACTGG GTCAAGTTAC TGGAGGCAGT CTGGATTTGA ATGTGCAAAT AAACAGAGGT 120
TGCTTTGATC CTTGAGGCTG ACAGGGAGGG GGAAGAAAAC GGAGTGCCCT GGTCAGAGAA 180
GTGCATGCTG GGCACTTGAA AGAGGGTTTG GGGGATGTGG AGCATGAGCT TGTCCTTATT 240
CCTTTGACTG GACCAAAAAC CTAATTTGTT AAAAAAAAAA AAAAATAGAG AGATCTTGAA 300
AGAGTCAGGG ACCCACATCA GACATTTCAG ACCTCCTCTG GGAACCAAAT ATTCCAATGG 360
CCTTTCTGCC TTGTCACCAG GAGGGGAGTG GGTTGCTTGA AGCCCACCCT CCCTCAAGGC 420
TCTCTTGCCT TTGGGACATC TTGGGTGCCA CTTGGGAGAA GGAGAAGCAG GATGGAACTA 480
TGAGGTGTGT GTGGTTCGGG GTGGGGCTGT AGGTTGGGAG GGGGTAGGGC CTATTGTCTC 540
CCTGGGCACC AATCCACAGC CACAGGCAGG CTTAGAGACG GAGAGACAAA GGAGGGAATG 600
GGAGAGCACA AAGGGAGCGG GAATGAAATG GTAAGTAAAG GCAAACAAAA GTGAGCCGGG 660
GGAGACAAAA GCTGGGAACA ATATTCCCCA GGCAATAGGC TCGGGAACAA TAGGGACACT 720
GACAGCCCCA CAAAGACACC AGTGTCTCCA AGTAGACGTT ATCTCAGGCA GTGGTTGGCA 780
GCCCCACTCT GGCTGCAGCT ATTTTCAGTG CCGCTTTTGT GCCATGCTGA ACAATATTCC 840
TTGCATGGCT GCTGATAGAA AGATGAGAAG GTTTCTGTTT GATTCTTCTC TTCCTTCCCT 900
CCCCCCTCCC CTTTTTCCAG CCCCCACCAG CTCCAGGCAG TCTGAGCTCA AGTCTCTGGC 960
CTGGTTAGGG GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTTG 1020
GGAAGAGACC AAGTGGGGAG GGTCTCTATC TGGGCTTCCA GTTGCCCTCA ATCTTATCAG 1080
GGCCTCCATG GAGGGAAGCT AGTAGAGTGG AGATTAGGGC TGGGCCAGTG GGGCTGAGAA 1140
CTGAGGTGTG CGAGGAGGAT CATCAGGGCA GTGGATTCTG CCCTTGCCCC AAATCACAAG 1200
ACCAGCCTGA GTGAGTGACT ATAAAAAGCC CTGCTTAGCA AAGGTTTTGC CTGTTGCTTG 1260
GCTATTCACA TACATAATAG CCAAGGCCAT AAGGGGTCCA CCCTGTCATT CCACCCCTTC 1320
CTCCTTTGTG CCCACAAGTG TTCCCCACTC TACCCCCATA GCCACTGCTT TCTCCCATTC 1380
TTGTTTGTAG TTTTACCAGC CCCTTGACTA GCTCCCAACT TCCCTCCCCA CCTCCGCCAC 1440
TGCCAGATGA ACCTAAGAGA TCGGGGAAAC TAGTCCTAGC TTGGGAAAAG ACTGGTATGC 1500
ACTGGCCCTT CCTTAGGCCT GATGGCCACT CCCACAGGGG TGTCCATGAT CTTCATCCAC 1560
AGTGCTGCTA TTCCCCACCA AGTATCTCCC CTGTGTTCCT CCCTAGAGGA ACTCTGACCC 1620
TAGAACATTG AGTCAGAGGT GTCCTTTCCC AGGGCCCCCT TGTGCATACG GCTGGTGTAC 1680
TCTTAGTTTT CTCAGTATCT TAGCCCACTA TGGCTGCCCC CGTGGGCTTA GATAAACTTT 1740
ACAGTTTTTC GTCTAGCTGG 1760