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

TagContent
EnhancerAtlas ID
HS139-38503 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr3:128316100-128317450 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs4328821chr3128316435hg19
rs2712431chr3128316890hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr3:128316619-128316638TGCCCAGCAGGGGGTGGTG+6.17
HES2MA0616.2chr3:128317270-128317280GGCACGTGCC+6.02
HES2MA0616.2chr3:128317270-128317280GGCACGTGCC-6.02
ZIC1MA0696.1chr3:128316621-128316635CCCAGCAGGGGGTG-6.06
ZIC3MA0697.1chr3:128316620-128316635GCCCAGCAGGGGGTG-6.26
ZIC4MA0751.1chr3:128316620-128316635GCCCAGCAGGGGGTG-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr3128316824128317064
Enhancer Sequence
AATCAGAGGA AGCACTGAGG AGCAGAGGCA GCGGTCCTGC TTGCAGGGTC TTAGGTCTAT 60
TGTCCCATTA CTCCTGACAA GGTAGTTGCT ATGAGTCCCC CCACTCCAAA GATGGAAAAG 120
CTGAGGCACA CAGAGGGTAA GTCATCTGCC AAAGGTCATT GAGCCAGGAG GTTGGCCAGG 180
GAGATCTCTG CTCACCGAGT TGGGACTGAG GAGTGGCAAG GGGGAGAGTA GTGTTTAGGG 240
AGACCCACTG CGTGCCTGCC ACCAGGCTAA GTGCCCTCTG CACTAAGCTA CTCTCATCCT 300
CGAGCAATAT TAAGAGGCTG GCATCGTGCA CCCAATTTTA GAGATGAAGA AGCAGGGCCT 360
CCGGGACCAG AAGCCTCAGC TCACACAGGA TTGAGTGCAG AGCTAAGGCT AGAGCCTGTC 420
TGCCTGGCTG CAGGGCCTAA CCCCTGGAGA GAGAAGACAA CATCACCCTG CTGGTGCTGT 480
CCTCTCAGCC CCCTCCATGC CCTGGGCACT GGGGCCGGAT GCCCAGCAGG GGGTGGTGGC 540
CTTGGCCCTG GGCAGACATT CTAGAAAGCC AGCAGTTCAT TAGGTCCCCT GCTCCAAAAC 600
ACAAGGGCCA TGCTTGAGAC TCATGGGTGA GGGCAGGGGT CTGCTGCTTC TTCCAACCCC 660
CACAACCAAG ATGGGCAGGG TGGACACTGG TGTTTCTCAG GCTCCTGTGA GTGCCCAGCC 720
CTTGCCATAC CAACCGGTGA CAGATGTTGC TGTCCCAGCT GCTTCTCCAC GCCTGGTGCA 780
GCCCTCCAGC GAGCTTTGTC AGGCCTACAT GGTGATTCAA ACACATCTGA GTCAACATAT 840
AAATATCAAA GGATTGCACT TTTTAAAATC CAAATTTCAC ATTTCTCTAG GAAAAAAGTA 900
GATCTGCCAG CCCTAGGCCC ATACTCTCAC AGATCCCCAG TCAGCTAGTG CTGAGCAGCA 960
GCTACCTCTT TGCGTGAAAC ATGTGAGCAT CAGTTTGCCC CAGTCCCCGC CACCTGCAGC 1020
CGAACTACTG TTTTCTTTCT TTTCTGGAGG CAGAGTCTTG CTCTTTCACC CAGGCTGGAA 1080
TGCAGCGGTG CGATCTCAGC TCACTTTAAC CTCCGCCTCC CGGGTTCAAG CGATTCTTCT 1140
GCCTCAGCCT CCCAAGTAGC TGGGATCACA GGCACGTGCC ACCACGCCCA GCTAATTTTT 1200
TGTACTTTAG AAGAGATGGA GTTTCACCAT GTTGCCCAGG CTGGCCTCGA ACTTCTGATC 1260
TCAGGCCTCC CAAAGTACTA GGATTACAGG TGTGAGCCAC CACACCCAAC CCTACTGTTT 1320
TCATTTTTAA GGGCCCTTAT GCTGTTGGTC 1350