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

TagContent
EnhancerAtlas ID
HS184-15610 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr19:45350660-45351620 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs41289512chr1945351516hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr19:45351228-45351238GCCCCGCCCC+6.02
KLF5MA0599.1chr19:45350977-45350987GGGGCGGGGC-6.02
SP1MA0079.4chr19:45351225-45351240CTGGCCCCGCCCCTT+6.16
SP4MA0685.1chr19:45351225-45351242CTGGCCCCGCCCCTTGC+6.19
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_01419chr19:45349343-45354856Adrenal_Gland
SE_28236chr19:45347674-45353520Fetal_Intestine
SE_29374chr19:45347891-45353882Fetal_Intestine_Large
SE_31891chr19:45347627-45353202Gastric
SE_38686chr19:45347491-45355155HUVEC
SE_43252chr19:45347579-45355377Lung
SE_47874chr19:45349269-45353110Pancreas
SE_54232chr19:45347544-45354362Spleen
SE_65607chr19:45347455-45353566Pancreatic_islets
SE_69164chr19:45348621-45353051H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194535077545351289
Enhancer Sequence
GTTTTCAGGG TTCCCGGCAG AACCGGGGGA CAGGAGACTC GATCTCGTGG GCTTCAGACT 60
TAATTGTAGG CAGAGGAACG TCTTCTGAGA TCCAAACAGA AGTGCGAGCA GCGGGCCCCG 120
TCTCTTGGGC TCCAGATATG ATCAAGGGTC GAAGGCTCTG TCTTGAGGCT GGAGTCTCAG 180
TCGCCTGAGT CCCAGATAGA ACGGGAGGCC CCGAGTCCCA GAGGCTGGGA GACTCCTCCC 240
TTTCCCTATG AATGGTCGGG GGCGACGGAG ACGTCGCCGG GGAAGTTTTC CTGGTTTCAC 300
TCTCGCCGAG CCAGGGAGGG GCGGGGCGGG CGCTCCTGGC TCCGGGTTCC GGACTCCCCG 360
GTTTCGGGAC CTTATCTATC CTCTGGTAGC GCCTTTGTCC TCAGAGCCAT AGCAGGAGGT 420
GGACGAGTGG AGCCGCCGCC CTTATCCCCC GTCCCTCCCA TTGCTATGCC TTGGACCCCC 480
TGGCGTCCTT CCATCCACCC CACTAGGGGA GGAGAGCGGC CCCCCTGGGG AGGGAGGGGC 540
TGGGAGGGAA CCCTTGAAAG AGGCGCTGGC CCCGCCCCTT GCAGGTGACC CGGTTGTGTA 600
TTCCCAGCGA CAAACTCTGG GATGCTAGAG TTTCCCGAGG GTTTGCGCAG AAGAGAGCTC 660
AGGGGGATCT TGGGGGAACC CCGGCCACCT CTCTGGCCTC ATTTCCCCCA GGATGGCTCT 720
CACTGGCCTC CCAGCTTTGA CCCAGAGCTG GGAACTCCGC TTCCATCCCC TGCCTCTCCC 780
TTCAGGCAGA AATAGGCAGA TGAGATCAGA ACTGGCACCT CTGGGTGAAT TCTCCGAACC 840
CACCAGACCC TGAGCCTACT GTTAGCTTGG TGCATGATCT CACCGAAGGC TCCAGCTTGC 900
CCTGGGAAAC AGGTCCTGTT TCTGTTTCCA TCTTAGAGAT GAGGAAACAG GCTCAGCAAA 960