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

TagContent
EnhancerAtlas ID
HS087-18122 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr7:1287810-1288850 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13241427chr71288639hg19
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr7:1288384-1288395GGGGGCGTGGC-6.62
SP3MA0746.2chr7:1288383-1288396GGGGGGCGTGGCG-7.22
SP8MA0747.1chr7:1288383-1288395GGGGGGCGTGGC-6.44
ZIC1MA0696.1chr7:1288254-1288268CACAGCGGGTGGGC-6.15
ZIC3MA0697.1chr7:1288253-1288268GCACAGCGGGTGGGC-6.23
ZIC4MA0751.1chr7:1288253-1288268GCACAGCGGGTGGGC-6.21
ZNF263MA0528.1chr7:1287889-1287910TCTCCCTCCCCTTCCTCCGCC-6.42
ZNF263MA0528.1chr7:1287895-1287916TCCCCTTCCTCCGCCTGCCCC-6.63
ZNF263MA0528.1chr7:1287886-1287907GCCTCTCCCTCCCCTTCCTCC-7.08
ZfxMA0146.2chr7:1288525-1288539CCGGCCTGGGCCTC+6.06
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr712880001288800
Number: 3             
IDChromosomeStartEnd
GH07I001248chr712882211288330
GH07I001249chr712883611288370
GH07I001250chr712884611288510
Enhancer Sequence
ATTCACTTAA TTAAAAAAGT GTAACTACAA CACTGCCCTC ATCAAGCTGC GGTTGCACCA 60
GCAGGGTTTC AAAGCCGCCT CTCCCTCCCC TTCCTCCGCC TGCCCCTGGG CCGCTTGGGG 120
CTGGAGCAAC CTTCCTCGTC CCCAGCCATG TCCCCCACCC TTAGGAGGGA CTATTGAAAA 180
CATATTCTTC CCCAACAGCC GGGACAGCTC CACCCACTGG TGTCCAGGGA CCTTCCCGGA 240
GGGGCCTGGG CACTCTGCCC TCCGCCTCTG CCTCAGTTTC CCCATTTCCA GGACCTGATT 300
TCGGTGCTGA GGTGCGTGTA GGCAGGGCAG TTTGGGTCCC CGCCTTTGTG GAACTGGTGT 360
TCTGTGCAGA AGGCGGGCGG GCAGTTGTCC CCTGGAAAAC AGGAAAGGAG AGGATAGTGT 420
TTGGGCCTCG GCGCCAGCTG TGAGCACAGC GGGTGGGCAT TCCTCACGCA GGCAGCCTTG 480
CGGAGCAGGG AGGTCCAGCA CAAGGGTGTG TTCCAAAGGC TCCACTGGTG GCCGGGTTTT 540
GAGTGGGATG AGAAGCTGGA GGATGCTGGG GCTGGGGGGC GTGGCGATAC CGTGGTGTCA 600
CTCCATCTCC CTGTGGGGCA GGTGCTTGTG GGGCTGAGGG GAGCTGCCTC TCCTAGCACT 660
GTGCTCCCGC TCTGGGCCAC CCACATCCAA CGCCCGCCTC CCTGCAGGTG CGAGGCCGGC 720
CTGGGCCTCT GGCTGGGCCA GCTCTGAGGG AGCTTTCCGT GGGATGGCTG GGCCTCTGTT 780
GCAGTTGCGA CCAATGCTGC GGTTTAAATT CTCCCTGGGT CCAATCCTGC TTCCCTCCCC 840
TAAGCCTCTC GCACACACAC CTCGGCTCAG GCTATTCACC GGGAAAGCCA CGCGGAGGCA 900
GGGCAGGCAG CGCCCCGCCA GAGACCCCCG GATGGTGGAG ATGGTGCGGT GGAGTCGGGA 960
CTGCTGGGGG CACCTGCTGA TGAGGTGGGA GGGTAAAGCC ACGGGGGATG CGGGTTTCTG 1020
GACTTGTTCG GGTGGGCGGG 1040