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

TagContent
EnhancerAtlas ID
HS048-38389 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr9:139540180-139541340 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs7854618chr9139540385hg19
rs61456361chr9139540519hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr9:139540518-139540537TATCCACCAGAGGGCAGCT+6.34
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_13025chr9:139541148-139542133CD34_Primary_RO01480
SE_13534chr9:139538759-139542381CD34_Primary_RO01536
SE_14136chr9:139539026-139542188CD34_Primary_RO01549
SE_30514chr9:139537658-139542042Fetal_Muscle
SE_37985chr9:139536233-139545050HUVEC
SE_49718chr9:139539678-139540844Right_Ventricle
SE_49718chr9:139541018-139541968Right_Ventricle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9139540454139540544
chr9139540778139541198
Number: 1             
IDChromosomeStartEnd
GH09I136642chr9139536653139542430
Enhancer Sequence
CGCCTACCCA TGGGTTTCAC GTGCTGGGGG CAGTCATCAC CCCAACCTCA AGAAGCCAAG 60
AGGACTGGAT GTGGCCCCAG CACCCCACCA GCAGCCATGT CCTCCCAGGG AGGGAGCATG 120
ACTTACGCCT GGGGCAGAAT AGGCTGCAGG GCCTGCTGGG AAGCCGTTCC CGGACCCCAG 180
CTCAGTCCTC CGGCAGATTC ACTCAGAGGA AGGTAGCACT GGTGACCTGG CCGGTGCTAG 240
GCCCCCAAGC CCGCCCGCCA GCGTTCTTCA AGTCTGCACG TCCGAGGGCG GGAGGGAGCA 300
TGGACCCTGT CAGCCCCACC CTGACTGGGG TGGCCCCATA TCCACCAGAG GGCAGCTGGG 360
CCCAGTCCGG GCCATCCCCT TCGGGAGCCA GCACAGCAGG AGGGCCCCTT GTCAGCCAGA 420
GCCTGGGTGG ACGGCAGAGC CCCCGGGGCC GCCTCTGGAC TGAGTTTGTG CCTCACCTAG 480
CTGGGGCCTG ACCTCGAGAG GTCACTGTTG CCCTGGGCCT CAGTTTCCCC ATCCAACAGG 540
TGGGGAGAGC GTTAGCACCC ACATCACGGC GGCCCCACAG ATCAGTGCAG CGTGAAGTAC 600
TCAGCTAACC CTCCAGACCC CGGAGGCTGG GCCTCCCACC CCGCTGCCCC TGACCCATCC 660
TGCACATCTG CCCCCACCTG GCTCCGCTCG CTCCCCTTGC TCCCCTCAGC CTCCCGTCCC 720
GCTGGGTGGG GGCCTCCAGC GCCTCCGCCT CCGCCTCCGG GCTTCCAGGC AGGAAGGCGG 780
CGGAGAGGAG CGTTTCCGCG CAGGCTGCTG TGCTGGGAGT GCAGCCTGTG ATAAGGACAC 840
ACATGGCCGG CTGCACGTCC GCCTTTTGTC CCTGGCTCCC GCCAGCCCTT CCTGCTCCGG 900
CCTGCAGGGT GGGGACTATG GGCCCGGCTG CAGCCCTCCC CCGACCCCCA CCTCCACTCT 960
GCCCCTGGCT CCACAGCCCC TGGGGTCCTG GCTGCCCTGG GGGAGTTTGA GGCCCCCAGT 1020
AGCAGCTACG GCTGGGGCCC CGGACAAACT GGGGGTGTAG GAGCTCTAGG AAATCAACCC 1080
CAGGGAGGCT GCTACGGCTA AACAGAAGCA TCAGCCCCAA CCCAGCAGGG CCAGATGTTC 1140
TGCTCTCCCT CCCCCAGTTT 1160