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

TagContent
EnhancerAtlas ID
HS030-00487 
Organism
Homo sapiens 
Tissue/cell
CyT49 
Coordinate
chr1:24430990-24432240 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3934861chr124431956hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr1:24431575-24431585GCCCCGCCCC+6.02
NKX2-3MA0672.1chr1:24431268-24431278TTCAAGTGGT-6.02
ZNF263MA0528.1chr1:24431890-24431911TTCCCATCTTCTCCCTGCCCC-6.13
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_27677chr1:24424566-24436755Fetal_Intestine
SE_28574chr1:24424526-24439807Fetal_Intestine_Large
SE_30016chr1:24427249-24433190Fetal_Muscle
SE_40929chr1:24431581-24433075Left_Ventricle
SE_51642chr1:24431481-24432773Skeletal_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12443184524432126
Enhancer Sequence
AGTCCTGTTC TGTCACCCAG GCTGAAGTGC AGTGGCACAA TCTCGGCTCA CTGCAACCTC 60
CGCCTCCCGG GTTCAAGCGA TTCTCTTGTC TCAGCCTCCC AAGTAGCTGG GATTACAGGC 120
ACCCGCCACC ATACCCAGCT AATTTTTGTA TTTTTAGTAG AGACAGGGTT TCCCAAGTAG 180
CTGGGACTAC AGGTGCAGGC CACATGCCCA GCTAATTTTT AAATTTCCTG TAGAGATGGG 240
GTCTCGCCAG CTGCCCAAGA TGTTCTCAAA CTCCTGGGTT CAAGTGGTCC TCCCTCCTTG 300
GCTTCCCAAA GTGCTGGAGG TGGGCCTGGG CTTGTTTGGT TATTTGTGTG CCCCAGTGCC 360
TCAGTCAGGT CCTGGGATAG ATGACACCCT CAGTAAATAT TTGTTGAAAG CCCTTCCTCA 420
TCCCCCAGGG TACTGGGCAA TGGGCCTTAG ACCCAGGGGG ATCTCAGGAA AGAGTAGCTT 480
AGCCATGTGA ATGACACGTC TCCTTCTGTG GTGAGACTGA GACCTGGGCC GCGGCCATGC 540
CTACTCCAAT GTGTGCCTGT GCAGGAGACC CCTGCCCCTG CCCCTGCCCC GCCCCTCCCC 600
AGGCGAGGCC TAGCCTCTGG GATTCTGCCA TGGTTCCCCT CCCAGGAAGG GCATCTCCTG 660
CTTTCCCAGC CCCCTTCAAG CCCTGAGGTT TCCATGCTGT TGTGGCGTTA AATTCTCATC 720
ACATGCAGGC CGGACAGGAG GTCTTCAATC CACTCTTCAG AACAGGAAAT GGAGTCAGGA 780
CCAGGCAGTT TAAGAGGCAT GGCTGAGACC TCACGCTGAG TGAGGAGAGA GGCAGAAAGC 840
GAGGCTGGGA ACACAAGGTT CTCGCTACAG GCGTGAGCTC CTTCTCCGTA GGCCCTTCCC 900
TTCCCATCTT CTCCCTGCCC CACCCACTGT CTCCCTGCTA CTTGGCCCCT GTCCTGCCTC 960
TCACCGTCAT CCTCAACCCT GGAGACGCCC AGCTTGCAGC ACCTGCCTTC TCATGAGACC 1020
AGAATCATAT TTTTATGAGG GCTGGCTCCC CAGGGGCCCA GTCTTCCAGC CCCAGGCTGG 1080
CTGCGGGGCA GCTAAGAATA ACCCAGGCCT AAGCTGGGCG TGGTGGCTTG TGCCTGTGGT 1140
CCCAGCTACT TGGGAGGCTG AGATGGGAGG ATCACTTGAG CCCAGGAGTC AAGACTGCAG 1200
TGAGCTATGA TTACTCCACT GCACACAGCA GCCTGAGCGA GGCCCCGCCT 1250