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

TagContent
EnhancerAtlas ID
HS104-00964 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr1:25468620-25470020 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2064251chr125469913hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr1:25469689-25469701AAACAAACAAAC-6.32
Foxd3MA0041.1chr1:25469693-25469705AAACAAACAAAC-6.32
RUNX1MA0002.2chr1:25468814-25468825AAACCACAGAG-6.14
ZfxMA0146.2chr1:25469445-25469459GAGGCCGAGGCGGG-6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12546877325469000
Enhancer Sequence
ATTTATATAT CGATTGTGAG TATATGCATT ACAAAGTTTT ATTTATTGAA TACTCTATGT 60
ACTAGGCATG GTGCCAACTG CTTTACCTGC ATTCTGTCAT TTCAGTTTCA TAAACAGTTC 120
AGAAATGAGA ACATTATTAT CCTCATTTCA TCTCTGGGAC AACTGAGCCT CCAGGAGGTG 180
AAGTGACCTG CTCCAAACCA CAGAGCTGGA AAGAGCCAGG ATTGCAACCC AGGCCTGTCT 240
GATTGCAGAG CCCGAACTCC TGGCTGTTAT GCTGGTCCTT GAGCTCTTGC TTCTCACCTC 300
AAAACCTGCC CTTCCATGTC TACTCTGTGA TGCTGGGGCA GGGACCCCAC AAACCAGTTT 360
CCGTTAACCA GCTAGTTTGT TTCTGCCTAC AGGGGACTAA TGGGAGGCTG GAAAGGCTGG 420
AGGAGGAAGG GACTCACTCC CTTCGCTTCC TGTTCCTGAA AGGGTCACCC TCGCAATGCT 480
CCTTCACCCT GGCAGGAGCA AGTCCTTCCT AAGCAGCAGC TGAATCTGCT TACAGTTTTT 540
CCAGCAATTG CAGAAGCAGC TTCATTGCCT GTCTTCCTTA AAAGTTTGGG TCCAGGGACC 600
ACGGGGCCTC TCCTGTGAGA TTAGGAATAC CAGCCCCAGC TGCGCAGTAC CCTCTCCTCA 660
GAAGGCCGAG TTTCTCTAAT TCCCACTTCT TCCTTTTCTT CTCCCAGCTC TAGGGGCTAT 720
TACTTCTATA ATACCTCAGC GTTCTATTTT GACCCTTTTG GTTACTTAAT TAACAACATC 780
AGAGGCCCGG CCTGGTGGCT CACGCCTGTA ATCTCAGCAC TTTGAGAGGC CGAGGCGGGC 840
GGATCACGAG GTCAGGAGTT CGAGACCAGC CTGGCCAACA TGATGAAACC CCGTCTCTAC 900
TAAAAATACA AAAATTAGTC GGGCATGGTG ACACGCACCT GTAATCCCAG CTACTCAGGA 960
GGCTGAGGCA GGAGAATCGC TTGAACCAGG GAGGCGGAGG TTGCAGTGAG CCAAGATCCC 1020
GCTACTGCAC TCCAGCCTGA GCAACAGAGC GAGACTCCGT CTCAAAACAA AACAAACAAA 1080
CAAACAAAAA ACAACCTCAT ACCTAATTAA CAATATATTA AATTCTGTCT CCTTCACCTT 1140
GGCAGCCACA GGTCTTTCTG GGAGTGGCAG CTGAATCCAC TTTATAGTTT TTCCAACAAT 1200
TGCAGAACAG CTTTATTGCC CCCACCCTCA CTCACCCAGA TCCCCACACT AGCCTGCCAG 1260
TGCCTCCTCC TCAGAGGTCT GGGTTCCAGT CCGATGGGCC TGTGGACCCA GAGATATGGG 1320
CACCAGCCAA GTGCACCTGA TGGATGTGAC CAATACATTA CATGGCACAG TTTAAGTCAC 1380
TAAAGATGTT TCAAATAACA 1400