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

TagContent
EnhancerAtlas ID
HS031-22176 
Organism
Homo sapiens 
Tissue/cell
Denditric_cell 
Coordinate
chr7:137881170-137882380 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7785014chr7137881690hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr7:137881254-137881275GGAGAAGGAGAAGGAGAAGCA+6.19
ZNF263MA0528.1chr7:137881248-137881269GAAGAAGGAGAAGGAGAAGGA+7.15
ZNF263MA0528.1chr7:137881251-137881272GAAGGAGAAGGAGAAGGAGAA+7.89
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7137881731137881787
Number: 1             
IDChromosomeStartEnd
GH07I138196chr7137880748137882745
Enhancer Sequence
TTGAATTCAG GAGGTGGAGG TTGCAGTGAG ATCGCACCAC TGCACTCCAG CCTGGGCGAC 60
AGAGCAAGAT TCTGTCAAGA AGAAGGAGAA GGAGAAGGAG AAGCAGAAGC AGAAGCAGAA 120
GCAGAAGCAG AAGCAGAAGC AGAAGCAGAA GCAGAAGCAG AAGCAGAAGC AGCAGAAGAA 180
GAAACAGTCA TGCCAATCTG TATAGCAAAA AAGTGAGGGG GAGTTAAAAA TCTGGTGGTG 240
TATCTATGGG GGTTGATGGT GTTGCTGAAA TGCCCCATAA TGGTTAATAT TGTGTCAACT 300
TGATTGGATT GAAGGACGCA AAGTACTGCT CCTGGGTGTG TCTGTGAGGG TGTTGCCAAA 360
GGAGATTAAC ATTTGAGTCG GTTGTCTGGG AAAGGCAGAC TCACCCTCAA TCTGGGCGAG 420
CACAATCTAA TCAGCTGCCA GTGTGGCCAG AATAAAAGCA GGCAGAAGAA TGTGGAAAGA 480
CTAGACTGGT TTAGCCTCCC AGTCTACATC TTTCTCCCAT GCTGGATGCT TCCTGCCCTT 540
AAACATCAGA CTCCAAGTTC TTCAGCTTTA GGACTTGCAC TGGCTTCCTT GCTCCTCAGC 600
TTGTAGATGG CCTATTGTGG GACCTTGTGA TTGTGTGAGT CAATACTCCT TAATAAACTC 660
CCCTTTATAT ATACATCTAT CCTATTTGTT CTGTCCCTCC AGAGAACCCT GACTAATACA 720
GCCCCCAAAA CCAACATTGA CCTCTTAGTT TAGAATTTGG AAAATGTGGG AAATCAGGCT 780
CTACTGGTCA GTGATTTTAA ATGGTTTGTA TTGGACTAAT TTCTTCAGAG AAGCTCTTTT 840
CTTTTTTCCA ATCTTTAAAG TGTCTATGAG ACAGAAAATA CTAATAATGG TGAACAACTT 900
TGCATGTATT TCTGTTTGTT TCCACATATG CTGTCTCAGT GACCCTCACC ATAACCCCAT 960
TACTGTATTA CAGAGAGGAA GCCAAGCCAC AGGGAGATTT AGTGATCTGC CTGTTGCCAC 1020
TTGTCTACTA TCCCTGTTGC CACTTGTCTA CTATGTGGAA TAGTAAAGAC AGAAAGACAG 1080
AACCAAAGTT TTTGACTTAC AGTCCTCAGT GTTTCGTTTC CTCCTTGGCT GGACACAGTT 1140
TACATTTCAA TACTATTACA TTCATATTTT AACACTGAGC CTTCTACTAA ATAGGGCATT 1200
CGATCTCATA 1210