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

TagContent
EnhancerAtlas ID
HS052-19940 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr2:28303100-28304410 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2337699chr228303713hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr2:28304296-28304313TGCTTTCTGTGAATCAA+6
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr22830364728304158
Number: 1             
IDChromosomeStartEnd
GH02I028080chr22830289828304815
Enhancer Sequence
TTTCAAAAGT GAACTAGATA ATCTCTGAGG TTCAGCCTTA AAATTCTGTG ATACTCATTT 60
AAAAATAACT GTACCATCCA GCATTTCAGA AAAAGCATTA AGGACATGTG TTTCATTTCC 120
TTAAATGAAA ACAGATTATA ATGTATGTAA TCAGAGCATT GAAAAGAGAA GGAGAGAGAG 180
GTGATTTCAG TACCAAAATT TGTCTATAGG ATAGACTACC TGGATGAGGC AAAAGGATCT 240
ATAGACTACC TGCCTCAAAA ATCTCTAGAT ATAATGAGAG AGATGGTAGG TACTCCTTGA 300
GATGAGATAC TAGTCTGATG ATGGCTTTTT TTGGTGATGG CTGTTGAACA ACATGTAAAT 360
AAAAGCAGTA ATCATGTTAG AAGAGACCAA TCTGTGCCTG TGTTCTGTAG ACTACATTGT 420
TAAGAGCATG GTTCAAATAT TTGAAAGAGA AAAGAAAACT GCTTTTAAAA CCACTTACAA 480
TTACCTTGGC ATTCTCATTT TAAGTAGCCA TCTGCAAGCA TATTAATTTT ATTATTTCAG 540
TGAACTCCCT ATTTGATTAA TCCGTGACCT GATTTAGTAA ACATTTGTCA GGATATATCT 600
TCCCTGGAGA TACATTAAGC TTGGAGCATG TAAGGCATCT TTTTTCCTAT TCAAACAGTG 660
AAGTTAGGAA AGTGTTGTGG TAATAATGTG AGCACAATTG TCTAAGAACA TTAAGAACCT 720
TCGTCTGGAT CTTTTGTTAC CATAAAAGGC AATGTATCAT GCTTTCCTGT TTTGCATGGA 780
TGAGAAGGGA GTAAAAAACA CCAAAAGAAT TTTTATTGCA TAGAAATATT TCCTTCCTAG 840
CAGTTGGTGA AGCAATAATG AGCCTACAAA ACAATCTTCC TATAGCTGGG GAGAGGAGGG 900
CAGGAAAACG TAGTGCAGCC AGCCACATAG ATTCGCAGAC TGGCAGGCTG GTCACAGAGC 960
GCCTGCTTCC ATCCAGAGTC CCTTCTACAT GTAACTCTCC CCAGGGCAAA GCGCCTGCAT 1020
GTGCTTCTTC TCACAGCCCT TTAAGATATA CAGGGCAAGT AGGAGCTGCT TCTTTTCTAG 1080
AAGAAGAACT TATCCAAGCC TGTGGTGCAG ACGATTGTTG TAGGCAGGCT AGAGCCACAC 1140
TTACCTGATT CCCAATTTGT ACGTAAGACC AGGCAAGGTC CACTGTGTTG AGAAGATGCT 1200
TTCTGTGAAT CAAATTACTT GGTACAGAAA ATGTTGCTTT CAGTGTATCT TGTGGCAACT 1260
TTAACATTGT AGACATCACC ACTGAATAAG ATGAATGCGT GGGAATTGTG 1310