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

TagContent
EnhancerAtlas ID
HS147-04199 
Organism
Homo sapiens 
Tissue/cell
NHEK 
Coordinate
chr1:200931720-200932870 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr1:200931993-200932007ATTCCCAAGGGACG+6.14
ZNF263MA0528.1chr1:200932691-200932712TCTTTCTCCTTCTCCTTCTTT-6.08
ZNF263MA0528.1chr1:200932685-200932706TCCTTCTCTTTCTCCTTCTCC-7.2
ZNF263MA0528.1chr1:200932688-200932709TTCTCTTTCTCCTTCTCCTTC-7.32
ZNF263MA0528.1chr1:200932682-200932703TTCTCCTTCTCTTTCTCCTTC-7.69
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1200932101200932549
Enhancer Sequence
AAAATGTAAA ATGCTGCGTA GATCAAACAA AAAAAAATAT CTTCAGGCTG GCTTTGCTCA 60
TGGACTGTCA GTGTGCAGTC CGGTCTGGGC AGGAGACACC AAGCAGGAAG CAGGAGGCTG 120
GGCCACACTG TGCTGTGGAG GTTTGGGCCC AGTGAGGAGC AGGACTTGAG GCTGTAGGCA 180
AGGGGAGTTG TTGAAGCGTT TTAAGCAAGT GGGTAGCATG GTTACAGAGC TGTGCATTTC 240
ACACAAATCA CCCAAGCTAC AGATCAGAGA AACATTCCCA AGGGACGGAA TTGGAGCCTG 300
TGCTGGAGAG TGTCTGGGGA GAAATGATGA AGTCAAGAAG ACAAAGGCAT GGGCGGGATT 360
AGCTAGTTGT GGAGATTGAT TTGATGTGAA CTGTGGAAGT AAAAGTTGCC TCTTGGCTTC 420
TGACATGGGT GAATGCTGGT GTCCTGGACT GAGGTCAGAA ATACAGAGGG AGGAACAGGT 480
GTGGAGGGGA AGGTGGTGGC TTGATTTTGG GCATGTTGAG CTTGTAAAAT CTGTGAGAAT 540
GCTAGTACAT CTATTCCATT GGAAGTTAGA TATGTATCAC TGAAGCTTGG AGAACAGGGC 600
TGTGTTTGGT GAACGCTGAG CATACCATTG GGTGGTAGAT GGAGATTGCA ACCCTAAGCC 660
CAGACATGCT CTCCTAAGGT AATTGTGTGG TGGGAGGAGT ATATGAGTCA ACACTGAGAT 720
TCCAGGAGAC ATCAGTTCCA AGGATCCCAC AGAGGAGACT AGAAAAGGAA ACCAGGCAGA 780
AAGTCAAAGG AGGACAACAA GAGAGGAGAG TCATGGTCAC CTAGGAAGGA CCATGACCAG 840
TTTCAGGAAG CAGTCAAGGG TACAAAAACC CAAGGGTTTC TCGGGTAACT TCAAAAGATG 900
GGAGAGATGA GCAGGCAGGC TAGGCTCAGC CTCCCCACCT CCTTCAACCC AAGCAGCCCC 960
ACTTCTCCTT CTCTTTCTCC TTCTCCTTCT TTTTTTTGTA GAGACAGGGT CTTGCCATGT 1020
TGCCCAGGCT GGTCTCCAAC TCCTGAGCTC AAGTGATCCT CCTGCCTTGG CTTTCCAAAG 1080
TGCTGGGATT ACAGGCGTGG GCCACCACAC CTGCCCCCCC ACCCCTTCTG TTAGTTTGGG 1140
ATATTGGGTT 1150